Loading
Loading…
Loading…
| # | Company | Amount | Rank | Status |
|---|---|---|---|---|
| 1 | L1₹20 LAccepted-AOC | ₹20 L | L1 | Accepted-AOC L1 |
| 2 | L1₹20 LAccepted-AOC 5 1 GROUND FLOOR BEES DUKAN ADARSH NAGAR JAIPUR 302004 | JAIPUR | RAJASTHAN | 302004 | ₹20 L | L1 | Accepted-AOC L1 |
| 3 | L1₹20 LAccepted-AOC | ₹20 L | L1 | Accepted-AOC L1 |
| 4 | L1₹20 LAccepted-AOC | ₹20 L | L1 | Accepted-AOC L1 |
| 5 | L1₹20 LAccepted-AOC | ₹20 L | L1 | Accepted-AOC L1 |
Tender Value
Refer Docs
EMD Value
₹50 L
Closing Date
29 Jun 2021, 5:00 pmClosed
Medical Superintendent cum Member Secretary, RMRS
SMS Hospital, Jaipur
Two Year Rate Contract for Drug Eluting Stents, Pacemakers, PTMC Balloon and other Consumable Items
2021_SMSMC_219815_1
1226_15.04.2021
Open Tender
Miscellaneous Goods
730 days
SMS Hospital
Please refer Tender documents.
3 documents required · 3 mandatory
₹1,000
Member Secretary, RMRS, SMS Hospital, Jaipur
₹50 L
Yes
SMS Hospital, Jaipur
12 Jan 2023
17 Apr 2021
30 Jun 2021
17 Apr 2021
29 Jun 2021
20 May 2021
23 Apr 2021
Group A-1 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (size 4 Fr. 9Fr.) (Standard Length) US FDA APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (size 4 Fr - 9Fr.)(Standard Length) -CE APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (size 4 Fr.- 9Fr.)(Standard Length) DCGI APPROVED Technical Specification as per Annexure-6
INTODUCER SHEATH FOR ADULTS (size 10 Fr. – 11 Fr.)(Standard Length) US FDA APPROVED Technical Specification as per Annexure-6
INTODUCER SHEATH FOR ADULTS (size 10 Fr. – 11 Fr.) (Standard Length) CE APPROVED- 10 Fr. – 11 Fr. Technical Specification as per Annexure-6
INTODUCER SHEATH FOR ADULTS (size 10 Fr. – 11 Fr.) (Standard Length) DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long) (Size 5Fr.-9Fr.) US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long) (Size 5Fr.-9Fr.) CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long) (Size 5Fr.-9Fr.) DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long)(Size 10Fr.-11Fr.) US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long)(Size 10Fr.-11Fr.) CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long) (Size 10Fr.-11Fr.) DCGI APPROVED Technical Specification as per Annexure-6
TRANS RADIAL INTRODUCER SHEETHS 4F-6F – US FDA APPROVED Technical Specification as per Annexure-6
TRANS RADIAL INTRODUCER SHEETHS 4F-6F – CE APPROVED Technical Specification as per Annexure-6
TRANS RADIAL INTRODUCER SHEETHS 4F-6F – DCGI APPROVED Technical Specification as per Annexure-6
STEERABLE INTRODUCER SHEETHS 5F-126F – US FDA APPROVED Technical Specification as per Annexure-6
STEERABLE INTRODUCER SHEETHS 5F/6F – CE APPROVED Technical Specification as per Annexure-6
STEERABLE INTRODUCER SHEETHS 5F/6F – DCGI APPROVED Technical Specification as per Annexure-6
LONG BRADED INTRODUCER SHEATH – US FDA APPROVED Technical Specification as per Annexure-6
LONG BRADED CONTRA LATERAL INTRODUCER SHEATH – CE APPROVED Technical Specification as per Annexure-6
LONG BRADED CONTRA LATERAL INTRODUCER SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (20-30 cm long) (Size 10:- 11Fr.) With Maximum 160 dig.Tip Deflation Technology – DCGI &US FDA Approved /CE Approved Technical Specification as per Annexure-6
INTRODUCER SHEATH (Size 08Fr:-18Fr.) DCGI& US FDA Approved /CE Approved Technical Specification as per Annexure-6
Group A-2 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
LONG INTRODUCER SHEATH (30-50 cm long)(Size 5Fr.-9Fr.) US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 5Fr.-9Fr.) CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 5Fr.-9Fr.) DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 10Fr.-11Fr.) US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 10Fr.-11Fr.) CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 10Fr.-11Fr.) DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 12Fr.and higher) US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 12Fr.and higher) CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH (30-50 cm long)(Size 12Fr.and higher) DCGI APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS US FDA APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS CE APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - US FDA APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS – CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS – DCGI APPROVED Technical Specification as per Annexure-6
LONG BRADED INTRODUCER SHEATH - US FDA/ CE APPROVED Technical Specification as per Annexure-6
LONG BRADED INTRODUCER SHEATH - DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH – US FDA/CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
LONG SUPPORT INTRODUCER SHEATH – US FDA / CE APPROVED Technical Specification as per Annexure-6
LONG SUPPORT INTRODUCER SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH – US FDA/CE APPROVED Technical Specification as per Annexure-6
LONG INTRODUCER SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
LONG CONTRA LATERAL INTRODUCER SHEATH – US FDA/CE APPROVED Technical Specification as per Annexure-6
LONG CONTRA LATERAL INTRODUCER SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
Group- A-3 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA-
PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH, REGULAR STIFFNESS) - US FDA APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH, REGULAR STIFFNESS) - CE APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH, REGULAR STIFFNESS) - DCGI APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - US FDA APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - CE APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - DCGI APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (REGULAR LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - US FDA APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (REGULAR LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - CE APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (REGULAR LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - DCGI APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (EXCHANGE LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - US FDA APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (EXCHANGE LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - CE APPROVED Technical Specification as per Annexure-6
PTFE COATED DIAGNOSTIC 0.032 INCH GUIDE WIRE – (EXCHANGE LENGTH, EXTRA STIFF SHAFT STRENGTH)-AMPLATZ TYPE - DCGI APPROVED Technical Specification as per Annexure-6
HYDROPHILIC DIAGNOSTIC GUIDE WIRE – RADIFOCUS TARUMO TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – US FDA APPROVED Technical Specification as per Annexure-6
HYDROPHILIC DIAGNOSTIC GUIDE WIRE – RADIFOCUS TARUMO TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – CE APPROVED Technical Specification as per Annexure-6
HYDROPHILIC DIAGNOSTIC GUIDE WIRE – RADIFOCUS TARUMO TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – DCGI APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (, REGULAR STIFFNESS) – US FDA APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (REGULAR LENGTH) – CE APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (REGULAR LENGTH) – DCGI APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (LONG LENGTH) – US FDA APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (LONG LENGTH) – CE APPROVED Technical Specification as per Annexure-6
RADIOFOCUS MINIPLASTIC GUIDEWIRE (LONG LENGTH) – DCGI APPROVED Technical Specification as per Annexure-6
Amplatz super-stiff Exchange Length PTFE COATED DIAGNOSTIC GUIDE WIRE – DCGI with US FDA / CE APPROVED Technical Specification as per Annexure-6
Group- A-4 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
JUDKINS CATHETER (JR JL & PIGTAIL) US FDA APPROVED • 4 French/5 French /6 French/7 French/8French size Left and Right judkins catheters in various standard curves and lengths.
JUDKINS CATHETER (JR JL & PIGTAIL) CE APPROVED • 4 French/5 French /6 French/7 French/8French size Left and Right judkins catheters in various standard curves and lengths.
JUDKINS CATHETER (JR JL & PIGTAIL) - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French size Left and Right judkins catheters in various standard curves and lengths.
MULTIPURPOSE CATHETER US FDA APPROVED • 4 French/5 French /6 French/7 French/8French size multipurpose catheters in various standard curves and lengths.
MULTIPURPOSE CATHETER- CE APPROVED • 4 French/5 French /6 French/7 French/8French size multipurpose catheters in various standard curves and lengths.
MULTIPURPOSE CATHETER - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French size multipurpose catheters in various standard curves and lengths.
AMPLATZ CATHETER - US FDA APPROVED • 4 French/5 French /6 French/7 French/8French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths.
AMPLATZ CATHETER - CE APPROVED • 4 French/5 French /6 French/7 French/8French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths.
AMPLATZ CATHETER DCGI APPROVED • 4 French/5 French /6 French/7 French/8French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths.
INTERNAL MAMMARY CATHETER- US FDA APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
INTERNAL MAMMARY CATHETER CE APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
INTERNAL MAMMARY CATHETER DCGI APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
BY-PASS GRAFT CATHETER US FDA APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
BY-PASS GRAFT CATHETER CE APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
BY-PASS GRAFT CATHETER - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – US FDA APPROVED • 4 French/5 French /6 French/7 French/8French diagnostic coronary catheters of TIG curves and lengths dedicated for trans radial coronary angiography and brachial approach also
TRANSRADIAL DIAGNOSTIC CORONARY CATHETER - CE APPROVED • 4 French/5 French /6 French/7 French/8French diagnostic coronary catheters of TIG curves and lengths dedicated for trans radial coronary angiography and brachial approach also.
TRANSRADIAL DIAGNOSTIC CORONARY CATHETER - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French diagnostic coronary catheters of TIG curves and lengths dedicated for trans radial coronary angiography and brachial approach also.
NIH CATHETER US FDA APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
NIH CATHETER - CE APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
NIH CATHETER - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
COURNARD CATHETER - US FDA APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
COURNARD CATHETER - CE APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
COURNARD CATHETER - DCGI APPROVED • 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.
Group- A-5 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
INJECTION NIKORANDIL (2 mg) – US FDA / CE APPROVED
INJECTION NIKORANDIL (2 mg) – DCGI APPROVED
INJECTION BIVALURIDIN – US FDA / CE APPROVED
INJECTION BIVALURIDIN – DCGI APPROVED
INJECTION ABCIXIMAB – US FDA / CE APPROVED
INJECTION ABCIXIMAB – DCGI APPROVED
INJECTION FONDARINAUX – US FDA / CE APPROVED
INJECTION FONDARINAUX – DCGI APPROVED
INJECTION ALTEPLASE 20mg– US FDA / CE /DCGI APPROVED
INJECTION ALTEPLASE 50 mg– US FDA / CE /DCGI APPROVED
Inj. Eptifibatide 75mg/100 ml (with hanger)
Inj. Eptifibatide 20mg/10 ml
Inj. Tenecteplase 40 mg
Inj. Tenecteplase 50 mg
Inj. Reteplase 18 mg
Group- A-6 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
INTRODUCER SHEATHS FOR PEDIATRIC USE (Size 4-6 Fr.) WITH J TIP/STRAIGHT INTRODUCER WIRE - US FDA APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATHS FOR PEDIATRIC USE (Size 4-6 Fr.) WITH J TIP/STRAIGHT INTRODUCER WIRE - CE APPROVED Technical Specification as per Annexure-6
INTRODUCER SHEATHS FOR PEDIATRIC USE (Size 4-6 Fr.) WITH J-TIP/STRAIGHT INTRODUCER WIRE - DCGI APPROVED Technical Specification as per Annexure-6
PIGTAIL CATHETER (PEDIATRIC) - US FDA APPROVED Technical Specification as per Annexure-6
PIGTAIL CATHETER (PEDIATRIC) - CE APPROVED Technical Specification as per Annexure-6
PIGTAIL CATHETER (PEDIATRIC) – DCGI APPROVED Technical Specification as per Annexure-6
JUDKINS CATHETER (PEDIATRIC) - US FDA APPROVED Technical Specification as per Annexure-6
JUDKINS CATHETER (PEDIATRIC) - CE APPROVED Technical Specification as per Annexure-6
JUDKINS CATHETER (PEDIATRIC) – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL JUDKINS CORONARY CATHETER WITH 2.5 CM CURVE (PEDIATRIC) - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL JUDKINS CORONARY CATHETER WITH 2.5 CM CURVE (PEDIATRIC) - CE APPROVED Technical Specification as per Annexure-6
SPECIAL JUDKINS CORONARY CATHETER WITH 2.5 CM CURVE (PEDIATRIC) - DCGI APPROVED Technical Specification as per Annexure-6
ANGIOGRAPHIC DOUBLE LEUMEN TRACKING CATHETER – 4 F/5F/ 6F
Group- A-7 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
MULTIPURPOSE CATHETER (PEDIATRIC) – US FDA/CE APPROVED • 4 Fr/ 5 Fr/ 6 Fr in various standard curves and lengths • Must be FDA approved
MULTIPURPOSE CATHETER (PEDIATRIC) – DCGI APPROVED • 4 Fr/ 5 Fr/ 6 Fr in various standard curves and lengths • Must be FDA approved
MULTIPURPOSE CATHETER (PEDIATRIC) – FDA/CE APPROVED • 4 Fr/ 5 Fr/ 6 Fr in various standard curves and lengths • Must be FDA approved
MULTIPURPOSE CATHETER (PEDIATRIC) – DCGI APPROVED • 4 Fr/ 5 Fr/ 6 Fr in various standard curves and lengths • Must be FDA approved
3- ‘FRENCH’ DIAGNOSTIC CATHETERS FOR NEONATAL USE - US FDA/CE APPROVED • Pigtail, Judkins, Multipurpose, Cobra and other diagnostic catheters of 3 Fr. size • Varying lengths and shapes
3- ‘FRENCH’ DIAGNOSTIC CATHETERS FOR NEONATAL USE –US FDA/ CE APPROVED • Pigtail, Judkins, Multipurpose, Cobra and other diagnostic catheters of 3 Fr. size • Varying lengths and shapes
3- ‘FRENCH’ DIAGNOSTIC CATHETERS FOR NEONATAL USE – DCGI APPROVED • Pigtail, Judkins, Multipurpose, Cobra and other diagnostic catheters of 3 Fr. size • Varying lengths and shapes
SWAN GANZ CATHETER - US FDA APPROVED - 6F/7F
SWAN GANZ CATHETER - CE APPROVED- 6F/7F
SWAN GANZ CATHETER - DCGI APPROVED- 6F/7F
SPECIAL SWAN GANZ CATHETER WITH : - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL SWAN GANZ CATHETER WITH : - CE APPROVED Technical Specification as per Annexure-6
SPECIAL SWAN GANZ CATHETER WITH : -DCGI APPROVED Technical Specification as per Annexure-6
BALLOON TIPPED ANGIOGRAPHY CATHETER- US FDA APPROVED- 5F-7F
BALLOON TIPPED ANGIOGRAPHY CATHETER- CE APPROVED- 5F-7F
BALLOON TIPPED ANGIOGRAPHY CATHETER - DCGI APPROVED- 5F-7F
BERMAN CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
BERMAN CATHETER - CE APPROVED Technical Specification as per Annexure-6
BERMAN CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
REVERSE BERMAN CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
REVERSE BERMAN CATHETER - CE APPROVED Technical Specification as per Annexure-6
REVERSE BERMAN CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
Group- A-8 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA-
ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) - US FDA APPROVED Technical Specification as per Annexure-6
ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) - CE APPROVED Technical Specification as per Annexure-6
ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – DCGI APPROVED Technical Specification as per Annexure-6
ACT TUBES - US FDA APPROVED Technical Specification as per Annexure-6
ACT TUBES - CE APPROVED Technical Specification as per Annexure-6
ACT TUBES – DCGI APPROVED Technical Specification as per Annexure-6
ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS - CE APPROVED Technical Specification as per Annexure-6
ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
HIGH – PRESURE INJECTOR LINES - US FDA APPROVED Technical Specification as per Annexure-6
HIGH – PRESURE INJECTOR LINES - CE APPROVED Technical Specification as per Annexure-6
HIGH – PRESURE INJECTOR LINES - DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE ECG ELECTRODES FOR ADULTS - US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE ECG ELECTRODES FOR ADULTS - CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE ECG ELECTRODES FOR ADULTS - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL RADIOLUCENT DISPOSABLE ECG ELECTRODES FOR ADULTS - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL RADIOLUCENT DISPOSABLE ECG ELECTODES FOR ADULTS - CE APPROVED Technical Specification as per Annexure-6
SPECIAL RADIOLUCENT DISPOSABLE ECG ELECTODES FOR ADULTS – DCGI APPROVED Technical Specification as per Annexure-6
SYRINGE FOR PRESSURE INJECTOR INSTALLED IN CATH LAB SMS HOSPITAL, JAIPUR - US FDA APPROVED • Should be compatible with existing machines at Cath Lab, SMSH
SYRINGE FOR PRESSURE INJECTOR INSTALLED IN CATH LAB SMS HOSPITAL, JAIPUR - CE APPROVED • Should be compatible with existing machines at Cath Lab, SMSH
SYRINGE FOR PRESSURE INJECTOR INSTALLED IN CATH LAB SMS HOSPITAL, JAIPUR – DCGI APPROVED • Should be compatible with existing machines at Cath Lab, SMSH
Group- A-9 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB IN SMS HOSPITAL - US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB IN SMS HOSPITAL - CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB IN SMS HOSPITAL – DCGI APPROVED Technical Specification as per Annexure-6
DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - US FDA APPROVED Technical Specification as per Annexure-6
DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - CE APPROVED Technical Specification as per Annexure-6
DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED Technical Specification as per Annexure-6
Group- A-10 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
ENDOMYOCARDIAL BIOPSY (EMB) FORCEPS SET - US FDA APPROVED Technical Specification as per Annexure-6
ENDOMYOCARDIAL BIOPSY (EMB) FORCEPS SET - CE APPROVED Technical Specification as per Annexure-6
ENDOMYOCARDIAL BIOPSY (EMB) FORCEPS SET – DCGI APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) - US FDA APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) - CE APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) –DCGI APPROVED Technical Specification as per Annexure-6
SHEATHS FOR INTRAVASCULAR SNARES - US FDA APPROVED Technical Specification as per Annexure-6
SHEATHS FOR INTRAVASCULAR SNARES - CE APPROVED Technical Specification as per Annexure-6
SHEATHS FOR INTRAVASCULAR SNARES – DCGI APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) - US FDA APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) - CE APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) – DCGI APPROVED Technical Specification as per Annexure-6
ACCESSORIES FOR INTRAVASCULAR MICROSNARE - US FDA APPROVED Technical Specification as per Annexure-6
ACCESSORIES FOR INTRAVASCULAR MICROSNARE - CE APPROVED Technical Specification as per Annexure-6
ACCESSORIES FOR INTRAVASCULAR MICROSNARE – DCGI APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – BASKET - US FDA APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – BASKET - CE APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER – BASKET – DCGI APPROVED Technical Specification as per Annexure-6
INTRAVASCULAR RETRIEVER SNARE KIT Goose Neck Type- US FDA/ CE/ DCGI Approved Technical Specification as per Annexure-6
Group- A-11 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA-
NON IONIC (LOW OSMOLAR) CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION - US FDA APPROVED Technical Specification as per Annexure-6
NON IONIC (LOW OSMOLAR) CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION - CE APPROVED Technical Specification as per Annexure-6
NON IONIC (LOW OSMOLAR) CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION – DCGI APPROVED Technical Specification as per Annexure-6
NON IONIC (ISOOSMOLAR) CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION - US FDA APPROVED Technical Specification as per Annexure-6
NON IONIC CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION - CE APPROVED Technical Specification as per Annexure-6
NON IONIC CONTRAST AGENTS USED DURING CARDIAC CATHETERIZATION - DCGI APPROVED Technical Specification as per Annexure-6
Group- A-12 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
RENAL DOUBLE CURVE CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
RENAL DOUBLE CURVE CATHETER - CE APPROVED Technical Specification as per Annexure-6
RENAL DOUBLE CURVE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
HEAD HUNTER CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
HEAD HUNTER CATHETER - CE APPROVED Technical Specification as per Annexure-6
HEAD HUNTER CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
SIMMONS/ SIDEWINDER CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
SIMMONS/ SIDEWINDER CATHETER - CE APPROVED Technical Specification as per Annexure-6
SIMMONS/ SIDEWINDER CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
PRESHAPED CATHETER FOR UTERINE ARTERY EMBOLISATION - US FDA APPROVED Technical Specification as per Annexure-6
PRESHAPED CATHETER FOR UTERINE ARTERY EMBOLISATION - CE APPROVED Technical Specification as per Annexure-6
PRESHAPED CATHETER FOR UTERINE ARTERY EMBOLISATION – DCGI APPROVED Technical Specification as per Annexure-6
VERTEBRAL CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
VERTEBRAL CATHETER - CE APPROVED Technical Specification as per Annexure-6
VERTEBRAL CATHETER - DCGI APPROVED Technical Specification as per Annexure-6
COELIAC AXIS CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
COELIAC AXIS CATHETER - CE APPROVED Technical Specification as per Annexure-6
COELIAC AXIS CATHETER -DCGI APPROVED Technical Specification as per Annexure-6
SHEPHERD’S HOOK CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
SHEPHERD’S HOOK CATHETER - CE APPROVED Technical Specification as per Annexure-6
SHEPHERD’S HOOK CATHETER - DCGI APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Coiled Stainless steel construction) - US FDA APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Coiled Stainless steel construction) - CE APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Coiled Stainless steel construction) – DCGI APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Braided Nitinol construction) - US FDA APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Braided Nitinol construction) - CE APPROVED Technical Specification as per Annexure-6
MICROCATHETER (Braided Nitinol construction) - DCGI APPROVED Technical Specification as per Annexure-6
VTK DIAGNOSTIC CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
VTK DIAGNOSTIC CATHETER - CE APPROVED Technical Specification as per Annexure-6
VTK DIAGNOSTIC CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
3D SPACE RCA ANGIOGRAPHIC CATHETER – US FDA /CE APPROVED Technical Specification as per Annexure-6
3D SPACE RCA ANGIOGRAPHIC CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
ANGIOGRAPHIC SIZING PIGTAIL CATHETER 5F/ 6F/ 7F – US FDA / CE APPROVED Technical Specification as per Annexure-6
ANGIOGRAPHIC SIZING PIGTAIL CATHETER 5F/ 6F/ 7F – DCGI APPROVED Technical Specification as per Annexure-6
DOUBLE LUMEN CATHETER FOR WIRE EXCHANGE FOR 0.014 GUIDEWIRE – US FDA/CE APPROVED Technical Specification as per Annexure-6
Group- A-13 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
STRAIGHT LONG INTRODUCER SHEATH WITH HYDROPHILIC INTRODUCER GUIDE WIRE - US FDA APPROVED Technical Specification as per Annexure-6
TRAIGHT LONG INTRODUCER SHEATH WITH HYDROPHILIC INTRODUCER GUIDE WIRE - CE APPROVED Technical Specification as per Annexure-6
STRAIGHT LONG INTRODUCER SHEATH WITH HYDROPHILIC INTRODUCER GUIDE WIRE – DCGI APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - US FDA APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - CE APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - DCGI APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING – US FDA APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING – CE APPROVED Technical Specification as per Annexure-6
STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING – DCGI APPROVED Technical Specification as per Annexure-6
Group- A-14 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Guiding catheter for Peripheral Vascular Use – US FDA APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – CE APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – DCGI APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – US FDA APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – CE APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – DCGI APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – US FDA APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – CE APPROVED Technical Specification as per Annexure-6
Guiding catheter for Peripheral Vascular Use – DCGI APPROVED Technical Specification as per Annexure-6
Long sheath for contra – lateral iliac/ femoral access – US FDA APPROVED Technical Specification as per Annexure-6
Long sheath for contra – lateral iliac/ femoral access – CE APPROVED Technical Specification as per Annexure-6
Long sheath for contra – lateral iliac/ femoral access –DCGI APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter both curve - US FDA APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter both curve - CE APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter both curve - DCGI APPROVED Technical Specification as per Annexure-6
Transradial Guiding Catheter right curve/ left curve – US FDA /CE APPROVED Technical Specification as per Annexure-6
Transradial Guiding Catheter right curve/ left curve – DCGI APPROVED Technical Specification as per Annexure-6
Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single curve – US FDA /CE APPROVED Technical Specification as per Annexure-6
Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single curve – DCGI APPROVED Technical Specification as per Annexure-6
Mother & Child Catheter – US FDA/CE APPROVED Technical Specification as per Annexure-6
Mother & Child Catheter – DCGI APPROVED Technical Specification as per Annexure-6
Intubation Catheter for Assisting Delivery of stent in difficult anatomies – US FDA/CE APPROVED Technical Specification as per Annexure-6
Intubation Catheter for Assisting Delivery of stent in difficult anatomies – DCGI APPROVED Technical Specification as per Annexure-6
Re-Entry Catheter for CTO for Coronary – US FDA/CE / DCGI APPROVED Technical Specification as per Annexure-6
Re-Entry Wire for CTO for Coronary – US FDA/CE / DCGI APPROVED Technical Specification as per Annexure-6
Re-Entry Balloon with Two exit Port for CTO for Coronary – US FDA/CE / DCGI APPROVED Technical Specification as per Annexure-6
RDC Shape Guiding Catheter for Renal & C-lilac artery Angioplasty – - US FDA/CE / DCGI APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter Jacky/Sarah curve - DCGI APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter Ikari curve - DCGI APPROVED Technical Specification as per Annexure-6
Group- A-15 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Femoral Compression Band – DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
I.C.D/P.I Compression Band - DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
Iodixanol 320mg/100ml in Plastic bottle - DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
Radial Compression Band - DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
Mullin’s Sheath for special Dilation - DCGI With US FDA /CE Approved Should be in All Sizes-6F & above septal puncture needle Technical Specification as per Annexure-6
Trans-Spetal puncture needle- DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
Rat Pad Type Radiation Protection Shield in All Type & all Sizes Technical Specification as per Annexure-6
PTCA/Coronary Angiography Drap Set Technical Specification as per Annexure-6
G- Kit Type Disposable surgeons Gown Set Technical Specification as per Annexure-6
Disposable Plastic Sheet of Size 1.5x2.5 mtr Technical Specification as per Annexure-6
Group-B-1 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
CORONARY STENT WITH CUSTOM-LENGTH STENT DEVIVERY SYSTEM WITH INDEPENDTLY OPERABLE EXPANSION ELEMENTS - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY STENT WITH CUSTOM-LENGTH STENT DEVIVERY SYSTEM WITH INDEPENDTLY OPERABLE EXPANSION ELEMENTS - CE APPROVED Technical Specification as per Annexure-6
CORONARY STENT WITH CUSTOM-LENGTH STENT DEVIVERY SYSTEM WITH INDEPENDTLY OPERABLE EXPANSION ELEMENTS – DCGI APPROVED Technical Specification as per Annexure-6
ATHERO-CATH DEVICES FOR DIRECTIONAL CORONARY ATHERECTOMY (DCA) - US FDA APPROVED Technical Specification as per Annexure-6
ATHERO-CATH DEVICES FOR DIRECTIONAL CORONARY ATHERECTOMY (DCA) - CE APPROVED Technical Specification as per Annexure-6
ATHERO-CATH DEVICES FOR DIRECTIONAL CORONARY ATHERECTOMY (DCA) – DCGI APPROVED Technical Specification as per Annexure-6
MOTOR FOR DCA - US FDA APPROVED Technical Specification as per Annexure-6
MOTOR FOR DCA - CE APPROVED Technical Specification as per Annexure-6
MOTOR FOR DCA - DCGI APPROVED Technical Specification as per Annexure-6
ROTALINK BURR - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab SMSH). Technical Specification as per Annexure-6
ROTALINK BURR - CE APPROVED (Compatible with existing Rota Machine Cath Lab SMSH). Technical Specification as per Annexure-6
ROTALINK BURR – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab SMSH). Technical Specification as per Annexure-6
ROTALINK ADVANCER - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab SMS H). Technical Specification as per Annexure-6
ROTALINK ADVANCER - CE APPROVED (Compatible with existing Rota Machine Cath Lab SMS H). . Technical Specification as per Annexure-6
ROTALINK ADVANCER – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab SMS H). Technical Specification as per Annexure-6
ROTALINK PLUS (ADVANCER AND BURR) - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab SMS H). Technical Specification as per Annexure-6
ROTALINK PLUS (ADVANCER AND BURR) - CE APPROVED (Compatible with existing Rota Machine Cath Lab SMSH Technical Specification as per Annexure-6
ROTALINK PLUS (ADVANCER AND BURR) – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab SMSH Technical Specification as per Annexure-6
ROTATIONAL ATHERECTOMY GUIDE WIRES - US FDA APPROVED Technical Specification as per Annexure-6
ROTATIONAL ATHERECTOMY GUIDE WIRES - CE APPROVED Technical Specification as per Annexure-6
ROTATIONAL ATHERECTOMY GUIDE WIRES –DCGI APPROVED pecification as per Technical Bid
ROTAGLIDE LUBRICANT - US FDA APPROVED Technical Specification as per Annexure-6
ROTAGLIDE LUBRICANT - CE APPROVED Technical Specification as per Annexure-6
ROTAGLIDE LUBRICANT – DCGI APPROVED Technical Specification as per Annexure-6
CATHETER FOR VIRTUAL HISTOLOGY - US FDA APPROVED Technical Specification as per Annexure-6
CATHETER FOR VIRTUAL HISTOLOGY - CE APPROVED Technical Specification as per Annexure-6
CATHETER FOR VIRTUAL HISTOLOGY – DCGI APPROVED Technical Specification as per Annexure-6
CATHETER FOR OPTICAL COHERENCE REFRACTOMETRY - US FDA APPROVED Technical Specification as per Annexure-6
CATHETER FOR OPTICAL COHERENCE REFRACTOMETRY - CE APPROVED Technical Specification as per Annexure-6
CATHETER FOR OPTICAL COHERENCE REFRACTOMETRY –DCGI APPROVED Technical Specification as per Annexure-6
DRUG DELIVERY/INFUSION CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
DRUG DELIVERY/INFUSION CATHETER - CE APPROVED Technical Specification as per Annexure-6
DRUG DELIVERY/INFUSION CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
CORONARY PROBING CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY PROBING CATHETER - CE APPROVED Technical Specification as per Annexure-6
CORONARY PROBING CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
CORONARY PERFUSION CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY PERFUSION CATHETER - CE APPROVED Technical Specification as per Annexure-6
CORONARY PERFUSION CATHETER –DCGI APPROVED Technical Specification as per Annexure-6
CORONARY TRAPEER CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY TRAPEER CATHETER - CE APPROVED Technical Specification as per Annexure-6
CORONARY TRAPEER CATHETER –DCGI APPROVED Technical Specification as per Annexure-6
IVUS CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
IVUS CATHETER - CE APPROVED Technical Specification as per Annexure-6
IVUS CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
CORONARY TAPERED STENT – US APPROVED Technical Specification as per Annexure-6
CORONARY TAPERED STENT - CE APPROVED Technical Specification as per Annexure-6
CORONARY TAPERED STENT – DCGI APPROVED Technical Specification as per Annexure-6
ROTAWIRE – US FDA APPROVED Technical Specification as per Annexure-6
ROTAWIRE – DCGI APPROVED Technical Specification as per Annexure-6
Group-B-2 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR ASD CLOSURE DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR ASD CLOSURE DEVICE – CE APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR ASD CLOSURE DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
PRELOADED ASD CLOSURE DEVICES – US FDA APPROVED Technical Specification as per Annexure-6
PRELOADED ASD CLOSURE DEVICES – CE APPROVED Technical Specification as per Annexure-6
PRELOADED ASD CLOSURE DEVICES – DCGI APPROVED Technical Specification as per Annexure-6
FENESTRATED SHEATH AND CLOSURE DEVICE US FDA APPROVED Technical Specification as per Annexure-6
FENESTRATED SHEATH AND CLOSURE DEVICE CE APPROVED Technical Specification as per Annexure-6
FENESTRATED SHEATH AND CLOSURE DEVICE DCGI APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICE US FDA APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICE CE APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICE DCGI APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APPENDAGE CLOSURE DEVICE US FDA APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APPENDAGE CLOSURE DEVICE CE APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APPENDAGE CLOSURE DEVICE DCGI APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PFO CLOSURE DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PFO CLOSURE DEVICE – CE APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PFO CLOSURE DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – CIRCULAR SHAPE - US FDA APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – CIRCULAR SHAPE - CE APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – CIRCULAR SHAPE – DCGI APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – OVAL SHAPED - US FDA APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – OVAL SHAPED - CE APPROVED Technical Specification as per Annexure-6
SIZING BALLOON FOR DEVICE CLOSURE – OVAL SHAPED –DCGI APPROVED Technical Specification as per Annexure-6
SIZING PLATE FOR DEVICE CLOSURE - US FDA APPROVED Technical Specification as per Annexure-6
SIZING PLATE FOR DEVICE CLOSURE - CE APPROVED Technical Specification as per Annexure-6
SIZING PLATE FOR DEVICE CLOSURE - DCGI APPROVED Technical Specification as per Annexure-6
DELIVERY CABLE FOR ASD/VSD/PDA DEVICES - US FDA APPROVED Technical Specification as per Annexure-6
DELIVERY CABLE FOR ASD/VSD/PDA DEVICES - CE APPROVED Technical Specification as per Annexure-6
DELIVERY CABLE FOR ASD/VSD/PDA DEVICES - DCGI APPROVED Technical Specification as per Annexure-6
RETRIEVERS FOR ASD/VSD/PDA DEVICES - US FDA APPROVED Technical Specification as per Annexure-6
RETRIEVERS FOR ASD/VSD/PDA DEVICES - CE APPROVED Technical Specification as per Annexure-6
RETRIEVERS FOR ASD/VSD/PDA DEVICES – DCGI APPROVED Technical Specification as per Annexure-6
SEATH FOR RETRIVAL OF DEVICES - US FDA APPROVED Technical Specification as per Annexure-6
SEATH FOR RETRIVAL OF DEVICES - CE APPROVED Technical Specification as per Annexure-6
SEATH FOR RETRIVAL OF DEVICES – DCGI APPROVED Technical Specification as per Annexure-6
Group B -3 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH /SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - CE APPROVED Technical Specification as per Annexure-6
TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) – DCGI APPROVED Technical Specification as per Annexure-6
Self Expandable Trans Catheter Aortic Valve Replacement System With All Required Accessories – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
Self Expandable Trans Catheter Tricuspid Valve Replacement System With All Required Accessories – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
Trans Catheter Tricuspid Valve Replacement System With All Required Accessories – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
TAVI (TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM (Retrievable) WITH ALL REQUIRED ACCESSORIES) – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
Shockwave I.V.L intravascular Lithotripsy Catheter system with connector cable - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Mitra-Clip (TRANS CATHETER Mitral VALVE Clip System) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
TAVI Guide-wire - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Group-B-4 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
VSD CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
VSD CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
VSD CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
VSD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
VSD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
VSD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR VSD CLOSURE DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR VSD CLOSURE DEVICE – CE APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR VSD CLOSURE DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –DCGI APPROVED Technical Specification as per Annexure-6
Group-B-5 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PDA CLOSURE DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PDA CLOSURE DEVICE – CE APPROVED Technical Specification as per Annexure-6
DELIVERY SHEATH FOR PDA CLOSURE DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – US FDA APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED Technical Specification as per Annexure-6
PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED Technical Specification as per Annexure-6
Group-B-6 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS - US FDA APPROVED Technical Specification as per Annexure-6
WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS - CE APPROVED Technical Specification as per Annexure-6
WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS – DCGI APPROVED Technical Specification as per Annexure-6
WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - US FDA APPROVED Technical Specification as per Annexure-6
WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - CE APPROVED Technical Specification as per Annexure-6
WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - DCGI APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS - CE APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH - CE APPROVED Technical Specification as per Annexure-6
SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH - CE APPROVED Technical Specification as per Annexure-6
SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH – DCGI APPROVED Technical Specification as per Annexure-6
Group-B-7 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - US FDA APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - CE APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - DCGI APPROVED Technical Specification as per Annexure-6
BALLOON CATHETERS (sizes 10 – 22 mm) - US FDA APPROVED Technical Specification as per Annexure-6
BALLOON CATHETERS (sizes 10 – 22 mm) - CE APPROVED Technical Specification as per Annexure-6
BALLOON CATHETERS (sizes 10 – 22 mm) - DCGI APPROVED Technical Specification as per Annexure-6
BALLOON IN BALLOON CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
BALLOON IN BALLOON CATHETERS - CE APPROVED Technical Specification as per Annexure-6
BALLOON IN BALLOON CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
FOGARTY EMBOLECTOMY CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
FOGARTY EMBOLECTOMY CATHETER - CE APPROVED Technical Specification as per Annexure-6
FOGARTY EMBOLECTOMY CATHETER - DCGI APPROVED Technical Specification as per Annexure-6
ATRIAL SEPTOSTOMY CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
ATRIAL SEPTOSTOMY CATHETER - CE APPROVED Technical Specification as per Annexure-6
ATRIAL SEPTOSTOMY CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
DETACHABLE BALLOON - US FDA APPROVED Technical Specification as per Annexure-6
DETACHABLE BALLOON - CE APPROVED Technical Specification as per Annexure-6
DETACHABLE BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
VASCULAR PLUGS – US FDA APPROVED Technical Specification as per Annexure-6
VASCULAR PLUGS – CE APPROVED Technical Specification as per Annexure-6
VASCULAR PLUGS IMPLANTATION– DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS TYSHEK TYPE (all sizes) - US FDA APPROVED Technical Specification as per Annexure-6
VALVOPLASTY BALLOON CATHETERS TYSHEK TYPE (all sizes) - CE APPROVED Technical Specification as per Annexure-6
Aortic Stent graft Abdominal - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
A U I Stent Graft System DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
iliac Stent Graft - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Multifunctional Occluder- DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Peripheral Snare with Tungsten Loop coated with Titanium Nitride - DCGI with CE/ US FDA Approved Technical Specification as per Annexure-6
Peripheral Snare with Tungsten loop Coated with Titanium Nitride (5mm to 35mm) Technical Specification as per Annexure-6
IVC Filter For Optimal Filtration of IVC Up to 23mm - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Coronary Snare with tungsten loop coated with Titanium Nitride (4mm&7mm) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Steerable Sheath with deflectable tip (190-160degree) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride Coated ASD Closure device with delivery system - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Delivery cable for ASD Closure device - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Delivery Sheath for Titanium Nitride coated ASD Closures Devices - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride Coated ASD Closures device without delivery system: - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Sizing balloon for device closure- Oval Shape - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Sizing balloon for device closure - Round Shape - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Delivery cable for VSD - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride coated Vascular Plugs- - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Occlusion balloon - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride Coated Left Aerial Appendage closure device with delivery: - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride Coated Left Aerial Appendage closure device without delivery- DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Delivery Sheath for Titanium Nitride coated VSD device closure system - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride coated VSD Closure device with delivery system - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride coated VSD Closure device with-out delivery system - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride coated PDA Closure device with delivery system - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Titanium Nitride coated PDA Closure device without delivery system Technical Specification as per Annexure-6
Delivery Sheath for Titanium Nitride coated PDA Closure device - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Delivery cable for PDA - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
TAA Stent Graft System - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Aortic stent system (AS series type) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Aortic stent system with balloon (AS series type) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Aortic stent system with balloon (ASC series type) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Aortic stent system with balloon (ASC series type) - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
High Pressure Balloons for Aortic coarctation - - DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Group-B-8 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - US FDA APPROVED Technical Specification as per Annexure-6
PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - CE APPROVED Technical Specification as per Annexure-6
PDA COILS MADE OF STEEL/ NITINOL/PLATINUM – DCGI APPROVED Technical Specification as per Annexure-6
0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - US FDA APPROVED Technical Specification as per Annexure-6
0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - CE APPROVED Technical Specification as per Annexure-6
0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM – DCGI APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.018 INCH) - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.018 INCH) - CE APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.018 INCH) – DCGI APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.035 INCH) - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.035 INCH) - CE APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.035 INCH) – DCGI APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.052 INCH) - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.052 INCH) - CE APPROVED Technical Specification as per Annexure-6
EMBOLISATION COILS (0.052 INCH) –DCGI APPROVED Technical Specification as per Annexure-6
PARK BLADE SEPTECTOMY CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
PARK BLADE SEPTECTOMY CATHETER - CE APPROVED Technical Specification as per Annexure-6
PARK BLADE SEPTECTOMY CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
Embolisation Coils - US FDA APPROVED Technical Specification as per Annexure-6
Embolisation Coils - CE APPROVED Technical Specification as per Annexure-6
Embolisation Coils – DCGI APPROVED Technical Specification as per Annexure-6
Embolisation Coils - US FDA APPROVED Technical Specification as per Annexure-6
Embolisation Coils - CE APPROVED Technical Specification as per Annexure-6
Embolisation Coils – DCGI APPROVED Technical Specification as per Annexure-6
Embolisation Coils - US FDA APPROVED Technical Specification as per Annexure-6
Embolisation Coils - CE APPROVED Technical Specification as per Annexure-6
Embolisation Coils – DCGI APPROVED Technical Specification as per Annexure-6
Coil pusher wire for 0.014/0.018” coils, compatible with the quoted micro catheters - US FDA APPROVED Technical Specification as per Annexure-6
Coil pusher wire for 0.014/0.018” coils, compatible with the quoted micro catheters - CE APPROVED Technical Specification as per Annexure-6
Coil pusher wire for 0.014/0.018” coils, compatible with the quoted microcatheters – DCGI APPROVED Technical Specification as per Annexure-6
Gelfoam sheet for vascular embollization - US FDA APPROVED Technical Specification as per Annexure-6
Gelfoam sheet for vascular embollization - CE APPROVED Technical Specification as per Annexure-6
Gelfoam sheet for vascular embollization – DCGI APPROVED Technical Specification as per Annexure-6
Liquid Embolization system available in Various sizes (2ml, 3ml & 6ml)– US FDA/ CE / DCGI APPROVED Technical Specification as per Annexure-6
Group-B-9 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – US FDA APPROVED Technical Specification as per Annexure-6
PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – CE APPROVED Technical Specification as per Annexure-6
PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – DCGI APPROVED Technical Specification as per Annexure-6
PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES – US FDA APPROVED Technical Specification as per Annexure-6
PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES –CE APPROVED Technical Specification as per Annexure-6
PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES –DCGI APPROVED Technical Specification as per Annexure-6
ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – US FDA APPROVED Technical Specification as per Annexure-6
ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – CE APPROVED Technical Specification as per Annexure-6
ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – DCGI APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– US FDA APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– CE APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– DCGI APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITHOUT ACCESSORIES – US FDA APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY/ MICROHOLES WITHOUT ACCESSORIES– CE APPROVED Technical Specification as per Annexure-6
PBMV BALLOON WITH SIDE SAFETY/ MICROHOLES WITHOUT ACCESSORIES– DCGI APPROVED Technical Specification as per Annexure-6
Group-B-10 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH, JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PTMC BALLOON WITH HOLE IN BALLOON – US FDA APPROVED Technical Specification as per Annexure-6
PTMC BALLOON WITH HOLE IN BALLOON – CE APPROVED Technical Specification as per Annexure-6
PTMC BALLOON WITH HOLE IN BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- US FDA APPROVED Technical Specification as per Annexure-6
PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- CE APPROVED Technical Specification as per Annexure-6
PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- DCGI APPROVED Technical Specification as per Annexure-6
Group-B-11 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
FFR WIRE WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR -CE APPROVED Technical Specification as per Annexure-6
FFR WIRE WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR –FDA APPROVED Technical Specification as per Annexure-6
FFR WIRE WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR –DCGI APPROVED Technical Specification as per Annexure-6
IVUS CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- CE APPROVED Technical Specification as per Annexure-6
IVUS CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- FDA APPROVED Technical Specification as per Annexure-6
IVUS CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- DCGI APPROVED Technical Specification as per Annexure-6
OCT CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- US FDA APPROVED Technical Specification as per Annexure-6
OCT CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- CE APPROVED Technical Specification as per Annexure-6
OCT CATHETER WITH ACCESSORIES COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- DCGI APPROVED Technical Specification as per Annexure-6
FFR WIRE WITH ACCESSORIES COMPITABLE TO ABBOTT IMAGING MACHINE INSTALLED WITH TOSHIBA CATH LAB IN CATH LAB, SMS HOSPITAL, JAIPUR –DCGI WITH US FDA / CE Approved Technical Specification as per Annexure-6
IVUS CATHETER WITH ACCESSORIES COMPITABLE TO TOSHIBA CATH LAB IMAGING MACHINE IN CATH LAB, SMS HOSPITAL, JAIPUR- DCGI WITH US FDA / CE Approved Technical Specification as per Annexure-6
NAME OF ITEMS : MECHANICAL ASPIRATION DEVICE (ALL TYPES) - CE / US FDA APPROVED Technical Specification as per Annexure-6
NAME OF ITEMS : MECHANICAL ASPIRATION DEVICE (ALL TYPES) - DCGI APPROVED Technical Specification as per Annexure-6
FFR WIRE (optical sensor based pressure wire) - DCGI WITH US FDA / CE Approved Technical Specification as per Annexure-6
IVUS CATHETER with 60 Mhz, HD IVUS catheter, Mechanical/Rotational catheter - DCGI WITH US FDA / CE Approved Technical Specification as per Annexure-6
Group-C-1 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PTCA INFLATION DEVICE - US FDA APPROVED Technical Specification as per Annexure-6
PTCA INFLATION DEVICE - CE APPROVED Technical Specification as per Annexure-6
PTCA INFLATION DEVICE -DCGI APPROVED Technical Specification as per Annexure-6
TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH Pull MECHANISM - US FDA APPROVED Technical Specification as per Annexure-6
TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH Pull MECHANISM - CE APPROVED Technical Specification as per Annexure-6
TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH Pull MECHANISM –DCGI APPROVED Technical Specification as per Annexure-6
TUOHY BORST – DOUBLE (HAEMOSTATIC Y-CONNECTOR) FOR BIFURCATION PTCA - US FDA APPROVED Technical Specification as per Annexure-6
TUOHY BORST – DOUBLE (HAEMOSTATIC Y-CONNECTOR) FOR BIFURCATION PTCA - CE APPROVED Technical Specification as per Annexure-6
TUOHY BORST – DOUBLE (HAEMOSTATIC Y-CONNECTOR) FOR BIFURCATION PTCA - DCGI APPROVED Technical Specification as per Annexure-6
RADIAL COMPRESION BAND (TR BAND TYPE)- US FDA Approved Technical Specification as per Annexure-6
RADIAL COMPRESION BAND (TR BAND TYPE) – CE Approved Technical Specification as per Annexure-6
RADIAL COMPRESION BAND (TR BAND TYPE) – DCGI Approved Technical Specification as per Annexure-6
Y- connector Kit (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH Pull MECHANISM (OKAY – 2 type) – DCGI Approved and US FDA / CE APPROVED Technical Specification as per Annexure-6
Group-C-2 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
MANIFOLD WITH ATTACHED TUBINGS (ANGIO KIT) with 3 Port - US FDA APPROVED Technical Specification as per Annexure-6
MANIFOLD WITH ATTACHED TUBINGS (ANGIO KIT) with 3 Port - CE APPROVED Technical Specification as per Annexure-6
MANIFOLD WITH ATTACHED TUBINGS (ANGIO KIT) with 3 Port - DCGI APPROVED Technical Specification as per Annexure-6
FEMORAL COMPRESSION DEVICES – DISC / DOME BASED COMPRESSION - US FDA APPROVED Technical Specification as per Annexure-6
FEMORAL COMPRESSION DEVICES – DISC / DOME BASED COMPRESSION - CE APPROVED Technical Specification as per Annexure-6
FEMORAL COMPRESSION DEVICES – DISC / DOME BASED COMPRESSION - DCGI APPROVED Technical Specification as per Annexure-6
DOMES OF FEMORAL COMPRESSION BAND - US FDA APPROVED Technical Specification as per Annexure-6
RADIAL COMPRESSION BAND - CE APPROVED Technical Specification as per Annexure-6
DOMES OF FEMORAL COMPRESSION DEVICE - DCGI APPROVED Technical Specification as per Annexure-6
PRESSURE TRANSDUTURE DOMES WITH PRESURE LINE LINK Technical Specification as per Annexure-6
PRESSURE TRANSDUTURE DOMES WITH PRESURE LINE LINK Technical Specification as per Annexure-6
PTCA GUIDING CATHETER – FDA/CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDING CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDING CATHETER – FDA/ CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDING CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDING CATHETER FOR DCA- US FDA/ CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDING CATHETER FOR DCA- DCGI APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter Jacky/Sarah curve - DCGI APPROVED Technical Specification as per Annexure-6
Radial Guiding catheter Ikari curve - DCGI APPROVED Technical Specification as per Annexure-6
Group-C-3 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
PTCA GUIDE WIRE – REGULAR LENGTH, REGULAR SHAFT SUPPORT AND FLOPPY TIP US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – REGULAR LENGTH, REGULAR SHAFT SUPPORT AND FLOPPY TIP CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – REGULAR LENGTH, REGULAR SHAFT SUPPORT AND FLOPPY TIP DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – REGULAR LENGTH, EXTRA - SUPPORT SHAFT AND FLOPPY TIP US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – REGULAR LENGTH, EXTRA - SUPPORT SHAFT AND FLOPPY TIP CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – REGULAR LENGTH, EXTRA - SUPPORT SHAFT AND FLOPPY TIP DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – EXCHANGE LENGTH US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – EXCHANGE LENGTH CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – EXCHANGE LENGTH DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, REGULAR LENGTH US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, REGULAR LENGTH CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, REGULAR LENGTH DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, EXCHANGE LENGTH US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, EXCHANGE LENGTH CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – HYDROPHILIC COATED, EXCHANGE LENGTH DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES WITH ELASTINITE CORE AND STAINLESS STEEL SHAFT SUPPORT US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES WITH ELASTINITE CORE AND STAINLESS STEEL SHAFT SUPPORT CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES WITH ELASTINITE CORE AND STAINLESS STEEL SHAFT SUPPORT DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH DUAL COATING US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH DUAL COATING CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH DUAL COATING DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH MULTIPLE MARKERS FOR MEASURING THE LENGTH OF STENOTIC SEGMENT - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH MULTIPLE MARKERS FOR MEASURING THE LENGTH OF STENOTIC SEGMENT - CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRE WITH MULTIPLE MARKERS FOR MEASURING THE LENGTH OF STENOTIC SEGMENT – DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES FOR CHRONIC TOTAL OCCLUSION (CTO) - US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES FOR CHRONIC TOTAL OCCLUSION (CTO) - CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES FOR CHRONIC TOTAL OCCLUSION (CTO) –DCGI APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) - US FDA APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) - CE APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) – DCGI APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) US FDA APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) CE APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) DCGI APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) US FDA APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) CE APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (REGULAR LENGTH) DCGI APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) - US FDA APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) - CE APPROVED Technical Specification as per Annexure-6
HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (EXCHANGE LENGTH) – DCGI APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE - US FDA APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE - CE APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE – DCGI APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE (Exchange) - US FDA APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE (Exchange) - CE APPROVED Technical Specification as per Annexure-6
STEERABLE HIGH SUPPORT .014 INCH GUIDEWIRE (Exchange) – DCGI APPROVED Technical Specification as per Annexure-6
PTCA WIRES WITH FACILITY OF BOOT LINKS FOR EXTENSION OF REGULAR WIRE - US FDA APPROVED Technical Specification as per Annexure-6
PTCA WIRES WITH FACILITY OF BOOT LINKS FOR EXTENSION OF REGULAR WIRE - CE APPROVED Technical Specification as per Annexure-6
PTCA WIRES WITH FACILITY OF BOOT LINKS FOR EXTENSION OF REGULAR WIRE - DCGI APPROVED Technical Specification as per Annexure-6
EXCHANGE LENGTH PTCA WIRE WITH MARKER WITH – US FDA APPROVED Technical Specification as per Annexure-6
EXCHANGE LENGTH PTCA WIRE WITH MARKER WITH – CE APPROVED Technical Specification as per Annexure-6
EXCHANGE LENGTH PTCA WIRE WITH MARKER WITH – DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE – DCGI With US FDA /CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE With Facility of Boot Links for Extension Of Regular Wire –DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
Micro-wire (0.008”-0.012” ) with Hydrophilic coating - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Special inflation device for high pressure (55 ATM), High Resolution - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Group-C-4 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
SPECIAL NON-TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL NON-TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - CE APPROVED Technical Specification as per Annexure-6
SPECIAL NON-TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - CE APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH PLATINUM IRIDIUM DISTAL SPRING COIL - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH HYDROCOAT-HYDROPHILIC COATING - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH HYDROCOAT-HYDROPHILIC COATING - CE APPROVED Technical Specification as per Annexure-6
SPECIAL TAPERING PTCA GUIDE WIRES FOR CTO WITH HYDROCOAT-HYDROPHILIC COATING - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL HYDROPHILIC PTCA GUIDE WIRES FOR CTO WITH SUPER ELASTIC ALLOY (Ni-Ti) CORE - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL HYDROPHILIC PTCA GUIDE WIRES FOR CTO WITH SUPER ELASTIC ALLOY (Ni-Ti) CORE - CE APPROVED Technical Specification as per Annexure-6
SPECIAL HYDROPHILIC PTCA GUIDE WIRES FOR CTO WITH SUPER ELASTIC ALLOY (Ni-Ti) CORE - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES FOR CTO, DEDICATED FOR RETROGRADE APPROACH - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES FOR CTO, DEDICATED FOR RETROGRADE APPROACH - CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA GUIDE WIRES FOR CTO, DEDICATED FOR RETROGRADE APPROACH – DCGI APPROVED Technical Specification as per Annexure-6
EXTENSIION (DOC) WIRE FOR APPROVED REGULAR LENGTH PTCA GUIDE WIRES - US FDA APPROVED Technical Specification as per Annexure-6
EXTENSIION (DOC) WIRE FOR APPROVED REGULAR LENGTH PTCA GUIDE WIRES - CE APPROVED Technical Specification as per Annexure-6
EXTENSIION (DOC) WIRE FOR APPROVED REGULAR LENGTH PTCA GUIDE WIRES – DCGI APPROVED Technical Specification as per Annexure-6
PENETRATION CATHETERS FOR CTO HAVING ROTATIONAL BLUNT PENETRATION - US FDA APPROVED Technical Specification as per Annexure-6
PENETRATION CATHETERS FOR CTO HAVING ROTATIONAL BLUNT PENETRATION - CE APPROVED Technical Specification as per Annexure-6
PENETRATION CATHETERS FOR CTO HAVING ROTATIONAL BLUNT PENETRATION – DCGI APPROVED Technical Specification as per Annexure-6
PENETRATION DEVICES FOR CTO BY BLUNT DISSECTION USING ACUATING JAWS - US FDA APPROVED Technical Specification as per Annexure-6
PENETRATION DEVICES FOR CTO BY BLUNT DISSECTION USING ACUATING JAWS - CE APPROVED Technical Specification as per Annexure-6
PENETRATION DEVICES FOR CTO BY BLUNT DISSECTION USING ACUATING JAWS - DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES WITH BIDIRECTIONAL DEFLECTABLE DISTAL TIP - US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES WITH BIDIRECTIONAL DEFLECTABLE DISTAL TIP - CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRES WITH BIDIRECTIONAL DEFLECTABLE DISTAL TIP – DCGI APPROVED Technical Specification as per Annexure-6
PTCA CATHETER WITH DEFLECTABLE DISTAL END - US FDA APPROVED Technical Specification as per Annexure-6
PTCA CATHETER WITH DEFLECTABLE DISTAL END - CE APPROVED Technical Specification as per Annexure-6
PTCA CATHETER WITH DEFLECTABLE DISTAL END – DCGI APPROVED Technical Specification as per Annexure-6
MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH. - US FDA APPROVED Technical Specification as per Annexure-6
MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH. - CE APPROVED Technical Specification as per Annexure-6
MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH. - DCGI APPROVED Technical Specification as per Annexure-6
GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - US FDA APPROVED Technical Specification as per Annexure-6
GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - CE APPROVED Technical Specification as per Annexure-6
GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - DCGI APPROVED Technical Specification as per Annexure-6
DOUBLE LEUMEN MICRO CATHETER (CRUSADE TYPE) – US FDA APPROVED Technical Specification as per Annexure-6
DOUBLE LEUMEN MICRO CATHETER (CRUSADE TYPE) – CE APPROVED Technical Specification as per Annexure-6
Special Guiding Catheter with HENKA 6fr/7fr- DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
MICRO CATHETER for Embolization – DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Group C-5 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA MUST QUOTE ONLY LATEST COMMERCIAL VERSION AVAILABLE IN INDIA.
PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVED Technical Specification as per Annexure-6
PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVED Technical Specification as per Annexure-6
PTCA BALLOON (SEMI-COMPLIANT) – DCGI APPROVED Technical Specification as per Annexure-6
PTCA BALLOON (NON-COMPLIANT) - US FDA APPROVED Technical Specification as per Annexure-6
PTCA BALLOON (NON-COMPLIANT) - CE APPROVED Technical Specification as per Annexure-6
PTCA BALLOON (NON-COMPLIANT) – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL LARGE PTCA BALLOONS OF UPTO 5 MM OR MORE IN DIAMETER - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL LARGE PTCA BALLOONS OF UPTO 5 MM OR MORE IN DIAMETER - CE APPROVED Technical Specification as per Annexure-6
SPECIAL LARGE PTCA BALLOONS OF MORE THAN 4 MM - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - CE APPROVED Technical Specification as per Annexure-6
SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL OTW PTCA BALLOON FOR SEPTAL ABLATION FOR HOCM - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL OTW PTCA BALLOON FOR SEPTAL ABLATION FOR HOCM - CE APPROVED Technical Specification as per Annexure-6
SPECIAL OTW PTCA BALLOON FOR SEPTAL ABLATION FOR HOCM – DCGI APPROVED Technical Specification as per Annexure-6
SPECIAL EXTRA LENGTH PTCA BALLOON CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL EXTRA LENGTH PTCA BALLOON CATHETERS - CE APPROVED Technical Specification as per Annexure-6
SPECIAL EXTRA LENGTH PTCA BALLOON CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
ZEROFOLD PTCA BALLOON - US FDA APPROVED Technical Specification as per Annexure-6
ZEROFOLD PTCA BALLOON - CE APPROVED Technical Specification as per Annexure-6
ZEROFOLD PTCA BALLOON - DCGI APPROVED Technical Specification as per Annexure-6
CORONARY PTCA BALLOON CUTTING BALLOON WITH FLEXTOMES - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY PTCA BALLOON CUTTING BALLOON WITH FLEXTOMES - CE APPROVED Technical Specification as per Annexure-6
CORONARY PTCA BALLOON CUTTING BALLOON WITH FLEXTOMES - DCGI APPROVED Technical Specification as per Annexure-6
RAPID EXCHANGE LOW PRESSURE ATRAUMATIC MICROSPORES PTFE BALLOON CATHETER FOR LOCAL INFUSION OF DRUG, CATHETER LENGTH > 130 CM. SIZE 1.5 – 4.0 MM – US FDA / CE APPROVED Technical Specification as per Annexure-6
RAPID EXCHANGE LOW PRESSURE ATRAUMATIC MICROSPORES PTFE BALLOON CATHETER FOR LOCAL INFUSION OF DRUG, CATHETER LENGTH > 130 CM. SIZE 1.5 – 4.0 MM – DCGI APPROVED Technical Specification as per Annexure-6
BEVELLED BALLON OF VARIOUS SIZES FOR ENTRY THROUGH THE STENT INTO SIDE BRANCH – US FDA / CE APPROVED Technical Specification as per Annexure-6
BEVELLED BALLON OF VARIOUS SIZES FOR ENTRY THROUGH THE STENT INTO SIDE BRANCH – DCGI APPROVED Technical Specification as per Annexure-6
HEMOSTATIC Y ADAPTER WITH PUSH PULL BUTTON – US FDA / CE APPROVED Technical Specification as per Annexure-6
HEMOSTATIC Y ADAPTER WITH PUSH PULL BUTTON – DCGI APPROVED Technical Specification as per Annexure-6
DEDICATED MICRO CATHETER FOR SIDE BRANCH ACCESS – US FDA/ CE APPROVED Technical Specification as per Annexure-6
DEDICATED MICRO CATHETER FOR SIDE BRANCH ACCESS – DCGI APPROVED Technical Specification as per Annexure-6
Special OTW PTCA Balloon For Retrograde Approach- DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
High Pressure Non Compliant Balloon- DCGI & US FDA/CE Approved Technical Specification as per Annexure-6
Ultra low Non Compliant CTO Balloon in diameter size 0.85mm - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Plaque Modification device for Highly calcified lesions -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Ultra low Non Compliant CTO Balloon in diameter size 0.85mm - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Group C-6 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
DRUG ELUTING PTCA BALLOON - US FDA APPROVED Technical Specification as per Annexure-6
DRUG ELUTING PTCA BALLOON - CE APPROVED Technical Specification as per Annexure-6
DRUG ELUTING PTCA BALLOON - DCGI APPROVED Technical Specification as per Annexure-6
PTCA BALLOON FOR RETROGRADE APPROACH OF CTO - US FDA APPROVED Technical Specification as per Annexure-6
PTCA BALLOON FOR RETROGRADE APPROACH OF CTO - CE APPROVED Technical Specification as per Annexure-6
PTCA BALLOON FOR RETROGRADE APPROACH OF CTO –DCGI APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) -000 US FDA APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - CE APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - DCGI APPROVED Technical Specification as per Annexure-6
SCORING BALLOON CATHETER FOR PTCA - US FDA APPROVED Technical Specification as per Annexure-6
SCORING BALLOON CATHETER FOR PTCA - CE APPROVED Technical Specification as per Annexure-6
SCORING BALLOON CATHETER FOR PTCA – DCGI APPROVED Technical Specification as per Annexure-6
DUAL WIRE PTCA BALLOON DILATATION CATHETER - US FDA APPROVED Technical Specification as per Annexure-6
DUAL WIRE PTCA BALLOON DILATATION CATHETER - CE APPROVED Technical Specification as per Annexure-6
DUAL WIRE PTCA BALLOON DILATATION CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
PTCA BIFURCATION BALLOON - US FDA APPROVED Technical Specification as per Annexure-6
PTCA BIFURCATION BALLOON - CE APPROVED Technical Specification as per Annexure-6
PTCA BIFURCATION BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - US FDA APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - CE APPROVED Technical Specification as per Annexure-6
CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - DCGI APPROVED Technical Specification as per Annexure-6
BALLOON DILATATION CATHETER FOR AORTA & IVC- US FDA APPROVED Technical Specification as per Annexure-6
BALLOON DILATATION CATHETER FOR AORTA & IVC- CE APPROVED Technical Specification as per Annexure-6
BALLOON DILATATION CATHETER FOR AORTA & IVC- DCGI APPROVED Technical Specification as per Annexure-6
BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - US FDA APPROVED Technical Specification as per Annexure-6
BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - CE APPROVED Technical Specification as per Annexure-6
BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - DCGI APPROVED Technical Specification as per Annexure-6
Z MED TYPE BALLOON FOR AORTIC COACTATION – US FDA/CE APPROVED Technical Specification as per Annexure-6
Z MED TYPE BALLOON FOR AORTIC COACTATION – DCGI APPROVED Technical Specification as per Annexure-6
Z MED TYPE BALLOON FOR AORTIC COACTATION – US FDA/CE APPROVED Technical Specification as per Annexure-6
Z MED TYPE BALLOON FOR AORTIC COACTATION – DCGI APPROVED Technical Specification as per Annexure-6
OTW BALLOON FOR PERIFERAL ANGIOPLASTY ALL SIZE AND DIAMETERS- CE/ FDA APPROVED Technical Specification as per Annexure-6
OTW BALLOON FOR PERIFERAL ANGIOPLASTY ALL SIZE AND DIAMETERS- DCGI APPROVED Technical Specification as per Annexure-6
Group C-7 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
STAINLESS STEEL CORONARY STENTS, PREMOUNTED ON BALLOON –US FDA APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL CORONARY STENTS, PREMOUNTED ON BALLOON –CE APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL CORONARY STENTS, PREMOUNTED ON BALLOON –DCGI APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM CORONARY STENTS, PREMOUNTED ON BALLOON – US FDA APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM CORONARY STENTS, PREMOUNTED ON BALLOON – CE APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM CORONARY STENTS, PREMOUNTED ON BALLOON –DCGI APPROVED Technical Specification as per Annexure-6
COVERED CORONARY STENTS – US FDA APPROVED Technical Specification as per Annexure-6
COVERED CORONARY STENTS – CE APPROVED Technical Specification as per Annexure-6
COVERED CORONARY STENTS – DCGI APPROVED Technical Specification as per Annexure-6
DEDICATED BARE METAL CORONARY STENTS FOR BIFURCATION LESIONS – US FDA APPROVED Technical Specification as per Annexure-6
DEDICATED BARE METAL CORONARY STENTS FOR BIFURCATION LESIONS – CE APPROVED Technical Specification as per Annexure-6
DEDICATED BARE METAL CORONARY STENTS FOR BIFURCATION LESIONS – DCGI APPROVED Technical Specification as per Annexure-6
DUAL COATED STENT , PREMOUNTED ON BALLOON – US FDA APPROVED Technical Specification as per Annexure-6
DUAL COATED STENT , PREMOUNTED ON BALLOON – CE APPROVED Technical Specification as per Annexure-6
DUAL COATED STENT , PREMOUNTED ON BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL COATED STENTS (ALL TYPES) – US FDA APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL COATED STENTS (ALL TYPES) – CE APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL COATED STENTS (ALL TYPES) – DCGI APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM COATED STENTS (ALL TYPES) – US FDA APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM COATED STENTS (ALL TYPES) – CE APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM COATED STENTS (ALL TYPES) – DCGI APPROVED Technical Specification as per Annexure-6
CARBON COATED STENTS WITH 2 PLATINUM MARKERS ON STENT ALSO - US FDA APPROVED Technical Specification as per Annexure-6
CARBON COATED STENTS WITH 2 PLATINUM MARKERS ON STENT ALSO - CE APPROVED Technical Specification as per Annexure-6
CARBON COATED STENTS WITH 2 PLATINUM MARKERS ON STENT ALSO – DCGI APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL RENAL STENTS, PREMOUNTED ON BALLOON – US FDA APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL RENAL STENTS, PREMOUNTED ON BALLOON – CE APPROVED Technical Specification as per Annexure-6
STAINLESS STEEL RENAL STENTS, PREMOUNTED ON BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM RENAL STENTS, PREMOUNTED ON BALLOON – US FDA APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM RENAL STENTS, PREMOUNTED ON BALLOON – CE APPROVED Technical Specification as per Annexure-6
COBALT CHROMIUM RENAL STENTS, PREMOUNTED ON BALLOON – DCGI APPROVED Technical Specification as per Annexure-6
DURG ELUTING PTA BALLOON FOR BELOW THE KNEE PERIPHERAL ARTERY – US FDA / CE APPROVED Technical Specification as per Annexure-6
DURG ELUTING PTA BALLOON FOR BELOW THE KNEE PERIPHERAL ARTERY – DCGI APPROVED Technical Specification as per Annexure-6
Group C-8 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SGPGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA DES STENT SHOULD HAVE AUTHENTIC CLINICAL SAFETY & EFFICACY DATA FOR 5 YEARS OR MORE IN RESPECT TO CONTEMPORARY-DES. MUST QUOTE ONLY LATEST COMMERCIAL VERSION AVAILABLE IN INDIA
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – US FDA APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – CE APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – DCGI APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – (WITH TALLER NON LEANIER LINKS) DRUG ELUTION - US FDA APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – (WITH TALLER NON LEANIER LINKS) - CE APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – (WITH TALLER NON LEANIER LINKS) - DCGI APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – WITH MULTI LAYER BALLOON AND INTRIGRATED TRANSITIONLESS TIP TECHNOLOGY –US FDA APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – WITH MULTI LAYER BALLOON AND INTRIGRATED TRANSITIONLESS TIP TECHNOLOGY - CE APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – WITH MULTI LAYER BALLOON AND INTRIGRATED TRANSITIONLESS TIP TECHNOLOGY - DCGI APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –US FDA APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – CE APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – DCGI APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH ULTRA THIN BIOABSORBABLE POLYMER COATED DES - US FDA APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH ULTRA THIN BIOABSORBABLE POLYMER COATED DES - CE APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH ULTRA THIN BIOABSORBABLE POLYMER COATED DES - DCGI APPROVED Technical Specification as per Annexure-6
EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH PVDF-HFP POLYMER AND WITH CUSTMISED STENT ARCHITECHTURE OF 4 CONNECTORS ON PROXIMAL END 2 THROUGH OUT – US FDA APPROVED Technical Specification as per Annexure-6
NAME OF ITEMS : EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH PVDF-HFP POLYMER AND WITH CUSTMISED STENT ARCHITECHTURE OF 4 CONNECTORS ON PROXIMAL END 2 THROUGH OUT - CE APPROVED Technical Specification as per Annexure-6
NAME OF ITEMS : EVEROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – WITH PVDF-HFP POLYMER AND WITH CUSTMISED STENT ARCHITECHTURE OF 4 CONNECTORS ON PROXIMAL END 2 THROUGH OUT - DCGI APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT US FDA APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT CE APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT DCGI APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT ON COBALT CHROMIUM - US FDA APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT ON COBALT CHROMIUM - CE APPROVED Technical Specification as per Annexure-6
SIROLIMUS COATED DRUG STENT ON COBALT CHROMIUM - DCGI APPROVED Technical Specification as per Annexure-6
SILICON CARBIDE AND SIROLIMUS DRUG ELUTING STENT – CE APPROVED Technical Specification as per Annexure-6
SILICON CARBIDE AND SIROLIMUS DRUG ELUTING STENT - US FDA APPROVED Technical Specification as per Annexure-6
SILICON CARBIDE AND SIROLIMUS DRUG ELUTING STENT – DCGI APPROVED Technical Specification as per Annexure-6
DUAL DRUG PACLITAXEL & TRIFUSAL INPOLIMER DUAL DRUG CORONARY STENTS – US FDA APPROVED Technical Specification as per Annexure-6
DUAL DRUG PACLITAXEL & TRIFUSAL INPOLIMER DUAL DRUG CORONARY STENTS – CE APPROVED Technical Specification as per Annexure-6
DUAL DRUG PACLITAXEL & TRIFUSAL INPOLIMER DUAL DRUG CORONARY STENTS – DCGI APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT –US FDA APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT – CE APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT – DCGI APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH CONTINUOUS SINOSODIAL TECHNOLOGY AND MICRO TRACK CATHETER – US FDA APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH CONTINUOUS SINOSODIAL TECHNOLOGY AND MICRO TRACK CATHETER – CE APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH CONTINUOUS SINOSODIAL TECHNOLOGY AND MICRO TRACK CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH > 120 DAYS DRUG ELUTION – US FDA APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH > 120 DAYS DRUG ELUTION – CE APPROVED Technical Specification as per Annexure-6
ZOTRALIMUS COATED DRUG ELUTING CORONARY STENT WITH > 120 DAYS DRUG ELUTION – DCGI APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED DRUG STENT – US FDA APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED DRUG STENT – CE APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED DRUG STENT – DCGI APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED POLIMER FREE DRUG STENT – US FDA APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED POLIMER FREE DRUG STENT – CE APPROVED Technical Specification as per Annexure-6
TACROLIMUS COATED POLIMER FREE DRUG STENT – DCGI APPROVED Technical Specification as per Annexure-6
SIROLIMUS ELUTING CORONARY STENT WITH BIODEGRADABLE POLYMER MOUNTED ON D.E. BALLOON (SIROLIMUS) – CE APPROVED Technical Specification as per Annexure-6
SIROLIMUS ELUTING CORONARY STENT WITH BIODEGRADABLE POLYMER MOUNTED ON D.E. BALLOON (SIROLIMUS) – US FDA APPROVED Technical Specification as per Annexure-6
SIROLIMUS ELUTING CORONARY STENT WITH BIODEGRADABLE POLYMER MOUNTED ON D.E. BALLOON (SIROLIMUS) – DCGI APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM – CE APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM – US FDA APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM – DCGI APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON NITINOL PLATFORM- CE APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON NITINOL PLATFORM –US FDA APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON NITINOL PLATFORM- DCGI APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT WITH AN ABLUMINAL BIODEGRADABLE POLYMER – CE APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT WITH AN ABLUMINAL BIODEGRADABLE POLYMER – FDA APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT WITH AN ABLUMINAL BIODEGRADABLE POLYMER – DCGI APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM, ABLUMINAL COATING - CE APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM, ABLUMINAL COATING - US FDA APPROVED Technical Specification as per Annexure-6
BIOLIMUS DRUG ELUTING STENT ON STAINLESS STEEL PLATFORM, ABLUMINAL COATING - DCGI APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH CO. CR. PLATFORM & BIODEGRADABLE POLYMER – CE APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH CO. CR. PLATFORM & BIODEGRADABLE POLYMER – US FDA APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH CO. CR. PLATFORM & BIODEGRADABLE POLYMER – DCGI APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH NITINOL PLATFORM & BIODEGRADABLE POLYMER – CE APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH NITINOL PLATFORM & BIODEGRADABLE POLYMER – US FDA APPROVED Technical Specification as per Annexure-6
DEDICATED BIFURCATION STENT WITH NITINOL PLATFORM & BIODEGRADABLE POLYMER – DCGI APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT (BIODEGRADABLE) - CE APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT (BIODEGRADABLE) - US FDA APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT (BIODEGRADABLE) – DCGI APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT BALLOON MOUNTED - CE APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT BALLOON MOUNTED - US FDA APPROVED Technical Specification as per Annexure-6
BIFURCATION DES STENT BALLOON MOUNTED – DCGI APPROVED Technical Specification as per Annexure-6
Drug eluting stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly -caprolactone(PCL) for accelerated and low concentration Sirolimus with Abluminal and specialized gradient coating .(Japan PMDA approved)- DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
Drug eluting stent with cobalt chromium platform - DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
SIROLIMUS ELUTING COBALT CHROMIUM PLATFORM, BIODEGRADABLE POLYMER, AND MICROPORUS SURFACE WITH SOFT COATING OF SHELLAC RASIN. Technical Specification as per Annexure-6
SIROLIMUS CLUTING, STAINLESS STEEL PLATFORM, BIODEGRADABLE POLYMER, MICROPORUS SURFACE WITH SOFT COATING OF SHELLAC RASIN WITH TEMPERATURE CONTROL PACKING & TEMPERATURE SENSITIVE CHECK METER. - DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
SIROLIMUS eluting biodegradable polymer (PLA) with Abluminal coating and 86 microns COBALT CHROMIUM PLATFORM with 10 microns polymer thickness embedded in 10 microns groves (IN-GROOVE TECHNOLOGY), which are created on the strut itself and close to 80 percent strut surface free of polymer and drug. – DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
SIROLIMUS eluting biodegradable polymer (PLA) with Abluminal coating and 86 microns COBALT CHROMIUM PLATFORM with 10 microns polymer thickness embedded in 10 microns groves (IN-GROOVE TECHNOLOGY), which are created on the strut itself and close to 80 percent strut surface free of polymer and drug. – DCGI With US FDA / CE Approved. Technical Specification as per Annexure-7
Sirolimus eluting Bio-Resorable scaffold Stent System - DCGI With US FDA / CE Approved Technical Specification as per Annexure-8
BA9 (Biolimus) Drug Polymer Free drug eluting stent with ultra short DAPT of 1 month as per ESC Guiding – DCGI With US FDA / CE Approved. Technical Specification as per Annexure-9
BA9 (Biolimus) Drug Polymer Free drug eluting stent – DCGI With US FDA / CE Approved. Technical Specification as per Annexure-10
Low Dose Sirolimus Eluting Stent- DCGI with US FDA /CE Approved Technical Specification as per Annexure-11
Sirolimus Drug Eluting Bifurcation Stent - DCGI with US FDA /CE Approved On Cobalt Chromium Platform and Biodegradable biocompatible Technical Specification as per Annexure-12
Sirolimus Drug Eluting Side branch Stent - DCGI with US FDA /CE Approved Technical Specification as per Annexure-13
Dual Drug Polymer free drug Eluting Stent - DCGI with US FDA /CE Approved Technical Specification as per Annexure-14
Sirolimus Eluting Stent – Cobalt chromium platform, Biostable polymer (Polysulfone polymer) provide uniform drug encapsulation and release. - DCGI APPROVED Technical Specification as per Annexure-15
Sirolimus Eluting Stent – Cobalt chromium platform, Biodegradable polymer matrix (PLGA polymer) with sirolimus drug open cell design with 3 interlinks per segment. - DCGI APPROVED Technical Specification as per Annexure-17
Group C-9 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
BALLOON EXPANDABLE PULMONARY ARTERY STENTS – US FDA APPROVED Technical Specification as per Annexure-18
BALLOON EXPANDABLE PERIPHERAL COVERED STENTS – CE APPROVED Technical Specification as per Annexure-19
BALLOON EXPANDABLE PULMONARY ARTERY STENTS – DCGI APPROVED Technical Specification as per Annexure-20
SELF EXPANDABLE PULMONARY ARTERY STENTS – US FDA APPROVED Technical Specification as per Annexure-21
SELF EXPANDABLE PULMONARY ARTERY STENTS – CE APPROVED Technical Specification as per Annexure-6
SELF EXPANDABLE PULMONARY ARTERY STENTS – DCGI APPROVED Technical Specification as per Annexure-6
IVC STENTS SELF EXPENDABLE - US FDA APPROVED Technical Specification as per Annexure-6
IVC STENTS SELF EXPENDABLE - CE APPROVED Technical Specification as per Annexure-6
IVC STENTS SELF EXPENDABLE – DCGI APPROVED Technical Specification as per Annexure-6
IVC STENTS BALLOON MOUNTED - US FDA APPROVED Technical Specification as per Annexure-6
IVC STENTS BALLOON MOUNTED - CE APPROVED Technical Specification as per Annexure-6
IVC STENTS BALLOON MOUNTED - DCGI APPROVED Technical Specification as per Annexure-6
PVA particles with consistent sized Particles - DCGI with US FDA/ CE APPROVED Technical Specification as per Annexure-6
Group C-10 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
STENTS WITH EPC CAPTURING TECHNOLOGY - US FDA APPROVED Technical Specification as per Annexure-6
STENTS WITH EPC CAPTURING TECHNOLOGY - CE APPROVED Technical Specification as per Annexure-6
STENTS WITH EPC CAPTURING TECHNOLOGY – DCGI APPROVED Technical Specification as per Annexure-6
BIODEGRADABLE CORONARY STENTS - US FDA APPROVED Technical Specification as per Annexure-6
BIODEGRADABLE CORONARY STENTS - CE APPROVED Technical Specification as per Annexure-6
BIODEGRADABLE CORONARY STENTS – DCGI APPROVED Technical Specification as per Annexure-6
TAPERED CORONARY STENT (DE) – US FDA APPROVED Technical Specification as per Annexure-6
TAPERED CORONARY STENT (DE) – CE APPROVED Technical Specification as per Annexure-6
TAPERED CORONARY STENT (DE) –DCGI APPROVED Technical Specification as per Annexure-6
TAPERED CAROTID STENT – US FDA APPROVED Technical Specification as per Annexure-6
TAPERED CAROTID STENT – CE APPROVED Technical Specification as per Annexure-6
TAPERED CAROTID STENT – DCGI APPROVED Technical Specification as per Annexure-6
DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CORONARY FILTER – US FDA/CE APPROVED Technical Specification as per Annexure-6
DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CORONARY FILTER – DCGI APPROVED Technical Specification as per Annexure-6
DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CAROTID ARTERY FILTER – US FDA/CE APPROVED Technical Specification as per Annexure-6
DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CAROTID ARTERY FILTER – DCGI APPROVED Technical Specification as per Annexure-6
DRUG ELUTING STENT FOR BELOW THE KNEE PERIPHERAL ARTERY – US FDA / CE APPROVED Technical Specification as per Annexure-6
DRUG ELUTING STENT FOR BELOW THE KNEE PERIPHERAL ARTERY – DCGI APPROVED Technical Specification as per Annexure-6
Group C-11 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
SPECIAL MICRO-CATHETER FOR CTO RETROGRADE APPROACH - US FDA APPROVED Technical Specification as per Annexure-6
SPECIAL MICRO-CATHETER FOR CTO RETROGRADE APPROACH - CE APPROVED Technical Specification as per Annexure-6
SPECIAL MICRO-CATHETER FOR CTO RETROGRADE APPROACH – DCGI APPROVED Technical Specification as per Annexure-6
IABP CATHETER WITH ACCESSORIES - US FDA APPROVED Technical Specification as per Annexure-6
IABP CATHETER WITH ACCESSORIES - CE APPROVED Technical Specification as per Annexure-6
IABP CATHETER WITH ACCESSORIES – DCGI APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - US FDA APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - CE APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA -DCGI APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH DISTAL BALLOON OCCLUSION AND AUTOMATED SUCTION DURING PTCA - US FDA APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH DISTAL BALLOON OCCLUSION AND AUTOMATED SUCTION DURING PTCA - CE APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH DISTAL BALLOON OCCLUSION AND AUTOMATED SUCTION DURING PTCA -DCGI APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MOTORIZED CUTTING AND SUCTION DURING PTCA - US FDA APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MOTORIZED CUTTING AND SUCTION DURING PTCA - CE APPROVED Technical Specification as per Annexure-6
THROMBECTOMY CATHETERS WITH MOTORIZED CUTTING AND SUCTION DURING PTCA - DCGI APPROVED Technical Specification as per Annexure-6
DOPPLER WIRE FOR PTCA - US FDA APPROVED Technical Specification as per Annexure-6
DOPPLER WIRE FOR PTCA - CE APPROVED Technical Specification as per Annexure-6
DOPPLER WIRE FOR PTCA – DCGI APPROVED Technical Specification as per Annexure-6
PRESSURE WIRE FOR PTCA - US FDA APPROVED Technical Specification as per Annexure-6
PRESSURE WIRE FOR PTCA - CE APPROVED Technical Specification as per Annexure-6
PRESSURE WIRE FOR PTCA – DCGI APPROVED Technical Specification as per Annexure-6
Group C-12 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
EMBOLIC PROTECTION DEVICES BASED ON FILTER TECHNOLOGY/MECHANISM - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES BASED ON FILTER TECHNOLOGY/MECHANISM - CE APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES BASED ON FILTER TECHNOLOGY/MECHANISM - DCGI APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY - CE APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY – DCGI APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH PROXIMAL BALLOON OCCLUSIVE TECHONOLOGY - US FDA APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH PROXIMAL BALLOON OCCLUSIVE TECHONOLOGY - CE APPROVED Technical Specification as per Annexure-6
EMBOLIC PROTECTION DEVICES WITH PROXIMAL BALLOON OCCLUSIVE TECHONOLOGY –DCGI APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – COLLAGEN PLUG BASED - US FDA APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – COLLAGEN PLUG BASED - CE APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – COLLAGEN PLUG BASED – DCGI APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – SUTURE BASED - US FDA APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – SUTURE BASED - CE APPROVED Technical Specification as per Annexure-6
ARTERIAL PUNCTURE CLOSURE DEVICES – SUTURE BASED –DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE FEMORAL COMPRESSION DEVICES – BALLOON BASED COMPRESSION - US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE FEMORAL COMPRESSION DEVICES – BALLOON BASED COMPRESSION - CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE FEMORAL COMPRESSION DEVICES – BALLOON BASED COMPRESSION – DCGI APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – BALLOON BASED COMPRESSION - US FDA APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – BALLOON BASED COMPRESSION - CE APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – BALLOON BASED COMPRESSION – DCGI APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – STRAP BASED COMPRESSION - US FDA APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – STRAP BASED COMPRESSION - CE APPROVED Technical Specification as per Annexure-6
COMPRESSION DEVICES FOR RADIAL ARTERY – STRAP BASED COMPRESSION – DCGI APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE RE-ENTRY CATHETER FOR CTO - US FDA APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE RE-ENTRY CATHETER FOR CTO - CE APPROVED Technical Specification as per Annexure-6
PTCA GUIDE WIRE RE-ENTRY CATHETER FOR CTO – DCGI APPROVED Technical Specification as per Annexure-6
CORONARY MICROCATHETER – US FDA APPROVED - US FDA APPROVED Technical Specification as per Annexure-6
CORONARY MICROCATHETER – CE APPROVED - CE APPROVED Technical Specification as per Annexure-6
CORONARY MICROCATHETER – DCGI APPROVED Technical Specification as per Annexure-6
Distal embolic protection device - US FDA APPROVED Technical Specification as per Annexure-6
Distal embolic protection device - CE APPROVED Technical Specification as per Annexure-6
Distal embolic protection device - DCGI APPROVED Technical Specification as per Annexure-6
Group C-13 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retro-grade approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide-wire for retrograde approach & – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide-wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & –DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –DCGI APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – CE APPROVED Technical Specification as per Annexure-6
Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED Technical Specification as per Annexure-6
Group C-14 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
High Pressure Angioplasty Balloon for peripheral vascular use – US FDA APPROVED Technical Specification as per Annexure-6
High Pressure Angioplasty Balloon for peripheral vascular use – CE APPROVED Technical Specification as per Annexure-6
High Pressure Non Compliant Balloon – DCGI APPROVED Technical Specification as per Annexure-6
High Pressure PTA Balloon For peripheral use – US FDA APPROVED Technical Specification as per Annexure-6
High Pressure Semi Compliant Balloon – CE APPROVED Technical Specification as per Annexure-6
High Pressure Angioplasty Balloon for peripheral vascular use – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Cutting Balloon catheter – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Cutting Balloon catheter – CE APPROVED Technical Specification as per Annexure-6
Peripheral Cutting Balloon catheter – DCGI APPROVED Technical Specification as per Annexure-6
Balloon in Balloon Catheter (BIB)- DCGI with US FDA /CE Approved Technical Specification as per Annexure-6
Semi Compliant Coronary balloon System OTW – DCGI with US FDA/ CE Approved Technical Specification as per Annexure-6
Semi Compliant Coronary balloon System OTW/ Monorail – DCGI with US FDA/ CE Approved Technical Specification as per Annexure-6
Semi Compliant Coronary balloon System– DCGI with US FDA/ CE Approved Technical Specification as per Annexure-6
Non Compliant Coronary Balloon System– DCGI with US FDA/ CE Approved Technical Specification as per Annexure-6
Sirolimus Eluting PTCA Balloon – DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Thrombo Suction Catheter - DCGI With US FDA / CE Approved. Technical Specification as per Annexure-6
Large Diameter PTA Balloon for Peripheral Use - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Plaque Modification device for Highly calcified lesions - DCGI With US FDA / CE Approved Technical Specification as per Annexure-6
Group C-15 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Peripheral Stent Balloon expandable (OTW/RX) – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable (OTW/RX) – CE APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable (OTW/RX) – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – CE APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – CE APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – CE APPROVED Technical Specification as per Annexure-6
Peripheral Stent Balloon expandable – (OTW/RX) – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Self expandable interwoven nitinol stent for popliteal artery – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Self expandable interwoven nitinol stent for popliteal artery – CE APPROVED Technical Specification as per Annexure-6
Peripheral Self expandable interwoven nitinol stent for popliteal artery –DCGI APPROVED Technical Specification as per Annexure-6
Group C-16 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent with tapered diameter – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent with tapered diameter – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent with tapered diameter – DCGI APPROVED Technical Specification as per Annexure-6
Balloon mounted stent with tapered diameter – US FDA APPROVED Technical Specification as per Annexure-6
Balloon mounted stent with tapered diameter for peripheral use – CE APPROVED Technical Specification as per Annexure-6
Balloon mounted stent with tapered diameter –DCGI APPROVED Technical Specification as per Annexure-6
Group C-17 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Self-Expanding peripheral stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent of large diameter – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent of large diameter – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral stent of large diameter – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral Drug eluting stent – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral Drug eluting stent – CE APPROVED Technical Specification as per Annexure-6
Peripheral Drug eluting stent – DCGI APPROVED Technical Specification as per Annexure-6
Peripheral bio-degradable or absorbable metal stent – US FDA APPROVED Technical Specification as per Annexure-6
Peripheral bio-degradable or absorbable metal stent – CE APPROVED Technical Specification as per Annexure-6
Peripheral bio-degradable or absorbable metal stent – DCGI APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral covered Stent – US FDA APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral covered Stent – CE APPROVED Technical Specification as per Annexure-6
Self-Expanding peripheral covered Stent –DCGI APPROVED Technical Specification as per Annexure-6
Venous Stent - DCGI With US FDA /CE Approved Technical Specification as per Annexure-6
Aortic Stent Graft – DCGI with US FDA / CE Approved Technical Specification as per Annexure-6
Group C-18 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/ SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
CAROTID SELF EXPENDABLE STENTS – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – CE APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – CE APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – CE APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – CE APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – CE APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – CE APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE STENT WITH TAPERED DIAMETER – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE STENT WITH TAPERED DIAMETER – CE APPROVED Technical Specification as per Annexure-6
CAROTID STENTS BALLOON EXPENDABLE STENT WITH TAPERED DIAMETER – DCGI APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER – US FDA APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER –CE APPROVED Technical Specification as per Annexure-6
CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER –DCGI APPROVED Technical Specification as per Annexure-6
Group C-19 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
IVC Filter – US FDA APPROVED Technical Specification as per Annexure-6
IVC Filter – CE APPROVED Technical Specification as per Annexure-6
IVC Filter – DCGI APPROVED Technical Specification as per Annexure-6
IVC Filter – US FDA APPROVED Technical Specification as per Annexure-6
IVC Filter – CE APPROVED Technical Specification as per Annexure-6
IVC Filter – DCGI APPROVED Technical Specification as per Annexure-6
IVC Filter – US FDA APPROVED Technical Specification as per Annexure-6
IVC Filter – CE APPROVED Technical Specification as per Annexure-6
IVC Filter – DCGI APPROVED Technical Specification as per Annexure-6
Group C-20 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Endovascular stent graft device for treatment of thoracic aortic aneurysms and dissections - US FDA APPROVED Technical Specification as per Annexure-6
Endovascular stent graft device for treatment of thoracic aortic aneurysms and dissections - CE APPROVED Technical Specification as per Annexure-6
Endovascular stent graft device for treatment of thoracic aortic aneurysms and dissections – DCGI APPROVED Technical Specification as per Annexure-6
Endovascular stent graft device for treatment of abdominal aortic aneurysms - US FDA APPROVED Technical Specification as per Annexure-6
Endovascular stent graft device for treatment of abdominal aortic aneurysms - CE APPROVED Technical Specification as per Annexure-6
Endovascular stent graft device for treatment of abdominal aortic aneurysms – DCGI APPROVED Technical Specification as per Annexure-6
Group C-21 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
RENAL DENERVATION DEVICE FOR RF ABLATION OF RENAL – CE / US FDA APPROVED Technical Specification as per Annexure-6
RENAL DENERVATION DEVICE FOR RF ABLATION OF RENAL –DCGI APPROVED Technical Specification as per Annexure-6
ASPIRATION DEVICE – CE APPROVED Technical Specification as per Annexure-6
ASPIRATION DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
ASPIRATION DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED – CE APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED – US FDA APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED – DCGI APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED– CE APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED – US FDA APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED– DCGI APPROVED Technical Specification as per Annexure-6
AMPLATZER PLUG – CE APPROVED Technical Specification as per Annexure-6
AMPLATZER PLUG – US FDA APPROVED Technical Specification as per Annexure-6
AMPLATZER PLUG – DCGI APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APENDAGE CLOSURE DEVICE – CE APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APENDAGE CLOSURE DEVICE –US FDA APPROVED Technical Specification as per Annexure-6
LEFT ATRIAL APENDAGE CLOSURE DEVICE – DCGI APPROVED Technical Specification as per Annexure-6
ABOVE KNEE AND BELLOW KNEE DIRECTIONAL ATHRECTOMY DEVICE – CE APPROVED Technical Specification as per Annexure-6
ABOVE KNEE AND BELLOW KNEE DIRECTIONAL ATHRECTOMY DEVICE – US FDA APPROVED Technical Specification as per Annexure-6
ABOVE KNEE AND BELLOW KNEE DIRECTIONAL ATHRECTOMY DEVICE –DCGI APPROVED Technical Specification as per Annexure-6
SNARE FOR CARDIOVASCULAR PURPOSE – US FDA/CE APPROVED Technical Specification as per Annexure-6
SNARE FOR CARDIOVASCULAR PURPOSE – DCGI APPROVED Technical Specification as per Annexure-6
SNARE FOR PERIFERAL USE – US FDA/CE APPROVED Technical Specification as per Annexure-6
SNARE FOR PERIFERAL USE – DCGI APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – BRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – BRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – UN BRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – UN BRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH UPTO 90 CM - BRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH UPTO 90 CM - BRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH UPTO 90 CM - UNBRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
LONG ARTRIAL SHEETH UPTO 90 CM - UNBRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
CROSS – OVER SHEETH - BRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
CROSS – OVER SHEETH - BRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
CROSS – OVER SHEETH - UNBRAIDED – US FDA/ CE APPROVED Technical Specification as per Annexure-6
CROSS – OVER SHEETH - UNBRAIDED – DCGI APPROVED Technical Specification as per Annexure-6
VISCERAL TYPE CATHETER – US FDA/ CE APPROVED Technical Specification as per Annexure-6
VISCERAL TYPE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
HEAD HUNTER TYPE CATHETER – US FDA/ CE APPROVED Technical Specification as per Annexure-6
HEAD HUNTER TYPE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
VTK TYPE CATHETER – US FDA/ CE APPROVED Technical Specification as per Annexure-6
VTK TYPE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
SIMMONS TYPE CATHETER – US FDA/ CE APPROVED Technical Specification as per Annexure-6
SIMMONS TYPE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
COBRA TYPE CATHETER – US FDA/ CE APPROVED Technical Specification as per Annexure-6
COBRA TYPE CATHETER – DCGI APPROVED Technical Specification as per Annexure-6
ACT TUBES FOR ACT MACHINE (MEDTRONIC ACT 200 MODEL)- US FDA/ CE APPROVED Technical Specification as per Annexure-6
ACT TUBES FOR ACT MACHINE (MEDTRONIC ACT 200 MODEL)- DCGI APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED BALLOON MOUNTED – CE APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED BALLOON MOUNTED – US FDA APPROVED Technical Specification as per Annexure-6
C.P. STENT COVERED BALLOON MOUNTED – DCGI APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED BALLOON MOUNTED – CE APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED BALLOON MOUNTED – US FDA APPROVED Technical Specification as per Annexure-6
C.P. STENT UNCOVERED BALLOON MOUNTED – DCGI APPROVED Technical Specification as per Annexure-6
Abdominal stent graft for treating Aortic Aneurysm– US FDA APPROVED Technical Specification as per Annexure-6
Abdominal stent graft for treating Aortic Aneurysm– CE APPROVED Technical Specification as per Annexure-6
Abdominal stent graft for treating Aortic Aneurysm– DCGI APPROVED Technical Specification as per Annexure-6
Thorosic stent graft for treating Thorasic Aneurysm and Thorosic dissection – US FDA APPROVED Technical Specification as per Annexure-6
Thorosic stent graft for treating Thorosic Aneurysm and Thorosic dissection– CE APPROVED Technical Specification as per Annexure-6
Thorosic stent graft for treating Thorosic Aneurysm and Thorosic dissection– DCGI APPROVED Technical Specification as per Annexure-6
Covered Aortic stent balloon mounted - US FDA APPROVED Technical Specification as per Annexure-6
Covered Aortic stent balloon mounted – CE Approved Technical Specification as per Annexure-6
Covered Aortic stent balloon mounted (Andra Stent Type) – DCGI Approved Technical Specification as per Annexure-6
Non-Covered Aortic stent balloon mounted - US FDA APPROVED Technical Specification as per Annexure-6
Non-Covered Aortic stent balloon mounted – CE Approved Technical Specification as per Annexure-6
Non-Covered Aortic stent balloon mounted (Endra Stent Type)– DCGI Approved Technical Specification as per Annexure-6
Group D-1 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
TEMPORARY PACING LEADS - US FDA APPROVED Technical Specification as per Annexure-6
TEMPORARY PACING LEADS - CE APPROVED Technical Specification as per Annexure-6
TEMPORARY PACING LEADS – DCGI APPROVED Technical Specification as per Annexure-6
TEMPORARY PACING LEADS: BALLOON FLOATABLE – US FDA APPROVED Technical Specification as per Annexure-6
TEMPORARY PACING LEADS: BALLOON FLOATABLE – CE APPROVED Technical Specification as per Annexure-6
TEMPORARY PACING LEADS: BALLOON FLOATABLE – DCGI APPROVED Technical Specification as per Annexure-6
RADIO FREQUENCY ABLATION CATHETER (7F,8MM)- Assorted Curves – US FDA APPROVED Technical Specification as per Annexure-6
RADIO FREQUENCY ABLATION CATHETER FOR VERICOSE VEIN – CE APPROVED Technical Specification as per Annexure-6
RADIO FREQUENCY ABLATION CATHETER (7F,4MM)- Assorted Curves – US FDA APPROVED Technical Specification as per Annexure-6
BIDIRECTIONAL ABLATION CATHETER 8MM- Assorted Curves - CE APPROVED/ US FDA APPROVED Technical Specification as per Annexure-6
M.F.M. DEVICE FOR AAA GRAFT STENT – US FDA APPROVED Technical Specification as per Annexure-6
M.F.M. DEVICE FOR AAA GRAFT STENT – CE APPROVED Technical Specification as per Annexure-6
M.F.M. DEVICE FOR AAA GRAFT STENT – DCGI APPROVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION BRANCHED ANDOGRAFT – US FDA APPRVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION BRANCHED ANDOGRAFT – CE APPRVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION BRANCHED ANDOGRAFT – DCGI APPRVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION CHIMNEY ANDOGRAFT – US FDA APPRVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION CHIMNEY ANDOGRAFT – CE APPRVED Technical Specification as per Annexure-6
AAA GRAFT STENT FOR AORTIC DISSECTION CHIMNEY ANDOGRAFT – DCGI APPRVED Technical Specification as per Annexure-6
AORTIC CUFFS – US FDA APPROVED Technical Specification as per Annexure-6
AORTIC CUFFS – CE APPROVED Technical Specification as per Annexure-6
AORTIC CUFFS – DCGI APPROVED Technical Specification as per Annexure-6
AORTIC STEPLES – US FDA APPROVED Technical Specification as per Annexure-6
AORTIC STEPLES –CE APPROVED Technical Specification as per Annexure-6
AORTIC STEPLES –DCGI APPROVED Technical Specification as per Annexure-6
O.C.T. CATHETERS FOR CORONARY ARTRIES – US FDA APPROVED Technical Specification as per Annexure-6
O.C.T. CATHETERS FOR CORONARY ARTRIES – US FDA APPROVED Technical Specification as per Annexure-6
O.C.T. CATHETERS FOR CORONARY ARTRIES – DCGI APPROVED Technical Specification as per Annexure-6
Pacing Lead retrievable system for P.P.I pacing leads – DCGI approved with US FDA/CE Approved Technical Specification as per Annexure-6
Group D-2 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/ SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVEDINTRODUCER SHEATHS FOR ELECTROPHYSIOLOGY Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
PACING LEAD STABLIZERS- US FDA APPROVED Technical Specification as per Annexure-6
PACING LEAD STABLIZERS- CE APPROVED Technical Specification as per Annexure-6
PACING LEAD STABLIZERS- DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC)- CE APPROVED Technical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC)- US FDA APPROVED Technical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC)- DCGI APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING- CE APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING- US FDA APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING- DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS -DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS -DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
PACING LEAD STABLIZERS- CE APPROVED Technical Specification as per Annexure-6
PACING LEAD STABLIZERS- US FDA APPROVED APPROVEDTechnical Specification as per Annexure-6
PACING LEAD STABLIZERS- DCGI APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - CE APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - US FDA APPROVED Technical Specification as per Annexure-6
LONG SHEATHS/INTRODUCERS - DCGI APPROVED Technical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC) - CE APPROVED APPROVEDTechnical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC) – US FDA APPROVED Technical Specification as per Annexure-6
SURFACE PATCH FOR 3 D MAPPING – NAV X (ADULT & PEDIATRIC) - DCGI APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING - CE APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING – US FDA APPROVED Technical Specification as per Annexure-6
BALLOON CATHETER FOR NON-CONTACT 3 D MAPPING – DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS -DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS -DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS -DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS -DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - CE APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
DIAGNOSTIC EP CATHETERS - DCGI APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK - CE APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – US FDA APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – DCGI APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK - CE APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – US FDA APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – DCGI APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK - CE APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – US FDA APPROVED Technical Specification as per Annexure-6
EP CATHETERS FOR PEDIATRIC EP WORK – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS – DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS - CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS –DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- DCGI APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN EP DIAGNOSTIC CATHETERS- DCGI APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS-DCGI APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- DCGI APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- CE APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- US FDA APPROVED Technical Specification as per Annexure-6
WOVEN PEDIATRIC EP CATHETERS- DCGI APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA - CE APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – US FDA APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – DCGI APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA - CE APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – US FDA APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – DCGI APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA - CE APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – US FDA APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – DCGI APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA - CE APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – US FDA APPROVED Technical Specification as per Annexure-6
CABLES FOR EP & RFA – DCGI APPROVED Technical Specification as per Annexure-6
3-D BRAIDED STEERABLE GUIDING INTRODUCER SHEATH, SUPPORTING TRANSSEPTAL - DCGI & US FDA/CE approved Technical Specification as per Annexure-6
Group –D-3 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA SPECIAL CATHETERS FOR AF, FLUTTER ETC (ITEMS 1-9) (quote all diameters, French size, different electrodes like Platinum, Paladium or stainless steel) All items should be compitable with existing EP RFA (BARD) Machine in Cath Lab, SMSH
DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- CE APPROVED Technical Specification as per Annexure-6
DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- US FDA APPROVED Technical Specification as per Annexure-6
DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- DCGI APPROVED Technical Specification as per Annexure-6
DEFLECTABLE DECAPOLAR (10) (PULM. VEIN) --- all diameters- CE APPROVED Technical Specification as per Annexure-6
DEFLECTABLE BIDIRECTIONAL RADIO FREQUENCY ABLATION CATHETER WITH CONNECTOR (7f,4MM) --- Med/ Large/Extra Large Curve- US FDA APPROVED Technical Specification as per Annexure-6
DEFLECTABLE DECAPOLAR (10) (PULM. VEIN) --- all diameters- DCGI APPROVED Technical Specification as per Annexure-6
DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- CE APPROVED Technical Specification as per Annexure-6
DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- US FDA APPROVED Technical Specification as per Annexure-6
DEFELCTABLE IRRIGATED ABLATION CATHETER WITH 6 PORT . (4MM)MED/LARGE/EXTRA LARGE CURVE Technical Specification as per Annexure-6
DEFLECTABLE RADIO FREQUENCY ABLATION CATHETER (7F,4MM) 2-5-2 ELECTRODE SPACING-TYPE SMALL/MEDIUM/LARGE CUR -CE APPROVED Technical Specification as per Annexure-6
DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- DCGI APPROVED Technical Specification as per Annexure-6
2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature- CE APPROVED Technical Specification as per Annexure-6
2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature- US FDA APPROVED Technical Specification as per Annexure-6
2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature-DCGI APPROVED Technical Specification as per Annexure-6
BASKET CATHETER WITH ACCESSORY- CE APPROVED Technical Specification as per Annexure-6
BASKET CATHETER WITH ACCESSORY- US FDA APPROVED Technical Specification as per Annexure-6
BASKET CATHETER WITH ACCESSORY- DCGI APPROVED Technical Specification as per Annexure-6
CRISTA CATHETER WITH ACCESSORY- CE APPROVED Technical Specification as per Annexure-6
CRISTA CATHETER WITH ACCESSORY- US FDA APPROVED Technical Specification as per Annexure-6
CRISTA CATHETER WITH ACCESSORY- DCGI APPROVED Technical Specification as per Annexure-6
PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- CE APPROVED Technical Specification as per Annexure-6
PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- US FDA APPROVED Technical Specification as per Annexure-6
PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECT. DECADUAPOLAR (20 poles) FOR A FLUTTER ---- all diameters- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECTABLE DECAPOLAR (10) (PULM. VEIN) --- all diameters- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECTABLE DECAPOLAR (10) (PULM. VEIN) --- all diameters- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFLECTABLE DECAPOLAR (10) (PULM. VEIN) --- all diameters-DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS DEFECTABLE DECADUAPOLAR (20) (PULM. VEIN) --- all diameters- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS 2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS 2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS 2F MULTIPOLAR (> TEN electrodes) for mapping through coronary vasculature- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS BASKET CATHETER WITH ACCESSORY- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS BASKET CATHETER WITH ACCESSORY- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS BASKET CATHETER WITH ACCESSORY- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS CRISTA CATHETER WITH ACCESSORY- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS CRISTA CATHETER WITH ACCESSORY- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS CRISTA CATHETER WITH ACCESSORY- DCGI APPROVED Technical Specification as per Annexure-6
PAEDIATRICS PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- CE APPROVED Technical Specification as per Annexure-6
PAEDIATRICS PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- US FDA APPROVED Technical Specification as per Annexure-6
PAEDIATRICS PACING CATHETER WITH ANGIOGROPHIC CAPABILITY- DCGI APPROVED Technical Specification as per Annexure-6
PEDIATRIC USE : ALL THE ABOVE CATHETERS, SHEATHS etc FOR PEDIATRIC USE. - CE APPROVED Technical Specification as per Annexure-6
PEDIATRIC USE : ALL THE ABOVE CATHETERS, SHEATHS etc FOR PEDIATRIC USE. – US FDA APPROVED Technical Specification as per Annexure-6
PEDIATRIC USE : ALL THE ABOVE CATHETERS, SHEATHS etc FOR PEDIATRIC USE. – DCGI APPROVED Technical Specification as per Annexure-6
Pentapolar Diagnostic Catheter – Fixed Curve US FDA APPROVED Technical Specification as per Annexure-6
Pentapolar Diagnostic Catheter – Fixed Curve CE APPROVED Technical Specification as per Annexure-6
Pentapolar Diagnostic Catheter – Fixed Curve DCGI APPROVED Technical Specification as per Annexure-6
Octapolar Diagnostic Catheter – Fixed Curve US FDA APPROVED Technical Specification as per Annexure-6
Octapolar Diagnostic Catheter – Fixed Curve CE APPROVED Technical Specification as per Annexure-6
Octapolar Diagnostic Catheter – Fixed Curve DCGI APPROVED Technical Specification as per Annexure-6
16 Pole Diagnostic Catheter – Fixed Curve US FDA APPROVED Technical Specification as per Annexure-6
16 Pole Diagnostic Catheter – Fixed Curve CE APPROVED Technical Specification as per Annexure-6
16 Pole Diagnostic Catheter – Fixed Curve DCGI APPROVED Technical Specification as per Annexure-6
20 Pole Diagnostic Catheter – Fixed Curve US FDA APPROVED Technical Specification as per Annexure-6
20 Pole Diagnostic Catheter – Fixed Curve CE APPROVED Technical Specification as per Annexure-6
20 Pole Diagnostic Catheter – Fixed Curve - DCGI APPROVED Technical Specification as per Annexure-6
24 Pole Diagnostic Catheter – Fixed Curve- US FDA APPROVED Technical Specification as per Annexure-6
24 Pole Diagnostic Catheter – Fixed Curve– CE APPROVED Technical Specification as per Annexure-6
24 Pole Diagnostic Catheter – Fixed Curve – - DCGI APPROVED Technical Specification as per Annexure-6
Bi-Directional Steerable Catheters US FDA APPROVED Technical Specification as per Annexure-6
Bi-Directional Steerable Catheters - CE APPROVED Technical Specification as per Annexure-6
Bi-Directional Steerable Catheters DCGI APPROVED Technical Specification as per Annexure-6
Atrial Mapping Catheters - US FDA APPROVED Technical Specification as per Annexure-6
Atrial Mapping Catheters - CE APPROVED Technical Specification as per Annexure-6
Atrial Mapping Catheters - DCGI APPROVED Technical Specification as per Annexure-6
Dual Curve RF Ablation Catheter - US FDA APPROVED Technical Specification as per Annexure-6
Dual Curve RF Ablation Catheter - CE APPROVED Technical Specification as per Annexure-6
Dual Curve RF Ablation Catheter - DCGI APPROVED Technical Specification as per Annexure-6
Gorup – D-4 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) - US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 1-10) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) –DCGI APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) - CE APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – US FDA APPROVED Technical Specification as per Annexure-6
ABLATION CATHETERS (ITEMS 11-20) – DCGI APPROVED Technical Specification as per Annexure-6
Group - D-5 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA- CATHETERS, CABLES, ACCESSORIES FOR ENDOCARDIAL SOLUTIONS (ESI) ACCESSORIES
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – US FDA APPROVED Technical Specification as per Annexure-6
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – CE APPROVED Technical Specification as per Annexure-6
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – DCGI APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – US FDA APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – CE APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – DCGI APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – US FDA APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – CE APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – DCGI APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – US FDA APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – CE APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – DCGI APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – US FDA APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – CE APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – DCGI APPROVED Technical Specification as per Annexure-6
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – CE APPROVED Technical Specification as per Annexure-6
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – US FDA APPROVED Technical Specification as per Annexure-6
REUSABLE DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE DEFIBRILLATION / TRANSCUTANEOUS PACING PATCHES (suitable for Equipment in Cath lab) – DCGI APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – CE APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – US FDA APPROVED Technical Specification as per Annexure-6
DEFIBRILLATION/TRANSCUTANEOUS PACING PATCHES for USE IN INFANTS AND CHILDREN – DCGI APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – CE APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – US FDA APPROVED Technical Specification as per Annexure-6
CRYO CATHETERS (AND ACCESSORIES)FOR ABLATION OF ARRHYTHMIAS IN CHILDREN AND ADULTS – DCGI APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – CE APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – US FDA APPROVED Technical Specification as per Annexure-6
INTRACARDIAC ULTRASOUND/ ECHO CATHETER FOR GUIDING RFA COMPATIBLE WITH THE EXISTING ECHO MACHINE AT SMS HOSPITAL, JAIPUR (QUOTE ALL PRICES OF THE CATHETERS and ACCESSORIES) – DCGI APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – CE APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – US FDA APPROVED Technical Specification as per Annexure-6
DISPOSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – DCGI APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – CE APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – US FDA APPROVED Technical Specification as per Annexure-6
REUSABLE ELECTROCAUTERY PATCHES FOR RFA (SUITABLE FOR STOCKERT AND EPT 1000 ablators) – DCGI APPROVED Technical Specification as per Annexure-6
Group - D-6 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Regular Radiofrequency ablation catheter, 6/ 7 Fr. Size with 4 mm tip electrode and multiple curves with connector. – CE APPROVED Technical Specification as per Annexure-6
Regular Radiofrequency ablation catheter, 6/ 7 Fr. Size with 4 mm tip electrode and multiple curves with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Regular Radiofrequency ablation catheter, 6/ 7 Fr. Size with 4 mm tip electrode and multiple curves with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter deflectable curved, 7 Fr size with 8 mm tip electode with connector. – CE APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter deflectable curved, 7 Fr size with 8 mm tip electode with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter deflectable curved, 7 Fr size with 8 mm tip electode with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter Bi-directional deflectable curve, 7 Fr size with 8mm tip electrode with connector. – CE APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter Bi-directional deflectable curve, 7 Fr size with 8mm tip electrode with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Radiofrequency ablation catheter Bi-directional deflectable curve, 7 Fr size with 8mm tip electrode with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Regular Irrigated tip ablation catheter 7 Fr size with 3.5mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode connector. – CE APPROVED Technical Specification as per Annexure-6
Regular Irrigated tip ablation catheter 7 Fr size with 3.5mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode connector. – US FDA APPROVED Technical Specification as per Annexure-6
Regular Irrigated tip ablation catheter 7 Fr size with 3.5mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode connector. –DCGI APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with bidirectional deflectable curve, 7 Fr size with 3.5 mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode with connector. – CE APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with bidirectional deflectable curve, 7 Fr size with 3.5 mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with bidirectional deflectable curve, 7 Fr size with 3.5 mm tip electrode, 6 side-holes for open loop irrigation at the tip electrode with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with half the flow rate of regular irrigated cath deflectable curve, 7Fr size with 3.5mm tip electrode with connector. – CE APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with half the flow rate of regular irrigated cath deflectable curve, 7Fr size with 3.5mm tip electrode with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Irrigated tip ablation catheter with half the flow rate of regular irrigated cath deflectable curve, 7Fr size with 3.5mm tip electrode with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Irrigated Navigation System Catheters for Mapping and Ablation compatible with magnetic based 3D electro anatomical system (7.5 F) with connector. – CE APPROVED Technical Specification as per Annexure-6
Irrigated Navigation System Catheters for Mapping and Ablation compatible with magnetic based 3D electro anatomical system (7.5 F) with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Irrigated Navigation System Catheters for Mapping and Ablation compatible with magnetic based 3D electro anatomical system (7.5 F) with connector. –DCGI APPROVED Technical Specification as per Annexure-6
Variable loop pulmonary vein Catheter with connector. – CE APPROVED Technical Specification as per Annexure-6
Variable loop pulmonary vein Catheter with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Variable loop pulmonary vein Catheter with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Fixed Loop pulmonary vein Catheter with connector. – CE APPROVED Technical Specification as per Annexure-6
Fixed Loop pulmonary vein Catheter with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Fixed Loop pulmonary vein Catheter with connector. – DCGI APPROVED Technical Specification as per Annexure-6
External Disposable non-sterile gel electrode compatible to magnetic based 3D Mapping System. – CE APPROVED Technical Specification as per Annexure-6
External Disposable non-sterile gel electrode compatible to magnetic based 3D Mapping System. – US FDA APPROVED Technical Specification as per Annexure-6
External Disposable non-sterile gel electrode compatible to magnetic based 3D Mapping System. – DCGI APPROVED Technical Specification as per Annexure-6
Tubing for Irrigated Catheters compatible with pump available in Cath Lab SMS H. – CE APPROVED Technical Specification as per Annexure-6
Tubing for Irrigated Catheters compatible with pump available in Cath Lab SMS H. – US FDA APPROVED Technical Specification as per Annexure-6
Tubing for Irrigated Catheters compatible with pump available in Cath Lab SMS H. – DCGI APPROVED Technical Specification as per Annexure-6
Fixed curve Quadripolar Electrophysiology Catheter (6F,4MM)CRD,2MM ELECTRODE SPACING- CE APPROVED Technical Specification as per Annexure-6
Fixed curve Quadripolar Electrophysiology Catheter (all Curve, 5-7F) with connector. – US FDA APPROVED Technical Specification as per Annexure-6
Fixed curve Quadripolar Electrophysiology Catheter (all Curve, 5-7F) with connector. – DCGI APPROVED Technical Specification as per Annexure-6
Deflectable Quadripolar Electrophysiology Catheter (all curve, with connector). – CE APPROVED Technical Specification as per Annexure-6
Deflectable Quadripolar Electrophysiology Catheter (6F,4MM)CRD/JSN/DAO,2-5-2 MM Electrode Spacing with assorted curves and compatible connector. – US FDA APPROVED Technical Specification as per Annexure-6
Deflectable Quadripolar Electrophysiology Catheter (all curve, with connector). –DCGI APPROVED Technical Specification as per Annexure-6
Fixed curve Decapolar catheter for Coronary sinus mapping (all curve, 5-7 F) with connector– CE APPROVED Technical Specification as per Annexure-6
Fixed curve Decapolar catheter for Coronary sinus mapping (all curve, 5-7 F) with connector– US FDA APPROVED Technical Specification as per Annexure-6
Fixed curve Decapolar catheter for Coronary sinus mapping (all curve, 5-7 F) with connector– DCGI APPROVED Technical Specification as per Annexure-6
Deflectable decapolar catheter for Coronary sinus mapping (all curve, 5-7F) with connector– CE APPROVED Technical Specification as per Annexure-6
Deflectable decapolar catheter for Coronary sinus mapping (all curve, 5-7F) with connector– US FDA APPROVED Technical Specification as per Annexure-6
Deflectable decapolar catheter for Coronary sinus mapping (all curve, 5-7F) with connector– DCGI APPROVED Technical Specification as per Annexure-6
Duo Decapolar Electrophysiology Catheter – 20 Poles with connector– CE APPROVED Technical Specification as per Annexure-6
Deflectable Decapolar Electrophysiology Catheter with connector (6F,4MM) revolving handle- DCGI APPROVED Technical Specification as per Annexure-6
Deflectable Quadripolar Electrophysiology Catheter with connector (6F,4MM)push puill handle. – US FDA APPROVED Technical Specification as per Annexure-6
Deflectable Decapolar Electrophysiology Catheter with Lumen, push puill handle connector Med/ Large(7F) - DCGI APPROVED Technical Specification as per Annexure-6
H- curve Duodecapolar Electrophysiology Catheter(7F) – 20 Poles with connector– US FDA APPROVED Technical Specification as per Annexure-6
Duo Decapolar Electrophysiology Catheter – 20 Poles with connector– DCGI APPROVED Technical Specification as per Annexure-6
Connecting cables for 3D mapping system. – CE APPROVED Technical Specification as per Annexure-6
Connecting cables for 3D mapping system. – US FDA APPROVED Technical Specification as per Annexure-6
Connecting cables for 3D mapping system. – DCGI APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free and light weight absorbable shield for protection from scattered radiation during interventional procedures like left sub-clavian EP/ device, CTO, Angioplasty and IR etc. – CE APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free and light weight absorbable shield for protection from scattered radiation during interventional procedures like left sub clavian EP/ device, CTO, Angioplasty and IR etc. – US FDA APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free and light weight absorbable shield for protection from scattered radiation during interventional procedures like left sub clavian EP/ device, CTO, Angioplasty and IR etc. – DCGI APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free, light weight absorbable shield for safety from scattered radiation, should be specific for Peripheral procedures like AAA. – CE APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free, light weight absorbable shield for safety from scattered radiation, should be specific for Peripheral procedures like AAA. – US FDA APPROVED Technical Specification as per Annexure-6
Sterilized packed, non Vinyl, lead-free, light weight absorbable shield for safety from scattered radiation, should be specific for Peripheral procedures like AAA. – DCGI APPROVED Technical Specification as per Annexure-6
Non vinyl, lead-free X-ray attenuation, light weight surgical cap for radiation safety in all fluoro labs and must be fit all head sizes. – CE APPROVED Technical Specification as per Annexure-6
Non vinyl, lead-free X-ray attenuation, light weight surgical cap for radiation safety in all fluoro labs and must be fit all head sizes. – US FDA APPROVED Technical Specification as per Annexure-6
Non vinyl, lead-free X-ray attenuation, light weight surgical cap for radiation safety in all fluoro labs and must be fit all head sizes. – DCGI APPROVED Technical Specification as per Annexure-6
Basket Catheter with accessories compatible with IBI compatible– CE APPROVED Technical Specification as per Annexure-6
Basket Catheter with accessories compatible with IBI compatible– US FDA APPROVED Technical Specification as per Annexure-6
Basket Catheter with accessories compatible with IBI compatible– DCGI APPROVED Technical Specification as per Annexure-6
Crista Catheter with accessories compatible with ablators– CE APPROVED Technical Specification as per Annexure-6
Crista Catheter with accessories compatible with ablators– US FDA APPROVED Technical Specification as per Annexure-6
Crista Catheter with accessories compatible with ablators–DCGI APPROVED Technical Specification as per Annexure-6
2F multi polar catheter (>10 poles) for mapping through coronary vasculature with IBI compatible connector– CE APPROVED Technical Specification as per Annexure-6
2F multi polar catheter (>10 poles) for mapping through coronary vasculature with IBI compatible connector– US FDA APPROVED Technical Specification as per Annexure-6
2F multi Polar catheter (>10 poles) for mapping through coronary vasculature with IBI compatible connector– DCGI APPROVED Technical Specification as per Annexure-6
Pacing catheter with angiographic capabilities with cables / connectors. – CE APPROVED Technical Specification as per Annexure-6
Pacing catheter with angiographic capabilities with cables / connectors. – US FDA APPROVED Technical Specification as per Annexure-6
Pacing catheter with angiographic capabilities with cables / connectors. – DCGI APPROVED Technical Specification as per Annexure-6
Temperature ablation catheter with fiber weave, Kevlar wrap and stainless steel center support for better curve formation, durability and tension knob for micro movements– CE APPROVED Technical Specification as per Annexure-6
Temperature ablation catheter with fiber weave, Kevlar wrap and stainless steel center support for better curve formation, durability and tension knob for micro movements– US FDA APPROVED Technical Specification as per Annexure-6
Temperature ablation catheter with fiber weave, Kevlar wrap and stainless steel center support for better curve formation, durability and tension knob for micro movements– DCGI APPROVED Technical Specification as per Annexure-6
Tip Deflecting coronary sinus catheter– CE APPROVED Technical Specification as per Annexure-6
Tip Deflecting coronary sinus catheter– US FDA APPROVED Technical Specification as per Annexure-6
Tip Deflecting coronary sinus catheter– DCGI APPROVED Technical Specification as per Annexure-6
Navistar compatible regular catheter with IBI compatible connector– CE APPROVED Technical Specification as per Annexure-6
Navistar compatible regular catheter with IBI compatible connector– US FDA APPROVED Technical Specification as per Annexure-6
Navistar compatible regular catheter with IBI compatible connector– DCGI APPROVED Technical Specification as per Annexure-6
Navistar compatible thermocol catheter with IBI compatible connector– CE APPROVED Technical Specification as per Annexure-6
Navistar compatible thermocol catheter with IBI compatible connector– US FDA APPROVED Technical Specification as per Annexure-6
Navistar compatible thermocol catheter with IBI compatible connector– DCGI APPROVED Technical Specification as per Annexure-6
Location/ reference patch for Navistar compatible catheters – CE APPROVED Technical Specification as per Annexure-6
Location/ reference patch for Navistar compatible catheters – US FDA APPROVED Technical Specification as per Annexure-6
Location/ reference patch for Navistar compatible catheters – DCGI APPROVED Technical Specification as per Annexure-6
Velocity Nav X surface Electrode kit– CE APPROVED Technical Specification as per Annexure-6
Velocity Nav X surface Electrode kit– US FDA APPROVED Technical Specification as per Annexure-6
Velocity Nav X surface Electrode kit– DCGI APPROVED Technical Specification as per Annexure-6
Ensite compatible array catheter– CE APPROVED Technical Specification as per Annexure-6
Ensite compatible array catheter– US FDA APPROVED Technical Specification as per Annexure-6
Ensite compatible array catheter– DCGI APPROVED Technical Specification as per Annexure-6
Disposable defibrillator/ Transcutaneous pacing patches– CE APPROVED Technical Specification as per Annexure-6
Disposable defibrillator/ Transcutaneous pacing patches– US FDA APPROVED Technical Specification as per Annexure-6
Disposable defibrillator/ Transcutaneous pacing patches– DCGI APPROVED Technical Specification as per Annexure-6
Cryocatheters for ablation with accessories – CE APPROVED Technical Specification as per Annexure-6
Cryocatheters for ablation with accessories – US FDA APPROVED Technical Specification as per Annexure-6
Cryocatheters for ablation with accessories – DCGI APPROVED Technical Specification as per Annexure-6
Preshaped, valved long sheeths for mapping and RF ablation of all curves (7F- 9F)> 80cm long– CE APPROVED Technical Specification as per Annexure-6
Preshaped, valved long sheeths for mapping and RF ablation of all curves (7F- 9F)> 80cm long– US FDA APPROVED Technical Specification as per Annexure-6
Preshaped, valved long sheeths for mapping and RF ablation of all curves (7F- 9F)> 80cm long– DCGI APPROVED Technical Specification as per Annexure-6
Introducer sheaths for electrophysiology of various curves (8F, 8.5 F, 9F) – CE APPROVED Technical Specification as per Annexure-6
Introducer sheaths for electrophysiology of various curves (8F, 8.5 F, 9F) – US FDA APPROVED Technical Specification as per Annexure-6
Introducer sheaths for electrophysiology of various curves (8F, 8.5 F, 9F) – DCGI APPROVED Technical Specification as per Annexure-6
Steerable introduction sheaths for mapping and RF ablation (7F – 9F) (Quote all lengths, curves and any other special feature) – CE APPROVED Technical Specification as per Annexure-6
Steerable introduction sheaths for mapping and RF ablation (7F – 9F) (Quote all lengths, curves and any other special feature) – US FDA APPROVED Technical Specification as per Annexure-6
Steerable introduction sheaths for mapping and RF ablation (7F – 9F) (Quote all lengths, curves and any other special feature) – DCGI APPROVED Technical Specification as per Annexure-6
Bidirectional steerable long sheaths with variable reach and autolock for EPS– CE APPROVED Technical Specification as per Annexure-6
Bidirectional steerable Introducer – Dual Reach- US FDA APPROVED Technical Specification as per Annexure-6
Bidirectional steerable long sheaths with variable reach and autolock for EPS– DCGI APPROVED Technical Specification as per Annexure-6
Trans Septal Puncture needle for BMV for adults use– CE APPROVED Technical Specification as per Annexure-6
Septal Puncture Neede – US FDA APPROVED Technical Specification as per Annexure-6
Trans Septal Puncture needle for BMV for adults use–DCGI APPROVED Technical Specification as per Annexure-6
Permanent venacava filter– CE APPROVED Technical Specification as per Annexure-6
Permanent venacava filter– US FDA APPROVED Technical Specification as per Annexure-6
Permanent venacava filter– DCGI APPROVED Technical Specification as per Annexure-6
Temporary venacava filter– CE APPROVED Technical Specification as per Annexure-6
Temporary venacava filter– US FDA APPROVED Technical Specification as per Annexure-6
Temporary venacava filter– DCGI APPROVED Technical Specification as per Annexure-6
Mullins sheaths – Kink resistant 6/7 F– CE APPROVED Technical Specification as per Annexure-6
Mullins sheaths – Kink resistant 6/7 F– US FDA APPROVED Technical Specification as per Annexure-6
Mullins sheaths – Kink resistant 6/7 F– DCGI APPROVED Technical Specification as per Annexure-6
Good quality disposable sterile patient drape for PTCA, impervious to fluids, with one absorbent sheet with hole and long size, two plastic sheet (long size) one sterile cloth towel– CE APPROVED Technical Specification as per Annexure-6
Good quality disposable sterile patient drape for PTCA, impervious to fluids, with one absorbent sheet with hole and long size, two plastic sheet (long size) one sterile cloth towel– US FDA APPROVED Technical Specification as per Annexure-6
Good quality disposable sterile patient drape for PTCA, impervious to fluids, with one absorbent sheet with hole and long size, two plastic sheet (long size) one sterile cloth towel– DCGI APPROVED Technical Specification as per Annexure-6
Group - D-7 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA VVI /VVIR PACEMAKER WITH ALL LEADS & ACCESSORIES.
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
V.V.I Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved Technical Specification as per Annexure-6
V.V.I.R Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved Technical Specification as per Annexure-6
V.V.I.R Pacemaker With All Accessories and Life time Warranty - DCGI & US FDA/CE approved Technical Specification as per Annexure-6
D.D.D Pacemaker With All Accessories and Life time Warranty - DCGI & FDA Approved /CE Approved Technical Specification as per Annexure-6
DDDR MRI Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved Technical Specification as per Annexure-6
DDDR MRI Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved Technical Specification as per Annexure-6
SICD (AICD) DF1 CONNECTOR--DCGI & US FDA Approved /CE Technical Specification as per Annexure-6
DICD-40J Deliver fable energy - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
BIPOLAR CRTP- latest and New Congestion monitoring algorithm - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
CRTP-QUADRIPOLAR-EGM Based Dynamic AV DELAY optimization -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
CRTP-MULTIPOINT EGM Based Dynamic AV DELAY optimization -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
CRT-D BIPOLAR DF1- -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
CRT-D QUADRIOPOLAR DF-4 FDA/CE approved latest and New 40J Deliver fable energy – -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
CRT-D MULTIPOINT DF-4 FDA/CE approved latest and New 40J Deliver fable energy- -DCGI & US FDA /CE Approved Technical Specification as per Annexure-6
Sub-cutenous ICD IMPLANT (SC- I.C.D.) with All Accessories - DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Digital Multi-Programmable Pacemaker with Life time warranty and All Accessories -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Group - D-8 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA – VDD/VDDR PACEMAKER WITH ALL LEADS &ACCESSORIES
PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA/CE APPROVED Technical Specification as per Annexure-6
PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI APPROVED Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
Group - D-9 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA DDD PACEMAKER
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
Group– D – 10 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA DDDR PACEMAKER
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES Technical Specification as per Annexure-6
Group – D – 11 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA AICD PACEMAKER (Single & Dual Chamber)
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS – DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS- US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS- US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS -US FDA/CE APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS- DCGI APPROVED ,ICD WITH ALL LEADS Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS -US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS- DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS- US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED, ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS -US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES Technical Specification as per Annexure-6
Group – D-12 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA Remote Monitoring device for HFT devices
REMOTE MONITORING DEVICE WITH INTERNATIONAL ROAMING- US FDA/ CE APPROVED Technical Specification as per Annexure-6
DCGI APPROVED AND US FDA/CE APPROVED- REMOTE MONITORING DEVICE WITH INTERNATIONAL ROAMING Technical Specification as per Annexure-6
AICD SINGLE CHAMBER DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
AICD DUAL CHAMBER DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
S/C ICD SINGLE CHAMBER DEVICE WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
S/C ICD SINGLE CHAMBER DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
D/C ICD SINGLE CHAMBER DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
D/C ICD SINGLE CHAMBER DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
Group – D-13 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA Arrhythmia Diagnostic Devices
US FDA/CE APPROVED IMPLANTABLE LOOP RECORDER Technical Specification as per Annexure-6
DCGI APPROVED IMPLANTABLE LOOP RECORDER Technical Specification as per Annexure-6
US FDA/CE APPROVED IMPLANTABLE LOOP RECORDER for AF DETECTION Technical Specification as per Annexure-6
DCGI APPROVED IMPLANTABLE LOOP RECORDER for AF DETECTION Technical Specification as per Annexure-6
US FDA/CE APPROVED MOBILE CARDIAC TELEMETRY SYSTEM FOR ARRHYTHMIA DIAGNOSIS Technical Specification as per Annexure-6
DCGI APPROVED MOBILE CARDIAC TELEMETRY SYSTEM FOR ARRHYTHMIA DIAGNOSIS Technical Specification as per Annexure-6
Group – D-14 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA BIVENTRICULAR PACEMAKER(CRT) WITH ALL ACCESSORIES AND LEADS
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
Group D-15 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA –(COMBO DEVICE) BIVENTRICULAR PACEMAKER + ICD WITH ALL LEADS
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION Technical Specification as per Annexure-6
Lead Less Pacemaker with All Accessories. –DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
CRT- D Combo DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
CRT- D Combo DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED Technical Specification as per Annexure-6
Group D-16 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUROR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA ALL TYPE OF PERMANENT PACEMAKER (GENERATOR ONLY) WITHOUT LEAD
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER (CRT) WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, BIVENTRICULAR PACEMAKER (CRT) WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, AICD DUAL CHAMBER PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, AICD DUAL CHAMBER PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, AICD SINGLE CHAMBER PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, AICD SINGLE CHAMBER PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, DDDR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, DDDR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, VDD/VDDR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, VDD/VDDR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, DDD PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, DDD PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, VVI PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, VVI PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
US FDA/CE APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
DCGI APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD Technical Specification as per Annexure-6
Group D-17 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA ALL TYPE OF LEADS FOR PERMANENT PACEMAKERS (WITHOUT GENERATOR)
US FDA/CE APPROVED, ATRIAL, RV. LV LEADS AND ALL ACCESSORIES FOR BIVENTRICULAR PACEMAKER (CRT) Technical Specification as per Annexure-6
DCGI APPROVED, ATRIAL, RV. LV LEADS AND ALL ACCESSORIES FOR BIVENTRICULAR PACEMAKER (CRT) Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEADS ATRIAL, RV. LV LEADS FOR BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEADS ATRIAL, RV. LV LEADS FOR BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ALL ACCESSORIES REQUIRED DURING IMPLANTATION Technical Specification as per Annexure-6
US FDA/CE APPROVED, RV LEAD FOR AICD SINGLE CHAMBER Technical Specification as per Annexure-6
DCGI APPROVED, RV LEAD FOR AICD SINGLE CHAMBER Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEADS FOR AICD DUAL CHAMBER Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEADS FOR AICD DUAL CHAMBER Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDDR PERMANENT PACEMAKER Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDDR PERMANENT PACEMAKER Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDD PERMANENT PACEMAKER Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDD PERMANENT PACEMAKER Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEADS FOR VDD/VDDR PACEMAKERS Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEADS FOR VDD/VDDR PACEMAKERS Technical Specification as per Annexure-6
US FDA/CE APPROVED, PACING LEADS FOR VVI/VVIR PACEMAKERS Technical Specification as per Annexure-6
DCGI APPROVED, PACING LEADS FOR VVI/VVIR PACEMAKERS Technical Specification as per Annexure-6
US FDA/CE APPROVED APICARDIAL LEAD FOR PACEMAKERS Technical Specification as per Annexure-6
DCGI APPROVED APICARDIAL LEAD FOR PACEMAKERS Technical Specification as per Annexure-6
Lead For VVI Pacemaker – DCGI & US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For VVIR Pacemaker - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For DDDR Pacemaker – RA Lead - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For DDDR Pacemaker – RV Lead - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For DDD Pacemaker – RA Lead - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For DDDR Pacemaker – RV Lead - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For VDD Pacemaker – DCGI APPROVED & US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For ICD Pacemaker – DCGI & US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For ICD Dual Chamber Pacemaker - DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRT Pacemaker –RA Lead DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRT Pacemaker –RV Lead DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRT Pacemaker –LV Lead DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRTD Pacemaker –RV Lead DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRTD Pacemaker –RA Lead DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Lead For CRTD Pacemaker –LV Lead -DCGI&US FDA/ CE Approved Technical Specification as per Annexure-6
Apicardial Pacing Lead – RV Lead Technical Specification as per Annexure-6
Apicardial Pacing Lead – RA Lead Technical Specification as per Annexure-6
Group D-18 ALL QUOTED ITEMS SHOULD BE APPROVED IN AIIMS DELHI/SG PGI- LAKHNOW/PGI-CHANDIGARH/SMSH,JAIPUR OR EQUAVALENT LEADING GOVT. INSTITUTIONS IN INDIA
Sub Cutenous I.C.D Device (S.I.C.D) with All Accessories – DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Ablation cable compatible with IBI Ablator - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Irrigated Ablation catheter with 12 Ports. (4mm) Med/ Large/Extra Large Curve – DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Irrigated ablation catheter for 3D Mapping with FLEXIBLE and LASER CUT TIP TECHNOLOGY - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Irrigated bidirectional ablation catheter for 3D Mapping with FLEXIBLE and LASER CUT TIP TECHNOLOGY - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Connector of duo decapolar catheter - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
PV Mapping Electrophysiology catheter with connector – deflectable variable circular mapping catheter 15mm-25mm diameter loop- DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Circular Diagnostic Catheter (5F) with 10 electrodes (for pulmonary veins), fixed diameter - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Circular Diagnostic Catheter (5F) with 10 electrode (for pulmonary veins), variable diameter - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Circular Diagnostic Catheter (7F) with 20 electrode (for pulmonary veins), variable diameter - DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Connector of PV mapping- -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Impedance patches for electro anatomical mapping (NavX Velocity Patches) for use with ENSITE Velocity Mapping System - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Balloon catheter for Non-Contact Mapping of Arrhythmias (Array Balloon) for use with ENSITE Velocity Mapping System - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Connector of decapolar catheter - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Fixed Curve Quadripolar Electrophysiology catheter (6F, 4 mm) CRD-2, 5mm electrode spacing - -DCGI & US FDA Approved /CE Approved. Technical Specification as per Annexure-6
Connector of quadripolar catheter- -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Special PTCA WIRE with nitinol alloy , PTFE Tapered tip - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
AGILIS Steerable Introducer - Dual Reach - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Bidirectional Steerable sheath with radio-opaque marker (8F,67cm) 0-180 degree turning with dilator - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Specialty Sheath For Atrial Flutter(SAFL) - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Swartz introducer sheath with haemostatic valve SL0/SL1/SL2/SL3 (8F, 63 cm) – DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Swartz Introducer sheath with haemostatic valve SR0/SR1/SR2 (8F, 81 cm) - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
BRK Needle-Adult - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Mullin Sheaths-Different Sizes - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Tacticath Catheter - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
HD Grid catheter for scar mapping - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Single port femoral sheath - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Duo port femoral sheath - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Tri port femoral sheath - -DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
MRI – ICD Single Chamber - US FDA/CE Approved Technical Specification as per Annexure-6
MRI ICD Dual Chamber - DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
MRI – CRT – D - DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
DDD/DDDR Pacemaker - DCGI & US FDA Approved /CE Approved Technical Specification as per Annexure-6
Group D-19 (Separate EMD) Miscellaneous Supporting Items (No need of Authorization letter from manufacturer/Supplier/Bidder
CD- R Media with Cover with SMSH & M.C logo printed over the cover Technical Specification as per Annexure-6
DVD- R Media with Cover with SMSH & M.C logo printed over the cover Technical Specification as per Annexure-6
G-Kit Type Disposable Sterile Surgeon Gowns Technical Specification as per Annexure-6
Disposable E.O. Sterile Angiography drap set kit (Radial), Technical Specification as per Annexure-6
Disposable E.O Sterile Angiography drap set kit (Femoral) Technical Specification as per Annexure-6
Long Disposable E.O Sterile Sheet (1.50 meter X 2.5 meter size) Technical Specification as per Annexure-6
Small Disposable E.O Sterile Sheet (1.50 meter X 1.0 meter size) Technical Specification as per Annexure-6
Transeptal Needle Technical Specification as per Annexure-6
Mullin’S sheath (10-18 fr) Technical Specification as per Annexure-6
Rat pad type Radiation Protection Device shield in all sizes Technical Specification as per Annexure-6
Coatry-Pencil for Coatry machine installed in SMSH Cath lab. Technical Specification as per Annexure-6
External Temporary Pacemaker Technical Specification as per Annexure-6
Bard India Healthcare Private Limited
GSS DISTRIBUTORS
Innvolution Healthcare Pvt Ltd
SAHAJANAND LASER TECHNOLOGY LTD
Envision Scientific Private Limited
Nano Therapeutics Pvt. Ltd
Relisys Medical Devices Limited
YES ASSOCIATES
Speciality Pharma
VEIVA SCIENTIFIC INDIA PRIVATE LIMITED
Horizon Healthcare Solutions
Shree Pacetronix Ltd.
Sahajanand Medical Technologies Pvt. Ltd.
Meril Life Sciences India Pvt.Ltd.,
KOX MED AND LAB PVT LTD
Vascular Concepts Ltd
Ace Cardiopathy Solutions Pvt. Ltd
SAHU SURGICAL EMPORIUM PVT .LTD.
Boston Scientific India Pvt Ltd
M/S SDS MEDICAL SYSTEMS
BIOTRONIK MEDICALDEVICES INDIA PVT LTD
India Medtronic Pvt. Ltd.
tech_eval.pdf
boq_comp_chart.xlsx
xlsx
fin_eval.pdf
aoc.pdf
Download all tender documents and submit your bid