Cardiology and Nephrology Consumable Item

Drug Eluting Stents, Pacemakers, PTMC Balloon and other Consumable Items

Group – A (Interventional Cardiology)

RADIAL INTRODUCER NEEDLE 18G, 70MM LENGTH & 20G, 40MM – USFDA/CE/DCGI Approved  Tip- Sharp Half-moon Bevel shape diamond cutting. 18 G 7 cm 20G 4 cm.

IV CANULA - 20G, /21G 3.2 CM AND 4 CM – USFDA/CE/DCGI APPROVED  Ultrasharp electropolished pointed tip. thin-walled construction, radiopaque in nature cannula made up of clear polyurethane. Hub shape Round mini wings/no wings with flash plug. 20G,21G 3.2 cm and 4 cm

TRANS RADIAL INTRODUCER KIT WITH PUNCTURE NEEDLE - 4F-7F – 7/10/15/25 CM, USFDA/PMDA APPROVED  Sizes - 4 – 7 French, Length – 7/10/15/25 cm  Pack must include 20 G/45mm entry needle, 0.025-inch x 45/80 cm hydrophilic mini guidewire.  Must have ETFE sheath tubing, dilator tube should be made up of polypropylene and should have silicon coating.  Should Contain haemostatic crosscut valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock.  With suture eye for securing sheath, Kink resistant, With Snap-on dilator-hub lock mechanism to prevent its back-out.

TRANS RADIAL INTRODUCER KIT WITH PUNCTURE NEEDLE - 4F-7F – 7/10/15/25 CM, CE/DCGI APPROVED  Sizes - 4 – 7 French, Length – 7/10/15/25 cm  Pack must include 20 G/45mm entry needle, 0.025-inch x 45/80 cm hydrophilic mini guidewire  Must have ETFE sheath tubing, dilator tube should be made up of polypropylene and should have silicon coating.  Should Contain haemostatic crosscut valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock.  With suture eye for securing sheath, Kink resistant, With Snap-on dilator-hub lock mechanism to prevent its back-out.

RADIAL INTRODUCER KIT - HYDROPHILIC CTO APPROACHABLE SLENDER PROFILE 4F-7F, 6.5F -Length - 7 cm, 11cm, 15cm, 25cm – CE Approved  Sizes - 4 – 7 French. Must include 6.5F special sheath, Length - 7 cm, 11cm, 15cm, 25cm.  Pack must include 22G/45mm plastic entry needle, 0.025-inch x 45/80 cm hydrophilic mini guidewire.  Must Have Metal Mesh Braided Structure  Must have 3 Layer sandwich of PTFE sheath tubing with Pebax inner layer and SS Braid, dilator tube should be made up of polypropylene and should have silicon coating.  Should Contain haemostatic crossover valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock.  With suture eye for securing sheath, Kink resistant, With Rotation-hub lock mechanism to prevent its back-out during insertion

SLENDER PROFILE HYDROPHILIC SHEATH 5-7 F (10, 16, CM) - USFDA/PMDA Approved  Must Have unique thin wall technology reducing the outer diameter by 1 Fr size whilst maintaining the one size lager inner diameter. 5Fr in 4, 6Fr in 5, 7Fr in 6 profile.  Must Have 7Fr Sheath with Outer diameter of 2.8mm, 6Fr with OD of 2.46 mm & 5Fr with OD of 2.13mm.  hydrophilic M coating with 20/21G Surflash needle and TIF tip technology which provide optimal tapering design.

FEMORAL INTRODUCER KIT 4-11F (10, 16 & 25 CM) - USFDA/PMDA APPROVED • Sizes - 4 – 11 French, Length – 10, 16 & 25 cm • Pack must include 18 G/20G, Surflash entry needle, 0.035- or 0.025-inch x 45 cm mini plastic guidewire • Must have ETFE sheath tubing, dilator tube should be made up of polypropylene and should have silicon coating. • Should Contain haemostatic crosscut valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock. • With suture eye for securing sheath, Kink resistant, With Snap-on dilator-hub lock mechanism to prevent its back-out during insertion

FEMORAL INTRODUCER KIT 4-11F (10, 16 & 25 CM) – CE/DCGI APPROVED  Sizes - 4 – 11 French, Length – 10, 16 & 25 cm  Pack must include 18 G/20G, Surflash entry needle, 0.035- or 0.025-inch x 45 cm mini plastic guidewire  Must have ETFE sheath tubing, dilator tube should be made up of polypropylene and should have silicon coating.  Should Contain haemostatic crosscut valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock.  With suture eye for securing sheath, Kink resistant, With Snap-on dilator-hub lock mechanism to prevent its back-out during insertion

FEMORAL INTRODUCER KIT - HYDROPHILIC CTO APPROACHABLE SLENDER PROFILE 4F-18F, Length - 11cm, 15cm, 25cm – CE Approved  Sizes - 4 – 18 French. Length - 11cm, 15cm, 25cm  Pack must include 18G/70 mm plastic entry needle, 0.038-inch x 45/80 cm & .035 for 4F hydrophilic mini guidewire.  Must Have Metal Mesh Braided Structure  Must have 3 Layer sandwich of PTFE sheath tubing with Pebax inner layer and SS Braid, dilator tube should be made up of polypropylene and should have silicon coating.  Should Contain haemostatic crossover valve to prevent back leak of blood and aspiration of air; With Integrated side arm with attached 3-way stopcock.  With suture eye for securing sheath, Kink resistant, With Rotation-hub lock mechanism to prevent its back-out during insertion

BRAIDED LONG SHEATH – 6-8F – 45CM - USFDA/PMDA APPROVED  Diameter 6,7,8F and length 45cm. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 6-8F – 45CM – CE/DCGI APPROVED  Diameter 6,7,8F and length 45cm. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 6-8F – 65CM - USFDA/PMDA APPROVED  Diameter 6,7,8F and length 65cm. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 6-8F – 65CM – CE/DCGI APPROVED  Diameter 6,7,8F and length 65cm. Atraumatic Tip for Carotid & Distal procedures • Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management) • Gold Coil Marker - For Distal Visibility • PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability • Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 6-8F – 90CM - USFDA/PMDA APPROVED  Diameter 6,7,8F and length 90cm. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 6-8F – 90CM – CE/DCGI APPROVED  Diameter 6,7,8F and length 90cm. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

BRAIDED LONG SHEATH – 8-18F – ALL LENGTH – CE/DCGI APPROVED  Diameter 8-18F and all length. Atraumatic Tip for Carotid & Distal procedures  Haemostatic Valves (Cross Cut Valve & TBV- detachable valves for thrombus management)  Gold Coil Marker - For Distal Visibility  PTFE Coating - Seamless Device Transition, Distal Hydrophilic Coated for navigability  Nylon Outer Layer with reinforced stainless-steel coil - Helps in Smooth & Anti-Kink effect

HYDROPHILIC GUIDEWIRE (LENGTH - 150) WITH MCOAT/HYDROCOAT TECHNOLOGY – PMDA/CE APPROVED  Standard tip & .035, .032, .038, .025. .018 diameter & 150 cm length - Straight / Angled / 1.5mm J shape  tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket  hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

HYDROPHILIC GUIDEWIRE (LENGTH - 150) WITH MCOAT/HYDROCOAT TECHNOLOGY – DCGI APPROVED  Standard tip & .035, .032, .038, .025. .018 diameter & 120 cm & 150 & 180 cm length - Straight / Angled / 1.5mm J shape, straight A, S, R-1.5mmJ, R-3mmJ in Standard and stiff support level  tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket  hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

HYDROPHILIC GUIDEWIRE (LENGTH - 180) WITH MCOAT/HYDROCOAT TECHNOLOGY – PMDA/CE APPROVED  Standard tip & .035, .032, .038, .025. .018 diameter & 180 cm length - Straight / Angled  tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket  hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

HYDROPHILIC GUIDEWIRE (LENGTH - 260) WITH MCOAT/HYDROCOAT TECHNOLOGY – PMDA/CE APPROVED  Standard tip & .035, .032, .038, .025. .018 diameter & 260 cm length - Straight / Angled  tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket  hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

HYDROPHILIC GUIDEWIRE (220 & 260) WITH MCOAT/HYDROCOAT TECHNOLOGY – DCGI APPROVED • Standard tip & .035, .032, .038, .025. .018 diameter & 220 cm & 260 cm length - Straight / Angled / 1.5mm J shape, straight A, S, R-1.5mmJ, R-3mmJ in Standard and stiff support level • tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

EXTRA STIFF - HYDROPHILIC GUIDEWIRE -150 CM USFDA/PMDA APPROVED • 0.035, .032, .038, .025, .018 diameter and 150 cm length - Straight / Angled -Half Stiff and stiff, Extra Stiff • with Mcoat technology tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

EXTRA STIFF - HYDROPHILIC GUIDEWIRE -260 CM USFDA/PMDA APPROVED • 0.035, .032, .038, .025, .018 diameter and 150 cm length - Straight / Angled -Half Stiff and stiff, Extra Stiff • with Mcoat technology tapered tip, single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat. One piece construction & Radiopaque polyurethane jacket.

PTFE GUIDEWIRE 150 CM - USFDA/PMDA APPROVED  150cm, 175 cm of lengths & 0.018'' to 0.038'' diameter With Silicon Coated tip.  Silicon Coated Tip with choice of Stainless-steel core or Nitinol core,  Should be available fixed as well as movable core.

PTFE GUIDE WIRE – 150 CM – CE/DCGI APPROVED  Should be available in 0.025, 0.032, 0.035 & 0.038 inches, 150 cm long, straight & J-Shaped tip  Should be available in variable lengths of flexible/floppy end, variable J tip sizes  Should be available fixed as well as movable core.

PTFE GUIDEWIRE – 260 CM - USFDA/PMDA APPROVED  260 cm of lengths & 0.018'' to 0.038'' diameter With Silicon Coated tip.  Silicon Coated Tip with choice of Stainless-steel core or Nitinol core,  Should be available fixed as well as movable core.

PTFE GUIDE WIRE – 260 CM – CE/DCGI APPROVED  Should be available in 0.025, 0.032, 0.035 & 0.038 inches, 150 cm long, straight & J-Shaped tip  Should be available in variable lengths of flexible/floppy end, variable J tip sizes  Should be available fixed as well as movable core.

AMPLATZ SUPER-STIFF GUIDE WIRE - 260 – USFDA/CE/DCGI APPROVED  Should be available in 0.035- and 0.038-inches size, 260/300 cm long, straight or J-Shaped tip  Should be available fixed as well as movable core.

DOUBLE CURVE EXTRA STIFF GUIDE WIRE – LANDERQUIST TYPE – REGULAR LENGTH

DOUBLE CURVE EXTRA STIFF GUIDE WIRE – LANDERQUIST TYPE – 260CM/300CM

PRE-SHAPED – TAVI SUPPORT WIRE – USFDA APPROVED  Outer Diameter: 0.035” (0.889 mm), Length: 275 cm  Core Material: Stainless Steel with LUBRIGREE PTFE coating  Unique Product Dimensions by Curve Size - Extra Small, Small, Large Curve

RADIAL ANGIOGRAPHIC CATHETER – TIG CURVE (4-6F) - USFDA/PMDA -APPROVED  Sizes - 4F, 5F, 6F, Shapes - TIG/3.5 JACKY/4-SARAH  Two-layer construction, double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers.  Must Have the shaft inner layer and outer layer contain barium sulphate with 32 Strands of stainless-steel braid  Must Have anti-kinking protector sleeve, with non-braided tip shaft (distal -2 cm).  Must have inner diameter of 4F = 1.03mm, 5F= 1.20mm, 6F = 1.30mm

RADIAL ANGIOGRAPHIC CATHETER HYDROPHILIC – TIG CURVE (4-6F) - DCGI APPROVED  Length - 80cm / 100cm / 110cm / 130cm, Sizes - 4F, 5F, 6F  Must Have triple-layer construction, double braided stainless-steel two-ply mesh sandwiched between layers of Nylon and Pebax.  Must Have anti-kinking protector sleeve, with uncoated non-braided tip shaft (distal -2 cm)  Must have inner diameter of 4F = 1.05mm, 5F= 1.20mm, 6F = 1.47mm with 1000psi flow rate.

RADIAL ANGIOGRAPHIC CATHETER HYDROPHILIC – TIG CURVE (4-6F) - DCGI APPROVED  Length - 80cm / 100cm / 110cm / 130cm, Sizes - 4F, 5F, 6F  Must Have triple-layer construction, double braided stainless-steel two-ply mesh sandwiched between layers of Nylon and Pebax.  Must Have anti-kinking protector sleeve, with uncoated non-braided tip shaft (distal -2 cm)  Must have inner diameter of 4F = 1.05mm, 5F= 1.20mm, 6F = 1.47mm with 1000psi flow rate.

FEMORAL DIAGNOSTIC CATHETER: 4 -6 FR (JL, JR, AL, AR, PIGTAIL) - CE APPROVED  Shapes - JL, JR, AL, AR, pigtail  Triple-layer construction, double braided stainless-steel two-ply mesh sandwiched between layers of Nylon and Pebax.  Inner diameter of 4F = 1.04mm, 5F= 1.20mm, 6F = 1.47mm with 1000psi flow rate.  Catheter should have slender profile ultra-thin wall that creates large lumen.  Catheter should have anti-kinking protector, with uncoated non-braided tip shaft (distal -2 cm).

FEMORAL DIAGNOSTIC CATHETER: 4 -6 FR (JL, JR, AL, AR, IM, PIGTAIL, MP) - USFDA/PMDA -APPROVED  Transfemoral catheter shapes JL, JR, AL, AR, IM, Pigtail, MP  braided Catheter with stainless steel mesh technology.  Inner diameter of 4Fr =1.03mm ,5Fr = 1.20mm, 6Fr = 1.30mm or more resulting in Higher flow rates.  The shaft inner layer and outer layer should contain BARIUM SULPHATE with 32 Strands of stainless-steel braid  Catheter should have ultra-thin wall that creates large lumen.  Catheter should have anti-kinking protector, with non-braided tip shaft (distal -2 cm).

JUDKINS CATHETER (JR & JL) – 4 – 6 FR  Size - 4 French/5 French /6 French size

AMPLATZ CATHETER – AL & AR – 4 6 FR  Size - 4 French/5 French /6 French

MULTIPURPOSE CATHETER (MP) 4-6 FR  Size - 4 French/5 French /6 French size

PIGTAIL CATHETER – 4 -6 FR  Size – 4 – 6 French

ANGIOGRAPHIC SIZING PIGTAIL CATHETER 5F/ 6F/ 7F –  SIZE – 5 F – 7 F

INTERNAL MAMMARY CATHETER – 4 -6 FR  Size - 4 French/5 French /6 French in various standard curves and lengths.

BY-PASS GRAFT CATHETER  Size - 4 French/5 French /6 French in various standard curves and lengths.

NIH CATHETER -  4 French/5 French /6 French/7 French/8French in various standard curves and lengths.

COURNARD CATHETER  4 French/5 French /6 French/7 French/8French in various standard curves and lengths.

DIAGNOSTIC CATHETERS FOR NEONATAL USE - 3- ‘FRENCH’  Pigtail, Judkins, Multipurpose, Cobra and other diagnostic catheters of 3 Fr. size  Varying lengths and shapes

DRUG DELIVERY/INFUSION CATHETER

CORONARY PROBING CATHETER

CORONARY PERFUSION CATHETER

CORONARY TRAPEER CATHETER

SWAN GANZ CATHETER - US FDA APPROVED - 6F/7F

SWAN GANZ CATHETER – CE/DCGI APPROVED- 6F/7F

SPECIAL SWAN GANZ CATHETER  Sizes - 4F, 5F, 6F and 7F and 8 Fr  4 F catheter should allow the passage of at least 0.021, 5 F – 0.025, 6 F – 0.035 and 7 F, 8F – 0.038-inch hydrophilic guide wire Catheter should be tapered at tip to ensure uniform diameter of the whole catheter, 10 cm marking along the catheter body.

BALLOON TIPPED ANGIOGRAPHY CATHETER

BERMAN CATHETER  Must be available in 4F, 5F, 6F and 7F sizes  Should have 6-8 holes proximal to the balloon for dye injection  Catheter should be tapered at tip to ensure uniform diameter of the whole catheter, 10 cm marking along catheter

REVERSE BERMAN CATHETER  Should be available in 4F, 5F, 6F & 7F sizes  Catheter should be tapered at tip to ensure uniform diameter of the whole catheter  Should have holes proximal to the balloon for dye injection  Should have a hole at the proximal tip to allow the passage over the wire

PIGTAIL CATHETER (PEDIATRIC)  Sizes 3 French/ 4 French/ 5 French/ 6 French  Smaller length for neonatal and pediatric use

SPECIAL JUDKINS CORONARY CATHETER WITH 2.5 CM CURVE (PEDIATRIC)  Sizes - 4 F/ 5 F/ 6 F

ANGIOGRAPHIC DOUBLE LEUMEN TRACKING CATHETER – 4 F/5F/ 6F

RENAL DOUBLE CURVE CATHETER  In various standard lengths and curves

HEAD HUNTER CATHETER  In various standard lengths and curves  035-038 compatible  100 cm long

SIMMONS/ SIDEWINDER CATHETER  In various standard lengths and curves  035-038 compatible  100 cm long

PRESHAPED CATHETER FOR UTERINE ARTERY EMBOLISATION  In various standard lengths and curves

VERTEBRAL CATHETER  In various standard lengths and curves

COELIAC AXIS CATHETER  In various standard lengths and curves

SHEPHERD’S HOOK CATHETER  In various standard lengths and curves

VTK DIAGNOSTIC CATHETER  In various standard lengths and curves 5f, 6f size

3D SPACE RCA ANGIOGRAPHIC CATHETER

ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS – USFDA Approved  Should meet highest medical industrial standards click-on  Quality certification should be provided from authorized agencies.

ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS - CE APPROVED  Should meet highest medical industrial standards  Quality certification should be provided from authorized agencies.

ADJUSTABLE HEMOSTASIS VALVE FOR CATHETERS - DCGI APPROVED  Should meet highest medical industrial standards  Quality certification should be provided from authorized agencies.

HEMOSTASIS VALVE - 8 FR. INNER LUMEN – USFDA Approved  star-shaped seal with Rotolock

HEMOSTASIS VALVE - 8 FR. INNER LUMEN – CE Approved  star-shaped seal with Rotolock

HEMOSTASIS VALVE - 8 FR. INNER LUMEN – DCGI Approved  star-shaped seal with Rotolock

PTCA PRESSURE CONSOLE – USFDA APPROVED

PTCA PRESSURE CONSOLE – CE APPROVED

PTCA PRESSURE CONSOLE – DCGI APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (DUAL-PATHWAY) – USFDA APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (DUAL-PATHWAY) -CE APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (DUAL-PATHWAY) -DCGI APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (TRI-PATHWAY) – USFDA APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (TRI-PATHWAY) – CE APPROVED

ANGIOPLASTY PRESSURE DIVERSION MODULE (TRI-PATHWAY) – DCGI APPROVED

HIGH – PRESURE INJECTOR LINES - DCGI APPROVED  Should be available in various lengths  Should have male and female luer locks  Should be transparent and kink resistant  Should be able to take high pressure of angiographic injections

DISPOSABLE ECG ELECTRODES FOR ADULTS - US FDA APPROVED  Adult diaphoretic foam electrodes.  Should be pre-gelled, peel and stick electrode with excellent adhesion  Should have no residue once removed  Should conform to or exceed the highest industrial standard for ECG electrodes,ation

SPECIAL RADIOLUCENT DISPOSABLE ECG ELECTODES FOR ADULTS – DCGI APPROVED  Radiolucent electrodes for Electro-physiologic Studies  Wet gel electrodes, Should be porous and breathable  Should conform to or exceed the highest industrial standard for ECG electrodes,  Quality certification from authorized agencies to be provided

SYRINGE FOR PRESSURE INJECTOR INSTALLED IN CATH LAB  Should be compatible with existing machines at Cath Lab, GMCK

HIGH-PRESSURE – CONTRAST DELIVERY INJECTOR – WITH LUER LOCK MECHANISM- 10 ML

HIGH-PRESSURE – CONTRAST DELIVERY INJECTOR – WITH LUER LOCK MECHANISM- 20 ML

ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long)  Should be available in sizes of 100, 150 & 200 cm Should have male luer lock connection at one end and a female luer lock connection at the other end

HIGH-FIDELITY PRESSURE MONITORING EXTENSION LINE – 200  medical-grade PVC or DEHP-free polyethylene, male and female Luer lock connectors,  must be DEHP-free (Diethylhexyl Phthalate-free) and latex-free.Pressure ratings – 1200 PSI

DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB IN GMCK HOSPITAL  Disposable transducers for invasive pressure monitoring  Should be compatible with available system in Cath Lab (IABP – Data Scope & Cath Lab transducer) and ICCU at GMCK  Should meet highest medical industrial standards  Quality certification should be provided form authorized agencies

DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED  Should be compatible with existing available system at Cath Lab and CCU at GMCK  Should meet or exceed highest standards  Quality certification from authorized agencies to be provided

PTCA INFLATION DEVICE - US FDA APPROVED  Efficient locking system to maintain high pressure  Rapid inflation and deflation, Clear barrel for easy visualization of de-bubbling  Luminescent analog pressure gauge (up to 30 atm), 20/30 Inflation Device registers pressures up to 30 atmospheres Ergometric and use friendly hand held design.

PTCA INFLATION DEVICE - CE APPROVED  Efficient locking system to maintain high pressure  Rapid inflation and deflation, Clear barrel for easy visualization of de-bubbling  Luminescent analog pressure gauge (up to 30 atm), 20/30 Inflation Device registers pressures up to 30 atmospheres Ergometric and use friendly hand held design.

PTCA INFLATION DEVICE - DCGI APPROVED  Efficient locking system to maintain high pressure  Rapid inflation and deflation, Clear barrel for easy visualization of de-bubbling  Luminescent analog pressure gauge (up to 30 atm), 20/30 Inflation Device registers pressures up to 30 atmospheres Ergometric and use friendly hand held design.

Y-CONNECTOR – PUSH PULL MECHANISM - US FDA/PMDA APPROVED  9F Bore Size for usage with a variety of devices  Should accommodate virtually all interventional devices  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end  Should have bleed back safety mechanism, Stepwise control for open, semi-open and closed position

Y-CONNECTOR – PUSH PULL MECHANISM – CE/DCGI APPROVED  9F Bore Size for usage with a variety of devices  Should accommodate virtually all interventional devices  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end  Should have bleed back safety mechanism, Stepwise control for open, semi-open and closed position

Y-CONNECTOR – PUSH CLICK MECHANISM –180 PSI PRESSURE SUSTENACE - DCGI APPROVED  9F Bore Size for usage with a variety of devices, with 180 Psi of pressure sustenance.  Should accommodate virtually all interventional devices  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end  Should have bleed back safety mechanism, Stepwise control for open, semi-open and closed position

Y-CONNECTOR – PUSH CLICK MECHANISM - 300 PSI PRESSURE SUSTENACE –DCGI APPROVED  9F Bore Size for usage with a variety of devices, with 300 Psi of pressure sustenance.  Should accommodate virtually all interventional devices  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end  Should have bleed back safety mechanism, Stepwise control for open, semi-open and closed position

Y- CONNECTOR KIT – PUSH PULL MECHANISM - STEPWISE CONTROL FOR OPEN, SEMI-OPEN AND CLOSED POSITION (OKAY – 2 type) - US FDA / CE APPROVED  Should accommodate virtually all interventional devices  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end  Should have bleed back safety mechanism

W-CONNECTOR - BIFURCATION PTCA – USFDA/CE//DCGI APPROVED  Two ports for insertion of two PTCA balloons or one balloon and one other part at the same time  Luer connector at the guiding catheter end, Rotating adapter at the guiding catheter end

MANIFOLD WITH ATTACHED TUBINGS (ANGIO KIT) with 3 Port LEFT-OFF /RIGHT OFF ORIENTATION - US FDA/CE/DCGI APPROVED  Pressure Integrity - 250 pascal per square inches -500 Pascal per square inches rating and wide port spacing. Clear polycarbonate body  Integrated pre-flushed transducer port  minimum flow rate of 85 ml/sec at 500 PSI. The design must minimize turbulence and air entrapment, evidenced by an 'airless rotator' mechanism for enhanced patient safety  Three side port manifold, One connector tubing for connecting Manifold to Tuohy Borst  One luer lock control syringe (10 or 12 ml) for contrast injection  Two large bore tubing (with flow regulating knob) for withdrawing contrast & Saline One 3 way stop-cock  Color Coded Manifold with left-off /right off orientation.

MANIFOLD WITH ATTACHED TUBINGS (ANGIO KIT) with 2 Port LEFT-OFF /RIGHT OFF ORIENTATION – USFDA/CE/DCGI APPROVED  Pressure Integrity - 250 pascal per square inches -500 Pascal per square inches rating and wide port spacing. Clear polycarbonate body  Integrated pre-flushed transducer port  minimum flow rate of 85 ml/sec at 500 PSI. The design must minimize turbulence and air entrapment, evidenced by an 'airless rotator' mechanism for enhanced patient safety  Two side port manifold, One connector tubing for connecting Manifold to Tuohy Borst  One luer lock control syringe (10 or 12 ml) for contrast injection  Two large bore tubing (with flow regulating knob) for withdrawing contrast & Saline One 3 way stop-cock  Color Coded Manifold with left-off /right off orientation.

GUIDING CATHETER WITH SPECIAL EXTRA BACKUP CURVE LENGTH (ABU 3.0, 3.25, 3.5, 3.75, 4.0) – CE Approved  Must have (ABU 3.0, 3.25, 3.5, 3.75, 4.0) and must include 6.5 French catheter  Must have triple layered SS braided sandwich structure with outer polymer blend layer & inner PTFE layer  Must Have Flat wire braided structure, Should have uncoated and non-braided atraumatic soft tip  Must have various tip shapes and curves – Extrabackup left, JL&JR, AL&AR, MP  Should have OD of 6F, 6.5F, 7F-8F.

SPECIAL 6.5 INTRODUCER & 6.5F GUIDING CATHETER (COMBO) – FOR TRI PROCEDURES – CE APPROVED  Must have triple layered SS braided sandwich structure with outer polymer blend layer & inner PTFE layer  Must Have Flat wire braided structure  Should have uncoated and non-braided atraumatic soft tip  Must have various tip shapes and curves – Extrabackup left, JL&JR, AL&AR, MP

RADIAL GUIDING CATHETER BOTH CURVE - US FDA APPROVED  Should be braided with low friction inner layer  Should have atraumatic soft tip  Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available  Should have the largest ID for each OD  Should have lengths ranging from 55-90 cm

RADIAL GUIDING CATHETER BOTH CURVE - CE APPROVED  Should be braided with low friction inner layer  Should have atraumatic soft tip  Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available  Should have the largest ID for each OD  Should have lengths ranging from 55-90 cm

RADIAL GUIDING CATHETER BOTH CURVE - DCGI APPROVED  Should be braided with low friction inner layer  Should have atraumatic soft tip  Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available  Should have the largest ID for each OD  Should have lengths ranging from 55-90 cm

TRANSRADIAL GUIDING CATHETER RIGHT CURVE/ LEFT CURVE – US FDA /CE APPROVED  Should be braided with low friction inner layer  Should have atraumatic soft tip  Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available  Should have the largest ID for each OD  Should have lengths ranging from 55-90 cm

RADIAL GUIDING CATHETER IKARI CURVE - DCGI APPROVED  Should be braided with low friction inner layer  Should have atraumatic soft tip  Should be available in various tip shapes and curves for access to different parts of the vasculature  Should have OD of 6F-8F available  Should have the largest ID for each OD  Should have lengths ranging from 90 cm or above

GUIDING CATHETER FOR PERIPHERAL VASCULAR USE – US FDA APPROVED  Should be available in various tip shapes and curves for access to different parts of the coronary vasculature, including judkins, multi – purpose and other shapes  Should have OD of 5F-8F available  Should have lengths ranging from 55-100 cm

GUIDING CATHETER FOR PERIPHERAL VASCULAR USE – CE APPROVED  Should be available in various tip shapes and curves for access to different parts of the coronary vasculature, including judkins, multi – purpose and other shapes  Should have OD of 5F-8F available  Should have lengths ranging from 55-100 cm

GUIDING CATHETER FOR PERIPHERAL VASCULAR USE – DCGI APPROVED  Should be available in various tip shapes and curves for access to different parts of the coronary vasculature, including judkins, multi – purpose and other shapes  Should have OD of 5F-8F available  Should have lengths ranging from 55-100 cm

GUIDING CATHETER FOR PERIPHERAL VASCULAR USE (5- 10F)– DCGI APPROVED  Should be available in various tip shapes and curves for access to different parts of the coronary vasculature, including judkins, multi – purpose and other shapes  Should have OD of 5F-10F available  Should have lengths ranging from 55-100 cm

LONG SHEATH FOR CONTRA – LATERAL ILIAC/ FEMORAL ACCESS – US FDA APPROVED  Should be low friction with inner coating to allow catheter manipulation  Should have distal radio-opaque tip for enhanced visibility on fluoroscopy  Should have a proximal hemostasis valve/ provision for tuohyborst valve  Shove be color coded for size identification  Should be available in 4F – 9 F size with the largest ID, lengths ranging from 40-110 cm

Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single curve – US FDA /CE APPROVED  Should be braided with low friction inner layer Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available, Should have lengths ranging from 55-90 cm

Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single curve – DCGI APPROVED  Should be braided with low friction inner layer Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal double curve, cobra, multi – purpose and other shapes  Should have OD of 6F-8F available, Should have lengths ranging from 55-90 cm

MOTHER & CHILD CATHETER – US FDA/CE APPROVED  With reliable support with large inner lumen and inner PTFE.

MOTHER & CHILD CATHETER – DCGI APPROVED  With reliable support with large inner lumen and inner PTFE.

INTUBATION CATHETER FOR ASSISTING DELIVERY OF STENT IN DIFFICULT ANATOMIES – US FDA/CE APPROVED

INTUBATION CATHETER FOR ASSISTING DELIVERY OF STENT IN DIFFICULT ANATOMIES – DCGI APPROVED

RDC SHAPE GUIDING CATHETER FOR RENAL & C-LILAC ARTERY ANGIOPLASTY – - US FDA/CE / DCGI APPROVED

GUIDE EXTENTION CATHETER: (GUIDE PLUS TYPE) – USFDA/PMDA APPROVED Guide Extension Catheter available in variable diameters of 4.7F and 5.0F for accessing distal anatomy and delivering high profile devices; Guide Extension Catheter with a tapered distal shaft for accessing distal and challenging coronary anatomy; Guide Extension Catheter with a Resinous atraumatic tip; Guide Extension Catheter with a large entry port design for easy device insertion

GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - US FDA APPROVED  120 proximal hypo-tube shaft  0.57 Inner diameter & 0.066” outer diameter  Should be with proximal marker and 1 x 1 braiding

GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - CE APPROVED  120 proximal hypo-tube shaft  0.57 Inner diameter & 0.066” outer diameter  Should be with proximal marker and 1 x 1 braiding

GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - DCGI APPROVED  120 proximal hypo-tube shaft  0.57 Inner diameter & 0.066” outer diameter Should be with proximal marker and 1 x 1 braiding

MANUAL ASPIRATION CATHETER Aspiration Catheter of 6F and 7F Guiding Catheter compatibility; 140 cm working length catheter with 140 cm stylet length; 90 cm and 100 cm depth markers; Provide 60ml aspiration syringe for high suction efficiency; large size collecting filter.

MECHANICAL ASPIRATION DEVICE – USFDA

MECHANICAL ASPIRATION DEVICE – CE/DCGI

THROMBECTOMY CATHETERS WITH DISTAL BALLOON OCCLUSION AND AUTOMATED SUCTION DURING PTCA - US FDA APPROVED

THROMBECTOMY CATHETERS WITH DISTAL BALLOON OCCLUSION AND AUTOMATED SUCTION DURING PTCA – CE/DCGI APPROVED

THROMBECTOMY CATHETERS WITH MOTORIZED CUTTING AND SUCTION DURING PTCA - US FDA APPROVED

THROMBECTOMY CATHETERS WITH MOTORIZED CUTTING AND SUCTION DURING PTCA – CE/DCGI APPROVED

ASPIRATION THROMBECTOMY CATHETER –1.30 MM SQUARE SUCTION AREA - USFDA/PMDA APPROVED • Available in Size 6F, 7F Both, Must have entry profile 0.019 inches • Braided polyamide elastomer shaft, stainless steel wire braiding and Guide wire type Stylet, • 6.0mm tip length for making aspiration inlet to come closer to the target thrombus and 10cm-length depth. • Must Have Distal 40 cm Hydrophilic coating.

ASPIRATION THROMBECTOMY CATHETER –1.30 MM SQUARE SUCTION AREA – CE APPROVED • Available in Size 6F, 7F Both, Must have entry profile 0.019 inches • Braided polyamide elastomer shaft, stainless steel wire braiding and Guide wire type Stylet, • 6.0mm tip length for making aspiration inlet to come closer to the target thrombus and 10cm-length depth. • Must Have Distal 40 cm Hydrophilic coating.

ASPIRATION THROMBECTOMY CATHETER –1.30 MM SQUARE SUCTION AREA – DCGI APPROVED • Available in Size 6F, 7F Both, Must have entry profile 0.019 inches • Braided polyamide elastomer shaft, stainless steel wire braiding and Guide wire type Stylet, • 6.0mm tip length for making aspiration inlet to come closer to the target thrombus and 10cm-length depth. • Must Have Distal 40 cm Hydrophilic coating.

COMPUTER AIDED VACCUM THROMBECTOMY CATHETER KIT FOR VTE MECHANICAL ASPIRATION WITH WORKING LENGTH OF 100/115/130 CM.  Should have multi-pitch, laser-cut stainless steel hypotube for 1:1 torque transfer & advance deliverability.  Catheter Should have ID of (3.33 mm), OD of 12 Fr with HTORQ tip with 50 mm circumferencial sweep.  compatible with 12 Fr sheath & wire platform (.014-.038) with proprietoryseperator technology.  Aspiration tubing Audio visual cues to help indicate location of clot in system & compatible with engine with (-29.2) inHg Deep vacuum

CATHETER -  Stainless steel hypotube at the proximal end, designed to enhance deliverability to the desired vessel with optimal visualization and placement.  Catheter size : 6 F Catheter type : Low crossing profile of 1.75mm with an ID of .044”.  Separator : proprietary separator technology for easy and quick aspiration, with 200 cm length and distal OD of .89 mm. Safety features : Ability to get the clot out and not macerate .

SEPARATOR COMPONANT:  150CM - proprietary separator technology for easy and quick aspiration, with 150 cm length and distal OD of 1.83 mm.  175 CM - proprietary separator technology for easy and quick aspiration, with 175 cm length and distal OD of 1.40 mm.

ASPIRATION SOURCE - ENGINE CANISTER _  1 litre capacity collecting jar with measuring marks. Integrated clot catcher with completely airtight and break resistant to – 2 ATM pressure. Single touch operation. LED Canister lighting.

ENGINE POWERFUL ASPIRATION PUMP  with 29-inch HG deep vacuum. Canister with integrated clot catheter. LED Canister should be sleek and simple design.

CORONARY MICRO-GUIDE CATHETER WITH GOLD MARKER– DISTAL 70 CM HYDROPHILIC COAT. USFDA/PMDA APPROVED • Must Have tapered stainless steel braid mesh construction and Inner PTFE Layer. • Must Have 13 CM floppy distal segment, 70cm distal hydrophilic coating • Must Have Distal outer diameter 1.8 Fr or less and Proximal Outer diameter 2.6Fr. • Catheter Length 130cm for antegrade approach and 150 cm for retrograde approach.

CORONARY MICRO-GUIDE CATHETER WITH GOLD MARKER– DISTAL 70 CM HYDROPHILIC COAT. CE/DCGI APPROVED • Must Have tapered stainless steel braid mesh construction and Inner PTFE Layer. • Must Have 13 CM floppy distal segment, 70cm distal hydrophilic coating • Must Have Distal outer diameter 1.8 Fr or less and Proximal Outer diameter 2.6Fr. • Catheter Length 130cm for antegrade approach and 150 cm for retrograde approach.

Re-Entry Catheter for CTO for Coronary – US FDA/CE / DCGI APPROVED

Re-Entry Wire for CTO for Coronary – US FDA/CE / DCGI APPROVED

Re-Entry Balloon with Two exit Port for CTO for Coronary – US FDA/CE / DCGI APPROVED

MICROCATHETER – TIP ENTRY – 1.3F - 135, 150 CM - USFDA APPROVED • Tapered soft tip, Tip entry 1.3 Fr distal 2.6 Fr & Proximal 2.8 Fr having SHINKA Shaft length 135 & 150 cm • USFDA approved

MICROCATHETER – TIP ENTRY – 1.3F -135, 150 CM – CE/DCGI APPROVED • Tapered soft tip, Tip entry 1.3 Fr distal 2.6 Fr & Proximal 2.8 Fr having SHINKA Shaft length 135 & 150 cm • USFDA approved

MICROCATHETER – TIP ENTRY – 1.4F -135, 150 CM - USFDA APPROVED • Tapered soft tip, Tip entry 1.4 Fr distal 1.9 Fr & Proximal 2.6 Fr having SHINKA Shaft length 135 & 150 cm • USFDA approved

MICROCATHETER – TIP ENTRY – 1.4F -135, 150 CM – CE/DCGI APPROVED • Tapered soft tip, Tip entry 1.4 Fr distal 1.9 Fr & Proximal 2.6 Fr having SHINKA Shaft length 135 & 150 cm • USFDA approved

MICROCATHETER - DOUBLE LUMEN – USFDA APPROVED

MICROCATHETER - DOUBLE LUMEN – USFDA APPROVED

COAXIAL MICROCATHETER SYSTEM FOR PERIPHERAL VESSELS – USFDA/PMDA APPROVED  2.8Fr and 2.4Fr - 2.4 and 2.0Fr Pre-Shaped Tip  tungsten coil pitch construction, PTFE inner layer, DMSO Compatible, Radiopaque 0.7 mm platinum/iridium markers

COAXIAL MICROCATHETER SYSTEM FOR PERIPHERAL VESSELS – CE/DCGI APPROVED  2.8Fr and 2.4Fr - 2.4 and 2.0Fr Pre-Shaped Tip tungsten coil pitch construction, PTFE inner layer, DMSO Compatible, Radiopaque 0.7 mm platinum/iridium markers

RADIAL ARTERY HAEMOSTASIS DEVICE- (TRANS RADIAL BAND) – USFDA/PMDA APPROVED  sizes – 24cm and 29cm, Must have belt magic tape for fast application.  Consists of two balloon specially designed for spot compression of the radial puncture site.  Must have curved support plate. Must have green Positioning marker

RADIAL ARTERY HAEMOSTASIS DEVICE- (TRANS RADIAL BAND) – CE/DCGI APPROVED  sizes – 24cm and 29cm, Must have belt magic tape for fast application.  Consists of two balloon specially designed for spot compression of the radial puncture site. Must have curved support plate. Must have green Positioning marker

FEMORAL COMPRESSION DEVICES – DISC / DOME BASED COMPRESSION - US FDA APPROVED

FEMORAL COMPRESSION DEVICES – DISC / DOME BASED COMPRESSION – CE/DCGI APPROVED

ICD/PI COMPRESSION DEVICES

PTCA/CORONARY ANGIOGRAPHY DRAP SET  Contains Absorbable Disposable Woven Cloth Sheet of Size 1.5 meter z 2.5 meter (2No)  Contains Absorbable Disposable Woven Cloth Sheet of Size 1.5 meter x 1metr (2No)

G- Kit Type Disposable surgeons Gown Set

Disposable Plastic Sheet of Size 1.5x2.5 mtr

ANGIOGRAPHY CINE RECORDABLE DISK- COMPACT R TYPE Media with Cover with Govt. Medical College Kota & M.C logo printed over the cover

ANGIOGRAPHY CINE RECORDABLE -DIGITAL VERSETILE – R TYPE Media with Cover with Govt. Medical College Kota & M.C logo printed over the cover

G-Kit Type Disposable Sterile Surgeon Gowns

Disposable E.O. Sterile Angiography drap set kit (Radial),  should have two long disposable sheet in both sizes  ( 1.50 meter X 1.0 meter with hole of 3 inch radius - 1 quantity)  ( 1.50 meter X 2.5 meter with hole of 3 inch radius – 2 in quantity)

Disposable E.O Sterile Angiography drap set kit (Femoral),  Should have two long disposable sheet in both sizes  ( 1.50 meter X 1.0 meter with hole of 3 inch radius - 1 quantity),  ( 1.50 meter X 2.5 meter with hole of 3 inch radius – 2 in quantity)

LONG DISPOSABLE E.O STERILE SHEET (1.50 METER X 2.5 METER SIZE)

SMALL DISPOSABLE E.O STERILE SHEET (1.50 METER X 1.0 METER SIZE)

RAT PAD TYPE RADIATION PROTECTION DEVICE SHIELD IN ALL SIZES

DISPOSABLE RADIATION PROTECTION SHIELDS & DRAPES  Disposable non fenestrated lead free absorbable sterile barrier pad for protection during fluoroscopy for coronary interventional procedures with a minimum thickness of 0.25 mm lead equivalence, with patented bi-layer homogenous sheet tested & certified to IEC 61331-1:2014, ASTM F3094-14, DIN 6857-1, USFDA approved, ISO 13485 & BARC certified with attenuation greater than 92% at 90kVp. Dimensions: 12” x 17”

DISPOSABLE RADIATION PROTECTION SHIELDS & DRAPES  Disposable scoop fenestrated lead free absorbable sterile barrier pad for protection during fluoroscopy for coronary interventional procedures with a minimum thickness of 0.25 mm lead equivalence, with patented bi-layer homogenous sheet tested & certified to IEC 61331-1:2014, ASTM F3094-14, DIN 6857-1, USFDA approved, ISO 13485 & BARC certified with attenuation greater than 92% at 90kVp. Dimensions: 12” x 17”, Fenestration: 3.5” x 1.5”

DISPOSABLE RADIATION PROTECTION SHIELDS & DRAPES  Disposable circular fenestrated lead free absorbable sterile barrier pad for protection during fluoroscopy for coronary interventional procedures with a minimum thickness of 0.25 mm lead equivalence, with patented bi-layer homogenous sheet tested & certified to IEC 61331-1:2014, ASTM F3094-14, DIN 6857-1, USFDA approved, ISO 13485 & BARC certified with attenuation greater than 92% at 90kVp. Dimensions: 12” x 17”, Fenestration: Circle Fenestration: 1.5”

DISPOSABLE RADIATION PROTECTION SHIELDS & DRAPES  Disposable non fenestrated lead free absorbable sterile barrier pad for protection during fluoroscopy for peripheral interventional procedures with a minimum thickness of 0.25 mm lead equivalence, with a minimum length of 34 inches and covering the length from hip to toe; with patented bi-layer homogenous sheet tested & certified to IEC 61331-1:2014, ASTM F3094-14, DIN 6857-1, USFDA approved, ISO 13485 & BARC certified with attenuation greater than 92% at 90kVp. Dimensions: 12” x 34”

DISPOSABLE RADIATION PROTECTION CAPS Disposable non fenestrated lead-free absorbable head cap for protection during fluoroscopy for interventional procedures with a minimum thickness of 0.25 mm lead equivalence and USFDA approved

External Temporary Pacemaker

PTCA Guide Wire – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm Length – USFDA/PMDA Approved • Must have Platinum coil at distal tip. Balance of Hydrophilic and Hydrophobic coating • Must have directly jointed SUS and Nitinol shaft through DuoCore technology and silicon coated joint. • Must have PTFE Coating from 25 to 180 cm length. & Mucus coat hydrophilic coating up to 248 mm • Should have 0.6 & 1.0 gram force tip loads

PTCA Guide Wire – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm Length – CE/DCGI Approved • Must have Platinum coil at distal tip. Balance of Hydrophilic and Hydrophobic coating • Must have directly jointed SUS and Nitinol shaft through DuoCore technology and silicon coated joint. • Must have PTFE Coating from 25 to 180 cm length. & Mucus coat hydrophilic coating up to 248 mm • Should have 0.6 & 1.0 gram force tip loads

CTO Stiff PTCA Wire - 3.6-gram Force tip load – 2 mm Silicon coated distal tip, 0.014” Diameter and 180 cm – USFDA/PMDA Approved • Must have Platinum coil at distal tip. Balance of Hydrophilic and Hydrophobic coating • Must have directly jointed SUS and Nitinol shaft through DuoCore technology and silicon coated joint. • Must have M coat hydrophilic coating up to 248 mm & PTFE Coating from 25 to 180 cm length.  Should have 3.6-gram fore tip load

CTO Stiff PTCA Wire - 3.6-gram Force tip load – 2 mm Silicon coated distal tip, 0.014” Diameter and 180 cm – CE/DCGI Approved • Must have Platinum coil at distal tip. Balance of Hydrophilic and Hydrophobic coating • Must have directly jointed SUS and Nitinol shaft through DuoCore technology and silicon coated joint. • Must have M coat hydrophilic coating up to 248 mm & PTFE Coating from 25 to 180 cm length. • Should have 3.6-gram fore tip load

PTCA GUIDEWIRE FOR SEPTAL NAVIGATION - 0.03 GM TIP LOAD– USFDA APPROVED • Tip load 0.3 gm, Hydrophilic coating with Sion Tec Technology, coil length 19 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR SEPTAL NAVIGATION - 0.03 GM TIP LOAD – CE/DCGI APPROVED • Tip load 0.3 gm, Hydrophilic coating with Sion Tec Technology, coil length 19 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD - 8.5 CM SPRING COIL - USFDA APPROVED • Stainless core, ACTONE technology, Polymer jacket with Hydrophilic coating, Tip load 3 gm, Radiopaque length 3 cm, Spring coil 8.5 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD - 8.5 CM SPRING COIL - CE/DCGI APPROVED • Stainless core, ACTONE technology, Polymer jacket with Hydrophilic coating, Tip load 3 gm, Radiopaque length 3 cm, Spring coil 8.5 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD – 3 CM SPRING COIL – USFDA APPROVED • Stainless core, ACTONE technology, Polymer jacket with Hydrophilic coating, Tip load 3 gm, Radiopaque length 3 cm, Spring coil 3 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD – 3 CM SPRING COIL – CE/DCGI APPROVED • Stainless core, ACTONE technology, Polymer jacket with Hydrophilic coating, Tip load 3 gm, Radiopaque length 3 cm, Spring coil 3 cm, Length 190 cm & 300 cm

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD – 11 CM SPRING COIL – USFDA APPROVED • Stainless core, ACTONE technology, Polymer jacket length 40 cm with Hydrophilic coating 50 cm, Tip Load 3 gm, Radiopaque length 3 cm, Spring coil 11 cm, Length 200 cm & 300 cm with straight tip & 1 mm pre shape

PTCA GUIDEWIRE FOR CTO – 3 GM TIP LOAD – 11 CM SPRING COIL – CE/DCGI APPROVED • Stainless core, ACTONE technology, Polymer jacket length 40 cm with Hydrophilic coating 50 cm, Tip Load 3 gm, Radiopaque length 3 cm, Spring coil 11 cm, Length 200 cm & 300 cm with straight tip & 1 mm pre shape

PTCA GUIDEWIRE FOR CTO – 0.6 GM TIP LOAD – 28 CM SPRING COIL – USFDA APPROVED Sion Tecc Technology, ACTONE Braiding, 17 cm Polymer Jacket 17 cm Slip coat coating, Radiopaque Length 16 cm 28 cm spring coil, Tapered tip 0.010-inch, Tip load 0.6 gm

PTCA GUIDEWIRE FOR CTO – 0.6 GM TIP LOAD – 28 CM SPRING COIL – CE/DCGI APPROVED Sion Tecc Technology, ACTONE Braiding, 17 cm Polymer Jacket 17 cm Slip coat coating, Radiopaque Length 16 cm 28 cm spring coil, Tapered tip 0.010-inch, Tip load 0.6 gm

PTCA GUIDEWIRE FOR CTO – 1.0 GM TIP LOAD – 28 CM SPRING COIL – USFDA APPROVED Sion Tecc Technology, ACTONE Braiding, 17 cm Polymer Jacket 17 cm Slip coat coating, Radiopaque Length 16 cm 28 cm spring coil, Tapered tip 0.010-inch, Tip load 1.0 gm

PTCA GUIDEWIRE FOR CTO – 1.0 GM TIP LOAD – 28 CM SPRING COIL – CE/DCGI APPROVED Sion Tecc Technology, ACTONE Braiding, 17 cm Polymer Jacket 17 cm Slip coat coating, Radiopaque Length 16 cm 28 cm spring coil, Tapered tip 0.010-inch, Tip load 1.0 gm

PTCA GUIDEWIRE FOR CTO – 1.7, 3.5, 4.5 GM TIP LOAD – 15 CM SPRING COIL – USFDA APPROVED  Sion Tecc Technology, ACTONE Braiding, spring coil length 15 cm, Radiopaque Length 15 cm, Tapered tip 0.010 inch  Gaia 1st tip load 1.7 gm Tapered tip 0.011 inch  Gaia 2nd tip load 3.5 gm, Tapered tip 0.012 inch  Gaia 3rd tip load 4.5 gm, • All are mini - pre shaped 1mm 45 degree angle , Micro cone tip used for CTO Cases

PTCA GUIDEWIRE FOR CTO – 1.7, 3.5, 4.5 GM TIP LOAD – 15 CM SPRING COIL – CE/DCGI APPROVED  Sion Tecc Technology, ACTONE Braiding, spring coil length 15 cm, Radiopaque Length 15 cm, Tapered tip 0.010 inch  Gaia 1st tip load 1.7 gm Tapered tip 0.011 inch  Gaia 2nd tip load 3.5 gm, Tapered tip 0.012 inch  Gaia 3rd tip load 4.5 gm,  All are mini - pre shaped 1mm 45 degree angle , Micro cone tip used for CTO Cases

PTCA GUIDEWIRE FOR CTO – 3.0 GM TIP LOAD  Single core , Core to tip , Tip load 3 gm , Tip radiopacity 3 cm , tip diameter 0.014 inch , Tip radiopacity 11 cm , slip coat over the spring coil used for CTO Lesion

PTCA GUIDEWIRE FOR CTO – 3.0, 6.0, 12 GM TIP LOAD  Single core , Core to tip , Tip load 3 gm ,6 gm , 12 gm Tip radiopacity 3 cm , tip diameter 0.014 inch , Tip radiopacity 11 cm , Silicone coating coat over the spring coil used for CTO Lesion

PTCA GUIDEWIRE FOR CTO – 9.0, 12, 20 GM TIP LOAD  Single core Core to tip , Tip load 9 gm tapered 0.090 , 12 gm tapered 0.090 inch & 20 gm Tapered tip 0.080 inch for CTO Lesion

PTCA GUIDEWIRE FOR CTO – 3.0 GM TIP LOAD Single core Core to tip , Tip load 3 gm, radiopacity 3 cm , guide wire length 330 cm , slip coat over the spring coil

PTCA GUIDEWIRE FOR CTO – 2.0, 4.0, 6.0 GM TIP LOAD  Sion Tecc Technology, ACTONE Braiding, spring coil length 15 cm , Radiopaque Length 15 cm , Tapered tip 0.010 inch  Gaia 1st tip load 2 gm Tapered tip 0.011 inch  Gaia 2nd tip load 4 gm, Tapered tip 0.012 inch  Gaia 3rd tip load 6 gm,  All are mini - pre shaped 1mm 45 degree angle , Micro cone tip , Xtrand Coil

PTCA WIRES WITH FACILITY OF BOOT LINKS FOR EXTENSION OF REGULAR WIRE - US FDA APPROVED

Micro-wire (0.008”-0.012” ) with Hydrophilic coating

Special inflation device for high pressure (55 ATM), High Resolution

PTCA WIRE – TIP LOAD - 0.5-0.7GM – USFDA Approved  Regular Workhorse Guidewire with Tapered Elastinite Nitinol Core, Durasteel Ribbon Tip and available in both hydrophilic and hydrophobic coatings between tip load 0.5-0.7gm

PTCA WIRE – TIP LOAD - 0.5-0.7GM –WITH INTERMEDIATE POLYMER SLEEVE - USFDA APPROVED  Regular Workhorse Guidewire with Elastinite Nitinol Core, Hyten Stainless Steel Tip, Intermediate polymer sleeve with Hydrocoat on distal tip between tip load 0.5-0.7gm

PTCA WIRE – TIP LOAD - 0.5-0.7GM –WITH INTERMEDIATE POLYMER SLEEVE - CE/DCGI APPROVED  Regular Workhorse Guidewire with Elastinite Nitinol Core, Hyten Stainless Steel Tip, Intermediate polymer sleeve with Hydrocoat on distal tip between tip load 0.5-0.7gm

PTCA WIRE – TIP LOAD - 0.5-0.7GM –WITH HYTEN STAINLESS STEEL TIP - USFDA APPROVED  Regular Workhorse Guidewire with Elastinite Nitinol Core, Hyten Stainless Steel Tip Intermediate polymer sleeve with Smoothglide coating on proximal and Turbocoat on distal tip between tip load 0.5-0.7gm

PTCA WIRE – TIP LOAD - 0.5-0.7GM –WITH HYTEN STAINLESS STEEL TIP - CE/DCGI APPROVED  Regular Workhorse Guidewire with Elastinite Nitinol Core, Hyten Stainless Steel Tip Intermediate polymer sleeve with Smoothglide coating on proximal and Turbocoat on distal tip between tip load 0.5-0.7gm

PTCA WIRE – TIP LOAD – 0.6 GM –WITH STAINLESS STEEL CORE WITH SHAPING RIBBON TIP - USFDA APPROVED  Regular Workhorse Guidewire with Tapered Stainless Steel Core and Shaping Ribbon Tip available in tip load of 0.6gm with Poly Tetra Fluoro Ethylene Coating on Proximal End

PTCA WIRE – TIP LOAD – 0.6 GM –WITH STAINLESS STEEL CORE WITH SHAPING RIBBON TIP – CE/DCGI APPROVED  Regular Workhorse Guidewire with Tapered Stainless Steel Core and Shaping Ribbon Tip available in tip load of 0.6gm with Poly Tetra Fluoro Ethylene Coating on Proximal End

PTCA WIRE – TIP LOAD – 0.8 GM – RESPONSEASE CORE GRIND WITH PALLADIUM-RHENIUM TIP – USFDA APPROVED  Regular Workhorse Guidewire with Responsease Core Grind Technology and 3cm Palladium-Rhenium Radiopaque Distal Tip available in tip load of 0.8gm with 190 and 300cm

PTCA WIRE – TIP LOAD – 0.8 GM – RESPONSEASE CORE GRIND WITH PALLADIUM-RHENIUM TIP – CE/DCGI APPROVED  Regular Workhorse Guidewire with Responsease Core Grind Technology and 3cm Palladium-Rhenium Radiopaque Distal Tip available in tip load of 0.8gm with 190 and 300cm

PTCA WIRE – TIP LOAD – 0.9 GM – RESPONSEASE CORE GRIND WITH UNCOATED TIP – USFDA APPROVED  Workhorse Guidewire with Durasteel Core, Responsease Core Grind Technology and 1.5 cm uncoated distal tip for tactile feedback available in multiple variants with exact same tip load of 0.9gm

PTCA WIRE – TIP LOAD – 0.9 GM – RESPONSEASE CORE GRIND WITH UNCOATED TIP – CE/DCGI APPROVED  Workhorse Guidewire with Durasteel Core, Responsease Core Grind Technology and 1.5 cm uncoated distal tip for tactile feedback available in multiple variants with exact same tip load of 0.9gm

PTCA WIRE – TIP LOAD – 0.6-.8 GM – TRIPLE SPRING WITH ROTARY SWAGGING TIP – USFDA APPROVED  Workhorse Guidewire with Triple Spring 304V Stainless Steel with NiTi Distal Core and Cold Working Rotary Swagging Tip available in tip loads between 0.6-0.8gm and lengths (190/300cm).

PTCA WIRE – TIP LOAD – 0.6-.8 GM – TRIPLE SPRING WITH ROTARY SWAGGING TIP – CE/DCGI APPROVED  Workhorse Guidewire with Triple Spring 304V Stainless Steel with NiTi Distal Core and Cold Working Rotary Swagging Tip available in tip loads between 0.6-0.8gm and lengths (190/300cm).

SPECIALITY PTCA WIRE – LOW SUPPORT - TIP LOAD 0.8-1.0 GM – USFDA APPROVED  Low Support Durasteel Guidewire with Full Polymer Coating available in tip loads between 0.8-1.0gm

SPECIALITY PTCA WIRE – LOW SUPPORT - TIP LOAD 0.8-1.0 GM – CE/DCGI APPROVED  Low Support Durasteel Guidewire with Full Polymer Coating available in tip loads between 0.8-1.0gm

SPECIALITY PTCA WIRE – MEDIUM SUPPORT - TIP LOAD 1.0-1.2 GM – USFDA APPROVED  Medium Support Durasteel Guidewire with Full Polymer Coating available in tiploads between 1.0-1.2gm

SPECIALITY PTCA WIRE – MEDIUM SUPPORT - TIP LOAD 1.0-1.2 GM – CE/DCGI APPROVED  Medium Support Durasteel Guidewire with Full Polymer Coating available in tiploads between 1.0-1.2gm

SPECIALITY PTCA WIRE – EXTRA SUPPORT - TIP LOAD 1.0-1.2 GM – USFDA APPROVED  Extra Support Durasteel Guidewire with Full Polymer Coating available in tiploads between 1.0-1.2gm

SPECIALITY PTCA WIRE – EXTRA SUPPORT - TIP LOAD 1.0-1.2 GM – CE/DCGI APPROVED  Extra Support Durasteel Guidewire with Full Polymer Coating available in tiploads between 1.0-1.2gm

SPECIALITY PTCA WIRE – EXTRA SUPPORT - TIP LOAD 1.3-1.5 GM – USFDA APPROVED  Extra Support Durasteel Guidewire with Full Polymer Cover, Marker at 4.5cm from distal tip and tipload between 1.3-1.5gm

SPECIALITY PTCA WIRE – EXTRA SUPPORT - TIP LOAD 1.3-1.5 GM – CE/DCGI APPROVED  Extra Support Durasteel Guidewire with Full Polymer Cover, Marker at 4.5cm from distal tip and tipload between 1.3-1.5gm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 1.0 GM – USFDA APPROVED  Stainless Steel Guidewire with Stainless Steel coils and hydrophilic coating availabe in tipload of 1gm with radioapaque tip of 3cm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 1.0 GM – CE/DCGI APPROVED  Stainless Steel Guidewire with Stainless Steel coils and hydrophilic coating availabe in tipload of 1gm with radioapaque tip of 3cm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 0.6 - 0.7 GM – USFDA APPROVED  Stainless Steel Guidewire with Intermediate polymer sleeve and hydrophobic coating availabe in tipload between 0.6-0.7gm with radioapaque tip of 3cm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 0.6 - 0.7 GM – CE/DCGI APPROVED  Stainless Steel Guidewire with Intermediate polymer sleeve and hydrophobic coating availabe in tipload between 0.6-0.7gm with radioapaque tip of 3cm

SPECIALITY PTCA WIRE – ELASTINITE NITINOL - TIP LOAD 0.7 - 0.8 GM – USFDA APPROVED  Elastinite Nitinol Guidewire with Shaping Ribbon Tip and Hydrophilic Coating avaialble in tipload between 0.7-0.8gm with radiopaque tip of 4.5cm

SPECIALITY PTCA WIRE – ELASTINITE NITINOL - TIP LOAD 0.7 - 0.8 GM – CE/DCGI APPROVED  Elastinite Nitinol Guidewire with Shaping Ribbon Tip and Hydrophilic Coating avaialble in tipload between 0.7-0.8gm with radiopaque tip of 4.5cm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 1.7, 4.7, 6.2, 8.7 GM – USFDA APPROVED  Stainless Steel Penetration Guidewire with Core-to-Tip design and hydrophilic coating available in tipload of 1.7, 4.7, 6.2, 8.7 gm

SPECIALITY PTCA WIRE – STAINLESS STEEL - TIP LOAD 1.7, 4.7, 6.2, 8.7 GM – CE/DCGI APPROVED  Stainless Steel Penetration Guidewire with Core-to-Tip design and hydrophilic coating available in tipload of 1.7, 4.7, 6.2, 8.7 gm

SPECIALITY PTCA WIRE – DURASTEEL - TIP LOAD 2.5-2.7 GM – USFDA APPROVED  Extra Support Durasteel CTO Guidewire with Full Polymer Cover, Gold Marker at 4.5cm from distal tip and tipload between 2.5-2.7gm

SPECIALITY PTCA WIRE – DURASTEEL - TIP LOAD 2.5-2.7 GM – CE/DCGI APPROVED  Extra Support Durasteel CTO Guidewire with Full Polymer Cover, Gold Marker at 4.5cm from distal tip and tipload between 2.5-2.7gm

PTCA WIRE FOR CTO TIP LOAD –4.5-4.8 – USFDA APPROVED  CTO Guidewire having Durasteel Core, Intermediate Polymer Sleeve available in tipload between 4.5-4.8gm Tipload and penetration power of 40 kgpsin

PTCA WIRE FOR CTO TIP LOAD –9.5-9.7– USFDA APPROVED  PTCA CTO Guidewire having Durasteel Core, Intermediate Polymer Sleeve available in tipload between 9.5-9.7gm Tipload and penetration power of 80 kgpsin

PTCA WIRE FOR CTO TIP LOAD –13.5-13.9 – USFDA APPROVED  PTCA CTO Guidewire having Durasteel Core, Intermediate Polymer Sleeve available in tipload between 13.5-13.9gm Tipload and penetration power of 120 kgpsin

PTCA WIRE FOR CTO TIP LOAD –12-12.5 – USFDA APPROVED CTO Guidewire having Durasteel Core, Intermediate Polymer Sleeve available in tipload between 12.0-12.5gm Tipload and penetration power of 140 kgpsin

PTCA WIRE FOR CTO TIP LOAD –12.8-13.0 – USFDA APPROVED CTO Guidewire having Durasteel Core, Intermediate Polymer Sleeve available in tipload between 12.8-13.0gm Tipload and penetration power of 200 kgpsin

PTCA WIRE FOR CTO – TIP LOAD – 11, 14 GM - USFDA APPROVED CTO Guidewire having having Durasteel Core, Hydrophilic coating (excluding the tip) for lubricity and ease of movement within a microcathete, textured tip with tip size of 0.009 Inches and tip angle of 25 degrees at 1 mm of tip. Should have the tip load of 11, 14GM

HIGH PRESSURE NON-COMPLIANT BALLOON – THREE PLEATS RE-WRAPPABLE STRUCTURE - PMDA APPROVED • with Innovative triple layer balloon technology with high pressure resistance of 22 ATM. • Must Have Elastomer outer layer, middle layer of Polyamide and inner most layer of Elastomer. • Must Have nominal pressure of 12atm and RBP of 22atm. • Shorter thin distal tip of 2.9mm with low entry profile of 0.43 mm. must have hydrophilic Mucus coating • Must Have 3.0 mm Short taper balloon shoulder & Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile. • Must have 2.6 French stainless steel core wire structured shaft & stainless-steel stylet in Mid Shaft. Must Have Hypotube without PTFE Coating.

HIGH PRESSURE NON-COMPLIANT BALLOON – THREE PLEATS RE-WRAPPABLE STRUCTURE – CE/DCGIAPPROVED  with Innovative triple layer balloon technology with high pressure resistance of 22 ATM.  Must Have Elastomer outer layer, middle layer of Polyamide and inner most layer of Elastomer.  Must Have nominal pressure of 12atm and RBP of 22atm.  Shorter thin distal tip of 2.9mm with low entry profile of 0.43 mm. must have hydrophilic Mucus coating  Must Have 3.0 mm Short taper balloon shoulder & Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile.  Must have 2.6 French stainless steel core wire structured shaft & stainless-steel stylet in Mid Shaft. Must Have Hypotube without PTFE Coating.

CTO Balloon with Ultra – Ultra Low Entry profile of 0.016" must have hydrophilic Mucus coating -PMDA APPROVED  Should have smallest diameter 1.00mm and 5mm length. - three pleats Re-wrappable structure.  Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile.  Must have Flexible Tip with short balloon bonding part of 0.4mm.  nominal pressure of 06 ATM and RBP of 14 ATM  Must have 2.4 to 2.7 French tapered stainless steel core wire structured shaft

CTO Balloon with Ultra – Ultra Low Entry profile of 0.016" must have hydrophilic Mucus coating -CE/DCGI APPROVED  Should have smallest diameter 1.00mm and 5mm length. - three pleats Re-wrappable structure.  Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile.  Must have Flexible Tip with short balloon bonding part of 0.4mm.  nominal pressure of 06 ATM and RBP of 14 ATM  Must have 2.4 to 2.7 French tapered stainless steel core wire structured shaft

PTCA BALLOON SEMI COMPLIANT FOR CTO – USFDA APPROVED  CTO Indicated Slim Seal Technology on distal tip with lesion entry profile of 0.016", crossing profile of 0.021" and single flexible Tungsten marker available in unique diameter of 1.2mm with variety of lengths  Diameter – 1.2, 1.5. 2.0  Length – 6, 8, 12, 15, 20 & in 2MM- 25, 30

PTCA BALLOON SEMI COMPLIANT FOR CTO – CE/DCGI APPROVED  CTO Indicated Slim Seal Technology on distal tip with lesion entry profile of 0.016", crossing profile of 0.021" and single flexible Tungsten marker available in unique diameter of 1.2mm with variety of lengths  Diameter – 1.2, 1.5. 2.0  Length – 6, 8, 12, 15, 20 & in 2MM- 25, 30

PTCA BALLOON SEMI COMPLIANT – USFDA APPROVED  with Slim Seal Technology on distal tip with crossing profile of 0.021”, Lesion entry profile of 0.017” and Microglide Coating available in diameter 2.25-5.00mm and lengths 6-30mm  Diameter – 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25, 30

PTCA BALLOON SEMI COMPLIANT – CE/DCGI APPROVED  with Slim Seal Technology on distal tip with crossing profile of 0.021”, Lesion entry profile of 0.017” and Microglide Coating available in diameter 2.25-5.00mm and lengths 6-30mm  Diameter – 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25, 30

PTCA BALLOON NON-COMPLIANT – USFDA APPROVED  with Multilayer CrossFlex Balloon Technology and Round Tip with Lesion Entry Profile of 0.018” available in diameter 1.5mm-5mm and lengths in 6mm-25mm with Skive Technology on Mid shaft of Dilatation Catheter  Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25

PTCA BALLOON NON-COMPLIANT – CE/DCGI APPROVED  with Multilayer CrossFlex Balloon Technology and Round Tip with Lesion Entry Profile of 0.018” available in diameter 1.5mm-5mm and lengths in 6mm-25mm with Skive Technology on Mid shaft of Dilatation Catheter  Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25

PTCA BALLOON NON-COMPLIANT – USFDA APPROVED  Multilayer and Single piece Outer member and Large Hypotube and Visible Hub Printing should have shorter deflation time and Shall come in sizes of 1.5 mm to 6 mm  Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 mm  Length - 6, 8, 12, 15, 20, 25

PTCA BALLOON NON-COMPLIANT – CE/DCGI APPROVED  Multilayer and Single piece Outer member and Large Hypotube and Visible Hub Printing should have shorter deflation time and Shall come in sizes of 1.5 mm to 6 mm  Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 mm  Length - 6, 8, 12, 15, 20, 25

PTCA BALLOON SEMI-COMPLIANT – CE APPROVED  balloon with laser bond technology on distal tip with crossing profile of 0.021” and tip entry profile of 0.017” available in diameter 2.25-5.00mm and lengths 6-30mm  Diameter –2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25, 30

PTCA BALLOON SEMI-COMPLIANT –DCGI APPROVED  balloon with laser bond technology on distal tip with crossing profile of 0.021” and tip entry profile of 0.017” available in diameter 2.25-5.00mm and lengths 6-30mm  Diameter –2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm  Length - 6, 8, 12, 15, 20, 25, 30

PTCA BALLOON NON-COMPLIANT – CE APPROVED  non-complaint coronary balloon with Tri-fold layers and Tip Entry Profile of 0.018” available in diameter 2.0-4.5mm and lengths in 8mm-25mm  Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5 MM  Length - 8, 12, 15, 20, 25 MM

PTCA BALLOON NON-COMPLIANT – DCGI APPROVED  non-complaint coronary balloon with Tri-fold layers and Tip Entry Profile of 0.018” available in diameter 2.0-4.5mm and lengths in 8mm-25mm  Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5 MM  Length - 8, 12, 15, 20, 25 MM

NON-COMPLIANT PTCA BALLOON – USFDA APPROVED  0.017” lesion entry profile, crossing profile - .031, Bi-Segmen inner shaft design with Hydrophilic coating, Over-the-inner tip design, Slop outer shaft  Platinum iridium marker bands, nominal pressure 12 ATM, RBP -18 ATM  Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 mm,  Length – 6, 8, 12, 15, 20, 30 mm

NON-COMPLIANT PTCA BALLOON – CE/DCGI APPROVED  0.017” lesion entry profile, crossing profile - .031, Bi-Segmen inner shaft design with Hydrophilic coating, Over-the-inner tip design, Slop outer shaft  Platinum iridium marker bands, nominal pressure 12 ATM, RBP -18 ATM  Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 mm,  Length – 6, 8, 12, 15, 20, 30 mm

SEMI-COMPLIANT PTCA BALLOON – USFDA APPROVED  0.017” lesion entry profile, crossing profile - .026, Bi-Segmen inner shaft design with Hydrophilic coating, Unique, over-the- inner tip design: outer tip material rides over the inner shaft material, Slop outer shaft, Optileap material with ZGlide hydrophilic coating  Platinum iridium marker bands, nominal pressure 12 ATM, RBP -18 ATM  Diameter –1.2, 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm,  Length – 8, 12, 15, 20, 30, 40 mm

SEMI-COMPLIANT PTCA BALLOON – CE/DCGI APPROVED  0.017” lesion entry profile, crossing profile - .026, Bi-Segmen inner shaft design with Hydrophilic coating, Unique, over-the- inner tip design: outer tip material rides over the inner shaft material, Slop outer shaft, Optileap material with ZGlide hydrophilic coating  Platinum iridium marker bands, nominal pressure 12 ATM, RBP -18 ATM  Diameter –1.2, 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 mm,  Length – 8, 12, 15, 20, 30, 40 mm

THINNEST WALL 0.08 SEMI COMPLIANT BALLOON – LONG LENGTH– CE APPROVED  NP -6 ATM, RBP – 18 ATM, Crossing profile .65  Diameter – 1.25, 1.5, 2.0, 2.25, 2.50, 2.75, 3.00, 3.25, 3.5, 4.00 & 4.5 MM  Length –10,12,15,20,25,30, 35, 40

ANGLED SHOULDER NON-COMPLIANT BALLOON – LONG LENGTH– CE APPROVED  Angled shoulder balloon with Trifold design, polyamide dual layer,  NP -8 ATM, RBP – 20 ATM, Entry profile -0.016, Crossing profile .70  Diameter – 1.25, 1.5, 2.0, 2.25, 2.50, 2.75, 3.00, 3.25, 3.5, 4.00 & 4.5 MM  Length –10,12,15,20,25,30, 35, 40

PTCA SCORING BALLOON – NITINOL HELICAL SHAPED SCORING ELEMENT – USFDA APPROVED  Tapered tip and three nitinol, helical shaped, electropolished scoring elements with rectangular edges, mounted on a balloon with a larger working range of 2 ATM - 20 ATM  Lesion entry profile .0172, hydrophilic coating, Laser cut hypotube, NP – 8 ATM, RBP – 16 ATM  Diameter -2.0mm, 2.5mm, 3.0mm, 3.5mm  lengths - 6mm, 10mm & 15mm, 20mm

PTCA SCORING BALLOON – NITINOL HELICAL SHAPED SCORING ELEMENT – CE/DCGI APPROVED  Tapered tip and three nitinol, helical shaped, electropolished scoring elements with rectangular edges, mounted on a balloon with a larger working range of 2 ATM - 20 ATM  Lesion entry profile .0172, hydrophilic coating, Laser cut hypotube, NP – 8 ATM, RBP – 16 ATM  Diameter -2.0mm, 2.5mm, 3.0mm, 3.5mm  lengths - 6mm, 10mm & 15mm, 20mm

PTCA SCORING BALLOON – TRIPLE TRIANGULAR MICROTOME – PMDA APPROVED  Scoring Balloon with triple triangular nylon microtomes 0.0155” in height with 120-degree angle between them.  An entry profile of O.0167 inch with 2.2Fr proximal shaft and 2.6F distal shaft.  NP-14 ATM RBP of 24 ATM  Diameter -2.0mm, 2.25mm, 2.5mm, 2.75mm, 3.0mm, 3.25mm, 3.5mm, 4.0mm.  Length – 13 mm

PTCA SCORING BALLOON NON-COMPLIANT – HIGH PRESURE - SINGLE WIRE – USFDA APPROVED  Scoring Balloon with single wire element, Tip length – 10mm, crossing profile .0350”.  Slider Hydrophilic Catheter and silicon coated lumen.  An entry profile of O.0167 inch with 2Fr proximal shaft and 3F distal shaft.  NP-12 ATM RBP of 22 ATM, Average burst pressure – 30ATM  Diameter -2.0mm, 2.25mm, 2.5mm, 2.75mm, 3.0mm, 3.25mm, 3.5mm, 3.75mm, 4.0mm.  Length – 6, 8, 10, 12, 15, 18, 20, 23, 25, 30 mm

PTCA SCORING BALLOON NON-COMPLIANT – HIGH PRESURE - SINGLE WIRE – CE/DCGI APPROVED  Scoring Balloon with single wire element, Tip length – 10mm, crossing profile .0350”.  Slider Hydrophilic Catheter and silicon coated lumen.  An entry profile of O.0167 inch with 2Fr proximal shaft and 3F distal shaft.  NP-12 ATM RBP of 22 ATM, Average burst pressure – 30ATM  Diameter -2.0mm, 2.25mm, 2.5mm, 2.75mm, 3.0mm, 3.25mm, 3.5mm, 3.75mm, 4.0mm.  Length – 6, 8, 10, 12, 15, 18, 20, 23, 25, 30 mm

PTCA CUTTING BALLOON – USFDA Approved  Bumper Tip, Acrylated urethane atherotome adhesive, Atherotomes , Z-Glide™ Hydrophilic Coating  Diameter -2.0mm, 2.25mm, 2.5mm, 2.75mm, 3.0mm, 3.25mm, 3.5mm, 3.75mm, 4.0mm.  Blade Length – 6, 10, 15 mm

PTCA CUTTING BALLOON – CE/DCGI Approved  Bumper Tip, Acrylated urethane atherotome adhesive, Atherotomes , Z-Glide™ Hydrophilic Coating  Diameter -2.0mm, 2.25mm, 2.5mm, 2.75mm, 3.0mm, 3.25mm, 3.5mm, 3.75mm, 4.0mm.  Blade Length – 6, 10, 15 mm

Triploblastic coated DRUG ELUTING PTCA BALLOON - CE/DCGI Approved  Must have optimum concentration of sirolimus – 2.75ug/mm  Diameter – 2 - 4mm, Length - 10 – 30mm  Must have nominal pressure 8ATM, RBP-16ATM

DURG ELUTING PTA BALLOON FOR BELOW THE KNEE PERIPHERAL ARTERY-DCGI APPROVED Paclitaxel Drug-Coated PTA Balloon Recommended guide wire- OTW (BTK): 0.018" Length (mm): 80,100,120 & 150 Diameter (mm): 2,2.5,3 & 4 Recommended guide wire- OTW (SFA): 0.035" Length (mm): 100,120 & 150 Diameter (mm): 5,6 & 7

DRUG ELUTING PTCA BALLOON - US FDA APPROVED  All types & sizes  Different types of drugs

DRUG ELUTING PTCA BALLOON - CE APPROVED  All types & sizes  Different types of drugs

DRUG ELUTING PTCA BALLOON - DCGI APPROVED  All types & sizes  Different types of drugs

BALLOON DILATATION CATHETER FOR AORTA & IVC- US FDA APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons  Available in the sizes and lengths

BALLOON DILATATION CATHETER FOR AORTA & IVC- CE APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons  Available in the sizes and lengths

BALLOON DILATATION CATHETER FOR AORTA & IVC- DCGI APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons  Available in the sizes and lengths

BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - US FDA APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons  Available in the sizes and lengths

BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - CE APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons  Available in the sizes and lengths

BIB (BALLOON IN BALLOON) TYPE BALLOONS FOR COARCTATION DILATATION - DCGI APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons Available in the sizes and lengths

Z MED TYPE BALLOON FOR AORTIC COACTATION – US FDA/CE APPROVED  5 to 20 cm diameter in all sizes Otw / Rapid exchange, compatible with 0.014”/0.035” and 0.038” wire

Z MED TYPE BALLOON FOR AORTIC COACTATION – DCGI APPROVED  5 to 20 cm diameter in all sizes  Otw / Rapid exchange, compatible with 0.014”/0.035” and 0.038” wire

Z MED TYPE BALLOON FOR AORTIC COACTATION – US FDA/CE APPROVED More than 20 cm diameter in all sizes Otw / Rapid exchange, compatible with 0.014”/0.035” and 0.038” wire

Z MED TYPE BALLOON FOR AORTIC COACTATION – DCGI APPROVED  More than 20 cm diameter in all sizes  Otw / Rapid exchange, compatible with 0.014”/0.035” and 0.038” wire

PROXIMAL OPTIMIZATION BALLOON – USFDA APPROVED  Specialised proximal optimisation balloon dilatation catheter with ultra short balloon shoulder of 0.6mm and an RBP of 22 atm with sizes ranging from a length of 6-15 mm and diameters ranging from 2.25-5 mm. Hydrophilic external surface coating from tip to adjacent guidewire port and silicone coating inside guidewire lumen.

PROXIMAL OPTIMIZATION BALLOON – CE/DCGI APPROVED  Specialised proximal optimisation balloon dilatation catheter with ultra short balloon shoulder of 0.6mm and an RBP of 22 atm with sizes ranging from a length of 6-15 mm and diameters ranging from 2.25-5 mm. Hydrophilic external surface coating from tip to adjacent guidewire port and silicone coating inside guidewire lumen.

PTCA HIGH PRESSURE CTO BALLOON – USFDA APPROVED  0.75 mm CTO balloon with a tip entry profile of 0.015” and ultra low crossing profile of 0.020” with a proprietary distal welding technology, 2.2F distal shaft, Rated Burst Pressure of 20 ATM and Average Burst Pressure of ≥ 28 ATM.  Diameters from 0.75mm, 1.0mm, 1.25mm, 1.50mm, 1.75mm & 2.0mm  lengths from 5mm, 8mm, 10mm, 15mm, 20mm, 25mm & 30mm.

PTCA HIGH PRESSURE CTO BALLOON – CE/DCGI APPROVED  0.75 mm CTO balloon with a tip entry profile of 0.015” and ultra-low crossing profile of 0.020” with a proprietary distal welding technology, 2.2F distal shaft, Rated Burst Pressure of 20 ATM and Average Burst Pressure of ≥ 28 ATM.  Diameters from 0.75mm, 1.0mm, 1.25mm, 1.50mm, 1.75mm & 2.0mm  lengths from 5mm, 8mm, 10mm, 15mm, 20mm, 25mm & 30mm.

ROTALINK BURR - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kots).

ROTALINK BURR – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota).

ROTALINK ADVANCER - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota).

ROTALINK ADVANCER - CE APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota).

ROTALINK ADVANCER – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota).

ROTALINK PLUS (ADVANCER & BURR) - US FDA APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota ).

ROTALINK PLUS (ADVANCER & BURR) - CE APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota

ROTALINK PLUS (ADVANCER AND BURR) – DCGI APPROVED (Compatible with existing Rota Machine Cath Lab GMC Kota

ROTATIONAL ATHERECTOMY GUIDE WIRES - US FDA APPROVED

ROTATIONAL ATHERECTOMY GUIDE WIRES - CE APPROVED

ROTATIONAL ATHERECTOMY GUIDE WIRES –DCGI APPROVED

ROTAGLIDE LUBRICANT - US FDA APPROVED

ROTAGLIDE LUBRICANT - CE APPROVED

ROTAGLIDE LUBRICANT – DCGI APPROVED

ROTAWIRE – US FDA APPROVED Should be compatible to Rota Machine in Cath Lab GMC Kota

ROTAWIRE – DCGI APPROVED Should be compatible to Rota Machine in Cath Lab GMC Kota.

HEART PUMP CATHETER AND SMARTASSIST SENSOR  USFDA & CE approved percutaneous heart pump capable of pumping blood @ 3.5-5 L/min to provide hemodynamic support for hemodynamic stabilization to enable Heart Recovery. Maintain patient hemodynamics during planned temporary coronary occlusions by maintaining mean arterial pressure (MAP), which may allow for a more thorough procedure and a more complete revisualization ma single session.

NIRS+IVUS CATHETER  USFDA & JAPAN PMDA APPROVED Near infrared spectroscopy & Intravascular Imaging catheter for detection of Lipid Core Plaques (LCP) and assessment of vessel structure with an automatically adjustable frequency bandwidth of 35-65 MHz depending on the need of the calcium with a pullback speed upto 2mm/sec and a pullback length if 150 mm. Catheter working length of 160 cm

IVUS CATHETER WITH ACCESSORIES - USFDA APPROVED  COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, Govt. Medical College Kota-

IVUS CATHETER WITH ACCESSORIES - CE/DCGI APPROVED  COMPITABLE TO VOLCANO IMAGING MACHINE IN CATH LAB, Govt. Medical College Kota-

SHOCKWAVE I.V.L INTRAVASCULAR LITHOTRIPSY CATHETER SYSTEM WITH CONNECTOR CABLE - DCGI WITH US FDA / CE APPROVED

I.V.L INDEGENOUS INTRAVASCULAR LITHOTRIPSY CATHETER SYSTEM WITH CONNECTOR CABLE – DCGI

IVUS CATHETER HD 60 MHZ CORONARY IMAGING CATHETERS. - US FDA APPROVED SHOULD BE COMPATIBLE WITH AVAILABLE MACHINE

IVUS CATHETER HD 60 MHz Coronary Imaging Catheters. – CE/DCGI APPROVED Should be compatible with available machine

IVUS CATHETER 40 MHz Coronary Imaging Catheters. - US FDA APPROVED Should be compatible with available machine

IVUS CATHETER 40 MHz Coronary Imaging Catheters. - US FDA APPROVED Should be compatible with available machine

LASER ATHERECTOMY CATHETER X-80 catheters with guidewire compatanility of 0.014 inch , Guiding catheter compatability of 6F, Maximum tip outer diameter ofm 0.038 inch , Maximum Shaft outer diameter of 0.049 inch with a working length of 100 mm , capability to generate a fluence of 30- 80 mJ/mm2 with a repitation rate of 25-80 Hertz. Available in 0.9 mm and 1.4 mm sizes.

Fractional Flow reserve Pressure Wire 1. Shouldbe0.014”guidewire. 2. Should have high-fidelity piezo electric pressure sensor technology for measurement of intravascular pressure. 3. The system should work wireless radio using Frequency-hopping spread spectrum to ensure secured radio connection with pressurewire 4. ThePressureWireshouldbecapableofwiredconnectiontoFFRmachine. 5. Shouldhavesensorhousingdesignwithmultiplelargewindows(Multiwindow Jacket). 6. Shouldhaveaflatcoretipdesignforabettershapeability&shaperetention. 7. Shouldpreferablyhavehydrophiliccoating 8. Shouldhavearadioopaquetip. 9. Shouldhaveoperatingpressurerangeof-30to+300mmHg. 10.Should have frequency response of DC to 25 Hz. 11.Should have radio range of at least 2m. 12.Should have Battery time of transmitter for at least 3 hours. 13.Should have a wireless transmission frequency range of 2.4000 – 2.4835 GHz

OCT Catheter: Catheter for intracoronary OCT, 0.014" guidewire and 6 F guide catheter compatibility. Lubricous hydrophilic coating and low tip entry profile for crossing tight, distal lesions.2.7 F crossing profile and supportive proximal shaft provide superb deliverability to the area of interest. Lens marker is immediately proximal to imaging lens and the distance of lens marker from tip should be 23 mm and proximal marker at 82 mm from the lens marker. Three radiopaque marker

TEMPORARY BIPOLAR PACING CATHETER- FLOW DIRECTED 1. Should be US FDA & DCGI approved 2. Should be latex balloon tipped, flow guided for stable insertion. 3. Should have 10 cm depth markers to enhance placement. 4. Should have smooth, polyurethane hemocompatible coating. 5. Should have clearly marked terminals. 6. Should have shrouded 2 mm pin connector leads. 7. Should have platinum electrodes 8. It should have flexible tip design for delicate placement.

TEMPORARY BIPOLAR PACING CATHETER- TORQUE CONTROL 1. Should be US FDA & DCGI approved 2. Should have 10 cm depth markers to enhance placement. 3. Should have smooth, polyurethane hemocompatible coating. 4. Should have clearly marked terminals. 5. Should have shrouded 2 mm pin connector leads. 6. Should have stainless steel centre conductor and stainless steel electrodes. 7. It should have solid core enables user to customize the curve. 8. Should have optimal torque control for challenging anatomy

ORBITAL ATHERECTOMY DEVICE 6F compatible Orbital Atherectomy device with 1.25mm diamond coated crown designed for bidirectional superficial calcium sanding and modify deep calcium through pulsatile forces to facilitates stent delivery and expansion in severely calcified lesions with durable nitinol guidewire with 0.12” proximal and 0.14” distal end along with viper slide lubricant

OAS Pump provides the saline pumping mechanism and power to the OAD with 250 V 4A SLOW BLOW, 1/4” x 1 - 1¼” meter fuse, ABS Plastic external housing, (100–240 VAC @ 50–60 Hz) external connector. Includes a bult in audible information signal for approximately every 25 sec of OAD spin time. Audible information signal every 5 sec for a total of 30 sec when the saline level falls below 200 mL.during a treatment period. The small, reusable, and portable OAS pump attaches to a standard five-wheel rolling intravenous (IV) pole or table mount pole.

Pressure Wire for FFR/DFR – USFDA

Pressure Wire for FFR/DFR – CE/DCGI

IABP CATHETER WITH ACCESSORIES - US FDA APPROVED Should be compatible with existing machine (Data Scope) in Cath Lab, GMCK

IABP CATHETER WITH ACCESSORIES - CE APPROVED Should be compatible with existing machine (Data Scope) in Cath Lab, GMCK

IABP CATHETER WITH ACCESSORIES DCGI APPROVED Should be compatible with existing machine (Data Scope) in Cath Lab, GMCK

TPI LEAD – USFDA APPROVED

TPI LEAD – CE APPROVED

TPI LEAD – DCGI APPROVED

Vascular closure device with Bio absorbable PGA suture that provide a secure seal • Bioabsorbable collagen designed, • low profile Bioabsorbable Anchor (50:50 blend glycolide and lactide polyer) • Must have bovine collagen plug. Must have 9 hole V-twist pattern suture weave. • Must be available in 6F and 8F sizes. USFDA+PMDA Approved

Vascular closure device with Bio absorbable PGA suture that provide a secure seal • Bioabsorbable collagen designed, • low profile Bioabsorbable Anchor (50:50 blend glycolide and lactide polyer) • Must have bovine collagen plug. Must have 9-hole V-twist pattern suture weave. • Must be available in 6F and 8F sizes. CE/DCGI Approved

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – USFDA APPROVED  Everolimus eluting cobalt chromium stent with peak to valley non-linear links with narrower and slimmer crests and ultra- low crossing profile of 0.039 inches for precise placement and zero transition distal shaft. Should have flourinated co- polymer. Should come in diameters from 2.00 mm to 4.00 mm with 5.5 mm post-dilatation capability for 3.5 mm and 4.0 mm stents

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – CE/DCGI APPROVED  Everolimus eluting cobalt chromium stent with peak to valley non linear links with narrower and slimmer crests and ultra-low crossing profile of 0.039 inches for precise placement and zero transition distal shaft. Should have flourinated co-polymer. Should come in diameters from 2.00 mm to 4.00 mm with 5.5 mm post-dilatation capability for 3.5 mm and 4.0 mm stents

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – USFDA APPROVED  everolimus eluting cobalt chromium stent with peak to valley taller non linear links and true centre tip technology for precise placement and zero transition distal shaft. Should have flourinated co-polymer. Should come in diameters from 2.00 mm to 4.00 mm

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – CE/DCGI APPROVED  everolimus eluting cobalt chromium stent with peak to valley taller non linear links and true centre tip technology for precise placement and zero transition distal shaft. Should have flourinated co-polymer. Should come in diameters from 2.00 mm to 4.00 mm

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – USFDA APPROVED  Everolimus eluting cobalt chromium stent with peak to valley taller non linear links and 5 Fold balloon technology and should have flourinated co polymer. Skive technology to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm.

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – CE/DCGI APPROVED  Everolimus eluting cobalt chromium stent with peak to valley taller non linear links and 5 Fold balloon technology and should have flourinated co polymer. Skive technology to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm.

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – LOGN LENGTH USFDA APPROVED  everolimus eluting cobalt chromium stent with peak to valley taller non linear links and 5 Fold balloon technology and should have flourinated co polymer. Skive technology to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm upto 48 mm length.

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – LOGN LENGTH - CE APPROVED  everolimus eluting cobalt chromium stent with peak to valley taller non linear links and 5 Fold balloon technology and should have flourinated co polymer. Skive technology to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm upto 48 mm length.

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – USFDA APPROVED  USFDA approved everolimus eluting cobalt chromium stent with peak to valley taller non linear links and dual layer pebax balloon technology and should have flourinated co polymer. SS junction support mandrel to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm.

EVEROLIMUS ELUTING COBALT CHROMIUM STENT – CE/DCGI APPROVED  USFDA approved everolimus eluting cobalt chromium stent with peak to valley taller non linear links and dual layer pebax balloon technology and should have flourinated co polymer. SS junction support mandrel to have a better pushability. Should come in diameters from 2.00 mm to 4.00 mm.

EVEROLIMUS ELUTING PLATINUM CHROMIUM STENT - DURABLE POLYMER– USFDA APPROVED

EVEROLIMUS ELUTING PLATINUM CHROMIUM STENT - DURABLE POLYMER – CE/DCGI APPROVED

EVEROLIMUS ELUTING PLATINUM CHROMIUM STENT – BIODEGRADABLE POLYMER - CE/DCGI APPROVED

EVEROLIMUS ELUTING PLATINUM CHROMIUM STENT – BIODEGRADABLE POLYMER - CE/DCGI APPROVED

Sirolimus Eluting Cobalt-Chromium stent with Abluminal Gradient coating - (L-605 Co-Cr Alloy) – USFDA/PMDA (should not have drug & Polymer coating on joints & Bends). 2 links – 8 Crown Design • Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Capro lactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. • Low concentration of Sirolimus (0.8ug/mmsq). • minimum tip entry profile of 0.42mm

Sirolimus Eluting Cobalt-Chromium stent with Abluminal Gradient coating - (L-605 Co-Cr Alloy) – CE/DCGI (should not have drug & Polymer coating on joints & Bends). 2 links – 8 Crown Design • Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Capro lactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. • Low concentration of Sirolimus (0.8ug/mmsq). minimum tip entry profile of 0.42mm

Optimized overexpansion, up to 6.25 mm for large Vessel- Sirolimus Eluting Cobalt-Chromium stent with Advanced Core wire shaft technology & Abluminal Gradient coating - (L-605 Co-Cr Alloy) – USFDA/PMDA  should not have drug & Polymer coating on joints & Bends. 2 links – 8 & 10 Crown Design  Must Have Advanced Core wire shaft technology.  should have an over expansion Limit of more than 1.5 mm of the stated Diameter  Must Have Rounded & Flexible Tip made up of Polyamide Elastomer.  Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Caprolactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. Low concentration of Sirolimus (0.8ug/mmsq), tip entry profile of 0.42mm.

Optimized overexpansion, up to 6.25 mm for large Vessel- Sirolimus Eluting Cobalt-Chromium stent with Advanced Core wire shaft technology & Abluminal Gradient coating - (L-605 Co-Cr Alloy) – CE/DCGI  should not have drug & Polymer coating on joints & Bends. 2 links – 8 & 10 Crown Design  Must Have Advanced Core wire shaft technology.  should have an over expansion Limit of more than 1.5 mm of the stated Diameter  Must Have Rounded & Flexible Tip made up of Polyamide Elastomer.  Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Caprolactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. Low concentration of Sirolimus (0.8ug/mmsq), tip entry profile of 0.42mm.

SIROLIMUS ELUTING WITH PROBIO COATING STENT – USFDA APPROVED Sirolimus Eluting Cobalt chromium stents, ultrathin struts 60 um. Should have coating passive probio coating (Amorphous Silicon Carbide). Should have active coating bio lute bioabsorbable ploy-L-Lactide. Should be USFDA approved.

SIROLIMUS ELUTING WITH PROBIO COATING STENT – CE/DCGI APPROVED Sirolimus Eluting Cobalt chromium stents, ultrathin struts 60 um. Should have coating passive probio coating (Amorphous Silicon Carbide). Should have active coating bio lute bioabsorbable ploy-L-Lactide. Should be USFDA approved.

SIROLIMUS ELUTING WITH SILICON CARBIDE COATING STENT – USFDA APPROVED Sirolimus eluting cobalt chromium stents with amorphous silicon carbide coating. Should be USFDA approved.

SIROLIMUS COATED STAINLESS STEEL STENT – CE APPROVED  Porus Surface, Shellac Resin (Wax-free), Bioresorbable Polymer

SIROLIMUS ELUTING COBALT CHROMIUM PLATFORM, - US FDA / CE Approved  BIODEGRADABLE POLYMER, AND MICROPORUS  SURFACE WITH SOFT COATING OF SHELLAC RASIN.

SIROLIMUS CLUTING, STAINLESS STEEL PLATFORM, - US FDA / CE Approved  BIODEGRADABLE POLYMER, MICROPORUS SURFACE WITH SOFT COATING OF SHELLAC RASIN WITH TEMPERATURE CONTROL PACKING & TEMPERATURE  SENSITIVE CHECK METER.

DUAL DRUG POLYMER FREE DRUG ELUTING STENT - DCGI WITH US FDA /CE APPROVED  Should have Cobalt Chromium Platform with Prubocol drug at place of polymer.  Should have no polymer.  Abluminal coating on MICROPORUS SURFACE WITH SOFT COATING OF SHELLAC RASIN.

DUAL DRUG POLYMER FREE DRUG ELUTING STENT - DCGI APPROVED  Should have Cobalt Chromium Platform with Prubocol drug at place of polymer.  Should have no polymer. Abluminal coating on MICROPORUS SURFACE WITH SOFT COATING OF SHELLAC RASIN.

BIO-RESORBABLE SCAFFOLD (BRS)  Sirolimus eluting Bio-Resorable scaffold Stent System - DCGI With US FDA / CE Approved  All Sizes and Diameter

SIROLIMUS COATED DRUG STENT - CE APPROVED • Open Cell Design only with two connectors between the rings, Stent material: CoCr per ASTM F562 • 60µ ultra-thin struts across all diameters and lengths • Crossing profile of ≤ 0.97MM Tip entry profile: 0.017”, LDZ Link: Long Dual ‘Z’ Link • RBP: 16 atm • Length (mm): 8 to 48 mm • Diameter(mm): 2.25 to 4.00 mm

SIROLIMUS COATED DRUG STENT - DCGI APPROVED • Open Cell Design only with two connectors between the rings, Stent material: CoCr per ASTM F562 • 60µ ultra-thin struts across all diameters and lengths • Crossing profile of ≤ 0.97MM Tip entry profile: 0.017”, LDZ Link: Long Dual ‘Z’ Link • RBP: 16 atm • Length (mm): 8 to 48 mm • Diameter(mm): 2.25 to 4.00 mm

EVEROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT - DCGI APPROVED • Everolimus Drug Eluting Stent, Open Cell Design only with two connectors between the rings • Stent Material & Design: L-605 Co-Cr Alloy with Laser cut seamless tubing in serpentine pattern. • 60µ ultra-thin struts across all diameters and lengths, Crossing profile of ≤ 0.97mm, Tip entry profile: 0.017” • LDZ Link: Long Dual ‘Z’ LinK, IFU labeled Overexpansion of the highest available diameter should be ≥ 5.50 mm • RBP: 16 atm • Length (mm): 8 to 48 mm • Diameter(mm): 2.25 to 4.00 mm

SIROLIMUS COATED DRUG STENT CE APPROVED • Open Cell Design only with two connectors between the rings • Stent Material & Design: L-605 Co-Cr Alloy with Laser cut seamless tubing in serpentine pattern. • 60µ ultra-thin struts across all diameters and lengths - Long Link DESIGN • Crossing profile of ≤ 0.97mm,M Tip entry profile: 0.41mm • RBP: 16 atm • Length (mm): 8 to 48 mm • Diameter(mm): 2.25 to 4.00 mm

SIROLIMUS COATED DRUG STENT DCGI APPROVED • Open Cell Design only with two connectors between the rings • Stent Material & Design: L-605 Co-Cr Alloy with Laser cut seamless tubing in serpentine pattern. • 60µ ultra-thin struts across all diameters and lengths - Long Link DESIGN • Crossing profile of ≤ 0.97mm,M Tip entry profile: 0.41mm • RBP: 16 atm • Length (mm): 8 to 48 mm • Diameter(mm): 2.25 to 4.00 mm

COVERED STENT USFDA APPROVED

COVERED STENT CE/DCGI APPROVED

COVERED CORONARY STENTS - US FDA APPROVED

COVERED CORONARY STENTS – CE/DCGI APPROVED Covered graft stent for dissected artery

GUIDEWIRE FOR PERIPHERAL INTERVENTION – NITINOL ALLOY REGULAR LENGTH  Tip Load Options of 6 g, nitinol lengths of 10 cm

GUIDEWIRE FOR PERIPHERAL INTERVENTION – NITINOL ALLOY REGULAR LENGTH  Tip Load Options of 4 g, nitinol lengths of 25 cm

GUIDEWIRE FOR PERIPHERAL INTERVENTION – NITINOL ALLOY REGULAR LENGTH–  Tip Load Options of 3.5 g, nitinol lengths of 40 cm

GUIDEWIRE FOR PERIPHERAL INTERVENTION – NITINOL ALLOY REGULAR LENGTH–  Tip Load Options of 2.8 g, nitinol lengths of 40 cm

GUIDEWIRE FOR PERIPHERAL INTERVENTION – STAINLESS STEEL, REGULAR LENGTH  .018Short taper, Bare coil, core to tip, tip load – 4.6 gm

PTA BALLOON – 12-200MM - USFDA  diameters 1.5, 2.0, 2.5, 3.0, and 4.0 mm, Length – 12, 20, 40, 60, 80, 120, 200  4F sheath compatible, Hydrophilic coating, tungsten markers, NP- 8, RBP - 14

PTA BALLOON - 12-200MM – CE/DCGI  diameters 1.5, 2.0, 2.5, 3.0, and 4.0 mm, Length – 12, 20, 40, 60, 80, 120, 200  4F sheath compatible, Hydrophilic coating, tungsten markers, NP- 8, RBP - 14

PTA BALLOON – 20-200MM - USFDA APPROVED  diameters 2.0, 2.5, 3.0, 4.0, 5.0, 5.5, 6.0, Length – 20, 40, 60, 80, 120, 150, 180, 200  4F/5F sheath compatible, Hydrophilic coating, tungsten markers, NP- 8, RBP – 14  Coaxial, over-the-wire design, One-piece catheter construction, Hydrophobic coating

PTA BALLOON – 20-200MM CE/DCGI  diameters 2.0, 2.5, 3.0, 4.0, 5.0, 5.5, 6.0, Length – 20, 40, 60, 80, 120, 150, 180, 200  4F/5F sheath compatible, Hydrophilic coating, tungsten markers, NP- 8, RBP – 14  Coaxial, over-the-wire design, One-piece catheter construction, Hydrophobic coating

PTA BALLOON – 20-250MM - USFDA  diameters 3 -12 MM, Length – 20, 40, 60, 80, 120, 150, 200, 250  5-7 F sheath compatible, Hydrophilic coating, tungsten markers,

PTA BALLOON – 20-250MM – CE/DCGI  diameters 3 -12 MM, Length – 20, 40, 60, 80, 120, 150, 200, 250  5-7 F sheath compatible, Hydrophilic coating, tungsten markers,

PTA BALLOON – 15-40MM – USFDA  diameters 4 -7 MM, lengths of 15 mm, 20 mm, 30 mm, and 40 mm  XCELON balloon material with a 14 atm RBP, Hydrophobic coated shaft and balloon, NP- 8, RBP – 14

PTA BALLOON – 15-40MM – CE/DCGI  diameters 4 -7 MM, lengths of 15 mm, 20 mm, 30 mm, and 40 mm XCELON balloon material with a 14 atm RBP, Hydrophobic coated shaft and balloon, NP- 8, RBP – 14

PTA BALLOON DILATATION CATHETER – USFDA  diameters 3 -12 MM, Length – 20, 30, 40, 60, 80, 100, 120, 150, 200 - Up to 24 ATM (2431 kPa) rated burst pressure  NyBax Balloon Material, 3 wings on 3-5 mm, 5 wings on 6 mm and plus, Mediglide hydrophilic coating

PTA BALLOON DILATATION CATHETER – CE/DCGI  diameters 3 -12 MM, Length – 20, 30, 40, 60, 80, 100, 120, 150, 200  Up to 24 ATM (2431 kPa) rated burst pressure NyBax Balloon Material, 3 wings on 3-5 mm, 5 wings on 6 mm and plus, Mediglide hydrophilic coating

ULTRA-HIGH-PRESSURE BALLOON - With pressures up to 40 ATM - USFDA  diameters 4 -12 MM, Length – 20, 30, 40, 60, 80, 100 -  Up to 40 ATM rated burst pressure

ULTRA-HIGH-PRESSURE BALLOON - With pressures up to 40 ATM -CE/DCGI  diameters 4 -12 MM, Length – 20, 30, 40, 60, 80, 100 Up to 40 ATM rated burst pressure

0.018” BALLOON DILATATION CATHETER - USFDA  0.020” lesion entry profile on a 0.018” wire  2-10 mm diameters, 10-220 mm lengths

0.018” BALLOON DILATATION CATHETER -CE/DCGI  0.020” lesion entry profile on a 0.018” wire 2-10 mm diameters, 10-220 mm lengths

0.035” BALLOON DILATATION CATHETER -USFDA  0.020” lesion entry profile on a 0.018” wire  12, 14, 16, 18 mm diameters, 20, 40, 60 mm lengths

0.035” BALLOON DILATATION CATHETER -CE/DCGI  0.020” lesion entry profile on a 0.018” wire 12, 14, 16, 18 mm diameters, 20, 40, 60 mm lengths

0.014” BALLOON DILATATION CATHETER -USFDA  0.017" lesion entry profile, NyBax Balloon Material

0.014” BALLOON DILATATION CATHETER -CE/DCGI 0.017" lesion entry profile, NyBax Balloon Material

CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - US FDA APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons Available in the sizes and lengths

CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - CE APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons Available in the sizes and lengths

CUTTING BALLOON FOR RENAL AND PERIPHERAL ARTERIES - DCGI APPROVED  Monorail (rapid exchange) and over-the-wire (OTW) balloons Available in the sizes and lengths

OTW BALLOON FOR PERIFERAL ANGIOPLASTY ALL SIZE AND DIAMETERS- CE/ FDA APPROVED

OTW BALLOON FOR PERIFERAL ANGIOPLASTY ALL SIZE AND DIAMETERS- DCGI APPROVED

BTK EVEROLIMUS ELUTING RESORBABLE SCAFFOLD SYSTEM – USFDA

BTK EVEROLIMUS ELUTING RESORBABLE SCAFFOLD SYSTEM – CE/DCGI

PERIPHERAL SELF EXPANDABLE INTERWOVEN NITINOL STENT FOR SUPERFICIAL FEMORAL ARTERY (SFA) AND / OR PROXIMAL POPLITEAL ARTERY - USFDA APPROVED

PERIPHERAL SELF EXPANDABLE INTERWOVEN NITINOL STENT FOR SUPERFICIAL FEMORAL ARTERY (SFA) AND / OR PROXIMAL POPLITEAL ARTERY - DCGI/CE APPROVED

SELF-EXPANDING PERIPHERAL STENT – USFDA Approved  Tri-Axial Technology Specifications, Flexible nitinol material

SELF-EXPANDING PERIPHERAL STENT – CE/DCGI Approved  Tri-Axial Technology Specifications, Flexible nitinol material

BALLOON-EXPANDING PERIPHERAL STENT – USFDA Approved  Cobalt chromium multi-link technology, Dual-layer balloon

BALLOON-EXPANDING PERIPHERAL STENT – USFDA Approved  Cobalt chromium multi-link technology, Dual-layer balloon

RENAL STENT SYSTEM – USFDA APPROVED  Cobalt chromium multi-link technology

RENAL STENT SYSTEM – CE/DCGI APPROVED Cobalt chromium multi-link technology

CAROTID STENT – USFDA  Closed-cell design for crush resistance, Rotational deployment handle with Freestyle, U- and S-shaped connectors

CAROTID STENT – CE/DCGI  Closed-cell design for crush resistance, Rotational deployment handle with Freestyle, U- and S-shaped connectors

CAROTID STENT – USFDA straight and tapered stent options, Nitinol material

CAROTID STENT – CE/DCGI Closed-cell design for crush resistance, Rotational deployment handle with Freestyle, U- and S-shaped connectors

EMBOLIC PROTECTION SYSTEM – USFDA Centered wire design, Circumferential nitinol frame, Platinum-tungsten frame coils, BareWir technology

EMBOLIC PROTECTION SYSTEM – CE/DCGI Centered wire design, Circumferential nitinol frame, Platinum-tungsten frame coils, BareWir technology

Vascular Plug – Single Lobe

Vascular Plug- Multi-layered mesh designed, Six planes of cross sectional coverage

Suture-Mediated Closure and Repair System – USFDA APPROVED

Suture-Mediated Closure (SMC) For Both Arterial And Venous Access – USFDA

Suture-Mediated Closure (SMC) For Both Arterial And Venous Access – CE/DCGI

Renal and Biliary Premounted Stent System – USFDA Macr Elements and additional proximal connectors

Renal and Biliary Premounted Stent System – CE/DCGI Macr Elements and additional proximal connectors

Drug Coated balloon for PTA – USFDA TransPax Coating, Paclitaxel-Coated PTA Balloon Catheter

Drug Coated balloon for PTA – USFDACE/DCGI TransPax Coating, Paclitaxel-Coated PTA Balloon Catheter

CAROTID STENT – USFDA APPROVED Closed cell design,

CAROTID STENT – CE/DCGI APPROVED Closed cell design,

Iliac and Biliary Premounted Stent System – USFDA Macro Elements engineered

Iliac and Biliary Premounted Stent System – CE/DCGI Macro Elements engineered

Renal and Biliary Premounted Stent System – USFDA Tandem Architectur Stent Design

Renal and Biliary Premounted Stent System – CE/DCGI Tandem Architectur Stent Design

SELF EXPANDING PERIPHERAL STENT – USFDA APPROVED

PERIPHAREL Drug-Eluting Vascular Stent -USFDA

PERIPHAREL Drug-Eluting Vascular Stent -CE/DCGI

Self-Expanding Stent System for Iliac – USFDA

Self-Expanding Stent System for Iliac – CE/DCGI

DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CORONARY FILTER - US FDA/CE APPROVED

DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CORONARY FILTER - DCGI APPROVED

DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CAROTID ARTERY FILTER - US FDA/CE APPROVED

DISTAL PROTECTION DEVICE 0.014 WIRE UMBRELLA TYPE CAROTID ARTERY FILTER - DCGI APPROVED

EMBOLIC PROTECTION DEVICES BASED ON FILTER TECHNOLOGY/MECHANISM - US FDA APPROVED

EMBOLIC PROTECTION DEVICES BASED ON FILTER TECHNOLOGY/MECHANISM - DCGI APPROVED

EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY - US FDA APPROVED

EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY-CE APPROVED

EMBOLIC PROTECTION DEVICES WITH DISTAL BALLOON OCCLUSIVE TECHONOLOGY - DCGI APPROVED

Distal embolic protection device - US FDA APPROVED  Should be made of polyurethane with radio-opaque nitinol loop  Should be suspended on the .014” wire with a suspension arm.  Should not occlude flow while in placement, Should be rapid exchange type  Should be compatible with a 6 F guiding catheter (0.066” ID) Should allow optimal filtration in vessels 3.5 - 5.5 mm size

Distal embolic protection device – CE/DCGI APPROVED  Should be made of polyurethane with radio-opaque nitinol loop  Should be suspended on the .014” wire with a suspension arm.  Should not occlude flow while in placement, Should be rapid exchange type  Should be compatible with a 6 F guiding catheter (0.066” ID) Should allow optimal filtration in vessels 3.5 - 5.5 mm size

Peripheral Cutting Balloon catheter - US FDA APPROVED  Should be available in balloon OD of 3-6 mm  Should have up to 15 mm or up to 20 mm working length

Peripheral Cutting Balloon catheter – CE/DCGI APPROVED  Should be available in balloon OD of 3-6 mm  Should have up to 15 mm or up to 20 mm working length Catheter shaft length should be up to 140 cm

Balloon in Balloon Catheter (BIB)- DCGI with US FDA /CE Approved

Plaque Modification device for Highly calcified lesions - DCGI With US FDA / CE Approved  Available in the sizes and length  Should be along with support Accessories  Super High pressure Balloon dialation catheter Non Compliant RBP -35 bar Must be twin layer in balloon with low lesion entry profile”0.16”

IVC Filter – US FDA APPROVED  For optimal filtration of IVC diameter of up to 40 mm  Made of either nitinol or stainless steel  Catheter carrier system inner diameter should be of maximum 12 F  It should be possible to insert from either jugular or femoral access Should be for permanent use

IVC Filter – CE APPROVED  For optimal filtration of IVC diameter of up to 40 mm  Made of either nitinol or stainless steel  Catheter carrier system inner diameter should be of maximum 12 F  It should be possible to insert from either jugular or femoral access Should be for permanent use

IVC Filter – DCGI APPROVED  For optimal filtration of IVC diameter of up to 40 mm  Made of either nitinol or stainless steel  Catheter carrier system inner diameter should be of maximum 12 F  It should be possible to insert from either jugular or femoral access Should be for permanent use

Endovascular stent graft device for treatment of thoracic aortic aneurysms and dissections - US FDA APPROVED  Device should be with proximal barbs, with or without distal bare spring configuration, and should be tapered or non – tapered.  The aortic device should be available in any one or more of the following sizes: OD 26-44mm; Length 4-24 cm. The device should be able to be advanced on up to 24 Fr shaft size. The manufacturer should agree to supply the size customized to the patient’s anatomy based on CT angiography

Endovascular stent graft device for treatment of thoracic aortic aneurysms and dissections – CE/DCGI APPROVED  Device should be with proximal barbs, with or without distal bare spring configuration, and should be tapered or non – tapered.  The aortic device should be available in any one or more of the following sizes: OD 26-44mm; Length 4-24 cm. The device should be able to be advanced on up to 24 Fr shaft size. The manufacturer should agree to supply the size customized to the patient’s anatomy based on CT angiography

Endovascular stent graft device for treatment of abdominal aortic aneurysms – USFDA APPROVED  Device should be with proximal barbs, with or without distal bare spring configuration, and should be either tapered or non – tapered  Devices with trans-renal or suprarenal fixation should be quoted.  The aortic device should be available in any 1 or more of the following sizes: OD 12-44mm; Length 4-24 cm. The device should be able to be advanced on up to 24 Fr shaft size.  The limb extensions of the main device for abdominal aortic applications should be available in 12-22 mm diameter, with or without flared ends and up to 12 cm in length The manufacturer should agree to supply the size customized to the patient’s anatomy based on CT angiography

Endovascular stent graft device for treatment of abdominal aortic aneurysms – CE/DCGI APPROVED  Device should be with proximal barbs, with or without distal bare spring configuration, and should be either tapered or non – tapered  Devices with trans-renal or suprarenal fixation should be quoted.  The aortic device should be available in any 1 or more of the following sizes: OD 12-44mm; Length 4-24 cm. The device should be able to be advanced on up to 24 Fr shaft size.  The limb extensions of the main device for abdominal aortic applications should be available in 12-22 mm diameter, with or without flared ends and up to 12 cm in length The manufacturer should agree to supply the size customized to the patient’s anatomy based on CT angiography

RENAL DENERVATION DEVICE FOR RF ABLATION OF RENAL – CE / US FDA APPROVED

RENAL DENERVATION DEVICE FOR RF ABLATION OF RENAL –DCGI APPROVED

C.P. STENT COVERED – CE APPROVED Should be balloon Mounted.

C.P. STENT COVERED – US FDA APPROVED

C.P. STENT COVERED – DCGI APPROVED

AMPLATZER PLUG – CE APPROVED

AMPLATZER PLUG – US FDA APPROVED

AMPLATZER PLUG – DCGI APPROVED

SNARE FOR PERIFERAL USE – US FDA/CE APPROVED

SNARE FOR PERIFERAL USE – DCGI APPROVED

LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – BRAIDED – US FDA/ CE APPROVED

LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – BRAIDED – DCGI APPROVED

LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – UN BRAIDED– US FDA/ CE APPROVED

LONG ARTRIAL SHEETH 6F/7F/8F LENGTH >= 90 CM – UN BRAIDED– DCGI APPROVED

LONG ARTRIAL SHEETH UPTO 90 CM - BRAIDED – US FDA/ CE APPROVED

LONG ARTRIAL SHEETH UPTO 90 CM - BRAIDED – DCGI APPROVED

LONG ARTRIAL SHEETH UPTO 90 CM - UNBRAIDED – US FDA/ CE APPROVED

LONG ARTRIAL SHEETH UPTO 90 CM - UNBRAIDED – DCGI APPROVED

CROSS – OVER SHEETH - BRAIDED – US FDA/ CE APPROVED

CROSS – OVER SHEETH - BRAIDED – DCGI APPROVED

CROSS – OVER SHEETH - UNBRAIDED – US FDA/ CE APPROVED

CROSS – OVER SHEETH - UNBRAIDED – DCGI APPROVED

VISCERAL TYPE CATHETER – US FDA/ CE APPROVED

VISCERAL TYPE CATHETER – DCGI APPROVED

HEAD HUNTER TYPE CATHETER – US FDA/ CE APPROVED

HEAD HUNTER TYPE CATHETER – DCGI APPROVED

VTK TYPE CATHETER – US FDA/ CE APPROVED

VTK TYPE CATHETER – DCGI APPROVED

SIMMONS TYPE CATHETER – US FDA/ CE APPROVED

SIMMONS TYPE CATHETER – DCGI APPROVED

COBRA TYPE CATHETER – US FDA/ CE APPROVED

Abdominal stent graft for treating Aortic Aneurysm– US FDA APPROVED

Abdominal stent graft for treating Aortic Aneurysm– CE APPROVED

Abdominal stent graft for treating Aortic Aneurysm– DCGI APPROVED

Thorosic stent graft for treating Thorasic Aneurysm and Thorosic dissection – US FDA APPROVED

Thorosic stent graft for treating Thorosic Aneurysm and Thorosic dissection– CE APPROVED

Thorosic stent graft for treating Thorosic Aneurysm and Thorosic dissection– DCGI APPROVED

Covered Aortic stent balloon mounted - US FDA APPROVED

Covered Aortic stent balloon mounted – CE Approved

Covered Aortic stent balloon mounted (Andra Stent Type) – DCGI Approved

Non-Covered Aortic stent balloon mounted - US FDA APPROVED

Non-Covered Aortic stent balloon mounted – CE Approved

Non-Covered Aortic stent balloon mounted (Endra Stent Type)– DCGI Approved

ASD Occluders, -percutaneous transcatheter closure for non-surgical closure of atrial septal defect. Device should be self-expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a waist between. Polyester fabric sewn into each disc and the waist to promote occlusion and tissue in growth. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. – USFDA Approved Sizes - 4mm, 5mm, 6mm, 7mm, 8mm, 9mm, 10mm, 11mm, 12mm, 13mm, 14mm, 15mm, 16mm, 17mm, 18mm, 19mm, 20mm, 22mm, 24mm, 26mm, 28mm, 30mm, 32mm, 34mm, 36mm, 38mm, and, 40mm

ASD - Multi Fenestrated (Cribriform) Occluders, percutaneous transcatheter closure for non-surgical closure of atrial septal defect. Device should be self-expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a very thin waist of 3mm. Device should have matched disc diameters to maximise the coverage of multiple fenestrations. Polyester fabric sewn into each disc promote occlusion and tissue in growth. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 18mm, 25mm, 30mm, 35mm, and 40mm

PDA Occluders, percutaneous transcatheter closure for non-surgical closure of patent ductus arteriosus. Device should be self- expandable made up of soft nitinol wire mesh, which has been heated and set to expand into T-Shape. Retention Skirt design should provide secure positioning with the ductus and reduce embolization. Polyester fabric sewn into the device to promote occlusion and tissue in growth. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 0405mm, 0406mm, 0608mm, 0810mm, 1012mm, 1214mm, and 1416mm

PDA Occluder with Double Disc, percutaneous transcatheter closure for non-surgical closure of moderate patent ductus arteriosus. Device should be self-expandable made up of soft nitinol compliant-multilayered mesh and dual articulating discs that provide high conformability to treat maximum types of PDA. Device should have symmetric design that offers procedural flexibility to choose Antegrade or Retrograde approach. Device should have fabric-free technology that allows for delivery through low-profile catheter while maintaining high rate of occlusion. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 0304mm, 0306mm, 0404mm, 0406mm, 0504mm, 0506mm, 0604mm, and 0606mm

PDA Occluder with Double Disc (for Neonates), percutaneous transcatheter closure for non-surgical closure of small patent ductus arteriosus in neonates while minimizing protrusion. Device should be self-expandable made up of soft nitinol compliant-multilayered mesh. Device should have low-profile dual articulating discs that provide high conformability to treat maximum types of small PDAs. Device should have symmetric design that offers procedural flexibility to choose Antegrade or Retrograde approach. Device must containt tightly woven, single layer mesh development to minimize residual shunt after placement. Device should be preloaded on delivery cable and comes with a special Low-Profile delivery catheter of 4Fr. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 0302mm, 0304mm, 0306mm, 0402mm, 0404mm, 0406mm, 0502mm, 0504mm, and, 0506mm

Muscular VSD Occluder, is a percutaenous transcatheter closure for non-surgical closure of a ventricular septal defect. The occluder is designed to close complex muscular VSDs in patients to be at high risk of surgical repair. The device should be self-expandable symmetric double disc made from a soft nitinol mesh. the device waist should be self-centered and fill the defect. The device should be filled with polyester material that promotes occlusion and tissue in growth. The waist length should be 7mm to accomodate the thickness of muscular ventricular septal wall. Symmetric design should allow both Antegrade and Retrograde Approach. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 4mm, 6mm, 8mm, 10mm, 12mm, 14mm, 16mm, and 18mm

P.I. Muscular VSD Occluder, is a percutaenous transcatheter closure for non-surgical closure of a ventricular septal defect. The occluder is designed to close complex muscular VSDs in patients to be at high risk post infarction caused due to MI. The device should be self-expandable symmetric double disc made from a soft nitinol mesh. the device waist should be self-centered and fill the defect. The device should be filled with polyester material that promotes occlusion and tissue in growth. The waist length should be 10mm to accomodate the thickness of apical ventricular septal wall. Symmetric design should allow both Antegrade and Retrograde Approach. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 16mm, 18mm, 20mm, 22mm, and 24mm

Membranous VSD Occluder, is a percutaneous transcatheter closure for non-surgical closure of peri-membranous ventricular septal defect. It should be non-concentric design allows for placement that avoida interference with aortic or AV valves. The device should be made up of soft nitinol meshwith interwoven polyester to promote occlusion and tissue in-growth. The device should be delievered using a Pusher Catheter from Venous Approach. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 4mm, 5mm, 6mm, 7mm, 8mm, 9mm, 10mm, 11mm, 12mm, 13mm, 14mm, 15mm, 16mm, 17mm, and 18mm

PFO Occluder, is a percutaneous transcatheter closure for non-surgical closure of patent foramen ovale. Device should be self- expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a very thin waist of 3mm. Device should have matched disc diameters to maximise the coverage of Foramen Ovale. Polyester fabric sewn into each disc promote occlusion and tissue in growth. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 18mm, 25mm, 30mm, and 35mm

ATV, Special Delivery System designed for ASD and PFO Cases. This delivery system comes with an ultra-flexible tip for better positioning of the device. Enhanced delivery cable improves the assessment of device final position prior to cable release. It is designed for no compromise on torque strength, sheath diameter and pushability. USFDA Approved Sizes - 6fr, 7fr, 8fr, 9fr, 10fr, 12fr, and 13fr

ITV, Special Delivery System with Delivery Cable angeled at 45°. Used for ASD and PFO cases USFDA Approved Sizes - 6fr, 7fr, 8fr, 9fr, 10fr, 12fr, and 13fr

ITV, Special Delivery System with Delivery Cable angeled at 180°. Used for VSD and PDA cases USFDA Approved Sizes - 5fr, 6fr, 7fr, 8fr, and 9fr

TVLP, Special Delivery System for PDA Occluder with Double Disc angeled at 90° (ADO II) USFDA Approved Sizes - 4fr and 5fr

TVLPC, Special Delivery Catheter for speical sizes of PDA Occluder with Double Disc angeled at 90° (Piccolo Device) USFDA Approved Sizes - 4fr

ITVP, Special Delivery System with Pusher Catheter angeled at 180° USFDA Approved Sizes - 7fr, 8fr and 9fr

LAA Closure, is a percutaneous transcatheter closure for non-surgical closure of Left Atrial Appendage. Having an innovative design of Cylindrical Plug attached with the retention skirt. Cylindrical Plug shaped head is designed to trap trabeculations. Device should be preloaded on the delivery cable with delivery profile of 12fr to 14fr. Devide should be made up of soft woven Nitinol mesh. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Sizes - 16mm, 18mm, 20mm, 22mm, 25mm, 28mm, 31mm, and, 34mm

TV, Special Delivery System with dual angeled sheath at 45° x 45° with the usable length of 80cm specially designed for LAA Occluders USFDA Approved Size - 12fr. And 14fr.

Sizing Balloon with a triple lumen balloon catheter with three radiopaque marker bands located inside the balloon to allow for radiographic measurement. The centre of the balloon should contains a pair of marker bands 0.4mm apart for corrent balloon alignment while measuing the defect and one marker band 15mm proximal of the pair. USFDA Approved Size - 18mm, 24mm. And 34mm

PVL Occluder is a percutaneour transcatheter closure of Para Valvular Leak which is a serious complication of valve replacement surgery. Devide should be made up of soft woven muti-layered Nitinol mesh designed to increase density and provide rapid occlusion. Low profile 4fr to 7fr sheath to facilitate defect crossing. Oblonged shape to improve wall apposition and enhance stability in PVL. Device orientation should be defined through a small platinum marker on the distal rim. The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults. USFDA Approved Size - 0204mm, 0306mm, 0408mm, 0310mm, 0510mm, 0312mm, 0512mm, 0314mm, and 0514mm.

PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM — CE/DCGI APPROVED Available in all the sizes • Hat-shaped designed PDA occluder device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Extended retention portion provides proper positioning of the device in the ductus arteriosus • Available Sizes- 4/6, 6/8, 8/10, 10/12, 12/14, 14/16, 16/18, 18/20mm

DELIVERY SHEATH FOR PDA CLOSURE DEVICE — CE /DCGI APPROVED

PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED/ DGCI APPROVED · Available in all the sizes • Hat-shaped designed PDA occluder device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Extended retention portion provides proper positioning of the device in the ductus arteriosus • Available Sizes- 4/6, 6/8, 8/10, 10/12, 12/14, 14/16, 16/18, 18/20mm

VSD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM — CE/DCGI APPROVED• Self-expanding, self-centering double-disc device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available Sizes- 4-4, 4-10, 6-4, 6-10, 8-4, 8-10, 10-4, 10-10, 12-4, 12-10mm • Certificates- CE & DCGI Approved • Shelf Life- 3 years

DELIVERY SHEATH FOR VSD CLOSURE DEVICE — CE APPROVED

VSD CLOSURE DEVICES WITH DELIVERY SYSTEM — CE/DCGI APPROVED• Self-expanding, self-centering double-disc device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available Sizes- 4-4, 4-10, 6-4, 6-10, 8-4, 8-10, 10-4, 10-10, 12-4, 12-10mm • Delivery cable available along with cable sheath in individual packaging • Soft and flexible distal end of delivery cable to navigate in various anatomies • Availability of ‘S-shaped’ sheath • Certificates- CE & DCGI Approved • Shelf Life- 3 years

Valve • Self-expanding frame, Supra-annular valve design, Bovine Pericardial Valve • Proprietary Anti-calcification tissue treatment • Extended internal sealing skirt • Two rows of Radio-opaque markers on the frame • Varying radial force frame – optimal forces at all 3 parts of the frame • Available in three sizes of 22, 26, and 30 mm, which cover the treatable annular diameter range from 17 to 27 mm • Post dilatation limits of valve frame equal to approved annulus diameter limit • Cell size of ≥ 15 French • Less metal at the inflow section • Certificates- CE & DCGI Approved

PFO CLOSURE DEVICES WITH DELIVERY SYSTEM — CE/DCGI APPROVED• Self-expanding, self-centering double-disc occluder • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available in 6 sizes, 5 sizes (18/18, 25/18, 25/25, 30/25, 30/30 mm) which are 8F compatible and 1 size (35/25 mm) which is 9F compatible • 6F delivery cable available in individual packaging • Certificates- CE & DCGI Approved • Shelf Life- 3 years

PFO CLOSURE DEVICES WITHOUT DELIVERY SYSTEM — CE/DCGI APPROVED• Self-expanding, self-centering double-disc occluder • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available in 6 sizes, 5 sizes (18/18, 25/18, 25/25, 30/25, 30/30 mm) which are 8F compatible and 1 size (35/25 mm) which is 9F compatible • Certificates- CE & DCGI Approved • Shelf Life- 3 years

DELIVERY SHEATH FOR PFO CLOSURE DEVICE — CE/DCGI APPROVED •Compatible with the device approved

ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – CE APPROVED/DCGI APPROVED · Approved for pediatric/adult use • Self-expanding, self-centering double-disc device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available in sizes- 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38 & 40mm

ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – CE APPROVED/DCGI APPROVED · Approved for pediatric/adult use · Self-centering, detachable device with delivery cable • Self-expanding, self-centering double-disc device • Platinum coating of ≤25 µ using nano fusion technology • Polypropylene fabric sewn inside the occluder device • Available in sizes- 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38 & 40mm and Delivery Sheath

DELIVERY SHEATH FOR ASD CLOSURE DEVICE - CE/DCGI APPROVED

DELIVERY CABLE FOR ASD/VSD/PDA/PFO DEVICES - CE/DCGI APPROVED

LEFT ATRIAL APPENDAGE CLOSURE DEVICE US FDA APPROVED

Occlusion balloon - DCGI with US FDA / CE Approved  Should be soft compliant balloon material with Radio-opaque markers at both distal and proximal end of balloon  Should be 14fr / 16fr Sheath and 0.035”/0.038” wire compatible. Should be available in diameter 20 mm/ 27 mm / 33 mm and 40 mm.

PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - US FDA APPROVED  0.035, 0.038 Inches Sizes ranging from 2 x 2 to 15 x 15

PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - CE APPROVED  0.035, 0.038 Inches Sizes ranging from 2 x 2 to 15 x 15

PDA COILS MADE OF STEEL/ NITINOL/PLATINUM – DCGI APPROVED  0.035, 0.038 Inches Sizes ranging from 2 x 2 to 15 x 15

0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - US FDA APPROVED Sizes ranging from 2 x 2 to 15 x 15

0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM - CE APPROVED Sizes ranging from 2 x 2 to 15 x 15

0.052 INCH PDA COILS MADE OF STEEL/ NITINOL/PLATINUM – DCGI APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.018 INCH) - US FDA APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.018 INCH) - CE APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.018 INCH) – DCGI APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.035 INCH) - US FDA APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.035 INCH) - CE APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.035 INCH) – DCGI APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.052 INCH) - US FDA APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.052 INCH) - CE APPROVED Sizes ranging from 2 x 2 to 15 x 15

EMBOLISATION COILS (0.052 INCH) –DCGI APPROVED Sizes ranging from 2 x 2 to 15 x 15

PARK BLADE SEPTECTOMY CATHETER - US FDA APPROVED

PARK BLADE SEPTECTOMY CATHETER - CE APPROVED

PARK BLADE SEPTECTOMY CATHETER – DCGI APPROVED

Embolisation Coils - US FDA APPROVED  Should be 0.014/0.018” compatible  Should be made of platinum with synthetic fibres  Should be non tapering/straight  Should be MR compatible  Should be available in any or the following diameters: 2-10 mm Should be of various lengths; the length of the coil at each diameter should be stated

Embolisation Coils - CE APPROVED  Should be 0.014/0.018” compatible  Should be made of platinum with synthetic fibres  Should be non tapering/straight  Should be MR compatible  Should be available in any or the following diameters: 2-10 mm Should be of various lengths; the length of the coil at each diameter should be stated

Embolisation Coils – DCGI APPROVED  Should be 0.014/0.018” compatible  Should be made of platinum with synthetic fibres  Should be non tapering/straight  Should be MR compatible  Should be available in any or the following diameters: 2-10 mm Should be of various lengths; the length of the coil at each diameter should be stated

Embolisation Coils - USFDA APPROVED  Should be 0.035/0.038” compatible  Should be made of platinum with synthetic fibres  Should be MR compatible  Should be tapering from a larger to a smaller end  Should be available in following sizes: diameters: 5-10 mm and length 2-15 cm The diameter to tapered end for tapering type coil should be mentioned

Embolisation Coils - CE APPROVED  Should be 0.035/0.038” compatible  Should be made of platinum with synthetic fibres  Should be MR compatible  Should be tapering from a larger to a smaller end  Should be available in following sizes: diameters: 5-10 mm and length 2-15 cm The diameter to tapered end for tapering type coil should be mentioned

Embolisation Coils – DCGI APPROVED  Should be 0.035/0.038” compatible  Should be made of platinum with synthetic fibres  Should be MR compatible  Should be tapering from a larger to a smaller end  Should be available in following sizes: diameters: 5-10 mm and length 2-15 cm The diameter to tapered end for tapering type coil should be mentioned

Embolisation Coils - US FDA APPROVED  Should be 0.035/0.038/0.052” compatible  Should be non tapering/straight  Should be made of stainless steel with synthetic fibres Should be available in the following sizes: diameters: 3-15 mm and length 2-15 cm

Embolisation Coils - CE APPROVED  Should be 0.035/0.038/0.052” compatible  Should be non tapering/straight  Should be made of stainless steel with synthetic fibres Should be available in the following sizes: diameters: 3-15 mm and length 2-15 cm

Embolisation Coils – DCGI APPROVED  Should be 0.035/0.038/0.052” compatible  Should be non tapering/straight  Should be made of stainless steel with synthetic fibres Should be available in the following sizes: diameters: 3-15 mm and length 2-15 cm

Coil pusher wire for 0.014/0.018” coils, compatible with the quoted micro catheters - US FDA APPROVED

Coil pusher wire for 0.014/0.018” coils, compatible with the quoted micro catheters - CE APPROVED

Coil pusher wire for 0.014/0.018” coils, compatible with the quoted microcatheters – DCGI APPROVED

Gelfoam sheet for vascular embollization - US FDA APPROVED

Gelfoam sheet for vascular embollization - CE APPROVED

Gelfoam sheet for vascular embollization – DCGI APPROVED

Liquid Embolization system available in Various sizes (2ml, 3ml & 6ml)– US FDA/ CE / DCGI APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – US FDA APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – CE APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITH ACCESSORIES – DCGI APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES – US FDA APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES –CE APPROVED

PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES –DCGI APPROVED

ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – US FDA APPROVED

ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – CE APPROVED

ACCESSORIES ONLY FOR THE ABOVE PBMV BALLOONS – DCGI APPROVED

PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– US FDA APPROVED

PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– CE APPROVED

PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITH ACCESSORIES– DCGI APPROVED

PBMV BALLOON WITH SIDE SAFETY / MICROHOLES WITHOUT ACCESSORIES – US FDA APPROVED

PBMV BALLOON WITH SIDE SAFETY/ MICROHOLES WITHOUT ACCESSORIES– CE APPROVED

PBMV BALLOON WITH SIDE SAFETY/ MICROHOLES WITHOUT ACCESSORIES– DCGI APPROVED

PTMC BALLOON WITH HOLE IN BALLOON – US FDA APPROVED

PTMC BALLOON WITH HOLE IN BALLOON – CE APPROVED

PTMC BALLOON WITH HOLE IN BALLOON – DCGI APPROVED

PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- US FDA APPROVED

PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- CE APPROVED

PTMC BALLOON (WITH HOLE IN BALLOON) WITH ALL ACESSORIES- DCGI APPROVED

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - – DCGI With US FDA /CE APPROVED

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - CE APPROVED

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) – DCGI APPROVED

Self Expandable Trans Catheter Aortic Valve Replacement System With All Required Accessories –US FDA /CE APPROVED  Should be in All Sizes Diameter Anti – Calcification and Chemical Dehydration Thin & Strong Low Profile With Delivery System.

Self Expandable Trans Catheter Aortic Valve Replacement System With All Required Accessories – DCGI APPROVED  Should be in All Sizes Diameter Anti – Calcification and Chemical Dehydration Thin & Strong Low Profile With Delivery System.

Self Expandable Trans Catheter Tricuspid Valve Replacement System With All Required Accessories – DCGI With US FDA /CE APPROVED  Should be in All Sizes Diameter Anti – Calcification and Chemical Dehydration Thin & Strong Low Profile With Delivery System.

Trans Catheter Tricuspid Valve Replacement System With All Required Accessories – DCGI With US FDA /CE APPROVED  Should be in All Sizes Diameter Anti – Calcification and Chemical Dehydration Thin & Strong Low Profile With Delivery System.

Mitra-Clip (TRANS CATHETER Mitral VALVE Clip System) - DCGI with US FDA / CE Approved

Mitra-Valve (TRANS CATHETER Mitral VALVE) - DCGI

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - usfda APPROVED

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - CE APPROVED

TAVI (|TRANS CATHETER AORTIC VALVE REPLACEMENT SYSTEM WITH ALL REQUIRED ACCESSORIES) - DCGI APPROVED

TAVI Guide-wire - DCGI with US FDA / CE Approved  Should be available in diameter 0.035, length 250-275 cm, Should have spring coil PTFE coating and Extra Small, small & large curves.

WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS - US FDA APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS - CE APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

WIRE 0.018” REGULAR LENGTH, REGULAR SHAFT STIFFNESS – DCGI APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - US FDA APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - CE APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

WIRE 0.018” REGULAR LENGTH, EXTRA – STIFF SHAFT - DCGI APPROVED Floppy Tip, Straight / J Shaped tip, 140-300cm long

VALVOPLASTY BALLOON CATHETERS - US FDA APPROVED  Varying sizes and diameters Approved for pediatric/adults use

VALVOPLASTY BALLOON CATHETERS - CE APPROVED  Varying sizes and diameters Approved for pediatric/adults use

VALVOPLASTY BALLOON CATHETERS – DCGI APPROVED  Varying sizes and diameters Approved for pediatric/adults use

SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH - US FDA APPROVED  Compatible with 0.018 inch guide wire Varying length and diamete

SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH - CE APPROVED  Compatible with 0.018 inch guide wire Varying length and diameter

SPECIAL BALLOON CATHETER COMPATIBLE WITH 4 FRENCH SHEATH – DCGI APPROVED  Compatible with 0.018 inch guide wire Varying length and diameter

SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH - US FDA APPROVED  Compatible with 0.025 inch guide wire Varying length and diameter

SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH - CE APPROVED  Compatible with 0.025 inch guide wire Varying length and diameter

SPECIAL PEDIATRIC VALVOPLASTY BALLOON CATHETERS COMPATIBLE WITH 4 FRENCH SHEATH – DCGI APPROVED  Compatible with 0.025 inch guide wire Varying length and diameter

VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - US FDA APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 4 ATM

VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - CE APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 4 ATM

VALVOPLASTY BALLOON CATHETERS (sizes 10 – 22 mm) - DCGI APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 4 ATM

BALLOON CATHETERS (sizes 10 – 22 mm) - US FDA APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 8 ATM

BALLOON CATHETERS (sizes 10 – 22 mm) - CE APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 8 ATM

BALLOON CATHETERS (sizes 10 – 22 mm) - DCGI APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 8 ATM

BALLOON IN BALLOON CATHETERS - US FDA APPROVED Quote in all sizes

BALLOON IN BALLOON CATHETERS - CE APPROVED Quote in all sizes

BALLOON IN BALLOON CATHETERS - DCGI APPROVED Quote in all sizes

FOGARTY EMBOLECTOMY CATHETER - US FDA APPROVED  4Fr./5Fr./6 Fr. sizes Metal rod at tip of the catheter to enable angulations up to 60 degrees

FOGARTY EMBOLECTOMY CATHETER - CE APPROVED  4Fr./5Fr./6 Fr. sizes Metal rod at tip of the catheter to enable angulations up to 60 degrees

FOGARTY EMBOLECTOMY CATHETER - DCGI APPROVED  4Fr./5Fr./6 Fr. sizes Metal rod at tip of the catheter to enable angulations up to 60 degrees

ATRIAL SEPTOSTOMY CATHETER - US FDA APPROVED 4Fr./5Fr./6 Fr. sizes

ATRIAL SEPTOSTOMY CATHETER - CE APPROVED 4Fr./5Fr./6 Fr. sizes

ATRIAL SEPTOSTOMY CATHETER – DCGI APPROVED 4Fr./5Fr./6 Fr. sizes

DETACHABLE BALLOON - US FDA APPROVED

DETACHABLE BALLOON - CE APPROVED

DETACHABLE BALLOON – DCGI APPROVED

VASCULAR PLUGS – US FDA APPROVED

VASCULAR PLUGS – CE APPROVED

VASCULAR PLUGS IMPLANTATION– DCGI with US FDA / CE Approved  should be Titanium Nitride Coated.  Should have PTFE layers for enhanced occlusion. Should be Available in various sizes (4.0- 24.0 MM.

VALVOPLASTY BALLOON CATHETERS TYSHEK TYPE (all sizes) - US FDA APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 4 ATM

VALVOPLASTY BALLOON CATHETERS TYSHEK TYPE (all sizes) - CE APPROVED  Approved for pediatric/adults use  Varying length and diameter Nominal pressure < 4 ATM

Aortic Stent graft Abdominal - DCGI with US FDA / CE Approved  Endovascular stent graft device for the treatment of thoracic aortic aneurysm or dissection with PTFE dual Membrane coating. With metal spine on the greater curvature to avoid stent shortening and provide axial support.

A U I Stent Graft System DCGI with US FDA / CE Approved  Specifically designed for treatment of endovascular Abdominal aortic Aneurysm A self – expandable nitinol stent with PTFE dual Membrane coating & offers axial support preventing foreshortening of stent.

iliac Stent Graft - DCGI with US FDA / CE Approved  Endo-vascular stent graft device for the treatment iliac aneurysm or dissection. With proximal bare spring configuration. It should be an extension to AAA graft system

Multifunctional Occluder- DCGI with US FDA / CE Approved  For Occlusion of muscular VSD peri-membranous VSD, RSOV, Apex window & AV Fistula Should be low profile (4F-6F) and Should come with a Elongatable waist.

Peripheral Snare with Tungsten Loop coated with Titanium Nitride - DCGI with CE/ US FDA Approved Loop Size 5MM to 35MM. Shaft Size up to 6F

Peripheral Snare with Tungsten loop Coated with Titanium Nitride (5mm to 35mm) - DCGI with US FDA / CE Approved

IVC Filter For Optimal Filtration of IVC Up to 23mm - DCGI with US FDA / CE Approved  Made of national and filter length up to 40  For Temporary Placement It Should be administrable from Jugular/ femoral route

Coronary Snare with tungsten loop coated with Titanium Nitride (4mm&7mm) - DCGI with US FDA / CE Approved

Steerable Sheath with deflectable tip (190-160degree) - DCGI with US FDA / CE Approved

PVA particles with consistent sized Particles - DCGI with US FDA/ CE APPROVED

ENDOMYOCARDIAL BIOPSY (EMB) FORCEPS SET - US FDA APPROVED Set should include  Should include an endomyo-cardial biopsy foreeps and compatible pre-shaped introducer sheath with side arm and its dilator

ENDOMYOCARDIAL BIOPSY (EMB) FORCEPS SET – CE/DCGI APPROVED Set should include  Should include an endomyo-cardial biopsy foreeps and compatible pre-shaped introducer sheath with side arm and its dilator  Variable lengths and sizes Should be available for both for jugular and femoral access

INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) - US FDA APPROVED Snare kit should include  A snare and its compatible sheath  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes of loop (5-35 mm)

INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) - CE APPROVED Snare kit should include  A snare and its compatible sheath  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes of loop (5-35 mm)

INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) –DCGI APPROVED Snare kit should include  A snare and its compatible sheath  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes of loop (5-35 mm)

SHEATHS FOR INTRAVASCULAR SNARES - US FDA APPROVED Should be compatible with item no. 3 &4

SHEATHS FOR INTRAVASCULAR SNARES - CE APPROVED Should be compatible with item no. 3 & 4

SHEATHS FOR INTRAVASCULAR SNARES – DCGI APPROVED Should be compatible with item no. 3 & 4

INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) - US FDA APPROVED Microsnare kit should include  A microsnare, compatible micro – catheter, micro – catheter introducer and a torque device  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes (2-7 mm)

INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) - CE APPROVED Microsnare kit should include  A microsnare, compatible micro – catheter, micro – catheter introducer and a torque device  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes (2-7 mm)

INTRAVASCULAR RETRIEVER – MICROSNARE (‘ AMPLATZ GOOSENECK’ TYPE) – DCGI APPROVED Microsnare kit should include  A microsnare, compatible micro – catheter, micro – catheter introducer and a torque device  Should have nitinol shaft  Should have 90 degree preformed snare loop Variable sizes (2-7 mm)

ACCESSORIES FOR INTRAVASCULAR MICROSNARE - US FDA APPROVED Should be compatible with item no. 7 & 8

ACCESSORIES FOR INTRAVASCULAR MICROSNARE - CE APPROVED Should be compatible with item no. 7 & 8

ACCESSORIES FOR INTRAVASCULAR MICROSNARE – DCGI APPROVED Should be compatible with item no. 7 & 8

INTRAVASCULAR RETRIEVER – BASKET - US FDA APPROVED Set should include  Basket retriever and its catheter Should be available in all sizes

INTRAVASCULAR RETRIEVER – BASKET - CE APPROVED Set should include  Basket retriever and its catheter Should be available in all sizes

INTRAVASCULAR RETRIEVER – BASKET – DCGI APPROVED Set should include  Basket retriever and its catheter Should be available in all sizes

INTRAVASCULAR RETRIEVER SNARE KIT Goose Neck Type – DCGI & US FDA / CE Approved

SIZING BALLOON FOR DEVICE CLOSURE — CIRCULAR SHAPE - CE APPROVED

Sizing balloon for device closure - Round Shape - DCGI /CE Approved

COBALT ClIROMIUM RENAL STENTS, PREMOUNTED ON BALLOON DCGI APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) · Available in the sizes and lengths Three Mid-strut to mid-strut connectors between two rings. • Two different crown design for diameters between 5- 7 mm. • Crossing profile ≤ 1.50 mm • Zero foreshortening • Available in 5,6 and 7mm diameters with length of 12,15 and 18 mm.

Permanent venacava filter– CE APPROVED

Permanent venacava filter– US FDA APPROVED

Permanent venacava filter– DCGI APPROVED

Temporary venacava filter– CE APPROVED

Temporary venacava filter– US FDA APPROVED

Temporary venacava filter– DCGI APPROVED

1 port Cath-Lock™ Introducer Sheath with Hemostasis Valve and Sideport, Dilator,and 50 cm Double Distal Guidewire with “J” and straight ends

2 Port Hemostasis Adapter with Sideports and Cath-Lock™ sealing mechanism, Venous Sheath,Dilator and 50 cm Double Distal guidewire with “J” and straight ends

3 Port Hemostasis Adapter with Sideports and Cath-Lock™ sealing mechanism, Venous Sheath,Dilator and 50 cm Double Distal Guidewire with “J” and straight ends

Introducer Sheath with Hemostasis Valve and Sideport, and Dilator , Mullins style curve 6/7/8 F size, 61cm usable length , 67cm Dilator usable length

Swartz lntroducer Braided sheath with hemostatic valve SL0/SL1/SL2/SL3 (8F, 63 cm usable length and 67cm Dilator usable length) accomodates maximum 0.32 Guidewire

Swartz lntroducer Non Braided sheath with hemostatic valve SR0/SR1/SR2/SR3 (8F, 63 cm),(8F, 63 cm usable length) accomodates maximum 0.38 Guidewire

8.5 F : 71 cm Bi-Directional (Assymetrical ) Deflectable sheath , Curl Dimension 16.8mm and 22.4 mm with Integrated hemostasis valve and Radiopaque tip marker and various curve options , compatible with 98 cm Transseptal Needle along with 180 cm Super Stiff Guidewire

8.5 F : 40 cm Bi-Directional (Assymetrical ) Deflectable sheath used for EPICARDIAL with Integrated hemostasis valve and Radiopaque tip marker and various curve options

BRK/BRK-1 Needle-Adult, 18 gauge, usable length 71 cm.

BRK/BRK-1 Needle-Adult, 18 gauge, usable length 98 cm.

Fixed Curve Quadripolar Electrophysiology catheter (6F/5F/4F, 1mm band electrode) CRD/JSN/DAO, 2-5-2 mm electrode spacing

Fixed Curve Quadripolar Electrophysiology catheter (6F) CRD-2, 5mm electrode spacing

Fixed Cuve (CSL) Decapolar Catheter (6F) -65 cm usable length with 5-5-5 Spacing with Tip Electrode 2mm

Fixed Cuve (CSL) Decapolar Catheter (6F) -120 cm usable length with 5-5-5 Spacing with Tip Electrode 2mm

Deflectable Decapolar Electrophysiology Catheter with connector (6F)-110cm usable length with 2-5-2 Spacing

Deflectable Decapolar Electrophysiology Catheter with connector (5F)-110cm usable length with 2-5-2 Spacing

Deflectable Decapolar Electrophysiology Catheter with connector (4F)-110cm usable length with 2-5-2 Spacing

DuoDecapolar Electrophysiology Catheter-20 Poles (7F) Usable Length 95cm with 5-5-5 Spacing, 1mm band electrode

8F Sensor Enabled Uni-Directional Circular Mapping Catheter with 3-3-3mm & 5-5-5mm electrode specification, 2mm tip & 1 mm band electrode with Fixed Loop

8F Sensor Enabled Bi-Directional Circular Mapping Catheter DF curve 3-3-3mm- & 5-5-5mm specification, 2mm tip & 1 mm band electrode with Fixed Loop

8F Sensor Enabled Uni-Directional Circular Mapping Catheter with 6.5mm electrode spacing Variable loop with 15-25 mm range

8F Sensor Enabled Bi-directional Circular Mapping Catheter with 1-4-1 mm electrode spacing Variable loop with 15-25 mm range

8F-Irrigated Bidirectional 16 Electrode ,2F Splines, 3 mm spacing , 1mm electrode size,High Density Sensor Enable Mapping Cathter Comaptible with Ensite Mapping system

Bi-D-Deflectable Radio Frequency Ablation Catheter (7 F, 4mm tip ) 2-5-2 electrode spacing - with Universal Temperature sensor (Thermocouple and Thermistor temperature monitoring capability),should be compatable to use with IBI T11 & Ampere RF

Uni-D-Deflectable Radio Frequency Ablation Catheter (7 F, 4mm tip ) 2-5-2 electrode spacing, Usable length 110cm ,should be compatable to use with IBI T11 & Ampere RF

Uni-D-Deflectable Radio Frequency Ablation Catheter (5 F, 4mm tip ) 2-5-2 electrode spacing ,should be compatable to use with IBI T11 & Ampere RF

Irrigated Bi- Directional ablation Catheter with Flexible tip 1-4-1, Symmetric and asymmetric option , should be compatable to use with IBI T11 & Ampere RF Generator

Irrigated Uni- Directional ablation Catheter with Flexible tip 1-4-1, D and F Curve , should be compatable to use with IBI T11 & Ampere RF Generator

Contact Force Sensor Enable Catheter with Fiber optic Technology for force detection 3.5 MM tip Electrode 8F , Six Saline irrigation hole, 2-2-2 ring spacing,should be compatable to use with IBI T11 & Ampere RF

Intracardiac ECHO Catheter-9F size ,Transducer type 64 element phased array , Viewing sector 80 degrees, Tip Deflection Anterior/Posterior, Left/Right +/- 120 degree flexion Compatible with Philips Cx50 Echo system

Magnetic & Impedance (Hybrid) Based patches for electroanotomical mapping for use with Ensite 3D mapping System.

Magnetic Based patches for electroanotomical mapping for use with Ensite 3D mapping System.

Cool Point Tubing Set for Irrigated RF Catheter with dedicated pressure sensor and compatible with Abbott Coolpoint Pump

Cables for Fixed Quadripolar electrophysiology catheters

Cables for Fixed Decapolar electrophysiology catheters

Cables for Deflectable Decapolar electrophysiology catheters

Cables for HighDensity mapping electrophysiology catheters compatible with Ensite mapping system

Cables for Ablation range of electrophysiology catheters compatible compatable to use with IBI T11 & Ampere RF

Cable for Fixed loop circular mapping catheters

Cable for Variable loop circular mapping catheters

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · VVIR · All single Chamber modes and basic pacing programmable parameters · Must have ventricular capture management · The Size of lead must be 7F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · VVIR · All single Chamber modes and basic pacing programmable parameters · Must have ventricular capture management · The Size of lead must be 7F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Life time replacement warranty. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

D.D.D Pacemaker With All Accessories - DCGI & FDA Approved /CE Approved

DDDR MRI Pacemaker With All Accessories -DCGI & US FDA/CE approved

DDDR MRI Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved · latest and New 3T Full body MRI, BEAT TO BEAT CAPTURE MGT, · Algorithm to manage neuro-cardiogenic syncope, · AF Suppression, Optimization of AV delay, Congestion Monitoring.

DICD-40J Deliver fable energy - -DCGI & US FDA Approved /CE Approved

CRTP-QUADRIPOLAR-EGM Based Dynamic AV DELAY optimization -DCGI & US FDA Approved /CE Approved · Congestion monitoring algorithm · Capture management for all chambers · Option of Triggered biv pacing during AF · Capable of Wireless telemetry

CRTP-MULTIPOINT EGM Based Dynamic AV DELAY optimization -DCGI & US FDA Approved /CE Approved · LV LEAD ABLE TO PACE AT TWO POINTS IN LV IN ONE CYCLE · QUDRIPOLAR LEAD WITH MRI COMPITABLE DEVICE · Congestion monitoring algorithm · Capture management for all chambers · Option of Triggered biv pacing during AF · Capable of Wireless telemetry

CRT-D QUADRIOPOLAR DF-4 FDA/CE approved latest and New 40J Deliver fable energy – -DCGI & US FDA Approved /CE Approved · FULL BODY MRI, CONGESTION MONITORINGNG RV LEAD 7F OR LESS · AF SUPPRESSION · EGM Based AV DELAY optimization · Mechanism for Narrow QRS by synchronizing intrinsic and paced pulses

CRT-D MULTIPOINT DF-4 FDA/CE approved latest and New 40J Deliver fable energy- -DCGI & US FDA /CE Approved · FULL BODY MRI, CONGESTION MONITORINGNG RV LEAD 7F OR LESS · AF SUPPRESSION · EGM Based AV DELAY optimization · Mechanism for Narrow QRS by synchronizing intrinsic and paced pulses

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDD · All modes and basic pacing programmable parameters including hystersis · The Size of lead must be 6F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDD · All modes and basic pacing programmable parameters including hystersis · The Size of lead must be 6F or less and with HIS bundal pacing lead · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDD · All modes and basic pacing programmable parameters including hystersis · The Size of lead must be 6F or less and with HIS bundal pacing lead · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDD · All modes and basic pacing programmable parameters including hystersis · The Size of lead must be 6F or less - HIS/LBBA PACING · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Life time replacement warranty. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDDR · All single modes and basic pacing programmable parameters and with special features · Must have approved algorithm for atrial fibrillation suppression with programmable automatic mode switch basel rate. · Must have ventricular capture management - Must have MRI Compitable · Must have P & R wave measurement · The Size of lead must be 6F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDDR · All modes and basic pacing programmable parameters and special features · Must have approved AF suppression algorithm & fluid Monitoring. · Must have ventricular capture management · Must have P & R wave measurement · The Size of lead must be 6F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Life time replacement warranty. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES · DDDR · All modes and basic pacing programmable parameters and special features · · Must have ventricular capture management · Must have P & R wave measurement - LBBA Pacing system - Style driven lead · The Size of lead must be 6F or less - Must have congestion monitoring · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Have feature for optimization of AV delay · Must have both active and passive fixation endocardial leads available · Life term replacement warranty. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS · Single chamber · RV lead must be 7F or less - Must have MRI Compitble · All basic programmable parameters · Lead should be steroid eluting · Should have both active and passive fixation leads · Should be minimum 8+2 year warranty · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS – DCGI APPROVED ,ICD WITH ALL LEADS · Single chamber · RV lead must be 7F or less - Must have MRI Compitble · All basic programmable parameters · Lead should be steroid eluting · Should have both active and passive fixation leads · Should be minimum 8+2 year warranty · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available.

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS -US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES · Dual chamber · RV lead must be 7F or less · All basic programmable parameters · Lead should be steroid eluting · Should have both active and passive fixation leads · Should be minimum 5+3 year warranty · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS- DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES · Dual chamber · RV lead must be 9F or less · All basic programmable parameters · Lead should be steroid eluting · Should have both active and passive fixation leads · Should be minimum 5+3 year warranty · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

AICD SINGLE CHAMBER DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED · Should have latest Bluetooth technology Low energy communication enabling smart phone connectivity through secured data encryption. · Should have multi point pacing delivers multiple LV pacing pulse/cardiac cycle in both LV and Biv pacing modes. · Should have Improvised SYNC-AV pulse CRT technology offer dynamic AV timing. · 40 J delivered energy for enhanced safety margin · Should have full body 3-Tesla MRI compatibility. · Direct presence of Parent Company in India (not only through the distributors) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required. · Company must provide at least one programmer exclusively to the cardiology dept., · Company must quote only the latest model of devices commercially available.

AICD DUAL CHAMBER DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED · Should have latest Bluetooth technology Low energy communication enabling smart phone connectivity through secured data encryption. · Should have multi point pacing delivers multiple LV pacing pulse/cardiac cycle in both LV and Biv pacing modes. · Should have Improvised SYNC-AV pulse CRT technology offer dynamic AV timing. · 40 J delivered energy for enhanced safety margin · Should have full body 3-Tesla MRI compatibility. · Direct presence of Parent Company in India (not only through the distributors) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required. · Company must provide at least one programmer exclusively to the cardiology dept., · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special features · Must have facility for EGM based optimization of AV, PV and VV delays · The size of atrial and RV leads should be 7F or less · The leads should be steroid eluting and should be bipolar and unkipolar configuration · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 5 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special features · Must have facility for EGM based optimization of AV, PV and VV delays · The size of atrial and RV leads should be 7F or less · The leads should be steroid eluting and should be bipolar and unkipolar configuration · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 5 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept.

US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have all basic programmable parameters · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay · The leads should be steroid eluting · Should have both active and passive fixation RA & RV endocardial leadsr - RV LEAD 7F OR LESS · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have all basic programmable parameters · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay · The leads should be steroid eluting · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have Quadripolar lead for LV pacing · Must have all basic programmable parameters with following special features · Facility of ATP during charging for defibrillation · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay · Must have fluid monitoring system - RV LEAD 7F OR LESS · The leads should be steroid eluting · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept.

DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have Quadripolar lead for LV pacing · Must have all basic programmable parameters with following special features · Facility of ATP during charging for defibrillation · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay · Must have fluid monitoring system · The leads should be steroid eluting · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special feature · The LV lead must be Quadripolar. - RV LEAD MUST BE 7F OR LESS · The leads should be steroid eluting and should be both bipolar and unipolar · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES RQUIRED DURING IMPANTATION · Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special feature · The LV lead must be Quadripolar. · The leads should be steroid eluting and should be both bipolar and unipolar · Should have both active and passive fixation RA & RV endocardial leads · Should have epicardial lead for epicardial LV lead implantation · Replacement warranty not less than 3 + 2 years · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

Lead Less Pacemaker with All Accessories. –DCGI AND US FDA/ CE APPROVED VVI, MRI COMPITABLE MUST HAVE RETRIEVABLE OPTION

Lead Less Pacemaker with All Accessories. –DCGI AND US FDA/ CE APPROVED DDD MRI COMPITABLE MUST HAVE RETRIEVABLE OPTION

CRT- D Combo DEVICE WITH ALL LEADS -ICD WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED · Should have latest Bluetooth technology Low energy communication enabling smart phone connectivity through secured data encryption. · Should have multi point pacing delivers multiple LV pacing pulse/cardiac cycle in both LV and BIV pacing modes. · Should have Improvised SYNC-AV pulse CRT technology offer dynamic AV timing. · 40 J delivered energy for enhanced safety margin · Should have full body 3-Tesla MRI compatibility.

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES VVI  All single Chamber modes and basic pacing programmable parameters  The Size of lead must be 7F or less  The Lead must be steroid eluting and should be both bipolar and unipolar configuration  Must have both active and passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES  VVIR  All single Chamber modes and basic pacing programmable parameters  Must have MRI Compatible  Must have programmable sensor control rest rate  Must have ventricular capture management  The Size of lead must be 8F or less  The Lead must be steroid eluting and should be both bipolar and uni-polar configuration  Must have both active and passive fixation endo-cardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES VVIR  All single Chamber modes and basic pacing programmable parameters  Must have MRI Compatible  Must have programmable sensor control rest rate  Must have ventricular capture management  The Size of lead must be 8F or less  The Lead must be steroid eluting and should be both bipolar and uni-polar configuration  Must have both active and passive fixation endo- cardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES • VVIR • All single Chamber modes and basic pacing programmable parameters • Must have MRI Compatible • Must have programmable sensor control rest rate • Must have ventricular capture management • The Size of lead must be 8F or less • The Lead must be steroid eluting and should be both bipolar and uni-polar configuration • Must have both active and passive fixation endo-cardial leads available • Life time replacement warranty. • Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required • Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available.

V.V.I Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved • latest and New Full body MRI, BEAT TO BEAT CAPTURE MGT,

D.D.D Pacemaker With All Accessories and Life time Warranty - DCGI & FDA Approved /CE Approved

DDDR MRI Pacemaker With All Accessories and Life time Warranty -DCGI & US FDA/CE approved

SICD (AICD) DF1 CONNECTOR--DCGI & US FDA Approved /CE

DICD-40J Deliver fable energy - -DCGI & US FDA Approved /CE Approved

CRTP-QUADRIPOLAR-EGM Based Dynamic AV DELAY optimization -DCGI & US FDA Approved /CE Approved  Congestion monitoring algorithm  Capture management for all chambers  Option of Triggered biv pacing during AF,  Capable of Wireless telemetry"

CRT-D QUADRIOPOLAR DF-4 FDA/CE approved latest and New 40J Deliver fable energy – -DCGI & US FDA Approved /CE Approved · FULL BODY MRI, CONGESTION MONITORINGNG · AF SUPPRESSION · EGM Based AV DELAY optimization · Mechanism for Narrow QRS by synchronizing intrinsic and paced pulses

CRT-D MULTIPOINT DF-4 FDA/CE approved latest and New 40J Deliver fable energy- -DCGI & US FDA /CE Approved · FULL BODY MRI, CONGESTION MONITORINGNG · AF SUPPRESSION · EGM Based AV DELAY optimization · Mechanism for Narrow QRS by synchronizing intrinsic and paced pulses

Sub-cutenous ICD IMPLANT (SC- I.C.D.) with All Accessories - DCGI & US FDA Approved /CE Approved

PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA/CE APPROVED  VDD  All VDD & single Chamber modes and basic pacing programmable parameters and with following special features  Must have ventricular capture management  The Size of lead must be 9F or less  The Lead must be steroid eluting and should be both bipolar configuration  Having passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained  technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available."

PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI APPROVED  VDD  All VDD & single Chamber modes and basic pacing programmable parameters and with following special features  Must have ventricular capture management  The Size of lead must be 9F or less  The Lead must be steroid eluting and should be both bipolar configuration  Having passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained  technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES  " DDD  All modes and basic pacing programmable parameters including hystersis  The Size of lead must be 7F or less  The Lead must be steroid eluting and should be both bipolar and unipolar configuration  Must have both active and passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES  " DDD  All modes and basic pacing programmable parameters including hystersis  The Size of lead must be 7F or less  The Lead must be steroid eluting and should be both bipolar and unipolar configuration  Must have both active and passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES  " DDDR  All single modes and basic pacing programmable parameters and with special features  Must have approved algorithm for atrial fibrillation suppression with programmable automatic mode switch basel rate.  Must have ventricular capture management  Must have P & R wave measurement  The Size of lead must be 7F or less  The Lead must be steroid eluting and should be both bipolar and unipolar configuration  Must have both active and passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED PERMANENT PACEMAKERS WITH ALL LEADS AND ACCESSORIES  DDDR  All modes and basic pacing programmable parameters and special features  Must have approved Atrial Tachycardia management algorithm & fluid Monitoring.  Must have ventricular capture management  Must have P & R wave measurement  The Size of lead must be 7F or less  The Lead must be steroid eluting and should be both bipolar and unipolar configuration  Must have both active and passive fixation endocardial leads available  Life time replacement warranty.  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS - US FDA/CE APPROVED ,ICD WITH ALL LEADS " Single chamber  RV lead must be 9F or less  All basic programmable parameters  Lead should be steroid eluting  Should have both active and passive fixation leads  Should be minimum 5+3 year warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

AICD SINGLE CHAMBER PACEMAKER WITH ALL LEADS – DCGI APPROVED ,ICD WITH ALL LEADS  " Single chamber  RV lead must be 9F or less  All basic programmable parameters  Lead should be steroid eluting  Should have both active and passive fixation leads  Should be minimum 5+3 year warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available."

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS -US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES  " Dual chamber  RV lead must be 9F or less  All basic programmable parameters  Lead should be steroid eluting  Should have both active and passive fixation leads  Should be minimum 5+3 year warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS- DCGI APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES  " Dual chamber  RV lead must be 9F or less  All basic programmable parameters  Lead should be steroid eluting  Should have both active and passive fixation leads  Should be minimum 5+3 year warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS- US FDA/CE APPROVED ,ICD WITH ALL LEADS AND ALL ACCESSORIES  Dual chamber  All basic programmable parameters  Must have shock reduction technology with fluid monitoring  Lead should be steroid eluting  Lead Should be DF-1& DF-4 compatible  Replacement warranty as per norms  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.

AICD DUAL CHAMBER PACEMAKER WITH ALL LEADS - DCGI APPROVED, ICD WITH ALL LEADS AND ALL ACCESSORIES  " Dual chamber  All basic programmable parameters  Must have shock reduction technology with fluid monitoring  Lead should be steroid eluting  Lead Should be DF-1& DF-4 compatible  Replacement warranty as per norms  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

D/C ICD SINGLE CHAMBER DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED  " Should have advanced feature of automatic AV Search, and Adjustable AV delay etc.  Direct presence of Parent Company in India (not only through the distributors) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required.  Company must provide at least one programmer exclusively to the cardiology dept.,  Company must quote only the latest model of devices commercially available."

S/C ICD SINGLE CHAMBER DEVICE MRI WITH ALL LEADS AND ALL ACCESSORIES - DCGI AND US FDA/ CE APPROVED  " Should have labelled PROJECTED longevity of > 12years with warranty not less than 8 + 2 years.  Direct presence of Parent Company in India (not only through the distributors) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required.  Company must provide at least one programmer exclusively to the cardiology dept.,  Company must quote only the latest model of devices commercially available."

US FDA/CE APPROVED IMPLANTABLE LOOP RECORDER  " Must be able to detect Asystole, Brady arrhythmia and VT/FVT  Must have the storage capacity of >45 minutes.  Must have dynamic sensing threshold for R wave sensing along with noise reversion  Must have a patient tool for symptomatic recording  Must have at least 35 months of longevity  Must be compatible with remote monitoring devices,  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED IMPLANTABLE LOOP RECORDER  " Must be able to detect Asystole, Bradyarrhythmia and VT/FVT  Must have the storage capacity of >45 minutes.  Must have dynamic sensing threshold for R wave sensing along with noise reversion  Must have a patient tool for symptomatic recording  Must have at least 35 months of longevity  Must be compatible with remote monitoring devices  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED IMPLANTABLE LOOP RECORDER for AF DETECTION  " Must be able to detect Asystole, Bradyarrhythmia, VT/FVT and AT/AF  Must have the storage capacity of >45 minutes.  Must have dynamic sensing threshold for R wave sensing along with noise reversion  Must have a patient tool for symptomatic recording along with alerts.  Must be able to give AF burden reports to monitor the progress of chronic AF patients.  Must have at least 35 months of longevity  Must be compatible with remote monitoring devices  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

 DCGI APPROVED IMPLANTABLE LOOP RECORDER for AF DETECTION  Must be able to detect Asystole, Brady-arrhythmia, VT/FVT and AT/AF  Must have the storage capacity of >45 minutes.  Must have dynamic sensing threshold for R wave sensing along with noise reversion  Must have a patient tool for symptomatic recording along with alerts.  Must be able to give AF burden reports to monitor the progress of chronic AF patients.  Must have at least 35 months of longevity  Must be compatible with remote monitoring devices,  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation whenever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

"US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION"  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special features  Must have facility for EGM based optimization of AV, PV and VV delays  The size of atrial and RV leads should be 7F or less  The leads should be steroid eluting and should be bipolar and unkipolar configuration  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, BIVENTRICULAR PACEMAKER WITH ATRIAL,RV, LV LEADS AND ALL ACCESSORIES REQUIRED DURING IMPLANTATION  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay and should have following special features  Must have facility for EGM based optimization of AV, PV and VV delays  The size of atrial and RV leads should be 7F or less  The leads should be steroid eluting and should be bipolar and unkipolar configuration  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL  ACCESSORIES RQUIRED DURING IMPANTATION"  Must have all basic programmable parameters  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay  The leads should be steroid eluting  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

"DCGI APPROVED BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITH ATRIAL, RV, LV LEADS AND ALL ACCESSORIES  RQUIRED DURING IMPANTATION"  Must have all basic programmable parameters  Must have separate programmable RV, LV lead amplitude, pulse width and VV delay  The leads should be steroid eluting  Should have both active and passive fixation RA & RV endocardial leads  Should have epicardial lead for epicardial LV lead implantation  Replacement warranty not less than 3 + 2 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITHOUT LEAD • Must have all basic programmable parameters • Should have all parameters shown in related group of pacemaker • Replacement warranty not less than 5 years • Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required • Company must provide at least one programmer exclusively to the cardiology dept. • Company must quote only the latest model of devices commercially available"

DCGI APPROVED, BIVENTRICULAR PACEMAKER + ICD (COMBO DEVICE) WITHOUT LEAD  Must have all basic programmable parameters • Should have all parameters shown in related group of pacemaker • Replacement warranty not less than 5 years • Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required • Company must provide at least one programmer exclusively to the cardiology dept.  • Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, BIVENTRICULAR PACEMAKER (CRT) WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

DCGI APPROVED, BIVENTRICULAR PACEMAKER (CRT) WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, AICD DUAL CHAMBER PACEMAKER WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, AICD DUAL CHAMBER PACEMAKER WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, AICD SINGLE CHAMBER PACEMAKER WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, AICD SINGLE CHAMBER PACEMAKER WITHOUT LEAD  Must have all basic programmable parameters  Should have all parameters shown in related group of pacemaker  Replacement warranty not less than 5 years  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

 US FDA/CE APPROVED, VDD/VDDR PERMANENT PACEMAKER WITHOUT LEA  VDD/VDDR  All VDD & single chamber modes and basic pacing programmable parameters and with following special features  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, VDD/VDDR PERMANENT PACEMAKER WITHOUT LEAD  VDD/VDDR  All VDD & single chamber modes and basic pacing programmable parameters and with following special features  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, DDD PERMANENT PACEMAKER WITHOUT LEAD  DDD  All modes and basic pacing programmable parameters including hysteresis  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

DCGI APPROVED, DDD PERMANENT PACEMAKER WITHOUT LEAD  DDD  All modes and basic pacing programmable parameters including hysteresis  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, VVI PERMANENT PACEMAKER WITHOUT LEAD  VVI  All single chamber modes and basic pacing programmable parameters  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, VVI PERMANENT PACEMAKER WITHOUT LEAD  VVI  All single chamber modes and basic pacing programmable parameters  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD  VVIR  All single chamber modes and basic pacing programmable parameters  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

DCGI APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD VVIR  All single chamber modes and basic pacing programmable parameters  Should have all parameters shown in related group of pacemaker  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD  DDDR  MRI compatible  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

DCGI APPROVED, VVIR PERMANENT PACEMAKER WITHOUT LEAD  DDDR  MRI compatible  Life term replacement warranty  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, ATRIAL, RV. LV LEADS AND ALL ACCESSORIES FOR BIVENTRICULAR PACEMAKER (CRT) A ATRIAL LEAD B RV LEAD C LV LEAD Should have all parameters shown in related group of pacemaker Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available

DCGI APPROVED, ATRIAL, RV. LV LEADS AND ALL ACCESSORIES FOR BIVENTRICULAR PACEMAKER (CRT)  A ATRIAL LEAD  B RV LEAD  C LV LEAD  Should have all parameters shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, RV LEAD FOR AICD SINGLE CHAMBER  Must have all specifications shown in related group of pacemaker  RV lead for AICD Single chamber  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.

DCGI APPROVED, RV LEAD FOR AICD SINGLE CHAMBER  Must have all specifications shown in related group of pacemaker  RV lead for AICD Single chamber  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, PACING LEADS FOR AICD DUAL CHAMBER  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available

DCGI APPROVED, PACING LEADS FOR AICD DUAL CHAMBER  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDDR PERMANENT PACEMAKER A ATRIAL LEAD B VENTRICULAR LEAD  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available. Company must quote only the latest model of devices commercially available"

DCGI APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDDR PERMANENT PACEMAKER A ATRIAL LEAD B VENTRICULAR LEAD  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

US FDA/CE APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDD PERMANENT PACEMAKERA A ATRIAL LEAD B VENTRICULAR LEAD  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

DCGI APPROVED, PACING LEAD (ATRIAL AND VENTRICULAR) FOR DDD PERMANENT PACEMAKER A ATRIAL LEAD B VENTRICULAR LEAD  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available"

US FDA/CE APPROVED, PACING LEADS FOR VDD/VDDR PACEMAKERS Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available

DCGI APPROVED, PACING LEADS FOR VDD/VDDR PACEMAKERS  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available

USFDA/CE APPROVED, PACING LEADS FOR VVI/VVIR PACEMAKERS  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept. Company must quote only the latest model of devices commercially available.

DCGI APPROVED, PACING LEADS FOR VVI/VVIR PACEMAKERS  Must have all specifications shown in related group of pacemaker  Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required  Company must provide at least one programmer exclusively to the cardiology dept.  Company must quote only the latest model of devices commercially available.

Lead For DDDR Pacemaker – RA Lead - DCGI&US FDA/ CE Approved

Lead For DDDR Pacemaker – RA Lead - DCGI&US FDA/ CE Approved

Lead For DDDR Pacemaker – RV Lead - DCGI&US FDA/ CE Approved

Lead For DDD Pacemaker – RA Lead - DCGI&US FDA/ CE Approved

Lead For DDDR Pacemaker – RV Lead - DCGI&US FDA/ CE Approved

Lead For VDD Pacemaker – DCGI APPROVED & US FDA/ CE Approved

Lead For ICD Pacemaker – DCGI & US FDA/ CE Approved

Lead For ICD Dual Chamber Pacemaker - DCGI&US FDA/ CE Approved

Lead For CRT Pacemaker –RA Lead DCGI&US FDA/ CE Approved

Lead For CRT Pacemaker –RV Lead DCGI&US FDA/ CE Approved

Lead For CRT Pacemaker –LV Lead DCGI&US FDA/ CE Approved

Lead For CRTD Pacemaker –RV Lead DCGI&US FDA/ CE Approved

Lead For CRTD Pacemaker –RA Lead DCGI&US FDA/ CE Approved

Lead For CRTD Pacemaker –LV Lead -DCGI&US FDA/ CE Approved

Epicardial Pacing Lead – RV Lead

Epicardial Pacing Lead – RA Lead

Latex Surgical Gloves (Powdered) – Thickness - 0.135 mm • Natural Rubber Latex , Beaded cuff, Protein Content Level: <200μg/dm2 (as per ASTM D 5712) • Size – 6. 6.5, 7, 7.5, 8

Latex Surgical Gloves (Powder Free) – Thickness - 0.135 mm • Natural Rubber Latex , Beaded cuff, Protein Content Level: <50μg/dm2 (as per ASTM D 5712) • Size – 6. 6.5, 7, 7.5, 8

SILICON COATED DIRECTLY JOINTED SUS & SITINOL SHAFT WIRE 0.7 GM, DUO CORE TECHNOLOGY – CE APPROVED

SILICON COATED DIRECTLY JOINTED SUS & SITINOL SHAFT WIRE – 0.7 GM - DUO CORE TECHNOLOGY DCGI APPROVED

SILICON COATED DIRECTLY JOINTED SUS & SITINOL SHAFT INTERMEDIATE WIRE 1 GM, DUO CORE TECHNOLOGY – CE APPROVED

SILICON COATED DIRECTLY JOINTED SUS & SITINOL SHAFT INTERMEDIATE WIRE – 1 GM - DUO CORE TECHNOLOGY DCGI APPROVED

STAINLESS STEEL GRINDED, CORE WIRE, ONE CORE CONSTRUCTION, PLATINUM TIP (3 CM) - 195 CM, STANDARD / 1.2 GF, INTERMEDIATE / 1.0 GF, FLOPPY / 0.8 GF, EXTRA FLOPPY / 0.6 GF – CE APPROVED

STAINLESS STEEL GRINDED, CORE WIRE, ONE CORE CONSTRUCTION, PLATINUM TIP (3 CM) - 195 CM, STANDARD / 1.2 GF, INTERMEDIATE / 1.0 GF FLOPPY / 0.8 GF, EXTRA FLOPPY / 0.6 GF – DCGI APPROVED

NITINOL DISTAL CORE WIRE -UNICORE- BOTH NITINOL - LE AND MULTIPLE STAINLESS-STEEL CONJUGATION - ULTRA-LOW (<0.7 G) – 3-6 GM CTO WIRE - CE APPROVED

NITINOL DISTAL CORE WIRE – UNICORE -BOTH NITINOL - LE AND MULTIPLE STAINLESS-STEEL CONJUGATION - ULTRA-LOW (<0.7 G) – 3-6 GM CTO WIRE - DCGI APPROVED

CONTROLLED VASCULAR LUMEN EXPANSION REGULATOR SYSTEM – CE APPROVED

CONTROLLED VASCULAR LUMEN EXPANSION REGULATOR SYSTEM – DCGI APPROVED

Post Vascular Intervention Coronary CVI-Balloon Catheters - Semi Crystalline Polymer Pressure Limit – 14-20

Pre Vascular Intervention Coronary CVI-Balloon Catheters - Semi Crystalline Co-Polymer EFT Shaft Pressure Limit – 7-14

Vascular Intervention Coronary CVI Drug-Coated Balloon - Lux coating technology blends paclitaxel with BTHC

Group – B (Interventional Neurology)

DISPOSABLE LUER LOCK SYRINGE • SHOULD BE COMPITABLE WITH CUANOACRYLATE. • SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C/ 50C.C

PICARD CATHETER • In various standard lengths and curves • 035-038 compatible 100 cm long

AMPLATZ CATHETER : • In various standard lengths and curves • 035-038 compatible 100 cm long

CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Exchange) • Should have hydrophilic coating • Should be available in various outer diameters and balloon lengths and various shaft lengths

CAROTID SELF EXPENDABLE STENTS • Should be 0.018” compatible • Should be over the wire and rapid exchange (OTW/RX) • Should be available in various diameters and length • Should be on a shaft length of 80-140 or above length

POLY VINYL ALCOHOL (PVA) PARTICLES FOR PRE-OPERATIVE TUMOUR EMBOLIZATION

ETHYL VINYL ALCOHOL EMBOLIC AGENT (WITH DMSO) FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION

DISTAL ACESS CATHETER FOR CO-AXIAL SYSTEMS • In various standerd length • Size 5fr 6fr 7fr • 0.035 to 0.070, 0.074 inner lumen

BALOON TOPPED GUIDING CATHETER • Size 6fr 7fr 8fr 9fr 10rf

SPECIAL MICRO GUIDWIRE WITH TORQUE DEVICE FOR USE WITH MICRO CATHETERS • Size 0.007” – 0.014”

SPECIAL MICRO GUIDWIRE (EXCHANGE LENGTH 260-300CM) WITH TORQUE DEVICE FOR USE WITH MICRO CATHETERS Size 0.010” – 0.014”

ELECTROLYTE DETACHABLE 3-D TYPE / HALICAL / 360 COILS FOR INTRACRANIAL ANEURYSM TREATMENT – BARE PLATINUM COILS

ELECTROLYTE DETACHABLE 3-D TYPE / HALICAL / 360 COILS FOR INTRACRANIAL ANEURYSM TREATMENT – COATED / BIO ACTIVE PLATINUM COILS

POWER SUPPLY ACESSIRIES AND CONNECTING CABLES FOR DETACHABLE COILS

OPEN CELL DESIGN INTRACRANIAL STENTS FOR STENT ASSISTED COILLING OF ANEURYSN • Should have open cell design • should be available in various size and diameter

FLOW DIVERTER FOR INTRACRANIAL ANEURISM TREATMENT

SINGLE LUMEN BALOON ANGIOPLASTY CATHETER FOR INTRECRANIAL USE

HYBRID CELL DESIGN INTRACRANIAL STENTS FOR STEN ASSISTED COILLENG OF ANEURUSM • Should have open cell design • should be available in various size and diameter

REVASCULIZATION DEVICE FOR MECHENICAL THROMBECTOMY

THROMBUS SUCTION CATHETERS FOR CLOT RETRIVALS FROM CAROTID AND VERTIBTALS

INFUSION CATHETER FOR MOTERISED FRAGMENTATION AND SUCTION FOR CLOT RETRIVAL WITH SEPERATER

STENT RETRIVAL FOR THROMBECTOMY

WEB DEVICE INTRASPECULAR – AVAILABLE ASSORTED SIZE

PRESSURE SALINE BAG 1000ML

PRESSURE INFUSION REUSABLE BAG 1000ML