Supply of Cardiology consumable and implants at RIMS, Ranchi

LIST OF OF CARDIAC & OTHER INSTRUMENTS / ACCESSORIES / CONSUMABLES ON RATE CONTRACT BASIS FOR AYUSHMANN BHARAT PMJAY SCHEME

A. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be USFDA approved.

B. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be CE approved .

C. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be DCGI approved.

3. PTCA GUIDEWIRE HYDROPHILIC

A. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". USFDA approved

B. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". CE approved

C. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". DCGI approved

4. PTCA GUIDEWIRE EXTRA SUPPORT

A. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". USFDA approved

B. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". CE approved

C. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". DCGI approved

5. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD < 1 GRAM

A. USFDA APPROVED

B. CE APPROVED

C. DCGI APPROVED

6. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD 1-3 GRAM

A. USFDA APPROVED

B. CE APPROVED

C. DCGI APPROVED

7. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD >3 GRAM

A. USFDA APPROVED

B. CE APPROVED

C. DCGI APPROVED

8. DRUG ELUTING STENTS OF VARIOUS DIAMETERS (all available diameter sizes) AND VARIOUS LENGTHS (all available lengths as per manufacturers) WITH THE FOLLOWING SPECIFICATIONS

A. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.

B. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.

C. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.

D. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.

E. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.

F. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.

G. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.

H. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.

I. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.

J. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.

K. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.

L. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.

M. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.

N. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.

O. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.

P. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.

Q. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.

R. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.

S. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.

T. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.

U. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.

V. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.

W. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.

X. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.

9. 035 PTFE CORONARY CATHETER GUIDEWIRE J TIP 145 TO 170 CM

10. PRESSURE MONITORING LINE 200 CM MALE TO FEMALE

11. HIGH PRESSURE LINE MALE TO FEMALE 120 CM WITH BRAIDED TUBING WITH MAXIMUM PRESSURE DELIVERY OF 1200 Psi

12. PTCA KIT WITH Y CONNECTOR, TUOHY BORST VALVE AND 25 CM EXTENSION CONTAINING TORQUER FOR PTCA WIRE AND PTCA WIRE INSETION TOOL

13. INDEFLATOR FOR CORONARY ANGIOPLASY WITH MAXIMUM PRESSURE CAPACITY OF 30 ATM.

14. CORONARY PRE DILATATION BALLOON CATHETER FOR CORONARY ANGIOPLASTY WITH FOLLOWING SPECIFICATIONS. 014 PTCA WIRE COMPATIBLE. MONORAIL DESIGN.

A. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):-1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. USFDA approved

B. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. CE approved

C. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5. Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. DCGI approved

15. CORONARY POST DILATATION BALLOON CATHETER FOR CORONARY ANGIOPLASTY WITH FOLLOWING SPECIFICATIONS. 014 PTCA WIRE COMPATIBLE. MONORAIL DESIGN.

A. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. USFDA approved

B. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. CE approved

C. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. DCGI approved

16. Paclitaxel coated drug eluting coronary balloon of carious size diameters and lengths.

A. USFDA approved

B. CE approved

C. DCGI approved

17. Cutting Balloons for coronary angioplasty of various diameter sizes and lengths.

A. USFDA approved

B. CE approved

C. DCGI approved

18. PRESSURE MONITORING LINE 200 CM MALE TO FEMALE

19. VASCULAR SHEATH FOR RADIAL ARTERY CANNULATION – 5 Fr, 6 Fr

a. USFDA approved

B. CE approved

C. DCGI approved

20. VASCULAR SHEATH FOR FEMORAL ARTERY CANNULATION – 6 Fr, 7 Fr, 8 Fr

a. USFDA approved

B. CE approved

C. DCGI approved

21. TEMPORARY PACING WIRE 6FR

a. USFDA approved

B. CE approved

C. DCGI approved

A.VVI PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22.A .VVIR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22C .DDD PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22D.DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22E VVIR PERMANENT IMPLANTABLE PACEMAKER MRI COMPATIABLE • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22F DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

22G ICD SINGLE CHAMBER • US FDA approved ICD , small and physiological Algorithm to eliminate over-sensing of R wave, T wave, fractionated QRS and other extraneous signals morphology bases,SVT discrimination algoritm ATP during charging wireless telemetry encourage intrinsic conduction more than 30 minutes of stored EGM, a) Device with all leads b) device without leads Permanent defibrillation lead, bipolar endocardial steroid eluting active and passive fixation lead Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. Company must provide its trained technical person for each implantation and for follow up programming whenever required. Company must quote only the latest model of devices commercially available.

22H ICD SINGLE CHAMBER MRI COMPATIABLE- Specifications as ICD single chamber with addition of MRI compatibility

23.DOUBLE LUMEN BALLOON DILATATION CATHETER OF VARIOUS SIZES FOR PERCUTANEOUS TRANSMITRAL MITRAL COMMISUROTOMY WITH ALL ACCESSORIES (ROUND WIRE, SEPTAL DILATOR, J-WIRE FOR PTMC BALLOON, FEMORAL SVENOUS SHEATH)

24.8 FR MULLINS SHEATH FOR TRANS-SEPTAL ACCESS

25.32 FE J TIPPED WIRE

26.TRANSEPTAL PUNCTURE NEEDLE 70 CM LONG, CURVED TIP, 18 GAUGE WITH A DISTAL TAPER TO 21 GAUGE, PREFERABLY BROCKENBROUGH NEEDLE.

27.PIGTAIL CARDIAC CATHETERISATION CATHETER 6 FR

28. LBBB AREA DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should be 7F or less. • The Lead must be configured for implantation at RA and LBB area. • Pre-configured sheath for placement of LBB area lead to be provided • Must have both active and passive fixation endocardial leads available. • Must have rate response which allows rate profile optimization. • Company should provide technical assistance for implantation and programming. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.

29. Artificial aortic valve for trans catheter placement (i) TRANSCATHETER HEART VALVE - 01 UNIT IT SHOULD BE MADE OF BOVINE/PORCINE PERICARDIUM TRI LEAFLET VALVE, MADE OF MEDICAL GRADE ALLOY WITH HYBRID CELL DESIGN .IT SHOULD HAVE INTERNAL/EXTERANL PET SKIRTING OR BOTH. THE SIZE OF THE VALVE SHOULD RANGE FROM 20 MM TO 32 MM OR MORE. (ii) VALVE DELIVERY SYSTEM - 01 UNIT THE VALVE SHOULD BE CRIMPED OR LOADED OVER THE DELIVERY SYSTEM PRIOR TO INSERTION INTO THE PATIENTS VASCULATURE. SHOULD BE 0.035 WIRE COMPATIBLE (iii) BALLOON DILATATION CATHETER - 01 UNIT BALLOON SIZE RANGES FROM 16 MM TO 25 MM WITH 30 MM LENGTH. THE BALLOON RBP SHOULD BE MINIMUM 6 atm. (iv) INTRODUCER SHEATH 01 UNIT SHOULD BE MINIMUM 14 FR AND LENGTH OF MINIMUM 30 CM, COMPATIBLE WITH ALL VALVE SIZES. SHOULD HAVE HAEMOSTATIC VALVE AND SIDE PORT WITH THREE WAY. SHOULD BE COMPATIBLE FOR FEMORAL ARTERY SIZE RANGING FROM 5 MM TO 7 MM. (v) INFLATION DEVICE - 02 UNITS (30ML/40ML/60ML) (vi) SYRINGES 50 CC - 02 UNITS THE FIRM SHOULD BE ABLE TO SUPPLY ANY SIZE OF VALVE, DELIVERY SYSTEM AND BALLOON SUITABLE FOR THE PATIENT.

30. Electrophysiology Catheter 6F and 4 Mm Crd 2 or 5Mm Electrode Spacing with Compatible Connector

31. 7 French Quadripolar Radio Frequency Ablation Catheter with a 4 Mm Tip and Bidirectional Deflection. should be Available in Small, Medium and Large Curves. should be Compatible with the available.

32. 7 French Quadripolar Radio Frequency Ablation Catheter with a 4 Mm Tip and unidirectional Deflection. should be Available in Small, Medium and Large Curves. should be Compatible with the available

33. 5 French fixed curve quadripolar catheter with 2-5-2 interelectrode spacing. One matching connector for every 5 catheters. Should be FDA'/CE'/DCGI approved

34. 6 French deflectable quadripolar catheter with 2-5-2 interelectrode spacing and matching connector. Should be FDA'/CE'/DCGI approved

35. 6 French deflectable decapolar catheter with 2-5-2 interelectrode spacing and matching connector. Should be FDA'/CE'/DCGI approved .

36. 6 or 7 French deflectable duodecapolar catheters (Halo) with matching connectors. Should be FDA'/CE'/DCGI approved

37. Long deflectable sheath with hemostatic valve, side port, atraumatic tip, braided shaft, uni- or bidirectional steerability, availability in small, medium or large curves, minimum inner diameter or 7F, minimum length of 65 cms. Should be FDA'/CE'/DCGI approved

38. 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, unidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA'/CE'/DCGI approved

39. 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, bidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and suitable connecting cables should be provided . Should be FDA'/CE'/DCGI approved

40. 7 French quadripolar Radiofrequency ablation catheter with a 8 mm tip, unidirectional deflection, availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA'/CE'/DCGI approved

41. 7 French quadripolar Radiofrequency ablation catheter with irrigated tip, uni- or bi-directional deflection and availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA'/CE'/DCGI approved

42. Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and unidirectional deflection for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system. Should be FDA'/CE'/DCGI approved

45. EMBOLIZATION COILS 035" all sizes. Should be FDA'/CE'/DCGI approved

46. EMBOLIZATION MICRO COILS 018 all sizes - Non Detachable and freely deliverable. Should be FDA'/CE'/DCGI approved

47. EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 2D. Should be FDA'/CE'/DCGI approved

48. EMBOLISATION PARTICLES Poly Vinyl Alcohol all sizes. Should be FDA'/CE'/DCGI approved

49. Gelfoam (Powder or granule form) for Embolization. Should be FDA'/CE'/DCGI approved

50. MICROCATHETERS with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery. Should be FDA'/CE'/DCGI approved

51. MICROCATHETERS - STEERABLE/ SHAPABLE with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery. Should be FDA'/CE'/DCGI approved

52. Soft Guideliner for mother and child technique. Should be FDA' or CE' and DCGI approved

53. Rotablator Wire 009. Should be FDA'/CE'/DCGI approved

54. Rotablator Advancer. Should be FDA'/CE'/DCGI approved

55. Rotablator Burr. Should be FDA'/CE'/DCGI approved

56. ASD AMPLATZER TYPE SELF CENTRE DEVICES WITH ALL sizes from 8mm and above . Should be FDA approved

57. COOK SHEATHS (all sizes 6F-15F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY. Should be FDA' or CE' and DCGI approved

58. PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE . Should be FDA'/CE'/DCGI approved

59. PDA DELIVERY SYSTEMS AND INTRODUCER CABLE SYSTEMS . Should be FDA'/CE'/DCGI approved

60. Ventricular septal Closure Devices All sizes ( 4mm to18 mm). Should be FDA'/CE'/DCGI approved

61. Delivery cable and sheath set for Ventricular septal defect closure. Should be FDA' or CE' and DCGI approved

Nano Therapeutics Pvt. Ltd

S3V Vascular Technologies Limited

Advanced MedTech Solutions Pvt. Ltd.

SAHAJANAND LASER TECHNOLOGY LIMITED

BOSTON SCIENTIFIC INDIA PVT LTD

B V ENTERPRISE

Ansh Therapeutics Pvt. Ltd

BHAWANI INDUSTRIES

India Medtronic Pvt. Ltd.

EVOLUTION HEALTH SCIENCE

Meril Life Science India Pvt Ltd

AKSHIT AGENCIES

St Jude Medical India Pvt Ltd

EVOLUTION HEALTH SCIENCE

Nano Therapeutics Pvt. Ltd

Ansh Therapeutics Pvt. Ltd

India Medtronic Pvt. Ltd.

B V ENTERPRISE

BOSTON SCIENTIFIC INDIA PVT LTD

AKSHIT AGENCIES

Meril Life Science India Pvt Ltd

BHAWANI INDUSTRIES