Supply Of Consumable Items For Cardiology And Neurointervention Cathlab At Associated Hospitals Of Medical College Kota

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Supply Of Consumable Items For Cardiology And Neurointervention Cathlab At Associated Hospitals Of Medical College Kota-1 Group –A: DIAGNOSTIC AND ACCESSORIES nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. 2 LONG INTRODUCER SHEATH: DCGI APPROVED n• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be Available in length from 65- 90 cm long n• 0.021 to 0.038-inch guide wire compatible n• Kink resistant 3 LONG INTRODUCER SHEATH: US FDA APPROVED n• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be Available in length from 65- 90 cm long n• 0.021 to 0.038-inch guide wire compatible n• Kink resistant 4 LONG INTRODUCER SHEATH: CE APPROVED n• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be Available in length from 65- 90 cm long n• 0.021 to 0.038-inch guide wire compatible n• Kink resistant 5 INTRODUCER SHEATH FOR ADULT: DCGI APPROVED n• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatible n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 6 INTRODUCER SHEATH FOR ADULT : US FDA APPROVED n• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatible n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 7 INTRODUCER SHEATH FOR ADULT : CE APPROVED n• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatible n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 8 LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : DCGI APPROVED nShould be available in 6fr,7fr,8fr 9 LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : US FDA APPROVED nShould be available in 6fr,7fr,8fr 10 LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : CE APPROVED nShould be available in 6fr,7fr,8fr 11 LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : DCGI APPROVED nShould be available in 6fr,7fr,8fr 12 LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : US FDA APPROVED nShould be available in 6fr,7fr,8fr 13 LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : CE APPROVED nShould be available in 6fr,7fr,8fr 14 PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : DCGI APPROVED 15 PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : US FDA APPROVED 16 PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : CE APPROVED 17 MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : DCGI APPROVED 18 MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : US FDA APPROVED 19 MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : CE APPROVED 20 HEAD HUNTER CATHETER : DCGI APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 21 HEAD HUNTER CATHETER : US FDA APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 22 HEAD HUNTER CATHETER : CE APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 23 SIMMONS/ SIDEWINDER CATHETER : DCGI APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 24 SIMMONS/ SIDEWINDER CATHETER : US FDA APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 25 SIMMONS/ SIDEWINDER CATHETER : CE APPROVED n• In various standard lengths and curves n• 035-038 compatible n• 100 cm long 26 VERTEBRAL CATHETER -In various standard lengths and curves : DCGI APPROVED 27 VERTEBRAL CATHETER -In various standard lengths and curves : US FDA APPROVED 28 VERTEBRAL CATHETER -In various standard lengths and curves : CE APPROVED 29 DISTAL ACCESS Catheter for CO- Axial Systems : DCGI APPROVED n• In various standard lengths n• 5f, 6f,7fr size n• 0.035” to .070”, .074 inner lumen. 30 DISTAL ACCESS Catheter for CO- Axial Systems : US FDA APPROVED n• In various standard lengths n• 5f, 6f,7fr size n• 0.035” to .070”, .074 inner lumen. 31 DISTAL ACCESS Catheter for CO- Axial Systems : CE APPROVED n• In various standard lengths n• 5f, 6f,7fr size n• 0.035” to .070”, .074 inner lumen. 32 SHEPHERD’S HOOK CATHETER : DCGI APPROVED nIn various standard lengths and curves 33 SHEPHERD’S HOOK CATHETER : US FDA APPROVED nIn various standard lengths and curves 34 SHEPHERD’S HOOK CATHETER : CE APPROVED nIn various standard lengths and curves 35 CEREBRAL ANGIOGRAPHY CATHETER : DCGI APPROVED n• In various standard lengths and curves n• 4FR, 5f, 6f size 36 CEREBRAL ANGIOGRAPHY CATHETER : US FDA APPROVED n• In various standard lengths and curves n• 4FR, 5f, 6f size 37 CEREBRAL ANGIOGRAPHY CATHETER : CE APPROVED n• In various standard lengths and curves n• 4FR, 5f, 6f size 38 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : DCGI APPROVED n• In various standard lengths and curves n• 4F, 5f, 6f size 39 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : US FDA APPROVED n• In various standard lengths and curves n• 4F, 5f, 6f size 40 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : CE APPROVED n• In various standard lengths and curves n• 4F, 5f, 6f size 41 PIGTAIL CATHETER : DCGI APPROVED n4 French/5 French /6 French/7 French/8French in various standard lengths. 42 PIGTAIL CATHETER : US FDA APPROVED n4 French/5 French /6 French/7 French/8French in various standard lengths. 43 PIGTAIL CATHETER : CE APPROVED n4 French/5 French /6 French/7 French/8French in various standard lengths. 44 COURNARD CATHETER : DCGI APPROVED n4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 45 COURNARD CATHETER : US FDA APPROVED n4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 46 COURNARD CATHETER : CE APPROVED n4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 47 COBRA TYPE CATHETER – DCGI APPROVED n• In various standard lengths and curves. n• 4Fr, 5fr, 6fr size 48 COBRA TYPE CATHETER – US FDA APPROVED n• In various standard lengths and curves. n• 4Fr, 5fr, 6fr size 49 COBRA TYPE CATHETER – CE APPROVED n• In various standard lengths and curves. n• 4Fr, 5fr, 6fr size 50 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – DCGI APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 120-150 cm long 51 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – US FDA APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 120-150 cm long 52 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – CE APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip nShould be between 120-150 cm long 53 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : DCGI APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 54 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : US FDA APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 55 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : CE APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have superelastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 56 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : DCGI APPROVEDZ n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 57 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : US FDA APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 58 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : CE APPROVED n• Must be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 180-260 cm long 59 BALLOON TIPPED GUIDING CATHETER : DCGI APPROVED nSIZES 6Fr,7 fr,8 fr,9fr,10 fr 60 BALLOON TIPPED GUIDING CATHETER : US FDA APPROVED nSIZES 6Fr,7 fr,8 fr,9fr,10 fr 61 BALLOON TIPPED GUIDING CATHETER : CE APPROVED nSIZES 6Fr,7 fr,8 fr,9fr,10 fr 62 INFLATION DEVICE WITH ANALOG DISPLAY : DCGI APPROVED 63 INFLATION DEVICE WITH ANALOG DISPLAY : US FDA APPROVED 64 INFLATION DEVICE WITH ANALOG DISPLAY : CE APPROVED 65 TUOHY BORST HAEMOSTATIC Y-CONNECTOR : DCGI APPROVED 66 TUOHY BORST HAEMOSTATIC Y-CONNECTOR : US FDA APPROVED 67 TUOHY BORST HAEMOSTATIC Y-CONNECTOR : CE APPROVED 68 TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : DCGI APPROVED 69 TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : US FDA APPROVED 70 TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : CE APPROVED 71 DISPOSABLE LUER LOCK SYRINGE : DCGI APPROVED n• SHOULD BE COMPITABLE WITH CUANOACRYLATE. n• SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C 72 DISPOSABLE LUER LOCK SYRINGE : US FDA APPROVED n• SHOULD BE COMPITABLE WITH CUANOACRYLATE. n• SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C 73 DISPOSABLE LUER LOCK SYRINGE : CE APPROVED n• SHOULD BE COMPITABLE WITH CUANOACRYLATE. n• SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C 74 Group –B: CAROTID ANGIOPLASTY nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. n 75 Guiding catheter for Neuro Vascular Use : DCGI APPROVED n• Should have atraumatic soft tip& flexible shaft n• Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature n• Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available n• Should have Inner Diameter of 4.2fr n• Should have various lengths from 90-110 cm 76 Guiding catheter for Neuro Vascular Use : US FDA APPROVED n• Should have atraumatic soft tip& flexible shaft n• Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature n• Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available n• Should have Inner Diameter of 4.2fr n• Should have various lengths from 90-110 cm 77 Guiding catheter for Neuro Vascular Use : CE APPROVED n• Should have atraumatic soft tip& flexible shaft n• Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature n• Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available n• Should have Inner Diameter of 4.2fr n• Should have various lengths from 90-110 cm 78 PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : DCGI APPROVED 79 PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : US FDA APPROVED 80 PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : CE APPROVED 81 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : DCGI APPROVED 82 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : US FDA APPROVED 83 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : CE APPROVED 84 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : DCGI APPROVED n• Should be on a .014” wire n• Should be made of polyurethane with radio-opaque nitinol loop n• Should be suspended on the .014” wire with a suspension arm n• Should not occlude flow while in placement n• Should be rapid exchange type n• Should be compatible with a 6 F guiding catheter (0.066” ID) n• Should allow optimal filtration in vessels 3.5 – 5.5 mm size 85 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : US FDA APPROVED n• Should be on a .014” wire n• Should be made of polyurethane with radio-opaque nitinol loop n• Should be suspended on the .014” wire with a suspension arm n• Should not occlude flow while in placement n• Should be rapid exchange type n• Should be compatible with a 6 F guiding catheter (0.066” ID) n• Should allow optimal filtration in vessels 3.5 – 5.5 mm size 86 DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : CE APPROVED n• Should be on a .014” wire n• Should be made of polyurethane with radio-opaque nitinol loop n• Should be suspended on the .014” wire with a suspension arm n• Should not occlude flow while in placement n• Should be rapid exchange type n• Should be compatible with a 6 F guiding catheter (0.066” ID) n• Should allow optimal filtration in vessels 3.5 – 5.5 mm size 87 CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : DCGI APPROVED n• Should have hydrophilic coating n• Should be available in various outer diameters and balloon lengths and various shaft lengths 88 CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : US FDA APPROVED n• Should have hydrophilic coating n• Should be available in various outer diameters and balloon lengths and various shaft lengths 89 CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : CE APPROVED n• Should have hydrophilic coating n• Should be available in various outer diameters and balloon lengths and various shaft lengths 90 CAROTID SELF EXPENDABLE STENTS: DCGI APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length nShould be on a shaft length of 80-140 or above length 91 CAROTID SELF EXPENDABLE STENTS: US FDA APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 92 CAROTID SELF EXPENDABLE STENTS: CE APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length nShould be on a shaft length of 80-140 or above length 93 CAROTID SELF EXPENDABLE STENTS: DCGI APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 94 CAROTID SELF EXPENDABLE STENTS: US FDA APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 95 CAROTID SELF EXPENDABLE STENTS: CE APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 96 CAROTID SELF EXPENDABLE STENTS – DCGI APPROVED n• Should be 0.035” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 97 CAROTID SELF EXPENDABLE STENTS – US FDA APPROVED n• Should be 0.035” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 98 CAROTID SELF EXPENDABLE STENTS – CE APPROVED n• Should be 0.035” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 99 CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 100 CAROTID STENTS BALLOON EXPENDABLE – US FDA APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 101 CAROTID STENTS BALLOON EXPENDABLE – CE APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 102 CAROTID STENTS BALLOON EXPENDABLE: DCGI APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 103 CAROTID STENTS BALLOON EXPENDABLE: US FDA APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 104 CAROTID STENTS BALLOON EXPENDABLE: CE APPROVED n• Should be 0.018” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 105 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: DCGI APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 106 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: US FDA APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 107 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: CE APPROVED n• Should be 0.014” compatible n• Should be over the wire and rapid exchange (OTW/RX) n• Should be available in various diameters and length n• Should be on a shaft length of 80-140 or above length 108 PERIPHERAL Balloon Expandable STENT – (OTW/RX): DCGI APPROVED n• Should be 0.014/0.018” compatible n• Should over the wire n• Should be made of cobalt chromium / Bare n• Should have balloon OD available in 4-7 mm n• Should have balloon/stent lengths of 12-18 mm n• Should have shaft lengths of 80-150 cm 109 PERIPHERAL Balloon Expandable STENT – (OTW/RX): US FDA APPROVED n• Should be 0.014/0.018” compatible n• Should over the wire n• Should be made of cobalt chromium / Bare• Should over the wire n• Should have balloon OD available in 4-7 mm n• Should have balloon/stent lengths of 12-18 mm n• Should have shaft lengths of 80-150 cm 110 PERIPHERAL Balloon Expandable STENT – (OTW/RX): CE APPROVED n• Should be 0.014/0.018” compatible n• Should over the wire n• Should be made of cobalt chromium / Bare n• Should have balloon OD available in 4-7 mm n• Should have balloon/stent lengths of 12-18 mm n• Should have shaft lengths of 80-150 cm 111 Group–C: ANEURYSMS COILS& ADHESIVES nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. 112 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : DCGI APPROVED 113 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : US FDA APPROVED 114 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : CE APPROVED 115 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : DCGI APPROVED 116 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : US FDA APPROVED 117 SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : CE APPROVED 118 SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : DCGI APPROVED 119 SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : US FDA APPROVED 120 SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : CE APPROVED 121 SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : DCGI APPROVED 122 SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : US FDA APPROVED 123 SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : CE APPROVED 124 ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : DCGI APPROVED 125 ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : US FDA APPROVED 126 ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : CE APPROVED 127 ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : DCGI APPROVED 128 ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : US FDA APPROVED 129 ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : CE APPROVED 130 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : DCGI APPROVED 131 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : US FDA APPROVED 132 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : CE APPROVED 133 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : DCGI APPROVED 134 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : US FDA APPROVED 135 THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : CE APPROVED 136 MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : DCGI APPROVED nSHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER 137 MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : US FDA APPROVED nSHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER 138 MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : CE APPROVED nSHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER 139 MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : DCGI APPROVED 140 MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : US FDA APPROVED 141 MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : CE APPROVED 142 PUSHABLE COILS TO BE USED WITH COIL PUSHERS : DCGI APPROVED 143 PUSHABLE COILS TO BE USED WITH COIL PUSHERS : US FDA APPROVED 144 PUSHABLE COILS TO BE USED WITH COIL PUSHERS : CE APPROVED 145 COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : DCGI APPROVED 146 COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : US FDA APPROVED 147 COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : CE APPROVED 148 SELECTIVE INFUSION MICROCATHETER FOR INTRACRANIAL ANEURYSM TREATMENT WITH 2 TIP MARKERS : DCGI APPROVED 149 SELECTIVE INFUSION MICROCATHETER FOR INTRACRANIAL ANEURYSM TREATMENT WITH 2 TIP MARKERS : US FDA APPROVED 150 SELECTIVE INFUSION MICROCATHETER FOR INTRACRANIAL ANEURYSM TREATMENT WITH 2 TIP MARKERS : CE APPROVED 151 SELECTIVE INFUSION MICROCATHETER FOR DEVPLOYING INTRACRANIAL DEVICE- DCGI APPROVED nSHOULD BE COMPITABLE FOR STENTS,FLOW DIVERTERS OR STENT RETRIEVERS OF VARIOUS SIZES. 152 SELECTIVE INFUSION MICROCATHETER FOR DEVPLOYING INTRACRANIAL DEVICE- US FDA APPROVED nSHOULD BE COMPITABLE FOR STENTS,FLOW DIVERTERS OR STENT RETRIEVERS OF VARIOUS SIZES. 153 SELECTIVE INFUSION MICROCATHETER FOR DEVPLOYING INTRACRANIAL DEVICE- CE APPROVED nSHOULD BE COMPITABLE FOR STENTS,FLOW DIVERTERS OR STENT RETRIEVERS OF VARIOUS SIZES. 154 POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : DCGI APPROVED 155 POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : US FDA APPROVED 156 POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : CE APPROVED 157 DETACHABLE BALLOON CATHETER : DCGI APPROVED 158 DETACHABLE BALLOON CATHETER : US FDA APPROVED 159 DETACHABLE BALLOON CATHETER : CE APPROVED 160 DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : DCGI APPROVED 161 DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : US FDA APPROVED 162 DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : CE APPROVED 163 TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : DCGI APPROVED 164 TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : US FDA APPROVED 165 TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : CE APPROVED 166 POLY VINYL ALCOHOL (PVA) PARTICLES FOR PRE-OPERATIVE TUMOUR EMBOLIZATION : DCGI APPROVED 167 POLY VINYL ALCOHOL (PVA) PARTICLES FOR PRE-OPERATIVE TUMOUR EMBOLIZATION : US FDA APPROVED 168 POLY VINYL ALCOHOL (PVA) PARTICLES FOR PRE-OPERATIVE TUMOUR EMBOLIZATION : CE APPROVED 169 ETHYL VINYL ALCOHOL EMBOLIC AGENT (WITH DMSO) FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION : DCGI APPROVED 170 ETHYL VINYL ALCOHOL EMBOLIC AGENT (WITH DMSO) FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION : US FDA APPROVED 171 ETHYL VINYL ALCOHOL EMBOLIC AGENT (WITH DMSO) FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION : CE APPROVED 172 LIPIDOL ULTRA FLUID : DCGI APPROVED 173 LIPIDOL ULTRA FLUID : US FDA APPROVED 174 LIPIDOL ULTRA FLUID : CE APPROVED 175 Group-D: STENTS& BALLOONS FOR CRANIAL USE nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. 176 DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : DCGI APPROVED 177 DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : US FDA APPROVED 178 DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : CE APPROVED 179 BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : DCGI APPROVED 180 BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : US FDA APPROVED 181 BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : CE APPROVED 182 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON) : DCGI APPROVED 183 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON) : US FDA APPROVED 184 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON): CE APPROVED 185 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : DCGI APPROVED 186 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : US FDA APPROVED 187 OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : CE APPROVED 188 OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED n• SHOULD HAVE OPEN CELL DESIGN n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 189 OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED n• SHOULD HAVE OPEN CELL DESIGN n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 190 OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED n• SHOULD HAVE OPEN CELL DESIGN n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 191 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED n• SHOULD BE COMPITABLE FOR LARGE VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 192 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED n• SHOULD BE COMPITABLE FOR LARGE VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 193 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED n• SHOULD BE COMPITABLE FOR LARGE VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 194 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED n• SHOULD BE COMPITABLE FOR SMALL VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 195 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED n• SHOULD BE COMPITABLE FOR SMALL VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 196 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED n• SHOULD BE COMPITABLE FOR SMALL VESSEL n• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 197 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : DCGI APPROVED 198 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : US FDA APPROVED 199 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : CE APPROVED 200 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : DCGI APPROVED 201 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : US FDA APPROVED 202 INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : CE APPROVED 203 INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : DCGI APPROVED 204 INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : US FDA APPROVED 205 INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : CE APPROVED 206 EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : DCGI APPROVED 207 EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : US FDA APPROVED 208 EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : CE APPROVED 209 EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : DCGI APPROVED 210 EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : US FDA APPROVED 211 EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : CE APPROVED 212 SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : DCGI APPROVED 213 SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : US FDA APPROVED 214 SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : CE APPROVED 215 BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : DCGI APPROVED 216 BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : US FDA APPROVED 217 BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : CE APPROVED 218 STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : DCGI APPROVED 219 STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : US FDA APPROVED 220 STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : CE APPROVED 221 FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : DCGI APPROVED 222 FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : US FDA APPROVED 223 FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : CE APPROVED 224 Group –E: CLOT RETRIEVAL DEVICES FOR THROMBACTOMY nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. 225 REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY: DCGI APPROVED 226 REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY : US FDA APPROVED 227 REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY : CE APPROVED 228 ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : DCGI APPROVED 229 ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : US FDA APPROVED 230 ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : CE APPROVED 231 THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : DCGI APPROVED 232 THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : US FDA APPROVED 233 THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : CE APPROVED 234 INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : DCGI APPROVED 235 INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : US FDA APPROVED 236 INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : CE APPROVED 237 STENT RETRIEVER FOR THROMBECTOMY : DCGI APPROVED 238 STENT RETRIEVER FOR THROMBECTOMY : US FDA APPROVED 239 STENT RETRIEVER FOR THROMBECTOMY : CE APPROVED 240 WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : DCGI APPROVED 241 WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : US FDA APPROVED 242 WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : CE APPROVED 243 Group – F: EMBOLIZATION/AVMs nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Lucknow, SMS Jaipur etc. 244 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH N-BUTYL CYANOACRYLATE) : DCGI APPROVED 245 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH N-BUTYL CYANOACRYLATE) : US FDA APPROVED 246 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH N-BUTYL CYANOACRYLATE) : CE APPROVED 247 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO) : DCGI APPROVED 248 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO): US FDA APPROVED 249 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO) : CE APPROVED 250 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO) WITH DETACHABLE TIPS : DCGI APPROVED 251 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO) WITH DETACHABLE TIPS : US FDA APPROVED 252 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH DMSO) WITH DETACHABLE TIPS : CE APPROVED 253 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH PARTICULATE EMBOLIC AGENTS SUCH AS PVA PARTICLEs) : DCGI APPROVED 254 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH PARTICULATE EMBOLIC AGENTS SUCH AS PVA PARTICLEs): US FDA APPROVED 255 SUPER SELECTIVE HIGH FLOW INFUSION CATHETERS – FOR CEREBRAL/SPINAL AVMS (COMPITABLE WITH PARTICULATE EMBOLIC AGENTS SUCH AS PVA PARTICLEs) : CE APPROVED 256 Group - G nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Luckhnow,SMS Jaipur etc. 257 INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length)-DCGI APPROVED n• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• 10-11 cm long for Femoral Access n• Pack must include 18 G or more, 6-7.5 cm long puncture needle n• 0.035 or 0.038 spring guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 258 INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - US FDA APPROVED n• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• 10-11 cm long for Femoral Access n• Pack must include 18 G or more, 6-7.5 cm long puncture needle n• 0.035 or 0.038 spring guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 259 INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - CE APPROVED n• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• 10-11 cm long for Femoral Access n• Pack must include 18 G or more, 6-7.5 cm long puncture needle n• 0.035 or 0.038 spring guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion nWith smooth and resistance free insertion 260 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - DCGI APPROVED n• 10-11 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 261 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - US FDA APPROVED n• 10-11 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 262 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - CE APPROVED n• 10-11 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 263 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) – DCGI APPROVED n• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• Sheath should be between 20-30 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 264 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - US FDA APPROVED n• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• Sheath should be between 20-30 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 265 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - CE APPROVED n• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. n• Sheath should be between 20-30 cm long n• 0.035 or 0.038 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 266 TRANS RADIAL INTRODUCER SHEETHS – DCGI APPROVED n• Sizes 4 French/5 French/ 6 French. n• 7.0 cm long for Radial & Brachial Access n• Pack must include 18/20 G, 6-7.5 cm long puncture needle n• 0.025-.038 inch guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 267 TRANS RADIAL INTRODUCER SHEETHS -US FDA APPROVED n• Sizes 4 French/5 French/ 6 French. n• 7.0 cm long for Radial & Brachial Access n• Pack must include 18/20 G, 6-7.5 cm long puncture needle n• 0.025-.038 inch guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 268 TRANS RADIAL INTRODUCER SHEETHS – CE APPROVED n• Sizes 4 French/5 French/ 6 French. n• 7.0 cm long for Radial & Brachial Access n• Pack must include 18/20 G, 6-7.5 cm long puncture needle n• 0.025-.038 inch guide wire compatible n• With cross cut design haemostatic valve prevent back leak and air aspiration n• snap on dialator lock with Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 269 LONG BRADED INTRODUCER SHEATH – DCGI APPROVED n• Sizes 6 French/7 French / 8 French 9 French and above n• Should be up to 90 cm n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 270 LONG BRADED INTRODUCER SHEATH – US FDA APPROVED n• Sizes 6 French/7 French / 8 French 9 French and above n• Should be up to 90 cm n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 271 LONG BRADED INTRODUCER SHEATH – CE APPROVED n• Sizes 6 French/7 French / 8 French 9 French and above n• Should be up to 90 cm n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 272 GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – DCGI APPROVED 273 GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – US FDA APPROVED 274 GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – CE APPROVED 275 STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - DCGI APPROVED n• Sizes from 4fr/5 fr/6Fr/ 7Fr n• Between 7-11 cm long n• With 0.025 - 0.038 inch guide wire compatible n• With Radio-opaque tip n• Should be for both Paediatric and Adult use 276 STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING –CE APPROVED n• Sizes from 4fr/5 fr/6Fr/ 7Fr n• Between 7-11 cm long n• With 0.025 - 0.038 inch guide wire compatible n• With Radio-opaque tip n• Should be for both Paediatric and Adult use 277 STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - US FDA APPROVED n• Sizes from 4fr/5 fr/6Fr/ 7Fr n• Between 7-11 cm long n• With 0.025 - 0.038 inch guide wire compatible n• With Radio-opaque tip n• Should be for both Paediatric and Adult use 278 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVED n• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Access n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 279 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DGCI APPROVED n• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Access n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 280 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS –US FDA APPROVED n• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Access n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• Integral side port with attached 3-way stopcock n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• With smooth and resistance free insertion 281 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - US FDA APPROVED n• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• Should have smooth and resistance free insertion 282 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVED n• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• Should have smooth and resistance free insertion 283 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DCGI APPROVED n• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspiration n• With integral side port with attached 3-way stopcock n• With suture eye for securing sheath n• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion n• Should have smooth and resistance free insertion 284 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - DCGI APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be between 145-180 cm long n• Should be available as straight & J-Shaped tip n• Should be available in variable lengths of flexible/floppy end n• Should be available in variable J tip sizes n• Should be available fixed as well as movable core. 285 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - US FDA APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be between 145-180 cm long n• Should be available as straight & J-Shaped tip n• Should be available in variable lengths of flexible/floppy end n• Should be available in variable J tip sizes n• Should be available fixed as well as movable core 286 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - CE APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be between 145-180 cm long n• Should be available as straight & J-Shaped tip n• Should be available in variable lengths of flexible/floppy end n• Should be available in variable J tip sizes n• Should be available fixed as well as movable core 287 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - DCGI APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be 240-300 cm long n• Should be available as straight or J-Shaped tip n• Should be available fixed as well as movable core. 288 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - US FDA APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be 240-300 cm long n• Should be available as straight or J-Shaped tip nShould be available fixed as well as movable core. 289 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - CE APPROVED n• Should be available in 0.025, 0.032, 0.035 and 0.038 inches size n• Should be 240-300 cm long n• Should be available as straight or J-Shaped tip nShould be available fixed as well as movable core. 290 HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) n– DCGI APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have Super elastic Nitinol alloy n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 120-150 cm long 291 HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) n– US FDA APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have Super elastic Nitinol alloy n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 120-150 cm long 292 HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) n– CE APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have Super elastic Nitinol alloy n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 120-150 cm long 293 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - DCGI APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 150-180 cm long 294 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - US FDA APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 150-180 cm long 295 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - CE APPROVED n• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• should be between 150-180 cm long 296 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - DCGI APPROVED n• Must be available in 0.018, 0.025, 0.032 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 260cm, 300 cm long 297 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - US FDA APPROVED n• Must be available in 0.018, 0.025, 0.032 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 260cm, 300 cm long 298 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - CE APPROVED n• Must be available in 0.018, 0.025, 0.032 and 0.038 inches size n• Should have super elastic alloy core n• Should have super flexible wire tip n• Should be available in straight and angled tip n• Should be between 260cm, 300 cm long 299 JUDKINS CATHETER (JR JL & PIGTAIL)-DCGI APPROVED n• 4 French/5 French /6 French/7 French/8French size n• Left and Right judkins catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 300 JUDKINS CATHETER (JR JL & PIGTAIL)- US FDA APPROVED n• 4 French/5 French /6 French/7 French/8French size n• Left and Right judkins catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 301 JUDKINS CATHETER (JR JL & PIGTAIL)-CE APPROVED n• 4 French/5 French /6 French/7 French/8French size n• Left and Right judkins catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 302 MULTIPURPOSE CATHETER - - DCGI APPROVED n• 4 French/5 French /6 French/7 Frenchsize n• Multipurpose catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 303 MULTIPURPOSE CATHETER - - US FDA APPROVED n• 4 French/5 French /6 French/7 Frenchsize n• Multipurpose catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 304 MULTIPURPOSE CATHETER - - CE APPROVED n• 4 French/5 French /6 French/7 Frenchsize n• Multipurpose catheters in various standard curves and lengths even for pediatric cases n• Must have Double mesh construction with Ultra-thin wall 305 TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – DCGI APPROVED n• 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths n• dedicated for angiography of right and left coronary arteries using either radial or brachial approach 306 TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – US FDA n• 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths n• dedicated for angiography of right and left coronary arteries using either radial or brachial approach 307 TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – CE APPROVED n• 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths n• dedicated for angiography of right and left coronary arteries using either radial or brachial approach 308 ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - DCGI APPROVED n• Should be soft and kink resistant n• Should give reliable pressure measurements n• Should be available in sizes of 100, 150 & 200 cm n• Should have male luer lock connection at one end and a female luer lock connection at the other end n• Should meet highest medical industrial standards for arterial pressure lines 309 ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - US FDA APPROVED n• Should be soft and kink resistant n• Should give reliable pressure measurements n• Should be available in sizes of 100, 150 & 200 cm n• Should have male luer lock connection at one end and a female luer lock connection at the other end n• Should meet highest medical industrial standards for arterial pressure lines 310 ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - CE APPROVED n• Should be soft and kink resistant n• Should give reliable pressure measurements n• Should be available in sizes of 100, 150 & 200 cm n• Should have male luer lock connection at one end and a female luer lock connection at the other end n• Should meet highest medical industrial standards for arterial pressure lines 311 ACT TUBES - DCGI APPROVED n• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota n• Should meet highest medical industrial standards n• Quality certification should be provided from authorized agencies. 312 ACT TUBES - US FDA APPROVED n• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota n• Should meet highest medical industrial standards nQuality certification should be provided from authorized agencies 313 ACT TUBES - CE APPROVED n• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota n• Should meet highest medical industrial standards nQuality certification should be provided from authorized agencies 314 MANIFOLD with 3 Port - DCGI APPROVED n• Three side port manifold n• One luer lock control syringe (10 or 15 ml) for contrast injection n• One three way stop-cock 315 MANIFOLD with 3 Port - US FDA APPROVED n• Three side port manifold n• One luer lock control syringe (10 or 15 ml) for contrast injection n• One three way stop-cock 316 MANIFOLD with 3 Port - CE APPROVED n• Three side port manifold n• One luer lock control syringe (10 or 15 ml) for contrast injection n• One three way stop-cock 317 HIGH – PRESURE INJECTOR LINES - DCGI APPROVED n• Should be available in various lengths n• Should have male and female luer locks n• Should be transparent and kink resistant n• Should be able to take high pressure of angiographic injections 318 HIGH – PRESURE INJECTOR LINES US FDA APPROVED n• Should be available in various lengths n• Should have male and female luer locks n• Should be transparent and kink resistant n• Should be able to take high pressure of angiographic injections 319 HIGH – PRESURE INJECTOR LINES - CE APPROVED n• Should be available in various lengths n• Should have male and female luer locks n• Should be transparent and kink resistant n• Should be able to take high pressure of angiographic injections 320 AMPLATZ CATHETER n• 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. n• Must be US FDA APPROVED 321 AMPLATZ CATHETER n• 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. n• Must be CE APPROVED 322 AMPLATZ CATHETER n• 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. n• Must be DCGI APPROVED 323 DISPOSABLE ECG ELECTODES FOR ADULTS – - DCGI APPROVED n• Wet gel electrodes n• Should be porous and breathable n• Should conform to or exceed the highest industrial standard for ECG electrodes, n• Quality certification from authorized agencies to be provided 324 DISPOSABLE ECG ELECTODES FOR ADULTS – US FDA APPROVED n• Wet gel electrodes n• Should be porous and breathable n• Should conform to or exceed the highest industrial standard for ECG electrodes, n• Quality certification from authorized agencies to be provided 325 DISPOSABLE ECG ELECTODES FOR ADULTS – - CE APPROVED n• Wet gel electrodes n• Should be porous and breathable n• Should conform to or exceed the highest industrial standard for ECG electrodes, n• Quality certification from authorized agencies to be provided 326 SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kota DCGI Approved n• Should be compatible with existing machines at GMC kota Cath Lab 327 SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaUS FDA APPROVED n• Should be compatible with existing machines at GMC kota Cath Lab 328 SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaCE APPROVED n• Should be compatible with existing machines at GMC kota Cath Lab 329 TRANS RADIAL ANGIOGRAPHY KIT – DCGI Approved n• Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. nKit Must include in one pack - n1. One Piece Trans-Radial Access sheath in 5fr/6fr/7fr, 7-10 Cm long (should have cross cut design haemostatic valve, 20G entry needle and 0.025 mini plastic guide wire in Sheath Pack) n2. One Piece RADIOFOCUS MINIPLASTiC GUIDEWIRE (Must have HYDROPHILIC Coating & Regular tip size 0.018, 0.025, 0.032 and 0.038 inches and in length 150CM) n3. One Piece TRANSRADIAL DIAGNOSTIC CORONARY CATHETER (Must have TIG curve dedicated for angiography of right and left coronary arteries using either radial or brachial approach) n4. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). n5. One Piece MANIFOLD with 3 Port (Three side port) n6. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection 330 TRANS RADIAL ANGIOGRAPHY KIT –US FDA Approved n• Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. nKit Must include in one pack - n7. One Piece Trans-Radial Access sheath in 5fr/6fr/7fr, 7-10 Cm long (should have cross cut design haemostatic valve, 20G entry needle and 0.025 mini plastic guide wire in Sheath Pack) n8. One Piece RADIOFOCUS MINIPLASTiC GUIDEWIRE (Must have HYDROPHILIC Coating & Regular tip size 0.018, 0.025, 0.032 and 0.038 inches and in length 150CM) n9. One Piece TRANSRADIAL DIAGNOSTIC CORONARY CATHETER (Must have TIG curve dedicated for angiography of right and left coronary arteries using either radial or brachial approach) n10. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). n11. One Piece MANIFOLD with 3 Port (Three side port) n12. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection 331 TRANS RADIAL ANGIOGRAPHY KIT – CE Approved n• Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. nKit Must include in one pack - n13. One Piece Trans-Radial Access sheath in 5fr/6fr/7fr, 7-10 Cm long (should have cross cut design haemostatic valve, 20G entry needle and 0.025 mini plastic guide wire in Sheath Pack) n14. One Piece RADIOFOCUS MINIPLASTiC GUIDEWIRE (Must have HYDROPHILIC Coating & Regular tip size 0.018, 0.025, 0.032 and 0.038 inches and in length 150CM) n15. One Piece TRANSRADIAL DIAGNOSTIC CORONARY CATHETER (Must have TIG curve dedicated for angiography of right and left coronary arteries using either radial or brachial approach) n16. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). n17. One Piece MANIFOLD with 3 Port (Three side port) n18. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection 332 PIGTAIL CATHETER (PEDIATRIC/Adult ) –DCGI Approved APPROVED n• Sizes 3 French/ 4 French/ 5 French/ 6 French n• Smaller length for neonatal and pediatric use 333 PIGTAIL CATHETER (PEDIATRIC/Adult ) –US FDA APPROVED n• Sizes 3 French/ 4 French/ 5 French/ 6 French n• Smaller length for neonatal and pediatric use 334 PIGTAIL CATHETER (PEDIATRIC/Adult ) –CE APPROVED n• Sizes 3 French/ 4 French/ 5 French/ 6 French n• Smaller length for neonatal and pediatric use 335 PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- DCGI Approved. n• Should be available in 0.032/0.035/0.038 inches size n• Should be between 240-300 cm long n• Should be available as straight & J-Shaped tip 336 PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- US FDA APPROVED. n• Should be available in 0.032/0.035/0.038 inches size n• Should be between 240-300 cm long n• Should be available as straight & J-Shaped tip 337 PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- CE APPROVED. n• Should be available in 0.032/0.035/0.038 inches size n• Should be between 240-300 cm long n• Should be available as straight & J-Shaped tip 338 INTERNAL MAMMARY CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be US FDA APPROVED 339 INTERNAL MAMMARY CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be CE APPROVED 340 INTERNAL MAMMARY CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be DCGI APPROVED 341 BY-PASS GRAFT CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be US FDA APPROVED 342 BY-PASS GRAFT CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be CE APPROVED 343 BY-PASS GRAFT CATHETER n• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. n• Must be DCGI APPROVED 344 Group-H nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Luckhnow,SMS Jaipur etc. 345 PTCA Guiding catheter– DCGI APPROVED . n• Should be braided with low friction Inner Layer of PTFE n• Should have atraumatic soft tip n• Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. n• Should have diameter 5 French/ 6 French/7 French/ 8French available n• Should have All various lengths 346 PTCA Guiding catheter–US FDA APPROVED n• Should be braided with low friction Inner Layer of PTFE n• Should have atraumatic soft tip n • Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. n• Should have diameter 5 French/ 6 French/7 French/ 8French available n• Should have All various lengths 347 PTCA Guiding catheter–CE APPROVED n• Should be braided with low friction Inner Layer of PTFE n• Should have atraumatic soft tip n• Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. n• Should have diameter 5 French/ 6 French/7 French/ 8French available n• Should have All various lengths 348 Radial Guiding catheter Ikari curve - DCGI APPROVED n• Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. n• Should be braided with low friction inner layer n• Should have atraumatic soft tip. n• Should have all the lengths and in diameter 5 French/ 6 French available 349 Radial Guiding catheter Ikari curve - DCGI APPROVED & US FDA/CE APPROVED n• Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. n• Should be braided with low friction inner layer n• Should have atraumatic soft tip. n• Should have all the lengths and in diameter 5 French/ 6 French available 350 Radial Guiding catheter Ikari curve - US FDA APPROVEDZ n• Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. n• Should be braided with low friction inner layer n• Should have atraumatic soft tip. n• Should have all the lengths and in diameter 5 French/ 6 French available 351 Mother & Child Catheter – - CE APPROVED n• With reliable support with large inner lumen and inner PTSE. 352 Mother & Child Catheter – - US FDA APPROVED n• With reliable support with large inner lumen and inner PTSE. 353 Mother & Child Catheter – - DCGI APPROVED n• With reliable support with large inner lumen and inner PTSE. 354 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - DCGI APPROVED n• 120 proximal hypotube shaft n0.57 Inner diameter & 0.066” outer diameter nShould be with proximal marker and 1 x 1 braiding 355 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - US FDA APPROVED n• 120 proximal hypotube shaft n0.57 Inner diameter & 0.066” outer diameter nShould be with proximal marker and 1 x 1 braiding 356 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - CE APPROVED n• 120 proximal hypotube shaft n0.57 Inner diameter & 0.066” outer diameter nShould be with proximal marker and 1 x 1 braiding 357 PTCA INFLATION DEVICE - DCGI APPROVED n• Efficient locking system to maintain high pressure n• Rapid inflation and deflation n• Clear barrel for easy visualization of de-bubbling n• Luminescent analog pressure gauge (up to 30 Atm) n• Ergomatric and use friendly hand held design. 358 PTCA INFLATION DEVICE - US FDA APPROVED n• Efficient locking system to maintain high pressure n• Rapid inflation and deflation n• Clear barrel for easy visualization of de-bubbling n• Luminescent analog pressure gauge (up to 30 Atm) n• Ergomatric and use friendly hand held design. 359 PTCA INFLATION DEVICE - CE APPROVED n• Efficient locking system to maintain high pressure n• Rapid inflation and deflation n• Clear barrel for easy visualization of de-bubbling n• Luminescent analog pressure gauge (up to 30 Atm) n• Ergomatric and use friendly hand held design. 360 TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –DCGI APPROVED n• Should accommodate virtually all interventional devices n• Luer connector at the guiding catheter end n• Rotating adapter at the guiding catheter end n• Should have bleed back safety mechanism n• Stepwise control for open, semi-open and closed position 361 TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –US FDA APPROVED n• Should accommodate virtually all interventional devices n• Luer connector at the guiding catheter end n• Rotating adapter at the guiding catheter end n• Should have bleed back safety mechanism n• Stepwise control for open, semi-open and closed position 362 TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –CE APPROVED n• Should accommodate virtually all interventional devices n• Luer connector at the guiding catheter end n• Rotating adapter at the guiding catheter end n• Should have bleed back safety mechanism n• Stepwise control for open, semi-open and closed position 363 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –DCGI APPROVED n• Should accommodate virtually all interventional devices n• Two ports for insertion of interventional devices n• Luer connector at the guiding catheter end 364 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –US FDA APPROVED n• Should accommodate virtually all interventional devices n• Two ports for insertion of interventional devices n• Luer connector at the guiding catheter end 365 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –CE APPROVED n• Should accommodate virtually all interventional devices n• Two ports for insertion of interventional devices n• Luer connector at the guiding catheter end 366 DRUG DELIVERY/INFUSION CATHETER - DCGI APPROVED 367 DRUG DELIVERY/INFUSION CATHETER - US FDA APPROVED 368 DRUG DELIVERY/INFUSION CATHETER - CE APPROVED 369 PTCA GUIDING CATHETER - DCGI APPROVED n• Should be available in Sizes of 5 French/6 fr/7fr/8fr n• Should be braided with low friction Inner Layer of PTFE n• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others n• Should also have availability of smaller length catheters (90 cm) & Regular length sizes. n• Should also have availability of catheters with side holes n• Should also have short tip catheters 370 PTCA GUIDING CATHETER - US FDA APPROVED n• Should be available in Sizes of 5 French/6 fr/7fr/8fr n• Should be braided with low friction Inner Layer of PTFE n• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others n• Should also have availability of smaller length catheters (90 cm) & Regular length sizes. n• Should also have availability of catheters with side holes n• Should also have short tip catheters 371 PTCA GUIDING CATHETER - CE APPROVED n• Should be available in Sizes of 5 French/6 fr/7fr/8fr n• Should be braided with low friction Inner Layer of PTFE n• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others n• Should also have availability of smaller length catheters (90 cm) & Regular length sizes. n• Should also have availability of catheters with side holes n• Should also have short tip catheters 372 PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. n- DCGI APPROVED 373 PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. n- US FDA APPROVED 374 PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. n- CE APPROVED 375 EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- DCGI APPROVED n• Should be Dedicated for externalization with tip load of 3g/force 376 EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- US FDA APPROVED n• Should be Dedicated for externalization with tip load of 3g/force 377 EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- CE APPROVED n• Should be Dedicated for externalization with tip load of 3g/force 378 Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating n -- DCGI APPROVED n• Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. n• Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures n• Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip. 379 Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating n -- US FDA APPROVED n• Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. n• Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures n• Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip. 380 Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating n -- CE APPROVED n• Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. n• Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures n• Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip. 381 Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED n• .014 One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve. 382 Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED n• .014 One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve. 383 Specialized PTCA Guide wire for Retrograde approach & CTO –CE APPROVED n• .014 One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve. 384 Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED n• PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g 385 Specialized PTCA Guide wire for Retrograde approach & CTO – US FDA APPROVED n• PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g 386 Specialized PTCA Guide wire for Retrograde approach & CTO –CE APPROVED n• PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g 387 Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO – DCGI APPROVED n• 0.010 One Piece core wire with joint less Spring coil with SION TECH technology n• cone tip with a tip load of 1.7gm and tip Radiopacity 15cm. 388 Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO – US FDA APPROVED n• 0.010 One Piece core wire with joint less Spring coil with SION TECH technology n• cone tip with a tip load of 1.7gm and tip Radiopacity 15cm. 389 Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO CE APPROVED n• 0.010 One Piece core wire with joint less Spring coil with SION TECH technology n• cone tip with a tip load of 1.7gm and tip Radiopacity 15cm. 390 • Special PTCA Guide Wire with Twister® core wire technology for facilitates navigation and torqueability for optimal precision- US FDA 391 • Special PTCA Guide Wire with Twister® core wire technology for facilitates navigation and torqueability for optimal precision-CE approved 392 • Spacial PTCA Guide Wire with Stainless Steel Spring Coil Design. US FDA /DCGI approved 393 • Spacial PTCA Guide Wire with Stainless Steel Spring Coil Design. CE/DCGI approved 394 HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – US FDA APPROVED. n• 0.014 inches n• Nitinol alloy n• With angled tip 3-5 cm long n• Tip with platinum/platinum alloy for optimum visualization n• With TFE coating n• 180 cm long 395 HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – CE APPROVED. n• 0.014 inches n• Nitinol alloy n• With angled tip 3-5 cm long n• Tip with platinum/platinum alloy for optimum visualization n• With TFE coating n• 180 cm long 396 HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – DCGI APPROVED. n• 0.014 inches n• Nitinol alloy n• With angled tip 3-5 cm long n• Tip with platinum/platinum alloy for optimum visualization n• With TFE coating n• 180 cm long 397 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED n• Disposable transducers for invasive pressure monitoring n• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota n• Should meet highest medical industrial standards n• Quality certification should be provided form authorized agencies 398 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - US FDA APPROVED n• Disposable transducers for invasive pressure monitoring n• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota n• Should meet highest medical industrial standards n• Quality certification should be provided form authorized agencies 399 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - CE APPROVED n• Disposable transducers for invasive pressure monitoring n• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota n• Should meet highest medical industrial standards n• Quality certification should be provided form authorized agencies 400 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED n• Should be compatible with existing available system n• Should meet or exceed highest standards n• Quality certification from authorized agencies to be provided 401 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - CE APPROVED n• Should be compatible with existing available system n• Should meet or exceed highest standards n• Quality certification from authorized agencies to be provided 402 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - US FDA APPROVED n• Should be compatible with existing available system n• Should meet or exceed highest standards n• Quality certification from authorized agencies to be provided 403 Group – I nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh, SGPGI-Luckhnow, SMS Jaipur etc. 404 PTCA BALLOON (SEMI-COMPLIANT) - DCGI APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Should have Hydrophilic coating and Fixed outer and inner tube. n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less n• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm n• Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above) 405 PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Should have Hydrophilic coating and Fixed outer and inner tube. n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less n• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm n• Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above) 406 PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Should have Hydrophilic coating and Fixed outer and inner tube. n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less n• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm n• Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above) 407 PTCA BALLOON (NON-COMPLIANT) – - DCGI APPROVED n• Quote both monorail (rapid exchange) and OTW balloons n• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm n• Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. n• Should have triple layer balloon technology for high pressure resistance 408 PTCA BALLOON (NON-COMPLIANT) – - US FDA APPROVED n• Quote both monorail (rapid exchange) and OTW balloons n• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm n• Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. n• Should have triple layer balloon technology for high pressure resistance 409 PTCA BALLOON (NON-COMPLIANT) – - CE APPROVED n• Quote both monorail (rapid exchange) and OTW balloons n• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm n• Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) n• With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. n• Should have triple layer balloon technology for high pressure resistance 410 SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - DCGI APPROVED n• Must have Ultra-low entry profile of 0.016” n• Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in all sizes& All variable lengths up to 20mm 411 SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - US FDA APPROVED n• Must have Ultra-low entry profile of 0.016” n• Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in all sizes& All variable lengths up to 20mm 412 SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - CE APPROVED n• Must have Ultra-low entry profile of 0.016” n• Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in all sizes& All variable lengths up to 20mm 413 SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - DCGI APPROVED n• Must have Ultra-low entry profile of 0.016” n• Should be available in variable balloon lengths minimum from 06mm - 20mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should have R.B.P -18atm or Above 414 SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - US FDA APPROVED n• Must have Ultra-low entry profile of 0.016” n• Should be available in variable balloon lengths minimum from 06mm - 20mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should have R.B.P -18atm or Above 415 SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - CE APPROVED n• Must have Ultra-low entry profile of 0.016” n• Should be available in variable balloon lengths minimum from 06mm - 20mm n• Quote both monorail (rapid exchange) and OTW balloons n• Should have R.B.P -18atm or Above 416 ZEROFOLD PTCA BALLOON - DCGI APPROVED APPROVED n• Available in all sizes and length n• Quote both monorail (rapid exchange) and OTW balloons 417 ZEROFOLD PTCA BALLOON - US FDA APPROVED n• Available in all sizes and length n• Quote both monorail (rapid exchange) and OTW balloons 418 ZEROFOLD PTCA BALLOON - CE APPROVED n• Available in all sizes and length n• Quote both monorail (rapid exchange) and OTW balloons 419 SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - DCGI APPROVED n• Must have Ultra-low entry profile of 0.016” n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. n• Should have high RBP -18 Atm or Above 420 SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - US FDA APPROVED n• Must have Ultra-low entry profile of 0.016” n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. n• Should have high RBP -18 Atm or Above 421 SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - CE APPROVED n• Must have Ultra-low entry profile of 0.016” n• Quote both monorail (rapid exchange) and OTW balloons n• Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. n• Should have high RBP -18 Atm or Above 422 CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) -DCGI APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 423 CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - US FDA APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 424 CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - CE APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 425 SCORING BALLOON CATHETER FOR PTCA - DCGI APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 426 SCORING BALLOON CATHETER FOR PTCA - US FDA APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 427 SCORING BALLOON CATHETER FOR PTCA - CE APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloons n• Available in the sizes and lengths 428 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) nWITH ENTRY PROFILE 1.4 FRENCH- DCGI APPROVED 429 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) nWITH ENTRY PROFILE 1.4 FRENCH- US FDA APPROVED 430 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) nWITH ENTRY PROFILE 1.4 FRENCH- CE APPROVED 431 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- DCGI APPROVED n• WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH n• Should be available from 130CM - 150 CM. 432 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- US FDA APPROVED n• WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH n• Should be available from 130CM - 150 CM. 433 MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- CE APPROVED n• WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH n• Should be available from 130CM - 150 CM. 434 IABP CATHETER WITH ACCESSORIES - DCGI APPROVED n• Should be compatible with existing machine at GMC Kota 435 IABP CATHETER WITH ACCESSORIES - US FDA APPROVED n• Should be compatible with existing machine at GMC Kota 436 IABP CATHETER WITH ACCESSORIES - CE APPROVED n• Should be compatible with existing machine at GMC Kota 437 THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - DCGI APPROVED 438 THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - US FDA APPROVED 439 THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - CE APPROVED 440 Special PTCA Balloon (Semi-Compliant) fat CTO Lesion. US FDAApproved. n• Must have low entry tip profile equal or less than 0.017 for crossing CTO or to difficult lesion. n• Must have lowest diameter starting from 1.0 mm . n• Must have lowest length starting from 5.0 mm . n• Monorail (rapid exchange) and the over-the-wire balloon. 441 Special PICA Balloon (Semi-compliant) for CTO Lesion. CE Approved. n• Must have low entry tip profile equal or less than 0.017 for crossing CTO or to difficult lesion. n• Must have lowest diameter starting from 1.0 mm. n• Must have lowest length starting from 5.0 mm . n• Monorail (rapid exchange) and the over-the-wire balloon. 442 Special PT. Balloon (Non-Compliant) lowest diameter in Post Dilation.-US FDA Approved. n• Must have diameter starting from 1.75 mm onwards. n• Monorail (rapid exchange) and the over-the-wire balloon. 443 Special PTCA Balloon (Non-Compliant) lowest diameter in Post Dilation. CE Approved. / US FDA / DCGI APPROVED n• Must have diameter starting from 1.75mm onwards. n• Monorail (rapid exchange) and the over-the-wire balloon. 444 Ultra-low entry profile (Semi-compliant) with 016 and entry, profile from 1.25*10 to 2.25*10 remain same for exceptional crossability. US FDA approved. n• Monorail (rapid exchange) and the over-the-wire balloon 445 Ultra-low entry profile (Semi-compliant) with 0.016 and entry profile from 1.25102o 2.2510 remain same for exceptional crossability. CE approved n• Monorail (rapid exchange) a. the over-the-wire balloon. 446 PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons n• Available in the size and lengths 447 PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons n• Available in the size and lengths 448 PTCA BALLOON (SEMI-COMPLIANT) - DCGI APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons n• Available in the size and lengths 449 PTCA BALLOON (NON-COMPLIANT) - US FDA APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons. n• Available in the size and lengths. 450 PTCA BALLOON (NON-COMPLIANT) - CE APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons. n• Available in the size and lengths . 451 PTCA BALLOON (NON-COMPLIANT) - DCGI APPROVED n• Monorail (rapid exchange) or over-the-wire (OTW) balloons. n• Available in the size and lengths . 452 Group J nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Luckhnow,SMS Jaipur etc. 453 COVERED CORONARY STENTS - DCGI APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) both n• Available in the sizes and lengths n• Covered graft stent for dissected artery n 454 COVERED CORONARY STENTS - US FDA APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) both n• Available in the sizes and lengths n• Covered graft stent for dissected artery 455 COVERED CORONARY STENTS - CE APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) both n• Available in the sizes and lengths n• Covered graft stent for dissected artery 456 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – DCGI APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 457 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 458 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 459 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – DCGI APPROVED n• WITH bioabsorbable or permanent polymer coated DES. n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 460 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –US FDA APPROVED n• WITH bioabsorbable or permanent polymer coated DES. n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 461 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –CE APPROVED n• WITH bioabsorbable or permanent polymer coated DES. n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 462 SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) nFor accelerated degradation and low concentration. - DCGI APPROVED. n• Sirolimus with Abluminal and specialized gradient coating (Japan PMDA approved technology). n• Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 463 SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) nFor accelerated degradation and low concentration. - USFDA APPROVED. n• Sirolimus with Abluminal and specialized gradient coating (Japan PMDA approved technology). n• Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 464 SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) or PLLA Polymer nFor accelerated degradation and low concentration. - CE APPROVED. n• Sirolimus with Abluminal and specialized gradient coating. n• Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 465 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packing n& temperature sensitive check meter. - DCGI APPROVED n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 466 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packing n& temperature sensitive check meter. -USFDA APPROVED n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 467 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packing & temperature sensitive check meter. - CE APPROVED n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 468 SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, nmicro-Porus surface with soft coating of shellac rasin- DCGI APPROVED n• Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 469 SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, nmicro-Porus surface with soft coating of shellac rasin- USFDA APPROVED n• Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 470 SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, nmicro-Porus surface with soft coating of shellac rasin- CE APPROVED n• Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 471 SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX n- DCGI APPROVED n• PROBUCOL WITH ABLUMINAL COATING. n• Should be available in diameter sizes from 2.25 mm- 4 mm n• Should be available in Lengths up to 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 472 SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX n-USFDA APPROVED n• PROBUCOL WITH ABLUMINAL COATING. n• Should be available in diameter sizes from 2.25 mm- 4 mm n• Should be available in Lengths up to 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 473 SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX n- CE APPROVED n• PROBUCOL WITH ABLUMINAL COATING. n• Should be available in diameter sizes from 2.25 mm- 4 mm n• Should be available in Lengths up to 48 mm n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES 474 SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – DCGI APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 475 SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 476 SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVED n• Must be Available in the sizes and lengths n• Must quote only the latest version commercially available n• Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) n• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES n 477 TEMPORARY PACING LEADS – DCGI APPROVED 478 TEMPORARY PACING LEADS –US FDA APPROVED 479 TEMPORARY PACING LEADS –CE APPROVED 480 • PERMANENTVVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI Approved n• All single Chamber modes and basic pacing programmable parameters n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for P.G. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. GMC KOTA n• Company must quote only the latest model of devices commercially available 481 • PERMANENTVVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA Approved n• All single Chamber modes and basic pacing programmable parameters n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for P.G. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. GMC KOTA n• Company must quote only the latest model of devices commercially available 482 • PERMANENTVVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES -CE Approved n• All single Chamber modes and basic pacing programmable parameters n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for P.G. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. GMC KOTA n• Company must quote only the latest model of devices commercially available 483 PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI Approved n• All single Chamber modes and with pediatric Base rate up to 160bpm and parameters n• Must have programmable sensor control rest rate n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available. 484 PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA Approved n• All single Chamber modes and with pediatric Base rate up to 160bpm and parameters n• Must have programmable sensor control rest rate n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available. 485 PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - CE Approved n• All single Chamber modes and with pediatric Base rate up to 160bpm and parameters n• Must have programmable sensor control rest rate n• Must have ventricular capture management n• The Size of lead must be 7F or less n• The Lead must be steroid eluting and should be both bipolar and unipolar configuration n• Must have both active and passive fixation endocardial leads available n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available. 486 VVIR PERMANENT PACEMAKER WITHOUT LEAD - DCGI Approved n• VVIR n• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemaker n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 487 VVIR PERMANENT PACEMAKER WITHOUT LEAD - US FDA Approved n• VVIR n• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemaker n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 488 VVIR PERMANENT PACEMAKER WITHOUT LEAD - CE Approved n• VVIR n• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemaker n• Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 489 PACING LEADS FOR VVI/VVIR PACEMAKERS - DCGI Approved n• Must have all specifications shown in related No. of pacemaker n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 490 PACING LEADS FOR VVI/VVIR PACEMAKERS - US FDA Approved n• Must have all specifications shown in related No. of pacemaker n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 491 PACING LEADS FOR VVI/VVIR PACEMAKERS - CE Approved n• Must have all specifications shown in related No. of pacemaker n• 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 n• Company must provide at least one programmer exclusively to the cardiology dept. n• Company must quote only the latest model of devices commercially available 492 SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER - CE Approved n• Must have modes AAI, AOO,VVI,VOO n• Basic Pacing rates 30-200. n• Electrode Type Unipolar or bipolar n• Services life more than 5 years n• Sensitivity 0.5-20 mV n• Output up to 5 volts 493 SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER - DCGI Approved n• Must have modes AAI, AOO,VVI,VOO n• Basic Pacing rates 30-200. n• Electrode Type Unipolar or bipolar n• Services life more than 5 years n• Sensitivity 0.5-20 mV n• Output up to 5 volts 494 SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER – US FDA Approved n• Must have modes AAI, AOO,VVI,VOO n• Basic Pacing rates 30-200. n• Electrode Type Unipolar or bipolar n• Services life more than 5 years n• Sensitivity 0.5-20 mV n• Output up to 5 volts 495 Group K nAll the consumable Items Must be approved/ being used in leading Govt. hospitals in India like AIIMS, New Delhi, PGI-Chandigarh,SGPGI-Luckhnow,SMS Jaipur etc. 496 Mullins sheaths – Kink resistant 6/7 F– DCGI APPROVED 497 ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes (6 mm – 40 mm) 498 ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –US FDA APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes (6 mm – 40 mm) 499 ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes (6 mm – 40 mm) 500 DELIVERY SHEATH FOR ASD CLOSURE DEVICE – DCGI APPROVED n• Compatible with the device approved in Item no. 2 501 DELIVERY SHEATH FOR ASD CLOSURE DEVICE –USFDA APPROVED n• Compatible with the device approved in Item no. 2 502 DELIVERY SHEATH FOR ASD CLOSURE DEVICE – CE APPROVED n• Compatible with the device approved in Item no. 2 503 ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED 504 ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM –USFDA APPROVED 505 ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM –CE APPROVED 506 PRELOADED ASD CLOSURE DEVICES – DCGI APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Preloaded device with delivery cable 507 PRELOADED ASD CLOSURE DEVICES –USFDA APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Preloaded device with delivery cable 508 PRELOADED ASD CLOSURE DEVICES – CE APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Preloaded device with delivery cable 509 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes 510 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –USFDA APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes 511 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVED n• Approved for pediatric/adult use n• Device made of biologically inert material n• Self-centering, detachable device with delivery cable n• Available in all the sizes 512 PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM - DCGI APPROVED 513 PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – USFDA APPROVED 514 PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM - CE APPROVED 515 • DELIVERY SHEATH FOR PDA CLOSURE DEVICE – DCGI APPROVED n• Should be Compatible with the device approved in Item no. 14 516 • DELIVERY SHEATH FOR PDA CLOSURE DEVICE –USFDA APPROVED n• Should be Compatible with the device approved in Item no. 14 517 • DELIVERY SHEATH FOR PDA CLOSURE DEVICE – CE APPROVED n• Should be Compatible with the device approved in Item no. 14 518 INJECTION NIKORANDIL (2 mg) – DCGI APPROVED 519 INJECTION NIKORANDIL (2 mg) – USFDA APPROVED 520 INJECTION NIKORANDIL (2 mg) – CE APPROVED 521 INJECTION TIROFIBAN – DCGI APPROVED 522 INJECTION TIROFIBAN –USFDA APPROVED 523 INJECTION TIROFIBAN –CE APPROVED 524 INJECTION SodiumNitro-Pruside– DCGI APPROVED 525 INJECTION SodiumNitro-Pruside–USFDA APPROVED 526 INJECTION SodiumNitro-Pruside–CE APPROVED 527 INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) – DCGI APPROVED nSnare kit should include n• A snare and its compatible sheath n• Should have nitinol shaft n• Should have 90 degree preformed snare loop n• Variable sizes of loop (5-35 mm) 528 INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) –US FDA APPROVED nSnare kit should include n• A snare and its compatible sheath n• Should have nitinol shaft n• Should have 90 degree preformed snare loop n• Variable sizes of loop (5-35 mm) 529 INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) – CE APPROVED nSnare kit should include n• A snare and its compatible sheath n• Should have nitinol shaft n• Should have 90 degree preformed snare loop n• Variable sizes of loop (5-35 mm) 530 SHEATHS FOR INTRAVASCULAR SNARES& MICROSNARE - US FDA / DCGI / CE APPROVED n• Should be compatible with item no 11. 531 CD – R MEDIA with atleast 700 MB storage and atleast 52x recordable speed with cover and printed “GMC kota.” on coverUS FDA / DCGI / CE APPROVED 532 DVD – MEDIA for Angiography sine and 3D Imaging system with cover and printed , GMC, kota on coverUS FDA / DCGI / CE APPROVED 533 SPECIAL VALVOPLASTY BALLOON CATHETER – DCGI APPROVED n1. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm n2. Should have dog boning for precise position 534 SPECIAL VALVOPLASTY BALLOON CATHETER –USFDA APPROVED n1. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm n2. Should have dog boning for precise position 535 SPECIAL VALVOPLASTY BALLOON CATHETER –CE APPROVED n3. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm n4. Should have dog boning for precise position 536 PBMV BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES – DCGI APPROVED 537 PBMV BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES –US FDA APPROVED 538 PBMV BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES –CE APPROVED 539 PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES - – DCGI APPROVED 540 PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES - –USFDA APPROVED 541 PBMV BALLOON (ALL TYPES AND SIZES) WITHOUT ACCESSORIES - –CE APPROVED 542 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES – DCGI APPROVED 543 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES –US FDA APPROVED 544 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH ALL ACCESSORIES –CE APPROVED 545 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH OUT ACCESSORIES – DCGI APPROVED 546 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH OUT ACCESSORIES –US FDA APPROVED 547 PTMC BALLOON (ALL TYPES AND ALL SIZES) WITH OUT ACCESSORIES –CE APPROVED 548 Trans Septal Puncture needle for BMV for adults use– DCGI APPROVED 549 Trans Septal Puncture needle for BMV for adults use–USFDA APPROVED 550 Trans Septal Puncture needle for BMV for adults use–CE APPROVED 551 SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED–CE APPROVED 552 SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED– USFDA APPROVED 553 SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED– DCGI APPROVED 554 DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– DCGI APPROVED 555 DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– CE APPROVED 556 DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– USFDA APPROVED