Supply Of Consumable Items For Cardiology And Neurointervention Cathlab At Associated Hospitals Of Medical College Kota Rate Contract Two Years, MBS HOSPITAL KOTA-Rajasthan

Supply Of Consumable Items For Cardiology And Neurointervention Cathlab At Associated Hospitals Of Medical College Kota Rate Contract Two Years-1 Group –A: DIAGNOSTIC AND ACCESSORIESnAll 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 APPROVEDn• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be Available in length from 65- 90 cm longn• 0.021 to 0.038-inch guide wire compatiblen• Kink resistant 3 LONG INTRODUCER SHEATH: US FDA APPROVEDn• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and aboven• Should be Available in length from 65- 90 cm longn• 0.021 to 0.038-inch guide wire compatiblen• Kink resistant 4 LONG INTRODUCER SHEATH: CE APPROVEDn• Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above n• Should be Available in length from 65- 90 cm longn• 0.021 to 0.038-inch guide wire compatiblen• Kink resistant 5 INTRODUCER SHEATH FOR ADULT: DCGI APPROVEDn• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and aboven• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatiblen• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 6 INTRODUCER SHEATH FOR ADULT : US FDA APPROVEDn• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and aboven• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatiblen• Kink resistantn• With dilator-hub lock mechanism to prevent its back-out during insertion 7 INTRODUCER SHEATH FOR ADULT : CE APPROVEDn• Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and aboven• Should be 10-24cm n• 0.021 or 0.038 inch guide wire compatiblen• 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 APPROVEDnShould be available in 6fr,7fr,8fr 9 LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : US FDA APPROVEDnShould be available in 6fr,7fr,8fr 10 LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : CE APPROVEDnShould 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 APPROVEDnShould be available in 6fr,7fr,8fr 13 LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : CE APPROVEDnShould 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 curvesn• 035-038 compatiblen• 100 cm long 21 HEAD HUNTER CATHETER : US FDA APPROVED n• In various standard lengths and curvesn• 035-038 compatiblen• 100 cm long 22 HEAD HUNTER CATHETER : CE APPROVED n• In various standard lengths and curvesn• 035-038 compatiblen• 100 cm long 23 SIMMONS/ SIDEWINDER CATHETER : DCGI APPROVEDn• In various standard lengths and curvesn• 035-038 compatiblen• 100 cm long 24 SIMMONS/ SIDEWINDER CATHETER : US FDA APPROVEDn• In various standard lengths and curvesn• 035-038 compatiblen• 100 cm long 25 SIMMONS/ SIDEWINDER CATHETER : CE APPROVEDn• In various standard lengths and curvesn• 035-038 compatiblen• 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 APPROVEDn• In various standard lengths n• 5f, 6f,7fr sizen• 0.035” to .070”, .074 inner lumen. 30 DISTAL ACCESS Catheter for CO- Axial Systems : US FDA APPROVEDn• In various standard lengths n• 5f, 6f,7fr sizen• 0.035” to .070”, .074 inner lumen. 31 DISTAL ACCESS Catheter for CO- Axial Systems : CE APPROVEDn• In various standard lengths n• 5f, 6f,7fr sizen• 0.035” to .070”, .074 inner lumen. 32 SHEPHERD’S HOOK CATHETER : DCGI APPROVEDnIn various standard lengths and curves 33 SHEPHERD’S HOOK CATHETER : US FDA APPROVEDnIn various standard lengths and curves 34 SHEPHERD’S HOOK CATHETER : CE APPROVEDnIn various standard lengths and curves 35 CEREBRAL ANGIOGRAPHY CATHETER : DCGI APPROVEDn• In various standard lengths and curvesn• 4FR, 5f, 6f size 36 CEREBRAL ANGIOGRAPHY CATHETER : US FDA APPROVEDn• In various standard lengths and curvesn• 4FR, 5f, 6f size 37 CEREBRAL ANGIOGRAPHY CATHETER : CE APPROVED n• In various standard lengths and curvesn• 4FR, 5f, 6f size 38 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : DCGI APPROVEDn• In various standard lengths and curvesn• 4F, 5f, 6f size 39 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : US FDA APPROVEDn• In various standard lengths and curvesn• 4F, 5f, 6f size 40 DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : CE APPROVEDn• In various standard lengths and curvesn• 4F, 5f, 6f size 41 PIGTAIL CATHETER : DCGI APPROVEDn4 French/5 French /6 French/7 French/8French in various standard lengths. 42 PIGTAIL CATHETER : US FDA APPROVEDn4 French/5 French /6 French/7 French/8French in various standard lengths. 43 PIGTAIL CATHETER : CE APPROVEDn4 French/5 French /6 French/7 French/8French in various standard lengths. 44 COURNARD CATHETER : DCGI APPROVEDn4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 45 COURNARD CATHETER : US FDA APPROVEDn4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 46 COURNARD CATHETER : CE APPROVEDn4 French/5 French /6 French/7 French/8French in various standard curves and lengths. 47 COBRA TYPE CATHETER – DCGI APPROVEDn• In various standard lengths and curves.n• 4Fr, 5fr, 6fr size 48 COBRA TYPE CATHETER – US FDA APPROVEDn• In various standard lengths and curves.n• 4Fr, 5fr, 6fr size 49 COBRA TYPE CATHETER – CE APPROVEDn• In various standard lengths and curves.n• 4Fr, 5fr, 6fr size 50 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – DCGI APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 120-150 cm long 51 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – US FDA APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 120-150 cm long 52 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – CE APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipnShould be between 120-150 cm long 53 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : DCGI APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 54 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : US FDA APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 55 HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : CE APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have superelastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 56 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : DCGI APPROVEDZn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 57 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : US FDA APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 58 PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : CE APPROVEDn• Must be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 180-260 cm long 59 BALLOON TIPPED GUIDING CATHETER : DCGI APPROVEDnSIZES 6Fr,7 fr,8 fr,9fr,10 fr 60 BALLOON TIPPED GUIDING CATHETER : US FDA APPROVEDnSIZES 6Fr,7 fr,8 fr,9fr,10 fr 61 BALLOON TIPPED GUIDING CATHETER : CE APPROVEDnSIZES 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 APPROVEDn• 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 APPROVEDn• 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 APPROVEDn• 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 ANGIOPLASTYnAll 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 APPROVEDn• Should have atraumatic soft tip& flexible shaftn• 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 availablen• Should have Inner Diameter of 4.2frn• Should have various lengths from 90-110 cm 76 Guiding catheter for Neuro Vascular Use : US FDA APPROVEDn• Should have atraumatic soft tip& flexible shaftn• 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 availablen• Should have Inner Diameter of 4.2frn• Should have various lengths from 90-110 cm 77 Guiding catheter for Neuro Vascular Use : CE APPROVEDn• Should have atraumatic soft tip& flexible shaftn• 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 availablen• Should have Inner Diameter of 4.2frn• 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 APPROVEDn• Should be on a .014” wiren• Should be made of polyurethane with radio-opaque nitinol loopn• Should be suspended on the .014” wire with a suspension armn• Should not occlude flow while in placementn• Should be rapid exchange typen• 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 APPROVEDn• Should be on a .014” wiren• Should be made of polyurethane with radio-opaque nitinol loopn• Should be suspended on the .014” wire with a suspension armn• Should not occlude flow while in placementn• Should be rapid exchange typen• 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 APPROVEDn• Should be on a .014” wiren• Should be made of polyurethane with radio-opaque nitinol loopn• Should be suspended on the .014” wire with a suspension armn• Should not occlude flow while in placementn• Should be rapid exchange typen• 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 APPROVEDn• Should have hydrophilic coatingn• 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 APPROVEDn• Should have hydrophilic coatingn• 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 APPROVEDn• Should have hydrophilic coatingn• Should be available in various outer diameters and balloon lengths and various shaft lengths 90 CAROTID SELF EXPENDABLE STENTS: DCGI APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthnShould be on a shaft length of 80-140 or above length 91 CAROTID SELF EXPENDABLE STENTS: US FDA APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 92 CAROTID SELF EXPENDABLE STENTS: CE APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthnShould be on a shaft length of 80-140 or above length 93 CAROTID SELF EXPENDABLE STENTS: DCGI APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 94 CAROTID SELF EXPENDABLE STENTS: US FDA APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 95 CAROTID SELF EXPENDABLE STENTS: CE APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 96 CAROTID SELF EXPENDABLE STENTS – DCGI APPROVEDn• Should be 0.035” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 97 CAROTID SELF EXPENDABLE STENTS – US FDA APPROVEDn• Should be 0.035” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 98 CAROTID SELF EXPENDABLE STENTS – CE APPROVEDn• Should be 0.035” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 99 CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• 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” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 101 CAROTID STENTS BALLOON EXPENDABLE – CE APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 102 CAROTID STENTS BALLOON EXPENDABLE: DCGI APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 103 CAROTID STENTS BALLOON EXPENDABLE: US FDA APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 104 CAROTID STENTS BALLOON EXPENDABLE: CE APPROVEDn• Should be 0.018” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 105 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: DCGI APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 106 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: US FDA APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 107 CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: CE APPROVEDn• Should be 0.014” compatiblen• Should be over the wire and rapid exchange (OTW/RX)n• Should be available in various diameters and lengthn• Should be on a shaft length of 80-140 or above length 108 PERIPHERAL Balloon Expandable STENT – (OTW/RX): DCGI APPROVEDn• Should be 0.014/0.018” compatiblen• Should over the wire n• Should be made of cobalt chromium / Baren• 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 APPROVEDn• Should be 0.014/0.018” compatiblen• 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 APPROVEDn• Should be 0.014/0.018” compatiblen• Should over the wire n• Should be made of cobalt chromium / Baren• 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& ADHESIVESnAll 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 APPROVEDnSHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER 137 MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : US FDA APPROVEDnSHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER 138 MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : CE APPROVEDnSHOULD 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 APPROVEDnSHOULD BE COMPITABLE FOR STENTS,FLOW DIVERTERS OR STENT RETRIEVERS OF VARIOUS SIZES. 152 SELECTIVE INFUSION MICROCATHETER FOR DEVPLOYING INTRACRANIAL DEVICE- US FDA APPROVEDnSHOULD BE COMPITABLE FOR STENTS,FLOW DIVERTERS OR STENT RETRIEVERS OF VARIOUS SIZES. 153 SELECTIVE INFUSION MICROCATHETER FOR DEVPLOYING INTRACRANIAL DEVICE- CE APPROVEDnSHOULD 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 USEnAll 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 APPROVEDn• SHOULD HAVE OPEN CELL DESIGNn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 189 OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVEDn• SHOULD HAVE OPEN CELL DESIGNn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 190 OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVEDn• SHOULD HAVE OPEN CELL DESIGNn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 191 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVEDn• SHOULD BE COMPITABLE FOR LARGE VESSELn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 192 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVEDn• SHOULD BE COMPITABLE FOR LARGE VESSELn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 193 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVEDn• SHOULD BE COMPITABLE FOR LARGE VESSELn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 194 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVEDn• SHOULD BE COMPITABLE FOR SMALL VESSELn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 195 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVEDn• SHOULD BE COMPITABLE FOR SMALL VESSELn• SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER 196 CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVEDn• SHOULD BE COMPITABLE FOR SMALL VESSELn• 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 THROMBACTOMYnAll 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/AVMsnAll 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 - GnAll 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 APPROVEDn• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• 10-11 cm long for Femoral Accessn• Pack must include 18 G or more, 6-7.5 cm long puncture needlen• 0.035 or 0.038 spring guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 258 INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - US FDA APPROVEDn• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• 10-11 cm long for Femoral Accessn• Pack must include 18 G or more, 6-7.5 cm long puncture needlen• 0.035 or 0.038 spring guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 259 INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - CE APPROVEDn• Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• 10-11 cm long for Femoral Accessn• Pack must include 18 G or more, 6-7.5 cm long puncture needlen• 0.035 or 0.038 spring guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionnWith smooth and resistance free insertion 260 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - DCGI APPROVED n• 10-11 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 261 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - US FDA APPROVEDn• 10-11 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 262 INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - CE APPROVEDn• 10-11 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 263 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) – DCGI APPROVEDn• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• Sheath should be between 20-30 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 264 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - US FDA APPROVEDn• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• Sheath should be between 20-30 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 265 LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - CE APPROVEDn• Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French.n• Sheath should be between 20-30 cm longn• 0.035 or 0.038 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• 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 Accessn• Pack must include 18/20 G, 6-7.5 cm long puncture needlen• 0.025-.038 inch guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 267 TRANS RADIAL INTRODUCER SHEETHS -US FDA APPROVEDn• Sizes 4 French/5 French/ 6 French.n• 7.0 cm long for Radial & Brachial Accessn• Pack must include 18/20 G, 6-7.5 cm long puncture needlen• 0.025-.038 inch guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 268 TRANS RADIAL INTRODUCER SHEETHS – CE APPROVEDn• Sizes 4 French/5 French/ 6 French.n• 7.0 cm long for Radial & Brachial Accessn• Pack must include 18/20 G, 6-7.5 cm long puncture needlen• 0.025-.038 inch guide wire compatiblen• With cross cut design haemostatic valve prevent back leak and air aspirationn• snap on dialator lock with Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 269 LONG BRADED INTRODUCER SHEATH – DCGI APPROVEDn• 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 compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 270 LONG BRADED INTRODUCER SHEATH – US FDA APPROVEDn• 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 compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertion 271 LONG BRADED INTRODUCER SHEATH – CE APPROVEDn• 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 compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• 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 APPROVEDn• Sizes from 4fr/5 fr/6Fr/ 7Frn• Between 7-11 cm longn• With 0.025 - 0.038 inch guide wire compatiblen• With Radio-opaque tipn• Should be for both Paediatric and Adult use 276 STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING –CE APPROVED n• Sizes from 4fr/5 fr/6Fr/ 7Frn• Between 7-11 cm longn• With 0.025 - 0.038 inch guide wire compatiblen• With Radio-opaque tipn• Should be for both Paediatric and Adult use 277 STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - US FDA APPROVEDn• Sizes from 4fr/5 fr/6Fr/ 7Frn• Between 7-11 cm longn• With 0.025 - 0.038 inch guide wire compatiblen• With Radio-opaque tipn• Should be for both Paediatric and Adult use 278 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVEDn• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Accessn• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 279 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DGCI APPROVEDn• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Accessn• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 280 INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS –US FDA APPROVEDn• Sizes 4 French/ 5 French/ 6 French/ 7 French n• Between 7-11 cm long for Radial & Brachial Accessn• 0.021 or 0.025 inch guide wire compatible n• With haemostatic valve to prevent back leak and air aspirationn• Integral side port with attached 3-way stopcockn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• With smooth and resistance free insertion 281 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - US FDA APPROVEDn• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• Should have smooth and resistance free insertion 282 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVEDn• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• Should have smooth and resistance free insertion 283 LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DCGI APPROVEDn• Sizes 4 French/5 French /6 French/7 French n• Between 16-24 cm long n• 0.021 or 0.025 inch guide wire compatiblen• With haemostatic valve to prevent back leak and air aspirationn• With integral side port with attached 3-way stopcockn• With suture eye for securing sheathn• Kink resistant n• With dilator-hub lock mechanism to prevent its back-out during insertionn• Should have smooth and resistance free insertion 284 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - DCGI APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be between 145-180 cm longn• Should be available as straight & J-Shaped tipn• Should be available in variable lengths of flexible/floppy endn• Should be available in variable J tip sizesn• Should be available fixed as well as movable core. 285 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - US FDA APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be between 145-180 cm longn• Should be available as straight & J-Shaped tipn• Should be available in variable lengths of flexible/floppy endn• Should be available in variable J tip sizesn• Should be available fixed as well as movable core 286 PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - CE APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be between 145-180 cm longn• Should be available as straight & J-Shaped tipn• Should be available in variable lengths of flexible/floppy endn• Should be available in variable J tip sizesn• Should be available fixed as well as movable core 287 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - DCGI APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be 240-300 cm longn• Should be available as straight or J-Shaped tipn• Should be available fixed as well as movable core. 288 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - US FDA APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be 240-300 cm longn• Should be available as straight or J-Shaped tipnShould be available fixed as well as movable core. 289 PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - CE APPROVEDn• Should be available in 0.025, 0.032, 0.035 and 0.038 inches sizen• Should be 240-300 cm longn• Should be available as straight or J-Shaped tipnShould 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 sizen• Should have Super elastic Nitinol alloyn• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 120-150 cm long 291 HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) n– US FDA APPROVEDn• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have Super elastic Nitinol alloyn• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 120-150 cm long 292 HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) n– CE APPROVEDn• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have Super elastic Nitinol alloyn• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 120-150 cm long 293 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - DCGI APPROVEDn• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 150-180 cm long 294 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - US FDA APPROVEDn• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 150-180 cm long 295 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - CE APPROVEDn• Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• 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 sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 260cm, 300 cm long 297 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - US FDA APPROVEDn• Must be available in 0.018, 0.025, 0.032 and 0.038 inches sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• Should be between 260cm, 300 cm long 298 RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - CE APPROVEDn• Must be available in 0.018, 0.025, 0.032 and 0.038 inches sizen• Should have super elastic alloy coren• Should have super flexible wire tipn• Should be available in straight and angled tipn• 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 sizen• Left and Right judkins catheters in various standard curves and lengths even for pediatric casesn• Must have Double mesh construction with Ultra-thin wall 300 JUDKINS CATHETER (JR JL & PIGTAIL)- US FDA APPROVEDn• 4 French/5 French /6 French/7 French/8French sizen• Left and Right judkins catheters in various standard curves and lengths even for pediatric casesn• Must have Double mesh construction with Ultra-thin wall 301 JUDKINS CATHETER (JR JL & PIGTAIL)-CE APPROVEDn• 4 French/5 French /6 French/7 French/8French sizen• Left and Right judkins catheters in various standard curves and lengths even for pediatric casesn• Must have Double mesh construction with Ultra-thin wall 302 MULTIPURPOSE CATHETER - - DCGI APPROVED n• 4 French/5 French /6 French/7 Frenchsizen• Multipurpose catheters in various standard curves and lengths even for pediatric casesn• Must have Double mesh construction with Ultra-thin wall 303 MULTIPURPOSE CATHETER - - US FDA APPROVEDn• 4 French/5 French /6 French/7 Frenchsizen• Multipurpose catheters in various standard curves and lengths even for pediatric casesn• Must have Double mesh construction with Ultra-thin wall 304 MULTIPURPOSE CATHETER - - CE APPROVEDn• 4 French/5 French /6 French/7 Frenchsizen• Multipurpose catheters in various standard curves and lengths even for pediatric casesn• 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 lengthsn• dedicated for angiography of right and left coronary arteries using either radial or brachial approach 306 TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – US FDAn• 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengthsn• 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 lengthsn• 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 APPROVEDn• Should be soft and kink resistantn• Should give reliable pressure measurementsn• Should be available in sizes of 100, 150 & 200 cmn• Should have male luer lock connection at one end and a female luer lock connection at the other endn• Should meet highest medical industrial standards for arterial pressure lines 309 ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - US FDA APPROVEDn• Should be soft and kink resistantn• Should give reliable pressure measurementsn• Should be available in sizes of 100, 150 & 200 cmn• Should have male luer lock connection at one end and a female luer lock connection at the other endn• Should meet highest medical industrial standards for arterial pressure lines 310 ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - CE APPROVEDn• Should be soft and kink resistantn• Should give reliable pressure measurementsn• Should be available in sizes of 100, 150 & 200 cmn• Should have male luer lock connection at one end and a female luer lock connection at the other endn• Should meet highest medical industrial standards for arterial pressure lines 311 ACT TUBES - DCGI APPROVEDn• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kotan• Should meet highest medical industrial standards n• Quality certification should be provided from authorized agencies. 312 ACT TUBES - US FDA APPROVEDn• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kotan• Should meet highest medical industrial standards nQuality certification should be provided from authorized agencies 313 ACT TUBES - CE APPROVEDn• Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kotan• 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 manifoldn• One luer lock control syringe (10 or 15 ml) for contrast injectionn• One three way stop-cock 315 MANIFOLD with 3 Port - US FDA APPROVEDn• Three side port manifoldn• One luer lock control syringe (10 or 15 ml) for contrast injectionn• One three way stop-cock 316 MANIFOLD with 3 Port - CE APPROVEDn• Three side port manifoldn• One luer lock control syringe (10 or 15 ml) for contrast injectionn• One three way stop-cock 317 HIGH – PRESURE INJECTOR LINES - DCGI APPROVED n• Should be available in various lengthsn• Should have male and female luer locksn• Should be transparent and kink resistantn• Should be able to take high pressure of angiographic injections 318 HIGH – PRESURE INJECTOR LINES US FDA APPROVEDn• Should be available in various lengthsn• Should have male and female luer locksn• Should be transparent and kink resistantn• Should be able to take high pressure of angiographic injections 319 HIGH – PRESURE INJECTOR LINES - CE APPROVEDn• Should be available in various lengthsn• Should have male and female luer locksn• Should be transparent and kink resistantn• Should be able to take high pressure of angiographic injections 320 AMPLATZ CATHETERn• 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 CATHETERn• 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 CATHETERn• 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 electrodesn• Should be porous and breathablen• 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 APPROVEDn• Wet gel electrodesn• Should be porous and breathablen• 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 APPROVEDn• Wet gel electrodesn• Should be porous and breathablen• 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 Approvedn• Should be compatible with existing machines at GMC kota Cath Lab 327 SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaUS FDA APPROVEDn• Should be compatible with existing machines at GMC kota Cath Lab 328 SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaCE APPROVEDn• Should be compatible with existing machines at GMC kota Cath Lab 329 TRANS RADIAL ANGIOGRAPHY KIT – DCGI Approvedn• 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 Approvedn• 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 Approvedn• 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 APPROVEDn• Sizes 3 French/ 4 French/ 5 French/ 6 Frenchn• Smaller length for neonatal and pediatric use 333 PIGTAIL CATHETER (PEDIATRIC/Adult ) –US FDA APPROVEDn• Sizes 3 French/ 4 French/ 5 French/ 6 Frenchn• Smaller length for neonatal and pediatric use 334 PIGTAIL CATHETER (PEDIATRIC/Adult ) –CE APPROVEDn• Sizes 3 French/ 4 French/ 5 French/ 6 Frenchn• 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 sizen• Should be between 240-300 cm longn• 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 sizen• Should be between 240-300 cm longn• 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 sizen• Should be between 240-300 cm longn• Should be available as straight & J-Shaped tip 338 INTERNAL MAMMARY CATHETERn• 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 CATHETERn• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths.n• Must be CE APPROVED 340 INTERNAL MAMMARY CATHETERn• 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 CATHETERn• 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 CATHETERn• 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 CATHETERn• 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths.n• Must be DCGI APPROVED 344 Group-HnAll 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 availablen• Should have All various lengths 346 PTCA Guiding catheter–US FDA APPROVEDn• Should be braided with low friction Inner Layer of PTFE n• Should have atraumatic soft tipn • 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 availablen• Should have All various lengths 347 PTCA Guiding catheter–CE APPROVEDn• 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 availablen• 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 layern• 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 APPROVEDn• Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route.n• Should be braided with low friction inner layern• 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 APPROVEDZn• Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route.n• Should be braided with low friction inner layern• Should have atraumatic soft tip.n• Should have all the lengths and in diameter 5 French/ 6 French available 351 Mother & Child Catheter – - CE APPROVEDn• With reliable support with large inner lumen and inner PTSE. 352 Mother & Child Catheter – - US FDA APPROVEDn• With reliable support with large inner lumen and inner PTSE. 353 Mother & Child Catheter – - DCGI APPROVEDn• With reliable support with large inner lumen and inner PTSE. 354 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - DCGI APPROVEDn• 120 proximal hypotube shaftn0.57 Inner diameter & 0.066” outer diameternShould be with proximal marker and 1 x 1 braiding 355 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - US FDA APPROVEDn• 120 proximal hypotube shaftn0.57 Inner diameter & 0.066” outer diameternShould be with proximal marker and 1 x 1 braiding 356 GUIDE EXTENTION CATHETER (GUIDEZILLA TYPE) - CE APPROVEDn• 120 proximal hypotube shaftn0.57 Inner diameter & 0.066” outer diameternShould be with proximal marker and 1 x 1 braiding 357 PTCA INFLATION DEVICE - DCGI APPROVEDn• Efficient locking system to maintain high pressuren• Rapid inflation and deflationn• Clear barrel for easy visualization of de-bubblingn• Luminescent analog pressure gauge (up to 30 Atm)n• Ergomatric and use friendly hand held design. 358 PTCA INFLATION DEVICE - US FDA APPROVEDn• Efficient locking system to maintain high pressuren• Rapid inflation and deflationn• Clear barrel for easy visualization of de-bubblingn• Luminescent analog pressure gauge (up to 30 Atm)n• Ergomatric and use friendly hand held design. 359 PTCA INFLATION DEVICE - CE APPROVEDn• Efficient locking system to maintain high pressuren• Rapid inflation and deflationn• Clear barrel for easy visualization of de-bubblingn• 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 APPROVEDn• Should accommodate virtually all interventional devicesn• Luer connector at the guiding catheter endn• Rotating adapter at the guiding catheter endn• Should have bleed back safety mechanismn• Stepwise control for open, semi-open and closed position 361 TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –US FDA APPROVEDn• Should accommodate virtually all interventional devicesn• Luer connector at the guiding catheter endn• Rotating adapter at the guiding catheter endn• Should have bleed back safety mechanismn• Stepwise control for open, semi-open and closed position 362 TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –CE APPROVEDn• Should accommodate virtually all interventional devicesn• Luer connector at the guiding catheter endn• Rotating adapter at the guiding catheter endn• Should have bleed back safety mechanismn• Stepwise control for open, semi-open and closed position 363 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –DCGI APPROVEDn• Should accommodate virtually all interventional devicesn• Two ports for insertion of interventional devicesn• Luer connector at the guiding catheter end 364 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –US FDA APPROVEDn• Should accommodate virtually all interventional devicesn• Two ports for insertion of interventional devicesn• Luer connector at the guiding catheter end 365 HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –CE APPROVEDn• Should accommodate virtually all interventional devicesn• Two ports for insertion of interventional devicesn• 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/8frn• Should be braided with low friction Inner Layer of PTFEn• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and othersn• Should also have availability of smaller length catheters (90 cm) & Regular length sizes.n• Should also have availability of catheters with side holesn• 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/8frn• Should be braided with low friction Inner Layer of PTFEn• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and othersn• Should also have availability of smaller length catheters (90 cm) & Regular length sizes.n• Should also have availability of catheters with side holesn• Should also have short tip catheters 371 PTCA GUIDING CATHETER - CE APPROVED n• Should be available in Sizes of 5 French/6 fr/7fr/8frn• Should be braided with low friction Inner Layer of PTFEn• All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and othersn• Should also have availability of smaller length catheters (90 cm) & Regular length sizes.n• Should also have availability of catheters with side holesn• 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 APPROVEDn• Should be Dedicated for externalization with tip load of 3g/force 377 EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- CE APPROVEDn• 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 coatingn -- 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 proceduresn• 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 coatingn -- US FDA APPROVEDn• 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 proceduresn• 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 coatingn -- CE APPROVEDn• 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 proceduresn• 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 APPROVEDn• .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 APPROVEDn• .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 technologyn• 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 APPROVEDn• 0.010 One Piece core wire with joint less Spring coil with SION TECH technologyn• 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 APPROVEDn• 0.010 One Piece core wire with joint less Spring coil with SION TECH technologyn• 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 inchesn• Nitinol alloyn• With angled tip 3-5 cm longn• Tip with platinum/platinum alloy for optimum visualizationn• With TFE coatingn• 180 cm long 395 HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – CE APPROVED.n• 0.014 inchesn• Nitinol alloyn• With angled tip 3-5 cm longn• Tip with platinum/platinum alloy for optimum visualizationn• With TFE coatingn• 180 cm long 396 HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – DCGI APPROVED.n• 0.014 inchesn• Nitinol alloyn• With angled tip 3-5 cm longn• Tip with platinum/platinum alloy for optimum visualizationn• With TFE coatingn• 180 cm long 397 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - DCGI APPROVEDn• Disposable transducers for invasive pressure monitoringn• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kotan• Should meet highest medical industrial standardsn• Quality certification should be provided form authorized agencies 398 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - US FDA APPROVEDn• Disposable transducers for invasive pressure monitoringn• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kotan• Should meet highest medical industrial standardsn• Quality certification should be provided form authorized agencies 399 DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - CE APPROVEDn• Disposable transducers for invasive pressure monitoringn• SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kotan• Should meet highest medical industrial standardsn• Quality certification should be provided form authorized agencies 400 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - DCGI APPROVEDn• Should be compatible with existing available systemn• Should meet or exceed highest standardsn• Quality certification from authorized agencies to be provided 401 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - CE APPROVEDn• Should be compatible with existing available systemn• Should meet or exceed highest standardsn• Quality certification from authorized agencies to be provided 402 DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - US FDA APPROVEDn• Should be compatible with existing available systemn• Should meet or exceed highest standardsn• Quality certification from authorized agencies to be provided 403 Group – InAll 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) balloonsn• 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 lessn• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mmn• Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above) 405 PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• 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 lessn• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mmn• Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above) 406 PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• 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 lessn• Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mmn• 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 balloonsn• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mmn• 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 APPROVEDn• Quote both monorail (rapid exchange) and OTW balloonsn• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mmn• 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 APPROVEDn• Quote both monorail (rapid exchange) and OTW balloonsn• Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mmn• 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- 2.25mmn• Quote both monorail (rapid exchange) and OTW balloonsn• Should be available in all sizes& All variable lengths up to 20mm 411 SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - US FDA APPROVEDn• Must have Ultra-low entry profile of 0.016”n• Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mmn• Quote both monorail (rapid exchange) and OTW balloonsn• Should be available in all sizes& All variable lengths up to 20mm 412 SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - CE APPROVEDn• Must have Ultra-low entry profile of 0.016”n• Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mmn• Quote both monorail (rapid exchange) and OTW balloonsn• 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 - 20mmn• Quote both monorail (rapid exchange) and OTW balloonsn• Should have R.B.P -18atm or Above 414 SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - US FDA APPROVEDn• Must have Ultra-low entry profile of 0.016”n• Should be available in variable balloon lengths minimum from 06mm - 20mmn• Quote both monorail (rapid exchange) and OTW balloonsn• Should have R.B.P -18atm or Above 415 SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - CE APPROVEDn• Must have Ultra-low entry profile of 0.016”n• Should be available in variable balloon lengths minimum from 06mm - 20mmn• Quote both monorail (rapid exchange) and OTW balloonsn• Should have R.B.P -18atm or Above 416 ZEROFOLD PTCA BALLOON - DCGI APPROVED APPROVEDn• Available in all sizes and lengthn• Quote both monorail (rapid exchange) and OTW balloons 417 ZEROFOLD PTCA BALLOON - US FDA APPROVEDn• Available in all sizes and lengthn• Quote both monorail (rapid exchange) and OTW balloons 418 ZEROFOLD PTCA BALLOON - CE APPROVEDn• Available in all sizes and lengthn• 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 balloonsn• 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 balloonsn• 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 balloonsn• 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) balloonsn• Available in the sizes and lengths 423 CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - US FDA APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• Available in the sizes and lengths 424 CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - CE APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• Available in the sizes and lengths 425 SCORING BALLOON CATHETER FOR PTCA - DCGI APPROVED n• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• Available in the sizes and lengths 426 SCORING BALLOON CATHETER FOR PTCA - US FDA APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• Available in the sizes and lengths 427 SCORING BALLOON CATHETER FOR PTCA - CE APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) balloonsn• 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 APPROVEDn• 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 APPROVEDn• 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 APPROVEDn• Should be compatible with existing machine at GMC Kota 436 IABP CATHETER WITH ACCESSORIES - CE APPROVEDn• 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 APPROVEDn• 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 APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloonsn• Available in the size and lengths 447 PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloonsn• Available in the size and lengths 448 PTCA BALLOON (SEMI-COMPLIANT) - DCGI APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloonsn• Available in the size and lengths 449 PTCA BALLOON (NON-COMPLIANT) - US FDA APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloons.n• Available in the size and lengths. 450 PTCA BALLOON (NON-COMPLIANT) - CE APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloons.n• Available in the size and lengths . 451 PTCA BALLOON (NON-COMPLIANT) - DCGI APPROVEDn• Monorail (rapid exchange) or over-the-wire (OTW) balloons.n• Available in the size and lengths . 452 Group JnAll 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 lengthsn• Covered graft stent for dissected arteryn 454 COVERED CORONARY STENTS - US FDA APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) both n• Available in the sizes and lengthsn• Covered graft stent for dissected artery 455 COVERED CORONARY STENTS - CE APPROVEDn• Monorail (rapid exchange) and over-the-wire (OTW) both n• Available in the sizes and lengthsn• 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 lengthsn• Must quote only the latest version commercially availablen• 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-DESn 457 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVEDn• Must be Available in the sizes and lengthsn• Must quote only the latest version commercially availablen• 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-DESn 458 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVEDn• Must be Available in the sizes and lengthsn• Must quote only the latest version commercially availablen• 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-DESn 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 availablen• 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-DESn 460 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –US FDA APPROVEDn• WITH bioabsorbable or permanent polymer coated DES.n• Must quote only the latest version commercially availablen• 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-DESn 461 EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –CE APPROVEDn• WITH bioabsorbable or permanent polymer coated DES.n• Must quote only the latest version commercially availablen• 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-DESn 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 Aboven• 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 Aboven• 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 Aboven• Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DESn 465 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packingn& 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-DESn 466 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packingn& temperature sensitive check meter. -USFDA APPROVEDn• 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-DESn 467 SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, nmicroporussurfacewith soft coating of shellac rasin with temperature control packing & temperature sensitive check meter. - CE APPROVEDn• 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 mmn• 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 APPROVEDn• Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mmn• 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 APPROVEDn• Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mmn• 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 mmn• 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 APPROVEDn• 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 mmn• 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 APPROVEDn• 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 mmn• 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 lengthsn• Must quote only the latest version commercially availablen• 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-DESn 475 SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVEDn• Must be Available in the sizes and lengthsn• Must quote only the latest version commercially availablen• 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-DESn 476 SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVEDn• Must be Available in the sizes and lengthsn• Must quote only the latest version commercially availablen• 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-DESn 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 Approvedn• All single Chamber modes and basic pacing programmable parametersn• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 KOTAn• Company must quote only the latest model of devices commercially available 481 • PERMANENTVVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA Approvedn• All single Chamber modes and basic pacing programmable parametersn• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 KOTAn• Company must quote only the latest model of devices commercially available 482 • PERMANENTVVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES -CE Approvedn• All single Chamber modes and basic pacing programmable parametersn• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 KOTAn• Company must quote only the latest model of devices commercially available 483 PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI Approvedn• All single Chamber modes and with pediatric Base rate up to 160bpm and parametersn• Must have programmable sensor control rest raten• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 Approvedn• All single Chamber modes and with pediatric Base rate up to 160bpm and parametersn• Must have programmable sensor control rest raten• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 Approvedn• All single Chamber modes and with pediatric Base rate up to 160bpm and parametersn• Must have programmable sensor control rest raten• Must have ventricular capture managementn• The Size of lead must be 7F or lessn• The Lead must be steroid eluting and should be both bipolar and unipolar configurationn• 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 Approvedn• VVIRn• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemakern• 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 Approvedn• VVIRn• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemakern• 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 Approvedn• VVIRn• All single chamber modes and basic pacing programmable parameters n• Should have all parameters shown in related No. of pacemakern• 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 Approvedn• Must have all specifications shown in related No. of pacemakern• 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 requiredn• 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 Approvedn• Must have all specifications shown in related No. of pacemakern• 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 requiredn• 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 Approvedn• Must have all specifications shown in related No. of pacemakern• 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 requiredn• 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 Approvedn• Must have modes AAI, AOO,VVI,VOOn• Basic Pacing rates 30-200.n• Electrode Type Unipolar or bipolarn• Services life more than 5 yearsn• Sensitivity 0.5-20 mVn• Output up to 5 volts 493 SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER - DCGI Approvedn• Must have modes AAI, AOO,VVI,VOOn• Basic Pacing rates 30-200.n• Electrode Type Unipolar or bipolarn• Services life more than 5 yearsn• Sensitivity 0.5-20 mVn• Output up to 5 volts 494 SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER – US FDA Approvedn• Must have modes AAI, AOO,VVI,VOOn• Basic Pacing rates 30-200.n• Electrode Type Unipolar or bipolarn• Services life more than 5 yearsn• Sensitivity 0.5-20 mVn• Output up to 5 volts 495 Group KnAll 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 usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• Available in all the sizes (6 mm – 40 mm) 498 ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –US FDA APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• Available in all the sizes (6 mm – 40 mm) 499 ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• 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 APPROVEDn• Compatible with the device approved in Item no. 2 502 DELIVERY SHEATH FOR ASD CLOSURE DEVICE – CE APPROVEDn• 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 usen• Device made of biologically inert materialn• Preloaded device with delivery cable 507 PRELOADED ASD CLOSURE DEVICES –USFDA APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Preloaded device with delivery cable 508 PRELOADED ASD CLOSURE DEVICES – CE APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Preloaded device with delivery cable 509 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED n• Approved for pediatric/adult usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• Available in all the sizes 510 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –USFDA APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• Available in all the sizes 511 PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVEDn• Approved for pediatric/adult usen• Device made of biologically inert materialn• Self-centering, detachable device with delivery cablen• 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 APPROVEDn• Should be Compatible with the device approved in Item no. 14 517 • DELIVERY SHEATH FOR PDA CLOSURE DEVICE – CE APPROVEDn• 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 includen• A snare and its compatible sheathn• Should have nitinol shaftn• Should have 90 degree preformed snare loopn• Variable sizes of loop (5-35 mm) 528 INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) –US FDA APPROVEDnSnare kit should includen• A snare and its compatible sheathn• Should have nitinol shaftn• Should have 90 degree preformed snare loopn• Variable sizes of loop (5-35 mm) 529 INTRAVASCULAR RETRIEVER – SNARE (‘AMPLATZ GOOSENECK’ TYPE) – CE APPROVEDnSnare kit should includen• A snare and its compatible sheathn• Should have nitinol shaftn• Should have 90 degree preformed snare loopn• Variable sizes of loop (5-35 mm) 530 SHEATHS FOR INTRAVASCULAR SNARES& MICROSNARE - US FDA / DCGI / CE APPROVEDn• 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 60mmn2. Should have dog boning for precise position 534 SPECIAL VALVOPLASTY BALLOON CATHETER –USFDA APPROVEDn1. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mmn2. Should have dog boning for precise position 535 SPECIAL VALVOPLASTY BALLOON CATHETER –CE APPROVEDn3. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mmn4. 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

Sr No	CorrigendumDate	Corrignedum	CorrigendumType	NewSubmissionDate
1	09-Oct-2020	Corrigendum	Technical Bid	26-10-2020

INR 1000 /-

INR 1200000.0 /-

INR 6 Crore /-