SUPPLY OF CONSUMABLE ITEMS FOR CARDIOLOGY AND NEUROINTERVENTION CATHLAB AT ASSOCIATED HOSPITALS OF MEDICAL COLLEGE KOTA RATE CONTRACT TWO YEARS

Group –A: DIAGNOSTIC AND ACCESSORIES All 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.

LONG INTRODUCER SHEATH: DCGI APPROVED · Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be Available in length from 65- 90 cm long · 0.021 to 0.038-inch guide wire compatible · Kink resistant

LONG INTRODUCER SHEATH: US FDA APPROVED · Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be Available in length from 65- 90 cm long · 0.021 to 0.038-inch guide wire compatible · Kink resistant

LONG INTRODUCER SHEATH: CE APPROVED · Sizes4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be Available in length from 65- 90 cm long · 0.021 to 0.038-inch guide wire compatible · Kink resistant

INTRODUCER SHEATH FOR ADULT: DCGI APPROVED · Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be 10-24cm · 0.021 or 0.038 inch guide wire compatible · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

INTRODUCER SHEATH FOR ADULT : US FDA APPROVED · Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be 10-24cm · 0.021 or 0.038 inch guide wire compatible · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

INTRODUCER SHEATH FOR ADULT : CE APPROVED · Sizes 4fr,5fr, 6fr,7Fr, 8Fr, &9 French and above · Should be 10-24cm · 0.021 or 0.038 inch guide wire compatible · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : DCGI APPROVED Should be available in 6fr,7fr,8fr

LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : US FDA APPROVED Should be available in 6fr,7fr,8fr

LONG INTRODUCER SHEATH 65 CM or Above ( UNBRAIDED) : CE APPROVED Should be available in 6fr,7fr,8fr

LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : DCGI APPROVED Should be available in 6fr,7fr,8fr

LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : US FDA APPROVED Should be available in 6fr,7fr,8fr

LONG INTRODUCER sheath 90 CM or Above (BRAIDED ) : CE APPROVED Should be available in 6fr,7fr,8fr

PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : DCGI APPROVED

PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : US FDA APPROVED

PUNCTURE NEEDLE FOR VASCULAR ACCESS IN ADULT (18G) : CE APPROVED

MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : DCGI APPROVED

MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : US FDA APPROVED

MICRO PUNCTURE NEEDLE FOR VASCULAR ACCESS IN CHILDREN- (20-22G) : CE APPROVED

HEAD HUNTER CATHETER : DCGI APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

HEAD HUNTER CATHETER : US FDA APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

HEAD HUNTER CATHETER : CE APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

SIMMONS/ SIDEWINDER CATHETER : DCGI APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

SIMMONS/ SIDEWINDER CATHETER : US FDA APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

SIMMONS/ SIDEWINDER CATHETER : CE APPROVED · In various standard lengths and curves · 035-038 compatible · 100 cm long

VERTEBRAL CATHETER -In various standard lengths and curves : DCGI APPROVED

VERTEBRAL CATHETER -In various standard lengths and curves : US FDA APPROVED

VERTEBRAL CATHETER -In various standard lengths and curves : CE APPROVED

DISTAL ACCESS Catheter for CO- Axial Systems : DCGI APPROVED · In various standard lengths · 5f, 6f,7fr size · 0.035” to .070”, .074 inner lumen.

DISTAL ACCESS Catheter for CO- Axial Systems : US FDA APPROVED · In various standard lengths · 5f, 6f,7fr size · 0.035” to .070”, .074 inner lumen.

DISTAL ACCESS Catheter for CO- Axial Systems : CE APPROVED · In various standard lengths · 5f, 6f,7fr size · 0.035” to .070”, .074 inner lumen.

SHEPHERD’S HOOK CATHETER : DCGI APPROVED In various standard lengths and curves

SHEPHERD’S HOOK CATHETER : US FDA APPROVED In various standard lengths and curves

SHEPHERD’S HOOK CATHETER : CE APPROVED In various standard lengths and curves

CEREBRAL ANGIOGRAPHY CATHETER : DCGI APPROVED · In various standard lengths and curves · 4FR, 5f, 6f size

CEREBRAL ANGIOGRAPHY CATHETER : US FDA APPROVED · In various standard lengths and curves · 4FR, 5f, 6f size

CEREBRAL ANGIOGRAPHY CATHETER : CE APPROVED · In various standard lengths and curves · 4FR, 5f, 6f size

DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : DCGI APPROVED · In various standard lengths and curves · 4F, 5f, 6f size

DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : US FDA APPROVED · In various standard lengths and curves · 4F, 5f, 6f size

DIAGNOSTIC CATHETER FOR SPINAL ANGIOGRAPHY : CE APPROVED · In various standard lengths and curves · 4F, 5f, 6f size

PIGTAIL CATHETER : DCGI APPROVED 4 French/5 French /6 French/7 French/8French in various standard lengths.

PIGTAIL CATHETER : US FDA APPROVED 4 French/5 French /6 French/7 French/8French in various standard lengths.

PIGTAIL CATHETER : CE APPROVED 4 French/5 French /6 French/7 French/8French in various standard lengths.

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

COURNARD CATHETER : US FDA APPROVED 4 French/5 French /6 French/7 French/8French in various standard curves and lengths.

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

COBRA TYPE CATHETER – DCGI APPROVED · In various standard lengths and curves. · 4Fr, 5fr, 6fr size

COBRA TYPE CATHETER – US FDA APPROVED · In various standard lengths and curves. · 4Fr, 5fr, 6fr size

COBRA TYPE CATHETER – CE APPROVED · In various standard lengths and curves. · 4Fr, 5fr, 6fr size

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – DCGI APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 120-150 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – US FDA APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 120-150 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (REGULAR LENGTH, REGULAR STIFFNESS) – CE APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip Should be between 120-150 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : DCGI APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : US FDA APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE – TYPE (EXCHANGELENGTH,EXTRA STIFFNESS) : CE APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have superelastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : DCGI APPROVEDZ · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : US FDA APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

PTFE COATED DIAGNOSTIC GUIDE WIRE – AMPLATZ TYPE (REGULARLENGTH,EXTRA STIFFNESS) : CE APPROVED · Must be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 180-260 cm long

BALLOON TIPPED GUIDING CATHETER : DCGI APPROVED SIZES 6Fr,7 fr,8 fr,9fr,10 fr

BALLOON TIPPED GUIDING CATHETER : US FDA APPROVED SIZES 6Fr,7 fr,8 fr,9fr,10 fr

BALLOON TIPPED GUIDING CATHETER : CE APPROVED SIZES 6Fr,7 fr,8 fr,9fr,10 fr

INFLATION DEVICE WITH ANALOG DISPLAY : DCGI APPROVED

INFLATION DEVICE WITH ANALOG DISPLAY : US FDA APPROVED

INFLATION DEVICE WITH ANALOG DISPLAY : CE APPROVED

TUOHY BORST HAEMOSTATIC Y-CONNECTOR : DCGI APPROVED

TUOHY BORST HAEMOSTATIC Y-CONNECTOR : US FDA APPROVED

TUOHY BORST HAEMOSTATIC Y-CONNECTOR : CE APPROVED

TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : DCGI APPROVED

TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : US FDA APPROVED

TUOHY BORSTHAEMOSTATIC Y-CONNECTOR WITH DOUBLE SIDE ARM : CE APPROVED

DISPOSABLE LUER LOCK SYRINGE : DCGI APPROVED · SHOULD BE COMPITABLE WITH CUANOACRYLATE. · SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C

DISPOSABLE LUER LOCK SYRINGE : US FDA APPROVED · SHOULD BE COMPITABLE WITH CUANOACRYLATE. · SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C

DISPOSABLE LUER LOCK SYRINGE : CE APPROVED · SHOULD BE COMPITABLE WITH CUANOACRYLATE. · SHOULD BE AVAILABLE IN 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C

Group –B: CAROTID ANGIOPLASTY All 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.

Guiding catheter for Neuro Vascular Use : DCGI APPROVED · Should have atraumatic soft tip& flexible shaft · Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature · Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available · Should have Inner Diameter of 4.2fr · Should have various lengths from 90-110 cm

Guiding catheter for Neuro Vascular Use : US FDA APPROVED · Should have atraumatic soft tip& flexible shaft · Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature · Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available · Should have Inner Diameter of 4.2fr · Should have various lengths from 90-110 cm

Guiding catheter for Neuro Vascular Use : CE APPROVED · Should have atraumatic soft tip& flexible shaft · Should be available in various tip shapes and curves for access to different parts of the Neuro vasculature · Should have Outer Diameter of 6Fr,7 fr,8 fr,9fr,10 fr available · Should have Inner Diameter of 4.2fr · Should have various lengths from 90-110 cm

PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : DCGI APPROVED

PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : US FDA APPROVED

PROXIMAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (PROXIMAL BALLOON OCCLUSION TECHNIQUE) : CE APPROVED

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : DCGI APPROVED

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : US FDA APPROVED

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER WITH PROXIMAL BALLOON OCCLUSION TECHNIQUE) : CE APPROVED

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : DCGI APPROVED · Should be on a .014” wire · Should be made of polyurethane with radio-opaque nitinol loop · Should be suspended on the .014” wire with a suspension arm · Should not occlude flow while in placement · Should be rapid exchange type · Should be compatible with a 6 F guiding catheter (0.066” ID) · Should allow optimal filtration in vessels 3.5 – 5.5 mm size

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : US FDA APPROVED · Should be on a .014” wire · Should be made of polyurethane with radio-opaque nitinol loop · Should be suspended on the .014” wire with a suspension arm · Should not occlude flow while in placement · Should be rapid exchange type · Should be compatible with a 6 F guiding catheter (0.066” ID) · Should allow optimal filtration in vessels 3.5 – 5.5 mm size

DISTAL NEURO-PROTECTION DEVICE FOR EMBOLIC PROTECTION (FILTER) : CE APPROVED · Should be on a .014” wire · Should be made of polyurethane with radio-opaque nitinol loop · Should be suspended on the .014” wire with a suspension arm · Should not occlude flow while in placement · Should be rapid exchange type · Should be compatible with a 6 F guiding catheter (0.066” ID) · Should allow optimal filtration in vessels 3.5 – 5.5 mm size

CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : DCGI APPROVED · Should have hydrophilic coating · Should be available in various outer diameters and balloon lengths and various shaft lengths

CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : US FDA APPROVED · Should have hydrophilic coating · Should be available in various outer diameters and balloon lengths and various shaft lengths

CAROTID ANGIOPALSTY BALLOON CATHETER (Over The Wire/Rapid Excahnge) : CE APPROVED · Should have hydrophilic coating · Should be available in various outer diameters and balloon lengths and various shaft lengths

CAROTID SELF EXPENDABLE STENTS: DCGI APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS: US FDA APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS: CE APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length Should be on a shaft length of 80-140 or above length

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

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

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

CAROTID SELF EXPENDABLE STENTS – DCGI APPROVED · Should be 0.035” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS – US FDA APPROVED · Should be 0.035” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS – CE APPROVED · Should be 0.035” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID STENTS BALLOON EXPENDABLE – DCGI APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID STENTS BALLOON EXPENDABLE – US FDA APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID STENTS BALLOON EXPENDABLE – CE APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

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

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

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

CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: DCGI APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: US FDA APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

CAROTID SELF EXPENDABLE STENTS WITH TAPERED DIAMETER: CE APPROVED · Should be 0.014” compatible · Should be over the wire and rapid exchange (OTW/RX) · Should be available in various diameters and length · Should be on a shaft length of 80-140 or above length

PERIPHERAL Balloon Expandable STENT – (OTW/RX): DCGI APPROVED · Should be 0.014/0.018” compatible · Should over the wire · Should be made of cobalt chromium / Bare · Should have balloon OD available in 4-7 mm · Should have balloon/stent lengths of 12-18 mm · Should have shaft lengths of 80-150 cm

PERIPHERAL Balloon Expandable STENT – (OTW/RX): US FDA APPROVED · Should be 0.014/0.018” compatible · Should over the wire · Should be made of cobalt chromium / Bare· Should over the wire · Should have balloon OD available in 4-7 mm · Should have balloon/stent lengths of 12-18 mm · Should have shaft lengths of 80-150 cm

PERIPHERAL Balloon Expandable STENT – (OTW/RX): CE APPROVED · Should be 0.014/0.018” compatible · Should over the wire · Should be made of cobalt chromium / Bare · Should have balloon OD available in 4-7 mm · Should have balloon/stent lengths of 12-18 mm · Should have shaft lengths of 80-150 cm

Group–C: ANEURYSMS COILS& ADHESIVES All 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.

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : DCGI APPROVED

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : US FDA APPROVED

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.007”- 0.010”) : CE APPROVED

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : DCGI APPROVED

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : US FDA APPROVED

SPECIAL MICRO GUIDEWIRE WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.014”). : CE APPROVED

SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : DCGI APPROVED

SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : US FDA APPROVED

SPECIAL MICRO GUIDEWIRE (EXCHANGE LENGTH- 260- 300 CMs) WITH TORQUE DEVICE FOR USE WITH MICROCATHETERS (SIZE: 0.010”- 0.014’) : CE APPROVED

SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : DCGI APPROVED

SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : US FDA APPROVED

SPECIAL MICRO GUIDEWIRE WITH DOCING DEVICE : CE APPROVED

ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : DCGI APPROVED

ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : US FDA APPROVED

ELECTROLYTE DETACHABLE 3-D TYPE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : CE APPROVED

ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : DCGI APPROVED

ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : US FDA APPROVED

ELECTROLYTE DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED/BIOACTIVE PLATINUM COILS : CE APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : DCGI APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : US FDA APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- NON-BIOACTIVE PLATINUM COILS : CE APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : DCGI APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : US FDA APPROVED

THERMO MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM COILS : CE APPROVED

MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : DCGI APPROVED SHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER

MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : US FDA APPROVED SHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER

MECHANICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- BARE PLATINUM : CE APPROVED SHOULD BE AVAILABLE FROM VARIOUS SIZES FROM 1.0 MM – 4.0MM DIAMETER

MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : DCGI APPROVED

MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : US FDA APPROVED

MACHENICAL DETACHABLE COILS FOR INTRACRANIAL ANEURYSMS TREATMENT- COATED PLATINUM COILS : CE APPROVED

PUSHABLE COILS TO BE USED WITH COIL PUSHERS : DCGI APPROVED

PUSHABLE COILS TO BE USED WITH COIL PUSHERS : US FDA APPROVED

PUSHABLE COILS TO BE USED WITH COIL PUSHERS : CE APPROVED

COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : DCGI APPROVED

COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : US FDA APPROVED

COIL PUSHERS FOR DETACHABLE PUSHABLE/EMBOLIZATION COILS : CE APPROVED

POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : DCGI APPROVED

POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : US FDA APPROVED

POWER SUPPLY ACCESSORIES AND CONNECTING CABLES FOR DETACHABLE COILS : CE APPROVED

DETACHABLE BALLOON CATHETER : DCGI APPROVED

DETACHABLE BALLOON CATHETER : US FDA APPROVED

DETACHABLE BALLOON CATHETER : CE APPROVED

DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : DCGI APPROVED

DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : US FDA APPROVED

DETACHABLE BALLOON MICROCATHETER FOR DETACHABLE BALLOONS : CE APPROVED

TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : DCGI APPROVED

TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : US FDA APPROVED

TISSUE ADHESIVE FOR AVMs/AVFs/DAVFs/TUMOR-EMBOLIZATION (N-BUTYL CYANOACRYLATE) : CE APPROVED

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

POLY VINYL ALCOHOL (PVA) PARTICLES FOR PRE-OPERATIVE TUMOUR EMBOLIZATION : US FDA APPROVED

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

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

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

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

LIPIDOL ULTRA FLUID : DCGI APPROVED

LIPIDOL ULTRA FLUID : US FDA APPROVED

LIPIDOL ULTRA FLUID : CE APPROVED

Group-D: STENTS& BALLOONS FOR CRANIAL USE All 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.

DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : DCGI APPROVED

DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : US FDA APPROVED

DOUBLE LUMEN BALLOON ANGIOPLASTY CATHETER FOR INTRA-CRANIAL USE : CE APPROVED

BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : DCGI APPROVED

BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : US FDA APPROVED

BALLOONANGIOPALSTY CATHETER FOR EXTRA-CRANIAL USE : CE APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON) : DCGI APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON) : US FDA APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : SINGLE LUMEN (FOR WIRE & BALLOON): CE APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : DCGI APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : US FDA APPROVED

OCCLUSION BALLOONS FOR FLOW MODIFICATION/ ASSISTANCE FOR TREATMENT OF WIDE NECK INTRACRANIAL ANEURYSM : DOUBLE LUMEN (FOR WIRE & BALLOON) : CE APPROVED

OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED · SHOULD HAVE OPEN CELL DESIGN · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED · SHOULD HAVE OPEN CELL DESIGN · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

OPEN CELL DESIGN INTRA-CRANIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED · SHOULD HAVE OPEN CELL DESIGN · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED · SHOULD BE COMPITABLE FOR LARGE VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED · SHOULD BE COMPITABLE FOR LARGE VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED · SHOULD BE COMPITABLE FOR LARGE VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – DCGI APPROVED · SHOULD BE COMPITABLE FOR SMALL VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – US FDA APPROVED · SHOULD BE COMPITABLE FOR SMALL VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

CLOSED CELL DESIGN INTRA-CRENIALSTENTS FOR STENT ASSISTED COILING OF ANEURYSMS – CE APPROVED · SHOULD BE COMPITABLE FOR SMALL VESSEL · SHOULD BE AVAILBLE IN VARIOUS SIZES & DIAMETER

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : DCGI APPROVED

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : US FDA APPROVED

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: COMPLETELY RETRIEVABLE : CE APPROVED

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : DCGI APPROVED

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : US FDA APPROVED

INTRA-CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLEFOR LARGE VESSEL : CE APPROVED

INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : DCGI APPROVED

INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : US FDA APPROVED

INTRA -CRANIAL STENT FOR STENT ASSISTED COILING OF ANEURYSMS: PARTIALLY RETRIEVABLE FOR SMALL VESSEL : CE APPROVED

EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : DCGI APPROVED

EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : US FDA APPROVED

EXTRA-CRANIAL STENT FOR CAROTID & VERTEBRAL ARTERIES & DURAL SINUSES: SELF EXPANDABLE & CLOSED CELL DESIGN : CE APPROVED

EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : DCGI APPROVED

EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : US FDA APPROVED

EXTRA-CRANIAL BARE METAL STENT FOR CAROTID & VERTEBRAL ARTERIES & OSTEAL LESIONS: BALLOON MOUNTED : CE APPROVED

SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : DCGI APPROVED

SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : US FDA APPROVED

SELF EXPANDABLE INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRANIAL VESSELS : CE APPROVED

BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : DCGI APPROVED

BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : US FDA APPROVED

BALLOON MOUNTED INTRA-CRANIAL STENT FOR TREATMENT OF ATHEROSCLEROTIC STENOTIC LESIONS OF INTRACRENIAL VESSELS : CE APPROVED

STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : DCGI APPROVED

STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : US FDA APPROVED

STENT-GRAFT (Covered Stent) FOR PSEUDO ANEURYSM OR FISTULA TREATMENT : CE APPROVED

FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : DCGI APPROVED

FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : US FDA APPROVED

FLOW DIVERTER FOR INTRACRANIAL ANEURYSM TREATMENT : CE APPROVED

Group –E: CLOT RETRIEVAL DEVICES FOR THROMBACTOMY All 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.

REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY: DCGI APPROVED

REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY : US FDA APPROVED

REVASCULARIZATION DEVICE FOR MECHANICAL THROMBECTOMY : CE APPROVED

ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : DCGI APPROVED

ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : US FDA APPROVED

ENDO VASCULAR SNARES FOR RETRIEVAL OF INTRAVASCULAR FORIEGN OBJECT : CE APPROVED

THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : DCGI APPROVED

THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : US FDA APPROVED

THROMBUS SUCTION CATHETERS FOR CLOT RETRIEVAL FROM CAROTID & VERTEBRALS : CE APPROVED

INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : DCGI APPROVED

INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : US FDA APPROVED

INFUSION CATHETERS FOR MOTORIZED FRAGMENTATION AND SUCTION FOR CLOT RETRIEVAL WITH SEPARATOR : CE APPROVED

STENT RETRIEVER FOR THROMBECTOMY : DCGI APPROVED

STENT RETRIEVER FOR THROMBECTOMY : US FDA APPROVED

STENT RETRIEVER FOR THROMBECTOMY : CE APPROVED

WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : DCGI APPROVED

WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : US FDA APPROVED

WEB DEVICE INTRA SACCULAR – AVAILABLE IN ASSORTED SIZES : CE APPROVED

Group – F: EMBOLIZATION/AVMs All 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.

Group - G All 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.

INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length)-DCGI APPROVED · Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. · 10-11 cm long for Femoral Access · Pack must include 18 G or more, 6-7.5 cm long puncture needle · 0.035 or 0.038" spring guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - US FDA APPROVED · Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. · 10-11 cm long for Femoral Access · Pack must include 18 G or more, 6-7.5 cm long puncture needle · 0.035 or 0.038" spring guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (4 Fr- 9Fr) (standard length) - CE APPROVED · Sizes 4 French/5 French/ 6 French/ 7 French/ 8 French/ 9 French. · 10-11 cm long for Femoral Access · Pack must include 18 G or more, 6-7.5 cm long puncture needle · 0.035 or 0.038" spring guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion With smooth and resistance free insertion

INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - DCGI APPROVED · 10-11 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - US FDA APPROVED · 10-11 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTODUCER SHEATH FOR ADULTS (10 Fr. – 11 Fr) - CE APPROVED · 10-11 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) – DCGI APPROVED · Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. · Sheath should be between 20-30 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - US FDA APPROVED · Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. · Sheath should be between 20-30 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

LONG INTRODUCER SHEATH (20-30 cm long)(Size 5Fr.-9Fr) - CE APPROVED · Sizes 5 French/ 6 French/ 7 French/ 8 French/ 9 French. · Sheath should be between 20-30 cm long · 0.035 or 0.038 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

TRANS RADIAL INTRODUCER SHEETHS – DCGI APPROVED · Sizes 4 French/5 French/ 6 French. · 7.0 cm long for Radial & Brachial Access · Pack must include 18/20 G, 6-7.5 cm long puncture needle · 0.025-.038 inch guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

TRANS RADIAL INTRODUCER SHEETHS -US FDA APPROVED · Sizes 4 French/5 French/ 6 French. · 7.0 cm long for Radial & Brachial Access · Pack must include 18/20 G, 6-7.5 cm long puncture needle · 0.025-.038 inch guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

TRANS RADIAL INTRODUCER SHEETHS – CE APPROVED · Sizes 4 French/5 French/ 6 French. · 7.0 cm long for Radial & Brachial Access · Pack must include 18/20 G, 6-7.5 cm long puncture needle · 0.025-.038 inch guide wire compatible · With cross cut design haemostatic valve prevent back leak and air aspiration · snap on dialator lock with Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

LONG BRADED INTRODUCER SHEATH – DCGI APPROVED · Sizes 6 French/7 French / 8 French 9 French and above · Should be up to 90 cm · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

LONG BRADED INTRODUCER SHEATH – US FDA APPROVED · Sizes 6 French/7 French / 8 French 9 French and above · Should be up to 90 cm · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

LONG BRADED INTRODUCER SHEATH – CE APPROVED · Sizes 6 French/7 French / 8 French 9 French and above · Should be up to 90 cm · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion

GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – DCGI APPROVED

GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – US FDA APPROVED

GLIDE SHEATH SLINDER WITH PUNCHAR NEEDLE 6 French/7French – CE APPROVED

STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - DCGI APPROVED · Sizes from 4fr/5 fr/6Fr/ 7Fr · Between 7-11 cm long · With 0.025 - 0.038 inch guide wire compatible · With Radio-opaque tip · Should be for both Paediatric and Adult use

STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING –CE APPROVED · Sizes from 4fr/5 fr/6Fr/ 7Fr · Between 7-11 cm long · With 0.025 - 0.038 inch guide wire compatible · With Radio-opaque tip · Should be for both Paediatric and Adult use

STRAIGHT REINFORCED SHEATH WITH HYDROPHILIC COATING - US FDA APPROVED · Sizes from 4fr/5 fr/6Fr/ 7Fr · Between 7-11 cm long · With 0.025 - 0.038 inch guide wire compatible · With Radio-opaque tip · Should be for both Paediatric and Adult use

INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVED · Sizes 4 French/ 5 French/ 6 French/ 7 French · Between 7-11 cm long for Radial & Brachial Access · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DGCI APPROVED · Sizes 4 French/ 5 French/ 6 French/ 7 French · Between 7-11 cm long for Radial & Brachial Access · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS –US FDA APPROVED · Sizes 4 French/ 5 French/ 6 French/ 7 French · Between 7-11 cm long for Radial & Brachial Access · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · Integral side port with attached 3-way stopcock · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · With smooth and resistance free insertion

LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - US FDA APPROVED · Sizes 4 French/5 French /6 French/7 French · Between 16-24 cm long · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · Should have smooth and resistance free insertion

LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - CE APPROVED · Sizes 4 French/5 French /6 French/7 French · Between 16-24 cm long · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · Should have smooth and resistance free insertion

LONG INTRODUCER SHEATH DEDICATED FOR TRANSRADIAL ACCESS - DCGI APPROVED · Sizes 4 French/5 French /6 French/7 French · Between 16-24 cm long · 0.021 or 0.025 inch guide wire compatible · With haemostatic valve to prevent back leak and air aspiration · With integral side port with attached 3-way stopcock · With suture eye for securing sheath · Kink resistant · With dilator-hub lock mechanism to prevent its back-out during insertion · Should have smooth and resistance free insertion

PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - DCGI APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be between 145-180 cm long · Should be available as straight & J-Shaped tip · Should be available in variable lengths of flexible/floppy end · Should be available in variable J tip sizes · Should be available fixed as well as movable core.

PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - US FDA APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be between 145-180 cm long · Should be available as straight & J-Shaped tip · Should be available in variable lengths of flexible/floppy end · Should be available in variable J tip sizes · Should be available fixed as well as movable core

PTFE COATED DIAGNOSTIC GUIDE WIRE – (REGULAR LENGTH & STIFFNESS) - CE APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be between 145-180 cm long · Should be available as straight & J-Shaped tip · Should be available in variable lengths of flexible/floppy end · Should be available in variable J tip sizes · Should be available fixed as well as movable core

PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - DCGI APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be 240-300 cm long · Should be available as straight or J-Shaped tip · Should be available fixed as well as movable core.

PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - US FDA APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be 240-300 cm long · Should be available as straight or J-Shaped tip Should be available fixed as well as movable core.

PTFE COATED DIAGNOSTIC GUIDE WIRE – (EXCHANGE LENGTH, REGULAR STIFFNESS) - CE APPROVED · Should be available in 0.025, 0.032, 0.035 and 0.038 inches size · Should be 240-300 cm long · Should be available as straight or J-Shaped tip Should be available fixed as well as movable core.

HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) – DCGI APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have Super elastic Nitinol alloy · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 120-150 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) – US FDA APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have Super elastic Nitinol alloy · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 120-150 cm long

HYDROPHILIC DIAGNOSTIC GUIDE WIRE –TARUMO TYPE M Coating (REGULAR LENGTH &STIFFNESS) – CE APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have Super elastic Nitinol alloy · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 120-150 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - DCGI APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 150-180 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - US FDA APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 150-180 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (REGULAR LENGTH) – - CE APPROVED · Must be available in 0.018, 0.025, 0.032, 0.035 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · should be between 150-180 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - DCGI APPROVED · Must be available in 0.018, 0.025, 0.032 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 260cm, 300 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - US FDA APPROVED · Must be available in 0.018, 0.025, 0.032 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 260cm, 300 cm long

RADIOFOCUS MINIPLASTIC GUIDEWIRE TARUMO TYPE M Coating (LONG LENGTH) – - CE APPROVED · Must be available in 0.018, 0.025, 0.032 and 0.038 inches size · Should have super elastic alloy core · Should have super flexible wire tip · Should be available in straight and angled tip · Should be between 260cm, 300 cm long

JUDKINS CATHETER (JR JL & PIGTAIL)-DCGI APPROVED · 4 French/5 French /6 French/7 French/8French size · Left and Right judkins catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

JUDKINS CATHETER (JR JL & PIGTAIL)- US FDA APPROVED · 4 French/5 French /6 French/7 French/8French size · Left and Right judkins catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

JUDKINS CATHETER (JR JL & PIGTAIL)-CE APPROVED · 4 French/5 French /6 French/7 French/8French size · Left and Right judkins catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

MULTIPURPOSE CATHETER - - DCGI APPROVED · 4 French/5 French /6 French/7 Frenchsize · Multipurpose catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

MULTIPURPOSE CATHETER - - US FDA APPROVED · 4 French/5 French /6 French/7 Frenchsize · Multipurpose catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

MULTIPURPOSE CATHETER - - CE APPROVED · 4 French/5 French /6 French/7 Frenchsize · Multipurpose catheters in various standard curves and lengths even for pediatric cases · Must have Double mesh construction with Ultra-thin wall

TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – DCGI APPROVED · 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths · dedicated for angiography of right and left coronary arteries using either radial or brachial approach

TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – US FDA · 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths · dedicated for angiography of right and left coronary arteries using either radial or brachial approach

TRANSRADIAL DIAGNOSTIC CORONARY CATHETER – CE APPROVED · 4 French/5 French /6 French diagnostic coronary catheters with TIG curved and All lengths · dedicated for angiography of right and left coronary arteries using either radial or brachial approach

ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - DCGI APPROVED · Should be soft and kink resistant · Should give reliable pressure measurements · Should be available in sizes of 100, 150 & 200 cm · Should have male luer lock connection at one end and a female luer lock connection at the other end · Should meet highest medical industrial standards for arterial pressure lines

ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - US FDA APPROVED · Should be soft and kink resistant · Should give reliable pressure measurements · Should be available in sizes of 100, 150 & 200 cm · Should have male luer lock connection at one end and a female luer lock connection at the other end · Should meet highest medical industrial standards for arterial pressure lines

ARTERIAL PRESSURE MONITOR LINES (100, 150 & 200 cm long) – - CE APPROVED · Should be soft and kink resistant · Should give reliable pressure measurements · Should be available in sizes of 100, 150 & 200 cm · Should have male luer lock connection at one end and a female luer lock connection at the other end · Should meet highest medical industrial standards for arterial pressure lines

ACT TUBES - DCGI APPROVED · Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota · Should meet highest medical industrial standards · Quality certification should be provided from authorized agencies.

ACT TUBES - US FDA APPROVED · Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota · Should meet highest medical industrial standards Quality certification should be provided from authorized agencies

ACT TUBES - CE APPROVED · Disposable ACT tubes compatible with existing machines at Cath lab at GMC Kota · Should meet highest medical industrial standards Quality certification should be provided from authorized agencies

MANIFOLD with 3 Port - DCGI APPROVED · Three side port manifold · One luer lock control syringe (10 or 15 ml) for contrast injection · One three way stop-cock

MANIFOLD with 3 Port - US FDA APPROVED · Three side port manifold · One luer lock control syringe (10 or 15 ml) for contrast injection · One three way stop-cock

MANIFOLD with 3 Port - CE APPROVED · Three side port manifold · One luer lock control syringe (10 or 15 ml) for contrast injection · One three way stop-cock

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

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

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

AMPLATZ CATHETER · 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. · Must be US FDA APPROVED

AMPLATZ CATHETER · 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. · Must be CE APPROVED

AMPLATZ CATHETER · 4 French/5 French/6 French/7 French/8 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. · Must be DCGI APPROVED

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

DISPOSABLE ECG ELECTODES FOR ADULTS – US FDA APPROVED · Wet gel electrodes · Should be porous and breathable · Should conform to or exceed the highest industrial standard for ECG electrodes, · Quality certification from authorized agencies to be provided

DISPOSABLE ECG ELECTODES FOR ADULTS – - CE APPROVED · Wet gel electrodes · Should be porous and breathable · Should conform to or exceed the highest industrial standard for ECG electrodes, · Quality certification from authorized agencies to be provided

SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kota DCGI Approved · Should be compatible with existing machines at GMC kota Cath Lab

SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaUS FDA APPROVED · Should be compatible with existing machines at GMC kota Cath Lab

SYRINGE FOR PRESSURE INJECTOR INSTALLED IN GMC kotaCE APPROVED · Should be compatible with existing machines at GMC kota Cath Lab

TRANS RADIAL ANGIOGRAPHY KIT – DCGI Approved · Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. Kit Must include in one pack - 1. 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) 2. 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) 3. 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) 4. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). 5. One Piece MANIFOLD with 3 Port (Three side port) 6. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection

TRANS RADIAL ANGIOGRAPHY KIT –US FDA Approved · Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. Kit Must include in one pack - 7. 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) 8. 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) 9. 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) 10. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). 11. One Piece MANIFOLD with 3 Port (Three side port) 12. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection

TRANS RADIAL ANGIOGRAPHY KIT – CE Approved · Should be compatible for Angiography of right and left coronary arteries using either radial or brachial approach. Kit Must include in one pack - 13. 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) 14. 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) 15. 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) 16. One Piece ARTERIAL PRESSURE MONITOR LINES (150 & 200 cm long). 17. One Piece MANIFOLD with 3 Port (Three side port) 18. One Pieceluer lock control syringe (10 or 12 ml) for contrast injection

PIGTAIL CATHETER (PEDIATRIC/Adult ) –DCGI Approved APPROVED · Sizes 3 French/ 4 French/ 5 French/ 6 French · Smaller length for neonatal and pediatric use

PIGTAIL CATHETER (PEDIATRIC/Adult ) –US FDA APPROVED · Sizes 3 French/ 4 French/ 5 French/ 6 French · Smaller length for neonatal and pediatric use

PIGTAIL CATHETER (PEDIATRIC/Adult ) –CE APPROVED · Sizes 3 French/ 4 French/ 5 French/ 6 French · Smaller length for neonatal and pediatric use

PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- DCGI Approved. · Should be available in 0.032/0.035/0.038 inches size · Should be between 240-300 cm long · Should be available as straight & J-Shaped tip

PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- US FDA APPROVED. · Should be available in 0.032/0.035/0.038 inches size · Should be between 240-300 cm long · Should be available as straight & J-Shaped tip

PTFE COATEDAMPLATZ TYPE GUIDE WIRE – (EXCHANGE LENGTH, SUPER STIFF SHAFT STRENGTH)- CE APPROVED. · Should be available in 0.032/0.035/0.038 inches size · Should be between 240-300 cm long · Should be available as straight & J-Shaped tip

INTERNAL MAMMARY CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be US FDA APPROVED

INTERNAL MAMMARY CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be CE APPROVED

INTERNAL MAMMARY CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be DCGI APPROVED

BY-PASS GRAFT CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be US FDA APPROVED

BY-PASS GRAFT CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be CE APPROVED

BY-PASS GRAFT CATHETER · 4 French/5 French/6 French/7 French/8 French in various standard curves and lengths. · Must be DCGI APPROVED

Group-H All 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.

PTCA Guiding catheter– DCGI APPROVED . · Should be braided with low friction Inner Layer of PTFE · Should have atraumatic soft tip · Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. · Should have diameter 5 French/ 6 French/7 French/ 8French available · Should have All various lengths

PTCA Guiding catheter–US FDA APPROVED · Should be braided with low friction Inner Layer of PTFE · Should have atraumatic soft tip · Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. · Should have diameter 5 French/ 6 French/7 French/ 8French available · Should have All various lengths

PTCA Guiding catheter–CE APPROVED · Should be braided with low friction Inner Layer of PTFE · Should have atraumatic soft tip · Should be available in various tip shapes and curves for access to different parts of the peripheral vasculature, including renal duble curve, cobra, multi-purpose and other shapes. · Should have diameter 5 French/ 6 French/7 French/ 8French available · Should have All various lengths

Radial Guiding catheter Ikari curve - DCGI APPROVED · Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. · Should be braided with low friction inner layer · Should have atraumatic soft tip. · Should have all the lengths and in diameter 5 French/ 6 French available

Radial Guiding catheter Ikari curve - DCGI APPROVED & US FDA/CE APPROVED · Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. · Should be braided with low friction inner layer · Should have atraumatic soft tip. · Should have all the lengths and in diameter 5 French/ 6 French available

Radial Guiding catheter Ikari curve - US FDA APPROVEDZ · Should be available in Ikari Left &Ikari Right Curve with Extra backup in Radial route. · Should be braided with low friction inner layer · Should have atraumatic soft tip. · Should have all the lengths and in diameter 5 French/ 6 French available

Mother & Child Catheter – - CE APPROVED · With reliable support with large inner lumen and inner PTSE.

Mother & Child Catheter – - US FDA APPROVED · With reliable support with large inner lumen and inner PTSE.

Mother & Child Catheter – - DCGI APPROVED · With reliable support with large inner lumen and inner PTSE.

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

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

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

PTCA INFLATION DEVICE - DCGI APPROVED · Efficient locking system to maintain high pressure · Rapid inflation and deflation · Clear barrel for easy visualization of de-bubbling · Luminescent analog pressure gauge (up to 30 Atm) · Ergomatric and use friendly hand held design.

PTCA INFLATION DEVICE - US FDA APPROVED · Efficient locking system to maintain high pressure · Rapid inflation and deflation · Clear barrel for easy visualization of de-bubbling · Luminescent analog pressure gauge (up to 30 Atm) · Ergomatric and use friendly hand held design.

PTCA INFLATION DEVICE - CE APPROVED · Efficient locking system to maintain high pressure · Rapid inflation and deflation · Clear barrel for easy visualization of de-bubbling · Luminescent analog pressure gauge (up to 30 Atm) · Ergomatric and use friendly hand held design.

TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –DCGI APPROVED · Should accommodate virtually all interventional devices · Luer connector at the guiding catheter end · Rotating adapter at the guiding catheter end · Should have bleed back safety mechanism · Stepwise control for open, semi-open and closed position

TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –US FDA APPROVED · Should accommodate virtually all interventional devices · Luer connector at the guiding catheter end · Rotating adapter at the guiding catheter end · Should have bleed back safety mechanism · Stepwise control for open, semi-open and closed position

TUOHY BORST (HAEMOSTATIC Y-CONNECTOR) FOR PTCA – PUSH PULL MECHANISM –CE APPROVED · Should accommodate virtually all interventional devices · Luer connector at the guiding catheter end · Rotating adapter at the guiding catheter end · Should have bleed back safety mechanism · Stepwise control for open, semi-open and closed position

HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –DCGI APPROVED · Should accommodate virtually all interventional devices · Two ports for insertion of interventional devices · Luer connector at the guiding catheter end

HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –US FDA APPROVED · Should accommodate virtually all interventional devices · Two ports for insertion of interventional devices · Luer connector at the guiding catheter end

HEMOSTATIC Y ADAPTER WITH Screw Type BUTTON –CE APPROVED · Should accommodate virtually all interventional devices · Two ports for insertion of interventional devices · Luer connector at the guiding catheter end

DRUG DELIVERY/INFUSION CATHETER - DCGI APPROVED

DRUG DELIVERY/INFUSION CATHETER - US FDA APPROVED

DRUG DELIVERY/INFUSION CATHETER - CE APPROVED

PTCA GUIDING CATHETER - DCGI APPROVED · Should be available in Sizes of 5 French/6 fr/7fr/8fr · Should be braided with low friction Inner Layer of PTFE · All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others · Should also have availability of smaller length catheters (90 cm) & Regular length sizes. · Should also have availability of catheters with side holes · Should also have short tip catheters

PTCA GUIDING CATHETER - US FDA APPROVED · Should be available in Sizes of 5 French/6 fr/7fr/8fr · Should be braided with low friction Inner Layer of PTFE · All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others · Should also have availability of smaller length catheters (90 cm) & Regular length sizes. · Should also have availability of catheters with side holes · Should also have short tip catheters

PTCA GUIDING CATHETER - CE APPROVED · Should be available in Sizes of 5 French/6 fr/7fr/8fr · Should be braided with low friction Inner Layer of PTFE · All possible shapes including : Judkin’s left and right, Extra back up support, Amplatz, Multipurpose, Hockey stick, and others · Should also have availability of smaller length catheters (90 cm) & Regular length sizes. · Should also have availability of catheters with side holes · Should also have short tip catheters

PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. - DCGI APPROVED

PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. - US FDA APPROVED

PTCA GUIDE WIRE - Entry profile Diameter 0.014” and 180 cm length and Hydrophilic coating. - CE APPROVED

EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- DCGI APPROVED · Should be Dedicated for externalization with tip load of 3g/force

EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- US FDA APPROVED · Should be Dedicated for externalization with tip load of 3g/force

EXTENSIIONPTCA WIRE WITHEXTRA LENGTH (Up to 330cm)- CE APPROVED · Should be Dedicated for externalization with tip load of 3g/force

Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating -- DCGI APPROVED · Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. · Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures · Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip.

Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating -- US FDA APPROVED · Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. · Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures · Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip.

Special PTCA GUIDE WIRE with 0.014” Diameter and 180 cm length with Hydrophilic coating -- CE APPROVED · Should have directly jointed SUS and Nitinol shaft throughDuo Core technology. · Should have one to one Torque Transmission and Hydrophilic M Type coating for Radial procedures · Should have Floppy tip, Tip load of 0.6gf - 1.0 gf with Silicon coating for 2mm from the tip.

Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED · .014" One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve.

Specialized PTCA Guide wire for Retrograde approach & CTO –US FDA APPROVED · .014" One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve.

Specialized PTCA Guide wire for Retrograde approach & CTO –CE APPROVED · .014" One Piece core wire with joint less spring coil 22cm polymer sleeve length with slip coat coating over the polymer Sleve.

Specialized PTCA Guide wire for Retrograde approach & CTO – DCGI APPROVED · PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g

Specialized PTCA Guide wire for Retrograde approach & CTO – US FDA APPROVED · PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g

Specialized PTCA Guide wire for Retrograde approach & CTO –CE APPROVED · PTCA Guide Wire with SION TECH Technology -Tapered Type, Polymer sleeve, Tip Load 1.0g

Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO – DCGI APPROVED · 0.010" One Piece core wire with joint less Spring coil with SION TECH technology · cone tip with a tip load of 1.7gm and tip Radiopacity 15cm.

Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO – US FDA APPROVED · 0.010" One Piece core wire with joint less Spring coil with SION TECH technology · cone tip with a tip load of 1.7gm and tip Radiopacity 15cm.

Specialized PTCA Guide wire (190cm length) for Retrograde approach & CTO CE APPROVED · 0.010" One Piece core wire with joint less Spring coil with SION TECH technology · cone tip with a tip load of 1.7gm and tip Radiopacity 15cm.

· Special PTCA Guide Wire with Twister® core wire technology for facilitates navigation and torqueability for optimal precision- US FDA

· Special PTCA Guide Wire with Twister® core wire technology for facilitates navigation and torqueability for optimal precision-CE approved

· Spacial PTCA Guide Wire with Stainless Steel Spring Coil Design. US FDA /DCGI approved

· Spacial PTCA Guide Wire with Stainless Steel Spring Coil Design. CE/DCGI approved

HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – US FDA APPROVED. · 0.014 inches · Nitinol alloy · With angled tip 3-5 cm long · Tip with platinum/platinum alloy for optimum visualization · With TFE coating · 180 cm long

HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – CE APPROVED. · 0.014 inches · Nitinol alloy · With angled tip 3-5 cm long · Tip with platinum/platinum alloy for optimum visualization · With TFE coating · 180 cm long

HEAVY DUTY NITINOL ALLOY EXTRA SUPPORT WIRE (RAGULAR LANGTH) – DCGI APPROVED. · 0.014 inches · Nitinol alloy · With angled tip 3-5 cm long · Tip with platinum/platinum alloy for optimum visualization · With TFE coating · 180 cm long

DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED · Disposable transducers for invasive pressure monitoring · SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota · Should meet highest medical industrial standards · Quality certification should be provided form authorized agencies

DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - US FDA APPROVED · Disposable transducers for invasive pressure monitoring · SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota · Should meet highest medical industrial standards · Quality certification should be provided form authorized agencies

DISPOSABLE TRANSDUCERS FOR INVASIVE PRESSURE MONITORING - CE APPROVED · Disposable transducers for invasive pressure monitoring · SHOULD BE COMPATIBLE WITH AVAILABLE SYSTEM IN CATH LAB at GMC kota · Should meet highest medical industrial standards · Quality certification should be provided form authorized agencies

DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - DCGI APPROVED · Should be compatible with existing available system · Should meet or exceed highest standards · Quality certification from authorized agencies to be provided

DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - CE APPROVED · Should be compatible with existing available system · Should meet or exceed highest standards · Quality certification from authorized agencies to be provided

DOMES FOR TRANSDUCER FOR INVASIVE PRESSURE MONITORING - US FDA APPROVED · Should be compatible with existing available system · Should meet or exceed highest standards · Quality certification from authorized agencies to be provided

Group – I All 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.

PTCA BALLOON (SEMI-COMPLIANT) - DCGI APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Should have Hydrophilic coating and Fixed outer and inner tube. · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less · Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm · Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above)

PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Should have Hydrophilic coating and Fixed outer and inner tube. · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less · Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm · Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above)

PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Should have Hydrophilic coating and Fixed outer and inner tube. · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less · Should be Available in the various diameter sizes from 1.25- 4 mm and lengthsminimum from 06mm - 20mm · Should have high nominal pressure and High Rated Burst Pressure too (RBP -18 atm or Above)

PTCA BALLOON (NON-COMPLIANT) – - DCGI APPROVED · Quote both monorail (rapid exchange) and OTW balloons · Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm · Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. · Should have triple layer balloon technology for high pressure resistance

PTCA BALLOON (NON-COMPLIANT) – - US FDA APPROVED · Quote both monorail (rapid exchange) and OTW balloons · Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm · Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. · Should have triple layer balloon technology for high pressure resistance

PTCA BALLOON (NON-COMPLIANT) – - CE APPROVED · Quote both monorail (rapid exchange) and OTW balloons · Available in all sizes from 2 – 5 mm, & All variable minimum from 06mm - 20mm · Should have a high nominal pressure and Very High Rated Burst Pressure (RBP -22 atm or Above) · With very thin distal tip with low entry profile of 0.43 mm or 0.16” or less. · Should have triple layer balloon technology for high pressure resistance

SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - DCGI APPROVED · Must have Ultra-low entry profile of 0.016” · Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm · Quote both monorail (rapid exchange) and OTW balloons · Should be available in all sizes& All variable lengths up to 20mm

SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - US FDA APPROVED · Must have Ultra-low entry profile of 0.016” · Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm · Quote both monorail (rapid exchange) and OTW balloons · Should be available in all sizes& All variable lengths up to 20mm

SPECIAL PTCA BALLOON CATHETER WITH LOW CROSSING PROFILE - CE APPROVED · Must have Ultra-low entry profile of 0.016” · Low crossingProfile should remain same for higher diameter sizes from 1.25 mm- 2.25mm · Quote both monorail (rapid exchange) and OTW balloons · Should be available in all sizes& All variable lengths up to 20mm

SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - DCGI APPROVED · Must have Ultra-low entry profile of 0.016” · Should be available in variable balloon lengths minimum from 06mm - 20mm · Quote both monorail (rapid exchange) and OTW balloons · Should have R.B.P -18atm or Above

SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - US FDA APPROVED · Must have Ultra-low entry profile of 0.016” · Should be available in variable balloon lengths minimum from 06mm - 20mm · Quote both monorail (rapid exchange) and OTW balloons · Should have R.B.P -18atm or Above

SPECIAL PTCA BALLOON CATHETER OF LESS THAN 1.5 MM - CE APPROVED · Must have Ultra-low entry profile of 0.016” · Should be available in variable balloon lengths minimum from 06mm - 20mm · Quote both monorail (rapid exchange) and OTW balloons · Should have R.B.P -18atm or Above

ZEROFOLD PTCA BALLOON - DCGI APPROVED APPROVED · Available in all sizes and length · Quote both monorail (rapid exchange) and OTW balloons

ZEROFOLD PTCA BALLOON - US FDA APPROVED · Available in all sizes and length · Quote both monorail (rapid exchange) and OTW balloons

ZEROFOLD PTCA BALLOON - CE APPROVED · Available in all sizes and length · Quote both monorail (rapid exchange) and OTW balloons

SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - DCGI APPROVED · Must have Ultra-low entry profile of 0.016” · Quote both monorail (rapid exchange) and OTW balloons · Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. · Should have high RBP -18 Atm or Above

SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - US FDA APPROVED · Must have Ultra-low entry profile of 0.016” · Quote both monorail (rapid exchange) and OTW balloons · Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. · Should have high RBP -18 Atm or Above

SPECIAL PTCA BALLOON FOR RETROGRADE & CTO – - CE APPROVED · Must have Ultra-low entry profile of 0.016” · Quote both monorail (rapid exchange) and OTW balloons · Should be available in variable balloon diameter from 1.0mm & lengths minimum from 06mm. · Should have high RBP -18 Atm or Above

CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) -DCGI APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - US FDA APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

CUTTING BALLOON FOR PTCA HAVING MICROSURGICAL ATHEROTOMES (BLADES) - CE APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

SCORING BALLOON CATHETER FOR PTCA - DCGI APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

SCORING BALLOON CATHETER FOR PTCA - US FDA APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

SCORING BALLOON CATHETER FOR PTCA - CE APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) balloons · Available in the sizes and lengths

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) WITH ENTRY PROFILE 1.4 FRENCH- DCGI APPROVED

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) WITH ENTRY PROFILE 1.4 FRENCH- US FDA APPROVED

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH (CARAVEL TYPE ) WITH ENTRY PROFILE 1.4 FRENCH- CE APPROVED

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- DCGI APPROVED · WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH · Should be available from 130CM - 150 CM.

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- US FDA APPROVED · WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH · Should be available from 130CM - 150 CM.

MICRO CATHETER TO BE USED FOR CTO ANTEGRADE AND RETROGATE APPORCH -- CE APPROVED · WITH PROXIMAL OUTER DIAMETER 2.6 FRENCH AND DISTAL OUTER DIAMETER 1.8 FRENCH · Should be available from 130CM - 150 CM.

IABP CATHETER WITH ACCESSORIES - DCGI APPROVED · Should be compatible with existing machine at GMC Kota

IABP CATHETER WITH ACCESSORIES - US FDA APPROVED · Should be compatible with existing machine at GMC Kota

IABP CATHETER WITH ACCESSORIES - CE APPROVED · Should be compatible with existing machine at GMC Kota

THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - DCGI APPROVED

THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - US FDA APPROVED

THROMBECTOMY CATHETERS WITH MANUAL SUCTION DURING PTCA - CE APPROVED

Special PTCA Balloon (Semi-Compliant) fat CTO Lesion. US FDAApproved. • Must have low entry tip profile equal or less than 0.017" for crossing CTO or to difficult lesion. • Must have lowest diameter starting from 1.0 mm . • Must have lowest length starting from 5.0 mm . • Monorail (rapid exchange) and the over-the-wire balloon.

Special PICA Balloon (Semi-compliant) for CTO Lesion. CE Approved. • Must have low entry tip profile equal or less than 0.017" for crossing CTO or to difficult lesion. • Must have lowest diameter starting from 1.0 mm. • Must have lowest length starting from 5.0 mm . • Monorail (rapid exchange) and the over-the-wire balloon.

Special PT. Balloon (Non-Compliant) lowest diameter in Post Dilation.-US FDA Approved. • Must have diameter starting from 1.75 mm onwards. • Monorail (rapid exchange) and the over-the-wire balloon.

Special PTCA Balloon (Non-Compliant) lowest diameter in Post Dilation. CE Approved. / US FDA / DCGI APPROVED • Must have diameter starting from 1.75mm onwards. • Monorail (rapid exchange) and the over-the-wire balloon.

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. • Monorail (rapid exchange) and the over-the-wire balloon

Ultra-low entry profile (Semi-compliant) with 0.016" and entry profile from 1.25102o 2.25'10 remain same for exceptional crossability. CE approved • Monorail (rapid exchange) a. the over-the-wire balloon.

PTCA BALLOON (SEMI-COMPLIANT) - US FDA APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons · Available in the size and lengths

PTCA BALLOON (SEMI-COMPLIANT) - CE APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons · Available in the size and lengths

PTCA BALLOON (SEMI-COMPLIANT) - DCGI APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons · Available in the size and lengths

PTCA BALLOON (NON-COMPLIANT) - US FDA APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons. · Available in the size and lengths.

PTCA BALLOON (NON-COMPLIANT) - CE APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons. · Available in the size and lengths .

PTCA BALLOON (NON-COMPLIANT) - DCGI APPROVED · Monorail (rapid exchange) or over-the-wire (OTW) balloons. · Available in the size and lengths .

Group J All 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.

COVERED CORONARY STENTS - DCGI APPROVED • Monorail (rapid exchange) and over-the-wire (OTW) both • Available in the sizes and lengths • Covered graft stent for dissected artery

COVERED CORONARY STENTS - US FDA APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) both · Available in the sizes and lengths · Covered graft stent for dissected artery

COVERED CORONARY STENTS - CE APPROVED · Monorail (rapid exchange) and over-the-wire (OTW) both · Available in the sizes and lengths · Covered graft stent for dissected artery

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – DCGI APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT – DCGI APPROVED • WITH bioabsorbable or permanent polymer coated DES. • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –US FDA APPROVED • WITH bioabsorbable or permanent polymer coated DES. • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

EVEROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING PLATINUM CHROMIUM CORONARY STENT –CE APPROVED • WITH bioabsorbable or permanent polymer coated DES. • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) For accelerated degradation and low concentration. - DCGI APPROVED. · Sirolimus with Abluminal and specialized gradient coating (Japan PMDA approved technology). · Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) For accelerated degradation and low concentration. - USFDA APPROVED. · Sirolimus with Abluminal and specialized gradient coating (Japan PMDA approved technology). · Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent with cobalt chromium platform, biodegradable polymer (PDLA) with poly caprolactone (PCL) or PLLA Polymer For accelerated degradation and low concentration. - CE APPROVED. • Sirolimus with Abluminal and specialized gradient coating. • Must have diameter sizes from 2.25 mm- 4 mm & up to long Lengths up to 38 mm or Above • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, microporussurfacewith soft coating of shellac rasin with temperature control packing & temperature sensitive check meter. - DCGI APPROVED • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, microporussurfacewith soft coating of shellac rasin with temperature control packing & temperature sensitive check meter. -USFDA APPROVED • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent - Stainless steel platform, biodegradable polymer, microporussurfacewith soft coating of shellac rasin with temperature control packing & temperature sensitive check meter. - CE APPROVED · Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, micro-Porus surface with soft coating of shellac rasin- DCGI APPROVED · Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, micro-Porus surface with soft coating of shellac rasin- USFDA APPROVED · Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS Eluting Stent- Cobalt chromium platform, biodegradable polymer, micro-Porus surface with soft coating of shellac rasin- CE APPROVED · Should be available in All diameter sizes from 2.25 mm- 4 mm & Lengths from 08- 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX - DCGI APPROVED · PROBUCOL WITH ABLUMINAL COATING. · Should be available in diameter sizes from 2.25 mm- 4 mm · Should be available in Lengths up to 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX -USFDA APPROVED · PROBUCOL WITH ABLUMINAL COATING. · Should be available in diameter sizes from 2.25 mm- 4 mm · Should be available in Lengths up to 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS COATED DRUG STENT WITH 100% POLIMER FREE DRUG DILIVERY BIORESORBABLE DRUG MATRIX - CE APPROVED · PROBUCOL WITH ABLUMINAL COATING. · Should be available in diameter sizes from 2.25 mm- 4 mm · Should be available in Lengths up to 48 mm · Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT – DCGI APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –US FDA APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

SIROLIMUS/ZOTAROLIMUS COATED DRUG ELUTING COBALT CHROMIUM CORONARY STENT –CE APPROVED • Must be Available in the sizes and lengths • Must quote only the latest version commercially available • Must have available in diameter sizes from 2.25 mm- 4 mm & up to long Lengths (38mm or Above) • Must have at least 2 years authentic clinical safety & efficacy data with respect to contemporary-DES

TEMPORARY PACING LEADS – DCGI APPROVED

TEMPORARY PACING LEADS –US FDA APPROVED

TEMPORARY PACING LEADS –CE APPROVED

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

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

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

PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - DCGI Approved · All single Chamber modes and with pediatric Base rate up to 160bpm and parameters · Must have programmable sensor control rest rate · Must have ventricular capture management · The Size of lead must be 7F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available.

PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - US FDA Approved · All single Chamber modes and with pediatric Base rate up to 160bpm and parameters · Must have programmable sensor control rest rate · Must have ventricular capture management · The Size of lead must be 7F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available.

PERMANENT VVIR PACEMAKERS WITH ALL LEADS AND ACCESSORIES - CE Approved · All single Chamber modes and with pediatric Base rate up to 160bpm and parameters · Must have programmable sensor control rest rate · Must have ventricular capture management · The Size of lead must be 7F or less · The Lead must be steroid eluting and should be both bipolar and unipolar configuration · Must have both active and passive fixation endocardial leads available · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available.

VVIR PERMANENT PACEMAKER WITHOUT LEAD - DCGI Approved · VVIR · All single chamber modes and basic pacing programmable parameters · Should have all parameters shown in related No. of pacemaker · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

VVIR PERMANENT PACEMAKER WITHOUT LEAD - US FDA Approved · VVIR · All single chamber modes and basic pacing programmable parameters · Should have all parameters shown in related No. of pacemaker · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

VVIR PERMANENT PACEMAKER WITHOUT LEAD - CE Approved · VVIR · All single chamber modes and basic pacing programmable parameters · Should have all parameters shown in related No. of pacemaker · Minimum 5 year replacement warranty for PG. If replacement warranty is More than 5 years the item will be considered separately for financial bid. · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

PACING LEADS FOR VVI/VVIR PACEMAKERS - DCGI Approved · Must have all specifications shown in related No. of pacemaker · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

PACING LEADS FOR VVI/VVIR PACEMAKERS - US FDA Approved · Must have all specifications shown in related No. of pacemaker · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

PACING LEADS FOR VVI/VVIR PACEMAKERS - CE Approved · Must have all specifications shown in related No. of pacemaker · Direct presence of Parent Company in India (not only through the distributors ) and company must provide its trained technical person for each implantation when ever required and for follow up programming when it is required · Company must provide at least one programmer exclusively to the cardiology dept. · Company must quote only the latest model of devices commercially available

SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER - CE Approved · Must have modes AAI, AOO,VVI,VOO · Basic Pacing rates 30-200. · Electrode Type Unipolar or bipolar · Services life more than 5 years · Sensitivity 0.5-20 mV · Output up to 5 volts

SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER - DCGI Approved · Must have modes AAI, AOO,VVI,VOO · Basic Pacing rates 30-200. · Electrode Type Unipolar or bipolar · Services life more than 5 years · Sensitivity 0.5-20 mV · Output up to 5 volts

SINGLE CHAMBER TEMPORARY EXTERNAL PACEMAKER – US FDA Approved · Must have modes AAI, AOO,VVI,VOO · Basic Pacing rates 30-200. · Electrode Type Unipolar or bipolar · Services life more than 5 years · Sensitivity 0.5-20 mV · Output up to 5 volts

Group K All 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.

Mullins sheaths – Kink resistant 6/7 F– DCGI APPROVED

ASD CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes (6 mm – 40 mm)

ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –US FDA APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes (6 mm – 40 mm)

ASD CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes (6 mm – 40 mm)

DELIVERY SHEATH FOR ASD CLOSURE DEVICE – DCGI APPROVED · Compatible with the device approved in Item no. 2

DELIVERY SHEATH FOR ASD CLOSURE DEVICE –USFDA APPROVED · Compatible with the device approved in Item no. 2

DELIVERY SHEATH FOR ASD CLOSURE DEVICE – CE APPROVED · Compatible with the device approved in Item no. 2

ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – DCGI APPROVED

ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM –USFDA APPROVED

ASD CLOSURE DEVICES WITHOUT DELIVERY SYSTEM –CE APPROVED

PRELOADED ASD CLOSURE DEVICES – DCGI APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Preloaded device with delivery cable

PRELOADED ASD CLOSURE DEVICES –USFDA APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Preloaded device with delivery cable

PRELOADED ASD CLOSURE DEVICES – CE APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Preloaded device with delivery cable

PDA CLOSURE DEVICES WITH DELIVERY SYSTEM – DCGI APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes

PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –USFDA APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes

PDA CLOSURE DEVICES WITH DELIVERY SYSTEM –CE APPROVED · Approved for pediatric/adult use · Device made of biologically inert material · Self-centering, detachable device with delivery cable · Available in all the sizes

PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM - DCGI APPROVED

PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM – USFDA APPROVED

PDA CLOSURE DEVICES WITHOUT DELIVERY SYSTEM - CE APPROVED

· DELIVERY SHEATH FOR PDA CLOSURE DEVICE – DCGI APPROVED · Should be Compatible with the device approved in Item no. 14

· DELIVERY SHEATH FOR PDA CLOSURE DEVICE –USFDA APPROVED · Should be Compatible with the device approved in Item no. 14

· DELIVERY SHEATH FOR PDA CLOSURE DEVICE – CE APPROVED · Should be Compatible with the device approved in Item no. 14

INJECTION NIKORANDIL (2 mg) – DCGI APPROVED

INJECTION NIKORANDIL (2 mg) – USFDA APPROVED

INJECTION NIKORANDIL (2 mg) – CE APPROVED

INJECTION TIROFIBAN – DCGI APPROVED

INJECTION TIROFIBAN –USFDA APPROVED

INJECTION TIROFIBAN –CE APPROVED

INJECTION SodiumNitro-Pruside– DCGI APPROVED

INJECTION SodiumNitro-Pruside–USFDA APPROVED

INJECTION SodiumNitro-Pruside–CE APPROVED

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

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

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

SHEATHS FOR INTRAVASCULAR SNARES& MICROSNARE - US FDA / DCGI / CE APPROVED · Should be compatible with item no 11.

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

DVD – MEDIA for Angiography sine and 3D Imaging system with cover and printed , GMC, kota on coverUS FDA / DCGI / CE APPROVED

SPECIAL VALVOPLASTY BALLOON CATHETER – DCGI APPROVED 1. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm 2. Should have dog boning for precise position

SPECIAL VALVOPLASTY BALLOON CATHETER –USFDA APPROVED 1. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm 2. Should have dog boning for precise position

SPECIAL VALVOPLASTY BALLOON CATHETER –CE APPROVED 3. Should be available in Diameter Sizes 4mm to 35mm and Length 20mm to 60mm 4. Should have dog boning for precise position

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

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

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

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

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

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

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

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

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

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

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

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

Trans Septal Puncture needle for BMV for adults use– DCGI APPROVED

Trans Septal Puncture needle for BMV for adults use–USFDA APPROVED

Trans Septal Puncture needle for BMV for adults use–CE APPROVED

SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED–CE APPROVED

SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED– USFDA APPROVED

SIZING BALLOON FOR DEVICE CLOSURE-OVAL SHAPED– DCGI APPROVED

DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– DCGI APPROVED

DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– CE APPROVED

DELIVERY CABLE FOR ASD/VSD/PDA DEVICES– USFDA APPROVED

Innvolution Healthcare Pvt Ltd

Sahajanand Medical Technologies Pvt. Ltd.

abbott healthcate pvt ltd

Meril Life Sciences India Pvt.Ltd.,

Boston Scientific India Pvt Ltd

Vascular Concepts Ltd

Ace Cardiopathy Solutions Pvt Ltd S

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