Jawaharlal Institute Of Postgraduate Medical Education And Research Tender
View complete overview of Puducherry JIPMER Tender
Jawaharlal Institute Of Postgraduate Medical Education And Research - JIPMER Tender
Eprocure
Opening Date24 Jul 2021
Closing Date24 Aug 2021
Tender AmountRefer Documents
Costs
EMD
Refer DocumentsDocument Cost
₹ 590Tender Fee
Refer Documents
Summary
Rate Contract For Supply Of Consumables And Non Consumables
Description
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Contact
Tender Id
2021_JIPMP_640145_1Bid Award Id
ViewTender No
JIP/PUR6(1)/OeT/Cardio/2021-22Tender Authority
Jawaharlal Institute Of Postgraduate Medical Education And Research ViewPurchaser Address
-Website
http://https://www.jipmer.edu.in/
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Documents
BOQ Items
(S) FEMORAL PCI SHEATH SYSTEMS SIZES 10, 12, 14 F with accessories for insertion.Should be FDA'/CE'/DCGI approved
100
-
-
(S)VASCULAR CLOSURE DEVICES Femoral all sizes.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 or 021 wires and 20G plastic cannula for puncture 5F, 6F,7F.Should be FDA'/CE'/DCGI approved
1500
-
-
(S) RADIAL ANGIO SET WITH PUNCTURE NEEDLE, SHEATH 6F, STRAIGHT GUIDEWIRE 025/021 AND TIG and TIG II CATHETER 5F, AND HYDROPHILIC POLYMER J tipped 035 145 cm WIRES.Should be FDA'/CE'/DCGI approved
1500
-
-
( S) RADIAL ANGIOGRAPHY KITS Comprising the following Items a.Radial Sheath Insertion System 6F b. Radial Angiography 5F TIG catheter c. 0.035 J Hydrophilic polymer wire, d.Disposable Sterile Drape for Radial/Femoral angiography e.Disposable Sterile Gowns -2, f.Disposable Gloves-2, g.Finger control syringe 20cc h.3/3 Rotating manifold i.pressure line j.100 mL Non Ionic contrast media.Should be FDA'/CE'/DCGI approved
500
-
-
( S)Flexible delivery sheaths with steerable and defelctable introducer systems ( 60 cm and above long).Should be CE' AND DCGI approved
50
-
-
( S)EXTRALONG ( more than 150 cm) pigtail catheters for illiac angiography from radial .Should be FDA'/CE'/DCGI approved
20
-
-
( S)Prolene sutured femoral access closure devices.Should be FDA' or CE' andDCGI approved
50
-
-
(S)Radial Compression Devices.Should be FDA'/CE'/DCGI approved
10
-
-
( S) COURNAND CATHETER 5F, 6F woven dacron.Should be FDA'/CE'/DCGI approved
50
-
-
( S) PIG TAIL CATHETERS 5F, 6F.Should be FDA'/CE'/DCGI approved
100
-
-
( S) MARKER PIGTAIL CATHETER 5F, 6F .Should be FDA'/CE'/DCGI approved
50
-
-
(S)JUDKINS LEFT CATHETER 4F,5F,6F all Curves.Should be FDA'/CE'/DCGI approved
200
-
-
(S)JUDKINS RIGHT CATHETER 4F,5F,6F all Curves.Should be FDA'/CE'/DCGI approved
200
-
-
(S)AMPLATZ LEFT CATHETER 4F, 5F,6F all Curves.Should be FDA'/CE'/DCGI approved
25
-
-
(S)AMPLATZ RIGHT CATHETER 4F,5F,6F all Curves.Should be FDA'/CE'/DCGI approved
25
-
-
(S)LEFT CORONARY BY PASS CATHETER 4F,5F,6F all Curves.Should be FDA'/CE'/DCGI approved
10
-
-
(S)RIGHT CORONARY BY PASS CATHETER 4F,5F,6F all Curves.Should be FDA'/CE'/DCGI approved
10
-
-
(S)INTERNAL MAMMARY ARTERY CATHETER 4F, 5F,6F all Curves.Should be FDA'/CE'/DCGI approved
25
-
-
(S)MULTIPURPOSE CATHETER A1,A2,B1,B2.Should be FDA'/CE'/DCGI approved
50
-
-
(S)PIG-TAIL CATHETER PEDIATRIC 4 F.Should be FDA'/CE'/DCGI approved
10
-
-
(S)RADIAL CAG TIG CATHETERS 5F ALL CURVES.Should be FDA'/CE'/DCGI approved
1200
-
-
(S) 2/3 ROTATING MANIFOLD FOR CAG.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) 3/3 ROTATING MANIFOLD FOR CAG/PTCA.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) Y CONNECTOR 10F Diameter having larger inner lumen with INTRODUCER NEEDLE for PTCA.Should be FDA'/CE'/DCGI approved
250
-
-
(S) 3 RING CONTROL SYRINGES 20cc.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)TEFLON COATED GUIDE WIRE145 CM 0.021" ST. & J.Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRE 145 CM 0.025" ST'& J.Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRES 0.032" 145 CM ST& J.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.035"ST & J.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.038" ST.Should be FDA'/CE'/DCGI approved
500
-
-
( S)Exchange length (260cm and above) 0.018'' peripheral guide wire .Should be FDA'/CE'/DCGI approved
50
-
-
( S)Lunderquist type high support exchange length 0.035'' (260cm and above) short and long tip guide wire .Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED EXCHANGEGUIDE WIRE 260 CM 0.032"ST. & J.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGEGUIDE WIRE 260 CM 0.035"ST. & J.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGEGUIDE WIRE 260 CM 0.038"ST& J.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO GUIDE WIRES 145 CM 018, 021.032,035 ST AND J ALL SIZES.Should be FDA'/CE'/DCGI approved
500
-
-
( S)TERUMO EXCHANGE GUIDE WIRES 018, 021.032,035 ST AND J ALL SIZES.Should be FDA'/CE'/DCGI approved
200
-
-
( S)TERUMO STIFF EXCHANGE GUIDE WIRES ALL SIZES.Should be FDA'/CE'/DCGI approved
500
-
-
( S)AMPLATZ TYPE SUPERSTIFF EXCHANGE GUIDE WIRES 0.035' AND .038''. 260 cm and above- Short floppy tip.Should be FDA'/CE'/DCGI approved
50
-
-
( S)AMPLATZ ULTRA STIFF GUIDE WIRES 0.035' AND 0.038'' J. 260 cm and above- LONG floppy tip.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)FEMORAL ANGIOPLASTY GUIDING CATHETER SYSTEMS 5F,6F,7F,8F ALL SHAPES AND SIZES.Should be FDA'/CE'/DCGI approved
1200
-
-
(EX)RADIAL ANGIOPLASTY -GUIDING CATHETER SYSTEMS 4F ALL SHAPES AND SIZES.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)RADIAL ANGIOPLASTY -GUIDING CATHETER SYSTEMS 5F,6F,7F ALL SHAPES AND SIZES.Should be FDA'/CE'/DCGI approved
500
-
-
( S)PTCA WIRES Floppy standard length .Should be FDA'/CE'/DCGI approved
300
-
-
( S)PTCA WIRES-Floppy exchange length.Should be FDA'/CE'/DCGI approved
300
-
-
( S) PTCA WIRES Intermediate Standard Length.Should be FDA'/CE'/DCGI approved
300
-
-
( S) PTCA WIRES Extra support Standard Length.Should be FDA'/CE'/DCGI approved
300
-
-
( S) PTCA DOC LINK EXTENSION WIRES.Should be FDA'/CE'/DCGI approved
300
-
-
( S)EXCHANGE WIRES FOR PTCA .Should be FDA'/CE'/DCGI approved
250
-
-
( S)Double core spring tip TYPE WIRES FOR PTCA.Should be FDA'/CE'/DCGI approved
300
-
-
( S)PTCA WIRES Tapering Tip Hydrophilic.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRE -TOTAL OCCLUSION WIRES-PLATINUM.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES for CTO-hydrophlic .Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES for CTO-hydrophlic Extra support.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES Polymer Coated Hydrophilic.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES Polymer Coated Hydrophilic Extra support.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES- Polymer coated tapering tip.Should be FDA'/CE'/DCGI approved
300
-
-
( S)PTCA WIRES - Specially Designed for Tortuous vessels.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA WIRES Extrasupport Polymer coated.Should be FDA'/CE'/DCGI approved
250
-
-
( S)LINK EXTENSION type 300 cm wires.Should be FDA'/CE'/DCGI approved
250
-
-
( S)PTCA 009 exchange length wires for Retrograde approach exchange length.Should be FDA'/CE'/DCGI approved
100
-
-
(EX)Rapid Exchange BalloonSystems with Semi-Compliant/Compliant Design with Excellent Trackability and High Inflation Pressures .Should be FDA' OR CE' AND DCGI approved
600
-
-
(EX)Rapid Exchange BalloonSystems with Semi-Compliant/Compliant Design with Excellent Trackability and High Inflation Pressures .Should be CE' AND DCGI approved
350
-
-
(EX)Non-Compliant Balloons for PTCA.Should be FDA' OR CE' AND DCGI approved
600
-
-
(EX)Non-Compliant Balloons for PTCA.Should be CE' AND DCGI approved
350
-
-
( S)Laser catheter coronary calcification intervention.Should be CE' AND DCGI approved
2
-
-
( S)Ultra low profile Non compliant balloons for PCI.Should be CE' AND DCGI approved
25
-
-
( S)Ultra low profile semi complaint baloons for PCI.Should be CE' AND DCGI approved
25
-
-
( S)Lithrotripsy balloons for heavy calcified proximal vessel PCI.Should be CE' AND DCGI approved
4
-
-
( S)High trackable 0.018'' embolisation coils for post op- visceral (GI and Renal artery pseudoaneurysm) .Should be CE' AND DCGI approved
25
-
-
( S)low profile CTO baloons for PCI starts at 0.75mm in diameter.Should be CE' AND DCGI approved
25
-
-
(EX)Over the wire Balloons for PTCA.Should be FDA' OR CE' AND DCGI approved
25
-
-
(EX)Over the wire Balloons for PTSMA.Should be FDA' OR CE' AND DCGI approved
10
-
-
( EX)Cutting Balloons Coronary.Should be FDA' OR CE' AND DCGI approved
50
-
-
( EX)Cutting Balloons Peripheral.Should be FDA' OR CE' AND DCGI approved
20
-
-
(EX)Drug Eluting Balloons Coronary.Should be FDA' OR CE' AND DCGI approved
20
-
-
(EX)Ultra high pressure Mustang type balloons Peripheral- sizes from 4mm to 10mm all lengths..Should be FDA' OR CE' AND DCGI approved
50
-
-
(EX)Drug eluting Balloons for in stent restenosis Coronary.Should be FDA' OR CE' AND DCGI approved
20
-
-
(EX) Scoring Balloons - for coronary and Peripheral- For severely calcified lesions.Should be FDA' OR CE' AND DCGI approved
10
-
-
(EX)BALLOON MOUNTED DRUG COATED stain less steel CORONARY STENTS.Should be CE' AND DCGI approved
50
-
-
(EX)Balloon expandable drug coated Cobalt chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
100
-
-
(EX)Balloon expandable drug coated Platinum chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
100
-
-
(EX)DRUG ELUTING STENTS FDA and DCGI APPROVED First Generation.Should be FDA approved
250
-
-
(EX)DRUG ELUTING STENTS FDA and DCGI APPROVED Second Generation.Should be FDA approved
250
-
-
(EX)DRUG ELUTING STENTS FDA and DCGI APPROVED Third Generation.Should be FDA approved
250
-
-
(EX)DRUG ELUTING STENTS CE and DCGI APPROVED.Should be CE' and DCGI approved
250
-
-
(EX)DRUG ELUTING STENTS DCGI APPROVED.Should be DCGI approved
250
-
-
( EX) DRUG ELUTING CORONARY STENTS TAPERING including longer legths.Should be FDA' OR CE' AND DCGI approved
250
-
-
( EX) DRUG ELUTING CORONARY STENTS EXTRA LENGTH ( beyond 38mm).Should be FDA' OR CE' AND DCGI approved
250
-
-
( EX) DRUG ELUTING STENTS- POLYMER FREE.Should be FDA' OR CE' AND DCGI approved
100
-
-
( EX) DRUG ELUTING STENTS- sizes above 48mm for diffuse lesions.Should be FDA' OR CE' AND DCGI approved
100
-
-
(S) Coronary micro snares ( 2mm to 5mm).Should be FDA' OR CE' AND DCGI approved
10
-
-
(EX)COVERED STENTS-CORONARY Low profile ad 0.014" compatable.Should be FDA'/CE'/DCGI approved
20
-
-
(S) FEMORAL ANGIOPLASTY KIT (1stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water'/ blood impenetrable front and hand shielding - 3 Nos; 2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY'' / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No; 3.DISPOSABLE GAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos; 4.TEFLON COATED GUIDE WIRES 145 CMS 0.035"ST & J - 1No; 5.Arterial Pressure monitoring Transducers (Disposable) - 1No; 6.INITIAL PUNCTURE NEEDLES18G - 1No; 7.FEMORAL PCI SHEATH SYSTEMS SIZE 5F to 9F with accessories for insertion - 2Nos; 8. PTCA WIRE - 1 No; 9.3 RING CONTROL SYRINGES FOR CAG'/PTCA 20cc - 1No; 10. 3'/3 ROTATING MANIFOLD FOR CAG'/PTCA-1No; 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No; 12.PTCA GUIDING CATHETER - 1No; 13.3 Ring Finger Control syringe 12 cc - 1No; 14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No; 15.Rapid Exchange BalloonSystems with Semi-Compliant'/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No; 16.Non-Compliant Balloons for PTCA - 1No; 17.DRUG ELUTING STENTS FDA/ DCGI /CE APPROVED -1 No; .Should be FDA'/CE'/DCGI approved
150
-
-
(S)FEMORAL ANGIOPLASTY KIT (2 Stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water'/ blood impenetrable front and hand shielding - 3 Nos; 2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY'' / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No; 3.DISPOSABLE GAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos; 4.TEFLON COATED GUIDE WIRES 145 CMS 0.035"ST & J - 1No; 5.Arterial Pressure monitoring Transducers (Disposable) - 1No; 6.INITIAL PUNCTURE NEEDLES18G - 1No; 7.FEMORAL PCI SHEATH SYSTEMS SIZE 5F to 9F with accessories for insertion - 2Nos; 8. PTCA WIRE- 1 No; 9.3 RING CONTROL SYRINGES FOR CAG'/PTCA 20cc - 1No; 10. 3'/3 ROTATING MANIFOLD FOR CAG'/PTCA-1No; 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No; 12.PTCA GUIDING CATHETER - 1No; 13.3 Ring Finger Control syringe 12 cc - 1No; 14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No; 15.Rapid Exchange BalloonSystems with Semi-Compliant'/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No; 16.Non-Compliant Balloons for PTCA - 1No; 17.DRUG ELUTING STENTS FDA/ DCGI /CE -2 Nos;.Should be FDA'/CE'/DCGI approved
150
-
-
(S)RADIAL ANGIOPLASTY KIT (1 Stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water'/ blood impenetrable front and hand shielding - 3 Nos; 2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY'' / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No; 3.DISPOSABLE GAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos; 4.TEFLON COATED GUIDE WIRES 145 CMS 0.035"ST & J - 1No; 5.Arterial Pressure monitoring Transducers (Disposable) - 1No; 6.INITIAL PUNCTURE NEEDLES18G - 1No; 7.TRANSRADIAL SHEATH SYSTEMS SIZE 6F with accessories for insertion - 1Nos
8. PTCA WIRE - 1 No; 9.3 RING CONTROL SYRINGES FOR CAG'/PTCA 20cc - 1No; 10. 3'/3 ROTATING MANIFOLD FOR CAG'/PTCA-1No; 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No; 12.PTCA GUIDING CATHETER - 1No; 13.3 Ring Finger Control syringe 12 cc - 1No; 14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No; 15.Rapid Exchange BalloonSystems with Semi-Compliant'/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No; 16.Non-Compliant Balloons for PTCA - 1No; 17.DRUG ELUTING STENTS FDA / DCGI/CE APPROVED -1 No; .Should be FDA'/CE'/DCGI approved
150
-
-
(S)RADIAL ANGIOPLASTY KIT (2 Stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water'/ blood impenetrable front and hand shielding - 3 Nos; 2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY'' / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No; 3.DISPOSABLE GAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos; 4.TEFLON COATED GUIDE WIRES 145 CMS 0.035"ST & J - 1No; 5.Arterial Pressure monitoring Transducers (Disposable) - 1No; 6.INITIAL PUNCTURE NEEDLES18G - 1No; 7.TRANSRADIAL SHEATH SYSTEMS SIZE 6F with accessories for insertion - 1Nos; 8. PTCA WIRE - 1 No; 9.3 RING CONTROL SYRINGES FOR CAG'/PTCA 20cc - 1No; 10. 3'/3 ROTATING MANIFOLD FOR CAG'/PTCA-1No; 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No; 12.PTCA GUIDING CATHETER - 1No; 13.3 Ring Finger Control syringe 12 cc - 1No; 14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No; 15.Rapid Exchange BalloonSystems with Semi-Compliant'/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No; 16.Non-Compliant Balloons for PTCA - 1No; 17.DRUG ELUTING STENT FDA/ DCGI/CE APPROVED -2 No;.Should be FDA'/CE'/DCGI approved
100
-
-
(S) 20CC INFLATION DEVICE AS ONE SET capable of inflation pressures upto 30 bar.Should be FDA'/CE'/DCGI approved
1000
-
-
( S)INFLATION DEVICE TO INFLATE LOW AND HIGH PRESSURE UPTO 40 ATM.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) PTCA MANIFOLD WITH FLUSH DEVICE.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) INFUSION ACCELERATOR ( PRESSURE BAG).Should be FDA'/CE'/DCGI approved
1000
-
-
( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 12cc.Should be FDA'/CE'/DCGI approved
1000
-
-
( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 20cc.Should be FDA'/CE'/DCGI approved
1000
-
-
( D) Thrombus Extraction Catheters for Primary PTCA.Should be FDA'/CE'/DCGI approved
100
-
-
( D) Coronary Microcatheters( 0.014" compatable).Should be FDA' or CE' andDCGI approved
100
-
-
( D)Shock wave assisted balloons for calcified lesions.Should be CE' AND DCGI approved
5
-
-
( D)Shock wave assembly and delivery system for ballooons.Should be CE' AND DCGI approved
5
-
-
( D)ULTRA HIGH PRESSURE (30 and above) non compliant CORONARY balloons for sevrely calcified stenosis (All sizes).Should be CE' AND DCGI approved
20
-
-
( D) Coronary Microcatheters for CTO entry- braided with cutting tip.Should be FDA' or CE' andDCGI approved
50
-
-
( D)Steerable Microguide catheters for sidebranch entry -Dual lumen type(over the wire and monorail).Should be FDA' or CE' and DCGI approved
20
-
-
( D)Micro catheters for visceral angio embolisation-Should be hydrophilic and 0.021" compatable.Should be FDA' OR CE' AND DCGI approved
50
-
-
(D)Retrograde coronary collateral Channel dilator .Should be FDA' or CE' and DCGI approved
20
-
-
( S)Superselective cathetor for Mother and Child technique.Should be FDA' or CE' and DCGI approved
20
-
-
(S) Soft Guideliner for mother and child technique.Should be FDA' or CE' and DCGI approved
20
-
-
(D) Intravascular Ultrasound Catheters compatible with Volcano IVUS system .Should be FDA'/CE'/DCGI approved
20
-
-
(D) Intravascular Ultrasound Catheters compatible with ILAB IVUS system with Pull back Slut.Should be FDA'/CE'/DCGI approved
25
-
-
(D)OCT Catheters .Should be FDA'/CE'/DCGI approved
10
-
-
(D)RADI 014 FFR WIRES.Should be FDA'/CE'/DCGI approved
50
-
-
(D)RADI 014 FFR WIRES wireless.Should be FDA'/CE'/DCGI approved
50
-
-
(D)VOLCANO 014 FFR WIRES.Should be FDA'/CE'/DCGI approved
10
-
-
(D) FFR WIRE Compatible with ILAB.Should be FDA'/CE'/DCGI approved
50
-
-
( D)Rotablator Wire 009.Should be FDA'/CE'/DCGI approved
25
-
-
( D)Rotablator Advancer.Should be FDA'/CE'/DCGI approved
25
-
-
( D)OPN type ultra high pressure highly non compliant balloon .Should be FDA' OR CE' AND DCGI approved
25
-
-
( D)Rotablator Burr.Should be FDA'/CE'/DCGI approved
25
-
-
(S)Swan Ganz capable of accommodating 0.038" Guide Wire Large Lumen Size 7F .Should be FDA'/CE'/DCGI approved
25
-
-
(S)Swan Ganz capable of accommodating 0.032/035" Guide Wire Large Lumen Size 6F .Should be FDA'/CE'/DCGI approved
25
-
-
(S)BERMAN BALLOON ANGIO CATHS WITH SIDE HOLES 5F,6F.Should be FDA'/CE'/DCGI approved
25
-
-
(S)BALLOON TEMPORARY PACING LEADS 5F,6F.Should be FDA'/CE'/DCGI approved
25
-
-
(S)Woven Dacron Catheter with platinum Tip Elecrode for Trasvenous Temporary pacing 5F/6F.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)Temporary Pacing Leads sizes with 5F/6F.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)Balloon Flow Assisted Temporary Pacing lead(5F and 6F .Should be FDA'/CE'/DCGI approved
100
-
-
(S)Accessories for Accura based Mitral valvuloplasty systems.Should be CE' AND DCGI approved
10
-
-
(EX)ALL SIZES OF PTMC Balloons- Reusable.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)ALL SIZES OF MITRAL VALVE BALLOON DILATATION SYSTEMS WITH REUSABLE LATEX RUBBER BALLOON DESIGN AND ACCESSORIES TO BE QUOTED.Should be FDA'/CE'/DCGI approved
25
-
-
( S)PRESSURE MANOMETER LINES MALE/FEMALE 150 CM.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)PRESSURE MANOMETER LINES MALE/MALE 150 CM.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)THREE WAY STOPCOCKS.Should be FDA'/CE'/DCGI approved
1500
-
-
(S)HIGH PRESSURE CONTRAST INJECTION TUBE.Should be FDA'/CE'/DCGI approved
250
-
-
(S)HIGH FLOW ANGIO FLUSH CATHS.Should be FDA'/CE'/DCGI approved
50
-
-
(S)LEFT INTERNAL MAMMARY GUIDE CATHETER 5 F,6F and & 7F .Should be FDA'/CE'/DCGI approved
50
-
-
(S)BRAIDED MULTIPURPOSE GUIDE CATHS(5F AND 6F).Should be FDA'/CE'/DCGI approved
60
-
-
(S) SOFT TIPPED braided Guide catheters for (4F,5F) for coronary/visceral use.Should be FDA' or CE' and DCGI approved
25
-
-
(S)BRAIDED SIMMONS SHAPED CEREBRAL CATHS.Should be FDA'/CE'/DCGI approved
50
-
-
(S)RENAL DOUBLE CURVE GUIDE CATHETER 4F, 5F 80CM , 120 CM, 140 CM.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TERUMO GLIDE CATHETER 4F,5F AND 6 F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)YASHIRO GLIDE CATHETER 4F, 5F 80 CM,120 CM,140CM.Should be FDA'/CE'/DCGI approved
50
-
-
( EX)PERIPHERAL BALLOONS(0.035" compatable) for femoro popliteal and iliac lesions.Should be FDA'/CE'/DCGI approved
50
-
-
( EX) RENAL BALLOON(0.014" compatable).Should be FDA'/CE'/DCGI approved
50
-
-
(S) 4 F AND 5 F catheter COMPATABLE PERI MEMBRANEUOUS VSD DEVICE with double screw design for antegrade and retrograde closure.Should be CE' AND DCGI approved
5
-
-
(EX)CAROTID and BTK BALLOONS(0.014" compatable) .Balloon Shaft length should be 160 CM AND ABOVE.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)SMALL VESSEL BALLOON( Diameters should be from 1mm to 4mm) All lengths.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PERIPH /RENAL/CAROTID GUIDING-100 cm and longer.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)RENAL STENTS -0.014' compatable Balloon Mounted Shaft Length 80 cm- All sizes.Should be FDA'/CE'/DCGI approved
50
-
-
(EX) Self expanding Femoro popliteal stents - all diameters.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)Dilators of Coons type for serial vascular dilation for large access .Should be CE' and DCGI approved
10
-
-
(EX) Balloon expandable STENTS PERIPHERAL- All sizes.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) Self expanding Iliac stents - all diameters.Should be FDA' or CE' and DCGI approved
25
-
-
( EX) CAROTID DISTAL PROTECTION DEVICES.Should be FDA'/CE'/DCGI approved
10
-
-
( EX) CAROTID STENTS TAPERING Self Expanding.Should be FDA'/CE'/DCGI approved
25
-
-
( EX)CAROTID STENTS Straight Self Expanding.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Nitinol Vascular plugs for embolisation.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)STENT GRAFTS FOR VISCERAL VASCULAR SYSTEM(Should be highy trackable,0.035" compatable).Should be FDA'/CE'/DCGI approved
25
-
-
(S) Sizing BALLOONS for ASD/PDA.Should be FDA'/CE'/DCGI approved
20
-
-
(D)VENA CAVA FILTER- Retrivable, Jugular Deployement.Should be FDA'/CE'/DCGI approved
10
-
-
(D)VENA CAVA FILTER- Retrivable, Femoral Deployement.Should be FDA'/CE'/DCGI approved
10
-
-
(D)VENA CAVA FILTER- RETRIVAL SYSTEM .Should be FDA'/CE'/DCGI approved
10
-
-
(S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange Length ( 0.018").Should be FDA'/CE'/DCGI approved
25
-
-
(S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange length(0.035").Should be FDA'/CE'/DCGI approved
25
-
-
(S)ROAD RUNNER POLYMER COATED WIRE 035 staright and J.Should be FDA'/CE'/DCGI approved
10
-
-
(S)PERIPHERAL CHRONIC TOTAL OCCLUSION WIRES 0.014, 0.0.35 diameter.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) EMBOLIZATION COILS 035" all sizes.Should be FDA'/CE'/DCGI approved
100
-
-
(EX) EMBOLIZATION COILS 0.038 to 052" all sizes.Should be FDA'/CE'/DCGI approved
100
-
-
( EX) EMBOLIZATION MICRO COILS 018 all sizes - Non Detachable and freely deliverable.Should be FDA'/CE'/DCGI approved
100
-
-
( EX)EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 2D.Should be FDA'/CE'/DCGI approved
100
-
-
(EX) Vascular embolisation nitinol based occluders all sizez with delivery system.Should be FDA' or CE' and DCGI approved
10
-
-
( EX) EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 3D.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)ENDOVASCULAR SNARES with Metal Tip.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)ENDOVASCULAR SNARES with Polymer Tip.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)ENDOVASCULAR SNARES Gooseneck.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)EMBOLISATION PARTICLES Poly Vinyl Alcohol all sizes.Should be FDA'/CE'/DCGI approved
50
-
-
(S)Super Absorbant Polymer Microspheres for Drug( Doxorubucin) Adsorption for TACE.Should be FDA'/CE'/DCGI approved
10
-
-
(S)Gelfoam (Powder or granule form) for Embolization.Should be FDA'/CE'/DCGI approved
10
-
-
(S)N-butyl cyanoacrylate GLUE for Embolization .Should be FDA'/CE'/DCGI approved
10
-
-
(EX)MICROCATHETERS with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)MICROCATHETERS - STEERABLE/ SHAPABLE with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)LARGE DIAMETER COVERED AORTA-ARCH AND ZONE 2 STENT GRAFTS TAA all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(EX) Aorto Uni iliac stent covered grafts All sizes.Should be CE' AND DCGI approved
2
-
-
(EX)AORTIC STENT covered GRAFTS for DTA aneurysm stenting .Should be FDA'/CE'/DCGI approved
5
-
-
(EX)Bare AORTIC STENTS FOR Coarctation (Sizes should be above 20mm up to 40mm) -Only Baloon expandable design.Should be FDA'/CE'/DCGI approved
2
-
-
(EX) Covered AORTIC stents (balloon expandable only) for aortic coarctation . Diameters should be 20mm and above.Should be CE' AND DCGI approved
2
-
-
(EX) Low profile Dacron / PTFE covered stent grafts ( 20-45mm) for sealing extensive aortic dissection .Should be CE' AND DCGI approved
5
-
-
(EX) Low profile hydrophilic sheaths for aortic procedures ( 12 F and above) .Should be FDA'/CE'/DCGI approved
10
-
-
(EX) Covered stent grafts for aortic arch aneurysm with onsite fenestraion capability.Should be FDA'/CE'/DCGI approved
5
-
-
(EX) Aortic covered Stent grafts (straight) capable for fenestration for justa renal and juxta subclavain aneurysms and traumatic aortic injury.Should be FDA'/CE'/DCGI approved
5
-
-
(EX) ABDOMINAL AORTIC ANEURYSM STENT GRAFTS WITH ILIAC LIMBS for abd aorta aneurysm.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)ASD DEVICES: All cutomised sizes from 8mm to 50 mm.Should be CE' AND DCGI approved
25
-
-
(EX) Ultra compliant linear Sizing balloons with markers (34mm to 44mm) for balloon asssited device deployment compatable with contralateral 8F sheath.Should be CE/DCGI approved
25
-
-
(EX) Ultra compliant linear Sizing balloons with markers (24mm to 34mm) for balloon asssited device deployment compatable with contralateral 7F sheath.Should be CE' and DCGI approved
25
-
-
(EX) COOK SHEATHS (all sizes 6F-15F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
100
-
-
(EX) Fenestrated ASD device for mutiple septal defects.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)ASD AMPLATZER TYPE SELF CENTRE DEVICES WITH ALL sizes from 8mm and above .Should be FDA approved
25
-
-
(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE .Should be FDA'/CE'/DCGI approved
25
-
-
(EX) Delivery System and cable set for PDA occlusion devie (4F- 12 F).Should be FDA'/CE'/DCGI approved
25
-
-
(EX)ADO-1 device for all morphology.Should be FDA' or CE' andDCGI approved
25
-
-
(EX) DUCT OCCLUSION DEVICE DELIVERY SYSTEM NONTAPERING SHEATHS with sidearm+INTRODUCER CABLE SET .Should be FDA'/CE'/DCGI approved
25
-
-
(EX)PDA OCCUSION DEVICE with Dual Discs of equal size .Should be FDA' or CE' andDCGI approved
5
-
-
(EX)PDA DELIVERY SYSTEMS AND INTRODUCER CABLE SYSTEMS .Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Ventricular septal Closure Devices All sizes ( 4mm to18 mm).Should be FDA'/CE'/DCGI approved
10
-
-
(EX) Delivery cable and sheath set for Ventricular septal defect closure.Should be FDA' or CE' and DCGI approved
10
-
-
(EX)Muscular VSD Closure Devices-All sizes and types .Should be FDA'/CE'/DCGI approved
10
-
-
(EX) Low profile Delivery sheath and cable for VSD closure devices( 5F to 14F).Should be CE' and DCGI approved
10
-
-
(EX) Low profile Duct occluder device for neonates and infants.Should be CE' AND DCGI approved
5
-
-
(EX)Ventricular septal Closure Devices All sizes with delivery system.Should be FDA' or CE' and DCGI approved
5
-
-
(EX) Atrial septal occluder(self centering) for complex morphology with balloon assisted delivery .Should be FDA' or CE' andDCGI approved
10
-
-
(EX) Post Infarct ventricular septal rupture Closure Devices- All sizes and types.FDA approved
10
-
-
(EX) PURPLE Recovery sheaths for embolised ASD devices-16 F and above size.Should be FDA approved
10
-
-
(EX) Large sized atrial septal occluders above 40mm size.Should be CE' AND DCGI approved
5
-
-
(EX) Vascular plug closure devices for coronary and Pulmonary AV fistula.Should be FDA'/CE'/DCGI approved
5
-
-
(EX) Ventricular septal defect (device alone) for antegrade closure .Should be FDA' or CE' and DCGI approved
5
-
-
(EX) Dual disc nitinol biocompatable layer coat secundum type atrial occluders (ALL SIZSES) for Pre assembled delivery system.Should be FDA' or CE' andDCGI approved
10
-
-
(EX) Extra soft Nitinol multi functional Closure Devices compatable with guide catheter delivery.Should be CE/DCGI approved
10
-
-
(EX)Left atrial appendage closure device.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)left atrial appendage closure delivery system.Should be FDA'/CE'/DCGI approved
10
-
-
(EX) Single disc occluders with device alone with sizes from 3mm onwards up to 20 mm ..Should be FDA' or CE' andDCGI approved
10
-
-
(EX)Trans catheter aortic valve (self expanding).Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Trans catheter aortic valve (balloon expanding).Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Trans catheter aortic valve delivery sheath(self expanding ).Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Trans catheter aortic valve delivery sheath(balloon expanding).Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Large diametre (14-20mm) balloon expanding aortic/ vena caval stents.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Large bore low profile manual aspiration system for high thrombus load.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Ultra low profile semi compliant coronary balloons for Chronic total occlusions.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Ultra High pressure above 25 atm non compliant balloon system for calcified lesions.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Balloon expandable covered stents(sizes 5-20mm) for fenestrated TEVAR/EVAR.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) Covered self expanding covered stent grafts for anurysm and leaks (4mm to 12mm).Should be FDA' or CE' andDCGI approved
10
-
-
(EX)Coda balloon for optimal Aortic Stent expansion .Should be FDA' or CE' and DCGI approved
10
-
-
(EX)Anzel sheaths for fenestarted EVAR .Should be FDA'/CE'/DCGI approved
20
-
-
(EX)Braided kink resistant long(100-120cm) delivery sheaths for VSD closure.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Braided kink resistant flexible sheaths (60-100cm) for fenestarted TEVAR and carotid interventions-straight and curved.Should be FDA'/CE'/DCGI approved
20
-
-
(S) Angioseal type-sponge based vascular closure system.Should be CE' AND DCGI approved
10
-
-
(EX)Radiation protection drape pads.Should be FDA'/CE'/DCGI approved
50
-
-
(S)GEL FOAM POWDER FOR ANGIO EMBOLISATION.Should be FDA' or CE' andDCGI approved
25
-
-
(EX)Cyanoacrylate glue for sealing coronary perforation.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Dissection re entry balloon for coronary CTO.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Sub intimal tracking device for CTO.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Large bore long femoral sheaths 12-18 F for aortic/TAVI interventions.Should be FDA'/CE'/DCGI approved
50
-
-
(EX)Suture based haemostasis device for large bore Femoral access.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Scoring balloons for debulking calcified lesions.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Vascular Plugs with delivery systems and sheaths.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Expandable femoral sheaths.Should be FDA'/CE'/DCGI approved
5
-
-
(S)STR shaped woven dacron intra coronary guide catheter( above 100 cm length).Should be CE' AND DCGI approved
10
-
-
(S)Slender sheaths for radial access -Should be expandable.Should be CE' AND DCGI approved
25
-
-
(S)Coronary micro snares.Should be CE' and DCGI approved
2
-
-
(EX)BIOPTOME for Coil Delivery.Should be FDA'/CE'/DCGI approved
10
-
-
( EX)Pulmonary'/Aortic balloon systems comprising of Pulmonary Valvuloplasty Balloons all sizs, curves and lengths .Should be FDA'/CE'/DCGI approved
10
-
-
( EX)Single diameter Aortic Valvuloplasty balloons of Cribier-Letac all sizes and lengths.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)High pressure non compliant peripheral balloons- (sizes from 4mm-10mm) 0.035'' compatable (All lengths).Should be CE' and DCGI approved
10
-
-
( EX)Stepped diameter balloons Cribier- Letac all sizes and lengths.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Pediatric Valvuloplasty balloons with accelerator, Bifoil balloons, Trifoil Balloons all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(S)Amplatz apex J extra stiff guide wire exchange lengths.Should be FDA'/CE'/DCGI approved
25
-
-
(S)14 F balloon introducer systems.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)COOK LONG SHEATHS CAPABLE OF ASD/VSD/PDA device deliverySIZES 6Fto 16F.Should be FDA'/CE'/DCGI approved
50
-
-
(S) INITIAL PUNCTURE NEEDLES18G.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) MICROPUNCTURE NEONATAL INTRODUCER SETS AND SHEATH SYSTEMS 4F,5F.Should be FDA'/CE'/DCGI approved
100
-
-
(S)GUIDE WIRE 38,A COOK HIWIRE 150CM.Should be FDA'/CE'/DCGI approved
25
-
-
(S)CARDIAC MULTIPACKS COMPRISING OF VENTRICULAR PIG TAIL CATHETER, LEFT CORONARY CATHETER, RIGHT CORONARY CATHETER, CATHETER INTRODUCER SHEATH ALL SIZES.Should be FDA'/CE'/DCGI approved
100
-
-
(S)Guide Extension Catheter,.Should be FDA'/CE'/DCGI approved
100
-
-
(S Balloon atrial septostomy catheter.Should be FDA'/CE'/DCGI approved
5
-
-
(S)TRANSSEPTAL CATHETER .Should be FDA'/CE'/DCGI approved
10
-
-
(S)BROCKENBOROUGH NEEDLE ADULT .Should be FDA'/CE'/DCGI approved
50
-
-
(S)BROCKENBOROUGH NEEDLE PEDIATRICS .Should be FDA'/CE'/DCGI approved
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 6F TO 14 F all sizes.Should be FDA'/CE'/DCGI approved
50
-
-
(S)MULLINS SHEATH with Matching Dilator with out sidearm 6F, 7F, 8F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)BALKAN CONTRALATERAL SHEATH 6F,7F,8F.Should be FDA'/CE'/DCGI approved
20
-
-
(S)MULLINS SHEATH CHILD.Should be FDA'/CE'/DCGI approved
10
-
-
(S)Bipolar temporary pacing electrodes, Sizes: 4F,5F,6F
.Should be FDA'/CE'/DCGI approved
50
-
-
(S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350'/370 100 ml Bottles).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350'/370 50 ml Bottles).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Iso Osmolar Contrast Media for Angiography and Angioplasty for Patients with Renal Dysfunction (Non-Ionic 350'/370 100 ml Bottles).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Iso Osmolar Contrast Media for Angiography and Angioplasty for Patients with Renal Dysfunction (Non-Ionic 350'/370 50 ml Bottles).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Myocardial Echocardiographic Contrast comprising of Sulphur Hexachloride or equivalent Micro Bubbles.Should be FDA'/CE'/DCGI approved
10
-
-
(S)Bioptomes for Endomyocardial biopsy : Bioptomes ; 5.2F. Should be FDA'/CE'/DCGI approved
10
-
-
(S)Radial Sheaths with Introducer needle, Guide wire and dilator: Complete Set:.Should be FDA'/CE'/DCGI approved
500
-
-
(S)Oximetry Cuvets for AVOXIMETER.Should be FDA'/CE'/DCGI approved
250
-
-
Inj TIROFIBAN 100 mL bottles.Should be FDA'/CE'/DCGI approved
50
-
-
Inj BIVALURIDIN.FDA approved
25
-
-
(S)TROPONIN I QUANTITATIVE BED SIDE TEST KIT .Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
250
-
-
(S)TROPONIN T QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
200
-
-
(S)HIGH SENSITIVE TROPONIN T QUANTITIVE QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
200
-
-
(S)HIGH SENSITIVE TROPONIN I QUANTITATIVE- FDA approved- Analyser Should be Supplied.Should be FDA' approved Measuring Device to be supplied
200
-
-
(S)N-TERMINAL PRO BNP QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(S)N-TERMINAL BNP QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(S)D-TIMER QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(S)NGAL QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
300
-
-
(S)Bedside Lipid Profile Measurement Kits.Reading Machine should be provided free
500
-
-
(S)Bedside INR Measurement Kits.Reading Machine should be provided free
250
-
-
(S)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACK SINGLE PIECE MEDIUM SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(S)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACK TWO PIECE SKIRT AND BLOUSE TYPE MEDIUM SIZE. .Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(S)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACK TWO PIECE SKIRT AND BLOUSE TYPE LARGE SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(S)Thyroid Collars Radiation Protection.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(S)Gonadal Shields Radiation Protection.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(S)Radaiation Protective Eye Goggles.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(S)Radaiation Protective Head Gear.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(S) Cath-Lab Cotton Dress Shirt with three pockets and Pyjama with pockets Large and medium Sized Light Blue Colour with label of “ Cath-Lab JIPMER” on both the shirt and the pyjama and Size printed.Sample to be supplied
100
-
-
(S) Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water/ blood impenetrable front and hand shielding.Should be FDA'/CE'/DCGI approved
500
-
-
(S) Glucometer Test Strips with four glucometers.Should be FDA'/CE'/DCGI approved
500
-
-
(D)Single Chamber Demand Cum Overdrive Temporary Pulse Generatorsin various Dual Chamber and Single Chamber modes.Should be FDA'/CE'/DCGI approved
5
-
-
(D)Dual Chamber Demand Cum Overdrive Temporary Pulse Generatorsin various Dual Chamber and Single Chamber modes.Should be FDA'/CE'/DCGI approved
5
-
-
5 French fixed curve quadripolar catheter with 2-5-2 interelectrode spacing. One matching connector for every 5 catheters.Should be FDA'/CE'/DCGI approved
20
-
-
6 French deflectable quadripolar catheter with 2-5-2 interelectrode spacing and matching connector.Should be FDA'/CE'/DCGI approved
6
-
-
6 French deflectable decapolar catheter with 2-5-2 interelectrode spacing and matching connector.Should be FDA'/CE'/DCGI approved
20
-
-
6 or 7 French deflectable duodecapolar catheters (Halo) with matching connectors.Should be FDA'/CE'/DCGI approved
10
-
-
Long deflectable sheath with hemostatic valve, side port, atraumatic tip, braided shaft, uni- or bidirectional steerability, availability in small, medium or large curves, minimum inner diameter or 7F, minimum length of 65 cms.Should be FDA'/CE'/DCGI approved
6
-
-
7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, unidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA'/CE'/DCGI approved
15
-
-
7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, bidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and suitable connecting cables should be provided .Should be FDA'/CE'/DCGI approved
10
-
-
7 French quadripolar Radiofrequency ablation catheter with a 8 mm tip, unidirectional deflection, availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA'/CE'/DCGI approved
4
-
-
7 French quadripolar Radiofrequency ablation catheter with irrigated tip, uni- or bi-directional deflection and availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA'/CE'/DCGI approved
4
-
-
Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and unidirectional deflection for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system.Should be FDA'/CE'/DCGI approved
20
-
-
Reusable indifferent electrode pad compatible with the Stockert ablator.Should be FDA'/CE'/DCGI approved
4
-
-
Surface electrode kit for use with the Ensite NavX system including 3 pairs of surface patches, 10 ECG electrodes and 1 system reference electrode .Should be FDA'/CE'/DCGI approved
4
-
-
SSIR - Single chamber rate responsive implantable multiprogrammable pacemaker with maximum programmable sensitivity of 0.5 mv or more with matching leads and subclavian introducer set to be quoted as one set. Active fixation leads should be supplied as atrial (50%) / ventricular (50%).Should be FDA'/CE'/DCGI approved
50
-
-
VDD implantable multiprogrammable pacemaker with shortest programmable AV delay of 50 ms, with matching single pass steroid eluting VDD lead and matching sublavian introducer. .Should be FDA'/CE'/DCGI approved
50
-
-
DDD - Dual chamber implantable multiprogrammable pacemaker with shortest programmable Av delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers..Should be FDA'/CE'/DCGI approved
50
-
-
DDDR - Dual chamber rate-responsive implantable multiprogrammable pacemaker with shortest programmable Av delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers..Should be FDA'/CE'/DCGI approved
25
-
-
Bipolar lead specially designed for placement in coronary sinus for LV pacing. Should be
supplied with 9F short sheath with valve, long preshaped slittable sheaths in various shapes for CS cannulation and inner subselective sheath. Lead, long sheath, subselective sheath and short sheath should be quoted as one set..Should be FDA'/CE'/DCGI approved
20
-
-
CRT - Triple chamber pacing system comprising pacemaker, active atrial and ventricular leads and bipolar, over the wire coronary sinus lead. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves '/ sizes..Should be FDA'/CE'/DCGI approved
20
-
-
AICD - Single chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of at least 35 J, with matching single and dual coil, integrated bipolar active fixation ventricular leads..Should be FDA'/CE'/DCGI approved
20
-
-
AICD - Dual chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J, with matching single and dual coil, integrated bipolar active fixation atrial and ventricular leads..Should be FDA'/CE'/DCGI approved
20
-
-
CRT-D - Triple Chamber Pacemaker System with cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for CRT pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J, with matching single and dual coil, integrated bipolar, active fixation atrial and ventricular leads. .Should be FDA'/CE'/DCGI approved
10
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-
Steroid eluting bipolar active fixation atrial leads with introducer sheath.Should be FDA'/CE'/DCGI approved
20
-
-
Steroid eluting bipolar active fixation ventricular leads with introducer sheath.Should be FDA'/CE'/DCGI approved
30
-
-
Single pass VDD leads with introducer sheath.Should be FDA'/CE'/DCGI approved
10
-
-
Single and Dual coil (50-50%), integrated bipolar active fixation ICD leads.Should be FDA'/CE'/DCGI approved
10
-
-
Active fixation epicardial leads .Should be FDA'/CE'/DCGI approved
10
-
-
Quadripolar lead specially designed for placement in coronary sinus for LV pacing. Should be supplied with 9F short sheath with valve, long preshaped slittable sheaths in various shapes for CS cannulation and inner subselective sheath. Lead, long sheath, subselective sheath and short sheath should be quoted as one set..Should be FDA'/CE'/DCGI approved
10
-
-
Implantable loop recorder for subcutaneous implantation, capable of recording at least one channel subcutaneous ECG. Matching hand-held activator should be provided. .Should be FDA'/CE'/DCGI approved
5
-
-
Steerable, long sheath introducer of at least 8F inner diameter, with atraumatic tip and bidirectional steering, designed for use in epicardial mapping.Should be FDA'/CE'/DCGI approved
2
-
-
Single chamber MRI conditional pacemaker with matching atrial or ventricular active or passive fixation lead and introducer sheath set. .Should be FDA'/CE'/DCGI approved
5
-
-
Dual chamber MRI conditional pacemaker with matching atrial and ventricular active or passive fixation leads and 2 introducer sheath sets..Should be FDA'/CE'/DCGI approved
5
-
-
Disposable Heartstart adult plus mutifunction defibrillation pads for use with the Philips defibrillator.Should be FDA'/CE'/DCGI approved
10
-
-
Disposable pads for defibrillation / transcutaneous pacing for use with the Zoll defibrillator.Should be FDA'/CE'/DCGI approved
10
-
-
(S)One set of high grade stainless steel surgical instruments for minor surgical procedure. Must include the following instruments – Sponge forceps 2 Nos, Towel clamp – 4, Hemostatic Crile forceps straight – 4, hemostatic Crile forceps curved – 6, Allis tissue forceps – 2, Mayo Hegar needle holder 6 inches – 1, Mayo Hegar needle holder 7 inches – 1, Mayo scissors straight – 1, Metzenbaum scissors curved – 1, Small curved scissors – 1, small straight scissors – 1, thumb forceps – 2, adsons toothed forceps – 2, Knife handle #7 – 1, knife handle #4 – 1, Weitlaner self retaining retractor sharp 5 inches – 1, double hook retractor – 2, right angle forceps – 1.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
2
-
-
(S)LEAD locking device for transvenous extraction of chronically implanted pacemaker and defibrillator leads with mechanical rotating dilator 9F/11F/13F diameter with a flexible shaft and dilator sheath set .Should be FDA'/CE'/DCGI approved
25
-
-
(S)SPO2 Probe Compaitable with Monitor Model : SPACE LABS.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG Probe Compaitable with Monitor Model : SPACE LABS.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff Compaitable with Monitor Model : SPACE LABS.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG leads Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (Adult)Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (paediatrics)Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (Adult) Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (paediatrics) Compaitable with Monitor Model : Mindray MEC 2000.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG leads Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (Adult)Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (paediatrics)Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (Adult) Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (paediatrics) Compaitable with Monitor Model : STAR 55.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG leads Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (Adult)Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP cuff (paediatrics)Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (Adult) Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
(S)BP Cuff (paediatrics) Compaitable with Monitor Model : Philips MP 30.Should be FDA'/CE'/DCGI approved
10
-
-
ACT Catridges compatible with medtronic ACT machine.Should be FDA'/CE'/DCGI approved
300
-
-
(S)Arterial Pressure monitoring Transducers (Disposable).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Syringe For pressure Injector (Disposable) - Liebel Flarsheim injector 100ml.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe disposable compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG Cable compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe disposable compaitable with Multi Purpose Monitor AGILENT.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG Cable compaitable with Multi Purpose Monitor AGILENT.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor AGILENT.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor AGILENT.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPO2 Probe disposable compaitable with Multi Purpose Monitor MEC 1200.Should be FDA'/CE'/DCGI approved
10
-
-
(S)ECG Cable compaitable with Multi Purpose Monitor MEC 1200.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor MEC 1200.Should be FDA'/CE'/DCGI approved
10
-
-
(S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor MEC 1200.Should be FDA'/CE'/DCGI approved
10
-
-
(S)Superior Quality ECG Jelly in bottles of 250 g long lasting .Should be FDA'/CE'/DCGI approved
2000
-
-
(S)Superior Quality ECG ECHO Jelly in bottles of 250 g long lasting .Should be FDA'/CE'/DCGI approved
2000
-
-
(S)Quick Clot - Hydrophilic non woven gauze roll impregnated with a naturally occuring inorganic mineral -Kaolin, Along with a unique direct pressure adhesive bandage packed in a foil pouch for aseptic removal..Should be FDA'/CE'/DCGI approved
1000
-
-
(S)MORTARA ELI-250 MACHINE cable.Should be FDA'/CE'/DCGI approved
5
-
-
(S)MORTARA ELI 350 MACHINE cable.Should be FDA'/CE'/DCGI approved
5
-
-
(S)CHEST BULBS ADULT.Should be FDA'/CE'/DCGI approved
5
-
-
(S)CHEST BULBS PEDIATRICS.Should be FDA'/CE'/DCGI approved
5
-
-
(S)LIMB LEADS ADULT.Should be FDA'/CE'/DCGI approved
5
-
-
(S)LIMB LEADS PEDIATRICS.Should be FDA'/CE'/DCGI approved
5
-
-
(S) BioCare ECG recorder paper.Should be FDA'/CE'/DCGI approved
2000
-
-
(S) Mortara ELI-250 ECG Recorder Head.Should be FDA'/CE'/DCGI approved
5
-
-
(S) Mortara ELI-350 ECG Recorder Head.Should be FDA'/CE'/DCGI approved
5
-
-
(S) Mortara TMT Paper.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) Mortara ELI-350 ECG Paper..Should be FDA'/CE'/DCGI approved
1000
-
-
(S) Mortara ELI-250 ECG Paper..Should be FDA'/CE'/DCGI approved
1000
-
-
(S) Edan Multichannel Machine Paper.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) NIHON KODEN Multichannel Machine Paper Roll Type.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) AG/AGCL IMPORTED PATIENT PREJELLED ELECTRODES FOR LONG-TERM MONITORING SUPERIOR QUALITY .Should be FDA'/CE'/DCGI approved
500000
-
-
(S)PATIENT TUBING SYSTEM COMPATIBLE WITH MAQUET S VENTILATOR.Should be FDA'/CE'/DCGI approved
10
-
-
(S)SPOT TEST KITS for HIV .Should be FDA'/CE'/DCGI approved
300
-
-
(S)SPOT TEST KITS for HBsAg .Should be FDA'/CE'/DCGI approved
300
-
-
(S)SPOT TEST KITS for HCV .Should be FDA'/CE'/DCGI approved
300
-
-
(S)StickyMats'/Tacky Mats 1 to 30 on 30 Peel Tags, anti ststic, with Holding Stick Time : 1000 mins, Price per box to be quoted with number of units per box.Should be FDA'/CE'/DCGI approved
300
-
-
(S) DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY'/ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES with absorbable material.Sample to be supplied for testing
1000
-
-
(S) DISPOSABLE STERILE DRAPES FOR PERMANENT PACEMAKER IMPLANTATION L and R Pectoral Approaches.Sample to be supplied for testing
250
-
-
(S) Tissue paperbased disposable bed covers in continious rolls of Width "90Cm" for use on trolleys & Cardiac Cath Lab Tables..Sample to be supplied for testing
5000
-
-
(S) DISPOSABLE STERILE ANGIOPLASTY DRAPES KITS WITH A. One Unit -DRAPE ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES with absorbable material B. Three Units DISPOSABLE STERILE GOWNS C. One Unit Disosable Centre Hole towel D. One Unit Cath Trolley Drape.Sample to be supplied for testing
5000
-
-
(S) DISPOSABLE GOWN & PYJAMA SET FOR CATH LAB PROCEDURE (SMALL/MEDIUM /LARGE).Sample to be supplied for testing
2000
-
-
(S) DISPOSABLE GAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures.Sample to be supplied for testing
10000
-
-
( D) BATTERY OPERATED AUTOMATED DIGITAL BP APPARATUS with ADULT,LARGE ADULT and PEDIATRIC CUFFS with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
10
-
-
( D ) DIGITAL BP APPARATUS HEAVY DUTY, with ADULT,LARGE ADULT and PEDIATRIC CUFFS RUNNING IN AC POWER FOR USE IN OPD AND WARD with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
2
-
-
( D)DIGITAL WEIGHING SCALE FOR PATIENT WEIGHT with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
2
-
-
( D) SYRINGE INFUSION PUMPS with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
4
-
-
(D)MULTIPARAMETER MONITORS ECG, SPO2,NIBP with 3yr warrranty and 2 sets of cables.Item to be Demonstrated to departmental selection committee.
10
-
-
( D) OT LIGHT- FLOOR MOUNTED, LED SOURCE , Brightness and Focus ADJUSTABLE with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
3
-
-
( D) SMALL SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee.
10
-
-
( D) INTERMEDIATE SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee.
10
-
-
( D) LARGE SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee.
10
-
-
( D) Battery Operated Pocket Sized SpO2 Probes.Item to be Demonstrated to departmental selection committee.
5
-
-
(D)Compact Disk- Recordable ( CD-R) with hard shell box.Item to be Demonstrated to departmental selection committee.
2000
-
-
(D)DVD- Recordable ( DVD-R) with hard shell box.Item to be Demonstrated to departmental selection committee.
200
-
-
(S)CD Sticker Labels with Department of Cardiology ,JIPMER Stickers, With Space for printing Angio No and CD No.Item to be Demonstrated and discussed to departmental selection committee.
3000
-
-
(S)Permanent Marker Pens- Thin Script- Black.Item to be Demonstrated and discussed to departmental selection committee.
50
-
-
(S)White Board Markers Black and Blue.Item to be Demonstrated and discussed to departmental selection committee.
50
-
-
(S)Batteries Compatible with Zoll M Series defibrillators.Should be FDA'/CE'/DCGI approved
15
-
-
(D)Catridge for HP 1020 series.Should be FDA'/CE'/DCGI approved
5
-
-
(S)Disposable Paper based Sterile Front Buttoned Black/ Brown/ Dark blue half sleeve shirt and pyjama for cath lab patient dress.Should be FDA'/CE'/DCGI approved
1000
-
-
(S)Rechargable Ni- MH Batteries 1.2 to 1.5 V AA 2500 mAh with 80 batteries and one fast charger which can charge 4 batteries at a time should be supplied with every 8 batteries..Should be FDA'/CE'/DCGI approved
80
-
-
(D)Long term external loop recorder with capability to record at least one ECG lead for a period of at least 7 days. Recording patch / electrodes should be water resistant allowing patient to bathe. Episodes should be identified automatically and it should also be possible to record patient triggered episodes. Transmission should be wireless and monitored in a 24x7 staffed monitoring center. Quoted cost should include disposable electrode set, recorder, hand-held activator, data transmission and reporting for the period of recording..Should be FDA'/CE'/DCGI approved
10
-
-
(S)Disposable, sterile cover for Fluoroscopy system Image Intensifier. Should fit Image Intensifier of different sizes and should have elastic band for easy retention..Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
100
-
-
(S)Washable and Autoclavable Cut Shoes (Clogs) Specially designed for wearing in Operation rooms /ICU's wear slippers at least 12 inch foot length.(roomy fit).should have non collapsible sole to support the arch of foot. The brochure mentioning the details of the product should be submitted .Mention various sizes available.(SPR).Item to be Demonstrated to departmental selection committee
150
-
-
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