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
Healthcare and Medicine
Eprocure
Opening Date4 Mar 2024
Closing Date11 Apr 2024
Tender AmountRefer Documents
Costs
EMD
₹ 5,000Document Cost
₹ 590Tender Fee
Refer Documents
Description
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Contact
Tender Id
2024_JIPMP_798650_1Bid Award Id
ViewTender No
JIP/Pur.2(7)/OeT/CARDI/2024-26Tender 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 SHEATH SYSTEMS SIZES 5F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
500
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(S) FEMORAL SHEATH SYSTEMS SIZES 5F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 6F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
100
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 6F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 7F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
100
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 7F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 8F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 8F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
100
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 9F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 9F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
100
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 10F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 10F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 11F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
-
-
(S) FEMORAL SHEATH SYSTEMS SIZES 11F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 12F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 12F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 14F 7.5 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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(S) FEMORAL SHEATH SYSTEMS SIZES 14F 11 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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(S) FEMORAL SHEATH SYSTEMS SIZES 5F 23 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 6F 23 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 7F 23 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
(S) FEMORAL SHEATH SYSTEMS SIZES 8F 23 cm with accessories for insertion.Should be FDA'/CE'/DCGI approved
50
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-
RADIAL ACCESS
-
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 018 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 021 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 025 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 018 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA'/CE'/DCGI approved
100
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 021 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA'/CE'/DCGI approved
100
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 025 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 6F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 6F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 6F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 6F 11cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 6F 11cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 6F 11cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA'/CE'/DCGI approved
400
-
-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA'/CE'/DCGI approved
400
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-
(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 10 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
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(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 10 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
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-
(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 16 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
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(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 6F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
-
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(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 6F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
-
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(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 6F 16 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 7F 10 cm capable of introducing 8F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
-
-
(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 7F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
-
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(S) TRANSRADIAL SLENDER SHEATH SYSTEMS 7F 16 cm capable of introducing 8F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA'/CE'/DCGI approved
100
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ACCESS CLOSURE
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(S) FEMORAL VASCULAR CLOSURE DEVICE Collagen Based Femoral 6F Should be FDA'/CE'/DCGI approved
40
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(S) FEMORAL VASCULAR CLOSURE DEVICE Collagen Based Femoral 8F Should be FDA'/CE'/DCGI approved
40
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(S) FEMORAL VASCULAR CLOSURE DEVICE Prolene sutured capable of closing upto 21F devices.Should be FDA' or CE' andDCGI approved
40
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(S) Collagen anchor based Femoral vascular closure device capable of closing large bore access ranging from 12 to 25 Fr.Should be FDA'/CE'/DCGI approved
40
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(S) Radial Compression Device Balloon Inflation type transparent .Should be FDA'/CE'/DCGI approved
25
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-
(S) Radial Compression Device Screw type .Should be FDA'/CE'/DCGI approved
25
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(S) Polymer reinforced adhesive skin closure strips 6mm x 100mm
500
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(S) Semipermeable waterproof plastic wound dressing with pad (Dressing size of 9 x 15cm and pad size 5 x 10cm)
200
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DIAGNOSTIC CATHETERS
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(S)COURNAND CATHETER 5F, 6F 110 cm woven dacron. Should be FDA'/CE'/DCGI approved
100
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(S)GOODALE-LUBIN CATHETER 6F, 7F 100/125 cm woven dacron. Should be FDA/CE/DCGI approved
50
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(S)JUDKINS LEFT CATHETER 4F 90/110 cm all Curves. Should be FDA'/CE'/DCGI approved
50
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(S)JUDKINS LEFT CATHETER 5F,6F 110 cm all Curves. Should be FDA'/CE'/DCGI approved
250
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-
(S)JUDKINS RIGHT CATHETER 4F, 90/110cm all Curves. Should be FDA'/CE'/DCGI approved
100
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(S)JUDKINS RIGHT CATHETER 5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
250
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(S)AMPLATZ LEFT CATHETER 4F 90/110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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(S)AMPLATZ LEFT CATHETER 5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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(S)AMPLATZ RIGHT CATHETER 4F 90/110 cmall Curves. Should be FDA'/CE'/DCGI approved
25
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(S)AMPLATZ RIGHT CATHETER 5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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-
(S)LEFT CORONARY BY PASS CATHETER 4F,5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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(S)RIGHT CORONARY BY PASS CATHETER 4F,5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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(S)INTERNAL MAMMARY ARTERY CATHETER 4F, 5F,6F 110cm all Curves. Should be FDA'/CE'/DCGI approved
25
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(S)MULTIPURPOSE CATHETER 4F 90/110cm A1,A2,B1,B2. Should be FDA'/CE'/DCGI approved
50
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(S)MULTIPURPOSE CATHETER 5F110cm A1,A2,B1,B2. Should be FDA'/CE'/DCGI approved
200
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(S)MULTIPURPOSE CATHETER 6F 110cm A1,A2,B1,B2. Should be FDA'/CE'/DCGI approved
200
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 100cm SMALL CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 110cm SMALL CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 100cm INTERMEDIATE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 110cm INTERMEDIATE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 100cm LARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 110cm LARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 100cm EXTRALARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 110cm EXTRALARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 100cm SMALL CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 110cm SMALL CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 100cm INTERMEDIATE CURVES.Should be FDA'/CE'/DCGI approved
250
-
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 110cm INTERMEDIATE CURVES.Should be FDA'/CE'/DCGI approved
250
-
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 100cm LARGE CURVES.Should be FDA'/CE'/DCGI approved
250
-
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 110cm LARGE CURVES.Should be FDA'/CE'/DCGI approved
250
-
-
(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 100cm EXTRALARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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(S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 110cm EXTRALARGE CURVES.Should be FDA'/CE'/DCGI approved
250
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( S) PIG TAIL CATHETERS 4F 90cm.Should be FDA'/CE'/DCGI approved
100
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( S) PIG TAIL CATHETERS 4F 110cm.Should be FDA'/CE'/DCGI approved
50
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-
( S) PIG TAIL CATHETERS 4F 150cm.Should be FDA'/CE'/DCGI approved
50
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( S) PIG TAIL CATHETERS 5F 90cm.Should be FDA'/CE'/DCGI approved
100
-
-
( S) PIG TAIL CATHETERS 5F 110cm.Should be FDA'/CE'/DCGI approved
400
-
-
( S) PIG TAIL CATHETERS 5F 150cm.Should be FDA'/CE'/DCGI approved
100
-
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( S) PIG TAIL CATHETERS 6F 90cm.Should be FDA'/CE'/DCGI approved
100
-
-
( S) PIG TAIL CATHETERS 6F 110cm.Should be FDA'/CE'/DCGI approved
400
-
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( S) PIG TAIL CATHETERS 6F 150cm.Should be FDA'/CE'/DCGI approved
100
-
-
( S) ANGLED PIG TAIL CATHETERS 4F 90cm.Should be FDA'/CE'/DCGI approved
50
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-
( S) ANGLED PIG TAIL CATHETERS 4F 110cm.Should be FDA'/CE'/DCGI approved
50
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( S) ANGLED PIG TAIL CATHETERS 4F 150cm.Should be FDA'/CE'/DCGI approved
50
-
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( S) ANGLED PIG TAIL CATHETERS 5F 90cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S) ANGLED PIG TAIL CATHETERS 5F 110cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S) ANGLED PIG TAIL CATHETERS 5F 150cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S) ANGLED PIG TAIL CATHETERS 6F 90cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S) ANGLED PIG TAIL CATHETERS 6F 110cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S) ANGLED PIG TAIL CATHETERS 6F 150cm.Should be FDA'/CE'/DCGI approved
50
-
-
( S)MARKER PIGTAIL CATHETER 4F 90cm. Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 4F 110cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 4F 150cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 5F 90cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 5F 110cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 5F 150cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 6F 90cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 6F 110cm .Should be FDA'/CE'/DCGI approved
50
-
-
( S) MARKER PIGTAIL CATHETER 6F 150cm .Should be FDA'/CE'/DCGI approved
50
-
-
NIH Angiography catheter 4F Should be FDA'/CE'/DCGI approved
50
-
-
NIH Angiography catheter 5F/6F Should be FDA'/CE'/DCGI approved
50
-
-
BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA'/CE'/DCGI approved
50
-
-
BERMAN Angiography catheter 5F and 6F 60/90/110 cm Should be FDA'/CE'/DCGI approved
50
-
-
REVERSE BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA'/CE'/DCGI approved
50
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-
REVERSE BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA'/CE'/DCGI approved
50
-
-
MULTITRACK Angiography Catheter capable of doing angiography with guidewire insitu 4F 80/100cm Should be FDA'/CE'/DCGI approved
25
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MULTITRACK Angiography Catheter capable of doing angiography with guidewire insitu 5F 80/100cm Should be FDA'/CE'/DCGI approved
25
-
-
MULTITRACK Angiography Catheter capable of doing angiography with guidewire insitu 6F 80/100cm Should be FDA'/CE'/DCGI approved
25
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ACCESSORIES
-
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-
(S) INITIAL PUNCTURE NEEDLES18G Should be FDA'/CE'/DCGI approved
1500
-
-
(S) MICROPUNCTURE NEONATAL INTRODUCER SETS AND SHEATH SYSTEMS 4F Should be FDA'/CE'/DCGI approved
100
-
-
(S) MICROPUNCTURE NEONATAL INTRODUCER SETS AND SHEATH SYSTEMS 5F.Should be FDA'/CE'/DCGI approved
100
-
-
(S) Micropuncture introducer set suitable for ultrasound guided vascular access. Should include one 21G 7cm micropuncture needle, one 0.18" guide wire and one 5F introducer sheath as one set
100
-
-
(S) 3/3 ROTATING MANIFOLD FOR CAG.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) 3/3 ROTATING MANIFOLD FOR 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) TOUHEY BORST Y CONNECTOR- SCREW TYPE and INTRODUCER NEEDLE for PTCA.Should be FDA'/CE'/DCGI approved
100
-
-
(S) Y CONNECTOR 10F Diameter having a larger inner lumen for peripheral interventions.Should be FDA'/CE'/DCGI approved
50
-
-
(S) Torquer device for 014 guide wire
250
-
-
(S) Torquer device for 018 guide wire
100
-
-
(S) Torquer device for 021 guide wire
50
-
-
(S) Torquer device for 025 guide wire
50
-
-
(S) Torquer device for 035 guide wire
50
-
-
(S) Torquer device for 038 guide wire
50
-
-
( 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
1000
-
-
(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) 3 RING CONTROL SYRINGES 20cc.Should be FDA'/CE'/DCGI approved
2000
-
-
(S) 3 RING CONTROL SYRINGES TRANSPARENT WITH MARKERS 20cc.Should be DCGI approved
1000
-
-
( S) FEMORAL ANGIOGRAPHY KITS Comprising the following Items a.Femoral Sheath Insertion System 6F 11cm b. Femoral Angiography 6F JL4 and JR3.5 catheters ( one each) c. 0.035 J Hydrophilic teflon 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 with 320 mg iodine/mL.Should be FDA'/CE'/DCGI approved
50
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-
(S) RADIAL ANGIO SET WITH PUNCTURE NEEDLE, SHEATH 6F 7cm, STRAIGHT GUIDEWIRE 025/021 AND TIG coronary diagnostic catheter 5F, AND HYDROPHILIC POLYMER J tipped 035 145 cm WIRES.Should be FDA'/CE'/DCGI approved
100
-
-
( S) RADIAL ANGIOGRAPHY KITS Comprising the following Items a.Radial Sheath Insertion System 6F 7cm 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 320mg iodine/mL.Should be FDA'/CE'/DCGI approved
50
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(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
5
-
-
(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
5
-
-
(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
5
-
-
(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
4
-
-
(S) 20CC INFLATION DEVICE AS ONE SET capable of inflation pressures upto 30 bar.Should be FDA'/CE'/DCGI approved
200
-
-
(S) 20CC INFLATION DEVICE AS ONE SET capable of inflation pressures upto 25 bar.Should be FDA'/CE'/DCGI approved
200
-
-
( S)INFLATION DEVICE TO INFLATE HIGH PRESSURE UPTO 50 ATM.Should be FDA'/CE'/DCGI approved
100
-
-
(S) PTCA MANIFOLD WITH FLUSH DEVICE.Should be FDA'/CE'/DCGI approved
100
-
-
(S) INFUSION ACCELERATOR ( PRESSURE BAG).Should be FDA'/CE'/DCGI approved
50
-
-
( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 12cc.Should be FDA'/CE'/DCGI approved
500
-
-
( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 20cc.Should be FDA'/CE'/DCGI approved
1000
-
-
GUIDEWIRES
-
-
-
(S)TEFLON COATED GUIDE WIRE 145 CM 0.021" ST. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRE 145 CM 0.021" J. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRE 145 CM 0.025" ST. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRE 145 CM 0.025" J. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRES 145 CM 0.032" ST. Should be FDA'/CE'/DCGI approved
300
-
-
(S)TEFLON COATED GUIDE WIRES 145 CM 0.032" J. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.035" ST. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.035" J. Should be FDA'/CE'/DCGI approved
1000
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.038" ST. Should be FDA'/CE'/DCGI approved
50
-
-
(S)TEFLON COATED GUIDE WIRES 145 CMS 0.038" J. Should be FDA'/CE'/DCGI approved
50
-
-
( S) TEFLON COATED EXCHANGE (260cm and above) 0.018'' ST peripheral guide wire .Should be FDA'/CE'/DCGI approved
25
-
-
( S) TEFLON COATED EXCHANGE (260cm and above) 0.018'' J peripheral guide wire .Should be FDA'/CE'/DCGI approved
25
-
-
( S) TEFLON COATED EXCHANGE (260cm and above) 0.021'' ST peripheral guide wire .Should be FDA'/CE'/DCGI approved
25
-
-
( S) TEFLON COATED EXCHANGE (260cm and above) 0.021'' J peripheral guide wire .Should be FDA'/CE'/DCGI approved
25
-
-
(S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above) 0.032"ST.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above) 0.032" J.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above) 0.035"ST.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above) 0.035" J.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGEGUIDE WIRE (260cm and above) 0.038"ST.Should be FDA'/CE'/DCGI approved
100
-
-
(S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above) 0.038"J.Should be FDA'/CE'/DCGI approved
100
-
-
( S)Lunderquist type high support exchange length 0.035'' (260cm and above) short and long floppy tip guide wire. Should be FDA'/CE'/DCGI approved
50
-
-
( S)Safari type high support exchange length 0.035'' (260cm and above)curved tip guide wire. Should be FDA'/CE'/DCGI approved
25
-
-
( S)Confida type intermediate support exchange length 0.035'' (260cm and above) J tip guide wire. Should be FDA'/CE'/DCGI approved
25
-
-
( S)Roadrunner type extrasupport exchange length 0.035'' (260cm and above) Straight tip guide wire with hydrophilic coating . Should be FDA'/CE'/DCGI approved
25
-
-
( S)Roadrunner type extrasupport exchange length 0.035'' (260cm and above) J tip guide wire with hydrophilic coating . Should be FDA'/CE'/DCGI approved
10
-
-
( S)AMPLATZ SUPERSTIFF EXCHANGE GUIDE WIRES 0.035'. 260 cm and above- Short floppy tip.Should be FDA'/CE'/DCGI approved
100
-
-
( S)AMPLATZ SUPERSTIFF EXCHANGE GUIDE WIRES .038''. 260 cm and above- Short floppy tip.Should be FDA'/CE'/DCGI approved
100
-
-
( S)AMPLATZ ULTRA STIFF EXCHANGE GUIDE WIRES 0.035' J. 260 cm and above- LONG floppy tip.Should be FDA'/CE'/DCGI approved
100
-
-
( S)AMPLATZ ULTRA STIFF EXCHANGE GUIDE WIRES 0.038'' J. 260 cm and above- LONG floppy tip.Should be FDA'/CE'/DCGI approved
100
-
-
( S) AMPLATZ NOODLE TYPE EXCHANGE Guidewire PTFE coated Stainless Steel wire 0.035" J. 260 cm and above
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 018 ST.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 018 J.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 021 ST.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 021 J.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 025 ST.Should be FDA'/CE'/DCGI approved
100
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 025 J.Should be FDA'/CE'/DCGI approved
175
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 032 ST.Should be FDA'/CE'/DCGI approved
150
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 032 J.Should be FDA'/CE'/DCGI approved
175
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 035 ST.Should be FDA'/CE'/DCGI approved
200
-
-
( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 035 J.Should be FDA'/CE'/DCGI approved
200
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 018 ST.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 018 J.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 021 ST.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 021 J.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 025 ST.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 025 J.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 032 ST.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 032 J.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 035 ST.Should be FDA'/CE'/DCGI approved
50
-
-
( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 035 J.Should be FDA'/CE'/DCGI approved
50
-
-
GUIDING CATHETERS
-
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JR 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S) (EX)PTCA GUIDING CATHETER 5F JR 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S) (EX)PTCA GUIDING CATHETER 6F JR 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JR 3.0 CURVE. Should be FDA'/CE'/DCGI approved
75
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JR 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JR 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JR 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JR 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JR 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JR 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JR 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JR 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JR 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JR 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JR 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JR 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JR 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JR 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JR 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JR 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 4.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JR 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JR 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JR 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JR 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JR 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F JL 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F JL 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F JL 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F JL 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F JL 5.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F EBU 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F EBU 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 5F EBU 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F EBU 2.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F EBU 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F EBU 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 8F EBU 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F EBU 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F EBU 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 6F EBU 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F EBU 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 8F EBU 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F EBU 3.75 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F EBU 3.75 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F EBU 3.75 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F EBU 3.75 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F EBU 3.75 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F EBU 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F EBU 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 6F EBU 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 7F EBU 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F EBU 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F XB 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F XB 2.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F XB 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 6F XB 2.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 6F XB 3.0 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F XB 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 8F XB 3.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F XB 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 5F XB 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 6F XB 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 7F XB 3.5 CURVE. Should be FDA'/CE'/DCGI approved
100
-
-
(S)(EX)PTCA GUIDING CATHETER 8F XB 3.5 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)PTCA GUIDING CATHETER 4F XB 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F XB 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F XB 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F XB 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F XB 4.0 CURVE. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F MP ALL CURVES. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F MP ALL CURVES. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F MP ALL CURVES. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F MP ALL CURVES. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F MP ALL CURVES. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F CLS 3.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F CLS 3.0 Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F CLS 3.0. Should be FDA'/CE'/DCGI approved
100
-
-
(EX)PTCA GUIDING CATHETER 7F CLS 3.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F CLS 3.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F CLS 3.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F CLS 3.5 Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F CLS 3.5. Should be FDA'/CE'/DCGI approved
100
-
-
(EX)PTCA GUIDING CATHETER 7F CLS 3.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F CLS 3.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AL 0.75. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AL 0.75 Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AL 0.75. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AL 0.75. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AL 0.75. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AL 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AL 1.0 Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AL 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AL 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AL 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AL 1.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AL 1.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AL 1.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AL 1.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AL 1.5. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AL 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AL 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AL 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AL 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AL 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AR 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AR 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AR 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AR 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AR 1.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 4F AR 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 5F AR 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 6F AR 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 7F AR 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX)PTCA GUIDING CATHETER 8F AR 2.0. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F 3D RDC GUIDING CATHETER . Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F 3D RDC GUIDING CATHETER . Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F RADIAL TIG 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F RADIAL TIG 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F RADIAL TIG 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F RADIAL TIG 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F RADIAL TIG 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F RADIAL TIG 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F RADIAL TIG 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F RADIAL TIG 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI LEFT 3.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI LEFT 3.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI LEFT 3.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI LEFT 3.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI LEFT 3.75 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI LEFT 3.75 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI LEFT 3.75 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI LEFT 3.75 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI LEFT 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI LEFT 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI LEFT 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI LEFT 4.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI LEFT 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI LEFT 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI LEFT 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI LEFT 4.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI RIGHT 1.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI RIGHT 1.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI RIGHT 1.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI RIGHT 1.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI RIGHT 1.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI RIGHT 1.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI RIGHT 1.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI RIGHT 1.5 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 4F IKARI RIGHT 2.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F IKARI RIGHT 2.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F IKARI RIGHT 2.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 7F IKARI RIGHT 2.0 PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F KIMMY PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F KIMMY PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 5F KIMMY MINOR PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(EX) 6F KIMMY MINOR PTCA GUIDING CATHETER. Should be FDA'/CE'/DCGI approved
50
-
-
(S)Sheathless PTCA guiding catheter for coronary interventions from radial access 5F. Should be FDA/CE/DGCI approved
25
-
-
(S)Sheathless PTCA guiding catheter for coronary interventions from radial access 6F. Should be FDA/CE/DGCI approved
25
-
-
(S)Sheathless PTCA guiding catheter for coronary interventions from radial access 7F. Should be FDA/CE/DGCI approved
25
-
-
(S)Sheathless PTCA guiding catheter for coronary interventions from radial access 8F. Should be FDA/CE/DGCI approved
25
-
-
(S)Coronary guide extension catheter 8 Fr .Should be FDA'/CE'/DCGI approved
10
-
-
(S)Coronary guide extension catheter with distal 2 mm radioluscent tip capable of doing OCT in coronary ostial lesion.Should be FDA'/CE'/DCGI approved
10
-
-
( S)Superselective cathether for Mother and Child technique.Should be FDA' or CE' and DCGI approved
10
-
-
(S)Coronary Guide Extension Catheter 6Fr. Should be FDA'/CE'/DCGI approved
10
-
-
(S)Coronary Guide Extension Catheter 7Fr. Should be FDA'/CE'/DCGI approved
10
-
-
(S)Soft Guideliner system for mother and child technique. Should be FDA' or CE' and DCGI approved
10
-
-
CORONARY WIRES
-
-
-
(S)PTCA WIRES Floppy standard length .Should be FDA'/CE'/DCGI approved
200
-
-
(S)PTCA WIRES Floppy extra support exchange length.Should be FDA'/CE'/DCGI approved
50
-
-
(S)PTCA WIRES Floppy extra support Intermediate Standard Length.Should be FDA'/CE'/DCGI approved
200
-
-
(S)PTCA WIRES Floppy Extra support Standard Length.Should be FDA'/CE'/DCGI approved
250
-
-
(S)PTCA DOC LINK EXTENSION Floppy extra support WIRES.Should be FDA'/CE'/DCGI approved
100
-
-
(S)Floppy extra support EXCHANGE WIRES FOR PTCA .Should be FDA'/CE'/DCGI approved
500
-
-
(S)Double core spring tip core to tip Floppy extra support TYPE WIRES FOR PTCA.Should be FDA'/CE'/DCGI approved
500
-
-
(S)PTCA WIRES Floppy extra support Tapering Tip Hydrophilic.Should be FDA'/CE'/DCGI approved
100
-
-
(S)PTCA WIRE - Floppy extra support CTO WIRES-PLATINUM.Should be FDA'/CE'/DCGI approved
100
-
-
(S)PTCA WIRES CTO- hydrophobic Floppy extra support .Should be FDA'/CE'/DCGI approved
100
-
-
(S)PTCA WIRES for CTO-hydrophlic without polymer coatingFloppy extra support Extra support.Should be FDA'/CE'/DCGI approved
50
-
-
(S)PTCA WIRES Polymer Coated Hydrophilic Floppy extra support .Should be FDA'/CE'/DCGI approved
75
-
-
(S)PTCA WIRES Polymer Coated Hydrophilic Floppy Extra support.Should be FDA'/CE'/DCGI approved
100
-
-
(S)PTCA WIRES- Polymer coated Floppy extra support tapering tip.Should be FDA'/CE'/DCGI approved
50
-
-
(S)PTCA WIRES - Specially Designed Floppy extra support for Tortuous vessels.Should be FDA'/CE'/DCGI approved
100
-
-
(S)PTCA WIRES Floppy extra support Hybrid coated.Should be FDA'/CE'/DCGI approved
60
-
-
(S)PTCA WIRES Floppy extra support Extrasupport Polymer coated.Should be FDA'/CE'/DCGI approved
60
-
-
(S)LINK EXTENSION Floppy extra support PTCA wire type 300 cm wires.Should be FDA'/CE'/DCGI approved
75
-
-
(S)PTCA 009 exchange length floppy wires for Retrograde approach exchange length.Should be FDA'/CE'/DCGI approved
40
-
-
(S)PTCA wire for CTO hydrophobic straight with tip loads available upto 12 gm.Should be FDA'/CE'/DCGI approved
40
-
-
(S)PTCA wire for collateral crossing with tip load of 0.3 gm.Should be FDA'/CE'/DCGI approved
40
-
-
(S)PTCA wire for CTO hydrophilic with a uncoated distal tip, preshaped.Should be FDA'/CE'/DCGI approved
40
-
-
(S)PTCA 009 exchange length floppy extra support wires for Retrograde approach exchange length.Should be FDA'/CE'/DCGI approved
40
-
-
CORONARY BALLOONS
-
-
-
(S) (EX)Rapid Exchange BalloonSystems with Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange BalloonSystems with Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange BalloonSystems with short overhang and Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be CE' and DCGI approved
80
-
-
(S) (EX)Rapid Exchange BalloonSystems with short overhang Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be CE' and DCGI approved
80
-
-
(S) (EX)Rapid Exchange BalloonSystems Low profile with Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange BalloonSystems with low profile Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of fibrotic lesions all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of calcific lesions all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of fibrotic lesions with short overhang all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of calcific lesions with short overhang all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons Low profile for PTCA of fibrotic lesions all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant Balloons Low profile for PTCA of calcific lesions all sizes.Should be FDA and DCGI approved
80
-
-
(S) (EX)Rapid Exchange Non-Compliant High-Pressure Balloons for PTCA all sizes.Should be FDA and DCGI approved
25
-
-
(S) (EX)Rapid Exchange Non-Compliant Ultrahigh pressure balloon for calcific lesions (30 atm and above for PTCA) all sizes .Should be FDA and DCGI approved
25
-
-
(S) (EX)Rapid Exchange Non-Compliant nominal pressure balloon for CTO intervention of all sizes.Should be FDA and DCGI approved
50
-
-
(S) (EX)Rapid Exchange Non-Compliant high pressure balloon for CTO intervention all sizes.Should be FDA and DCGI approved
50
-
-
(S) (EX)Rapid Exchange Non-Compliant Ultrahigh pressure balloon for CTO intervention all sizes.Should be FDA and DCGI approved
50
-
-
(S) (EX) Rapid Exchange Non-Compliant Balloons for PTCA all sizes.Should be CE' and DCGI approved
80
-
-
(S) (EX)Rapid Exchange ULTRA HIGH PRESSURE (upto 35atm) Non-Compliant Balloons for PTCA.Should be FDA and DCGI approved
25
-
-
(S) (EX) Rapid Exchange ULTRA HIGH PRESSURE (upto 45atm)Non-Compliant Balloons for PTCA.Should be CE' and DCGI approved
25
-
-
(S)( EX)Ultra low profile Non compliant balloons for PCI.Should be CE' AND DCGI approved
25
-
-
(S)( EX)Ultra low profile compliant balloons for PCI.Should be CE' AND DCGI approved
25
-
-
(S)( EX)Ultra low profile semi complaint baloons for PCI.Should be CE' AND DCGI approved
25
-
-
(S)( EX)low profile CTO baloons for PCI 0.65mm in diameter.Should be CE' AND DCGI approved
25
-
-
(S)( EX)low profile CTO baloons for PCI 0.75mm in diameter.Should be CE' AND DCGI approved
25
-
-
(S) (EX)Over the wire Balloons for PTCA compliant .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S) (EX)Over the wire Balloons for PTCA Semicompliant .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S) (EX)Over the wire Balloons for PTCA Semicompliant for CTO .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S) (EX)Over the wire Balloons for PTCA Non-compliant .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S) (EX)Over the wire Balloons for PTCA Noncompliant for CTO .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S)(EX)Over the wire Balloons for PTSMA.Should be FDA' OR CE' AND DCGI approved
50
-
-
(S)( EX)Cutting Balloons Coronary.Should be FDA' OR CE' AND DCGI approved
10
-
-
(S)(EX) Scoring Coronary Balloons For severely calcified lesions.Should be FDA' OR CE' AND DCGI approved
12
-
-
(S) (EX)Drug eluting Coronary Balloons for in stent restenosis Coronary PACLITAXEL ELUTING Should be FDA' OR CE' AND DCGI approved
12
-
-
(S) ( EX) Dedicated non compliant coronary balloon for proximal optimisation technique (POT balloon) with shoulder length of 0.6 mm or less. Should be FDA'/CE'/DCGI approved
15
-
-
(S) ( EX) Coronary perfusion balloon catheter.Should be FDA'/CE'/DCGI approved
10
-
-
(S) (EX)Drug eluting Coronary Balloons for in stent restenosis Coronary SIROLIMUS ELUTING Should be FDA' OR CE' AND DCGI approved
30
-
-
CORONARY STENTS
-
-
-
(S)(EX)Balloon expandable BARE METAL Cobalt chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
25
-
-
(S)(EX) Balloon expandable sirolimus eluting second generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expadable everolimus eluting second generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expadable zoratolimus eluting second generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expadable sirolimus eluting third generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expadable everolimus eluting third generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expadable zotarolimus eluting third generation coronary stents.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Cobalt chromium alloy LESS than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Cobalt chromium alloy MORE than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Cobalt chromium alloy LESS than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Cobalt chromium alloy MORE than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Cobalt chromium alloy LESS than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Cobalt chromium alloy MORE than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Cobalt chromium alloy LESS than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Cobalt chromium alloy MORE than 70micrometer strut CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Platinum chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Platinum chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Platinum chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Platinum chromium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Platinum iridium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Platinum iridium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Platinum iridium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Platinum iridium alloy CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Polymer free CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Polymer free CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Polymer free CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Polymer free CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Sirolimus coated Biodegradable polymer CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Everolimus coated Biodegradable polymer CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Zotarolimus coated Biodegradable polymer CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)Balloon expandable Biolimus coated Biodegradable polymer CORONARY STENTS .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)DRUG ELUTING STENTS CE and DCGI APPROVED.Should be CE' and DCGI approved
500
-
-
(S)(EX)DRUG ELUTING STENTS DCGI APPROVED.Should be DCGI approved
500
-
-
(S)(EX)DRUG ELUTING CORONARY STENTS TAPERING .Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX) DRUG ELUTING CORONARY STENTS EXTRA LENGTH ( beyond 38mm).Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)DRUG ELUTING STENTS- POLYMER FREE.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)DRUG ELUTING STENTS- sizes above 48mm for diffuse lesions.Should be FDA' OR CE' AND DCGI approved
500
-
-
(S)(EX)DRUG ELUTING CORONARY STENTS 4 and 4.5mm diamater expandable at least to 5.75 all lengths.Should be FDA' OR CE' AND DCGI approved
100
-
-
(S)(EX)Drug eluting stent mounted on drug coated balloon.Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)Drug eluting bioresorbable vascular scaffold system for coronaries.Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)COVERED STENTS-CORONARY Cobalt Chromium 5F guiding compatible Low profile all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(S)(EX)COVERED STENTS-CORONARY Cobalt Chromium 6F guiding compatible Low profile all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(S)(EX)COVERED STENTS-CORONARY Stainless Steel 6F guiding compatible Low profile all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(S)(EX)COVERED STENTS-CORONARY Stainless steel 7F guiding compatible Low profile all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
THROMBUS EXTRACTION
-
-
-
(S)(EX)Thrombus Extraction Catheters for Primary PTCA without stillette.Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)Thrombus Extraction Catheters for coronary thrombus extraction floppy soft tip without stillette.Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)Thrombus Extraction Catheters for Primary PTCA with stillette .Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)Thrombus Extraction Catheters for Primary PTCA without stillette.Should be FDA'/CE'/DCGI approved
20
-
-
(S)(EX)Thrombus Extraction Catheters for Peripheral venous /Pulmonary thrombi 8F with a suction device provided by the company on demand .Should be FDA'/CE'/DCGI approved
5
-
-
(S)(EX)Thrombus Extraction Catheters for Peripheral arterial-venous thrombi 6F with a suction device provided by the company on demand .Should be FDA'/CE'/DCGI approved
5
-
-
(S)(EX)Thrombus Extraction Catheters for Peripheral arterial thrombi4F with a suction device provided by the company on demand .Should be FDA'/CE'/DCGI approved
5
-
-
MICROCATHETER
-
-
-
( D) Coronary Microcatheters( 0.014" compatable) with distal entry profile 1.8F.Should be FDA' or CE' andDCGI approved
15
-
-
( D) Coronary Microcatheters( 0.014" compatable) with distal entry profile 1.8F floppy tip .Should be FDA' or CE' andDCGI approved
15
-
-
( D) Coronary Microcatheters( 0.014" compatable) with distal entry profile 1.4F.Should be FDA' or CE' andDCGI approved
15
-
-
( D) Coronary Microcatheters( 0.014" compatable) with distal entry profile 1.4F Floppy tip.Should be FDA' or CE' andDCGI approved
15
-
-
( D) Coronary Microcatheters for CTO entry- braided with cutting tip.Should be FDA' or CE' andDCGI approved
15
-
-
( D) Coronary Microcatheters torquable ( 0.014" compatable).Should be FDA' or CE' andDCGI approved
15
-
-
( D)Dual lumen Coronary microguide catheters for sidebranch entry(over the wire and monorail).Should be FDA' or CE' and DCGI approved
15
-
-
(D)Angled tip coronary microcatheter for side branch access.Should be FDA' or CE' andDCGI approved
15
-
-
(D)Retrograde coronary collateral Channel dilator .Should be FDA' or CE' and DCGI approved
15
-
-
( D) Peripheral Micro catheters for visceral angio embolisation-Should be hydrophilic and 0.021" compatable.Should be FDA' OR CE' AND DCGI approved
15
-
-
( D) Peripheral Micro catheters for visceral angio embolisation-Should be hydrophilic with attached 0.018" hydrophilic wire.Should be FDA' OR CE' AND DCGI approved
15
-
-
IMAGING & PHYSIOLOGY
-
-
-
(D) Intravascular Ultrasound Catheters compatible with Volcano IVUS system .Should be FDA'/CE'/DCGI approved
25
-
-
(D) Intravascular Ultrasound Catheters compatible with ILAB IVUS system with Pull back Sled.Should be FDA'/CE'/DCGI approved
25
-
-
(D) Intravascular Ultrasound Catheters compatible with ILAB IVUS system.Should be FDA'/CE'/DCGI approved
25
-
-
(D)OCT Catheters .Should be FDA'/CE'/DCGI approved
10
-
-
(D)FFR WIRES compatible with Abbott FFR systems.Should be FDA'/CE'/DCGI approved
50
-
-
(D)FFR WIRES wireless, compatible with Abbott FFR systems.Should be FDA'/CE'/DCGI approved
50
-
-
(D) FFR WIRES compatible with Volcano FFR system .Should be FDA'/CE'/DCGI approved
50
-
-
(D) FFR WIRE Compatible with Boston FFR system.Should be FDA'/CE'/DCGI approved
50
-
-
CTO PCI
-
-
-
(EX)Ultra low profile semi compliant coronary balloons for Chronic total occlusions.Should be FDA'/CE'/DCGI approved
60
-
-
(EX)Dissection re entry balloon for coronary CTO.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)Sub intimal tracking device for CTO.Should be FDA'/CE'/DCGI approved
5
-
-
DEBULKING SYSTEMS CORONARY
-
-
-
( D)Rotablator Wire 009 Floppy.Should be FDA'/CE'/DCGI approved
25
-
-
( D)Rotablator Wire 009 Extra support .Should be FDA'/CE'/DCGI approved
25
-
-
(D) (EX) Rotational atherectomy Burr all sizes
25
-
-
(D) Rotational atherectomy advancer
25
-
-
(D) (EX) Rotational atherectomy Burr and Advancer system integrated all sizes
25
-
-
(D) (EX)Coronary orbital atherectomy system for calcified coronary lesions all sizes.Should be FDA'/CE'/DCGI approved
5
-
-
(D) (EX) Coronary Laser Atherectomy catheter for intervention in calcified coronaries all sizes.Should be CE' AND DCGI approved
5
-
-
(D) (EX)CORONARY intravascular Lithrotripsy balloons for heavy calcified proximal vessel PCI all sizes.Should be CE' AND DCGI approved
5
-
-
IABP
-
-
-
(D) (EX)Intra aortic balloon pump balloons small, medium and large SIZES compatible with Datascope IABP systems.Should be FDA'/CE'/DCGI approved.
50
-
-
(D)Helium with tank for IABP Machine Datascope model.
5
-
-
BALOON VALVULOPLASTY
-
-
-
(S)(EX)ALL SIZES OF PTMC Balloons- Reusable.Should be FDA'/CE'/DCGI approved
50
-
-
(S)Accessories for PTMC Balloons.Should be CE' AND DCGI approved, the accessories will be procured from the same company is selected for PTMC balloons . Accessories include a) Coiled LA guide wire for tracking the balloon into LA b) 21F black dilator c) LV entry wire d) metal stretching tube e) stylet f) syringe for inflation g) ruler/calliper for measuring balloon size
25
-
-
(D)(EX)ALL SIZES OF PTMC Balloons with Accessories- Reusable.Should be FDA'/CE'/DCGI approved
5
-
-
(D)(EX)All sizes of Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design and accessories are to be quoted. Should be FDA'/CE'/DCGI approved
8
-
-
(D)(EX)All sizes of Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design. Should be FDA',CE'/DCGI approved
25
-
-
(D)(EX) Accessories for Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design . the accessories will be procured from the same company is selected for Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design.a) Coiled LA guide wire for tracking the balloon into LA b) 21F black dilator c) LV entry wire d) metal stretching tube e) stylet f) syringe for inflation g) ruler/calliper for measuring balloon size Should be FDA,CE'/DCGI approved
15
-
-
(D)( EX) Aortic valvuloplasty balloon systems with accessories of all sizes and lengths.Should be FDA'/CE'/DCGI approved
10
-
-
(D)( EX)Pulmonary valvuloplasty balloon systems with accessories all sizs and lengths .Should be CE'/DCGI approved
10
-
-
(D)( EX)Stepped diameter balloons Cribier- Letac with accessories all sizes and lengths.Should be FDA'/CE'/DCGI approved
10
-
-
(D)(EX)Pediatric Valvuloplasty Tyshak MINI 014 compatible balloons with accelerator, Bifoil balloons, Trifoil Balloons with accessories all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(D)(EX)Pediatric Valvuloplasty Tyshak-II balloons with accelerator, Bifoil balloons with accessories all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(D)(EX)Pediatric Valvuloplasty Tyshak-II balloons with accelerator, Trifoil Balloons with accessories all sizes.Should be FDA'/CE'/DCGI approved
10
-
-
(D) (EX)Low profile non-compliant pediatric valvuloplasty balloons 4-10 mm diameter, with introducer size starting at 4 Fr with accessories.Should be FDA'/CE'/DCGI approved
10
-
-
PERIPHERAL INTERVENTION
-
-
-
(S)BALKAN CONTRALATERAL SHEATH 6F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)BALKAN CONTRALATERAL SHEATH 7F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)BALKAN CONTRALATERAL SHEATH 8F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)(EX)High pressure non compliant peripheral balloons- (sizes from 4mm-10mm) 0.035'' compatable (All lengths).Should be CE' and DCGI approved
50
-
-
(S)( EX)Cutting Balloons Peripheral. 6mm to 8mm diamter all lengths Should be FDA' OR CE' AND DCGI approved
50
-
-
(S)(EX) Scoring Balloons - Peripheral- For severely calcified lesions.Should be FDA' OR CE' AND DCGI approved
50
-
-
(S)(EX)Drug Eluting Balloons Peripheral.Should be FDA' OR CE' AND DCGI approved
50
-
-
(S)(EX)Drug Eluting Balloons Peripheral for ISR .Should be FDA' OR CE' AND DCGI approved
50
-
-
(S) (EX)Ultra high pressure Mustang type balloons Peripheral- sizes from 4mm to 10mm all lengths..Should be FDA' OR CE' AND DCGI approved
10
-
-
(EX) Covered self expanding covered stent grafts for Peripheral anurysm and leaks (4mm to 12mm).Should be FDA' or CE' andDCGI approved
10
-
-
(S)LEFT INTERNAL MAMMARY GUIDE CATHETER 5F, 6F and & 7F .Should be FDA'/CE'/DCGI approved
10
-
-
(S)BRAIDED MULTIPURPOSE GUIDE CATHS(5F AND 6F).Should be FDA'/CE'/DCGI approved
50
-
-
(S) SOFT TIPPED braided Guide catheters for (4F,5F) for coronary/visceral use.Should be FDA' or CE' and DCGI approved
50
-
-
(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)RENAL DOUBLE CURVE GUIDE CATHETER 4F, 5F 80CM , 120 CM, 140 CM.Should be FDA'/CE'/DCGI approved
50
-
-
(S)RENAL DOUBLE CURVE GUIDE CATHETER 6F 80CM , 120 CM, 140 CM.Should be FDA'/CE'/DCGI approved
50
-
-
(S)RENAL DOUBLE CURVE GUIDE CATHETER 7F 80CM, 120 CM, 140 CM.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TERUMO GLIDE CATHETER HEAD HUNTER 4F.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TERUMO GLIDE CATHETER HEAD HUNTER 5F AND 6 F.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TERUMO GLIDE CATHETER COBRA 4F.Should be FDA'/CE'/DCGI approved
50
-
-
(S) TERUMO GLIDE CATHETER 4F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)YASHIRO GLIDE CATHETER 5F 6F 80 CM,120 CM, 140 CM.Should be FDA'/CE'/DCGI approved
50
-
-
(S)YASHIRO GLIDE CATHETER 4F 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
-
-
(S) Fogarty arterial embolectomy catheter 4&5F.Should be FDA'/CE'/DCGI approved
10
-
-
( EX) RENAL BALLOON(0.014" compatable).Should be FDA'/CE'/DCGI approved
25
-
-
(EX)CAROTID and BTK BALLOONS(0.014" compatable) .Balloon Shaft length should be 160 CM AND ABOVE.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)SMALL VESSEL BALLOON( Diameters should be from 1mm to 4mm) All lengths.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)PERIPH /RENAL/CAROTID GUIDING-100 cm and longer.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)RENAL STENTS -0.014' compatable Balloon Mounted Shaft Length 80 cm- All sizes.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) Self expanding Femoro popliteal stents - all diameters.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Dilators of Coons type for serial vascular dilation for large access .Should be CE' and DCGI approved
25
-
-
(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
10
-
-
( EX)CAROTID STENTS Straight Self Expanding.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
10
-
-
(S) (EX)Sizing BALLOONS for ASD/PDA.Should be FDA'/CE'/DCGI approved
10
-
-
(S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange Length ( 0.018").Should be FDA'/CE'/DCGI approved
100
-
-
(S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange length(0.035").Should be FDA'/CE'/DCGI approved
100
-
-
(S)ROAD RUNNER POLYMER COATED WIRE 035 staright and J.Should be FDA'/CE'/DCGI approved
10
-
-
Peripheral intravascular lithotripsy catheter for treating calcified lesions in peripheral arteries like illiac, femoral and popliteal artery.Should be FDA'/CE'/DCGI approved
5
-
-
Highly flexible kink resitant peripheral stents suitable for deploying in superficial femoral artery and poplliteal artery.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
10
-
-
RENAL DENERVATION
-
-
-
Renal artery denervation catheter system for management of resistant hypertension. Should be FDA/CE/DGCI approved
5
-
-
EMBOLIZATION
-
-
-
(S)(EX)Cyanoacrylate glue for sealing coronary perforation.Should be FDA'/CE'/DCGI approved
10
-
-
(S)(EX)EMBOLISATION PARTICLES Poly Vinyl Alcohol all sizes.Should be FDA'/CE'/DCGI approved
100
-
-
(S) Lipoidol for embolization Should be FDA'/CE'/DCGI approved
25
-
-
(S)Super Absorbant Polymer Microspheres for Drug( Doxorubucin) Adsorption for TACE.Should be FDA'/CE'/DCGI approved
5
-
-
(S)Gelfoam (Powder or granule form) for Embolization.Should be FDA'/CE'/DCGI approved
25
-
-
(S)N-butyl cyanoacrylate GLUE for Embolization .Should be FDA'/CE'/DCGI approved
10
-
-
(S)(EX)MICROCATHETERS with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA'/CE'/DCGI approved
15
-
-
(S)(EX)MICROCATHETERS - STEERABLE/ SHAPABLE with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA'/CE'/DCGI approved
15
-
-
(S)GEL FOAM POWDER FOR ANGIO EMBOLISATION.Should be FDA' or CE' and DCGI approved
25
-
-
(EX) EMBOLIZATION COILS 035" all sizes.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) EMBOLIZATION COILS 0.038 to 052" all sizes.Should be FDA'/CE'/DCGI approved
25
-
-
(EX) EMBOLIZATION COILS 052" all sizes.Should be FDA'/CE'/DCGI approved
25
-
-
( EX) EMBOLIZATION MICRO COILS 018 all sizes - Non Detachable and freely deliverable.Should be FDA'/CE'/DCGI approved
50
-
-
( EX)EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 2D.Should be FDA'/CE'/DCGI approved
50
-
-
( S) EMBOLIZATION COILS Highly trackable 0.018'' embolisation coils for post op- visceral (GI and Renal artery pseudoaneurysm) .Should be CE' AND DCGI approved
50
-
-
( EX) EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 3D.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Nitinol Vascular plugs for embolisation.Should be FDA'/CE'/DCGI approved
10
-
-
EX)Bi lobed Nitinol Vascular plugs for embolisation.Should be FDA'/CE'/DCGI approved
10
-
-
EX)Tri lobed ( should have retention disk on both sides)Nitinol Vascular plugs for embolisation.Should be FDA'/CE'/DCGI approved
5
-
-
EX)Nitinol Vascular plugs for embolisation deliverable through smallest Fr diagnostic catheter supporting 0.038 guidewire .Should be FDA'/CE'/DCGI approved
10
-
-
SNARES
-
-
-
(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)ENDOVASCULAR SNARES Needle Eye. Should be FDA'/CE'/DCGI approved
5
-
-
(S)Coronary micro snares. Should be CE' and DCGI approved
5
-
-
(EX)ENDOVASCULAR SNARES Basket. Should be FDA'/CE'/DCGI approved
5
-
-
COARCTATION STENTING
-
-
-
(D)(EX)Bare AORTIC STENTS FOR Coarctation (Sizes should be above 20mm up to 40mm) - Baloon expandable design.Should be FDA'/CE'/DCGI approved
10
-
-
(D) (EX) Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with specially designed links for non-foreshortening on balloon-dilatation with low crimping profile capable of being deliverable through sheath sizes starting from 9F.
10
-
-
(D)(EX)Non pre-mounted ePTFE covered aortic stents with semi-open cell design made of cobalt-chromium with specially designed links for non-foreshortening on balloon-dilatation with low crimping profile capable of being deliverable through sheath sizes starting from 12F or smaller.Capable of being expanded to sizes starting from 14 mm to more than or equal to 22 mm
2
-
-
(D)(EX)Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with minimum foreshortening on balloon-dilatation with low crimping profile capable
2
-
-
(D)(EX)Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with minimum foreshortening on balloon-dilatation with low crimping profile
2
-
-
(D)(EX) Premounted ePTFE covered stents made of cobalt-chromium made for aortic coarctation stenting with low foreshortening on dilatation capable of being expanded from 12 to 24 mm capable of being delivered through sheath sizes starting from 9 F
2
-
-
(D)(EX) Premounted ePTFE covered stents made of cobalt-chromium with low foreshortening on dilatation capable of being expanded from 5mm to 10 mm capable of being delivered through sheath sizes starting from 6F meant for use in peripheral vessels, renal artery, arteriovenous fistulas for dialysis etc
3
-
-
(D)(EX) Non-premounted bare aortic stents made of platinum-iridium capable of being expanded from 8mm to 24 mm capable of being delivered through sheath sizes starting from 9F meant for use in aorta
2
-
-
(D)(EX) Non-premounted PTFE covered aortic stents made of platinum-iridium capable of being expanded from 8mm to 24 mm capable of being delivered through sheath sizes starting from 12F meant for use in aorta
1
-
-
(D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 12 to 20 mm) - Baloon expandable design.Should be FDA'/CE'/DCGI approved
10
-
-
(D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 20mm up to 40mm) - Self-expanding design.Should be FDA & DCGI approved
10
-
-
(D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 12 to 20 mm) - Self expanding design.Should be FDA & DCGI approved
10
-
-
(D)(EX) Covered AORTIC stents (balloon expandable only) for aortic coarctation (Sizes from 12 to 30mm). Should be CE' AND DCGI approved.
10
-
-
(D) (EX) Balloon in Balloon Stent Placement Catheter for aortic coarcation (Sizes from 12 to 30mm). Should be CE' AND DCGI approved.
10
-
-
(D)(EX) Covered Mounted AORTIC stents (balloon expandable only) for aortic coarctation (Sizes from 12 to 30mn). Should be CE' AND DCGI approved
10
-
-
DEVICE CLOSURE ACCESSORIES
-
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 6F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 7F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 8F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 9F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 10F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 11F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 12F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 14F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
(S)MULLINS SHEATH with Matching Dilator with sidearm 16F all sizes.Should be FDA'/CE'/DCGI approved ( Length to be specified)
50
-
-
( S) 5F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
( S) 6FFlexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
( S) 8F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
( S) 10F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
( S) 12F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
( S) 14F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE' AND DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 6F-7F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 8F-9F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 10F-11F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 12F-13F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 14F-15F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) COOK SHEATHS (all sizes 16F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA' or CE' and DCGI approved
50
-
-
(EX) Ultra compliant linear Sizing balloons with markers for ASD balloon sizing (18mm,24mm 34mm).Should be CE/DCGI approved
10
-
-
(EX)Haursdorf delivery sheaths for ASD device closure all sizes. Should be FDA'/CE'/DCGI approved
25
-
-
ATRIAL SEPTAL DEVICES
-
-
-
(EX)ASD DEVICES: All customised sizes from 8mm to 50 mm.Should be FDA/CE' AND DCGI approved ( Device only)
50
-
-
(EX) Delivery cable for ASD Device 5F/6F for sizes 8mm to 50mm (the cable will be procured from the same company who is selected as L1 in the category : " ASD DEVICES: All customised sizes from 8mm to 50 mm Should be FDA,CE' AND DCGI approved" as indicated in the row above
25
-
-
((EX)ASD DEVICES: All customised sizes from 8mm to 50 mm.Should be FDA/CE' AND DCGI approved ( Device only)
50
-
-
(EX) Delivery cable for ASD DEVICES: All customised sizes from 4 mm waist diameter onwards (the cable will be procured from the same company which is selected as L1 in the category "ASD DEVICES: All customised sizes from 8mm to 50 mm.Should be FDA & CE' AND DCGI approved" as indicated in the row above
25
-
-
(EX)ASD DEVICES All customised sizes from 8mm to 50 mm with Delivery cable and delivery system ( loading sheath and long sheath for device delivery): All customised sizes from 8mm to 50 mm.Should be FDA/CE' AND DCGI approved
50
-
-
(EX)ASD DEVICES All customised sizes from 8mm to 50 mm with Delivery cable and delivery system ( loading sheath and long sheath for device delivery): All customised sizes from 8mm to 50 mm.Should be FDA &CE' AND DCGI approved
8
-
-
(EX) Fenestrated ASD device for mutiple septal defects with cable and accesories All sizes.Should be FDA'/CE'/DCGI approved
5
-
-
(EX)ASD AMPLATZER TYPE SELF CENTRE DEVICES WITH ALL sizes from 8mm and above .Should be FDA approved
8
-
-
(EX) Atrial septal occluder(self-centering) for complex morphology with balloon-assisted delivery with cable and accesories.Should be FDA' or CE' andDCGI approved
20
-
-
(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 with delivery sheath and cables.Should be CE' AND DCGI approved
8
-
-
(EX) Dual disc nitinol biocompatable layer coated secundum type atrial occluders (ALL SIZSES) with Pre assembled delivery system.Should be FDA' or CE' andDCGI approved
8
-
-
(EX)Cribriform multifenestrated septal occluder with a narrow waist -various sizes; disc diameters upto 40 mm meant for occlusion of multifenestrated ASDs. Should be FDA /CE/DGCI approved
5
-
-
(EX)Atrial flow regulator device with delivery cable and accesories.Should be FDA/CE/DGCI approved
5
-
-
(EX)Patent foramen ovale (PFO) closure device with delivery cable and accesories.Should be FDA/CE/DGCI approved
5
-
-
PDA DEVICES
-
-
-
(D)(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 3MM TO 20MM WAIST SIZE .Should be FDA'/CE'/DCGI approved ( Device only)
50
-
-
(D)(EX) Delivery Cable for PDA Occlusion Device (the cable will be procured from the same company who is selected as L1 in the category " PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 3MM TO 20MM WAIST SIZE .Should be FDA'/CE'/DCGI approved"
25
-
-
(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 4MM TO 20MM WAIST SIZE . 4x6 device should be deliverable by 5Fr delivery system.Should be FDA'&CE'/DCGI approved ( Device only)
50
-
-
(EX) Delivery Cable set for PDA occlusion device (the cable will be procured from the same company that is selected as L1 in the category " PDA OCCLUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 4MM TO 20MM WAIST SIZE. 4x6 device should be deliverable by 5Fr delivery system. Should be FDA'&CE'/DCGI approved"
25
-
-
(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE with Delivery Cable .Should be FDA'/CE'/DCGI approved
25
-
-
(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE with Delivery Cable .Should be FDA'&CE'/DCGI approved
10
-
-
(EX)ADO-1 device with delivery cable for all morphology.Should be FDA' or CE' andDCGI approved
10
-
-
(EX) DUCT OCCLUSION DEVICE with DELIVERY SYSTEM NONTAPERING SHEATHS with sidearm+INTRODUCER CABLE SET .Should be FDA'/CE'/DCGI approved
10
-
-
(EX)PDA OCCUSION DEVICE with Dual Discs of equal size and delivery cable .Should be FDA' or CE' andDCGI approved
7
-
-
(EX)PDA DELIVERY SYSTEMS AND INTRODUCER CABLE SYSTEMS .Should be FDA'/CE'/DCGI approved.
8
-
-
(EX) Low profile Duct occluder device for neonates and infants with delivery cable and 4F delivery systems. Should be FDA/CE' AND DCGI approved
7
-
-
(EX) Low profile Duct occluder device for neonates compatible with 4F delivery system.Should be FDA CE' AND DCGI approved ( Device Only)
7
-
-
(D)Delivery cable AND 4F sheath (the cable and sheath will be procured from the same company who is selected as L1 in the category "Low profile Duct occluder device for neonates and infants compatible with 4F delivery system"
25
-
-
(EX) Single disc duct occluders with with sizes from 3mm onwards up to 20 mm ..Should be FDA' or CE' andDCGI approved ( DEVICE alone)
15
-
-
(D) (EX) Delivery cable for Single disk duct occluders (the cable will be procured from the same company who is selected as L1 in the category"Single disc duct occluders with sizes from 3mm onwards up to 20 mm ..Should be FDA' or CE' and DCGI approved"
25
-
-
VSD DEVICES
-
-
-
(EX)Ventricular septal defect Closure Devices All sizes ( 4mm to18 mm).Should be FDA'/CE'/DCGI approved ( DEVICE only)
8
-
-
(EX) Delivery cable Ventricular septal defect closure (the cable will be procured from the same company who is selected as L1 in the category- " Ventricular septal defect Closure Devices All sizes ( 4mm to18 mm).Should be FDA'/CE'/DCGI approved"
4
-
-
(EX)Muscular VSD Closure Devices-All sizes with delivery cable - cost of cable and device should be mentioned separately.Should be FDA'/CE'/DCGI approved
8
-
-
(EX) Low profile Delivery sheath for VSD closure devices( 5F to 14F).Should be CE' and DCGI approved
8
-
-
(EX)Ventricular septal defect Closure Devices All sizes with delivery system and delivery cable.Should be FDA'/CE' and DCGI approved
8
-
-
(EX)Ventricular septal defect Closure Devices ( ONLY Device) All sizes .Should be FDA' /CE' and DCGI approved
5
-
-
(EX)Delivery cable for the item "Ventricular septal defect Closure Devices ( ONLY Device) All sizes.Should be FDA' /CE' and DCGI approved (the cable will be procured from the same company who is selected as L1 in the item mentioned above
5
-
-
(EX) Post Infarct ventricular septal rupture Closure Devices- All sizes and types.FDA approved
5
-
-
(EX) Ventricular septal defect (device alone) for antegrade closure .Should be FDA' or CE' and DCGI approved
5
-
-
(EX) Extra soft Nitinol multi-functional Closure Devices ( ONLY DEVICE) compatible with guide catheter and delivery cables attachable to both ends of the device.deliverable with a minimum of atleast 4Fr delivery system .Should be CE/DCGI approved
10
-
-
(S) 4 F AND 5 F catheter COMPATABLE PERI MEMBRANEUOUS VSD DEVICE with double screw design for antegrade and retrograde closure ( DEVICE ONLY).Should be CE' AND DCGI approved
5
-
-
(S)(EX)Braided kink resistant long(100-120cm) delivery sheaths for VSD closure all sizes.Should be FDA'/CE'/DCGI approved
25
-
-
(S)(EX)COOK LONG SHEATHS CAPABLE OF ASD/VSD/PDA device delivery SIZES 6Fto 16F.Should be FDA'/CE'/DCGI approved
50
-
-
LA APPENDAGE EXCLUSION
-
-
-
(D)(EX)Left atrial appendage closure device with delivery system all sizes.Should be FDA'/CE'/DCGI approved
5
-
-
TRANSCATHETER VALVE REPLACEMENT & REPAIR
-
-
-
(EX)Trans catheter aortic valve (self-expanding) with delivery systems and all accessories .Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Trans catheter aortic valve (balloon expanding)with delivery systems and all accessories.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Trans catheter aortic valve delivery sheath( for 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)Transcatheter mitral valve repair system with accessories.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Transcatheter tricuspid valve repair system with accessories.Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Percutaneous bicaval self expanding valve system for severe tricuspid regurgitation with accessories. Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Transcatheter balloon expandable pulmonary valve with delivery system. Should be FDA/CE/DGCI approved
10
-
-
(EX)Transcatheter self expanding pulmonary valve with delivery system. Should be FDA/CE/DGCI approved
10
-
-
(EX)Large bore long femoral sheaths 12-18 F for aortic/TAVI interventions.Should be FDA'/CE'/DCGI approved
10
-
-
TEVAR/EVAR
-
-
-
(EX)Large diameter (14-20mm) balloon expanding aortic/ vena caval stents.Should be FDA'/CE'/DCGI approved
5
-
-
(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)Balloon expandable covered stents(sizes 5-20mm) for fenestrated TEVAR/EVAR.Should be FDA'/CE'/DCGI approved
25
-
-
(EX)Expandable femoral sheaths for balloon expandable valves .Should be FDA'/CE'/DCGI approved
10
-
-
(EX)Braided kink resistant flexible sheaths (60-100cm) for fenestarted TEVAR and carotid interventions-straight and curved.Should be FDA'/CE'/DCGI approved
25
-
-
(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) 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
-
-
SPECIAL CATHETERS & IMPLANTS
-
-
-
Impella catheter for percutaneous cardiopulmonary support 2.5 LPM
2
-
-
Impella catheter for percutaneous cardiopulmonary support 5 LPM
2
-
-
(EX)Large bore low profile manual aspiration system for high thrombus load from peripheral arteries/veins .Should be FDA'/CE'/DCGI approved
15
-
-
(S)Bioptomes for Endomyocardial biopsy : Bioptomes ; 5.2F .Should be FDA'/CE'/DCGI approved
2
-
-
(EX)BIOPTOME for Endomyocardial biopsy 6F.Should be FDA'/CE'/DCGI approved
2
-
-
(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 Balloon atrial septostomy catheter.Should be FDA'/CE'/DCGI approved
5
-
-
(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
-
-
Intracardiac echocardiography catheter is compatible with ILAB Echo system.
10
-
-
Intracardiac echocardiography catheter compatible with Philips Echo system.
10
-
-
TRANS SEPTAL PUNCTURE
-
-
-
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
-
-
CATH LAB INJECTABLES
-
-
-
(S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350 mg I/ml, 100 ml Bottles).Should be FDA'/CE'/DCGI approved
100
-
-
(S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350 mg I/ml, 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 320 mg I/ml, 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 320 mg I/ml 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
-
-
Inj TIROFIBAN 100 mL bottles.Should be FDA'/CE'/DCGI approved
50
-
-
Injection sildenafil 10 mg vial.Should be FDA'/CE'/DCGI approved
50
-
-
Injection Nicorandil 48 mg vial.Should be FDA'/CE'/DCGI approved
10
-
-
Injection Nicorandil 2 mg vial.Should be FDA'/CE'/DCGI approved
100
-
-
Injection milrenone 10 mg vial. Should be FDA'/CE'/DCGI approved
20
-
-
Injection Cangrelor 50 mg vial. Should be FDA'/CE'/DCGI approved
20
-
-
Injection BIVALURIDIN 250 mg vial .Should be FDA'/CE'/DCGI approved
10
-
-
Injection TENECTAPLASE 30mg Should be FDA'/CE'/DCGI approved
10
-
-
Injection TENECTAPLASE 40mg Should be FDA'/CE'/DCGI approved
10
-
-
Injection TENECTAPLASE 50mg Should be FDA'/CE'/DCGI approved
10
-
-
BIOMARKERS
-
-
-
(D)TROPONIN I QUANTITATIVE BED SIDE TEST KIT .Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
250
-
-
(D)TROPONIN T QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
200
-
-
(D)HIGH SENSITIVE TROPONIN T QUANTITIVE QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
200
-
-
(D)HIGH SENSITIVE TROPONIN I QUANTITATIVE- FDA approved- Analyser Should be Supplied.Should be FDA' approved Measuring Device to be supplied
200
-
-
(D)N-TERMINAL PRO BNP QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(D)N-TERMINAL BNP QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(D)D-TIMER QUANTITATIVE BED SIDE TEST KIT.Should be FDA'/CE'/DCGI approved Measuring Device to be supplied
50
-
-
(D)Bedside Lipid Profile Measurement Kits.Reading Machine should be provided
500
-
-
(D)Bedside INR Measurement Kits.Reading Machine should be provided
250
-
-
(D) ACT cartridges. Reading Machine should be provided
500
-
-
RADIATION PROTECTION
-
-
-
(D)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
-
-
(D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACK SINGLE PIECE LARGE SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to the departmental selection committee
20
-
-
(D)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
-
-
(D)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
-
-
(D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE SMALL SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE MEDIUM SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE LARGE SIZE.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(D)Sterile lead-free disposable radiation protection shield.Should be FDA'/CE'/DCGI approved
5
-
-
(D)Soft flexible Thyroid Collars Radiation Protection.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
20
-
-
(D)Gonadal Shields Radiation Protection.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(D)Radaiation Protective Eye Goggles.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(D)Radaiation Protective Head Gear.Should be FDA'/CE'/DCGI approved & Item to be Demonstrated to departmental selection committee
10
-
-
(D)Radiation protection drape pads.Should be FDA'/CE'/DCGI approved
50
-
-
ELECTROPHYSIOLOGY
-
-
-
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
40
-
-
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
30
-
-
4 or 5 French fixed curve decapolar catheter with 2-5-2 interelectrode for coronary sinus placement. Should be FDA'/CE'/DCGI approved
2
-
-
7 French deflectable duodecapolar catheters with 2-5-2 interelectrode spacing with matching connectors.Should be FDA'/CE'/DCGI approved
5
-
-
7 French deflectable duodecapolar catheters with 2-8-2-(60)-2-8-2 interelectrode spacing with matching connectors.Should be FDA'/CE'/DCGI approved
10
-
-
6 French fixed curve 20-pole catheter with 2-2-2 spacing for mapping in Crista region
4
-
-
20-pole variable diameter circular mapping catheter for mapping in pulmonary veins
10
-
-
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
20
-
-
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
20
-
-
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 a 8 mm tip, bidirectional 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
2
-
-
7 French quadripolar Radiofrequency ablation catheter with irrigated tip, unidirectional 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. Tubing set for irrigation to be provided with each catheter. Should be FDA'/CE'/DCGI approved
10
-
-
7 French quadripolar Radiofrequency ablation catheter with irrigated tip, bidirectional 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. Tubing set for irrigation to be provided with each catheter. Should be FDA'/CE'/DCGI approved
10
-
-
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
-
-
Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and bidirectional 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
10
-
-
Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip, bidirectional deflection and contact force sensing 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
5
-
-
Multipolar mapping catheter for use with the CARTO mapping system (Pentaray Nav)
10
-
-
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
20
-
-
Multipolar mapping catheter suitable for omnipolar mapping with the Ensite NavX system
10
-
-
Reusable indifferent electrode pad compatible with the Stockert ablator.Should be FDA'/CE'/DCGI approved
4
-
-
Balloon catheter for cryoablation of pulmonary veins with all required accessories including mapping catheter and steerable sheath
4
-
-
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
30
-
-
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
4
-
-
IMPLANTS Single Chamber
-
-
-
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
20
-
-
MRI SSIR - Single chamber rate responsible implantable multiprogrammable MRI conditional pacemaker with matching MRI conditional atrial or ventricular active fixation lead and introducer sheath set. .Should be FDA'/CE'/DCGI approved
20
-
-
IMPLANT DUAL CHAMBER
-
-
-
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
-
-
MRI DDDR - Dual chamber MRI conditional pacemaker with matching MRI conditional atrial and ventricular active fixation leads and 2 introducer sheath sets. Should be FDA'/CE'/DCGI approved
50
-
-
AICD
-
-
-
Single chamber, Single Coil DF4 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 coil, integrated bipolar active fixation ventricular leads. Should be FDA'/CE'/DCGI approved
10
-
-
Single chamber, Dual coil DF4 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 dual coil, integrated bipolar active fixation ventricular leads..Should be FDA'/CE'/DCGI approved
5
-
-
Single chamber, Single Coil MRI conditional DF4 AICD - Single chamber, MRI conditional 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 coil, integrated bipolar active fixation MRI conditional ventricular leads. Should be FDA'/CE'/DCGI approved
10
-
-
Dual chamber Single coil DF4 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 coil, integrated bipolar active fixation atrial and ventricular leads..Should be FDA'/CE'/DCGI approved
5
-
-
Dual chamber Dual Coil DF4 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 dual coil, integrated bipolar active fixation atrial and ventricular leads..Should be FDA'/CE'/DCGI approved
2
-
-
Dual chamber Single coil MRI conditional DF4 AICD - Dual chamber, MRI conditional 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 coil, integrated bipolar active fixation MRI conditional atrial and ventricular leads..Should be FDA'/CE'/DCGI approved
5
-
-
Single chamber subcutaneous ICD with lead designed for subcutaneous placement, introducer and other accessories
2
-
-
CRT-P & D
-
-
-
CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and passive bipolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, 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
5
-
-
CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and passive quadripolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, 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
10
-
-
CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, 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
10
-
-
MRI CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial, active fixation MRI conditional RV leads and passive quadripolar over the wire MRI conditional coronary sinus lead (LV lead). Should include compatible short sheaths with valve, 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
10
-
-
MRI CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, MRI conditional active fixation atrial, MRI conditional active fixation RV leads and MRI conditional active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, 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
10
-
-
Single coil DF-4 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 comprising active fixation atrial lead, single coil with integrated bipolar active fixation RV lead and passive Quadripolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, 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
5
-
-
Single coil DF-4 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 comprising active fixation atrial lead, single coil with integrated bipolar active fixation ventricular RV lead and active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, 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
5
-
-
MRI conditional Single coil DF-4 CRT-D - Triple Chamber MRI conditional 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 comprising active fixation MRI conditional atrial lead, single coil with integrated bipolar active fixation MRI conditional RV lead and passive Quadripolar over the wire MRI conditional coronary sinus lead (LV lead). Should include compatible short sheaths with valve, 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
5
-
-
MRI conditional Single coil DF-4 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 comprising active fixation MRI conditional atrial lead, single coil with integrated bipolar active fixation MRI conditional RV lead and active fixation Quadripolar over the wire MRI conditional coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, 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
5
-
-
CONDUCTION SYSTEM PACING
-
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-
Single chamber SSIR for Conduction system pacing-Single chamber rate responsive implantable multiprogrammable pacemaker with lead and specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories required for conduction system pacing. Should be FDA'/CE'/DCGI approved.
5
-
-
MRI conditional Single chamber SSIR for Conduction system pacing-Single chamber rate responsive implantable multiprogrammable pacemaker with lead and specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories required for conduction system pacing. Should be FDA'/CE'/DCGI approved.
5
-
-
MRI conditional Dual chamber DDDR for Conduction system pacing-Dual chamber rate-responsive implantable multiprogrammable MRI conditional pacemaker with active fixation MRI conditional atrial lead, lead with specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories for conduction system pacing. Should be FDA'/CE'/DCGI approved
10
-
-
Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial lead, quadripolar coronary sinus lead, lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves '/ sizes. Should be FDA'/CE'/DCGI approved
10
-
-
MRI conditional Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial lead, quadripolar MRI conditonal coronary sinus lead, lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves '/ sizes. Should be FDA'/CE'/DCGI approved
10
-
-
MRI conditional Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial lead, active fixation & screw in type of quadripolar MRI conditional coronary sinus lead (LV lead), MRI conditional lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves '/ sizes. Should be FDA'/CE'/DCGI approved
5
-
-
PACING LEADS
-
-
-
Steroid eluting bipolar active fixation atrial leads with introducer sheath.Should be FDA'/CE'/DCGI approved
50
-
-
Steroid eluting bipolar active fixation ventricular leads with introducer sheath.Should be FDA'/CE'/DCGI approved
50
-
-
Single and Dual coil (50-50%), integrated bipolar active fixation DF4 type ICD leads.Should be FDA'/CE'/DCGI approved
20
-
-
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
20
-
-
Quadripolar lead specially designed for placement in coronary sinus for LV pacing with built in screw in type of active fixation mechanism for maintaining stable position. Should be supplied with compatible 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
-
-
Lumenless Lead with preshaped sheath (specifically designed for conduction system pacing) along with slitter and short subclavian sheath as one set.
20
-
-
Stylet driven ventricular lead for conduction system pacing with sheath and other compatible accessories.
10
-
-
Unipolar epicardial pacing leads
10
-
-
Bipolar epicardial pacing leads
10
-
-
LEADLESS PACEMAKER
-
-
-
Miniaturised pacemaker for use as leadless pacemaker with delivery system and other required accessories
5
-
-
TEMPORARY PACING
-
-
-
(S)Temporary Pacing Leads sizes with 5F/6F.Should be FDA'/CE'/DCGI approved
50
-
-
(S)Balloon Flow Assisted Temporary Pacing lead(5F and 6F .Should be FDA'/CE'/DCGI approved
30
-
-
(D)Single Chamber Demand Cum Overdrive Temporary Pulse Generators with various Dual Chamber and Single Chamber modes, capable of overdrive pacing.Should be FDA'/CE'/DCGI approved
10
-
-
(D)Dual Chamber Demand Cum Overdrive Temporary Pulse Generators with various Dual Chamber and Single Chamber modes, capable of overdrive pacing.Should be FDA'/CE'/DCGI approved
10
-
-
LOOP RECORDERS/REMOTE MONITORING
-
-
-
(D) IMPLANTABLE loop recorder - long term ( ILR) 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
10
-
-
(D) EXTERNAL DISPOSABLE 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
-
-
(D) Wrist Wearable, reusable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with android OS. Waterproof with a year warranty.
10
-
-
(D) Wrist Wearable, reusable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with iOS . Waterproof with a year warranty.
10
-
-
(D) Wrist Wearable, reusable rechargable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with both Android and iOS . Waterproof with a year warranty.
10
-
-
(D) Medical grade reusable rechargeable monitoring wrist wearable device for remote monitoring of continuous pulse rate, physical activity, respiration rate and patient triggered ECG and SpO2. Automated arrhythmia warning on PPG and automated Arrhythmia diagnosis on ECG. Remote recording of PPG and ECG waveforms should be possible. Battery life should be a minimum 48 hours and waterproof at IP67 or above. Patient data should be visible to the patient via an Android or iOS smartphone and to the physician via a web interphase. The unit should be CDSCO certified and US FDA approved for PPG-based arrhythmia and ECG arrhythmia diagnosis and if not human clinical trial data indicating a specificty and sensitivity of 95% or above should be submitted. The unit should have 3-year warranty.
2
-
-
SURGICAL INSTRUMENTS
-
-
-
(D)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
4
-
-
LEAD EXTRACTION
-
-
-
(D)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
5
-
-
(D)Lead locking device for extraction of chronically implanted leads
20
-
-
MONITOR/ECG/TMT/DEFIBRILLATOR CONSUMABLES
-
-
-
(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 : 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
-
-
(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)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) BioCare ECG cable.Should be FDA'/CE'/DCGI approved
5
-
-
(S) Mortara ELI-250 ECG Recorder Head.Should be FDA'/CE'/DCGI approved
1000
-
-
(S) Mortara ELI-350 ECG Recorder Head.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) Mortara TMT Paper.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
-
-
(D)Disposable Heartstart adult plus mutifunction defibrillation pads for use with the Philips defibrillator.Should be FDA'/CE'/DCGI approved
50
-
-
(D)Disposable pads for defibrillation / transcutaneous pacing for use with the Zoll defibrillator.Should be FDA'/CE'/DCGI approved
50
-
-
(D)Disposable pads for defibrillation for use with the Zoll AED.Should be FDA'/CE'/DCGI approved
2
-
-
(D)Reusable pads for defibrillation for use with the Zoll AED.Should be FDA'/CE'/DCGI approved
2
-
-
VENTILATOR CONSUMABLES
-
-
-
(S)PATIENT TUBING SYSTEM COMPATIBLE WITH MAQUET S VENTILATOR.Should be FDA'/CE'/DCGI approved
10
-
-
TEST KITS
-
-
-
(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
-
-
CLEANING/CUTTING DISPOSABLES
-
-
-
(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
-
-
Surgical Hair clipper (General Blade) - cleaning regular area battery operated for pre-operative preparational.Hair removal from body with no risk of cuts on the skin.To be supplied with suitable charger and blade.Hair clipper machine should be used in wet or dry condition and recharger for the machine should be provided.(One machine for 400 hair clipping blades)
2000
-
-
Surgical Hair clipper (Sensitive blade) - cleaning sensitive area battery operated for pre-operative preparational.Hair removal from body with no risk of cuts on the skin.To be supplied with suitable charger and blade.Hair clipper machine should be used in wet or dry condition and recharger for the machine should be provided.(One machine for 400 hair clipping blades)
2000
-
-
DRAPES/COVERS/PACKING/STORE DISPOSABLE
-
-
-
(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 IN DARK COLOURS - Brown/Dark Blue/ (SMALL/MEDIUM /LARGE).Sample to be supplied for testing
2000
-
-
( 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
-
-
(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)Disposable, sterile cover for Fluoroscopy system Radiation shield. 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
400
-
-
(D) Disposable sterile ultrasound probe cum cable "long" cover made of polyethene or similar translucent material with a flat end. A small pouch of sterile ultrasound jelly, elastic bands and or paper adhesive bands for binding the probe and cable to be provided as a sterile set. Different sizes that are compatible with adult and pediatric cardiac/vascular/abdominal probes to be supplied.
200
-
-
(D) Reuasable Cath-Lab Cotton Dress Shirt with three pockets and Pyjama with two pockets Large and medium Sized Light Blue Colour with the 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)Disposable Paper-based Sterile Front Buttoned Black/ Brown/ Dark blue half sleeve shirt and pyjama for cath lab patient dress.SMALL, MEDIUM,LARGE sizes Should be FDA'/CE'/DCGI approved
500
-
-
(S)Compact Disk- Recordable ( CD-R) with hard shell box.Sample to be submitted to departmental selection committee.
2000
-
-
(S)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.Sample to be submitted to departmental selection committee.
50
-
-
(S)White Board Markers Black and Blue.Sample to be submitted to departmental selection committee.
50
-
-
(D)Washable and Autoclavable Cut Shoes (Clogs) Specially designed for wearing in Cathlabs/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.(Small, Medium, Large and Extra large).Item to be Demonstrated to the departmental selection committee
150
-
-
MONITORING DEVICES - NON CONSUMABLES
-
-
-
( 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 with rechargable Lithium ion batters FOR USE IN OPD AND WARD with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
2
-
-
( D ) DIGITAL BP, SpO2, Respiratory Rate, Temperature Measuring APPARATUS HEAVY DUTY, with ADULT, LARGE ADULT and PEDIATRIC CUFFS RUNNING IN AC POWER with rechargeable Lithium-ion Battery FOR USE IN OPD AND WARD 3 yr warranty.Item to be Demonstrated to the departmental selection committee.
2
-
-
(D) DIGITAL Automated BP apparatus for use with TMT machine with automatic noise detection and artefact cancellation and ability for ECG gating
1
-
-
( D)DIGITAL WEIGHING SCALE FOR PATIENT WEIGHT with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
2
-
-
( D) Battery Operated Pocket Sized SpO2 Probes.Item to be Demonstrated to departmental selection committee.
5
-
-
(D) Digital Stadiometer for height measurement.
7
-
-
(D) Temperature and Humidity monitors for Cathlabs and ICU. Should have maximum and minimum values for 24 hours on display and ability to store 30 days data for export.
4
-
-
(D) Dual zone Temperature monitors for Refrigerators for monitoring freezer and cabin temperatures. Should have maximum and minimum values for 24 hours on display and ability to store 30 days data for export.
8
-
-
(D)MULTIPARAMETER MONITORS ECG, SPO2,NIBP with 3yr warrranty and 2 sets of cables.Item to be Demonstrated to the departmental selection committee.
10
-
-
( D) SYRINGE INFUSION PUMPS with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
4
-
-
( D) OT LIGHT- FLOOR MOUNTED, LED SOURCE , Brightness and Focus ADJUSTABLE with 3 yr warranty.Item to be Demonstrated to departmental selection committee.
2
-
-
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