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| Sl. No. | Item Description |
| 1 | RATE CONTRACT OF CARDIAC ITEMS :- |
| 2 | Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm, 5Fr. =1.20 mm, 6 Fr.=1.30 mm or more with flow rates of 12, 21,25 ml per second respectively. Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) Amplatz left & right, (AL1 & 2, AR 1 & 2) multipurpose, hockey stick, IMA, pigtail- 4Fr.-5Fr.-6Fr.USFDA/PMDA approved |
| 3 | Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm, 5Fr. =1.20 mm, 6 Fr.=1.30 mm or more with flow rates of 12, 21,25 ml per second respectively. Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) Amplatz left & right, (AL1 & 2, AR 1 & 2) multipurpose, hockey stick, IMA, pigtail- 4Fr.-5Fr.-6Fr.CE approved |
| 4 | Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm, 5Fr. =1.20 mm, 6 Fr.=1.30 mm or more with flow rates of 12, 21,25 ml per second respectively. Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) Amplatz left & right, (AL1 & 2, AR 1 & 2) multipurpose, hockey stick, IMA, pigtail- 4Fr.-5Fr.-6Fr.DCGI approved |
| 5 | PTFE Angiography WireGuide wire with V stick, with choice of stainless steel core or nitinol coreMust have 250 cm to 300 cm of length and.018” to .038” diameterWith silicon coated tip and bevel indicator USFDA/PMDA approved |
| 6 | PTFE Angiography WireGuide wire with V stick, with choice of stainless steel core or nitinol coreMust have 250 cm to 300 cm of length and.018” to .038” diameterWith silicon coated tip and bevel indicator• CE approved |
| 7 | PTFE Angiography WireGuide wire with V stick, with choice of stainless steel core or nitinol coreMust have 250 cm to 300 cm of length and.018” to .038” diameterWith silicon coated tip and bevel indicator• DCGI approved |
| 8 | Sirolimus eluting Drug Eluting BalloonRapid exchange with nanotech novel drug delivery having solid lipid nanospheres platinum/Iridium RO markerdiameter from 2.0-4.5 mm length 9-41 mm.• USFDA/PMDA approved |
| 9 | Sirolimus eluting Drug Eluting BalloonRapid exchange with nanotech novel drug delivery having solid lipid nanospheres platinum/Iridium RO markerdiameter from 2.0-4.5 mm length 9-41 mm.• CE Approved |
| 10 | Sirolimus eluting Drug Eluting BalloonRapid exchange with nanotech novel drug delivery having solid lipid nanospheres platinum/Iridium RO markerdiameter from 2.0-4.5 mm length 9-41 mm.DCGI Approved |
| 11 | Paclitaxel Drug Eluting Balloon Trans Pax coatingWing seal technologyAvailable in variable Lengths and diameters USFDA/PMDA Approved |
| 12 | Paclitaxel Drug Eluting Balloon Trans Pax coatingWing seal technologyAvailable in variable Lengths and diameters CE Approved |
| 13 | Paclitaxel Drug Eluting Balloon Trans Pax coatingWing seal technologyAvailable in variable Lengths and diameters• DCGI Approved |
| 14 | Directional Cutting balloon Microsurgical atherotomes Monorail catheterBi-segment inner lumen shaft Hydrophilic coating Proximal shaft- 1.8FrSize 2-4 Diameter Length 6,10,15mmUSFDA/PMDA Approved |
| 15 | Directional Cutting balloon Microsurgical atherotomes Monorail catheterBi-segment inner lumen shaft Hydrophilic coating Proximal shaft- 1.8FrSize 2-4 Diameter Length 6,10,15mm CE Approved |
| 16 | Directional Cutting balloon Microsurgical atherotomes Monorail catheterBi-segment inner lumen shaft Hydrophilic coating Proximal shaft- 1.8FrSize 2-4 Diameter Length 6,10,15mm• DCGI Approved |
| 17 | PTCA Inflation Device-Efficient locking system to maintain high pressureRapid inflation and deflationClear barrel for easy visualization of de-bubbling Luminescent analog pressure gauge (up to 30 atm)Ergomatric and use friendly hand held design Company’s name & logo has to be there on indeflator itselfUSFDA/PMDA approved |
| 18 | PTCA Inflation Device-Efficient locking system to maintain high pressureRapid inflation and deflationClear barrel for easy visualization of de-bubbling Luminescent analog pressure gauge (up to 30 atm)Ergomatric and use friendly hand held design Company’s name & logo has to be there on indeflator itselfCE approved |
| 19 | PTCA Inflation Device-Efficient locking system to maintain high pressureRapid inflation and deflationClear barrel for easy visualization of de-bubbling Luminescent analog pressure gauge (up to 30 atm)Ergomatric and use friendly hand held design Company’s name & logo has to be there on indeflator itself• DCGI approved |
| 20 | Two port manifold set with pressure line 200 cm, luer lock 10cc syringe and IV set.USFDA/PMDA approved |
| 21 | Two port manifold set with pressure line 200 cm, luer lock 10cc syringe and IV set.CE approved |
| 22 | Two port manifold set with pressure line 200 cm, luer lock 10cc syringe and IV set.• DCGI approved |
| 23 | ASD CLOSURE DEVICES WITH DELIVERY SYSTEM• Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes 4mm to 20 mm all sizes and 22-40 mm all even sizes) •45 Degree Angle BraidedDelivery system with Flexible Screwing cable• USFDA/PMDA approved |
| 24 | ASD CLOSURE DEVICES WITH DELIVERY SYSTEM• Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes 4mm to 20 mm all sizes and 22-40 mm all even sizes) •45 Degree Angle BraidedDelivery system with Flexible Screwing cableCE - approved |
| 25 | ASD CLOSURE DEVICES WITH DELIVERY SYSTEM• Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla Available in all the sizes 4mm to 20 mm all sizes and 22-40 mm all even sizes) •45 Degree Angle BraidedDelivery system with Flexible Screwing cable•DCGI approved |
| 26 | ASD Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh sewn with PTFE membrane available in all sizesUSFDA /PMDA approved |
| 27 | ASD Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh sewn with PTFE membrane available in all sizesCE - approved |
| 28 | ASD Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh sewn with PTFE membrane available in all sizesDCGI - approved |
| 29 | ASD - Multi Fenestrated (Cribriform) Occluders,• self-expandable double disc made up of soft nitinol wire mesh••two flat discs and waist of 3mm.matched disc diameters Polyester fabric sewn into each discChemically Intaglio treated to improve biocompatibility & reduce nickel(Ni)leaching-MR. conditional up to 3 TeslaAvailable in all the sizes (18 mm - 40 mm)• USFDA /PMDA approved |
| 30 | ASD - Multi Fenestrated (Cribriform) Occluders,• self-expandable double disc madeup of soft nitinol wire mesh ••two flat discs and waist of 3mm. matched disc diametersPolyester fabric sewn into each discChemically Intaglio treated to improve biocompatibility & reduce nickel(Ni)leaching-MR. conditional up to 3 Tesla.Available in all the sizes (18 mm - 40 mm)CE - approved |
| 31 | ASD - Multi Fenestrated (Cribriform) Occluders,• self-expandable double disc made up of soft nitinol wire mesh••two flat discs and waist of 3mm.matched disc diameters Polyester fabric sewn into each discChemically Intaglio treated to improve biocompatibility & reduce nickel(Ni)leaching-MR. conditional up to 3 Tesla Available in all the sizes(18 mm - 40 mm)• DCGI - approved |
| 32 | LEFT ATRIAL APPENDAGE CLOSUREDEVICE with Delivery set• Disc and Lobe mechanism•Polyester fabric sewn into eachdiscPre loaded on delivery cable Chemically Intaglio treated to improve biocompatibility & reduce nickel(Ni) leaching-MR. conditional up to 3 Tesla •Pre mounteddevice USFDA /PMDA approved |
| 33 | LEFT ATRIAL APPENDAGE CLOSUREDEVICE with Delivery set• Disc and Lobe mechanism•Polyester fabric sewn into eachdiscPre loaded on delivery cable Chemically Intaglio treated to improve biocompatibility & reduce nickel(Ni) leaching-MR. conditional up to 3 Tesla •Pre mounteddeviceCE - approved |
| 34 | LEFT ATRIAL APPENDAGE CLOSUREDEVICE with Delivery set• Disc and Lobe mechanism•Polyester fabric sewn into eachdiscPre loaded on delivery cable Chemically Intaglio treated to improve biocompatibility & reduce nickel(Ni) leaching-MR. conditional up to 3 Tesla •Pre mounteddevice• DCGI - approved |
| 35 | PFO CLOSURE DEVICES WITH DELIVERY SYSTEM• Available in all the sizes (18- 35 mm)• Device should be self-expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a very thin waist of 3mm.•Polyester fabric sewn into each disc promoteocclusion and tissue in growth.The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching.•Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics andadults.• Device should be pre mounted to delivery cable and Delivery system should be Braided and 45 degree angled• USFDA PMDA approved |
| 36 | PFO CLOSURE DEVICES WITH DELIVERY SYSTEM• Available in all the sizes (18- 35 mm)• Device should be self-expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a very thin waist of 3mm.•Polyester fabric sewn into each disc promoteocclusion and tissue in growth.The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching.•Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults.• Device should be pre mounted to delivery cable and Delivery system should be Braided and 45 degree angledCE - approved |
| 37 | PFO CLOSURE DEVICES WITH DELIVERY SYSTEM• Available in all the sizes (18- 35 mm)• Device should be self-expandable double disc made up of soft nitinol wire mesh that is shaped into two flat discs and a very thin waist of 3mm.•Polyester fabric sewn into each disc promoteocclusion and tissue in growth.The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching.•Device should be MR Conditional upto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults.• Device should be pre mounted to delivery cableand Delivery system should be Braided and 45 degree angled• DCGI approved |
| 38 | SIZING BALLOON FOR DEVICE CLOSURE –CIRCULAR SHAPE• Sizing Balloon with a triple lumen balloon catheter with three radiopaque marker bands located inside the balloon to allow for radiographic measurementUSFDA /PMDA approved |
| 39 | SIZING BALLOON FOR DEVICE CLOSURE –CIRCULAR SHAPE• Sizing Balloon with a triple lumen balloon catheter with three radiopaque marker bands located inside the balloon to allow for radiographic measurementCE - approved |
| 40 | SIZING BALLOON FOR DEVICE CLOSURE –CIRCULAR SHAPE• Sizing Balloon with a triple lumen balloon catheter with three radiopaque marker bands located inside the balloon to allow for radiographic measurementDCGI- approved |
| 41 | SIZING BALLOON FOR DEVICE CLOSURE –OVAL SHAPEDUSFDA /PMDA approved |
| 42 | SIZING BALLOON FOR DEVICE CLOSURE –OVAL SHAPEDCE- approved |
| 43 | SIZING BALLOON FOR DEVICE CLOSURE –OVAL SHAPED• DCGI approved |
| 44 | RETRIEVERS FOR ASD/VSD/PDA DEVICES–USFDA /PMDA approved |
| 45 | RETRIEVERS FOR ASD/VSD/PDA DEVICES–CE- approved |
| 46 | RETRIEVERS FOR ASD/VSD/PDA DEVICES–DCGI - approved |
| 47 | SHEATH FOR RETRIVAL OF DEVICES –USFDA /PMDA approved |
| 48 | SHEATH FOR RETRIVAL OF DEVICES –CE- approved |
| 49 | SHEATH FOR RETRIVAL OF DEVICES –DCGI - approved |
| 50 | VSD CLOSURE DEVICES WITH DELIVERY SYSTEM• • Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes4 - 18 mm and 7 mm Central Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• USFDA /PMDA approved |
| 51 | VSD CLOSURE DEVICES WITH DELIVERY SYSTEM• • Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes4 - 18 mm and 7 mm Central Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• CE-approved |
| 52 | VSD CLOSURE DEVICES WITH DELIVERY SYSTEM• • Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery • Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes4 - 18 mm and 7 mm Central Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• DCGI- approved |
| 53 | VSD Closure device with delivery system :- Elongatable waistSoft Woven meshLow delivery profile as low as 4F and maximum upo to 7 F Double sided screw for retrograde or antegrade approach Available in all sizesUSFDA /PMDA approved |
| 54 | VSD Closure device with delivery system :- Elongatable waistSoft Woven meshLow delivery profile as low as 4F and maximum upo to 7 F Double sided screw for retrograde or antegrade approach Available in all sizesCE-approved |
| 55 | VSD Closure device with delivery system :- Elongatable waistSoft Woven meshLow delivery profile as low as 4F and maximum upo to 7 F Double sided screw for retrograde or antegrade approach Available in all sizesDCGI- approved |
| 56 | Membranous VSD Closure device with delivery system :-Soft woven nitinol mesh; sewn with PTFE membraneNon concentric designThe device should be delivered using a pusher catheter from venous approchChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizes USFDA /PMDA approved |
| 57 | Membranous VSD Closure device with delivery system :-Soft woven nitinol mesh; sewn with PTFE membraneNon concentric designThe device should be delivered using a pusher catheter from venous approchChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesCE-approved |
| 58 | Membranous VSD Closure device with delivery system :-Soft woven nitinol mesh; sewn with PTFE membraneNon concentric designThe device should be delivered using a pusher catheter from venous approchChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesDCGI – approved |
| 59 | Muscular VSD Closure device with delivery system :- coated with titanium nitride (TiN) Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, Asymmetric and eccentric forms Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesUSFDA /PMDA approved |
| 60 | Muscular VSD Closure device with delivery system :- coated with titanium nitride (TiN) Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, Asymmetric and eccentric forms Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesCE-approved |
| 61 | Muscular VSD Closure device with delivery system :- coated with titanium nitride (TiN) Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, Asymmetric and eccentric forms Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesDCGI - approved |
| 62 | Muscular VSD Closure device with delivery system :- Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, double disc Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesUSFDA /PMDA approved |
| 63 | Muscular VSD Closure device with delivery system :- Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, double disc Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesCE-approved |
| 64 | Muscular VSD Closure device with delivery system :- Soft woven nitinol mesh; sewn with PTFE membraneSymmetric, double disc Waist length should be 7 mmChemically treated to improve biocompatibility & reduce nickel (Ni) leaching.MR. conditional up to 3 Tesla available in all sizesDCGI- approved |
| 65 | Post infarction Muscular VSD Closure device with delivery system :-• • Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes 18-24 mm and 10 mm Central Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• USFDA/PMDA approved |
| 66 | Post infarction Muscular VSD Closure device with delivery system :-• Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes 18-24 mm and 10 mmCentral Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• CE-approved |
| 67 | Post infarction Muscular VSD Closure device with delivery system :-• • Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 TeslaAvailable in all the sizes 18-24 mm and 10 mm Central Waist •45 Degree Angle Braided Delivery system with Flexible Screwing cable• DCGI- approved |
| 68 | PDA CLOSURE DEVICES WITH DELIVERY SYSTEMApproved for pediatric/adult use• Device made of biologically inert material(nitinol)• Self-centering, detachable device with delivery• cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR conditional up to 3 Tesla Available in all the sizes • 180 Degree angle braided delivery system without Hemostasis valve attached on delivery sheathUSFDA /PMDA approved |
| 69 | PDA CLOSURE DEVICES WITH DELIVERY SYSTEMApproved for pediatric/adult use• Device made of biologically inert material(nitinol)• Self-centering, detachable device with delivery• cable• Polyester fabric integrated in each disc. • Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR conditional up to 3 Tesla Available in all the sizes • 180 Degree angle braided delivery system without Hemostasis valve attached on delivery sheathCE-approved |
| 70 | PDA CLOSURE DEVICES WITH DELIVERY SYSTEMApproved for pediatric/adult use• Device made of biologically inert material(nitinol)• Self-centering, detachable device with delivery• cable• Polyester fabric integrated in each disc.• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR conditional up to 3 Tesla Available in all the sizes • 180 Degree angle braided delivery system without Hemostasis valve attached on delivery sheathDCGI- approved |
| 71 | PDA Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh; sewn with PTFE membraneAvailable in all sizesUSFDA /PMDA approved |
| 72 | PDA Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh; sewn with PTFE membraneAvailable in all sizes CE-approved |
| 73 | PDA Closure device with delivery system :- coated with titanium nitride (TiN)Soft woven nitinol mesh; sewn with PTFE membraneAvailable in all sizes DCGI - approved |
| 74 | PDA occluder with double disc :-Low Profile devices, Symmetric design, Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Suitable for Retrograde or antegradeapproach• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla , Available in all the sizes Compitable with Low profile Deliverys systemUSFDA /PMDA approved |
| 75 | PDA occluder with double disc :-Low Profile devices, Symmetric design, Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Suitable for Retrograde or antegradeapproach• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla , Available in all the sizes Compitable with Low profile Deliverys systemCE-approved |
| 76 | PDA occluder with double disc :-Low Profile devices, Symmetric design, Approved for pediatric/adult use• Device made of biologically inert material• Self-centering, detachable device with delivery• Cable• Suitable for Retrograde or antegradeapproach • Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla , Available in all the sizes Compitable with Low profile Deliverys systemDCGI - approved |
| 77 | PDA occluder with double disc (for neonates) :- Made up of biologically inert material (nitinol)• Symmetric disc design -low profile with low profiledelivery catheter of 4 Fr.• Tightly woven single layer mesh• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Premounted deviceUSFDA /PMDA approved |
| 78 | PDA occluder with double disc (for neonates) :- Made up of biologically inert material (nitinol)• Symmetric disc design -low profile with low profiledelivery catheter of 4 Fr.• Tightly woven single layer mesh• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Premounted device CE-approved |
| 79 | PDA occluder with double disc (for neonates) :- Made up of biologically inert material (nitinol)• Symmetric disc design -low profile with low profiledelivery catheter of 4 Fr.• Tightly woven single layer mesh• Chemically Intaglio treated to improve biocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Premounted device DCGI- approved |
| 80 | Valvular Plug for Paravalvular leak closure -• Made up of biologically inert material (nitinol)• Oblong design -Compatible with low profile delivery catheter.• Tightly woven single layer mesh• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Pre mounteddevice All sizes•USFDA/PMDA approved |
| 81 | Valvular Plug for Paravalvular leak closure -• Made up of biologically inert material (nitinol)• Oblong design -Compatible with low profile delivery catheter.• Tightly woven single layer mesh• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Pre mounteddevice All sizes•CE approved |
| 82 | Valvular Plug for Paravalvular leak closure -• Made up of biologically inert material (nitinol)• Oblong design -Compatible with low profile delivery catheter.• Tightly woven single layer mesh• Chemically Intaglio treated to improvebiocompatibility & reduce nickel (Ni) leaching.• MR. conditional up to 3 Tesla • Pre mounteddevice All sizes•DCGI - approved |
| 83 | Coil pusher wire for 0.014/0.018” coils, (compatible with the quoted micro catheters )With delivery systemUSFDA /PMDA approved |
| 84 | Coil pusher wire for 0.014/0.018” coils, (compatible with the quoted micro catheters )With delivery system CE-approved |
| 85 | Coil pusher wire for 0.014/0.018” coils, (compatible with the quoted micro catheters )With delivery system DCGI -approved |
| 86 | Pediatric Femoral Sheath 4 Fr.Removable cap which has hexacuspid valveExcellent kink resistantSideport extension with 3-way stopcock Optimized catheter manoeuvrability with minimal leakageCannula made of two (thinner) layers of polyethyleneColor codes for easy french size identification0.21’’ Guide wire compatible Diameter: 4 FrLengths: 11 cm with 21G needleUSFDA /PMDA approved |
| 87 | Pediatric Femoral Sheath 4 Fr.Removable cap which has hexacuspid valveExcellent kink resistantSideport extension with 3-way stopcock Optimized catheter manoeuvrability with minimal leakageCannula made of two (thinner) layers of polyethyleneColor codes for easy french size identification0.21’’ Guide wire compatible Diameter: 4 FrLengths: 11 cm with 21G needleCE- approved |
| 88 | Pediatric Femoral Sheath 4 Fr.Removable cap which has hexacuspid valveExcellent kink resistantSideport extension with 3-way stopcock Optimized catheter manoeuvrability with minimal leakageCannula made of two (thinner) layers of polyethyleneColor codes for easy french size identification0.21’’ Guide wire compatible Diameter: 4 FrLengths: 11 cm with 21G needleDCGI -approved |
| 89 | Catheters for paediatric intervention Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm,Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) multipurpose, IMA, pigtail- 4Fr.USFDA /PMDA approved |
| 90 | Catheters for paediatric intervention Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm,Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) multipurpose, IMA, pigtail- 4Fr.CE-approved |
| 91 | Catheters for paediatric intervention Angiographic Catheter comprised of a two- layer construction featuring double braided stainless-steel two-ply mesh sandwiched between layers of polyurethane and polyamide elastomers allowing 1:1 torque transmission.The shaft inner layer and outer layer contain barium sulfate for visibility and contrast under fluoroscopy.Inner diameter of 4 Fr.= 1.03 mm,Diagnostic catheter comes with anti-kinking protector, with non-braided tip shaft (distal -2 cm) offering soft & round tip with co-axial alignment.Transfemoral Angiography catheter – Judkin Left and Right, (JL3-JL5,JR3-JR5) multipurpose, IMA, pigtail- 4Fr.DCGI - approved |
| 92 | Mullin sheath with dilator USFDA /PMDA approved |
| 93 | Mullin sheath with dilator CE-approved |
| 94 | Mullin sheath with dilator DCGI- approved |
| 95 | Trans- septal needle.USFDA /PMDA approved |
| 96 | Trans- septal needle.CE-approved |
| 97 | Trans- septal needle. DCGI -approved |
| 98 | PTMC Balloon With all accessories (mullin sheath, coiled wire, dilator, stretching tube, stylet, trans-septal needle)balloon material: Fabric extruded with Latex 12F balloon catheter,80cm in lengthTri-layered balloonAvailable size range of inflation diameter are 19- 22mm, 23-26mm,25-28mm,26-29mm,and 27- 30mm.Accessories available individually in a separate packing: Metal balloonstretching tube-medical grade stainless steel 80cm Dilator medical grade polymer -12FLA guide wire – medical grade stainless steel Stylet –Medical grade stainless steelSyringe with markings of 19-22mm,21- 24mm,23-26mm,25-28mm,26-29mm,and 27-30mm.Small tip to avoid perforation3 lumens at proximal end.USFDA/PMDA approved |
| 99 | PTMC Balloon With all accessories (mullin sheath, coiled wire, dilator, stretching tube, stylet, trans-septal needle)balloon material: Fabric extruded with Latex 12F balloon catheter,80cm in lengthTri-layered balloonAvailable size range of inflation diameter are 19-22mm, 23-26mm,25-28mm,26-29mm,and 27- 30mm.Accessories available individually in a separate packing: Metal balloonstretching tube-medical grade stainless steel 80cm Dilator medical grade polymer -12FLA guide wire – medical grade stainless steel Stylet –Medical grade stainless steelSyringe with markings of 19-22mm,21- 24mm,23-26mm,25-28mm,26-29mm,and 27-30mm.Small tip to avoid perforation3 lumens at proximal end.CE- approved |
| 100 | PTMC Balloon With all accessories (mullin sheath, coiled wire, dilator, stretching tube, stylet, trans-septal needle)balloon material: Fabric extruded with Latex 12F balloon catheter,80cm in lengthTri-layered balloonAvailable size range of inflation diameter are 19- 22mm, 23-26mm,25-28mm,26-29mm,and 27- 30mm.Accessories available individually in a separate packing: Metal balloonstretching tube-medical grade stainless steel 80cm Dilator medical grade polymer -12FLA guide wire – medical grade stainless steel Stylet –Medical grade stainless steelSyringe with markings of 19-22mm,21- 24mm,23-26mm,25-28mm,26-29mm,and 27-30mm.Small tip to avoid perforation3 lumens at proximal end. DCGI – approved |
| 101 | INTRAVASCULAR RETRIEVER-Micro SNARE(‘AMPLATZ GOOSENESK’ TYPE)-Snare kit should include with all accessories like sheath etc.A snare and its compatible sheath Should have nitinol shaft Titanium nitride coated tungsten loop Should have 90 degree preformed snare loop Radiopaque marker at distal tipVariable size of loop (2-4 mm) USFDA/PMDA approved |
| 102 | INTRAVASCULAR RETRIEVER-Micro SNARE(‘AMPLATZ GOOSENESK’ TYPE)-Snare kit should include with all accessories like sheath etc.A snare and its compatible sheath Should have nitinol shaftTitanium nitride coated tungsten loop Should have 90 degree preformed snare loop Radiopaque marker at distal tipVariable size of loop (2-4 mm) CE -approved |
| 103 | INTRAVASCULAR RETRIEVER-Micro SNARE(‘AMPLATZ GOOSENESK’ TYPE)-Snare kit should include with all accessories like sheath etc.A snare and its compatible sheath Should have nitinol shaftTitanium nitride coated tungsten loop Should have 90 degree preformed snare loop Radiopaque marker at distal tipVariable size of loop (2-4 mm) DCGI - approved |
| 104 | Vacular device closure Proglide TypeUSFDA/PMDA approved |
| 105 | Vacular device closure Proglide TypeCE approved |
| 106 | Vacular device closure Proglide TypeDCGI -approved |
| 107 | Temporary pacemaker leadBalloon tipped 5Fr/6FrUSFDA/PMDA approved |
| 108 | Temporary pacemaker leadBalloon tipped 5Fr/6FrCE approved |
| 109 | Temporary pacemaker leadBalloon tipped 5Fr/6FrDCGI - approved |
| 110 | TAVI Guide wireOuter Diameter 0.035” (0.889mm),Length 275 cm,Core Material Stainless Steel, Spring Coil Material Stainless Steel, Spring Coil Coating LUBRIGREENTM PTFE,Curves Extra Small (16cm X 2.9cm) Small (16cm x 4.2cm x 4.2cm),Large (18cm x5.0cm x 4.9cm) |
| 111 | TAVI Guide wireOuter Diameter 0.035” (0.889mm),Length 275 cm,Core Material Stainless Steel, Spring Coil Material Stainless Steel, Spring Coil Coating LUBRIGREENTM PTFE,Curves Extra Small (16cm X 2.9cm) Small (16cm x 4.2cm x 4.2cm),Large (18cm x 5.0cm x 4.9cm) |
| 112 | TAVI Guide wireOuter Diameter 0.035” (0.889mm),Length 275 cm,Core Material Stainless Steel, Spring Coil Material Stainless Steel, Spring Coil Coating LUBRIGREENTM PTFE,Curves Extra Small (16cm X 2.9cm) Small (16cm x 4.2cm x 4.2cm),Large (18cm x 5.0cm x 4.9cm) |
| 113 | Peripheral wire 0.014- Stainless steel core wire Hydrophilic & hydrophobic coating Tip load – 3 gm & 6 gmUS FDA approvedWire length- 190 cm & 300 cm USFDA /PMDA approved |
| 114 | Peripheral wire 0.014- Stainless steel core wireHydrophilic & hydrophobic coating Tip load – 3 gm & 6 gmUS FDA approvedWire length- 190 cm & 300 cm CE - approved |
| 115 | Peripheral wire 0.014- Stainless steel core wireHydrophilic & hydrophobic coating Tip load – 3 gm & 6 gmUS FDA approvedWire length- 190 cm & 300 cm DCGI - approved |
| 116 | Peripheral wire 0.018-0.018” guide wire with Stainless steel core wireHydrophilic & hydrophobic coating Tip load – 7.6 gm & 6.5 gmUS FDA approvedWire length- 150 cm, 200 & 300 cm USFDA /PMDA approved |
| 117 | Peripheral wire 0.018-0.018” guide wire with Stainless steel core wireHydrophilic & hydrophobic coating Tip load – 7.6 gm & 6.5 gmUS FDA approvedWire length- 150 cm, 200 & 300 cm CE – approved |
| 118 | Peripheral wire 0.018-0.018” guide wire with Stainless steel core wireHydrophilic & hydrophobic coating Tip load – 7.6 gm & 6.5 gmUS FDA approved Wire length- 150 cm, 200 & 300 cm DCGI - approved |
| 119 | Peripheral Balloons -0.018”/0.014” wire compatible –Should be 4F/5F sheath and 0.018”/0.014” wire compatible with choice of OTW/Monorail delivery systemShould be non-compliant/ semi compliant. Should have high rated burst pressure with scratch/puncture resistant pebax material Should have lowest tip entry profile of not more than 0.022” and good 5 fold re-wrap designShould have excellent coulum support with balloon laser bonded and short atraumatic tapered tipShould have full length tapered core wire for enhancd pushability and kink resistance Should have balloon length starting from 10 mm – 60mm and balloon diameter from 3 mm to 10 mm.USFDA /PMDA approved |
| 120 | Peripheral Balloons -0.018”/0.014” wire compatible –Should be 4F/5F sheath and 0.018”/0.014” wire compatible with choice of OTW/Monorail delivery systemShould be non-compliant/ semi compliant. Should have high rated burst pressure with scratch/puncture resistant pebax material Should have lowest tip entry profile of not more than 0.022” and good 5 fold re-wrap designShould have excellent coulum support with balloon laser bonded and short atraumatic tapered tipShould have full length tapered core wire for enhancd pushability and kink resistance Should have balloon length starting from 10 mm – 60mm and balloon diameter from 3 mm to 10 mm.CE - approved |
| 121 | Peripheral Balloons -0.018”/0.014” wire compatible –Should be 4F/5F sheath and 0.018”/0.014” wire compatible with choice of OTW/Monorail delivery systemShould be non-compliant/ semi compliant. Should have high rated burst pressure with scratch/puncture resistant pebax material Should have lowest tip entry profile of not more than 0.022” and good 5 fold re-wrap designShould have excellent coulum support with balloon laser bonded and short atraumatic tapered tipShould have full length tapered core wire for enhancd pushability and kink resistance Should have balloon length starting from 10 mm – 60mm and balloon diameter from 3 mm to 10 mm.DCGI- approved |
| 122 | Regular length,0.035, straight tipped , Teflon coated Guide wireUSFDA /PMDA approved |
| 123 | Regular length,0.035, straight tipped , Teflon coated Guide wireCE approved |
| 124 | Regular length,0.035, straight tipped , Teflon coated Guide wireDCGI- approved |
| 125 | Regular length,0.035, straight tipped , Hydrophilic coated Guide wireUSFDA /PMDA approved |
| 126 | Regular length,0.035, straight tipped , Hydrophilic coated Guide wireCE- approved |
| 127 | Regular length,0.035, straight tipped , Hydrophilic coated Guide wireDCGI- approved |
| 128 | Lander quist Super Stiff wire 0.035 “ - Exchange lengthUSFDA /PMDA approved |
| 129 | Lander quist Super Stiff wire 0.035 “ - Exchange lengthCE - approved |
| 130 | Lander quist Super Stiff wire 0.035 “ - Exchange lengthDCGI - approved |
| 131 | Micropuncture set needle set 5F 7Cm needle USFDA /PMDA approved |
| 132 | Micropuncture set needle set 5F 7Cm needle CE- approved |
| 133 | Micropuncture set needle set 5F 7Cm needle DCGI - approved |
| 134 | Abdominal aortic aneurysm- covered stent USFDA /PMDA approved |
| 135 | Abdominal aortic aneurysm- covered stent CE - approved |
| 136 | Abdominal aortic aneurysm- covered stent DCGI - approved |
| 137 | Abdominal aortic aneurysm- non covered stent USFDA /PMDA approved |
| 138 | Abdominal aortic aneurysm- non covered stent CE - approved |
| 139 | Abdominal aortic aneurysm- non covered stent DCGI - approved |
| 140 | Covered stent grafts- various lengths and diameter USFDA /PMDA approved |
| 141 | Covered stent grafts- various lengths and diameter CE - approved |
| 142 | Covered stent grafts- various lengths and diameter DCGI - approved |
| 143 | Non Covered stent grafts- various lengths and diameterUSFDA /PMDA approved |
| 144 | Non Covered stent grafts- various lengths and diameterCE - approved |
| 145 | Non Covered stent grafts- various lengths and diameterDCGI - approved |
| 146 | Distal embolic protection device- Carotid/SVG-(One size for all carotids)Eccentric filter with nitinol loop for 360 degree wall apposition Rx.014 6F sheath compatible 190 cm extra support wire Uniform micro pore size of110 micron pore size with 1 mm pore free zoneNon thrombogenic nylon membrane with hydrophilic coatingShouls allow optimal filtration in vessels 3-5.5 mm sizeUSFDA /PMDA approved |
| 147 | Distal embolic protection device- Carotid/SVG-(One size for all carotids)Eccentric filter with nitinol loop for 360 degree wall appositionRx.014 6F sheath compatible 190 cm extra support wire Uniform micro pore size of110 micron pore size with 1 mm pore free zoneNon thrombogenic nylon membrane with hydrophilic coatingShouls allow optimal filtration in vessels 3-5.5 mm size CE - approved |
| 148 | Distal embolic protection device- Carotid/SVG-(One size for all carotids)Eccentric filter with nitinol loop for 360 degree wall appositionRx.014 6F sheath compatible 190 cm extra support wire Uniform micro pore size of110 micron pore size with 1 mm pore free zoneNon thrombogenic nylon membrane with hydrophilic coatingShouls allow optimal filtration in vessels 3-5.5 mm size DCGI - approved |
| 149 | Peripheral self expanding drug eluting stent- Paclitaxel eluting self-expanding stent with a polymer that releases paclitaxel over 12 month with lowest dose density of 0.167ug/mm2 for SFA and PPATriaxial delivery systemHybrid cell architecture with open and close celldesisnEasy deployment with thumbwheel & pull grip6F sheath compatibility Dia-6 &10 mmLength – 40,60,80,100,120 mmUSFDA /PMDA approved |
| 150 | Peripheral self expanding drug eluting stent- Paclitaxel eluting self-expanding stent with a polymer that releases paclitaxel over 12 month with lowest dose density of 0.167ug/mm2 for SFA and PPATriaxial delivery systemHybrid cell architecture with open and close celldesisnEasy deployment with thumbwheel & pull grip6F sheath compatibility Dia-6 &10 mmLength – 40,60,80,100,120 mmCE approved |
| 151 | Peripheral self expanding drug eluting stent- Paclitaxel eluting self-expanding stent with a polymer that releases paclitaxel over 12 month with lowest dose density of 0.167ug/mm2 for SFA and PPATriaxial delivery systemHybrid cell architecture with open and close celldesisnEasy deployment with thumbwheel & pull grip6F sheath compatibility Dia-6 &10 mmLength – 40,60,80,100,120 mmDCGI - approved |
| 152 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Life long battery warranty.Auto capture mode Minimize ventricular pacingmodeBeat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath3.0 T MRI compatible (full body) USFDA/PMDA-approved |
| 153 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Life long battery warranty.Auto capture modeMinimize ventricular pacing mode Beat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath3.0 T MRI compatible (full body) CE-approved |
| 154 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Life long battery warranty.Auto capture mode Minimize ventricular pacing mode Beat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath3.0 T MRI compatible (full body) DCGI -approved |
| 155 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Auto capture modeMinimize ventricular pacing modeBeat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath1.5 T and above MRI compatible (full body) USFDA/PMDA-approved |
| 156 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Auto capture modeMinimize ventricular pacing modeBeat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath1.5 T and above MRI compatible (full body) CE - approved |
| 157 | Dual Chamber Pacemaker (DDD) with peel away sheath 6 Fr. –with conduction system pacing (CSP)Screw in and tined lead as per operator’s wish Auto capture modeMinimize ventricular pacing modeBeat to Beat capture mechanism AF suppressionOptimization of AV delayPacemaker lead profile should be maximum up to 5 .8 Fr.Lead should be compatible with 6 Fr. peel away sheath1.5 T and above MRI compatible (full body) DCGI-approved |
| 158 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AFFacility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optionalUSFDA /PMDA approved |
| 159 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AFFacility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optional CE- approved |
| 160 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AFFacility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optional DCGI - approved |
| 161 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. Sheath Atrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AFFacility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optional USFDA /PMDA approved |
| 162 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AFFacility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optionalCE - approved |
| 163 | CRT-P with conduction system pacing (CSP) –with all accessoriesCRT-P with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-PLV lead-upto 5 Fr.RV lead up to 5.8 Fr. and compatible with 6 Fr. SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. SheathHeart Failure Congestion Monitoring Trends with AlertsFacility for overdriving Atrium for prevention of Atrial Arrythmias Electrocardiogram based AV Optimization for suggesting optimized AV Delays warranty : Minimum 5 years on Device Special Algorithms to Predict Lead failure and Protection inappropriate shocks during failed leadProgrammable AT/AF Alerts with AF Burden trendingFacility of specially coated Device for avoiding lead abrasion (optional)Special Trigger Mode Biventricular Pacing in Presence of AT/AF Facility of RF TelemetryShould be supplied with 6 compatible leads and Introducers for RA & RVLV lead delivery systems should be compatible with 7 Fr. EP catheters optional DCGI- approved |
| 164 | CRT-D with conduction system pacing (CSP) –with all accessoriesCRT-D with with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-DLV lead-upto 5 Fr.RV defibrillator lead : Should be supplied up to 7.6 Fr. Defibrillator lead compatible with 8 Fr. Peel away SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. Sheath40J delivered energyPulse width and Tilt : Programmable as per DFTHeart Failure Congestion Monitoring Trends with AlertsSmall size below 35cc Warranty : Minimum 5 yearsFacility of Changing the shocking vector based on Over Current sensingSpecial Sensing filter protection for T Wave over sensing (optional)Special Algorithms to Predict Lead failure and Protection from inappropriate shocks during failed lead with vibratory patient Alert optionalFacility of specially coated Device for avoiding lead abrasion (optional) USFDA/PMDA- approved |
| 165 | CRT-D with conduction system pacing (CSP) –with all accessoriesCRT-D with with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-DLV lead-upto 5 Fr.RV defibrillator lead : Should be supplied up to 7.6 Fr. Defibrillator lead compatible with 8 Fr. Peel away SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. Sheath40J delivered energyPulse width and Tilt : Programmable as per DFTHeart Failure Congestion Monitoring Trends with AlertsSmall size below 35cc Warranty : Minimum 5 yearsFacility of Changing the shocking vector based on Over Current sensingSpecial Sensing filter protection for T Wave over sensing (optional)Special Algorithms to Predict Lead failure and Protection from inappropriate shocks during failed lead with vibratory patient Alert optionalFacility of specially coated Device for avoiding lead abrasion (optional)CE- approved |
| 166 | CRT-D with conduction system pacing (CSP) –with all accessoriesCRT-D with with all accessories - RA, RV and Quadripolar LV leads and catheters CRT-DLV lead-upto 5 Fr.RV defibrillator lead : Should be supplied up to 7.6 Fr. Defibrillator lead compatible with 8 Fr. Peel away SheathAtrial lead up to 5.8 Fr. and compatible with 6 Fr. Sheath40J delivered energyPulse width and Tilt : Programmable as per DFTHeart Failure Congestion Monitoring Trends with AlertsSmall size below 35cc Warranty : Minimum 5 yearsFacility of Changing the shocking vector based on Over Current sensingSpecial Sensing filter protection for T Wave over sensing (optional)Special Algorithms to Predict Lead failure and Protection from inappropriate shocks during failed lead with vibratory patient Alert optionalFacility of specially coated Device for avoiding lead abrasion (optional) DCGI - approved |
| 167 | Subcutaneous ICD with all accessories USFDA/PMDA approved |
| 168 | Subcutaneous ICD with all accessories CE - approved |
| 169 | Subcutaneous ICD with all accessories DCGI - approved |
| 170 | Lead Less Pacemaker with all accessories USFDA/PMDA approved |
| 171 | Lead Less Pacemaker with all accessories CE - approved |
| 172 | Lead Less Pacemaker with all accessories DCGI - approved |
| 173 | Rota wire and wire clip torquer 330cm 0.009”, for rotational atherectomy system Compatible with existing rota blator machine in cath labUSFDA/PMDA approved |
| 174 | Rota wire and wire clip torquer 330cm 0.009”, for rotational atherectomy system Compatible with existing rota blator machine in cath labCE - approved |
| 175 | Rota wire and wire clip torquer 330cm 0.009”, for rotational atherectomy system Compatible with existing rota blator machine in cath labDCGI - approved |
| 176 | FFR Pressure WireShould be 0.014” guide wire.System should work both wired and wireless radio using frequency hopping spread spectrum to ensure secure radioconnection with Pressure Wire. Should be compatible with available QUANTIEN FFR Measurement System. USFDA/PMDA approved |
| 177 | FFR Pressure WireShould be 0.014” guide wire.System should work both wired and wireless radio using frequency hopping spread spectrum to ensure secure radio connection with Pressure Wire.Should be compatible with available QUANTIEN FFR Measurement System. CE Approved |
| 178 | FFR Pressure WireShould be 0.014” guide wire.System should work both wired and wireless radio using frequency hopping spread spectrum to ensure secure radio connection with Pressure Wire.Should be compatible with availableQUANTIEN FFR Measurement System. DCGI- Approved |
| 179 | OCT CatheterThe imaging catheter should be able to emit near infra red light to produce high resolution real time image.Catheter should be compatible with 0.014” guide wire.Should be compatible with available Optis Integrated Next OCT System USFDA/PMDA Approved |
| 180 | OCT CatheterThe imaging catheter should be able to emit near infra red light to produce high resolution real time image.Catheter should be compatible with 0.014” guide wire.Should be compatible with available Optis Integrated Next OCT System CE Approved |
| 181 | OCT CatheterThe imaging catheter should be able to emit near infra red light to produce high resolution real time image.Catheter should be compatible with 0.014” guide wire.Should be compatible with available Optis Integrated Next OCT SystemDCGI- Approved |
| 182 | IVL. Catheter and Connector cable Intravascular lithotripsy intuitive catheter with Rx system for treating highly Calcified lesionsIntegrated 12mm SC balloon NP- 6 ATMRBP – 10ATMDiameter – 2.5,3.0,3.5,4.0mm2 Emitters( 80 Pulses per Catheter ) Registry with minimum 300 patients published in a peer reviewed journal USFDA/PMDA approved |
| 183 | IVL. Catheter and Connector cable Intravascular lithotripsy intuitive catheter with Rx system for treating highly Calcified lesionsIntegrated 12mm SC balloon NP- 6 ATMRBP – 10ATMDiameter – 2.5,3.0,3.5,4.0mm2 Emitters( 80 Pulses per Catheter ) Registry with minimum 300 patientspublished in a peer reviewed journal CE – approved |
| 184 | IVL. Catheter and Connector cable Intravascular lithotripsy intuitive catheter with Rx system for treating highly Calcified lesionsIntegrated 12mm SC balloon NP- 6 ATMRBP – 10ATMDiameter – 2.5,3.0,3.5,4.0mm2 Emitters( 80 Pulses per Catheter ) Registry with minimum 300 patientspublished in a peer reviewed journal DCGI - approved |
| 185 | Mitral ClipTrans catheter edge to edge repair (TEER) SystemCobalt chromium covered with polyester fabric and national graspersClip arm- 3-7 mmClip arm length – 9 and 12 mmWith guide catheter and delivery system and all accessoriesUSFDA/PMDA approved |
| 186 | Mitral ClipTrans catheter edge to edge repair (TEER) SystemCobalt chromium covered with polyester fabric and national graspersClip arm- 3-7 mmClip arm length – 9 and 12 mmWith guide catheter and delivery system and all accessoriesCE- approved |
| 187 | Mitral ClipTrans catheter edge to edge repair (TEER) SystemCobalt chromium covered with polyester fabric and national graspersClip arm- 3-7 mmClip arm length – 9 and 12 mmWith guide catheter and delivery system and all accessoriesDCGI - approved |
| 188 | Tricuspid valve- THVBalloon expandable THV system Hybrid honey comb cell design Size 20,21.5,23.0,24.5,26.0,27.5,29.0,30.5,32.0mm14 Fr Python sheathNavigator THV delivery system Mammoth predication balloon Crimping toolUSFDA/PMDA approved |
| 189 | Tricuspid valve- THVBalloon expandable THV system Hybrid honey comb cell design Size20,21.5,23.0,24.5,26.0,27.5,29.0,30.5,32.0mm14 Fr Python sheathNavigator THV delivery system Mammoth predication balloon Crimping toolCE -approved |
| 190 | Tricuspid valve- THVBalloon expandable THV system Hybrid honey comb cell design Size20,21.5,23.0,24.5,26.0,27.5,29.0,30.5,32.0mm14 Fr Python sheathNavigator THV delivery system Mammoth predication balloon Crimping toolDCGI - approved |
| 191 | IVC filter Various sizesWith all accessories USFDA/PMDA approved |
| 192 | IVC filter Various sizesWith all accessories CE -approved |
| 193 | IVC filter Various sizesWith all accessories DCGI - approved |
| 194 | Peripheral drug coated balloon 0.035” CompatibleDiameter 4 to 6 mm Length 60-150mm USFDA/PMDA approved |
| 195 | Peripheral drug coated balloon 0.035” CompatibleDiameter 4 to 6 mmLength 60-150mm CE -approved |
| 196 | Peripheral drug coated balloon 0.035” CompatibleDiameter 4 to 6 mm Length 60-150mm DCGI - approved |
| 197 | Inj. Inclisiran 284 mgSmall interfering RNA ( si RNA) that lowers LDL cholesterol by targeting the PCSK 9 protein in the liverUSFDA/PMDA approved |
| 198 | Inj. Inclisiran 284 mgSmall interfering RNA ( si RNA) that lowers LDL cholesterol by targeting the PCSK 9 protein in the liverCE – approved |
| 199 | Inj. Inclisiran 284 mgSmall interfering RNA ( si RNA) that lowers LDL cholesterol by targeting the PCSK 9 protein in the liverDCGI – approved |
| 200 | Inj. Iodixanol 100 mlIso- osmolar, Non ionic, dimeric, iodinecontaining contrast agent USFDA/PMDA approved |
| 201 | Inj. Iodixanol 100 mlIso- osmolar, Non ionic, dimeric, iodine containing contrast agentCE -approved |
| 202 | Inj. Iodixanol 100 mlIso- osmolar, Non ionic, dimeric, iodine containing contrast agentDCGI- approved |
| 203 | Inj. Tirzepatide USFDA/PMDA approved |
| 204 | Inj. Tirzepatide CE -approved |
| 205 | Inj. Tirzepatide DCGI- approved |
| 206 | Inj. Cangrelor USFDA/PMDA approved |
| 207 | Inj. Cangrelor CE -approved |
| 208 | Inj. Cangrelor DCGI- approved Please Enable Macros to View BoQ information |
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