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| Sr No | Corrigendum Date | Corrigendum | Type | New Submission Date |
|---|---|---|---|---|
| 1 | 25-08-2022 | CARDIOTHORACIC | Other | 01-09-2022 |
| 2 | 24-08-2022 | Corrigendum for date | Date | 01-09-2022 |
| 3 | 22-08-2022 | Corrigendum for CTVS | Other | 25-08-2022 |
| 4 | 20-08-2022 | Corrigendum Regarding technical sheet | Other | 25-08-2022 |
| Sl. No. | Item Description |
| 1 | ITEM LIST |
| 2 | Iohexol for Vascular Procedures350 x 50 ML in Plastic Polypropylene Bottle. |
| 3 | Iohexol for Vascular Procedures350 x 100 ML in Plastic Polypropylene Bottle. |
| 4 | Iohexol for Vascular Procedures350 x 200 ML in Plastic Polypropylene Bottle. |
| 5 | Iohexol for Vascular Procedures350 x 500 ML in Plastic Polypropylene Bottle. |
| 6 | Iodixanol Vascular Procedure 320 x 100 ML in plastic Polypropylene bottle. |
| 7 | Syringe for pressure Injector compatible with Imaxon injector ZY6322 |
| 8 | Syringe for pressure Injector compatible with Imaxon injector ART-700 |
| 9 | Y Adoptor for pressure injector compatible with Imaxon injector |
| 10 | Pnumbra Catheter for Thrombosuction compatible to Pnumbra machine CAT6 |
| 11 | Pnumbra Catheter for Thrombosuction clottingcompatible to Pnumbra machine CAT8 |
| 12 | Seprator for Thrombosuction clotting compatible to CAT 6 catheter and Pnumbra machine |
| 13 | Seprator for Thrombosuction clotting compatible to CAT 8 catheter and Pnumbra machine |
| 14 | Canister for Thrombosuction cloting Exudate compatible to Pnumbra machine1000 ML |
| 15 | Tubing for Thrombosuction clotting compatible to Pnumbra machine |
| 16 | PUR Catheter 16G Length 15 and 20 CM with Guide wire 0.9x400mm Introducing Needle |
| 17 | Drug Delivery System |
| 18 | 2.45% activated glutaraldehyde with a powder activator, 510k Cleared and effective against Human CoronaVirus. It should be endorsed by minimum fiveMDM’s: Karl Storz, Pentax, Stryker, Richard wolf , Philips for their– Rigid & Flexible Telescopes, Fiber optic cables, TEE probes . Should have Disinfectant manufacturer compatible tray made ofglass filled polypropylene which can be steam sterilized. Should also have test strip which consists of sodium sulfite and dyes impregnated and dried on filter paper . PACK SIZE= 5 LITRE JAR |
| 19 | Solution containingBenzotriazole, N-(hydroxyethyl) -ethylenediaminetriacetic acid (HEDTA),Dipotassium hydrogen phosphate, Potassium Dihydrogen Phosphate and0.55% w/v opa .510k Cleared and effective against Human CoronaVirus and cytomegalo virus . It should be endorsed by minimum fiveMDM’s: Karl Storz, Pentax, Stryker, Richard wolf , Olympus for their– Rigid & Flexible Telescopes, Fiber optic cables, . Also should be endorsed by AER manufacturers.Should also have test strip which consists of sodium sulfite and dyes impregnated and dried on filter paper . PACK SIZE= 5 Litre |
| 20 | Effervescent 50% troclosene Sodium tablet 5g each tablet. PACK SIZE : 50 Tab/bt. |
| 21 | Traystrays made of glass filled polypropylene which can be steam sterilize and CE approvedfor Disinfection. |
| 22 | Dacron Graft Y6X12 |
| 23 | Dacron Graft Y7X14 |
| 24 | Dacron Graft st 6X20/30 |
| 25 | Dacron Graft st 6X40/60 |
| 26 | Dacron Graft st 6X70 |
| 27 | Dacron Graft St 7x20/30 |
| 28 | Dacron Graft St 7x40/60 |
| 29 | Dacron Graft St 7x70 |
| 30 | Dacron Graft St 8x40/60 |
| 31 | PTFE Graft 6x20 |
| 32 | PTFE Graft 6x65/50 |
| 33 | PTFE Graft 6x75/80 |
| 34 | PTFE Graft 4x40 |
| 35 | PTFE Graft 5x20 |
| 36 | PTFE Graft 7x40/80 |
| 37 | PTFE Graft 8x40/50 |
| 38 | IABP Balloon compatible to maquet machine |
| 39 | Cardiac Stablizer MICS |
| 40 | Platipus |
| 41 | Picco catheter Continious cardiac output Moniter catheter with injector housing 3 fr x 7 cm |
| 42 | Picco catheter Continious cardiac output Moniter catheter with injector housing 4 fr x 8 cm |
| 43 | Picco catheter Continious cardiac output Moniter catheter with injector housing 5 fr x 20 cm |
| 44 | Embolactomy catheter |
| 45 | PTFE Felt |
| 46 | Femoral Arterial canula |
| 47 | Venous Arterial canula |
| 48 | PTFE Bifergated Graft |
| 49 | Lineaar Cuttur Stapler 60 mm . Universal instrument 2 rows on both cut line side with B form Staple Technology |
| 50 | Linear Cutter Reloadfor Medium tissue, No of Staples 84 , Open Staple Height 3.8mm, Formed Closed Stapple Height 1.5mm Blue, Cut line 60mm, Staple line 63 mm ,Compatible with |
| 51 | Linear Cutter Reloadfor Thicktissue, Staples 84 , Open Staple Height 4.8mm, Formed Closed Stapple Height 2.0mm Green, Cut line 60mm, Staple line 63 mm, Compatible with Linear Cutter 60mm Universal instrument 2 rows on both cut line side with B form Staple Technology |
| 52 | Disposable Curved Cutter Stapler ,Open Leg length 40mm , Formed closed staple Height 2.0 mm Blue or green |
| 53 | Single Use Circular Stapler Outer Diameter 25mm, Inner Diameter 17mm, No of Staples 22 , Open Height 4.8mm, Formed Height 2.0 mm |
| 54 | Single Use Circular Stapler Outer Diameter 29mm, Inner Diameter 21mm, No of Staples 26, Open Height 4.8 mm, Formed Height 2.0mm |
| 55 | Single Use Circular Stapler Outer Diameter 31mm, Inner Diameter 23mm, No of Staples 28, Open Height 5.0 mm, Formed Height 2.2 mm |
| 56 | Single Use Circular Stapler Outer Diameter 33mm, Inner Diameter 25mm, No Of Staples 32, Open Height 5.2 mm, Formed Height 2.2 mm |
| 57 | Transducer - Open Surgery (Multi-Use without Counter limitation.) |
| 58 | Transducer - Thorocoscopic (Multi-Use without Counter limitation.) |
| 59 | Probe 6 mm Hand Activated Cutting & Coagulating Shears with 360 degrees of shaft rotation, capable of sealing blood vessels up to 5mm in diameter with 36 cm shaft length. Compatible with existing Rf Generators ,Ultrasonic generator and transducer(Multi-Use without Counter limitation.) |
| 60 | Probe 9 cm shaft, curved, tapered tip for precise dissection, seals 5 mm vessels, as well as lymphatic ,360-degree of shaft rotation, triggers support multiple hand positions.Compatible with Ultrasonic generator and transducer for(Multi-Use without Counter limitation.) |
| 61 | Probe 17cm shaft, curved, tapered tip for precise dissection, seals 5 mm vessels, as well as lymphatic , 360-degree of shaft rotation, triggers support multiple hand positions.Compatible with Ultrasonic generator and transducer (Multi-Use without Counter limitation.) |
| 62 | Probe with Bipolar 6mm Hand Activated Curved Cutting &Coagulating Shears with 360 degrees of shaft rotation, capable of sealing blood vessels up to 5mm in diameter with 23 cm shaft length . Compatible with existing Rf Generators & Ultrasonic generator and transducer(Multi-Use withoutCounter limitation.) which can be used as both ultrasonic & Bipolar Laparoscopic shears . |
| 63 | VIROFIL Smoke,Plume and Pathogen Filter with Universal Luer Lock + 3 Luer Caps |
| 64 | NOVA 5 mm, 5-10mm,5-12 mm , Bladeless Trocar w/ VIEWFINDER 100mm with VIROFIL Pathogen Filter |
| 65 | Cartidge small Titanium Red Trans verac Grooves Heart shape wire usfda Cartdige of 6 clip |
| 66 | Cartidge small TitaniumTrans verac Grooves Heart shape wire usfda Cartdige of 6 clip |
| 67 | Cartidge Medium Titanium Trans verac Grooves Heart shape wire usfdaCartdige of 6 clip |
| 68 | Cartidge Medium-Large Titanium Trans verac Grooves Heart shape wire usfdaCartdige of 6 clip |
| 69 | Cartidge Large TitaniumTrans verac Grooves Heart shape wire usfda Cartdige of 6 clip |
| 70 | Polymer Ligation Clip With Locking machanism. Cover 3mm to 16mm vessels. Medium Large Class 3 for CE |
| 71 | Polymer Ligation Clip With Locking machanism. Cover 3mm to 16mm vessels. Large Class 3 for CE |
| 72 | Polymer Ligation Clip With Locking machanism. Cover 3mm to 16mm vessels. Extra Large Class 3 for CE |
| 73 | Poliglecaprone 25) USP Size 3-0 ,Suture Lenght 70cm , Needle Length 25 mm , 3/8 Circle Reverse Cutting |
| 74 | Monofilament Poly (P-dioxanone) Uni-Directional with End Loop barbed suture, Violet 1/2 Circle Taper Point , USP Size 2-0 ,Suture Length 30cm , Needle Length 37 mm |
| 75 | Undyed, Braided Coated Short Term Poly (Glycolide-Co-L-Lactide) (Polyglactin -910) 1/2 Circle Taper Cut , USP Size 2-0 ,Suture Length 90cm , Needle Length 36 mm |
| 76 | Undyed, Braided Coated Short Term Poly (Glycolide-Co-L-Lactide) (Polyglactin -910)1/2 Circle Round Bodied, 1/2 Circle Reverse Cutting Double Armed , USP Size 2-0 ,Suture Length 140cm , Needle Length 40 mm |
| 77 | Polyester 1 |
| 78 | Polyester 2 |
| 79 | Polyester5 |
| 80 | Endoscopic Linear Cutter stapler 60 mm Short Shaft (Open+Thoracic) |
| 81 | Endoscopic Linear Cutter stapler 160mm Standard Shaft (Regular Laparoscopy) |
| 82 | Endoscopic Linear Cutter stapler260mm Extra LongShaft |
| 83 | Reload 45 mm White & BlueEndoscopic Linear CutterArticulating Reload for Vascular Tissue,Staple Height 2.5mm, 3.5 mm |
| 84 | Reload 60 mm White & Blue Endoscopic Linear Cutter Articulatingfor Vascular Tissue,- Staple Height 2.5mm, 3.5 mm |
| 85 | Reload60 mm GoldEndoscopicLinear CutterArticulatingfor Medium Thick Tissue,- Staple Height 4.1mm |
| 86 | Reload 60 mm GreenEndoscopic Linear CutterArticulatingfor Thick Tissue,Staple Height 4.8mm |
| 87 | Reload 60 mm GreenEndoscopic Linear CutterArticulatingfor Extra Thick Tissue,Staple Height 5.0mm |
| 88 | Pre-fitted with polyester sutures : visual mark printed on polyester for easy Mesh centring. 3D Honeycomb knitted structure for superior tissue integration and patient comfort.Dual Side Mesh with Composition ofPolyester with polyurethane. Mesh Came with circular sizes also 12cm and 15cm circular . Sizes:6*11cm,7.6*15cm,10*15cm,15*15cm,15*20cm |
| 89 | Central 4 Lumen catheter |
| 90 | Transperent dressings Tegaderm |
| 91 | Talc powder for Pleurodesiss |
| 92 | Multi hole Multipurpouse catheter for Thrombolysis |
| 93 | Skin stapler |
| 94 | Vascular stapler |
| 95 | Bronceal stapler |
| 96 | Bovine pericardial bioprosthesis for the aortic position.FDA and European CE. The leaflets (made from a single strip of pericardium) are externally mounted over a titanium stent and this allows complete opening of the leaflets and aids in proper coaptation. Pericardial cover on the stent helps in mitigating the tissue abrasion with tissue to tissue contact. A propriety fixation procedure aids in proper leaflet shaping for proper leaflet coaptation. Presence of LinX anticalcification treatment resists tissue calcification and degradation of the valve.It is available in sizes 19mm, 21mm,23mm,25mm,27mm and 29mm. |
| 97 | Tissue Heart Valve - Biological tissue heart valves for Mitral and Aortic Heart position available in sizes 19-33mm . Design: Triple composite porcine valves. Valves have patented Anti-calcification treatment ( Linx AC technology). Lowest profile-9mm (lowest in the market). Sewing ring is made of polyester with markers for helping in suturing . Suture-friendly cuff minimizes suture drag & parachuting forces . Fixation Method: Low Pressure glutarldehyde fixation . Flexfit stent to reduce leaflet stress.The flexfit system reduces the rinse time to 2x10 seconds. Mitral Ratcheting system facilitates insertion into the mitral annulus and avoids suture looping. Scalloped inflow surface optimizes valve seating. USFDA approved. |
| 98 | ( Regent Flex cuff)- Aortic Mechanical heart valve- Mechanical Heart Valve for Aortic position.Individually sterilized and ready for use in individual patients. Expiration date: Five years from the date of manufacturing.Bi-leaflet and rotatable. Supra-annular placement.Low Profile.Maximum protrusion of leaflets from the housing is 3.4mm. Minimizes need for root enlargement. Up to 84% orifice to annulus ratio. Single-digit Pressure Gradients. Opening angle of 85 degrees. Significantly larger EOA’s than other mechanical heart valves. Significant reduction in LV mass.Disc: Pyrolytic carbon/graphite substrate. Housing: Pyrolytic carbon/titanium with Pyrolytic carbon coating. Sewing ring: made from polyester with markers for helping in suturing. The Flex Cuff is flanged and more pliable than the standard cuff. Patented butterfly upstream pivot design that lowers thrombogenicity, results in larger opening angles for improved laminar flow and a reduction in turbulence .Radio opaque for improved visualization during X-ray and fluoroscopy. The valve is MRI conditional. Controlled torque rotation mechanism . Available in sizes 17 mm to 29mm . U.S FDA approved and CE approved. |
| 99 | Bileaflet Aortic with Conduit -Double-velour woven fabric offers excellent sealing handling and healing characteristics .Collagen impregnation provides uniform tissue in-growth and biocompatibility .Rotatable valve attached .Allows for upstream placement of leaflets resulting in a wide opening angle .Enhanced Cuff Configuration Offers excellent implantability ,Conforms to the annulus,Designed to minimize potential for paravalvular leak . Low porosity graft eliminates the need for pre-clotting and reduces surgical time.No pleats allows for easy positioning and attachment of coronaries.Available in sizes: 19mm to 33 mm .US. FDA approved. |
| 100 | Rings Rigid Repair solutions available in rigid forms. The rigid ring is a full 3D ring which creates natural saddle shape.The ring has a complete titanium alloy core.Mimics healthy mitral anatomy and provides full remodeling which reduces stress. The ring helps in redistributing leaflet stress and chordal tension and increases repair durability. Encourages tissue in-growth through use of double velour polyester cuff. Facilitates in suturing with the EZ suture cuff supported by a unique triangular core. Available in sizes 22mm to 34mm. usfda |
| 101 | Pericardial Patch:-Indicated for cardiac and great-vessel reconstruction and repair and pericardial closure. 2. Designed Should be for ease of use, soft, pliable tissue conforms to uneven surfaces and minimizes suture hole leaks for more reliable repairs. 3. Should have EnCap™ technology, reduces adhesions enabling easier re-access and structure identification.4. Should have EnCap™ anti-calcification technology to minimize calcification and promote host endothelialization resulting in a more biocompatible material.5. Should be Glutaraldehyde and EnCap™ technology treated, bovine pericardium resists shrinkage and aneurysm formation—potentially reducing the chance of re-operation.6. Should be Rinse less Preparation, Ready to use. Thinner patch to accommodate pediatric applications.8. Available Sizes Should be : 2x5, 5x10, 9x14, 4x5 |
| 102 | Contigra |
| 103 | Vascular Mimetic Implant ( Supera)• For distal SFA, popliteal & across joints • 018 Nitinol interwoven design4—7mm Diametervarious lengthsupto 200mm |
| 104 | Renal Balloon expandable stent ( Herculink Elite) Rx .014 compatible Cobalt Chromium 3-3-Multi- link design •5 F Compatible across all sizes 5 , 5.5, 6 , 6.5 & 7 in length 12, 15 & 18 mm USFDA |
| 105 | Peripheral Balloon expandable stent system ( Omnilink Elite).OTW .035 guide wire compatible. 6F Sheath compatible across all sizes ( 7mm to 10 mm dia).L-605 Cobalt chromium Multi-Link stent design. Thin struts lowest crimped profile. Dual-layer, five-fold balloon. USFDA |
| 106 | Self expanding nitinol stent for carotid angioplasty - assorted sizes (X.Act).Rx Tapered Closed cell design with flared ends. 6F Sheath Compatible across all sizes. Freestyle technology. USFDA |
| 107 | Self expanding nitinol stent for peripheral angioplasty - assorted sizes. Absolute Pro & Absolute Pro LL). 035 OTW 6F sheath compatible across all sizes. 135mm usable catheter length for all sizes.Triaxial delivery system with I beam Technology to ensure accurate stent placement. USFDA |
| 108 | Vascular closure device. ( Perclose Proglide).5-22F polypropylene monofilament suture mediated vessel closure. With no re - access restriction. Immediate re-access advantage. Flexibility to pre-close and close over the wire. For small hole and large hole closure both. USFDA |
| 109 | 035 Peripheral Angioplasty Balloon ( Armada 35).CrossFlex Dual-layer balloon technology. OTW .035 guide wire compatible. 5F-7F sheath compatible to 12mm-14mm diameter faster deflation. Usable Catheter length 135cm for all sizesdia 4mm to 14mmup to 250mm length. USFDA |
| 110 | 014 Peripheral Angioplasty Balloon ( Armada 14). CrossFlex Dual-layer balloon technology. OTW 014 guide wire compatible.4F sheath compatible for dia 1.5 to 5 mm length upto 200mm. Usable Catheter length 150cm for all sizes .. USFDA |
| 111 | .018 Peripheral Angioplasty Balloon ( Armada 18). CrossFlex Dual-layer balloon technology. OTW 018 guide wire compatible.5F sheath compatible to diameters from 2mm to5.5 mm. Usable Catheter length 135cm for all sizes .USFDA |
| 112 | CarotidAngioplasty Balloon ( Viatrac 14 plus). Rx 014 Carotid Balloon. 014 guide wire compatible.5F sheath compatible to 4 to 7 mm diameter with 20mm length available in half sizes of diameter 4.5 & 5.5. Usable Catheter length 135cm for all sizes .USFDA |
| 113 | Distal embolic protection device ( Emboshield Nav6). One size for all carotids.Filter should be independent of wire. Rx .014 6F Sheath compatible.190 cm Bare wire workhorse wire preloaded delivery catheter.Uniform micro pore size of 120 micron pore size with 1mm pore free zone.Non-thrombogenic Nylon Membrane with hydrophilic coating. USFDA |
| 114 | Clip Based Closure Device – ( Star Close).5-8 F Nitinol Clip basedvessel closure Device.With no re - access restriction. USFDA |
| 115 | 035 extra support type Guidewire.Supportive .035 wire with soft atraumatic tip. 1:1 torque response provides exceptional steering. Hydrophobic coating to reduce friction. Wire lengths of 190 cm, and 300 cm |
| 116 | Peripheral CTO guide wire. . 014 with various tip load stiffness from 4.8- 13.0 mg.. Durasteel Core material. Transitionless Core Taper. Exposed shapable tip coils. Wire lengths of 190 cm and 300 cm. |
| 117 | 018 stainless support guide wire . various tip length 3cm / 5cm with shapeable straight & j tip.Supportive stainless steel shaft for excellent tactile feedback.1:1 torque for navigation around vessel bends. |
| 118 | 014 hybrid peripheral guide wire . Distal nitinol tip and proximal Stainless steel.Tip load 2.8 & 3.5g.Hydrophilic coating and radiopaque polymer cover.1:1 torque for navigation around vessel bends. Wire lengths of 190 cm and 300 cm. |
| 119 | 018 hybrid peripheral guide wire . Distal nitinol tip and proximal Stainless steel. Tip load 4g. Hydrophilic coating and radiopaque polymer cover. Available in Short taper and long taper both types of Tips. Transitionless Weld between Nitinol and Steel part. 1:1 torque for navigation around vessel bends. Wire lengths of 190 cm and 300 cm |
| 120 | Peripheral Vascular Plug ( Amplatzer AVP II ). Multi-layered, multiple-lobed Nitinol mesh design for rapid embolization within the vessel4. to embolize medium and high-flow vessels. Guide Catheter or Sheath Deliverable: Compatible with 4-7 F sheaths. or 5-9 F guide catheters depending on device size |
| 121 | Bioprosthetic heart valve. Triple composite bovine pericardium with elgiloy/alloy frame stent. Should have polymer support ring inside the polyester knit fabric for stent posts covering. Should have Anti calcification treatment done. Should have tenting system for avoiding suture looping in mitral position. Only latest version is acceptable. Should have sizes for aortic position from 19 to 25mm and for mitral position from 25 to 31mm.DGCI/CE Approved |
| 122 | Disposable Bladeless Trocar with Bird Wing Tip Design, 5mm in Diameter, 95mm Standard Sleeve Length, Self -Adjusting & Detachable Secondary Seal which can accommodate instruments diameter upto 5mm |
| 123 | Disposable Bladeless Trocar with Bird Wing Tip Design, 10mm in Diameter, 95mm Standard Sleeve Length, Self -Adjusting & Detachable Secondary Seal which can accommodate instruments diameter ranging from 5mm to 10mm |
| 124 | Disposable Bladeless Trocar with Bird Wing Tip Design & Optical Entry Feature, 12mm in Diameter, 95mm Standard Sleeve Length, Self -Adjusting & Detachable Secondary Seal which can accommodate instruments diameter ranging from 5mm to 12mm |
| 125 | Disposable Bladeless Trocar with Bird Wing Tip Design, 15mm in Diameter, 110mm Standard Sleeve Length, Self -Adjusting & Detachable Secondary Seal which can accommodate instruments diameter ranging from 5mm to 15mm |
| 126 | Ultrasonic scalpel for cutting and coagulating, 36 cm shaft length, 5 mm diameter Double layer non-stick (Teflon) coating pad on Jaw. 14cm/ 23cm/ 36cm/ 45cm |
| 127 | Radial arterial cannula With built in sliding lock system-sizes 20 |
| 128 | Retrograde Cannula catheter self -inflating smooth ballon with pre-shaped stylet and handle 14FR. Overall length should approx 27cm & should have 18 2mm sized smooth balloon. Shouldbe FDA Approved |
| 129 | Aortic Perfusion Cannulae; wire reinforced dispersion tip sizes: 21Fr and 24Fr overall length Approx. 35cm and vent Should be US FDAApproved |
| 130 | P.A. Catheter with 3, lumens & color coding for each lumen. Should be able to means P.A. pressure flow directed insertion & should be supplied with all accessorises. Like guid wire op sheath etc. bulb near end hole. Should be US FDA Approved |
| 131 | Flo trac sensor to measure contionuous cardiac output monitoring (To be compatible with Vigileo/EV 1000 cardiac output monitoring machine) Should be US FDA Approved |
| 132 | Arterial Transducer for measuring invasive blood pressure and CVP. Should be US FDA Approved |
| 133 | Disposable yellow Bulldog Clamp small size of 1-2 cm with metallic spring good occluding capacity. Should be US FDA Approved |
| 134 | Proximal aortic anastomosis device - It should provide the surgeon with a stable, blood field. It allows for up to three anastomosis form one insertionsite. It eliminates the need for partial occlusion clamping during coronary artery bypass grafting. size 3.5mm/4.0mm/4.5mm |
| 135 | Sternum and ribslock plate Should be available in different sizes and shapes to be supplied with Applier (gun) Sample based selection. Should be US FDA approved |
| 136 | Sternum and ribs lock plate 2.4mm and 2.7mm dimaeter cancellous self drilling locking with applier. Should be available in different sizes sample based selection. Should be US FDA approved |
| 137 | Ultra high pressure non compilant pta dilation Balloon Catheter -High performance balloon,Non-Complaint,multilayer balloon with Coaxial shaft and working pressure range ofupto 12atm, highest rated burst pressure of 18 atm Sizes: Diameter (12mm to 26 mm) & Lengths (2cm & 4cm ) with Shaft lengths of 75and 120cms. |
| 138 | Retrieval IVC Filter (window period 300 day)-Clinically tested in Largest longest IDE filter demonstrated safely implanted to provide immediate protection againts PE,Optional IVC Filter, two levels of filtration with the legs aproviding the lower level of filtration and the arms providing and the arms providing the upper level of filtration, Highly visible snare tip seamlessly welded to the body for easy filter retrieval even after long in-dwell time. the upper level of filtration |
| 139 | Self expandable (electro polished ) with radiopic markers- The Stent (implant ) Should equipped with four highly visible radiopaque PUZZLE Tantalum Markers on both the proximal and distal end for ACCURATE. It Should a self-expanding flexible nitinol (nickel-titanium alloy ) stent that expands to its preset diameter upon exposure to body temperature. The stent has a segmental repeating pattern and an open cell geometry with flared ends to help prevent dislocation or migration partial cuts around the circumference of the stent cylinder provide enhanced flexibility and allow segment-by segment expansion It shouldindicated for the treatment of illiac occlusive disease in patients with symptomatic vascular diseaseof the common and/or externaliliac arteries up to 126/200 mm in length with a reference vessel diameter of 5 to 9mm Perfect metalic length delivery thumb delibery 60-120 4 deployment for physicians convenience in deploying stent - Trigger, Slide, Combination and conventional. |
| 140 | self expending and popliteal Nitinol Stent with UniqueTriple Helix design Structure- Self Expending USFDA approved for SFA and Popliteal Stent with Unique Triple Helix design Structure for Multi-dimensional Flexibilty with unique Delivery system having both thumb wheel and pin & pull mechanism it should 5F Vascular Stent System and intended to improve luminal diameter in the treatment of symptomatic de novo or restenostic lesions up to 240 mm in length in the native superficial femoreal arterty (SFA)and popliteal artery with reference vessel diameters rangingfrom 5.0-7.0 mm USFDA approved |
| 141 | Ultra high pressure non complaint balloon-It Should for use in Percutaneous Transluminal Angioplasty of the femoral, iliac and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. High performence balloon catheter consistingof an overthe-wire catheter with a balloon fixed at the distal tip.The proprietary ultr non-compliant low profile balloon is designed to provide consistent balloon diameters and lengths even at high pressures.Tow radiopaque markers delineate the working length of the balloon and aid in balloon placement.The coaxial catheter includes a tapered atraumatic tip to facilitate advancement of the catheter to and through the stenosis |
| 142 | Balloon Expandable Vascular Covered Stent -It should for treatment of atherosclerotic lesious in commonand external iliac arterise with reference vessel diameters between 4.5 mm, and 12.0mm and lengths up to 100mm Balloon Expandable Vascular Covered Stent should comprised of an electropolished balloon-expandable stent made from 316L stainless steel, encapsulated between two layers of ePTFE. The covered stent should supplied pre-mounted on an over-the-wire delivery system with a non-compliant balloon |
| 143 | Drug Coated Balloon-Drug Coated Balloon With 2ug-3ug mm 2 dose paclitaxble with polysorbate & sorbitol as Carrier which will Deliver an optimal, therapeutic drug dose to the target vessel wall after a minimum 30 second inflation time Available in size -035guidewire compatible-120 cm shaft -4mm -6mm dia, lenght upto 150mm, 035 guidewire compatible -75cm shaft -5mm-12mm dia,length 60mm 014 guidewire compatible -150cm shaft -2mm to 3.5mm dia length 120mm |
| 144 | PTA Dilatation Catheter semi-compliant consisting of an over the wire (otw)-It should semi-compliant balloon catheter consisting of an over the wire (otw) catheter with an angioplasty balloon fixed at the distal tip. Two radiopaque markers delineate the working the length of the balloon and aid in balloon placement inteded to dilate stenoses in the peripheral arteries to treat obstructive lesions of native or synthetic AV Fistulae and /or re-expand endoluminal stent graft elements in the iliac arteries. 3-12 diameter range and 20-300 balloon length. |
| 145 | PTA Dilatation Catheter semi-compliant hydrophyclic balloon cathater consisting of an our the wire (OTW)- It should for use in percutaneous transluminal angioplasty (PTA) of the renal, popliteal, tibial femoral and peroneal arteries. To facilitate catheter advancementthrougs the vasculature and the viessal stenosis, dual layer hydrophlic coating should present on the distal segment of the shaft and the balloon. |
| 146 | Dual Sheath 9Fr and, ideal for IVC Filter rectrieval -Dual sheath 9fr and 11frideal for Denali retreval Kink Resistant Nitinol Construction with Radiopaque Loop for EnhancedVisibility 90\" loop snarefor proper placementwith Precise 1:1toeque facilitates filter easy hook capture marker Bands for Accurate Positioning Convenientall-in-kit includes new coaxial Sheaths and hemostaic valve |
| 147 | Percutaneous Transluminal Valvuloplasty of the pulmonary valve -It Should for Percutaneous Transluminal Valvuloplasty of the pulmonary valve in the following patient with isolated pulmonary valve stenosisA patient with valvular pulmonary stenosis with other minor congenital heart disease that dose not require surgical intervention The Proprietay non compliant low profile balloon is designed to provide consistent balloon diameters and length ecen at high pressure. |
| 148 | Ulta high pressure non complaint balloon -It should for use in precutaneous Transluminal Angioplasty of the peripheral vasculature including the ilac arteries and ilac femoral veins and for the treatment of obstructive lesions or synthetic arteriovenous dialysis fistulae a high performance balloon catheter consisting od an over thewire with a balloon fixed at the distal tip The proprietary non-compliantlow profile balloon is designed to provide consistent balloon diameters and lengths even at high pressure |
| 149 | Ultra high pressure large volume inflation device (30ml)-An ultra high pressure, larhge volume inflation device used to inflate monitor pressure and deflate angioplasty balloon dilatation catheters.It should a onepiece, 30ml disposable inflation device rated for 40 atm with a lever-lock design that controls the piston a manometer and a high-pressure conncting tube with a male luer rotating adapter. Also enclosed is a high-pressure 3-way stopcock to aid in preparation and use of the device.The manometer measures pressures ranging from 0 atm up to 40 atm in 1 atm increments. The accuracy of the manometer has been determined to be within +1.6 ATM. These products are not made with natural rubber latex |
| 150 | Flexible self-expanding prosthesis comprising of dual layer Eptef encapsulation with carbon impregnation-Flexible self expanding prosthesis comprising of dual layer Eptef encapsulation with carbon impregnation on luminal surface to reduce intimal hyperplasia. The inner lumen of covered stent (blood contacting surface) is carbon impregnated. The highly and fracture rasistant base stent architecture for tortous vessel like cephalic arch and SFA. The stent is availble in straight and flared configurations avilable from variety sizes for AVF and iliac /SFA indication diameter (6-10mm). Safety lock system on delivery system prevents premature release and two-wheel deployment to ensure accurate placement of stent at the lesion site. No stent migration |
| 151 | High-performance rossing catheter -High- performance catheter in 014\" , 018\" , 035\" Platfrom desigend to be first line aid to cross stenotic lesions and chronic occlusions when standard wires fail.Radiopaque marking system , 1cmradiopaque markers positioned 1 cm apartwityh doble markers dilenate 10 cm and 20 cm |
| 152 | Self expanding nitinol stent - It should self expanding nitional stent is FDA approved for treament of iliac occlusive disease in patients with symptomatic vascular disease of common or exteenal iliac arteerise residual stenoses with impaired perfusion followong balloon dilatation- It shouldhas optimized pin and pull delivery system for precise placement .High visibility for stent deployment and relocation under fluroscopy 0.035\" guidewire compatible, diameter sizing of stent to target lesion reduces stent migration |
| 153 | Self expandable cover stent graft, dual layer Eptfe- It should Vascular stent graft is used in Residual Stenosis with impaired perfusion following balloon dilation especially in stages III & IV according to Fontaine dissection; detached arteriosclerotic plaque material luminal obstruction following balloon dilatation occlusion after thrombolysis or after aspiration or dilatation restenosis or re-occlusion proven dual layer ePTFR encapsulation demonstrated a significant reduction at 90 day in the incidence of in stent restenosis compared to PTA Proprietary bioactive carbon impregnation designed to reduce early stage platelet adhesion Flexible implant that demonstrated kink resistance placement in tortuos lesions presenting with in-stent restenosis or non stented in patients |
| 154 | Multiconnecting tube with 150 cm tube for connecting to the patient end, 2 nos 100cm connecting tube with drip chamber to connect to the contrast and saline bottles/pack and 2 connectors for connecting the 2 syringes in the dual head injector system. |
| 155 | Custom made Pressure Garment below Knee stockings Pair. |
| 156 | Custom made Pressure Garment Full Knee stockings Pair. |
| 157 | Custom made Pressure Garment Fore arm |
| 158 | Custom made Pressure Garment Fullarm |
| 159 | Custom made Pressure Garment Fore arm with Guantlet |
| 160 | Custom made Pressure Garment Fullarm with guantlet |
| 161 | Tegaderm CHG Clorhexedine Gluconate IV Securement Dressing 1657R |
| 162 | Tegaderm CHG Clorhexedine Gluconate IV Securement Dressing 1660R |
| 163 | Sterile Collagen sheets in Wet & meshedform. PureType 1&3triple helicalMembrane Bovine Originpreserved in a mixture of Iso Propyl alcohol and waterGamma sterilized and supplied in double sterile pouches. Biocompatibleas per ISO 9001/ ISO13485 n10x10 |
| 164 | Sterile Collagen sheets in Wet & Meshedform. PureType 1&3triple helicalMembrane Bovine Originpreserved in a mixture of Iso Propyl alcohol and waterGamma sterilized and supplied in double sterile pouches. Biocompatibleas per ISO 9001/ ISO13485 n10x10 |
| 165 | Sterile Collagen sheets in Dryform. PureType 1&3triple helicalMembrane Bovine OriginGamma sterilized and supplied in double sterile pouches. Biocompatibleas per ISO 9001/ ISO13485 n10x10 |
| 166 | Sterile Collagen sheets in Dryform. PureType 1&3triple helicalMembrane Bovine OriginGamma sterilized and supplied in double sterile pouches. Biocompatibleas per ISO 9001/ ISO13485 n10x20 |
| 167 | Sterile Porus Collagen Sheet in Dry form (Fish Origin)10x10 cm |
| 168 | Sterile Porus Collagen Sheet in Dry form (Fish Origin)8\" x 12\" |
| 169 | Silicone sheetPure Poly Siloxanebased silicone scar managementproduct in sheet form.10x10 |
| 170 | Biofil AB Sterils medicated collegan Particles5 ML |
| 171 | Biofil AB Sterils medicated collegan Particles10 ML |
| 172 | Lipido-Colloid contact layer impregnated with silver salts Urgotul AG Silver Sterilenon-occulusive woundcontact layer consists of silver healing Matrix made of polyester mesh impregnated with hydrocolloid particles( CMC),petroleum jelly, polymers and silver salts with demonstrated in vitro antibacterial activity upto 7 days, using patented Lipido- colloid technology 10x12 |
| 173 | Lipido-Colloid contact layer impregnated with silver salts Urgotul AG Silver Sterilenon-occulusive woundcontact layer consists of silver healing Matrix made of polyester mesh impregnated with hydrocolloid particles( CMC),petroleum jelly, polymers and silver salts with demonstrated in vitro antibacterial activity upto 7 days, using patented Lipido- colloid technology 15x20 |
| 174 | Lipido-Colloid foam dressing with adhesive border Urgotul sterile self -adherentpatented TLC matrix (lipido colloid technology) wound contact layer combined withabsorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outer film with soft silicone adhesive border on the edges for atraumatic removal and repositioning of dressing.13x13 |
| 175 | Lipido-Colloid foam dressing with adhesive border Urgotul sterile self -adherentpatented TLC matrix (lipido colloid technology) wound contact layer combined withabsorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outer film with soft silicone adhesive border on the edges for atraumatic removal and repositioning of dressing.15x20 |
| 176 | Lipido-Colloid foam dressing with adhesive border Urgotul sterile self -adherentpatented TLC matrix (lipido colloid technology) wound contact layer combined withabsorbent polyurethane foam pad , a superabsorbent layer ,a vapour permeable waterproof outer film with soft silicone adhesive border on the edges for atraumatic removal and repositioning of dressing.20x20 |
| 177 | CABG Kit Off Pump (Annexure 1) |
| 178 | Single valve surgery kit (Annexure 2) |
| 179 | ASD/VSD kit(Annexure3 ) |
| 180 | Dry suction wet seal with Air flow capacity of 16LPM. Should maintain suction level of (-10)(-43) c.m.Should have single chamber with capacity of 250ml. |
| 181 | IABP BALLON 30cc/35cc/40cc with 8fr sheath. |
| 182 | PTFA Graft 10*90cm |
| 183 | Decron Graft 8*80cm |
| 184 | Fibrillar |
| 185 | Oxdised Regenerated Cellulose 4*8 |
| 186 | Oxdised Regenerated Cellulose 2*14 |
| 187 | Antibactirial coated polyglactine 910,2-0,70cm for port closure |
| 188 | PTFE PATCHES 10*90mm, 0.2mm THICKNESS |
| 189 | PTFE PATCHES 10*90mm, 0.4mm THICKNESS |
| 190 | Needleless 2 way connector with 12cm extension |
| 191 | Burette IVset measured volume fluid administration set with bacteria retentive air inlet |
| 192 | Triple pressure monitoring kit with option of closed loop blood sampling kit including needleless sampling site |
| 193 | Pur central venous catheter triple lumen 7Fr ,13cm & 16cm lengthand nitonel guidewire with anti blood flow connector on introducer needle. |
| 194 | Pur central venous catheter four lumen 8.5Fr ,13cm length and nitonel guidewire with anti blood flow connector on introducer needle. |
| 195 | Central venous catheter setsingle lumen 24G with nitonel guidewire |
| 196 | cardioplegia fusion adapter |
| 197 | PUR HD catheter kit double lumen 11.5fr 13cm with 9fr X 10cm dialator |
| 198 | Rifampcin and Miconazole Impregnated Triple lumen polyurethane catheter, L-16cm, 7.5 Fr, G- 14*18*18 |
| 199 | CVC Line Pediatric Triple lumen Polyurethane catheter with double introducer one cannula and one needle, 4.5 Fr, 6 cm, G-20*23*23 |
| 200 | Radial Arterial catheter with guide wire • Should have PE material to prevent dampning • Should have anti kinking coller to prevent kinking of catheter • 20 G/8 and 18G/10 cm PE catheter with introducer needle and guidewire |
| 201 | Polyurethane femoral arterial catheter with guide wire, without integral extention to avoid damping, 16G, 15cm |
| 202 | Silver ion impregnated central venous catheter triple lumen 7.5 fr 16cm/20cm. |
| 203 | PUR XRO catheter 20CM with 22G seldinger techniwue with straight guidewire with a flexible tip and one 50*50 cm drape |
| 204 | PUR XRO catheter 20CM with 22G seldinger techniwue with straight guidewire with a flexible tip and one 50*50 cm drape |
| 205 | Disposable Curved Circular Stapleral sizes with Three Circular Staggered Staple-Lines ( 3 Rows ) and Optimized Staple Formation Technique, Tissue Compression Indicator, Open Staple Leg Length of 4.5mm which can accommodates compressed tissue thickness from 1.0- 2.5mm BIS / 4 digit European CE Certified |
| 206 | Powered endoscopic linear cutter blue reload 45mm having six row of staple line, round staple wire with the open staple height of 3.5mm and closed staple height of 1.5mm BIS / 4 digit European CE Certified |
| 207 | Powered endoscopic linear cutter green reload 45mm having six row of staple line, round staple wire with the open staple height of 4.1mm and closed staple height of 2mm BIS / 4 digit European CE Certified |
| 208 | Powered endoscopic linear cutter white reload 45mm having six row of staple line, round staple wire with the open staple height of 2.5mm and closed staple height of 1mm BIS / 4 digit European CE Certified |
| 209 | Powered endoscopic linear cutter blue reload 60mm having six row of staple line, round staple wire with the open staple height of 3.5mm and closed staple height of 1.5mm BIS / 4 digit European CE Certified |
| 210 | Powered endoscopic linear cutter Gold reload 60mm having six row of staple line, round staple wire with the open staple height of 3.8mm and closed staple height of 1.8mm BIS / 4 digit European CE Certified |
| 211 | Powered endoscopic linear cuttergreen reload 60mm having six row of staple line, round staple wire with the open staple height of 4.1mm and closed staple height of 2mm |
| 212 | Powered endoscopic linear cutter white reload 60mm having six row of staple line, round staple wire with the open staple height of 2.5mm and closed staple height of 1mm BIS / 4 digit European CE Certified |
| 213 | Powered Endoscopic Linear cutter 45mm with 60 Degree Articulation on both side, Having Safety button to prevent accidental firing, with Manual override spanner, Stepped anvil for compression, 360 degree rotating shaft and having 280mm shaft length BIS / 4 digit European CE Certified |
| 214 | Powered Endoscopic Linear cutter 60mm with 60 Degree Articulation on both side, Having Safety button to prevent accidental firing, with Manual override spanner, Stepped anvil for compression, 360 degree rotating shaft and having 280mmshaft length BIS / 4 digit European CE Certified |
| 215 | DISP. CIRCULAR STAPLER NON DETACHABLE ANVIL - Varient- Row 3External diameter- 34/32 mmNo of rows- 3Staple quality- 48Closed staple hight- 0.75- 1.6 mmShaft length- 14 CMKinfe diameter- 23mm BIS / 4 digit European CE Certified |
| 216 | 811 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 217 | 812 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 218 | 813 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 219 | 814 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 220 | 815 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 221 | 816 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 222 | 817 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 223 | 818 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 224 | 819 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 225 | 820 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 226 | 821 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 227 | 822 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 228 | 823 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 229 | 824 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 230 | 825 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 231 | 826 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 232 | 827 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 233 | 828 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 234 | 829 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 235 | 830 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 236 | 831 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 237 | 832 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 238 | 833 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 239 | 834 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 240 | 835 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 241 | 836 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 242 | 837 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 243 | 838 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 244 | 839 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 245 | 840 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 246 | 841 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 247 | 842 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 248 | 843 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 249 | 844 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 250 | 845 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 251 | 846 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 252 | 847 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 253 | 848 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 254 | 849 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 255 | 850 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 256 | 851 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 257 | 852 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 258 | 853 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 259 | 854 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 260 | 855 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 261 | 856 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 262 | 857 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 263 | 858 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 264 | 859 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 265 | 860 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 266 | 861 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 267 | 862 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 268 | 863 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 269 | 864 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 270 | 865 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 271 | 866 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 272 | 867 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 273 | 868 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 274 | 869 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 275 | 870 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 276 | 871 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 277 | 872 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 278 | 873 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 279 | 874 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 280 | 875 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 281 | 876 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 282 | 877 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 283 | 878 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 284 | 879 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 285 | 880 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 286 | 881 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 287 | 882 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 288 | 883 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 289 | 884 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 290 | 885 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 291 | 886 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 292 | 887 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 293 | 888 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 294 | 889 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 295 | 890 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 296 | 891 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 297 | 892 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 298 | 893 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 299 | 894 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 300 | 895 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 301 | 896 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 302 | 897 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 303 | 898 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 304 | 899 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 305 | 900 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 306 | 901 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 307 | 902 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 308 | 903 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 309 | 904 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 310 | 905 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 311 | 906 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 312 | 907 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 313 | 908 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 314 | 909 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 315 | 910 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 316 | 911 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 317 | 912 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 318 | 913 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 319 | 914 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 320 | 915 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 321 | 916 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 322 | 917 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 323 | 918 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 324 | 919 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 325 | 920 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 326 | 921 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 327 | 922 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 328 | 923 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 329 | 924 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 330 | 925 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 331 | 926 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 332 | 927 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 333 | 928 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 334 | 929 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 335 | 930 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 336 | 931 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 337 | 932 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
| 338 | 933 Item No. (Detailed Description as per Technical Specification and Compliance Sheet) |
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