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Dr Sampurnanand Medical College Tender

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If you're looking for Rajasthan tenders online and are tired of typing tender ID over and again or going through the cumbersome government websites for it, you are in luck. We have collated every Eproc Rajasthan tender on BidAssist. And for any queries related to an e-tender Rajasthan, like bidding process, registration process, etc., are explained below. Read on.

Dr Sampurnanand Medical College - SNMC Tender

Goods
Healthcare and Medicine
Eprocure
Jodhpur, Rajasthan
Opening Date24 Jan 2023
Closing Date9 Feb 2023
Tender Amount₹ 75,00,000 
Notes
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Costs

  • EMD

    ₹ 1,50,000

  • Document Cost

    ₹ 500

  • Tender Fee

    ₹ 1,000

Description

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BOQ Items

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Braided Long Sheath *Atraumatic Tip for Carotid & Distal procedures *Hemostatic Valves to prevent back leak and air aspiration. With TBV detachable valve for thrombus management *Gold Coil Marker – For Distal Visibility, Distal hydrophilic coating *PTFE Coating – Seamless Device Transition * Available in Diameter 6,7,8 f and length 45cm,65cm & 90cm. * With suture eye for securing sheath. Nylon out layer with stainless steel coil * With internal side port with attached 3 way stopcock.

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Radial Artery Haemostasis Device- (T.R. Band) • Consists of two balloons specially designed for spot compression of the radial puncture site. • Must have belt magic tape for fast application. • Must have curved support plate. Must have green Positioning marker. • Must be available in 2 sizes – 24cm and 29cm • USFDA/PMDA approved

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Hydrophilic Guidewire with Mcoat technology tapered tip, (Regular Length) • single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat.One piece construction & Radiopaque polyurethane jacket. • Must be available in standard and stiff. • Must be available in .032, .038, .025, .018 diameter and 150 cm, 180 cm length - Straight / Angled / 1.5 mm J shape • USFDA approved

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Hydrophilic Guidewire with Mcoat technology tapered tip, (Exchange Length) • single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat.One piece construction & Radiopaque polyurethane jacket. • Must be available in standard and stiff. • Must be available in .032,.035, .038, .025, .018 diameter and 260 cm length - Straight / Angled / 1.5 mm J shape • USFDA approved

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Hydrophilic Guidewire with Mcoat technology tapered tip, (Regular Length) • single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat.One piece construction & Radiopaque polyurethane jacket. • Must be available in standard and stiff. • Must be available in .032, .038, .025, .018 diameter and 150 cm, 180 cm length - Straight / Angled / 1.5 mm J shape • PMDA approved

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Hydrophilic Guidewire with Mcoat technology tapered tip, (Exchange Length) • single Nitinol core alloy, Tungsten-infused polyurethane jacket • hydrophilic polymer coat.One piece construction & Radiopaque polyurethane jacket. • Must be available in standard and stiff. • Must be available in .032,.035, .038, .025, .018 diameter and 260 cm length - Straight / Angled / 1.5 mm J shape • PMDA approved

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Baby J wire (180 cm) with radius of 1.5mm J tip, (Regular Length) • Must Have Tungsten-infused polyurethane jacket. • Baby J Curve Must have radius of 1.5 mm. • Super elastic Nitinol alloy, M coat hydrophilic coat, • One piece construction for 1:1 torque & Radiopaque polyurethane jacket. • USFDA/PMDA approved

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Baby J wire (300 cm) with radius of 1.5mm J tip, (Exchange Length) • Must Have Tungsten-infused polyurethane jacket. • Baby J Curve Must have radius of 1.5 mm. • Super elastic Nitinol alloy, M coat hydrophilic coat, • One piece construction for 1:1 torque & Radiopaque polyurethane jacket. • USFDA/PMDA approved

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Guide wire Hydrophillic coated 0.0 32x150 cm Polyurathane Jacket. Glider Torque Devices. Super elastic Nitinol core. Eurepean CE

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Special Slender Sheath (GSS) For trans radial root Must Have unique thin wall technology reducing the outer diameter by 1 Fr size whilst maintaining the one size lager inner diameter. Must Have 7Fr Sheath with Outer diameter of 2.8mm, 6Fr with OD of 2.46 mm & 5Fr with OD of 2.13mm. hydrophilic M coating with 20/21G Surflash needle and TIF tip technology which provide optimal tapering design. USFDA/PMDA Approved

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Radial Sheath with Puncture Needle Standard Length includesurflash 20G*2 entry needle (plastic IV catheter) and 0.025” mini plastic guidewire. Radial Introducer Sheath with patent unique cross-cut design haemostatic valve with Integrated side arm with attached 3-way stopcock. Must have ETFE sheath tubing, polypropylene dilator tube with silicon coating. Must have Snap-on / click-off dilator lock, anti-kinking sleeve & must have suture eye. USFDA/PMDA approved

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Radial Sheath with Puncture Needle Standard Length includesurflash 20G*2 entry needle (plastic IV catheter) and 0.025” mini plastic guidewire. Radial Introducer Sheath with patent unique cross-cut design haemostatic valve with Integrated side arm with attached 3-way stopcock. Must have ETFE sheath tubing, polypropylene dilator tube with silicon coating. Must have Snap-on / click-off dilator lock, anti-kinking sleeve & must have suture eye. DCGI approved

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Tiger Shaped Angiographic Catheter Comprised of a two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers. Must Have the shaft inner layer and outer layer contain barium sulphate. Must Have anti-kinking protector sleeve, with non-braided tip shaft (distal -2 cm). Trans radial catheter must have shapes designed to cannulate left and right coronary arteries TIG, TIG II, JACKY, SARAH. Must have inner diameter of 4F = 1.03mm, 5F= 1.20mm, 6F = 1.30mm with flow rates of 4Fr - 10ml/Sec, 5Fr – 22.6ml/Sec, 6Fr – 25.6ml/Sec. USFDA/PMDA approved

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Tiger Shaped Angiographic Catheter Comprised of a two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers. Must Have the shaft inner layer and outer layer contain barium sulphate. Must Have anti-kinking protector sleeve, with non-braided tip shaft (distal -2 cm). Trans radial catheter must have shapes designed to cannulate left and right coronary arteries TIG, TIG II, JACKY, SARAH. Must have inner diameter of 4F = 1.03mm, 5F= 1.20mm, 6F = 1.30mm with flow rates of 4Fr - 10ml/Sec, 5Fr – 22.6ml/Sec, 6Fr – 25.6ml/Sec. DCGI approved

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Manifold: 2 port manifold, Leur lock system, with inert material non slippery, with pressure rating up to 250 to 500psi, Right on. clear body allowing easy visibility for de-bubbling,easy rotating handles, rotating leur for secure connection, airtight.optional extension tubing and on/off handle for options

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Leurlock plastic single use syringe, 10ml, 20 ml

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Pressure monitoring iv lines, 200 cm

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Needle 26 G 0.45mm x 13mm

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Diagnostic femoral Catheter consistent ID from hub to tip Stainless steel wire braided body wrapped with thrombi-resistant material Color codes for easy french size identification Soft, atraumatic, radiopaque tip (radiopaque marker from the origin of the tip) 4F/5F/6F Lengths: 65 cm/80 cm/100 cm/110 cm/125 cm All regular shape (Curve 3.5, 4, 4.5) JL, JR, AL, AR Special - SRC, 3DRC, Straight, Pigtail, IM USFDA approved

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PIGTAIL CATHETER - (Sizes 4 French/5 French/6 French) Adult regular length for adult use, Smaller length for neonatal and paediatric use. two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers. Must be DCGI Approved

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Sheathless Access System  Available in 5F/6F/7F Smaller access profile than any radial sheath of the same french size 7F guiding catheter is equal to OD profile of a 5F sheathless access system up to 2F arteriotomy reduction compared to a conventional sheath system Options for single/dual long dilators (135 cm each) of 0.021” / 0.035” wire compatible Contains hydrophilic nitinol mini-guidewire (45 cm) Contains IV cannula (Angiocath) needle (20 G) Hydrophilic coating covering the distal 20 cm of the vessel dilator DCGI/CE/USFDA approved

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JUDKINS CATHETER (JR & JL) – (5 French /6 French/7 French) Left and Right Judkin’s catheters in various standard curves and lengths. (3.0-5.0) two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers.contain barium sulphate. Must be DCGI APPROVED

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PTCA Guide catheter uniform diameters from hub to tip Catheter range should have short tip, long tip (16 mm long) for active and passive support, side holes Braiding design should be hybrid ideally flat-on-round wire braiding PTFE lining for lubricious lumen from hub to tip Tip should be radiopaque (radiopaque marker from the origin of the tip) Large lumen (minimum of 0.070'' inner lumen for 6F) 5F Long Vista Brite TIP: 16 mm ultrasoft, atraumatic tip for deep seating, additional support and stability Diameters: 5, 6, 7, 8, 9 Fr Lenghts: 55 cm/90 cm/95 cm/100 cm Available in wide range of shapes including all regular shapes, transradial-specific shapes, other speciality shapes Unique extra back up shapes for right coronary and left coronary: XB, XBC, XBLAD, XBR, XBRCA Speciality shapes: LCB, IM, RCB, MPA, 3DRC, Hockey stick (HS) Special radial shapes: Barbeue Curve 3, 3.5, 4, 4.5, 5 cm USFDA approved

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MULTIPURPOSE CATHETER – (4 French/5 French /6 French/7 French) Multipurpose catheters in various standard curves and lengths. (0.75/1.0/1.5/2.0) two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers.contain barium sulphate. Must be USFDA APPROVED

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MULTIPURPOSE CATHETER – (4 French/5 French /6 French/7 French) ·Multipurpose catheters in various standard curves and lengths. (0.75/1.0/1.5/2.0) ·two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers.contain barium sulphate. · Must beDCGI APPROVED

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AMPLATZ CATHETER - 4 French/5 French /6 French/7 French Amplatz left (AL) and Amplatz right (AR) catheter in various standard curves and lengths. two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers. contain barium sulphate Must be DCGI APPROVED

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INTERNAL MAMMARY CATHETER - 5 French /6 French In various standard curves and lengths. Two-layer construction, 50µm double braided 32 Strands of stainless-steel two-ply mesh sandwiched layers of polyurethane and polyamide elastomers. contain barium sulphate· Must be DCGI APPROVED

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No torque Right Coronary Catheter length - 5 French /6 French Must be USFDA APPROVED

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Marker Pigtail ; 5F/ 6F

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Angled Pig Tail catheter 110cm– 5 French /6 French 145degere angle and both 6 and 12 side holes. Must be USFDA APPROVED

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Special Guiding Catheter – IKARI Curve •         Must Have Ikari curve for radial route. •         Must have stainless steel flat wire braid •         High Strength Wired braided catheter with Inner Layer of PTFE with fluoro Polymer. •         Must have Zone technology - five Zone each fabricated from a material of different stiffness. •         Must have larger lumen. 6Fr ID - .071" •         USFDA/PMDA approved

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Guiding Catheter– Must have stainless steel flat wire braid High Strength Wired braided catheter with Inner Layer of PTFE with fluoro Polymer. Must have Zone technology - five Zone each fabricated from a material of different stiffness. Must have larger lumen. 6Fr ID - .071" Flat 2 over 2, stainless steel wire Guiding catheter with hydrophilic coating (Uncoated distal 7 cm & Proximal 25 cm) with superior backup control & larger lumen size with shapes like TIG/EBU/XBRA USFDA/PMDA approved.

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Micro Puncture access set 4/5Fr with .018 wire and 21 G needle..

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Femoral Artery Puncture needle 18 G 70cm with 0.038 or smaller guide wire compatible in sterile and non pyrogenicpacking.

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PTCA accessories -10 cm tube with 3 way stop cork at one end and leur lock on other end.

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PTCA Needle – for carrying 0.014” coronary wire

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Torquer for 0.014 wire

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Co-Pilot Bleed back control valve with twin seals: Bleed back seal wand clam psealprmits high pressure injection up to 400PSI Easygrip push pull knob for single operator use and complete hemostasis.

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Rota Wire – (USFDA/CE APPROVED) Floppy / Extra Support (Should be compatible with Existing Rota Machine)

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IVUS Catheter - (USFDA/CE APPROVED) Available with 60 Mhz, HD IVUS Catheter, mechanical/ Rotational Catheter

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IVUS SLED Pullback sled with available IVUS machine in cath lab

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IVUS Should be compatible in 6 french with existing IVUS system in MDMH cathlab. IVUS catheter US FDA/CE approved (ivus machine available in MDMH cathlab)

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Guide extension catheter: Guide Extension Catheter - (USFDA approved) Stainless steel hypotube, polymer catheter segment 1x1 wire braiding, Glide coating 0.57” Inner diameter & 0.067” Outer Diameter 6/7, 25cm and 40cm.

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Thrombectomy Catheter •       Available in Size 6F, 7F, must have entry profile 0.019 inches with 1.30 mm square suction area •       Braided polyamide elastomer shaft, stainless steel wire braiding and Guide wire type Stylet, •       6.0mm tip length for making aspiration inlet to come closer to the target thrombus and 10cm-length depth. •       Must Have Distal 40 cm Hydrophilic coating. •      USFDA /CE/ DCGI Approved

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Thrombectomy Catheter •       Available in Size 6F, 7F, must have entry profile 0.019 inches with 1.30 mm square suction area •       Braided polyamide elastomer shaft, stainless steel wire braiding and Guide wire type Stylet, •       6.0mm tip length for making aspiration inlet to come closer to the target thrombus and 10cm-length depth. •       Must Have Distal 30 cm Hydrophilic coating. •      USFDA /CE/ DCGI Approved

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Dedicated Microcatheter Dedicated dual lumen micro catheter for side branch access

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Micro channel dilator tapered soft tip of 1.3 Fr with tungsten Braiding and hydrophilic polymer shaft with OD of 2.6Fr; Length 135 cm and 150cm.

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Wire braided catheter works with rotation movements for CTO penetration catheter, length 135cms

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Coronary Micro catheter: Must Have tapered stainless steel braid mesh construction and Inner PTFE Layer. Must Have 13 CM floppy distal segment.70cm distal hydrophilic coating Must Have Distal outer diameter 1.8 Fr or less and Proximal Outer diameter 2.6Fr. Must be available in Catheter Length 130cm for antegrade&150 cm for retrograde Must have Gold marker for the tip visibility USFDA/PMDA approved

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Cutting Balloon for PTCA having Microsurgical Atherotomes – (USFDA APPROVED) Monorail catheter, Bi-segment Inner Lumen Shaft Proximal Shaft – 1.8 Fr, Hydrophilic Coating Available in the Sizes - 2-4mm dia x 6,10,15 mm lengths

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Coronary scoring balloon with 3 helical nitinol elements over a semi compliant balloon with RBP of 20 atm available in sizes of 2.0, 2.5,3.0 and 3.5mm diameter and length of 6,10 and 15mm. USFDA Approved

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Sirolimous Drug eluting cobalt chromium plateform biodegradable polymer DCGI approved coronary stent

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Sirolimous Drug eluting cobalt chromium coronary stent strut thickness of ≤ 60 um with Hybrid Amorphous Silicon Carbide &Biodegradeable Polymer USFDA approved.

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Biolimus A9 coated Cobalt-chromium platform Coronary stent with biodegradable polymer

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Biolimus A9 coated Coronary stent system ( without any carrier or polymer) USFDA approved

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Sirolimus Eluting Cobalt-Chromium stent with Abluminal Gradient coating- (L-605 Co-Cr Alloy) (should not have drug & Polymer coating on joints & Bends). 2 links – 8 Crown Design Must Have Advanced Core wire shaft technology. should have an over expansion Limit of more than 1.5 mm of the stated Diameter Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Capro lactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. Low concentration of Sirolimus (0.8ug/mmsq), tip entry profile of 0.42mm. PMDA+CE Approved

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Sirolimus Eluting Cobalt-Chromium stent with Abluminal Gradient coating - (L-605 Co-Cr Alloy) (should not have drug & Polymer coating on joints & Bends). 2 links – 8 Crown Design Bioresorbable polymer of PLCL (Poly Lactic Acid + Poly Capro lactone PCL) with degradation time of 3-4 months. Should have Bioinspired Open cell in phase design. Low concentration of Sirolimus (0.8ug/mmsq). minimum tip entry profile of 0.42mm PMDA+CE Approved

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Zotarolimus Eluting Stent 4.5 and 5.0 mm in diameter and in varing length. USFDA approved.

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Zotarolimus Eluting Stent 2mm in diameter in varing length. USFDA approved.

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Everolimus Eluting Cobalt chromium platform stent with Multilayer Pebex with balloon. Peak to valley 3-3-3 taller Non Linear Link Multilink-8 Platform, With Slim seal technology. Fluorinated copolymer with strut thickness of 0.0032” USFDA Approved

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Everolimus Eluting Cobalt chromium platform stent Peak to valley 3-3-3 taller Non Linear Link Multilink-8 Platform, Fluorinated copolymer with strut thickness of 0.0032” Diameter above 2.5mm and more Length above 38mm USFDA/ CE Approved

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Everolimus eluting, Platinum chromium platform stent with diameter 4.0, 4.5 and 5.0 mm , different avaialble length, USFDA approved, Bioabsorable polymer

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Sirolimus Eluting BioResorbable Vascular Scaffold System with 100µm strut Thickness Scaffold Diameters: 2.75 - 4.00 mm ; Scaffold Lengths : 16 - 40 mm DCGI & CE Approved

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Fractional Flow Reserve Pressure wire Should be 0.014” guide wire. Should have high-fidelity piezo electric pressure sensor technology for measurement of intravascular pressure. The system should work wireless radio using Frequency-hopping spread spectrum to ensure secured radio connection with pressurewire. The PressureWire should be capable of wired connection to FFR machine. Should have sensor housing design with multiple large windows (Multi window Jacket). Should have a flat core tip design for a better shapeability& shape retention. Should preferably have hydrophilic coating Should have a radio opaque tip. Should have operating pressure range of -30 to +300 mmHg. Should have frequency response of DC to 25 Hz. Should have radio range of at least 2m.Should have Battery time of transmitter for at least 3 hours. Should have a wireless transmission frequency range of 2.4000 – 2.4835 GHz (ISM Band) 14.Should not have a total signal time delay of 30 ms

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Optical Coherence Tomography (OCT) Catheter The imaging catheter should be able to emit near infrared light to produce high-resolution real-time images. The imaging catheter Should be compatible with 0.014” guidewire. It should have outer diameter (distal) that is less than 3.0 French . The imaging catheter should have usable length of 135 mm. The imaging catheter should have radiopaque markers at the distal tip, imaging lens and 50 mm proximal to the lens marker to help physician in aligning pullback to region of interest. The imaging catheter should be hydrophilic coated. It should have rapid exchange tip for guidewire loading. The imaging catheter should have shaft markers to notify physician when the distal tip exiting the guide catheter

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High pressure Non compliant PTCA balloon Diameter 1.5 mm to 5.0 mm in various length RBP 24 and above Mono rail Should be CE approved

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Non-Compliant CTO balloon diameter 0.85mm Hydrophilic coating Single proximal marker RBP 16atm or above. Lesion Entry Profile - 0.016 ഼or less.

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Non-Compliant CTO balloon diameter 0.85mm to 4mm RBP 16atm or above. Lesion Entry Profile - 0.015 ഼or less. Balloon hypotube must be spiral cut design.

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Non Compliant Coronary Balloon Cross Flex technology and flexible dual tungsten marker Lesion entry profile 0.018” Micro glide coating Available in diameter 1.5 to 5.0 mm In Mono rail plate form. US FDA approved

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Semi Compliant Coronary Balloon Slim seal technology on distal tip Crossing profile of 0.021” Lesion entry profile 0.017” Micro glide coating Available in diameter 1.2 mm to 5mm OTW plate form. In varying length US FDA approved

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Semi Compliant Coronary Balloon Slim seal technology on distal tip Crossing profile of 0.021” Lesion entry profile 0.017” Micro glide coating Available in diameter 1.2 to 5.0 mm In Mono rail plate form. USFDA approved

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High pressure non-compliant balloon with Innovative triple layer balloon technology with high pressure resistance of 22 ATM. Must Have Elastomer outer layer, middle layer of Polyamide and inner most layer of Elastomer. Must Have nominal pressure of 12atm and RBP of 22atm. Shorter thin distal tip of 2.9mm with low entry profile of 0.43 mm. must have hydrophilic Mucus coating Must Have 3.0 mm Short taper balloon shoulder & Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile. Must have 2.6 French stainless steel core wire structured shaft & stainless-steel stylet in Mid Shaft. Must Have Hypotube without PTFE Coating. Must Have three pleats Re-wrappable structure. PMDA+CE Approved

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CTO Balloon with Ultra – Ultra Low Entry profile of 0.016" must have hydrophilic Mucus coating. Should have smallest diameter 1.00mm and 5mm length. Must Have 0.8mm Shorter and 25μm Thinner radiopaque marker for lower crossing profile. Must have Flexible Tip with short balloon bonding part of 0.4mm. nominal pressure of 06 ATM and RBP of 14 ATM Must have 2.4 to 2.7 French tapered stainless steel core wire structured shaft. Must Have three pleats Re-wrappable structure. PMDA+CE Approved

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USFDA approved semi-complaint coronary balloon With EFT Technology diameter 1.25 - 4.00mm and lengths 6-30mm

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USFDA approved Non-complaint coronary balloon With Patch work coating and semi crystalline polymer material Should have diameter 2.0 – 5.0mm and lengths 8-30mm

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Non-complaint coronary balloon Should have diameter 5.5 mm in various length.

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PTCA Guide Wire – Core material ElastiniteNitinol for excellent flexibility and durability, Shaping ribbon for excellent shape retention and atraumatic tip load less than 0.5 gm to 0.7gm with Regular Length, Regular Shaft Support and Floppy TIP

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PTCA Guide Wire-DuraSteel Stainless Steel for durability and excellent torque control, Full polymer jacket, Core to Tip Design for precise steering and tip control, various tip Loads 1.5 gm to 4.1.gm for complex anatomies, Hydrophilic coating for longer lasting Lubricity.

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PTCA Guide Wire-DuraSteel Stainless Steel for durability and excellent torque control, Full polymer jacket, Core to Tip Design for precise steering and tip control, various tip Loads 0.8 gm to 1.2 gm for complex anatomies, Hydrophilic coating for longer lasting Lubricity.

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Workhorse Guidewire with Triple Spring 304V Stainless Steel with Nitinol Distal Core and Cold Working Rotary Swagging Tip available in tip loads between 0.6-0.8gm and lengths (190/300cm).

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DOC Extension Wire Regular length PTCA guidewire-USFDA Approved.

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.014" One Piece core workhorse wire with jointless spring coil 20cm polymer sleeve length with slip coat coating over the polymer sleeve, tip load 0.8g ,180cm length tip radiopacity 3cm

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.014" One Piece core Extra-support wire with jointless spring coil, PTFE coating over the shaft, tip load .7g,180cm length with tip radiopacity 3cm

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.014" One Piece core CTO wire with jointless spring coil PTFE coating over the shaft, tip load 3g, 6g and 12g ,180cm length with tip radiopacity 11cm

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.014" One Piece core wire with jointless spring coil and slip coat on the spring coil, PTFE coating over the shaft, tip load 3g, ,180cm length with tip radiopacity 11cm

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Dedicated guidewire for externalization with tip load of 3g length 330cm

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One Piece core wire with jointless Spring coil with slip coat coating over the spring coil tapering to .009", tip load 9g ,180cm length tip radiopacity 20cm

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One Piece core wire with jointless Spring coil with slip coat coating over the spring coil tapering to .009", tip load 12g ,180cm length tip radiopacity 20cm

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One Piece core wire with jointless Spring coil with slip coat coating over the spring coil tapering to .008", tip load 20g ,180cm length tip radiopacity 17cm

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.010" One Piece core wire with joint less Spring coil length 15cm, cone tip with a tip load of 1.7gm .190cm length tip radiopacity 15cm,

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.011" One Piece core wire with joint less Spring coil length 15cm, cone tip with a tip load of 3.5gm190cm length tip radiopacity 15cm

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.012" One Piece core wire with joint less Spring coil length 15cm, cone tip with a tip load of 4.5 gm 190cm length tip radiopacity 15cm

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.014" Extra support One Piece core wire with jointless Spring coil with Sion Tech, having composite core with ACTONE Inside, lowest tip load .3g, length tip radiopacity 3cm, pre-shaped tip, 52 cm hydrophilic coating, available in 190 and 300cm lengths

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PTCA Guide Wire – 2 mm Silicon coated distal tip, 0.014” Diameter and 180 cm length PTCA wire Must have Platinum coil at distal tip. Must have directly jointed SUS and Nitinol shaft through DuoCore technology and silicon coated joint. Must have M coat hydrophilic coating upto 248 mm. Must have PTFE Coating from 25 to 180 cm length. Should be Available in both 0.6 and 1gm tip load Should be available in extra floppy andFloppy tip PMDA + USFDA

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PTCA Guide Wire -DuraSteel Stainless Steel for durability and excellent torque control, Full polymer jacket, Core to Tip Design for precise steering and tip control various tip Loads 0.8 gm to 1.2 gm for complex anatomies, Hydrophilic coating for longer lasting Lubricity.

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Vascular Closure Device for 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 (USFDA Approved) For small hole and large hole closure both.

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Special Inflation Device Special Inflation Device for high pressure (55 ATM), Swiss Made, High Resoultion.

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Cerebral protection system used as an embolic decive to capture and remove thrombus/ debries during endovascular process or transcatheter aortic valve implantation. 6Fr. Length 95cm.

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LEFT ATRIAL APPENDAGE CLOSURE DEVICE CE APPROVED Braided Pebax with PTFE Liner and platinum/iridium marker bands

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Stainless Steel Brockenbrough needle used to make the transseptal puncture for adults. Size - 18G shaft with 21G Tip Length - 71cms

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LAA Closure Device- percutaneous transcatheter closure for non-surgical closure of Left Atrial Appendage. Having an innovative design of Cylindrical Plug attached with the retention skirt. Cylindrical Plug shaped head designed to trap trabeculations. Device should be preloaded on the delivery cable with delivery profile of 12fr to 14fr. Device should be made up of soft woven Nitinol mesh. The matellic material should be treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MRConditionalupto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults.

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Special Delivery System with dual angeled sheath with the usable length of 80cm specially designed for LAA Occluders. Sizes Available 12Fr. & 14Fr.

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PFO Occluder- a percutaneous transcatheter closure for non-surgical closure of patent foramen ovale. 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. Device should have matched disc diameters to maximise the coverage of Foramen Ovale. Polyester fabric sewn into each disc promote occlusion and tissue in growth. The matellic material should be treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MRConditionalupto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults.

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Special Delivery System designed for PFO Cases. This delivery system comes with an ultra-flexible tip for better positioning of the device. Enhanced delivery cable improves the assessment of device final position prior to cable release. It is designed for no compromise on torque strength, sheath diameter and pushability.

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Para valvular leak Occluder - a percutaneourtranscatheter closure of Para Valvular Leak. Device should be made up of soft woven muti-layered Nitinol mesh designed to increase density and provide rapid occlusion. Low profile 4fr to 7fr sheath to facilitate defect crossing. Oblonged shape to improve wall apposition and enhance stability in PVL. Device orientation should be defined through a small platinum marker on the distal rim. The matellic material should be treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MRConditionalupto 3Tesla or less. Device should be backed by strong clinical study with proven success rate for pediatrics and adults.

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TranscatherBicaval valve systems, dry tissue technology and preloaded on delivery sytem, readily available for implantation, with different sizes, CE/DCGI approved

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Balloon Expandable transcathater aortic valve replacement system with all standard accessories for implantation. Should be available in standard, intermediate sizes and XL sizes. Should be quoted with all accessories (Delivery system, Dilitation balloon catheter and introducer sheath) CE& DCGI Approved

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Self ExpandingRecapturable and Supra Annular Transcatheter Aortic Porcine Pericardium Valve Nitinol frame Should be available to treat annulus size from 17-30 mm. USFDA approved. Should be quoted with all accessories (Delivery system, Dilitation balloon catheter and introducer sheath)

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Self ExpandingRecapturable and Supra Annular Transcatheter Aortic Porcine Pericardium Valve with External Pericardial Skirt

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A balloon-expandable, radiopaque, cobalt-chromium alloy frame a trileaflet bovine pericardial tissue valve, a polyethylene terephthalate (PET) inner skirt, and a PET outer skirt. USFDA approved. Available in different sizes (20-30mm) Should be available with delivery system which consists of a balloon catheter for deployment of the valve, and a Flex Catheter to aid in valve alignment to the balloon, tracking, and positioning of the valve, Stylet, Crimping accessory removable Loader and inflation device

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BMV BALLOON Specially designed balloon perfectly shaped for mitral valve Short inflation/ deflation cycle New small and soft tip Large size matrix and three lumen at proximal end Longer guide wire to increase safety in taller patients and available sizes of 20-30.

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BMV Balloon with accessories BMV Balloon with accessory set should containing Guide Wire, Stylet, Stretching Tube, Ruler, dilator, syringe.

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Mullin Sheath for Mitral Valvuloplasty Balloon

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ASD Closer device should be self-centering detachable double disc made up of biologically inert material The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MRConditionalupto 3Tesla or lessand safe under static magnetic feild. intaglio coated to prevent nickel Leaching. Provan clinical data for safety and efficacy. USFDA

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ASD Closer device for Fenestrated Defects should be self-centering detachable double disc made up of biologically inert matarial The matellic material should be Intaglio treated to improve biocompatibilty and reduce nickel (Ni) leaching. Device should be MRConditionalupto 3Tesla or lessand safe under static magnetic feild. intaglio coated to prevent nickel Leaching. Provan clinical data for safety and efficacy. USFDA

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Delivery system for ASD Device USFDA approved. All sizes Ped and Adult. Comprise of 45° curve delivery sheath with a check valve mechnisim. Kink resistant with reinforcement with intrenal braided layer of stainless steel. Soft radiopaque tip. Dialtor with tapering tip should be fit in the sheath locking mechnisim. Loader plastic wise and delivery cable.

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VSD Closure Device Muscular With delivery system Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system. All sizes. USFDA.

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VSD Closure device Special Muscular for post infarctionwith delivery system. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system. All sizes with waist length of 10mm. USFDA.

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PDA Closure Device. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system. All sizes . USFDA.

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Symmetrical PDA Closue Device with Discs on both sides. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system.Should have a symmetric design enabling both antegrade and retrograde delivery. All sizes . USFDA.

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Symmetrical PDA Closue Device with Retension Discs on both sides for use in preterm neonates. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less. Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system.Should have a symmetric design enabling both antegrade and retrograde delivery. All sizes . USFDA.

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Delivery system for PDA Device. Approved for use of infants, children and adults. Should comprise of 180 degree curve delivery sheath with chck valve mechaism. Should be kink resistant with reinforcement with internal braided layer. Soft Rdiopaque tip. Dilator with taperig tip should fit in the sheath locking mechanism. Loader, plastic vise and delivery cable should be included.All sizes(including 4 and 5 Fr).USFDA.

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Delivery system for PDA Device with symmetrical Disc on both sides Approved for use of infants, children and adults. Should comprise of 180 degree curve delivery sheath with chck valve mechaism. Should be kink resistant with reinforcement with internal braided layer. Soft Rdiopaque tip. Dilator with taperig tip should fit in the sheath locking mechanism. Loader, plastic vise and delivery cable should be included.All sizes(including 4 and 5 Fr).USFDA.

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PFO Closure Devices with Delivery system. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system. All sizes . USFDA.

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LAA Closure Device with delivery system. Self centering detachable device. Device and all accessories must be made up of biologically inert material. Proven MR conditional and safe under static magnetic field of 3 Tesla or less.Intaglio coated to prevent nickel leaching. Proven clinical data should be available for the safety and efficacy of the device. Vendor should be able to supply all the components of the delivery system. All sizes . USFDA

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Sizing Balloon for ASD Device closure Oval Shaped. Compliant balloon material flexible shaft and soft tip. Radio-opaque markers bands. Available in all approved sizes. Over the wire: compatible with 0.035 wire.

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Titanium Nitride coated ASD Closure device with delivery System Approved for Paediatric/Adult use Device made up of biologically inert material Available in all sizes (06mm to 42mm) Titanium Nitride (TiN) coating should be there to prevent Nickel Leaching. Should come with compatible delivery system

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Titanium Nitride coated VSD Closure Device with Delivery System -Approved for pediatric/Adult use -Device made up of biologically inert material -Available in all sizes (06mm to 24mm) -Titanium Nitride (TiN) coating should be there to prevent Nickel Leaching. -Should come with compatible delivery system

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Titanium Nitride coated PDA Closure device with delivery system -Approved for pediatric/Adult use -Device made up of biologically inert material -Available in all sizes (03-05mm to 20-22mm) -Titanium Nitride (TiN) coating should be there to prevent Nickel Leaching. -Should come with compatible delivery system

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Multifunctional Occluder -For Occlusion of Muscular VSD, Perimembranous VSD, RSOV, Apex window & AV Fistula - Should be Low profile (4F-6F) -Should come with a elongatable waist and can be used in Retrograde and Antegrade approach.

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Covered Coronary Stent USFDA approved Monorail Available in variable sizes Covered graft stent for dissected artery.

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Peripheral Drug Delivery / Infusion Catheter Flexible, self-expanding prosthesis comprising of dual layer ePTFE 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 flexible and fracture resistant base stent architecture for tortous vessel like cephalic arch and SFA.The stent is available in straight and flared configurations available 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

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Long sheaths for contra-lateral iliac/femoral access -should be kink resistantwith a reinforcement mechanism. -should have distal raido-opadque tip for enhanced visibiltiy on fluoroscope. -should have smooth transition from dilator to sheath. -should have a proximal hemostasis valve/ provision for touhybborst valve. -Should be color coded for size identification. -should be avilable in 5 Fr -9 Fr size with the largest ID -Should have lengths ranging from 40-60cm.

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Preipheralbaloon expandable system OTW 0.035 guide wire compatible 6f sheath compatible across all sizes 97mm to 10 mm dia) l-605 Cobalt chromium crimped profile Thin struts lowest crimped profile Dual later, five fold balloon USFDA Approved

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High -performance crossing catheter in .014'', .018'', .035'' platform designed to be first line aid to cross stenotic lesions and chronic total occlusions when standard wires fail. Radiopaque marking system , 1cm radiopaque markers positioned 1cm apart with double markers dilenate 10cm and 20cm.

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Peripheral support catheter • Double braided stainless-steel shaft with 0.035” guidewire with one embedded two swaged radiopaque markers. Comes in 0.035 & 0.018 wire compatibity

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Micro catheter Available as 2fr& Co-axial in 2.4fr,2.7fr with hydrophilic coating protruding through 0.018& 0.021 hydrophilic guidewire.

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Snare kit 2-35mm diameter, 90-degree nitinol& gold-plated tungsten loop) single and Multiloop snare kit(2-45mm diameter, three interlaced nitinol loops) for foreign body retrieval, should come with flexible, reinforced, strain relief hub to reduce buckling and unique peel away insertion tool. USFDA Approved

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PACLITAXEL COATED DRUG ELUTING BALLOON FOR Below Knee intervention Paclitaxel coating should be 2ug/ mm2 Should have Hydrophobic coating for Minimizing Drug Loss Must be compatible with 0.018 -inch wire Loading Tool should be available Must be compatible with 4 Fr sheath Balloon length should be 20mm – 200mm Dia - 2-4 mm

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PACLITAXEL COATED DRUG ELUTING BALLOON FOR ILIAC & SFA Paclitaxel coating should be 2ug/ mm2 Should have Hydrophobic coating for minimizing Drug Loss Must be compatible with 0.018 -inch wire Loading Tool should be available Must be compatible with 4 Fr sheath Balloon length should be 20mm – 200mm Dia - 4-7 mm

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Balloon for Below Knee Intervention With an ultra-low lesion entry profile (0.017”/0.43 mm) and best-in-class crossing profile (0.030”/0.76 mm) With deflation times of less than 10 seconds and balloon lengths up to 220 mm Balloon Dia from 1.5 mm to 4mm with 4 F sheath compatibility across sizes. Monorail/ Over the Wire.

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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 of 110 micron pore size with 1mm pore free zone · Non-thrombogenic Nylon Membrane with hydrophilic coating · Should allow optimal filtration in vessels 3– 5.5 mm size · USFDA Approved

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Embolization Coils - 0.035" Detachable Should be Platinum coils and MRI compatible Fibered coils to have Dacron to promote thrombogenicity Should have various shapes like helical, complex helical, diamond, vortex, double apex design, etc. Should have round proximal and distal coil ends with tapered introducer pusher Should have dense fibre(dacron) to locate more coil and fibre inside the vessel and reduce tail formation.

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Embolization Coils - 0.035" Detachable Should have platinum coil material with or without fibers (dacron) Should have controlled deployment and ability to reposition before full deployment Should have interlocking arm mechanism Easy transfer from dispenser coil to microcatheter. Should have various shapes like helical, complex helical, diamond, vortex, double apex design, etc.

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Embolization Coils - 0.018" Pushable Should be Platinum coils and MRI compatible Fibered coils to have dacron to promote thrombogenicity Should have various shapes like helical, complex helical, diamond, vortex, double apex design, multiloop, etc. Should have round proximal and distal coil ends with tapered introducer pusher Should have dense fiber(dacron) to locate more coil and fiber inside the vessel and reduce tail formation. Should have a choice of fibered and detachable

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Embolization Coils - 0.018" Detachable Should have platinum coil material with or without fibers (dacron) Should have controlled deployment and ability to reposition before full deployment Should have interlocking arm mechanism Easy transfer from dispenser coil to microcatheter. Should have various shapes like helical, complex helical, diamond, vortex, double apex design, etc.

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PVA Particles Should be made of polyvinylalcohol Should have uniquely shaped and consistent sized particles All available size particle should be quoted.

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Stent Graft System for Thoracic Aorta - Nitinol Stent Graft system with mono filament polyester graft material, braided polyester sutures and platinum iridium sutures - With Tip capturing mechanism for precise positioning, - With Proximal, middle, and distal markers, - With Proximal Bare/Covered part. - Available in 22 mm to 46 mm diameter. - Available in 100 mm to 200 mm length - Available with 4 mm tapering

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Graft Stent for Aneurysm of Abdominal Aorta – Bifurcated Graft - Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - With Proximal Barbs and anchoring pins, With Tip Capturing Mechanism, Good Conformability, Self-expanding, Flexible, With markers - Proximal & Distal - Available in 23 mm to 36 mm proximal diameter and upto 166 mm ipsilateral length and up to 20F Compatible

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Graft Stent for Aneurysm of Abdominal Aorta – Contralateral Limb/Iliac Extension - Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - Available from 16 mm to 24 mm Diameter and up to 199 mm length, upto 18F Compatible - Has proximal Bare part, - To be used with Bifurcated graft in abdominal aortic aneurysm

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Graft Stent for Aneurysm of Abdominal Aorta – Abdominal Tube - Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - With Proximal Barbs and anchoring pins, With Tip Capturing Mechanism, Good Conformability, Self-expanding, Flexible, With markers - Proximal & Distal - Available in 23 mm to 36 mm proximal diameter 70 mm length and up to 20F Compatible

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Graft Stent for Aneurysm of Abdominal Aorta – Abdominal Cuff - Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - With Proximal Barbs and anchoring pins, With Tip Capturing Mechanism, Good Conformability, Self-expanding, Flexible, With markers - Proximal & Distal - Available in 23 mm to 36 mm proximal diameter 49 mm length and up to 20F Compatible

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Graft Stent for Aneurysm of Abdominal Aorta – AortoUni Iliac - Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - With Proximal Barbs and anchoring pins, With Tip Capturing Mechanism, Good Conformability, Self-expanding, Flexible, With markers - Proximal & Distal - Available in 23 mm to 36 mm proximal diameter, 14 mm distal diameter, 102 mm length and up to 20F Compatible

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Compliant Balloon for endograftmolding, Appotition of stent grafts in seal zone, for temporary aortic occlusion 12F Compatible, Can get dilated from 10 mm to 46 mm

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Introducer sheaths for access. Available from 12F to 26F diameter and various length

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Retrieval system for IVC filter Dual Sheath 9Fr and 11Fr, ideal for IVC filter retrieval. Kink Resistant Nitinol Construction with Radiopaque Loop for Enhanced Visibility, 90° loop snare for proper loop placement with Precise 1:1 torque facilitates easy filter hook capture , Marker Bands for Accurate Positioning Convenient all-in-one kit includes new coaxial sheaths and hemostatic valve

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IVC Filter Low profile 5F inner diameter delivery system IVC Filter Body available in femoral and jugular approach having conical shape & dual level filtration with curved Anchors help prevent cranial and caudal migration. Easy and accurate delivery system promotes self-centering. Highly visible snare tip seamlessly welded to filter body, with Smooth neck design encourages easy snare capture. Same filter assembly for both femoral and jugular approach.

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Venous stents Designed specially for the Venous anatomy, 3 mm flared stent ends are designed to reduce the risk of stent migration and maximize wall apposition, Venous Stent is available in 10 mm to 20 mm stent diameters and 40 mm to 160 mm stent lengths, triaxial delivery system for deployment accuracy,Tantalum markers for high stent visibility under fluoroscopy

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Renal Balloon Expandable Stent 0.014” compitable cobalt chromium 3-3 multi link design 5Fr compatible across all sizes 5, 5.5, 6, 6.5 and 7mm in diameter 12, 15 and 18mm in length USFDA approved

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Vascular Mimetic Implant for distal SFA, popliteal & across joints 018 Nitinol interwoven design without joints. 4.5, 5.5, 6.5 &—7.5mm Diameter various lengthsupto 200mm

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Peripheral Angioplasty Balloon CrossFlex Dual-layer balloon technology OTW .035 guide wire compatible 5Fsheath compatible to 4 to 7 mm diameter with faster deflation Usable Catheter length 135cm for all sizesdia 4mm to 14mm up to 250mm length USFDA Approved

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Peripheral Angioplasty Balloon 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 Approved

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Peripheral Angioplasty Balloon CrossFlex Dual-layer balloon technology OTW 018 guide wire compatible 5F sheath compatible to diameters from 2mm to 5.5 mm& 6mmLength- 20mm to 200mm Usable Catheter length 150cm for all sizes . USFDA Approved

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Self expandingnitinol stent for carotid angioplasty Rx Tapered carotid stent with Closed cell design with flared ends 6F Sheath Compatible across all sizes Freestyle ergonomic deployment technology USFDA Approved

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Self expandingnitinol stent for peripheral angioplasty - assorted sizes .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 Approved

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Guide Wire – 035 extra support type 190cm/exchange length.

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Guide Wire – 014 dedicated peripheral CTO guide wire with various tip load upto 13.5 mg.

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Guide wire- 018 stainless support guide wire with various tip length 3cm / 5cm with shapeable straight & j tip.

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Guide wire- 014 hybrid peripheral guide wire with distal nitinol tip and proximal Durasteel with 1:1 torque.

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Guide wire- 018 hybrid peripheral guide wire with distal nitinol tip and proximal Durasteel with 1:1 torque.

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Carotid Angioplasty Balloon 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 Approved

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Peripheral Vascular Plug Multi-layered, multiple-lobed Nitinol mesh design for rapid embolization within the vessel 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

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Stent for Coarctation of the Aorta Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Un-Covered and Unmounted Length : 28/34/39/45mm

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Stent for Coarctation of the Aorta Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Un-Covered and Unmounted Length : 50/55/60mm

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Stent for Coarctation of the Aorta Balloon Expandable Stent up to 30mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 10 zig pattern. Un-Covered and Unmounted Length : 50/55/60mm

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Covered Stent for Coarctation of the Aorta /RVOT Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Covered and Unmounted Length : 28/34/39/45 mm

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Covered Stent for Coarctation of the Aorta /RVOT Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Covered and Unmounted Length : 50/55/60mm

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Covered Stent for Coarctation of the Aorta /RVOT Balloon Expandable Stent up to 30mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 10 zig pattern. Covered and Unmounted Length : 50/55/60mm

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Pre-mounted Stent for Coarctation of the Aorta Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Un-Covered and Pre-mounted on Balloon in Balloon (Two Balloons on same shaft) Length : 28/34/39/45 mm

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Pre-mounted Covered Stent for Coarctation of the Aorta /RVOT Balloon Expandable Stent up to 24mm in Diameter Stents should be Composed of 0.013” platinum-iridium wire arranged in 8 zig pattern. Covered and Pre-mounted on Balloon in Balloon (Two Balloons on same shaft) Length : 28/34/39/45mm

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High Pressure Percutaneous Transluminal Valvuloplasty (PTV) Balloon Catheter High pressure balloon. Maximum steering and trackability. Coaxial catheter. Configurations ranging from 4.0 to 30.0 mm in diameter Non-Compliant Thermoplastic Elastomer Balloon.

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Balloon in Balloon Stent Placement catheter inner balloon 1/2 of the balloon diameter of the outer balloon. Four image bands that match the functional length of each balloon. A usable length of 110 cm Balloons are for use with a 0.035" guidewire. Inner balloon acts as a tool to hold the stent in place while outer balloon is inflated. Allows for controlled and incremental expansion of the Stent.

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High performance balloon, Non- Complaint, multilayer balloon with Coaxial Shaft and working pressure range of upto 12 atm, highest rated burst pressure of 18 atm Sizes: Diameter (12mm to 26mm) & Lengths (2cm & 4cm) with Shaft length of 75and 120cms.

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Common and external iliac arteries stent with reference vessel diameters between 4.5 mm and 12.0 mm, and lesion lengths up to 100 mm. Balloon Expandable Vascular Covered Stent i comprised of an electropolished balloon-expandable stent made from 316L stainless steel, encapsulated between two layers of ePTFE. The covered stent is supplied pre-mounted on an over-the-wire delivery system with a non-compliant balloon

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VVI/VVIR LeadLess Pacemaker with All Accessories. US FDA approved, permanent leadless pacing capsule providing VVI/VVIR pacing • The weight of the device should be less than 2 gms and volume less than 1 cc • Must be MRI conditional pacemaker for full body scan - 1.5T & 3T • Must have ventricular capture management • Should have the ability to transmit data through remote monitor

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VDD LeadLess Pacemaker with All Accessories. – US FDA/ CE APPROVED, Global 7 year warranty. permanent leadless pacing capsule providing VVI/VVIR/VDD pacing • The weight of the device should be less than 2 gms and volume less than 1 cc • Must be MRI conditional pacemaker for full body scan - 1.5T & 3T • Must have ventricular capture management • Should have the ability to transmit data through remote monitor

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Antibacterial Envelope • US FDA approved fully absorbable antibacterial envelope which elutes antibiotics effective against common infections • Maintains MIC of the antibiotics at the pocket site for at least a week from implant date • The envelope should be completely absorbed within 3 months

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DDDR pacemaker US FDA/ CE and DCGI approved permanent pacemaker for physiological pacing (his bundle and left bundle pacing ) with all leads and accessories with life time warranty. MRI Compatible/ Safe Stylet driven lead for conduction system pacing. Delivery sheath/ system for conduction system pacing.

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DDDR pacemaker US FDA/ CE and DCGI approved permanent pacemaker for physiological pacing (his bundle and left bundle pacing ) with all leads and accessories with life time warranty. MRI Compatible/ Safe lead for conduction system pacing. Delivery sheath/ system for conduction system pacing.

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Dual Chamber Rate Response Pacemaker US FDA approved Dual Chamber pacemaker, MRI Safe Lead size 6Fr or less Optim coating on lead All modes are inbuilt – VVI, VOO, DOO,DDDR etc Smallest in size and volume should be 10cc or less Features like AF suppression algorithm and optimization of A-V delay.

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Balloon tipped floating catheter for tempporarytransvenous pacing 5Fr, 110cm,Non heparin coated Depth marking to aid placement of electrode. Intra electrode spacing 1cm. Balloon inflation syringe 1.5 cc ECG adapter, needle- cannula balloon inflation syringe. Balloon pacing electrode shaft made up of woven Dacron fiver material and includes heparin bonding.

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Balloon acclusion angiographic catheter injecting contrast medica proximal to balloon 4 Fr to 6 Fr 110mm length

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Pulmonary artery catheter for measurement of pulmonary artery and wedge pressure having balloon port and infusion port

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Distal embolic protection device - Carotid /SVG · Rapid Exchange, Fire fixed. 0.018” or 0.014” wire compatible, Used in Carotid, peripheral and coronary intervention. Delivery End 3.2 F, Recovery End 4.2 F.

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Radioopque Marker Tape applied on skin for marking and lesion length measurement.

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2 port manifold, Leur lock system, With inert material non slippery with pressure rating up to 250 to 550psi, Right on. clear body allowing easy visibility for de-bubbling, easy rotating handles, rotating leur for secure connection, airthight. optional extension tubing and on/off handle for options

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item 16

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811 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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812 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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813 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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814 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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815 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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816 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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817 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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818 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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819 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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820 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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821 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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822 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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823 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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824 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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825 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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826 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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827 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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828 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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829 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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830 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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831 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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832 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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833 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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834 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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835 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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836 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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837 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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838 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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839 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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840 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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841 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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842 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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843 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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844 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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845 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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846 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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847 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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848 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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849 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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850 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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851 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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852 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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853 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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854 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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855 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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856 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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857 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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858 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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859 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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860 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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861 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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862 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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863 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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864 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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865 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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866 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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867 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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868 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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869 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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870 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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871 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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872 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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873 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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874 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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875 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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876 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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877 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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878 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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879 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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880 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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881 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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882 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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883 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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884 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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885 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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886 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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887 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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888 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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889 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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890 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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891 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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892 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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893 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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894 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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895 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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896 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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897 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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898 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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899 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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900 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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901 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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902 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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903 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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904 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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905 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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906 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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907 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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908 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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909 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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910 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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911 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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912 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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913 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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914 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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915 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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916 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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917 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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918 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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919 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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920 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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921 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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922 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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923 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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924 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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925 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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926 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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927 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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928 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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929 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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930 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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931 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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932 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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933 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

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