02(2025-26) Item No.01. Supply Of Cardiology Implants

Cardiology Implants and Equipmets

High Pressure Line Available in 150cm and 200cm, made of branded PVC, very flexible and pressure should hold up to 1200psi with leur lock on one side and collerfillting on other side.

Radial introducer needle · 18G, 32mm length, · Inner diameter 1.3mm

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.

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

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

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

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

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

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

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

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

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

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

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

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

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

AngioKit 2 Port: 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

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

Leurlock plastic single use syringe, 10ml, 20 ml

Pressure monitoring iv lines, 200 cm

Needle 26 G 0.45mm x 13mm

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

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

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 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

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

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

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

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

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

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

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

Marker Pigtail ; 5F/ 6F

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

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

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

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

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

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

PTCA Needle – for carrying 0.014” coronary wire

Torquer for 0.014 wire

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.

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

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

IVUS SLED Pullback sled with available IVUS machine in cath lab

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)

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.

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/ PMDA/DCGI Approved

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

Dedicated Microcatheter Dedicated dual lumen micro catheter for side branch access

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.

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

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

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

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

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

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

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

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

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 Must Have Rounded & Flexible Tip made up of Polyamide Elastomer.Should have Bioinspired Open cell in phase design. Low concentration of Sirolimus (0.8ug/mmsq), tip entry profile of 0.42mm. PMDA+CE Approved

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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.

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.

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).

DOC Extension Wire Compatible with Abbott PTCA wire Regular length PTCA guidewire-USFDA Approved.

DOC Extension Wire Compatible with Asahi PTCA wire Regular length PTCA guidewire-USFDA Approved

.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

.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

.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

.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

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

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

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

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

.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,

.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

.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

.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

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

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.

Vascular Closure Device for 5-22F polypropylene monofilament suture mediated vessel closure With no re - access restriction Flexibility to pre-close and close over the wire (USFDA Approved) Immediate re-access advantage For small hole and large hole closure both.

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

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.

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

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

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.

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

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.

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.

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.

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

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

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)

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

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

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.

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

Mullin Sheath for Mitral Valvuloplasty Balloon

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

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

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.

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.

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.

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.

Symmetrical PDAClosue 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.

Symmetrical PDAClosue 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.

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.

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.

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.

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

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.

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

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

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

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.

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

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

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.

Peripheralballoon 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

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.

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

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

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

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

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

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.

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

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.

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.

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

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.

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.

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.

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.

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

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

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

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

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.

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.

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.

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.

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

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

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.

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

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

Hydrophilic Guidewire with tapered tip, (Regular Length -150 CM) single Nitinol core alloy, Tungsten-infused polyurethane jacket *hydrophilic polymer coat. One piece construction & Radiopaque polyurethan jacket. * Must be available in standard and stiff. * Must be available in ..035, diameter and 150 cm, - Straight / Angled / 1.5 mm J shape * USFDA/PMDA approved

0.035" over the wire system stainless steel , One piece laser cut stainless steel slotted tube, Closed cell design,N shaped flex segments for minimal foreshortening, excellent contourability, High radial strength, Assorted sizes - length 19mm, 25 mm, 39 mm, 55mm and 79 mm

Bare Metal Stainless Steel Stent - can be expanded from 14mm to 25mm, unexpended stent length 50 mm

Large Diameter Balloon, Coaxial 7F over the wire shaft, Braided inner body, 5 and 6 atm rated burst pressure. Diamter of balloon 14 mm, 15 mm,16mm , 18 mm, 20 mm, 22 mm and 25 mm

Sirolimus El uting DES ,Co-Cr platform/ Biodegradable Polymer/ Microporous Surface/ Shellac Resin/ Ablumin al Coating/ Strut Th ickness 68μm (SY), 79μm (MY) CE Approved

Dual layer coronary balloon / RBP 35 bars/ ABP 45 bars / Strictly non-compliant (only 10% growth)/ and for super high pressure PTCA , a Manometer of 55 atm

One Piece core specialty wire with jointless spring coil tapering to .009"; 0.6gf,0.8gf & 1.0gf of tip load; 16cm polymer sleeve length with slip coat coating over the polymer sleeve, 190cm length; tip radiopacity 16cm, available for atengrade/retrograde approch.

.014" One Piece core workhorse wire with jointless spring coil 22cm polymer sleeve length with slip coat coating over the polymer sleeve, tip load 0.8gf, 1.0gf ,180cm length tip radiopacity 3cm

IVL Catheter and Connector Cable,- Intravascular Lithotripsy Intuitive Catheter with Rx system for treating highly calcified lesions,- Integrated 12mm SC balloon ,- NP - 4atm/ RBP - 10 atm,- Diameters:2.5 ,3.0,3.5,4.0mm ,- 2 emitters (80 pulses per catheter),B. Portable and Rechargeable IVL Generator,Intravascular lithotripsy catheter generator, po1iable, IV-Pole mountable, rechargeable battery for intuitive IVL Catheter

sensor guided TAVI wire, Single wire working as a guide wire, for Hemodynamic Measurement and for Rapid LV pacing

Recommended for use in Percutaneous Transluminal Angioplasty of the femoral, iliac, and renal arteries and for the arteriovenous dialysis fist,ulae. High performance balloon catheter consisting of an / overthe-wire catheter with a balloon fixed at the distal tip. The proprietary ultra noncompliant, low profile balloon is designed to provide consistent balloon diameters and lengths even at high pressures. Two 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.

PTA Dilatation Catheters are recommended for use in percutaneous transluminal angioplasty (PTA) of the renal, popliteal, tibial, femoral, and peroneal arteries. To facilitate catheter advancement through the vasculature and the vessel stenosis,Dual Layer Hydrophilic Coating is present on the distal segment of the shaft and the balloon

The Stent (Implant) is equipped with four highly visible radiopaque Tantalum Markers on both the proximal and distal end for ACCURATE PLACEMENT. 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 . indicated for the treatment of illiac occlusive disease in patients with symptomatic vascular disease of the common and/or external iliac arteries up to 126 mm in length with a reference vessel diameter of 5 to 9 mm. Perfect metalic length, unique delivery, thumb delivery , 60-120. 4 deployment method for physicians convenience in deploying stent - Trigger, Slide, Combination and conventional.

Indicated for the treatment of atherosclerotic lesions in common and external iliac arteries with reference vessel diameters between 4.5 mm and 12.0 mm, and lesion lengths up to 100 mm.Balloon Expandable Vascular Covered Stent is 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-thewire delivery system with a non-compliant balloon

CAROTID SELF EXPANDING STENTAuto Tapered (Self Tapered and Non Tapered) Stent Rapid ExchangeGuide wire Compatibility- 0.014Guiding Catheter Compatibility- 7F (S-8 mm) 8F (9-10 mm) Length of Delivery System- l3ScmDiameter: 6,7,8,9 & 10 mmLength: 20, 30 & 40mmSheath Compatibility- 5 F (5-8 mm) 6F (9-10 mm)

Embolic Protection Device Distal Protection Device Carotid Filter Rapid ExchangeSheath Compatibility: 6FGuide wire Compatibility-0.014 Guiding Catheter Compatibility- 8F Diameter: S ,6 &7 mmLength: 180cm

Temporary Bipolar Pacing Catheter- Torque Control1. Should be US FDA & DCGI approved2. Should have 10 cm depth markers to enhance placement.3. Should have smooth, polyurethane hemocompatible coating. 4. Should have clearly marked terminals.5. Should have shrouded 2 mm pin connector leads.6. Should have stainless steel centre conductor and stainless steel electrodes.7. It should have solid core enables user to customize the curve.8. Should have optimal torque control for challenging anatomy

Temporary Bipolar Pacing Catheter- Flow directed1. Should be US FDA & DCGI approved2. Should be latex balloon tipped , flow guided for stable insertion.3. Should have 10 cm depth markers to enhance placement.4. Should have smooth, polyurethane hemocompatible coating. 5. Should have clearly marked terminals.6. Should have shrouded 2 mm pin connector leads.7. Should have platinum electrodes8. It should have flexible tip design for delicate placement.

PTMC Balloon With all accessories dilator, stylet, Guide wire, Syringe, Ruler,Stretching Tube)• *Specially Designed balloon , perfectly shaped to for the mitral valve• *Short inflation/deflation cycle• *New small and soft tip• *Large size matrix and With Three Lumen at proximal End.• *Longer guide wire to increase safety in tallerpatients available sizes of 19- 30 • CE- approved

Self-Expandable Nitinol stent with radial force fixation, e PTFE dual Membrane coating for (excellent biocompatibility and durabilityand No suture on the main body to prevent pin hole Leakage). SPINE - ONNECTINGBAR -(Gives Axial support , - Avoids shortening). Size OD - 20mm to 44mm; Length - 80mm, l OOmm, 120mm, 140mm 160mm and 200mm. Tapering - 4/6/8mm

Iliac Stent Graft Endovascular stent graft device for the treatment iliac aneurysm or dissection. with proximal bare spring configuration.It should be an extension to AAA Graft System. OD - l Omm to18mm Length - 60mm to 120mm

Steerable sheath with deflectable tip (90-180 degree)Size Available upto - 5/6/7/8/9/10/12/14Fr. in 80cm 90cm Length

AUI Stent Graft System specifically designed for treatment of endovascular Abdominal Aortic Aneurysm. A self-expandable nitinol Stent with ePTFE dual Membrane coating with connectingspine bar for flexibility &offers axial support preventing foreshortening of stent.

BIODEGRADABLE POLYMER /MICROPOROUS SURFACE STAINLESS STEEL PLATFORM/SIROLIMUS DRUG & SHELLAC RESIGN/ABLUMINAL COATING I TEMPERATURE CONTROL DEVICE-AG ALERT US FDA I CE & DCGI APPROVED

Biodegradable Polymer Sirolimus Eluting Coronary Stent with Co-Cr Platform having Microporous surface, abluminal coating and shellac resin with Strut Thickness 68pm (SV), 79pm (MV) CE/DCGI

Self Expending USFDA approved for SFA and Popliteal Nitinol Stent with Unique triple Helix design Structure for Multi-dimensional Flexibility with unique Delivery system having both thumb wheel and pin & pull mechanism. 5F Vascular Stent System is 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 femoral artery (SFA) and popliteal artery with reference vessel diameters ranging from 5.0 - 7.0 mm.

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

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 Design- Dual layer ePTFE encapsulation demonstrated a significant reduction at 90 days 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 after placement in tortuous lesions presenting with in-stent restenosis or non stented lesions in patients

Rapid inflation and deflation, Clear barrel for easy visualization of de-bubbling, Luminescent analog pressure gauge (up to 30 atm), Ergomatric and use friendly hand held design. Volume: 25ml, Range of Positive Pressure: 0 to 30 bar Plunger: Screw Type plunger"

Ridaforolimus Eluting Stent System on cobalt Chromium Platform with Flexx2 delivery system, tapered spring tip and reinforced hypotube With Elastomeric coating. Unique WiZe cell architecture

seventh-generation Ridaforolimus eluting coronary stent featuring a unique stent design which utilizes a distinctive CoCr framework composed of struts with varying widths and integrates radiopaque markers into its structure.

Broad Based QR for Thrombosuction under pressure containing (a)CAT6,6FR length 135cm catheter(b) Aspirationtubing (c)Canister 1000ml · It Should be Mechanical thrombectomy Catheter 6FR · It Should be 132CM · It should be distal od5.0F/1.65mm · It Should be USFDA certified in aid with 6fr catheter · It Should be to maintain the lumen of the catheter & for removal of blood clot. · It should be Mechnical Thrombolysis.

Broad Based QR for Thrombosuction under pressure (8mm kit) containing (a)Cat 8, 8 FR catheter (b) Aspiration tubing (c) Canister 1000ml 1. It Should be Mechanical thrombectomy Catheter 8 FR 2. It Should be 115 CM 3. It should be distal od 8.0 F /2.67 mmmm 4. It Should be USFDA certified in aid with 8fr catheter 5. It Should be to maintain the lumen of the catheter & for removal of blood clot. 6. It should be Mechnical Thrombolysis.

Broad Based QR for Thrombosuction under pressure containing (a) Cat 3, 3 FR length 150 cm catheter (b) Aspiration tubing (c) Canister 1000ml 1.It Should be Mechanical thrombectomy Catheter 3 FR 2. It Should be length 150 CM 3. It should be proximal OD 4.1 F (1.37 mm) distal od 3.4 f (1.14 mm) 4. It Should be USFDA certified in aid with 3 fr catheter 5. It Should be to maintain the lumen of the catheter & for removal of blood clot. 6. It should be Mechnical Thrombolysis.

Broad Based QR for Thrombosuction under pressure containing (a) Cat D, 8 FR length 50 cm catheter (b) aspiration tubing (c) conister 1000ml 1. It Should be Mechanical thrombectomy Catheter 8 FR 2. It Should be length 50 CM 1. It Should be distal od 0.055"/1.40mm 3. It Should be USFDA certified in aid with 8 fr catheter 4. It Should be to maintain the lumen of the catheter & for removal of blood clot. 5. It should be Mechnical Thrombolysis.

Broad Based QR for Separator 8Fr – 150 cm 1. It Should be Mechanical thrombectomy separator 8fr-150 cm 2. It Should be distal od 0.055"/1.40mm 3. It Should be USFDA certified in aid with 6fr catheter 4. It Should be to maintain the lumen of the catheter & for removal of blood clot.

Broad Based QR for Separator 6Fr – 175 cm 1. It Should be Mechanical thrombectomy separator 6fr-175 cm 2. It Should be distal od 0.055"/1.40mm 3. It Should be USFDA certified in aid with 6fr catheter 4. It Should be to maintain the lumen of the catheter & for removal of blood clot. 5. It should be Mechnical Thrombolysis.

J Tip Normal length Teflon Guide wire for femoral angiography PTFE coated, Must be 0.035” in diameter and 150cm in length

Exchange length J Tip exchange length Teflon Guide wire for femoral angiography PTFE coated, Must be 0.035” in diameter and 260cm/300 cmin length

PTCA guide wire- 2 mm Silicon coated distal tip, 0.0014” Diameter and 300cm 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 hydrophilic coating upto 248mm. Must have PTFE Coating from 25 to 180cm length. Should be Available in both 0.6 and 1gm tip load Should be available in extra floppy and Floppy tip PMDA + USFDA

PTCA Guide Wire - Core material Elastinite Nitinol for excellent flexibility and durability, Shaping ribbon for excellent shape retention and atraumatic tip load less than 0.65 gm with Length 300cm, Regular Shaft Support Floppy tip

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 1.3 to 2.5gm for complex anatomies,Hydrophilic coating for longer lasting Lubricity.

Amplatz Super stiff wire 0.035, Exchange langth 260cm, J.Tip

Amplatz Extra stiff wire 0.035, Exchange langth 260cm, J.Tip

Femoral Sheath Length (cm): 11 French Sizes (Fr.): 4F FEMORAL INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR ADULTS (Sizes 4F Fr.)- Excellent kink resistant,Side port extension with 3-way stopcock,Cannula made of two (thinner) layers of polyethylene,Removable cap which has hexacuspid valve 0.38’’ Guide wire compatible ,Lengths: 11 cm, DCGI/CE/USFDA approved

Paediatric Sheath Length (cm): 7.5 French Sizes (Fr.): 4F/5F/6F FEMORAL INTRODUCER SHEATH WITH PUNCTURE NEEDLE FOR PAEDIACTRIC - Excellent kink resistant,Side port extension with 3-way stopcock,Cannula made of two (thinner) layers of polyethylene,Removable cap which has hexacuspid valve, 0.21’’ Guide wire compatible, Lengths: 7.5 cm, Diameters: 4,5 & 6 Fr DCGI/CE/USFDA approved

Diagnostic catheterFrench Sizes 4FDiagnostic catheter,Technology ensures consistent ID from hub to tip ,Three-segment polyurethane construction ,Stainless steel wire braided body wrapped with thrombi-resistant material,soft, atraumatic, radiopaque tip (radiopaque marker from the origin of the tip), Lengths: 65 cm/80 cm/100 cm/110 cm,Radial - RBL TG, TG, RBL JK,special - SRC, 3DRC, Straight, Pigtail, IM,Shapes: JL, JR, AL, AR, IM, LIMA, EGB, MPA, NIH, PIG, RCB, SON &RBL,Available in 4F,DCGI/CE/USFDA approved

Peripheral Vascular Plug Multi-layered, multiple-lobed Nitinol mesh design for rapid embolization within the vessel4to embolize medium and high-flow vesselsGuide Catheter or Sheath Deliverable: Compatible with 4-7 F sheathsor 5-9 F guide catheters depending on device size

10F Lumen compatible Y Connector for complex procedures including IVUS,Rota ,OCT etc , Should have Dual Valve - Hemostatic& Fixed Valve USFDA Approved

PTCA wire doc extension * Extension wire 0.014 diameter and 150 cm length, PTFE Coated * Must have modified distal end that enables to attach the RUNTHROUGH NS Wire * USFDA/PMDA approved

Double Lumen Micro catheter to for CTO and bifurcation angioplasty, monorail and over the wire design.

dilators: Dilators for atrial septal / femoral dilation 8-38-20, 10.0-38-20,12.0-38-20,140.-38-20,16.0-38-20, 18.0-38-20, 20.0-38-20, 22-38-20, 24-38-20,

Guiding catheter - (USFDA/CE APPROVED) PTFE coating, 4x2 Braided , Atraumatic tip, Available in 5F,6F,7F,8F,9F Hydrophilic coating, in diameter 0.75 to 4.0 Available with JL, JR, CLS, FL, FR, AL, AR, IM, MP, VL, ART3, LBU, KR, Kimny, Cobra, SIM, NTR Q Curve

TAVI Device Specification – Percutaneous Transcatheter Self-expanding bovine tissue heart valve for Aortic Heart position available in sizes 23mm-29mm with low profile Delivery System - Unique Valve design with Intra-annular leaflets - Valves should have Anti-calcification treatment - Polyethylene fabric material with dynamic cuff that synchronizes with the cardiac cycle - Should have USFDA, EU-MDR, Canada and Japan approved.

Micro catheter to perform CTO procedure with pre-shaped tip of 45/90/120 deg, 0.014 guidewire compatible, stainless -steel braid, coiled shaft, 130CM & 150CM working length.

A unique Five-layer shaft construction that provides flexibility, torque and tracking over a 0.014'' guidewire , Distal 3 cm nylon coil provides rotational assistance for impressive trackability for complex antegrade. Radiopaque tip. 60 cm hydrophilic coating. Distal tip OD 1.6F & Distal tip length 11mm.

Micro catheter with spiral shaft and gold tip. Gold tip should provide leading edge rotational advancement with visibility under fluoroscopy.

Radial angiography Puncture Sheath, 18 & 20G with plastic body and stainless steel puncture needle JELKO Type Needle and Sheath

Computer Aided Vaccum thrombectomy catheter kit for VTE Mechanical Aspiration with working length of 100/115/130 cm. Should have multi-pitch, laser-c ut stainless steel hypotube for 1:1 torque transfer & advance deliverability. Catheter Should have ID of (3.33 mm), OD of 12 Fr with HTORQ tip with 50 mm circumferencial sweep. It should be compatible with 12 Fr sheath & wire platform (.014-.038) with proprietoryseperator technology. Aspiration tubing Audio visual cues to help indicate location of clot in system & compatible with engine with (-29.2) inHg Deep vaccum

Catheter: Stainless steel hypotube at the proximal end, designed to enhance deliverability to the desired vessel with optimal visualization and placement. Catheter size : 6 F Catheter type : Low crossing profile of 1.75mm with an ID of .044”. Separator : proprietary separator technology for easy and quick aspiration, with 200 cm length and distal OD of .89 mm. Safety features : Ability to get the clot out and not macerate .

Separator : proprietary separator technology for easy and quick aspiration, with 150 cm length and distal OD of 1.83 mm. Separator : proprietary separator technology for easy and quick aspiration, with 175 cm length and distal OD of 1.40 mm.

Engine Canister _1 litre capacity collecting jar with measuring marks. Integrated clot catcher with completely airtight and break resistant to – 2 ATM pressure. Single touch operation. LED Canister lighting.

BA9(Biolimus) eluting coronary stent with CoCr platform and biodegradable polymer.

BA9 (Biolimus) eluting coronary stent with Stainless steel platform and biodegradable polymer. Length upto 48 mm

BA9(Biolimus) drug, polymer free drug eluting stent with ultra short DAPT of one month as per ESC guidelines and stainless steel platform. USFDA APPROVED

BA9(Biolimus) drug, polymer free drug eluting stent with ultra short DAPT of one month as per ESC guidelines and CoCr platform. PMDA(Japanese Fda) APPROVED.

Everolimus CoCr DES, Unique hybrid stent design and Biodegradable polymer (PLGA) coated, Uniform 60µm Strut Thickness across all diameter 2.25 to 5mm, length 8 to 48mm

Sirolimus CoCr DES, Unique hybrid stent design and Biodegradable polymer Uniform 63µm Strut Thickness across all diameter 2.25 to 4 mm, length 8 to 48mm

Everolimus CoCr DES, open and closed cell design, Special Electro- Polishing Technique along with Uniform 59µm Strut Thickness across all diameter 2.25 to 4 mm, length 8 to 48mm

Sirolimus CoCr DES, open and closed cell design, Special Electro- Polishing Technique along with Uniform 59µm Strut Thickness across all diameter 2.25 to 4 mm, length 8 to 48mm

Semi Compliant balloon catheters with hydrophilic coating, low entry profile of 0.016" having size- 1.00 mm to 4.00 mm, lengths 5 mm to 40 mm

Non Compliant balloon catheters with hydrophilic coating, low entry profile of 0.016" having size- 1.50 mm to 5.00 mm, lengths 8 mm to 40 mm

Stainless steel Hypotube , Polymer Cathater Segment 1:1 wire braiding, hydrophilic coated with radical coller, 0.57" Inner Diameter,& 0.067" outer diameter. Available size 5 fr. 5.5fr, 6 fr, 6fr longer,7 fr

Self Expandable Transcathater Bicaval System with dry Tissue technology, Pre loaded delivery system, Available in different sizes

cathater should have latex silicon balloon, infusion capacity 1.5cc,7Fr seath compatibility, effective Length 1100 mm.

Self Expandable Transcathater aortic valve implantation (Tavi) with dry tissue technology, preloaded delivery system, available in different sizes.

cathater should be radio opaque marker and tip, compataible with 0.0035" Guidewire. The Catheter should have CVD Proximal lumen port distance from tip 10cm The Catheter should have CVD Proximal lumen port distance from tip 10cm. should have additional Lubricity, availabe in various configration & come with introducr &Cathater straightner.

Biodegradable Polymer Sirolimus Eluting Coronary Stent with Stainless- Steel Platform having Microporous surface, abluminal coating and shellac resin with diameters of 2.0 mm to 4.0 mm of varying length.

Biodegradable Polymer Sirolimus Eluting Coronary Stent with Co-Cr Platform having Microporous surface, abluminal coating and shellac resin with Strut Thickness 68µm (SV), 79µm (MV).

Biodegradable Polymer Sirolimus Eluting Coronary Stent with Co-Cr Platform having Microporous surface, abluminal coating and shellac resin with Strut Thickness 68µm (SV), 79µm (MV).

Biodegradable Polymer Sirolimus Eluting Coronary Stent with Stainless- Steel Platform having Microporous surface, abluminal coating and shellac resin with Temperature Control Device - TAG ALERT

Micro catheter to perform CTO procedure with pre-shaped tip of 45/90/120 deg, 0.014 guidewire compatible, stainless -steel braid, coiled shaft, 130CM & 150CM working length.

Guide extension having half-pipe technology for smooth device entry with coil reinforced tip and PTFE inner lining, mother & child catheter, Size 5Fr, 5.5Fr, 6Fr, 7Fr, 8Fr, 150CM working length

A unique Five-layer shaft construction that provides flexibility, torque and tracking over a 0.014'' guidewire ,Flexible, tapered tip for superior tracking for antegrade & retrograde. Radiopaque tip. 60 cm hydrophilic coating. Distal tip OD 1.6F & Distal tip length 11mm.

A unique Five-layer shaft construction that provides flexibility, torque and tracking over a 0.014'' guidewire, Distal 3 cm nylon coil provides rotational assistance for impressive trackability for complex antegrade. Radiopaque tip. 60 cm hydrophilic coating. Distal tip OD 1.6F & Distal tip length 11mm.

A unique Five-layer shaft construction that provides flexibility, torque and tracking over a 0.014'' guidewire, Dual coil tapers down to single coil 21cm from distal tip for lower profile for frontline retrograde. Radiopaque tip. 60 cm hydrophilic coating. Distal tip OD 1.6F & Distal tip length 10mm.

Micro catheter with spiral shaft and gold tip. Gold tip should provide leading edge rotational advancement with visibility under fluoroscopy.

14 Fr Biomechanical Vascular Closure Device designed specifically for large bore femoral arterial access site closure following the use of 10-14 Fr. devices or sheaths (maximum O.D. of 18 Fr.), An over the wire design with a resorbable anchor & Collagen, sliding suture knot, Visual and auditory cues and simple lever rotation. The Vascular device comes along with depth locator, sheath &introducer.

18 Fr Biomechanical Vascular Closure Device designed specifically for large bore femoral arterial access site closure following the use of 15-18 Fr. devices or sheaths (maximum O.D. of 25 Fr.)., An over the wire design with a resorbable anchor & Collagen, sliding suture knot, Visual and auditory cues and simple lever rotation. The Vascular device comes along with depth locator, sheath & introducer.

CE Approved Collagen based 3-step mechanical Vascular Closure Device , available in 6F & 8F, compatible with the standard existing introducer sheath used during the interventional procedure.

Everolimus Eluting Coronary Stent System (EECSS) includes: L-605 cobalt chromium (CoCr) alloy Mounted on Thin, single-layer balloon enables high pressure deployment while maintaining flexibility and strength. Pebax‡72D True center tips: Designed with co-axial positioning system (CPS) Coating that consists of a blend of the anti-proliferative drug Everolimus and Fluroniated Co-polymers Ultra-low crimped stent crossing profile of 0.039 inch and Tip entry profile of 0.017”(3.0x18mm). Post dilatation capabilities up to 3.75 mm for diameters 2.0 – 3.25 mm and 5.5mm for diameters 3.5 – 4.0mm. Nominal Pressure 2.0 – 2.5 mm balloon diameter: 9 ATM & 2.75 – 4.0 mm balloon diameter: 12 ATM RBP of 16ATM Offers exceptional deliverability from the re-engineered stent delivery system featuring a single-piece outer member for added pushability and trackability. Safety of Sent in high bleeding risk (HBR) patients treated with 1-month (as short as 28 days) dual antiplatelet therapy (DAPT)

Bare metal Covered Coronary stent -US FDA approved

Minoxidil 2%

Minoxidil 5%

Minoxidil 10 %

Podophyliin Toxin

Sulphur + Calamine

sunscreen (octinoxate,avobenzone , oxybenzone) spf 30

Clotrimazole 10Mg

(Medium Chain Triglyceride)

Budesonide 200 mcg.

Formeterol 6mcg.+ Fluticasone 250 mcg. Inhalation

Formoterol 6 mcg. + Budesonide 200 mcg.

Formoterol 6 mcg. + Budesonide 400 mcg.

Leosalbutamol 50mcg.+ Ipratopium 40mcg.

Levosalbutamol inhalation Solution 50ml/gm

Lignocaine 1%

1.5% Hydrogen Peroxide

Fluticasone FT

Midazolam 0.5mg/5ml

Neomycin sulphate and Bacitracin Zinc ointment USP 5 mg + 500 IU/gm

Sodium Chloride 0.9% 3000ML(N.S)

Sodium Chloride bottel 100ML

Magnesium sulphate, Sulphacetamide, Urea 75 gm

Clobetasol+Salicylic acid 0.5%+6%

Heparin 50 IU Benzyl Nicotinate 2 mg

Fluticasone

Neomycin, Polmyxin and Bacitracin zinc ophthalmic 15 gm IP

Tacrolimus 0 .03% 15 gm

Tacrolimus 0 .1% 15 gm

Zinc Oxide +Alo Vera +Semethicone

Omega 3Fatty Acid 50ML

Caffiene Citrate Oral Solution

Mercunium Chloride

salicylic acid 16.7% + lactic acid 16.7%

Coloplast 60 Gm

EEG 400GM

Diclofenac Each Transdermal patch contain 200 mg Diclofenac

povidone iodine

Milk Low Birth Formula

Recombinant Human Growth Hormone 4IU vial With Syringe

Enterogermina 2billion spores 5ml

Formeterol 20mcg +Budesonide 0.5mg

Levosalbutamol 2.5 mg + Ipratropium 500 mcg 2.5 ml

N-acetylcysteine (NAC) 200mg/ml

Budesonide 0.5mg/ml

Budesonide 1ml

Glycopyrronium 25mcg. Inhalation 2ml.

Sodium Chloride 3 %

Tiotropium Bromide dry powder 30/pack

Revolizer/ rotahaler Device

Root Canal Sealer (Calcium Carbonate)

Fosfomycin 3gm

HMF for Pretem

L-Arginine+proanthocynadine granules 3mg

Polyethyene glycol + Sodium Chloride+Sodium Bi Carbonate+Potassium Chloride

Racecadotril Sachet 30 mg

Etanercept 25MG/0.5ML

Polyethyene glycol with Elctrolyte approx 130gm

Lidocaine 10% 20Ml

Superoxidized

Mesalazine

Glycerin 2 gm/ml

Paracetamol 170 mg Each Suppsitory contain paracetamol 170 Mg

Cefaclor Each 5 ml contain Cefaclor 125 Mg

Codiene Phosphate

Amlodipine oral solution 1 MG/ ML

Artemether 40mg + Lumefantrine 240 mg 30ml

B. complex

Baclofen Oral Solution 5 MG /ML

Calcium Phosphate 200 ml

Cefixime Oral Suspension 50MG

Cefixime Oral Suspension 100MG

Cefpodoxime Proxetil Oral suspension 50MG

Cefpodoxime Proxetil Oral suspension 100MG

Cefuroxime Axetil oral suspension 125mg/5ml

Clarithromycin for oral suspension 125mg/5ml

Cefoperazone 1mg Inj.

Cyclosporine Oral solution 100mg/ml

Rabbit-ATG (Anti Thymocyte Globulin) 250 mg

Cyproheptadine 200ML

Dextromethorphan Hcl + Chlorpheniramine

Diatrizoic Acid Salts & Meglumine 66% & Sodium 10% & Iodine content 370 mg/ml 30 ml

Drotavarine

Each 15 ml contains: Milk of Magnesia 11.25 ml+ Liquid Paraffin 3.75 ml 170 ml

each 5 ml Containing : Paracetamol 125 mg + Ibuprofen 100 mg 60 ml

Enzyme 100 ML

Esomperazole

Fluconazole oral suspension

Furosemide Oral Solution 10mg/30ml

L-Carnitine 500mg/5ml in 30 ml

L-Carnosine 100mg/5ml in 200ml

Levofloxacin Oral Solution

Linezolid 100mg/5ml in 30ml

Mefenamice Acid 100mg/5ml

Mefenemic Acid 50 mg + Paracetamol 250 mg /60 ml

Melatonin 60 ml

Montelucast+Levocetrizine

Nitrofurantoin oral suspension 25mg/5ml in 100

Ondansetron oral suspension

Oxybutynin oral suspension5 ml

Phenobarbitone 20mg/5ml in 100ml

Prednisolone IP 50mg

Piracetam 500mg/5ml in 100ml

Potassium Magnesium citrate

Ranitidine oral suspension

Rifaximin

Sodium Bicarbonate oral suspension

Sodium Picosulphate oral suspension

Sorbitol + Tricholine Citrate

Sucralphate

Triclofos oral suspension500 mg/ 5ml in 30ml

Ursodeoxycholic oral suspension 125mg/5ml in 100ml

Zinc oral suspension 20 mg/100 Ml

/Susp. Azithromycin oral suspension 100mg/5ml

/Susp. Azithromycin oral suspension 200mg/5ml

Midodrine 5mg

Hydroxyurea 500mg

CoQ 300mg(Capsule of Co-enzyme Q10 with Lycopene,Selenium & omega 3 fatty acid )

Everolimus 5mg

Everolimus 10mg

Tacrolimus 0.25

Nintedanib 150MG

6-Mercaptopurine 20 mg

Acebrophylline SR 200 Mg

Aceclofenac + Thiocolchicoside

Aceclofenac SR 200 mg

Aceclofenac+Paracetamol+ Serratiopeptidase (100+325+15 mg)

Afatinib 20 mg

Afatinib 30 mg

Afatinib 40 mg

Alendronate Sodium 70 mg

Alfuzosin 10 mg

Alpelisib 150 mg (Monopoly)

Alpelisib 200 mg (Monopoly)

Alpelisib 250 mg (Monopoly)

Amantidine 100mg

Amisulpride 50 mg

Apixaban 2.5 mg

Apixaban 5mg

Aripiprazole 10 mg

Aripiprazole 5 mg

Aspirin IP 300 mg

Aspirin Dispresible 325mg

Atomoxetin 10 mg

Atomoxetin 18 mg

Atomoxetin 25 mg

Atroxentine 250mg (Trientine HCL)

Axitinib 5 Mg

Bilastin 20 MG

Biotin 5 MG

Bosentan 62.5 mg

Bosutinib 500 mg

Brivaracetam 50mg

Buprinorphine 2 mg

Calcium Acetate 667

Calcium Folinate 15 mg

Capmatinib 200 mg (Monopoly)

Carbimazole 10 mg

Cefixime + Potassium Clavulanate 200+125mg

Cefpodoxime proxetil 100mg

Cefpodoxime 200mg

Cefpodoxime CV 375

Chlordiazepoxide 25 mg

Chlordiazsepoxide 10 Mg + Clidinium 25 mg

Chlorthalidone 6.25 mg

Cholchicine 0.5mg

Cilostazol 50mg

Cilostazol 100mg

Clarithromycin 250 MG

Clarithromycin 500mg

Cilnidipine 5 mg

Cilnidipine10 mg

Cilnidipine 20 mg

Clonazepam 0.25

Clonazepam 1Mg

Clozapine 25 mg

Clozapine 50 mg

Clozapine 100 mg

Cotriamazole 480MGs

Cyproheptadine 4Mg

Cyproterone Acetate 2 mg +Ethynil Estradiol. 035mg

Dabigatran 150 mg

Dabigatran 110 mg

Dabrafenib 50 mg

Dacomitinib 15 mg (Monopoly)

Dacomitinib 30 mg (Monopoly)

Dapagliflozin 10 MG

Dapoxetine 30 mg

Dapsone 100 mg

Deflazacort 6mg

Deflazacort 12 MG

Desvenlafaxine 50mg

Diclo & Sera& Para.

Diclofenac + Thiocolchicoside

Dienogest 2mg

Diltiazem prolonged released 90mg

Dimethyl Fumarate120 mg

Dimethyl Fumarate 240mg

Disulfiram 125 mg

Disulfiram 250mg

Donepezil 5 mg

Duloxetine gastro resistant 20 mg

Duloxitine gastro resistant30 mg

Dydrogesterone 10mg

Eltrombopag 25MG

Eltrombopag 50MG

Empagliflazone 10mg

Empagliflazone 25mg

Entacapone 200 mg

Erlotinib 150 mg

Erlotinib 100mg

Esomeprazole 40 Mg

Estradiol Valerate 2 mg

Estradiol Valerate

Enzalupamide 40mg

Ethynil Estradiol 0.02mg+ Tab Desogestral 0.15mg

Etizolam 0.5 mg

Etoricoxib+thiocolchicoside(60+8 mg)

Exemestane 25 mg

Febuxostat 40 mg

Febuxostat 80 mg

Fexofenadine 120 MG

Fexofenadine 180 MG

Fingolimod 0.5 mg

Fludrocortisone 100Mcg

Flunarizine 10mg

Fluvoxamine 100 mg

Fluvoxamine 50 mg

Folinic Acid 15mg

Formaline

Furosemide 20mg + Spironolactone 50mg

Glucosamine hydrocloride + Diacerin 50 mg

Ibrutinib 140mg

Indomethacin 75 mg SR

Inositol + Myoinositol 1000mg

Ivermectin 6 mg + Albendazole 400 mg

Ivermectin 6mg

Ivermectin 12mg

Ketoconazole 200 MG

Lacosamide 50 mg

Lamotrigine Dispersible 100MG

Lapatinib 500mg

Lenalidomide 25MG

Lenalidomide 10 mg

Lenvatinib 4 mg

Lenvatinib 10 mg

Levetiracetam IP 250 mg

Levodopa+Carbidopa 125

Levodopa+Carbidopa+Entacapone 100mg/25mg/200mg

Levofloxacin 750 mg

Levosulpride 75mg

Levothyroxine Sodium 25 mcg

Levothyroxine Sodium 75 mcg

Linaglipitin 2.5mg

Linaglipitin 5mg

Lopinavir 200Mg+Ritonavir 50 mg

Loratadine 10 mg

Lorlatinib 25 mg

Lorlatinib 100 mg

Megestrol Acetate 160 mg

Melatonin 3 mg

Melphalan 2mg

Metolazone 5mg

Methimazole 5 mg

Methimazole 10mg

Methotrexate 7.5MG

Methotrexate 15mg

Methylphenidate 10 mg

Methylprednisolone 4mg

Methylprednisolone 16mg

Methylprednisolone 8mg

Meverberine 135 mg + Chlordiazepoxide 10 mg

Midostaurin 25 mg (Monopoly)

Mirabegeron 25 mg

Mirabegeron 50 mg

Mirtazapine 7.5mg

Mirtazapine 15mg

Mifepristone 25mg

Montelukast 4 mg

Montelukast 5 mg

Montelukast 10 mg

Morphine 10MG

Morphine 30MG

Moxifloxacin 400 Mg

Moxonidine 0.2 mg

Moxonidine 0.3 mg

N-Acetylecystine effervescent form, orange flavour, 600 mg

Naltrexone 50 mg

Nebivolol 5mg

Nebivolol 10mg

Nicorandil 5mg

Nicoumalone 1 Mg

Nicoumalone 3 Mg

Nicoumalone 4 Mg

Nifidipine 20MG

Nifidipine 20MG SR

Nilotinib 150 mg (Monopoly)

Nilotinib 200 mg (Monopoly)

Nilotinib 300mg (Monopoly)

Nitazoxanide 500mg

Nitrazepam 5mg

Nitrazepam 10 mg

Olaparib 50 mg (Monopoly)

Olaparib 150 mg (Monopoly)

Olmesartan medoxomil 20 MG

Orciprenaline 10 Mg

Osimertinib 80 mg (Monopoly)

Oxcarbazepine 300MG

Oxcarbazepine 450MG

Oxazepam 15mg

Pancreatin Gastroresistant 10,000MG(with proteiase & amylase)

Pantoprazole 20MG

Paracetomol 650 mg

Paroxetine 12.5mg

Paroxetine 25mg

Pazopanib 200mg

Pazopanib 400mg

Penicillin V 400MG

Pentoxifylline Extended Release/SR 400mg

Perampanel 2 mg

Perampanel 4mg

Pheniramine 25 MG

Phenozopyridine 200Mg

Pirfenidone 200 mg

Pirfenidone 400 mg

Piroxicam DT 20mg

Pomalidomide 2 mg

Pomalidomide 4 mg

Posacozazole 100mg

Posacozazole 40mg/ml

Prasugrel 10MG TAB

Prazosin 5MG

Prednisolone IP 40mg

Primidone 50 mg

Primidone 250 mg

Prochlorperazine 5mg

Progesterone only Pills

Propranolol 10mg

Propranolol 40 mg SR

Propylthiouracil 100 mg

Pyridoxine 100 mg

Ranolazine 500MG

Rasagiline1MG

Regorafenib 40 mg

Repaglinamide 0.5mg

Repaglinamide 1mg

Ribociclib 200 mg (Monopoly)

Rifampicin 150 mg

Rifampicin 450 mg

Rifampicin 600 mg

Rifaximin 200

Rifaximin 550mg

Rivaroxaban 10mg

Rivaroxaban 15mg

Rivaroxaban 20mg

Rizatriptan 10mg

Ropinirole 0.25mg

Rosuvastatin 10mg + Fenofibrate 160mg

Ruxolitinib 5 mg

Ruxolitinib 10 mg

Ruxolitinib 15 mg

Ruxolitinib 20 mg

Selegiline 5mg

Serratiopeptidase 10mg

Serratiopeptidase 20 mg

Sevelamer Carbonate 800 mg

Sildosin + Dutasteride

Silymarin 70mg.

Sitagliptine + Metformin (50/500)

Sildenafil 20 mg

Sofosbuvir 400 mg+ Velpatasvir 100 mg

Solifenacin succinate 10 mg

Sorafenib 200 mg

Sultamicin 375 MG

Sunitinib 12.5 mg

Sunitinib 25 mg

Sunitinib 50 mg

Tacrolimus 1MG

Tamsulosin + Dutasteride

Tapentadol 50mg

Tegafur + Uracil 100 mg

Tetrabenazine 25mg

Ticagrelor 90mg

Tofacitinib 5 mg

Tolvapatan 15mg

Topiramate 50MG

Torsemide 20mg

Tramadol 37.5mg + Paracetamol 325mg

Trametinib 0.5mg + Davarafenide 150mg (Monopoly)

Trimetazidine 35mg

Trimetazidine 60mg

Trypsin + Rutoside+Bromelain

Verapamil Hydrochloride Sustained Release 40

Verapamil Hydrochloride Sustained Release 120

Vildagliptin 50mg

Voglibose 0.2 mg Tab

Voglibose 0.3 mg Tab

Warfarin 1MG

Warfarin 2MG

Warfarin 3MG

Zinc 50MG

Zolpidem 10mg

Zonisamide 50mg

Zonisamide 100 mg

Tiotropium 9mcg Inhaler

Human Albumin 20% in 50 ml Vial

Tetanus Vaccine (Adsorbed) IP in 0.5 ml

Inj. Piperacillin 400mg & Tazobactam 500mg

Inj. Meropenam 1gm

Inj. Ceftriaxone 1gm

USG guided nerve stimilation needle (360 ultra)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

852 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)

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

857 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)

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

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

862 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)

865 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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870 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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894 Item No. (Detailed Description as per Technical Specification and Compliance Sheet)

895 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)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

915 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)

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

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

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

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

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

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

927 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)

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

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

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

Veiva Scientific India Pvt Ltd (BID ID -3167155)

Abbott Healthcare Pvt. Ltd. (BID ID -3172169)

Terumo India Pvt Ltd (BID ID -3172392)

Sahajanand Medical Technologies Limited (BID ID -3171597)

Ace Cardiopathy Solutions Pvt Ltd S (BID ID -3172105)

M/S SINGAPORE MEDICARE SYSTEM (BID ID -3172717)

Meril Life Sciences India Pvt.Ltd., (BID ID -3163693)

BOSTON SCIENTIFIC INDIA PRIVATE LIMITED (BID ID -3167943)

M/s St Jude Medical India Pvt Ltd (BID ID -3160471)

R R DISTRIBUTORS (BID ID -3170426)

LIFETECH SCIENTIFIC INDIA PRIVATE LIMITED (BID ID -3147926)

Trinika Healthcare (BID ID -3167740)

RENIX (BID ID -3171107)

India Medtronic Pvt. Ltd. (BID ID -3149994)

India Medtronic Pvt. Ltd.

M/s St Jude Medical India Pvt Ltd

Meril Life Sciences India Pvt.Ltd.,

PURPLE MICROPORT CARDIOVASCULAR PVT LTD

Veiva Scientific India Pvt Ltd

Trinika Healthcare

BOSTON SCIENTIFIC INDIA PRIVATE LIMITED

R R DISTRIBUTORS

RENIX

Sahajanand Medical Technologies Limited

Ace Cardiopathy Solutions Pvt Ltd S

Abbott Healthcare Pvt. Ltd.

Terumo India Pvt Ltd

M/S SINGAPORE MEDICARE SYSTEM