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Tender For 01 (2025-26) 01 (2025-26) Item No. 01 Cardeothoracic Equipments And Implants - Titanium Ligaclips small with Small diamond shape pyramidal heads, similar to needle holder Inserts, ensuring a firm multi-directional atraumatic grip. Interlocking atraumatic teeth designed for non-slip closure on the vessels. Triangular shape of the titanium wire for the precision of the positioning of the clip into the jaws of the applier. Should be US FDA Approved. Titanium Ligaclips medium with Small diamond shape pyramidal heads. similar to needle holder Inserts, ensuring a firm multi-directional atraumatic grip. Interlocking atraumatic teeth designed for non-slip closure on the vessels. Triangular shape of the titanium wire for the precision of the positioning of the clip into the jaws of the applier. Should be US FDA Approved. Titanium Ligaclips large with Small diamond shape pyramidal heads, similar to needle holder Inserts, ensuring a firm multi-directional atraumatic grip. Interlocking atraumatic teeth designed for non-slip closure on the vessels. Triangular shape of the titanium wire for the precision of the positioning of the clip into the jaws of the applier. Should be US FDA Approved. Proximal aortic anastomosis device. It should provide stable blood field It allows for up to three anastomosis from one insertion. Size -3.5mm/4.0mm/4.5mm Membrane Oxygenator (Plasma resistant) with integrated arterial filter. Should have surface area with surface area of 1.4 m2. It should have radial blood flows design to give efficient gas transfer. It should have quick priming inlet and vacuum assisted venous drainage. Oxygenator Should have self-venting facility. Integrated arterial filter should be polyester/polycarbonate/equivalent material. Integrated arterial filter pore size should be less than 40 micron with the surface area of around 60-80cm2. Priming volume of around of less than 285ml visible path top to bottom should have maximum flow for large body surface area patient ranging from 0.5 to 6 L/M. Should have phosphoryl choline (PC) coating like phisio. Should be able to operate at venous reservoir level of minimum 150 ml. Oxygenator reservoir should have polycarbonate/polyester/equivalent screen type venous filter with pore size less than 50 micron. Should be US FDA Approved. Should be supplied with Appropriate stand. UW Solution for organ transplant use. Dacron Graft knitted Bioseal Grafts diameter 6mm to 8mm length 30 cm Dacron Grafts knitted Bioseal diameter 6mm to 8mm length 60 cm Dacron Grafts woven Bioseal diameter 20mm to 32mm length 30 cm Aortobifemoral bioscal graft dacron sizes-6x12x45/7x14x45/8x16x45 CORONARY OSTEAL CANNULA 10FR/12FR/14FR INTRA CARDIAC SUMP 20FR/12FR ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 20 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 40 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 50 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 60 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 70 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 100 cm US FDA Approved ePTFE Grafts Plain Straight diameter 6mm/7mm/8mm length 75 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 20 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 40 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 50 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 60 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 70 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 75 cm US FDA Approved ePTFE Grafts ring reinforced diameter 6mm/7mm/8mm length 100 cm US FDA Approved Jodine Impregnated Incision Drape, Size 55cm x 45 cm (Ahesive Area) Should be Gamma Sterilize. Should be polyurethane adhesive coated surgical film with povidone iodine. Transparent and breathable surface and hold drape securely in place. Test report from NABL certified lab to be submitted. The product should be CE/IS certified lah. The company should be EN 1499:2013. It Should be ISO 13485:2016 & ISO 9001:2015 approved. Certificate of Registrations issued by United Registrar of Systems. Document recognised by Member of Multilateral Recognition Arrangement. Certified by UKAS Management Systems Surface and Air Sterilizer for ICUs and OTs sterilization. It should be next generation photocatalytic oxidation technology based sterilizer. It should be without chemical. It should offer surface sterilization, air sterilization and air purification. It should be without any physical filter. Should have zero maintenance. Servator HTK solution for organ transplant uses. Perfadex lung preservation Solution for lung transplant use. SMMS Surgical Gowns (ILXL): CE,ISO, TUV, EN13795 marked, GOWN AAMI Level 4 Blood Penetration test ASTM F1670 & Viral Penetration test ASTM F1671 Transparent Carrier film 100% polyurethane, skin-friendly polyacrylate adhesive with free of colophony and colophony derivatives and Wound pad with absorbent layer made of viscose/polyester, polyester/poly-ethylene wound contact 4x10 Inch, CE & ISO Certified Nonwoven base material: white, 100% polyester, polyacrylate adhesive with free of colophony and colophony derivatives Wound pad with absorbent layer made of viscose and polyethylene/poly-propylene, wound contact layer made from polyethylene 4x13.6 Inch,CE & ISO Certified Class 1 EC Medical Device with Accuracy and waterproof adhesive thermochromic temperature indicator with three colour code Rectangular shape and rounded corners with monitoring window, having MVTR in the area of fixation: 964 g/24h/m² die-cut opening. lengthwise elasticity additional sterile cushioning pad with fixation size-5.5x6.5 CM.CE & ISO Certified CVC Dressing with ergonomic shape film with porous adhesive coating. monitoring window large film-nonwoven laminate counter fixation element with V-shaped cutout lengthwise elasticity additional sterile cushioning pad size 9x11 CM,CE & ISO Certified wide retention polyester wound dressing having polyacrylate strip patterned adhesive coating with MVTR more than 5000 g/m2/24hr and air permeability more than 4000 g/m2/24hr. SIZE 10cmx10m,CE & ISO Certified Graduated compression stockings with Below Thigh having pressure gradient 16-18mmhs/material composition 91% nylon polyamide, 9% lycra elastane, Color coding with extra gussette Size S,M,L,XL,XXL Central Venous Catheter adult 3 lumen 5,5.5 & 7Fr & 14,15 & 16 cm length with raulerson syringe to reduce blood loss, Non kinking guide wire made up of 45% titanium & 55% nickel, with CE,ISO & HTCert certified Vacuum line cleaner, contains qac with non ionic surfactant 2.5, with 92.76 inert ingredients should accumulate bio film and kill biofilm forming microorganisms should have recommendation of Ada pack size 1 ltr. Should be ISO 13485:2016 & ISO 9001:2015 approved. Certificate of Registrations issued by United Registrar of Systems. Document recognised by Member of Multilateral Recognition Arrangement. Certified by UKAS Management Systems Paraffin Ip grade, non ionic surfactant contains butane, base should be highly purified mineral oil, for optimum lubrication. Should be ISO 13485:2016 & ISO 9001:2015 approved. Certificate of Registrations issued by United Registrar of Systems. Document recognized by Member of Multilateral Recognition Arrangement. Certified by UKAS Management Systems Sterile hands for rub CHG 2,5% v/v, Ethanol 70% v/v Broad spectrum bacteriacidal including MRSA, VRE. Should be ISO 13485:2016 & ISO 9001:2015 approved. Certificate of Registrations issued by United Registrar of Systems. Document recognised by Member of Multilateral Recognition Arrangement. Certified by UKAS Management Systems 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/Hiac Extension Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethlene - Available from 10 mm to 28 mm Diameter and up to 199mm 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 70mm 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 Graft Stent for Aneurysm of Abdominal Aorta Aorto Uni Iliac -Nitinol Stent Graft System with multi filament polyester graft material, Ultra High Molecular Weight Polyethiene 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 endograft molding. Apposition of stent grafts in seal zone, for temporary aortic occlusion 12F Compatible, Balloon can get dilated from 10 mm to 46 mm. Introducer sheaths for access. Available from 12F to 16F Available with 28 cm Length and valves Introducer sheaths for access. Available from 18F to 26F Available with 28 cm Length and valves Venous self-expanding stent system is intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction. Tri-axial shaft design controls friction and stabilizes stent position during deployment. Rotating thumb wheel offers predictable placement and auditory feedback. Patented open-cell design with offset connection points delivers flexibility. Three connection points between cells optimize flexibility with stable deployment. nique strut design, rigorous finishing, optimized heat-treating processes and the highest quality nitinol-help us deliver durability over time, consistent 9 F delivery system across our full matrix for a simplified procedure Catheter length of 90 cm that supports all three access sites and can be used with a standard length guidewire. Self Expandable Nitionol venous stent. Sizes Available 10,12,14,16,18,20mm(Diameter) 40,60,80,100,120,150mm(Length) AORTIC ROOT CANNULAE 4FR AORTIC ROOT CANNULA WITH VENT LINE 7FR 0.021 platinum coils, Hellicaly designed detachable coils, Detachable coils enclaced with Nylon/ PGLA fiber, Available in diameter of 2-20mm and lengths upto 50 cm. To be delivered through a microcatheter, Fully resheatable after partial deployment and repositionable, Instant mechanical detachment Microcatheter, End hole single lumen catheter, usable length ranging from 13 cm 153 cm depending on catheter profile, available in 021 and 027 distal diameter, continuous staineless steel construction, Hydrophilic outer coating, PTFE inner liner, DMSO Compatible Self-Expanding Nitinol stent to treat Carotid stenosis. 0.014 system with 6 Fr crossing profile. No foreshortening. Proprietary EXPRT Release technology to prevent stent jumping. Anatomically designed tapered stent. Tantalum Marker on catheter to indicate tapered location CE Mark, DCGI and FDA approval CE Mark, DCGI and FDA approval Embolic protection device with Rx exchange system. Available in diameters from 3 mm 7 mm sizes. Works with 014 & 018 system. Heparin coated filter. Braided Nitinol design filter for full wall apposition. Proximal mouth indicator for visualization of filter mouth. Longitudinal and rotational filter movement. 6Fr guide and 5 Fr sheath compatible. Preloaded capture wire of 320 cms CE Mark, DCGI & FDA approval Self-Expanding Nitinol Stent Spiral cell connection for flexible design. Available in diameters from 5mm to 10mm. Lengths available from 40 mm to 200 mm. 0.035 compatible 6 Fr delivery system CE Mark, DCGI & FDA approval Balloon Expandable stent Stainless steel stent, Proximal & Distal stent markers. Available in Diameter of Smm to 10 mm. 0.035 Compatible OTW system. 6 fr & 7 fr delivery system CE Mark, DCGI & FDA approval 0.035 Balloon with OTW system Flexitec xtreme halloon material for high pressure dilatation. Hydrophilic coating to facilitate crossing. Diameters from 4 mm to 12 mm. Lengths available 20mm-200 mm. Large inflation lumen for fast deflation time CE Mark, DCGI & FDA approval 0.014 atherectomy device system in 6Fr & 7 Fr. Plaque excision system. Torquer knob to directionally target eccentric and concentric plaque Cutter rotation speed at 12000 rpm CE Mark, DCGI & FDA approval Paclitaxel coated balloon for SFA & Fem pop lesions. Drug concentration 3.5micro gm/mm square. Excipient Urea to facilitate drug transfer. Diameter from 4mm-7mm balloon. Lengths from 40 150 mm. Syr follow up on clinical trials CE Mark, DCGI & FDA approval, Nitinol wire, Silicone coating. 0.014, 018, 035 diameter, 180 cm, 300 cm length CE Mark, DCGI & FDA approval,0.014 OTW halloon, Tapered tip for better control on navigation. Tapered balloon in long lengths. 4 Fr & 5 Fr device profile. Diameter 1.5mm 6mm. Lengths 20 mm-210 mm CE Mark & FDA approval,0.035 OTW balloon, High pressure balloon with RBP 16-24 atm. Device profile 6 Fr-7 Fr. Diameter 4mm 12mm. Length 20mm-100mm 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 SFr, 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, 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. 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. Two in one device, Guide-extension with trapping capabilities, Trapping balloon positioned proximal to the half-pipe channel, pushrod, Gold marker band under proximal end of balloon, Hypotube pushrod, Half pipe channel, Hydrophilic coating, coil reinforced guide extension, Radio-opaque marker 2mm from distal tip & 4mm from collar, White positioning markers at 95cm & 105cm, Sizes-6F, 7F & 8F, Working length-150cm, 13cm Rapid exchange length, Nominal pressure -12atm. Rated burst pressure-14 atm, Trapping Balloon length -11mm, 3.1 mm unrestricted balloon OD. IABP balloon catheter. Should be compatible with existing machine Balloon volumes 40cc Catheter profile of 7/7.5/8fr with guide wire and introducer sheath and dilators. Should be kink resistance with wire-reinforced catheter body. Should be CE and USFDA Approved Biomechanical vascular closure device for large bore femoral arterial access site closure. Should be available in 14 Fr. and 18 Fr. It should be effectively closes femoral arterial access sites following the use of sheaths ranging from 12 Fr. to 25 Fr. O.D. Endobronchial blocker tube with auto inflation button. Should available in 5fr.7fr and 9fr. Hybrid Stent Graft System for aortic arch and descending thoracic aorta repair with the frozen elephant trunk (EFT). Should be available in straight, branched and trifurcation configurations. Surgical sealant should seal, adhere and reinforce tissue, and it should be used in a variety of indications and applications. Mechanical Bileafleat prosthetic Heart Valve. Bileafleat prosthetic Heart valve with opening angle 90 degree made of pyrolytic carbon (mitral aortic) of all sizes. Should have minimal gradient across the valve in vitro and vivo. The housing of prosthesis should be rotatable to give optimal positioning for the valve with titanium stiff ring, should be in use for more than 20 year and acceptability by cardiac surgeon, low profile sewing ring made up of polyester, should be radio opaque during X-ray and fluoroscopy Expiration date should be 3 years from the date of purchase. Should be USFDA approved. Tissue Heart Stabilizer should have flexible arm, which can mount a malleable vacuum suction foot for beating heart surgery, and a flexible mounting to fit on all size of retractors either for Mid sternotomy or thoracotomy. The arm should also be able to mount malleable retractor for retracting lung other tissue as well. The arm should also be able to mount Starfish. The Foots, Starfish and retractor should also be separately available. Heart Stabilizing system for Minimally Invasive coronary artery bypass surgery Tissue Heart Stabilizer arm shall facilitate approach from left thoracotomy to stabilize desired area of the heart. The foot attachment end must be flexible for adjustment inside the cavity for better positioning during minimally invasive coronary artery bypass surgery. The arm must be able to attach both foot and starfish. The Foot and starfish should be available separately. The mounting arm shall be sperate. Rotational atherethrombectomy catheter for removal of thrombus and atheroma to treat native vessels, stenosed stent and stent graft from acute to chronic materials, system that comes in 3 sizes 6F and 8F to treat vessels from 3-12 mm available in catheter length 110 cm, 135 cm and 85 cm in combination of Nitinol guide wire, collecting bag (2000 ml) and sterile drape (for motor or footswitch Dimension: 3400 mm x 185 mm) Mechanical thrombectomy catheter for removal of acute thrombus from native vessels, stenosed, stent graft and bypass graft, system that comes in 3 sizes 6F, 8F and 10F to treat vessels from 3-12mm available in catheter length 110cm. 135cm and 85cm in combination of Nitinol guide wire, collecting bags (2000ml) and sterile drape (for motor or footswitch Dimension: 3400 mm x 185 mm) Portable drive system, combination of a motorized control unit and handle clubbed with catheter system for rotational atherethrombectomy and mechanical thrombectomy procedures. The system should have foot switch padel for operator convenience. Ulta high pressure non compilant PTA dilation Balloon Catheter - 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. Retrieval IVC Filter (window period 300 days)- Clinically tested in Largest, longest IDE filter study demonstrated safely implanted to provide immediate protection against PE,Optional IVC Filter, two levels of filtration with the legs providing the lower level of filtration and the arms providing and the arms providing the upper level of filtration, Highly visible snare tip seamlessly welded to the body for easy filter retrieval even after long in-dwell times. the upper level of filtration Self expandable (electro polished) with 4 radiopic markers - The Stent (Implant) should equipped with four highly visible radiopaque PUZZLE Tantalum Markers on both the proximal and distal end for ACCURATE PLACEMENT. It Should a self-expanding, flexible, nitinol (nickel-titanium alloy) stent that expands to its preset diameter upon exposure to body temperature. The stent has a segmental repeating pattern and an open cell geometry with flared ends to help prevent dislocation or migration. Partial cuts around the circumference of the stent cylinder provide enhanced flexibility and allow segment-by-segment expansion. It should 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. Self expending and Popliteal Nitinol Stent with Unique triple Helix design Structure 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. It should 5F Vascular Stent System and intended to improve luminal diameter in the treatment of symptomatic de novo or restenostic lesions up to 240 mm in length in the native superficial femoral artery (SFA) and popliteal artery with reference vessel diameters ranging from 5.0-7.0 mm. USFDA approved Ulta high pressure non complaint balloon-It should for use in Percutaneous Transluminal Angioplasty of the femoral, iliac, and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. High performance balloon catheter consisting of an overthe-wire catheter with a balloon fixed at the distal tip. The proprietary ultra non-compliant, low profile halloon 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 Balloon Expandable Vascular Covered Stent-It should 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 should comprised of an electropolished balloon-expandable stent made from 316L stainless steel, encapsulated between two layers of ePTFE. The covered stent should supplied pre-mounted on an over-the-wire delivery system with a non-compliant balloon Drug Coated Balloon-Drug Coated Balloon with 2 µg/mm2 dose of paclitaxel with polysorbate & Sorbitol as Carrier which will Deliver an optimal, therapeutic drug dose to the target vessel wall after a minimum 30 second inflation time. Available in sizes-035 guidewire compatible 120 cm shaft-4mm-6mm dia, length upto 150mm, 035 guidewire compatible 75cm shaft-5mm 12 mm dia, length 60mm, 014 guidewire compatible 150 cm shaft-2mm to 3.5mm dia, length 120 mm PTA Dilatation Catheter semi-compliant balloon catheter consisting of an over the wire (OTW)- It should semi-compliant balloon catheter consisting of an over the wire (OTW) catheter with an angioplasty balloon fixed at the distal tip. Two radiopaque markers delineate the working length of the balloon and aid in balloon placement. intended to dilate stenoses in the peripheral arteries, to treat obstructive lesions of native or synthetic AV fistulae and/or re-expand endoluminal stent graft elements in the iliac arteries. 3-12 diameter range and 20-300 balloon length. PTA Dilatation Catheter semi-compliant hydrophylic balloon catheter consisting of an over the wire (OTW) It should 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 should present on the distal segment of the shaft and the balloon Dual Sheath 9Fe and 11Fr, ideal for IVC filter retrieval Dual Sheath 9Fr and 11Fr, ideal for Denali 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 Ulta high pressure non complaint balloon It should for use in Percutaneous Transluminal Angioplasty of the peripheral vasculature, including the iliac arteries and iliac and femoral veins, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae, a high performance balloon catheter consisting of an over-thewire catheter with a balloon fixed at the distal tip. The proprietary non-compliant, low profile balloon is designed to provide consistent balloon diameters and lengths even at high pressures Ultra high pressure large volume inflation device (30 ml)- An ultra high pressure, large volume inflation device used to inflate, monitor pressure, and deflate angioplasty balloon dilatation catheters. It should a onepiece, 30 ml disposable inflation device rated for 40 atm with a lever-lock design that controls the piston, a manometer, and a high-pressure connecting tube with a male Luer rotating adapter. Also enclosed is a high-pressure 3-way stopcock to aid in preparation and use of the device. The manometer measures pressures ranging from 0 atm up to 40 atm in 1 atm increments. The accuracy of the manometer has been determined to be within 1.6 ATM. These products are not made with natural rubber latex Flexible self-expanding prosthesis comprising of dual layer ePTFE encapsulation with carbon impregnation-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 High-performance crossing catheter-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, lem radiopaque markers positioned lem apart with double markers dilenate 10cm and 20cm. Self expanding nitinol stent It should self expanding nitinol stent is FDA approved for treatment of Iliac Occlusive disease in patients with Symptomatie vascular disease of common or external iliac arteries, residual stenoses, with impaired perfusion following balloon dilatation. It should has optimized pin and pull delivery system for precise placement. High visibility for stent deployment and relocation under fluroscopy. 0.035 guidewire compatible, diameter sizing of stent to target lesion reduces stent migration Self expandable cover stent graft, Dual layer ePTFE It should Vascular Stent Graft is used in Residual Stenosis with impaired perfusion following balloon dilation especially in stages III & IV according to Fontaine dissection; detached arteriosclerotic plaque material luminal obstruction following balloon dilatation; occlusion after thrombolysis or after aspiration or dilatation, restenosis or re-occlusion, Proven 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 den onstrated kink resistance after placement in tortuous lesions presenting with in-stent restenosis or non stented lesions in patients Embolectomy catheter no. 2,3,4,5,6 and 7 colour code balloon capacity 2 ml with steel wire. Should be US FDA Approved. Flo Trac Sensor Arterial Pressure Cardiac Output sensor compatible with VIGILEO/EV1000/Hemosphere monitor to provide CO.CI,SV.SVISVV,SVR & SVRI on continuous basis when connected with patient arterial pressure line. Should be US FDA Approved. One Disposable pressure transducer with flush device & vent stopcock. IV set, 2 three way stopcocks & 48 12 pressure tubings. Gold-plated connector wires for high-fidelity signal transmission Design features a straight fluid path across the pressure sensor for easy priming and minimal waveform distortion. Available with a Snap-Tab flush device that can be easily gripped and stretched 360 to quickly and casily flush the system and generate a square-wave test pattern. Fluid-resistant cable connector. It should have a flow rate of 3+/-1 m/hr under 300 mm Hg IV bag pressure. Should be US FDA Approved. Double Disposable pressure transducer with 2 flush devices & vent stopcocks, trifurcated IV set, 4 three way stopcocks & 2 sets of 48+ 12 pressure tubings. Gold-plated connector wires for high-fidelity signal transmission. Design features a straight fluid path across the pressure sensor for easy priming and minimal waveform distortion. Available with a Snap-Tab flush device that can be easily gripped and stretched 360° to quickly and easily flush the system and generate a square-wave test pattern. Fluid-resistant cable connector. It should have a flow rate of 3+/- 1 ml/hr under 300 mm Hg IV hag pressure. Should be US FDA Approved etc.
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