| | Sector | abcEducation And Research Institute | Tender Value | INR 10 Crore | | Location | Rajasthan - India | Ref.No | 82967873 | | Closing Date | 08 - May - 2025 | | | | Supply of 01(2025-26) Item No. 01 Cardiothoracic 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 Bioseal 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, Iodine 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 Lab. the Company Should Be En 14992013. It, Should Be Iso 134852016 & Iso 90012015 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 (llxl) Ce, Iso, Tuv, En13795 Marked, Gown Aami Level 4 - Blood, |
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