tender for evacuated closed blood collection tubes , evacuated closed blood collection tubes :- , 1) clot activator for serum with gel 3.5 ml, 13 x 75mm with yellow cap • should be sterile, evacuated and pet and single hand operation for capping and decapping. • it should be recommended of therapeutic drug monitoring. • it should be iso 13485 and us-fda /european ce approved. product code should be mentioned which is quoted and supplied to the institution. • it should be gamma sterile /eb as per current iso11137 guidelines. • batch wise sterility, pyrogenicity and toxicity certificate should be given. , 2) evacuated blood collection tube with spray dried k2edta with lavender cap • it should be made of clear latex free polyethylene terephthalate. size 13 x 75 mm with 3.0 ml(5.4 mg), volume capacity. • batch wise sterility, pyrogenicity and toxicity certificate should be given • it should be iso 13485 and us-fda /european ce approved. product code should be mentioned which is quoted and supplied to the institution. • it should be gamma sterile /eb as per current iso11137 guidelines. , 3) sodium citrate evacuated tube with tube-in-tube technology sealed from the top to avoid citrate leakage for coagulation test with vacuum (with na citrate - 0.109 mi ,3.2%) • it should be made of clear latex free polyethylene terephthalate with light blue hemogard, 13 mm x 75mm vol. 2.7 ml. • batch wise sterility, pyrogenicity and toxicity certificate should be given. • it should have tube-in-tube technology for full draw volume that reduced headspace thereby minimize platelet activation and provide accurate appt result • it should be iso 13485 and us-fda /european ce approved. product code should be mentioned which is quoted and supplied to the institution. • it should be gamma sterile /eb as per current iso11137 guidelines. , 4) evacuated tube for silica-clot activator/silicon coated made of clear latex polyethylene terephthalate with hemogard 13 mm x 75 mm, vol. 4.0 ml. o it should be iso 13485 and us-fda/european ce approved. product code should be mentioned which is quoted and supplied to the institution. o it should be gamma sterile /eb as per current iso11137 guidelines. • batch wise sterility, pyrogenicity and toxicity certificate should be given • adequate combustion data to prove that it is safe for the environment upon incineration. , 5) blood collection needle 21 or 22 gauge with cap and safety lock for evacuated tube. • it should be iso 13485 and us-fda /european ce approved. product code should be mentioned which is quoted and supplied to the institution. • it should be gamma sterile/eb as per current iso11137 guidelines. • batch wise sterility, pyrogenicity, toxicity certificate should be given. • it should have facility to lock the needle to reduce needle stick injuries and help in one handed use. • as per clsi recommendation it should be from same manufacturer of vacuumed blood collection tube and holder. , 6) evacuated tube for spray coated with sodium fluoride (3mg.), na2edta (6mg.) made of clear latex polyethylene terephthalate with hemogard 13 mm x 75 mm, vol. 2.0 ml. • it should be iso 13485 and us-fda/european ce approved. product code should be mentioned which is quoted and supplied to the institution. it should be gamma sterile /eb as per current iso11137 guidelines. • batch wise sterility, pyrogenicity and toxicity certificate should be given. , 7) evacuated tube needle holder with disposable release button • it should be iso 13485 and us-fda/european ce approved. product code should be mentioned which is quoted and supplied to the institution. • it should be gamma sterile /eb as per current iso11137 guidelines. • it should have release button to dispose the needle automatically. • as per clsi recommendation it should be from same manufacturer of vacuumed blood collection tube and holder. , 8) blood lancet for high blood flow. • medical grade, stainless steel and polymer blood lancet, super sharp tip for instant incision. sterile and individually pee label pouch pack. • needle gauge and depth (mm) should be at least 23g x 1.8 mm. • blood volume should be 100 - 250μl. • batch wise sterility, pyrogenicity and toxicity certificate should be given. o it should be iso 13485 and us-fda /european ce approved. product code should be mentioned which is quoted and supplied to the institution it should be gamma sterile as per current iso11137 guidelines.