Name of Work:- SHORT TERM E-BID FOR RATE CONTRACT CUM SUPPLY AND EMPANELMENT OF SURGICAL ITEMS
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Item Description
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\\"SyphilisAntibody (Rapid) detection kits1. The assay should be based on Rapid chromatographic immunoassay for qualitative detection of Antibodies (lgG, lgA & lgM) to TP in serum, plasma & whole Blood.2. The assay should utilize recombinant Treponemal antigens i.e. Tp15, Tpl7, Tp47 against Syphilis.3. The assay should be in card format.4. Adequate documents detailing the principle components, bio- safety methodologies, validity criteria, interpretation of results, performance characteristics storage conditions, limitation of assays manufacturing & expiry dates should be provides with each kit.5. The kit should have approval of the statutory authority in its country of origin.6. In case of imported kits it should be registered and licensed under the provisions of Drugs & Cosmetics act and rules and/or medical devices rules 2017 in India.7. In case of indigenous manufacturers should be licensed under the provisions of Drugs & cosmetics Act and rules and or medical devices rules 2017 issued by the competent authority defined under Drugs and cosmetics act, 1940.8. The kit should have minimum shelf- life of 5/6th or 12 months (whichever is more) at the port of discharge of consignees.9. Read result time should not be more than 20 minutes.10. Assay should have Sensitivity 100% & specificity 99 %or more with documentary evidence.11. The storage & transport temperature of the Kit should be 2-30°C.12. The pack size should not be more than 50 tests wherein each test is individually\\"
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Bed Side Leucodepletion Filters for Blood Transfusion (For 2 unit of Red Cell) [NE32B] 1. Filters should be able to leucodepletered cells form leukocytecontamination separately for 1 unitof red cells and for 2 units of redcells each.2. Filters should be having thecapacity of log 4 reduction(99.99%)3. Filters should not carry anycharges it should be neutrallycharged.4. Filters material should bepolyester woven / non- woven.5. Leukocytes should beconsistently averaging less than0.5x105 residual leucocytes forone unit of red cell and 0.2*106for two units of red cell. RBCrecovery should be averaging morethan 90%.6. Filters should have hard / softhousing for optical monitoring.7. Filtration loss should not bemore than 35 ml for one unit redcell.8. Should have integrated ≥ 40 μm,micro aggregate filter.9. Should be US FDA/ EuropeanCE Certified.
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Hepatitis B Surface Antigen (Elisa) Testing Kits IV Generation/High sensitiveShould have Microplate ELISA Coated with either polyclonal or monoclonal antibodies to HBsAg and either polyclonal or monoclonal antibodies in conjugate. The assay should be able to detect all the 11 subtypes (ad & ay subtype) including mutant strains. The assay should be able to detect surface antigen to hepatitis B virus.
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HBsAg (Rapid Test) Please Enable Macros to View BoQ information
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