Rate Contract For Lab Kits/Reagents/Consumable Items For Blod Bank Department At Jhalawar Hospital And Medical College, Jhalawar , Lab Kits/Reagents/Consumables , Anti A Blood Grouping (Anti A Monoclonal Serum) -10 Ml , Anti A Lectin -1X10 Ml , Anti Ab Antisera -1X10 Ml , Anti B Blood Grouping (Anti B Monoclonal Serum) -10 Ml , Anti D (Rn) Blood Grouping Serum -10 Ml , Anti H Lectin -1X10 Ml , Adhesive Plaster 4 Inch Wide , Band Aid Adhesive Strip , Blood Weighing Machine (0-1 Kg) , Bovine Albumin -1X10 Ml , Coombs Antisera -1X10 Ml , Double Blood Bag , Lancet , Multi Channel Tips (0.5-10 Ul-Compatible) -1X1000 , Multi Channel Tips (10-100 Ul-Compatible) -1X1000 , Multi Channel Tips (30-300 Ul-Compatible) -1X1000 , Multi Channel Tips (50-50 Ul- Compatible) -1X1000 , Pediatric Blood Bag , Rpr/Vdrl Test Kit , Rubber Ball For Donor Use , Signal Cpda 350 Ml Blood Bag Blood Collection Bag Made Up Of Dehp(Di-2-Ethyihexylphthalate)Plasticized Pvc Collapsible Non Vented Sterile Containers With Collecting Tube For Completely Closed System To Avoid The Chances Of Contaminating .Single Blood Bag Capacity -350Ml. Needle-16 Gauge Ultra Thin Walled And Straight . Blood Bagtube Should Have Multiple Printed Id/Segment Numbers . (External Port Should Be Tamper Proof And Shouldnt Be Recapped .Anticoagulant _Cpda-1(49Ml.)It Should Be Clear & Colour Less.) , Tissue Paper Roll , Torniquet Belt , Triple Blood Bag 450 Ml With Sagm Mother Bag Of Triple Blood Bag Should Have 450Ml Capacity With 63Ml Cpd Solution And Is Connected To One Satellite Transfer Bag Of 400Ml Capacity And One Satellite Transfer Bag Of 400Ml With 100Ml Sagm. Mother Bag Should Be 35Mm To 50Mm Thickness To Prevent Breakage During Centrifugation And The Inner Diameter Of The Tube Should Be Standard Measurement. Needle Should Be 16G With Triple. Bevel Design To Reduce Penetration Force And Enable Painless Vain Puncture. Blood Bags And Its Packing Should Be Properly Labeled With Batch No. Mfg Date And Date Of Expiry. Product Labels Should Be Bar-Coded As Per Rule. Complies To Iso 3826 And Quality Of Components Stored As Per Indian Drugs And Cosmetics Act. For The Manufacturers Have To Produce Documentary Evidence From The Laboratories Approved By Government Of India. , Weighing Machine (Donor) , Disposable Blue Tips For Microplpettes (2-200Ul) -1X1000 , Disposable Yello Tips For Microplpettes (200-10010Ul)- 1X1000 , Finn Pipette Variable Volume (100-1000 Ul) , Finn Pipette Variable Volume (10-100 Ul) , Hbsag Elisa Test Kit 4Th Gen. Hbsag Elisa Test Kits (Specification-Sensitivity & Specificity Should Be100% Must Be Able To Detect 0.5 Or Less Ng/Ml. 4Th Generation Hbsag)- Test Kits Must Have A Long Shelf Life. Detects All Known 11 Sub-Types Of Hbv And Also Mutant Strains Can Be Used On Any Manual/Semi-Automatic System Of Elisa. 1X96 Test. 1. The Kit To Be Procured Should Have Approval Of The Statutory Authority In Its Country Of Origin. 2. In Case Of Imported Kits It Should Have Been Registered And Licensed In India By Dcg (I). 3. In Case Of Indigenous Manufacturers They Shall Have License Issued By The Competent Authority Defined Under Drugs And Cosmetics Act, 1940, After Appropriate Evaluation By The Centers Approved By Dcg (I). , Hbsag Rapid Test Kit (Rapidtest) 4Th Gen. Specification-Sensitivity & Specificityshould Be100% Must Be Able To Detect 0.1 Or Less Iu/Ml . It Should Detects Major Vaccine Escape Mutants14t126n,T126s,Q129r,Q129hq129l,M133h,M133l,K141e,P142s,T143k,D144a,G145r,T123a,P120q It Should Have Single Step Procedure ,Subtype Serotype-A/H,A/E,A/F,D/G,D/F,D/G Specimen : Serum/Plasma, Finger Stick Whole Blood And Vein Puncture Whole Blood , Hcv Elisa Test Kit, 4Th Generation 1. Microplate Elisa Coated With Recombinant/Synthetic Peptide Antigens For Core, Ns3, Ns4 And Ns5 And Antibody To Hcv Core Antigen. 2. 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 Provided With Each Kit. 3. The Kit To Be Procured Should Have Approval Of The Statutory Authority In Its Country Of Origin. 4. In Case Of Imported Kits It Should Have Been Registered And Licensed In India By Dcg(I). 5. In Case Of Indigenous Manufacturers They Shall Have License Issued By The Competgent Authority Defined Under Drugs And Cosmetics Act 1940. After Appropriate Evaluation By The Centers Approved By Dcg(I). 6. The Kit Should Have Minimum Shelf-Life Of 5/6Th Or 12 Months (Whichever Is More) At The Port Of Discharge Of Consignees. 7. The Assay Component Should Include Reactive (For Both Antibody And Antigen) And Non-Reactive Controls. 8. The Assay Should Have A Sensitivity More Thanor Equal To 100% And Specificity Of More Than Or Equal To 98%. 9. The Manufacturer/Authorized Agent Should Ensure Maintenance Of Cold Chain During Storage & Transport The Kits At 20C-80C. The Cumulative Time Temperature Indicator Technology Used Should Be Pre-Qualified By Who And Placed On Every Pack Of Kits. 10. The Pack Size Should Be 96 Tests/Kit. , Hcv Rapid Dot Test(Must Be 100% Sensitivity And Up To 100%. – 4Th Generation Hcvshould Be Based On Flow Through Technology Results In Less Than 3 Minutes, Highly Purified Hcv Antigens For Core, Ns3, Ns4, Ns5 Immobilized On The Device). Hcv Should Be Able For The Detect Antigen Core Ns3, Ns4, Ns5 Regions , Hivelisa(Competitive) Test Kit, 4Th Generation 1. Should Be Solid Phase Micro Plate Coated Hiv I & Ii Recombinant And/Or Synthetic Peptide Antigens And Antibody To Hiv 1 P 24. 2. The Assay Should Detect Hiv I And Ii Antibodies And Hiv 1P24 Antigen. 3. Adequate Documents Detailing The Principle, Components, Details Of Antigen For Antibody Detection Of Hiv 1 And 2 And P24antigenm Bio-Safety, Methodologies, Validity Criteria, Interpretation Of Results, Performance Characteristics, Storage Conditions, Limitation Of Assays, Manufacturing & Expiry Dates Should Be Provided With Each Kit. 4. The Kit Should Have Approval Of The Statutory Authority In Its Country Of Origin. 5. 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. 6. In Case Of Indigenous Manufacturers Should Be Licensed Under The Provisions Of Drugs & Cosmetics Act And Rules Or Medical Devices Rules 2017 Issued By The Competent Authority Defined Under Drugs And Cosmetics Act, 1940. 7. The Kit Should Have Minimum Remaining Shelf0life Of 5/6Th Or 12 Months (Whichever Is More) At The Port Of Discharge Of Consignees. 8. The Assay Component Should Include Reactive (For Both Antibody As Well As Antigen) And Non-Reactive Controls With Each Kit. 9. The Assay Should Have Sensitivity Level Of 100% And Specificity Level Of More Than Or Equal To 98%. 10. The Manufacturer/Authorized Agent Should Ensure Maintenance Of Cold Chain During Storage And Transport The Kits At 20C-80C. The Cumulative Time Temperature Indicator Technology Used Should Be Pre-Qualified By Sho And Placed On Every Pack Of Kits. 11. The Pack Size Should Be 96 Tests/Kit. , Hiv Rapid Dot Test (Specification – 4Th Generation 1. Should Be A Solid Phase Coated Hiv I & Hiv Ii Recombinant And/Or Synthetic Peptide Antigens And Antibody To Hiv I P24. 2. The Assay Should Destec Hiv I And Ii Antibodies And Hiv 1 P24 Antigen In Plasma, Serum Or Whole Blood. 3. Adequate Documents Detailing The Principle, Components, Details Of Antigen For Antibody Detection Of Hiv 1 And 1 And P24 Antigen, Biko-Safety, Methodologiesm, Validity Criteria, Assays, Manufacturing & Expiry Dates Should Be Provide With Each Kit. 4. The Kit Should Have Approval Of The Statutory Authority From The Country Of Origin. 5. In Case Of Improtd Kits, It Should Be Registered And Licensed Under The Provisions Of Drugs & Conmetics Act And Rules And/Or Medical Devices Rules 2017 In India. 6. In The Case Of Indigenous Manufactuers Should Be Licensed Under The Provisions Of Drugs & Cosmetics Act And Rules And/Or Medical Devices Rules 2017 & Also Be Evaluated By The Centers Approved By Dcg(I). 7. The Kit Should Have Minimum Shelf-Life Of 5/6 Or 12 Months (Whichever Is More)At The Port Of Discharge Of Consignees. 8. The Time Required For Performing The Test Should Not Be More Than 30 Minutes. 9. The Control Dot/Band Should Be Able To Detect The Presence Of Human Immunoglobulins And Should Not Be Just A Procedural Control Or Meant For Merely Checking The Flow Of Reagents Or Intergrity Of The Antigen. 10. The Assay Should Have Sensitivity Of 100% And Specificity Of More Than Or Equal To 98%. 11. The Manufacturers Should Ensure That : A) The Test Kits Should Be Packed Such That There Is A Provision To Conduct Single Test At A Time. B) The Assay Components Should Include Hiv Positive (Both Antigern And Antibody Positive) And Negative Serum Control Sufficient For Conducting 20% Of The Test (10% Negative And 10% Positive Controls) : And C) The Pack Size Of Hiv Rapid Test Kits Should Not Be More Than 50 Tests Per Kits. 12. The Manufacture/Authorized Agent Should Ensure Maintenance Of Cold Chain During Storage & Transport The Kits At 200C-800C. The Cumulative Time Temperature Indicator Technology Used Should Be Pre-Qualified By Who And Placed On Every Pack Of Kits. , K-3 Edta Vial 1X100 , K-2 Edta Vial 1X100 , Parle Biscuits - 20 20 Cashew Butter Cookies (75Gm) Butter Bite Parle Gold , Malaria Card Detection Of P Falciparum (Hrp-2) And P Vivax (Pldh) Malaria Antigen , Test Tube Stand 48 Hole Plastic , Test Tube Stand 96 Hole Plastic , Plain Vial , Rh View Box , Microscope Slide , Small Test Tube , Dropper , Graduated Flask And Beaker – 100Ml. , Graduated Flask And Beaker – 500Ml. , Graduated Flask And Beaker – 1000Ml. , Orange Juice , Microscope Slide Cover Slips , Leukocyte Reduction Filter System For Red Blood Cells. Features 1. Easy To Operate, Without Amendment User Habits. 2. Even At 40C Low Temperature, Puriblood Leukocyte Reduction Filter Still Have High Filtration Speed, High Leukocyte Filtration Efficacy, High Rbcs Recovery And Low Hemolysis Ratio. 3. High Filtration Speed Can Applicable To Emergency Surgery Transfusion Requirements Needs. Specifications Capacity : 1~2 Unit Blood (1 Unit=250Ml) Flow Rate : Approximately 50Ml/Min. Leukocytes Reduction Rate >99.9% Rbcs Recovery Rate> 95% Application: Hospital Bedside, Direct Transfusion. , Ice Pack Gel , Distlled Water 5 Ltr. , Stand For Blood Grouping Antisera , Blood Bag Multifunction Hand Stripper Should Certified By Ce & Ios9001 , Ph Strips 0.0-6.0 Ph, Resolution : 0.5Ph Unit (50 Strips) , Ph Strips 6.0-7.7Ph, Resolution : 0.3-0.4Phunit )50 Strips) , Ph Strips 7.0-14.0 Ph, Resolution: 0.5Ph Unit (50 Strips) , Ph Buffer Capsules (3 Standard Buffers- Ph4, Ph7 & Ph10)-2 Each , Specific Gravity Meter , Sodium Hypochlorite Solution 4% (5 Liters Per Bottle) , Copper Sulphate Cuso4.5 H2o-Ar Grade (500 Gm Sper Pack
