Tender For Kits Chemical Reagent Glassware Etc - Anti-A antisera, Monoclonal blood grouping IgM antibody for slide and tube method For ABO blood grouping Vial of 10 ml and storage at +2to +8°C. Titer >1:256 with A cell and negative with B cell.avidity should be 4sec. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-B antisera, Monoclonal blood grouping IgM antibody for slide and tube method For ABO blood grouping Vial of 10 ml each and storage at +2 to+8°C. Titer >1:256 with B cell and negative with A cell. avidity should be 4sec. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-D antisera, IgM and IgG combination,, Monoclonal IgM and IgG blood typing antibody for slide and tube method For RH blood typing Vial of 10 ml cach and storage at + 2 to +8°C. Titre 1:256 with Rh positive cell, avidity should be < 10 sec. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-AB antisera, Monoclonal blood grouping IgM antibody for slide and tube method For ABO blood grouping Vial of 10 ml each and storage at +2 to +8°C. Titer >1:256 with A cell and with B cell. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-D antisera, monoclonal IgG only, antibody only for tube method For weak D testing. Titre 1:32 and specificity: 100% to Rho(D antigen). avidity should be < 5 sec. Vial of 10 ml each. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-Al lectin, monoclonal IgM antibody for tube method To differentiate Al red cell antigen from A2 antigen. Vial of 5 ml cach. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti H lectin, monoclonal IgM antibody for tube method Vial of 5ml each and storage of 2 to 8°C. Titre 1:16 with O group cells and negative reaction with Oh phenotype. Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Anti-Human Globulin (coombs sera) polyspecific, containing anti-IgG and anti C3d To detect IgG antibodies as in Cross matching, DAT and IAT tests Vial of 10 ml each and storage at 2 to 8 deg * C AIG should give 2 +/3+/4+ reaction with Coombs Control Cell and negative reaction with any std cell Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval. Bovine serum Albumin 22% solution for serological applications, protein concentration and pH should be adjusted to 22% and 7.1(+/ (- 0.2)% ) respectively To enhance immunological reactions and increase test sensitivity. Should be validated by NIB/EC/AABB/FDA. Vial of 10 ml each and storage at+ 2 to +8°C. Demonstration of item is must for final technical approval. Fourth generation ELISA Kit for anti-HCV Microplate coated with recombinant/Synthetic peptide antigens for core NS3, NS4 & NSS and antibody to HCV Core Antigen.NIV/ WHO GMP qualified sensitivity: >= 99.5% and specificity: > 99.8% Antibody (IgG and IgM detection. Demonstration of item is must for final technical approval. Fourth generation ELISA kit for detection of HIV p24 antigen & anti-HIV 1/2 antibody. NIV/ WHO GMP qualified sensitivity: ≥ 99.5% and specificity: > 99.8% Antibody (IgGi and IgM detection). Analytical sensitivity 08 IU/ml for p24 antigen Demonstration of item is must for final technical approval. Fourth generation/ Third generation ELISA Kit for Hepatitis B Surface Antigen and IgG and IgM detection. NIV/ WHO GMP qualified sensitivity:299.5% and specificity: 99.8% Antibody (IgG and IgM detection). Analytic sensitivity <50 picogram/ml Demonstration of item is must for final technical approval. Rapid test kits anti-HIV fourth generation for P24 antigen & antibody detection. (Principal of Enzyme Immuno Assay, Agglutination, or any other principal) Should be a solid phase coated HIVI & HIV II recombinant and synthetic peptide antigen and antibody to HIV I P24.Assay should detect HIV I & HIV II Antibodies and HIV I P24 Antigen in plasma, serum or whole Blood. Supplier must provide Negative & Positive control free of cost as and when require by the department. NARI/NIV/ WHO evaluated sensitivity >= 99.5% and specificity: > 98% Should be solid phase coated HIV I & HIV II Recombinant and/or synthetic peptide antigens Demonstration of item is must for final technical approval. Rapid test Kits for HCV antibody (Should be solid phase/particle coated with recombinant and /or/synthetic peptide antigen for Core. NS3, NS4, NS5) Supplier must provide Negative & Positive control free of cost as and when require by the department. NARI/NIV/ WHO evaluated sensitivity: >= 99% and specificity: >= 98% Demonstration of item is must for final technical approval. Rapid test kits for Hepatitis B Surface Antigen (Should be solid phase/particle coated with monoclonal antibodies to 11BsAg) Supplier must provide Negative & Positive control free of cost as and when require by the department. NARI/NIV/ WHO evaluated sensitivity >= 99% and specificity: >= 98% Analytical sensitivity/limit of detection should be < 3.13 IU as per WHO performance acceptance criteria for screening of Blood Donors. Demonstration of item is must for final technical approval. Rapid test kit for malaria antigen PI/Pan (HRP-II PI/pLDH Pan), sensitivity: 100% and specificity: 99% for both P. Falciparum & P. Vivax. Kits should be WHO/NARI/NIV/ICMR Prequalified Demonstration of item is must for final technical approval. TPHA rapid immune chromatography test kit. sensitivity: 100% and specificity: 99.8% Antibody (IgG and IgM)detection Demonstration of item is must for final technical approval. Single Blood Collection Bag 350 ml (CPDA) Specification Attached. Demonstration of item is must for final technical approval. Triple Blood collection bag 350 ml with diversion pouch (SAGM) Specification Attached. Demonstration of item is must for final technical approval. Triple Blood collection bag 450 ml with diversion pouch (SAGM) Specification Attached. Demonstration of item is must for final technical approval. Triple Blood collection bag 450 ml with diversion pouch and with inline leucodepletion filter (SAGM) Specification Attached. Demonstration of item is must for final technical approval. Lab side leucodepletion filter 1. The predeosit storage leucodepletion filter for the leucodepletion of packed red blood 2. Filtration of whole blood and red cells must be completed for 90% of bags wi minutes from time at which flow of blood into the filter is opened. 3. The filter should be able to reduce the final count of leucocyte in the product to < 5 * 1 bag. 4. The filtration process should not reduce red cell to less than 85% of the initial red ce percentage of haemolysis < 1% 5. Usable for RBC Blood of core temperature in the range 20 deg * C - 24 deg * C 6. Filter material should be highly porous polyurethane/ polyester material to ensure qu red cell during filtration. 7. Filter should have a Pre filter 200 micro meter to ensure two step filtration of (Optional) 8. Filter housing Material should be polycarbonated/ PVC soft housing with housing vol max 40 ml. 9. Bag should be sterilized be Beta irradiation or ETO or gamma sterilization. 10. The device should have drip chamber with by pass or intergrated airvent to remove ai the bag. 11. Transfer bag should be attached and have minimum 500 ml. capacity. 12. Each Dockable filter should be in a separate casing to maintain integarity and shape filters. 13. Market standing of more than 4 years. 14. Should have expiry of more than 18 months at the time of supply. Product labels barcoded as per ISBT128. Dengue Rapid test kit should be solid phase immunochromatographic principle for qualitative detection of dengue NSI antigen with detection of IgG and IgM antibody to dengue virus in human serum/plasma. WHO/NARI/NIV/ICMR Prequalified Demonstration of item is must for final technical approval. ELISA kit for Dengue NSI ( 1. The ELISA kit should be designed for qualitative detection of dengue NS1 antigen of all 4 dengue serotypes in human serum 2. The assay should be based on Sandwich method 3. Microwells should be coated with monoclonal antibodies against dengue NSI 4. The conjugate should contain to Anti-NS1 monoclonal antibody labelled with horseradish peroxidase 5. All the reagents should be in ready to use form. Only wash buffer concentrate to be reconstituted before use. 6. The assay components should include positive and negative controls with each kit. 7. The time required for performing the test should range between 1-2 1/2 hours 8. The ELISA kit for detection of dengue NS1 antigen should have a sensitivity of >99% and a specificity of >99% 9. The shelf life of the kit should be 18 months or longer 10. The pack size of the kits should be 96 tests/kit 11. Adequate documents detailing the principle components, bio-safety methodologies, validity criteria, procedure flowchart, interpretation of results, performance characteristics, storage conditions, limitation of assays, manufacturing & expiry dates should be provided with each kit Should be validated by ICMR/NIV. Demonstration of item is must for final technical approval. elisa kit for syphilis elisa kit for pan (ldh) malaria Cuvettes for Rapid Haemoglobin test HB301 (should be compatible with Make Hemocue Model 301) Evacuated blood collection (plastic) tube with Silica-clot activator for serum chemistry with red Safety Cap. It should be made of clear latex free polyethylene terepthalate. 13mm×100mm with 6.0ml volume.product should be European CE or USFDA Approved with Notified Body. Batch wise sterility, pyrogenicity and toxicity certificate should be given, Ciamma sterilize with certificate proof of pervious training record Firm should submit consent letter in BOQ to provide training to technicians/nurses regularly. Adequate combustion data to prove that it is safe for environment upon incineration. Evacuated blood collection (plastic) tube with spray dried K2 EDTA/K3 EDTA with lavender Safety Cap. It should be made of clear latex free polyethylene terepthalate. 13mm-75mm with 3.0ml volume. product should be European CE or USFDA Approved with Notified Body. Batch wise sterility, pyrogenicity and toxicity certificate should be given. Gamma sterilize with certificate proof of pervious training record Firm should submit consent letter in BOQ to provide training to technicians/nurses regularly. (1×100) Evacuated Sodium citrate blood collection (Gamma Irradiated Glass) tube for coagulation test (with Na citrate 0.109 M/3.2%) with LIGHT BLUE Safety Cap. It should be made of clear latex free polyethylene terepthalate, 13mm×75mm with 2.7 ml volume. product should be European CE or USFDA Approved with Notified Body. Batch wise sterility, pyrogenicity and toxicity certificate should be given. Gamma sterilize with certificate proof of pervious training record Firm should submit consent letter in BOQ to provide training to technicians/nurses regularly. (1×100) Disposable Evacuated blood collection needle with/without Flash 226.*1 inch. Gamma sterilize with certificate proof of pervious training record (1×100), product should be European CE or USFDA Approved with Notified Body. Batch wise sterility, pyrogenicity and toxicity certificate should be given. Evacuated tube blood collection Needle Holders for holding needle and tube. (1×100) Variable volume multichannel micro pipette (8 channels) 5-50 µl Variable volume multichannel micro pipette (8 channel)-5-50 µl clean graduated. Fully autoclavable. Certification: European CE, IVD Certified and provide certificate of calibration at time supply of item. Company should have facility for in lab calibration of pipette as per NABL-ISO 17025, In India at multiple locations and should have facility for onsite calibration as per NABL guideline. The company should submit technical compliance sheet as per technical specifications mentioning the make & model of quoted item along with catalogue in the Technical bid. Firm should supply stand frack to hold the pipette free of cost. Guarantee: Two years on equipment from the date of installation/supply. Two Preventive Maintenance services annually during Guarantee. Demonstration of item is must for final technical approval. Variable volume multichannel micro pipette (8 channels) 100 µl 1. Variable volume multichannel micro pipette (8 channel)-100 µl clean graduated. 2. Fully autoclavable. 3. Certification: European CE, IVD Certified and provide certificate of calibration at time supply of item. 4. Compon should have facility for in lab calibration of pipette as per NABI-150 17025, In India at maltiple locations and should have facility for onsite calibration as per NABI. guideline. 5. The company should subrit technical compliance sheet as per technical specifuations. meniloning the make & mood of quoted item along with catalogue in the Technical bid. . Firm should supply stand/rack to hold the pipette free of cost. f 7. Guarantee: Two years on eqepenent from the date of installatiory/supply. 8. Two Preventive Maintenance services annually during Guarantee. 9. Demonszution of item is mist for final technica approval Variable volume single channel niera pipette )20-200 لم Variable volume multichanne: micro pipette (20-100 µl) clean graduated. Fully amclavable. Certificathe European CE, IVD Certified and provide certificate of calibration at supply of tem time Company should have facility for in lab calibrasion of pipette as per NABL ISO 17025, In India at multiple locations ans should have facility Er onsite calibration as per NABL guideline. The consanny should submit technical compliance sheet as per technical specifications mentioning the make & model of quoted item along with catalogue in the Technical bid. Firm should supply stand/rock to hold the pipette free of cost. Guarantee: Two years on equpracat from the dats of installation/supply. Two Preventive Maintenance services annually during Guarantee. Demonstration of item is must for find techniest approval. Variable volume single channel nkra pipette (5-503 Variable volume single chaanel micro pipette-5-50 µl clean gradaated. Fully autoclavable. Certifiction: Earopean CE, IVD Certified and provide certificate of calibration at time supply item. Compary should have factity for in lab calibration of pipette as per NA.BI-ISO 17025, In India a maltiple locatinne and should have facility for onsite calibration as per NABL guidclisc The company should submit technical compliance sheet as per technical specifications mentioring the make & model of quoted item aong with catalogucin the Technical bid Firm should supply stand frack to hold the pipete free of cost. Guananec: Two years on equipament from the case of installation/supply. Two Preventive Maintenance services annually during Guarantee. Demonstration of item is must for final technical approval Fixed volume single channel mico pipette 100 μ Fixed voume single channel micro pipeite 100 på. Fully autoclavable. Certification European CE, IVD Certified and provide certificate of calibration a time supply of tem Company should have facility for in lab calibration of pipette an pe NABL-ISO 17025, In India at nultiple locations and should have ficility for onsite calibration as per NABL guideline. The company should submt technical complance sheet as per technical specifications mentioning the make & mode of quoted item alorg with catalogue in the Technical bid. Firm shoud supply stand rack to hold the pipette free of cost. Guarantee Two years on equbment from the date of installation/supply. Two Preventive Maintenance services annually during Guarantee. Demonstration of item is must for final technical approval. Fired volume single channel miers pipette 1000 με Fixed volume single channel nicro pipette 1000 a Fally autoclavable. Certification European CE, IVD Certified and provide certificate of calibration at time supply of item Company should have facility for in lab calibraton of pipette as per NABL ISO 17025, to India at multiple locations and should have facility for onsite calibration as per NABL. guideline. The company should suhmt technical compliance sheet as per technical specifications mentioning the make & model of quoted item along with catalogue in the Technical bid. Firm shoud supply stand frack to hold the pipette free of cost. Guarantee Two years on equioment from the date of installation/supply. Two Preventive Maintenance services annually during Guarantee. Demonstration of iters is muss for final technical approval Disposable micropipette Tips up to 5-50 µl (Yellow colour). Disposable micropipette Tips up to 20-200 µl (Yelles colour). Disposable meropipette Tips up to 100-1000 µl (Blue Colour). Test tube stard 96 boles, 13mm diameter in two shelves fully autoclavable. Test tube stand 48 boles, 13mm clameter in two shelves fully autoclavable Dropper plaste short sae I ml crpacity Foroops Plastic big Glass Slides 75x25x1.35 mm (Side made up of high quality transparent and color less glass with ground edgesand parallelism hetsoon the surfaces and should be IS I merked. Demonstrationol tem is must for inal technical approval. ID Coombs Card for cross-matching by Gel Technology Cormpatible with Microprocessor Controlled micro typing centrifuge machineinodel-4) centrifuge 12 SII) and incubater(model ID incubator 37 SI) (Maike B10-RAD) ID Diluents-2 for Gel Technology Compatible with Compatible with Microprocessor Controlled micro typing centrifuge machine(nodel-ID centrifuge 12 SIT) and incubator(model ID incubator 37 SI) (Make BIO-RAD) ID forward and reverse grouping card for Gel Technobgy Compatible with Microprocessor Controlled miro typing centrifugs machino(model-ID centrifuge 12 811) and incubator mode II) incubator 37 SI) (Maike BIO-RAD ID Forward grup card for Gel Todinology Compatibl: with Compatible with Microprocessor Controlled mire typing centrifuge raschino(model-II centrifuge 12 SII) and incubator(model ID incubator 379) (Make BIO-RAD (1X96 test) Make BIO-RAD) ID New born crouping by Gel Technology Coompatible with Microprocessor Controlled micro typing centrifuge machine model-ID cestrifuge 12 Sil) and incubator(model ID incubator 37 ST. (Make BIO-RAD) 11) Gel card or catended RH phenotyping(C,E,ce&K with etl.) Computible with Microprocesszor Controlled mero typing contrifige machinetmodel D centrifuge 12 SII) and incubator(rvodel ID incubator 37 11) (Make BIO-RAD) ID 3 cell panel (0.8% cell suspersions for irregular antibody detection. 3 X 10 ml) should be sterile pyrogen free. Should be CE mark CTVD approved, traccability certificate should be avaiable and minimum expiry date should be 3-4 weeks at the time of supply. (Make BIO-RAD) ID 11 cell pasel (0.8% cell suspension) for irregular antibody detection. (11 X 4 ml) should be sterile pyrogen free. Should be C. mask/CIVD approved. Traceability certificate should be available and minimum expiry date should be 3-4 weeks at the time of supply. (Make BIO-RAD) Labeled Disposable Plastic Test Tube for cross matching: Size-13x100 mm: Capacity-5 ml Labeled Disposable Plastic Test Tube for cross matching Size-13x75 mm: Capacity- 5 ml. etc
