Kits chemical reagent glassware etc

Reagents/Kits/ Chemical/Glassware/ Polyware etc Items

Anti-A antisera, Monoclonal blood grouping lgM 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 lgM 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, lgM and lgG combination, , Monoclonal lgM and lgG blood typing antibody for slide and tube method For RH blood typing Vial of 10 ml each 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 lgM 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 lgG 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-A1 lectin, monoclonal lgM antibody for tube method To differentiate A1 red cell antigen from A2 antigen. Vial of 5 ml each . Should be validated by NIB/EC/AABB/FDA. Demonstration of item is must for final technical approval.

Anti – H lectin, monoclonal lgM 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 – lgG and anti C3d To detect lgG antibodies as in Cross matching, DAT and IAT tests Vial of 10 ml each and storage at+ 2 to + 8˚C. AHG 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 & NS5 and antibody to HCV Core Antigen.NIV/ WHO GMP qualified sensitivity: ≥ 99.5% and specificity: > 99.8% Antibody (lgG and lgM 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 (lgG and lgM 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 lgG and lgM detection . NIV/ WHO GMP qualified sensitivity:≥99.5% and specificity: > 99.8% Antibody (lgG and lgM 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 HIV I & 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 HBsAg) 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 <0.130 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 Pf/Pan (HRP-II Pf/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 (lgG and lgM )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 cells. 2. Filtration of whole blood and red cells must be completed for >90% of bags within 45 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 <5x10^6 per bag. 4. The filtration process should not reduce red cell to less than 85% of the initial red cell mass percentage of haemolysis < 1% . 5. Usable for RBC Blood of core temperature in the range 20o C- 24o C. 6. Filter material should be highly porous polyurethane/ polyester material to ensure quality of red cell during filtration. 7. Filter should have a Pre filter 200 micro meter to ensure two step filtration of blood. (Optional) 8. Filter housing Material should be polycarbonated/ PVC soft housing with housing volume of 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 air inside 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 of the 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 should barcoded as per ISBT128.

Dengue Rapid test kit -should be solid phase immunochromatographic principle for qualitative detection of dengue NS1 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 NS1 ( 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 NS1 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 • Should be an ELISA reader based qualitative test • Microwells should be coated with a mixture of recombinant Treponemal antigens- TpN 15, TpN 17 & 47. • Should be based on Sandwich ELISA • Total incubation time should be only 105 mins • Reagents should be ready to use, with no reconstitution required • The assay components should include positive and negative controls with each kit • The assay should have sensitivity of 100% and specificity of 99.8% or more • Adequate documents detailing the principle components, bio-safety methodologies, validity criteria, procedure flowchart, interpretation of results , performance characteristics, storage conditions , limition of assays, manufacturing & expiry dates should be provided with each kit • The kit should be evaluated approved by National Insitute of Biologicals (NIB) • The pack size of the kits should be 96 tests/ kit • Should be validated by ICMR/NIV • Demonstation of item is must for final technical approval.

Elisa kit for PAN (LDH) Malaria • Should be an ELISA reader based qualitative test • Microwells should be coated with monoclonal antibodies to LDH of all Plasmodium species (pLDH) • The assay should detect pLDH from all 4 species of Plasmodium in human whole blood • Should be based on Sandwich ELISA • Total incubation time should be only 90 mins • Reagents should be ready to use, with no reconstitution required • The assay components should include positive and negative controls with each kit • The assay should have sensitivity of 100% and specificity of 99.8% or more • 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 • The pack size of the kits should be 96 tests / kit Should be validated by ICMR/NIV. Demonstration of item is must for final technical approval.

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. Gamma 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 22G.*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 1. Variable volume multichannel micro pipette (8 channel ) –5 – 50 µl clean graduated. 2. Fully autoclavable. 3. Certification :- European CE , IVD Certified and provide certificate of calibration at time supply of item. 4. 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. 5. 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. 6. Firm should supply stand /rack to hold the pipette free of cost. 7. Guarantee: Two years on equipment from the date of installation/supply. 8. Two Preventive Maintenance services annually during Guarantee. 9. 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. 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. 5. 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. 6. Firm should supply stand /rack to hold the pipette free of cost. 7. Guarantee: Two years on equipment from the date of installation/supply. 8. Two Preventive Maintenance services annually during Guarantee. 9. Demonstration of item is must for final technical approval

Variable volume single channel micro pipette (20-200 μl) • Variable volume multichannel micro pipette–(20-200 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 /rack 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 single channel micro pipette (5-50μl) • Variable volume single channel micro pipette– 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 /rack 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.

Fixed volume single channel micro pipette 100 μl • Fixed volume single channel micro pipette 100 μl . • 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 /rack 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.

Fixed volume single channel micro pipette 1000 μl • Fixed volume single channel micro pipette 1000 μl 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 /rack 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.

Disposable micropipette Tips up to 5-50 µl (Yellow colour).

Disposable micropipette Tips up to 20-200 µl (Yellow colour).

Disposable micropipette Tips up to 100 -1000 µl (Blue Colour).

Test tube stand 96 holes, 13mm diameter in two shelves fully autoclavable .

Test tube stand 48 holes, 13mm diameter in two shelves fully autoclavable.

Dropper plastic short size 1 ml capacity

Forceps Plastic big

Glass Slides 75x25x1.35 mm (Slide made up of high quality transparent and color less glass with ground edges and parallelism between the surfaces and should be IS I marked. Demonstration of item is must for final technical approval.

ID Coombs Card for cross-matching by Gel Technology Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)

ID Diluents-2 for Gel Technology Compatible with Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)

ID forward and reverse grouping card for Gel Technology Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)

ID forward group card for Gel Technology Compatible with Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD) (1 X 96 test) Make BIO-RAD)

ID New born Grouping by Gel Technology Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)

ID Gel card for extended RH phenotyping(C,E,c,e&K with ctl.) Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)

ID 3 cell panel (0.8% cell suspension) for irregular antibody detection. (3 X 10 ml) should be sterile pyrogen free. Should be CE mark/CIVD approved. traceability certificate should be available and minimum expiry date should be 3-4 weeks at the time of supply. (Make BIO-RAD)

ID 11 cell panel (0.8% cell suspension) for irregular antibody detection. (11 X 4 ml) should be sterile pyrogen free. Should be CE mark/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.

Lancet with sharp Tip & smooth margins. Batch wise sterility/ pyrogenicity /toxicity certificate should be given. () Demonstration of item is must for final technical approval.

Medicated adhesive tape for Blood donors. . Demonstration of item is must for final technical approval.

Thermal paper roll (55 mm X 30 mt) for 3 part hematology analyzer

Roll of tissue paper

Sod. Hypo Chloride Solution (6%)

D.M. Water

Pressure sensitive thermo graph for BBR & Platelet Agitator (Terumo Penpol) ( 1 X 50)

Pressure sensitive thermo graph for Deep Freezer (Terumo Penpol) ( 1 X 50)

Normal Thermo graph for BBR & Platelet Agitator (Terumo Penpol) (1 X 50)

Normal Thermo graph for Deep freezer (Terumo Penpol) (1 X 50)

Normal Thermo graph for BBR (REMI) (1 X 50)

Writing pen for Normal Thermo Graph

Bulb for Micro scope 6 volt, 20 watt

Chewable Calcium with Vitamin D3 Tablets for SDP Donors

Exchange Set (product Should be compatible with Apheresis Machine , Make Terumo Penpol, Model-Spectra Optia)

platelet plasma set (product Should be compatible with Apheresis Machine , Make Terumo Penpol, Model-Spectra Optia)(1x6)

ACD Solution Make Terumo Penpol

Disposable ESR pipette

Leishman stain liquid

methylene blue

tourniquete

Brilliant cresyl blue

Giemsa staining powder

Neubaur counting chamber

Reticulocyte count stain

field stain I

field stain II

Sterile connecting device wafers Should be compatible with sterile connecting device make-Terumo penpol,model-TSCD-2 serial no - 1612026 Proprietary item

Re-agents for 3 part cell counter analyzer (Make-Transasia model- Erba H-360 S.N.-K10012220345 ) (a) Erba H360 Diluent

Re-agents for 3 part cell counter analyzer (Make-Transasia model- Erba H-360 S.N.-K10012220345 ) (b) Erba H360 lyse

Re-agents for 3 part cell counter analyzer (Make-Transasia model- Erba H-360 S.N.-K10012220345 ) (c) Erba H Clean

Re-agents for 3 part cell counter analyzer (Make-Transasia model- Erba H-360 S.N.-K10012220345 ) (d) H360 control tri level

Re-agents for 3 part cell counter analyzer (Make-Transasia model- Erba H-360 S.N.-K10012220345 ) (e) H360 calibrator

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) I. Erba H560 Diluent ,(1 X 20 ltr)

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) II. Erba H560 lyse-1 ,( 4 X 200 ml)

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) III. Erba H560 lyse-2 ,( 3 X 500 ml)

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) IV..Erba H Clean ,(4 X 50 ml)

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) V. H560 control tri level ,(3x 3 ml)

Re-agents for 5 part cell counter analyzer (Make-Transasia model- Erba H-560 S.N.-K1104213055 ) VI. H560 calibrator , (1x3 ml)

ID Gel card for antigen profile 1 (P1,Lea,Leb,Lua,Lub with ctl.) Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator Make BIO-RAD)

ID Gel card for antigen profile II (k,Kpa,Kpb,Jka,Jkb with ctl.) Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator Make BIO-RAD)

ID Gel card for antigen profile III (M,N,S,s,Fya,Fyb) first 2 microtubule contain neutral gel and last 4, gel with polyspecific anti human globulin; the corresponding antibodies (ID- test sera, specially adapted for ID system) are added after red cell suspension(in ID Diluent-2) Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator (Make BIO-RAD) pack size-ID card(1 X 12 test) Test sera-24 profile( 6x1.4ml)

ID Gel -Card (NaCl, Enzyme Test and Cold Agglutinins) suitable for antibody screening and identification procedures, compatibility testing and reverse Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator (Make BIO-RAD) grouping.(1x4x12 test)

ID Gel card for Anti-A1 Absorbed Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator . 72 test (1 X 12 ) Make BIO-RAD)

ID Gel card for anti-H, monoclonal,Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator . 72 test (1 X 12 ) Make BIO-RAD)

ID gel card for Partial RhD Typing Set consists of 6 monoclonal anti-D which can aid in the further characterization of the RhD antigen after routine RhD typing. Compatible with Microprocessor Controlled micro typing centrifuge machine and incubator (Make BIO-RAD)

ID gel card for DC-Screening I ( IgG, IgA, IgM, C3c, C3d, ctl) Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD) 12 test (1 x 12 gel card)

ID gel card for DC-Screening II (IgG, C3d, ctl/IgG, C3d, ctl) Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD) 24 test (1 x 12 gel card)

ID gel Card for DAT IgG-Dilution Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD) 12 test (1 x 12 gel card)

ID gel Card for DAT IgG subclasses (IgG1/IgG3 )Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD) 12 test (1 x 12 gel card)

ID-CellStab - glycine buffered saline which stabilizes red cells at 0.8% suspension for use in the ID-System for up to 4 weeks after preparation. (2x100ml)

ID Diluents-1 for Gel Technology Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)( 2x100ml)

ID-Papain - standardized liquid papain solution and used for pre-treating red cells to prepare red cell reagents, or used as an enzyme additive reagent in a one stage technique. Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)(1x10 ml)

ID-CellWash-P to wash the RBC After treatment of the red cells with papain. Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)(1x500ml)

Neutral ID gel card for cross matching ,antibody screening and identification, phenotyping and IGg titre. Compatible with Microprocessor Controlled micro typing centrifuge machine(model-ID centrifuge 12 SII) and incubator(model ID incubator 37 SI) (Make BIO-RAD)(1x100 gel card)

ANTI -C (Anti -RH2) monoclonal antibody for C antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.(make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -c (Anti -RH4) monoclonal antibody for c antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval(make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -E (Anti -RH3) monoclonal antibody for E antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -e (Anti -RH5) antibody for e antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Kell monoclonal antibody for K antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Cellano(KEL2) antibody for k antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Fya (FY1) antibody for Fya antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Fyb (FY2) antibody for Fyb antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Jka (JK1) monoclonal antibody for Jka antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Jkb (JK2) monoclonal antibody for Jkb antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Lea (LE1) antibody for Lea antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -Leb (LE2) antibody for Leb antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval(make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -M antibody for M antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -N antibody for N antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -S antibody for S antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

ANTI -s antibody for s antigen detection on RBC(extended phenotyping) by coloumn tube technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval(make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -K for K antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Fya for Fya antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Fyb for Fyb antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Jka for Jka antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Jkb for Jkb antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Lea for Lea antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -Leb for Leb antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -M for M antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -N for N antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -S for S antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -s for s antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 5 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Ortho sera ANTI -P1 for P1 antigen detection on RBC(extended phenotyping) by coloumn agglutination technique. . Should be validated by NIB/EC/AABB/FDA . Vial of 3 ml each and storage at+ 2 to + 8˚C. Demonstration of item is must for final technical approval.((make- ortho clinical diagnostic, model- orthoworkstation BioVue )

Glycine acid elution kit for red cell. 1) it should have clearly defined end point color change. 2) should be validated for both tube and gel techniques. 3) acid and buffer provided in dropper vials to reduce risk of contamination. 4) vials should have color coded caps to differentiate acid step and buffer step. 5) wash bottle should have fill line to allow easy preparation of working wash solution. 6) should be FDA cleared.

ZZAP kit for adsorption IGg antibodies from RBC. 1) kit containing 0.2 M DTT and 1% papain activated by L- cysteine. 2) supplied as a kit as 0.2 M DTT 5 ml and 1% papain 1 ml volume, to be used directly from the vial.

Sickle cell (A,S.C) rapid test card with all essentials buffer and consumables for qualitative screening, in vitro diagnostic immunochromatographic assay foe the detection and differentiation of A,S and C type of hemoglobin phenotype in human whole blood. sensitivity ≥99%, specificity ≥99%.

Microcuvette for hemoCue plasma /Low Hb photometer for quantitative determination of low lwvwl hemoglobin in plasma and serum specimen (Make- HemoCue, ) product should be CE/IVD approved.

PRP kits compatible with Autologous platelet concentrate machine , Model- PRP Ultra, Make Remi. kits should be sterile , closed system based and Disposable having sample volume of 20 ml.

HbsAg ES Reagent Pack / Testing Kit (A)Proprietary Item Should be Compatiable Fully Automated Immunoassay Analyzer Machine (Make – Ortho clinical Diagnosis, Model – VITROS 3600) ( B) All Test Kits should be supplied with relevant Calibrators, Controls & Consumables (C) Test kit must not be near expiry at the time of supply

Anti HCV Kit / Reagent Pack (A)Proprietary Item Should be Compatiable Fully Automated Immunoassay Analyzer Machine (Make – Ortho clinical Diagnosis, Model – VITROS 3600) ( B) All Test Kits should be supplied with relevant Calibrators, Controls & Consumables (C) Test kit must not be near expiry at the time of supply

HIV (I & II) Combo kit (A)Proprietary Item Should be Compatiable Fully Automated Immunoassay Analyzer Machine (Make – Ortho clinical Diagnosis, Model – VITROS 3600) ( B) All Test Kits should be supplied with relevant Calibrators, Controls & Consumables (C) Test kit must not be near expiry at the time of supply

Syphilis TPA Reagent kit (A)Proprietary Item Should be Compatiable Fully Automated Immunoassay Analyzer Machine (Make – Ortho clinical Diagnosis, Model – VITROS 3600) ( B) All Test Kits should be supplied with relevant Calibrators, Controls & Consumables (C) Test kit must not be near expiry at the time of supply

Medi Lifecare Govind (BID ID -3210988)

salasar distributor (BID ID -3226094)

KRISHIV ASSOCIATE (BID ID -3223674)

M/S Garg Scientific and Surgical Co (BID ID -3226361)