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supply of laboratory equipments ihbt 1 anti a • monoclonal antisera formulated cell culture supernatant containing murine igm anti a, suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003.• should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 10 ml vial. 2 anti a • monoclonal antisera formulated cell culture supernatant containing murine igm anti a, suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003.• should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 5 ml vial. 3 anti b • monoclonal antisera formulated cell culture supernatant containing murine igm anti b, suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003.• should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 10 ml vial. 4 anti b • monoclonal antisera formulated cell culture supernatant containing murine igm anti b, suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003. • should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 5 ml vial. 5 anti ab • monoclonal antisera formulated cell culture supernatant containing murine igm anti ab suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003.• should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 10 ml vial. 6 anti ab • monoclonal antisera formulated cell culture supernatant containing murine igm anti ab suitable for slide, tube and plates.• a blend of monoclonal antibodies.• potency, specificity and avidity shall be as per the criteria of dghs 2003.• should preferably detect common weaker variants. • reagent to be suitable for slide, tube and micro plate assay• packed in 5 ml vial. 7 anti d • monoclonal antisera formulated cell culture supernatant containing human igm anti d antibodies• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • should preferably detect common d variants. • packed in 5 ml vial. 8 anti d • monoclonal antisera formulated cell culture supernatant containing human igm anti d antibodies• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • should preferably detect common d variants. • packed in 10 ml vial. 9 anti d • monoclonal antisera formulated cell culture supernatant containing human igg anti d antibodies• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • should preferably detect common d variants. • packed in 5 ml vial. 10 anti d •polyclonal antisera formulated cell culture supernatant containing human blend igg + igm anti d antibodies• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • should preferably detect common d variants. • packed in 10 ml vial. 11 anti a 1 • should be either lectin obtained from dolicus biflorus diluted in buffered saline or polyclonal / monoclonal antiserum• neutral ph• ready to use• should differentiate clearly between a1 and a2 as well as a1b and a2b• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • packed in 5ml vial. 12 anti a 1 •should be either lectin obtained from dolicus biflorus diluted in buffered saline or polyclonal / monoclonal antiserum• neutral ph• ready to use• should differentiate clearly between a1 and a2 as well as a1b and a2b• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • packed in 10 ml vial. 13 anti h • should be either lectin obtained from ulex europeus diluted in buffered saline or polyclonal / monoclonal antiserum• neutral ph• ready to use• should recognize “h†antigen on all human red cells• should differentiate clearly between “bombay phenotype†(oh] and others.• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • packed in 5 ml vial. 14 anti h • should be either lectin obtained from ulex europeus diluted in buffered saline or polyclonal / monoclonal antiserum• neutral ph• ready to use• should recognize “h†antigen on all human red cells• should differentiate clearly between “bombay phenotype†(oh] and others.• reagent to be suitable for slide, tube and micro plate assay• potency, specificity and avidity shall be as per the criteria of dghs 2003 • packed in 10 ml vial. 15 anti human globulin • polyspecific anti human globulin prepared from a pool of rabbit anti igg serum and mouse monoclonal anti c3b and anti c3d.• should be a blend of polyspecific rabbit anti human igg and murine monoclonal anti c3b and c3d antibodies.• should be for the detection of cell bound blood group antibody and/or components of complement based on direct antiglobulin test and indirect antiglobulin test.• potency and specificity shall be as per the criteria of dghs 2003 • packed in 5ml vial. 16 anti human globulin • polyspecific anti human globulin prepared from a pool of rabbit anti igg serum and mouse monoclonal anti c3b and anti c3d.• should be a blend of polyspecific rabbit anti human igg and murine monoclonal anti c3b and c3d antibodies.• should be for the detection of cell bound blood group antibody and/or components of complement based on direct antiglobulin test and indirect antiglobulin test.•potency and specificity shall be as per the criteria of dghs 2003. • packed in 10 ml vial. 17 anti human globulin •monospecific anti human globulin prepared from a pool of rabbit anti igg serum .• should be monospecific rabbit anti human igg .• should be for the detection of cell bound blood group antibody based on direct antiglobulin test and indirect antiglobulin test.•potency and specificity shall be as per the criteria of dghs 2003. • packed in 10 ml vial. 18 anti human globulin •monospecific anti human globulin prepared from a pool of rabbit anti c3 serum .• should be monospecific rabbit anti human c3.• should be for the detection of cell bound blood group antibody based on direct antiglobulin test and indirect antiglobulin test.• potency and specificity shall be as per the criteria of dghs 2003.• packed in 10 ml vial. 19 22% bovine albumin • suitable for enhancement of red cell agglutination reactions.• should be derived from raw bovine serum.• protein concentration should be 22%• should be free from potential infectious risk as the source is bovine serum.• the ph should be neutral.• should be suitable for use with direct as well as indirect agglutination tests.• the conductivity should be controlled for serological applications• packed in 10 ml vial• storage temperature should be 2+ to 8+oc 20 22% bovine albumin •suitable for enhancement of red cell agglutination reactions• should be derived from raw bovine serum• protein concentration should be 22%• should be free from potential infectious risk as the source is bovine serum • the ph should be neutral• should be suitable for use with direct as well as indirect agglutination tests.• the conductivity should be controlled for serological applications• packed in 5 ml • storage temperature should be 2+ to 8+oc 21 anti c antisera monoclonal igm antibodies ,liquid, ready to use in 5ml vials preservative: <0.1% nan3 cell line: ms 24 22 anti c antisera monoclonal igm antibodies ,liquid, ready to use in 10ml vials preservative: <0.1% nan3 cell line: ms 24 23 anti c antisera monoclonal igm antibodies ,liquid, ready to use in 5ml vials preservative: <0.1% nan3 cell line: ms 33 24 anti c antisera monoclonal igm antibodies ,liquid, ready to use in 10ml vials preservative: <0.1% nan3 cell line: ms 33 25 anti e antisera monoclonal igm antibodies ,liquid, ready to use in 5ml vials preservative: <0.1% nan3 cell line: ms 260 26 anti e antisera monoclonal igm antibodies ,liquid, ready to use in 10ml vials preservative: <0.1% nan3 cell line: ms 260 27 anti e antisera monoclonal igm antibodies ,liquid, ready to use in 5ml vials preservative: <0.1% nan3 cell line: ms 16, ms 21, ms 63 28 anti e antisera monoclonal igm antibodies ,liquid, ready to use in 10ml vials preservative: <0.1% nan3 cell line: ms 16, ms 21, ms 63 29 anti fya antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 30 anti fyb antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 31 anti lea antisera igm class antibody, ready to use in 2ml vial preservative: <0.1% nan3 32 anti leb antisera igm class antibody, ready to use in 2ml vial preservative: <0.1% nan3 33 anti lua antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 34 anti lub antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 35 anti p antisera monoclonal igm antibodies ,liquid,ready to use in 1ml vials preservative: <0.1% nan3 , cell line 650 36 anti k, antisera igm class antibody, ready to use in 5ml vial preservative: <0.1% nan3 37 anti k antisera igm class antibody, ready to use in 2ml vial preservative: <0.1% nan3 38 antikpa antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 39 antikpb antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 40 anti s antisera igm class antibody, ready to use in1ml vial preservative: <0.1% nan3 41 anti s antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 42 anti m antisera monoclonal antibodies (mouse hybridoma),liquid, ready to use in 2 ml vials preservative: <0.1% nan3 43 anti n antisera monoclonal antibodies (mouse hybridoma),liquid,ready to use in 2 ml vials preservative: <0.1% nan3 44 anti jsa antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 45 anti jsb antisera igm class antibody, ready to use in 1ml vial preservative: <0.1% nan3 46 anti jka antisera igm class antibody, cell line:ms 15, ready to use in 2ml vial preservative: <0.1% nan3 47 anti jkb antisera igm class antibody, cell line:ms 15, ready to use in 2ml vial preservative: <0.1% nan3 48 anti cde antisera monoclonal igm antibodies ,liquid, ready to use in 5ml vials preservative: <0.1% nan3 49 anti cde antisera monoclonal igm antibodies ,liquid, ready to use in 10ml vials preservative: <0.1% nan3 cell line: ms 26,ms 201,ms 80 50 coombs control cells coombs control igg , red cell sensitised with igg, in a 4%+/ 1% suspension, ready to use, in 10 ml vials. 51 acid elution kit • for rapid acid elution of antibodies from intact rbcs.• containing wash solution (concentrated) containing glycine nacl buffer, elution solution containing a low ph glycine buffer with colour indicator in 10 ml vial. buffer solution containing tris buffer with bovine albumin(1 2%) in 10 ml vial.storage temperature of kit : 2 8 0 c.• shelf life : 1 year 52 edta glycine elution kit •for elution of igg from rbcs.•the kit should contain concentrated solution of sodium edta, low ph glycine solution, tris(hydroxymethyl) aminomethane solution.•storage temperature of kit : 2 8 0 c.•shelf life : 1 year 53 adsorption kit for warm autoantibody •should remove warm reactive autoantibody from red blood cells to facilitate resolution of serological complexities.•the reagent is based on the zzap reagent.•should have lyophilized dithiothreitol and cysteine activated papain in a phosphate buffer.•50 or 100 tests/ kit.•shelf life of reconstituted reagent should be at least 5 days. •storage temperature of kit : 2 8 0 c.•shelf life : 1 year 54 adsorption kit for cold autoagglutinins •should use rabbit erythrocyte stroma for adsorption of cold agglutinins anti i, anti h or anti ih.•should contains a saline suspension of rabbit erythrocyte stroma for autoadsorption of cold autoagglutinin.•should have long expiry and stability. 55 duolys (diagast qwalys 3) with free supply of required quality controls hema cqi for qwalys diagast test compatible on qwalys diagast microplate should have (anti a, anti b, anti ab, anti d, anti e, anti e, anti c, anti c, anti kell, neg control, a1, b (cells) including all reagent use in this test. 56 crosslys (diagast qwalys 3) test compatible on qwalys diagast microplate should have ( igg/c3d/clt) including all reagent use in this test. 57 screenlys (diagast qwalys 3) test compatible on qwalys diagast 11 cell panel for antibody identification including all reagent use in this test. 58 abdlys(diagast qwalys 3) with free supply of required quality controls hema cqi for qwalys diagast test compatible on qwalys diagast microplate should have (anti a, anti b, anti d, neg control, a1, b (cells) including all reagent use in this test. 59 groupa2lys (diagast –qwalys 3) with free supply of required quality controls hema cqi for qwalys diagast test compatible on qwalys diagast microplate should have (anti a, anti b, anti ab, anti d1, anti d2, neg control, a1,a2, b,o (cells) including all reagent use in this test. 60 crosslys (diagast qwalys 3) test compatible on qwalys diagast microplate for cross matching including all reagent use in this test. 61 screenlys (diagast qwalys 3) with free supply of required quality controls sera cqi for qwalys diagast •test compatible on qwalys diagast microplate for antibody screening testing including all reagent use in this test. 62 abd pad device for blood grouping • for performing blood grouping test within 30 40 seconds.• use of patented m trap technology. • ce mark product and approved by nib. • use of whole blood, finger prick, samples drawn in edta, citrate, blood bag segments, • 5 70µl of rbcs can be used per well, no volume specific,• pre dispensed monoclonal antibodies on the device.• can be used up to 37 degree c and 90 % humidity.• no risk of contamination between samples, results. • pre dispensed monoclonal antibodies on the device. •. multipletests per single pad.• expiry 1 to 6 months 63 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for pre transfusion testing coombs, iat & dat with anti igg , & anti c3 compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have facility to perform antibody screening three cell panel, and antibody identification eleven cell panel & cross match.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 64 column agglutination antibody screening consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •the test system should be based on the principle of column agglutination technology compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system should able to detect igm, igg, iga, c3c, c3d components.•the test system should be coated with appropriate monospecific antisera for the detection of unexpected antibody eg. anti igm, anti igg, anti iga, anti c3c, anti c3d.•the test system should be supplied with accessories required to perform the test.•shelf life : minimum 12 months. 65 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for determination of the abo/rh blood grouping combined with reverse grouping and compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have monoclonal anti a, anti b, anti d(dvi ), control and a1 and b cell.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 66 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for determination of the antigen profile for p1, lea, leb, lua, lub and control and compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have monoclonal anti p1, anti lea, anti leb, anti lua, anti lub, control.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 67 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for determination of the antigen profile for k, kpa, kpb, jka, jkb and control and compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have monoclonal anti k, anti kpa, anti kpb, anti jka, anti jkb, control.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 68 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for determination of the antigen profile for m, n, s, s, fya, fyb and control and compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have monoclonal anti m, anti n, anti s, anti s, anti fya, and anti fyb.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 69 column agglutination test consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 sii •column agglutination test, required for determination of the rh subgroup and k and compatible with bio rad gel card incubator 37 si and bio rad gel card centrifuge 12 sii.•the test system shall have required consumables like liss solution and other reagents, dispensers for test. •the test system should be compatible with equipment technology & reagents. •the test system should have monoclonal anti c, anti c, anti e, anti e, anti k, control.•the reagent red cell panels for antibody screening & identification should be available with the company.•all media and consumables for setting up and standardization should be provided free of cost. •shelf life : minimum 12 months. 70 column agglutination antibody screening two cell panel consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 •for antibody screening containing 2 cells panel i,ii and should be compatible with bio rad gel card, bio rad incubator 37 si and bio rad gel card centrifuge 12 sii. • should be able to screen all clinically significant antibodies against antigen system of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg . •medium reagent red blood cells suspended in isotonic medium (red cell preserving solution) •stability at least six weeks (42 days)•storage 2 – 8° c 71 column agglutination antibody screening three cell panel consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 •for antibody screening containing 3 cells panel i,ii,iii and should be compatible with bio rad gel card, bio rad incubator 37 si and bio rad gel card centrifuge 12 sii. • should be able to screen all clinically significant antibodies against antigen system of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg . •medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c 72 column agglutination antibody identification eleven cell panel consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 for antibody identification containing elevan cell panel of 3% reagent red blood cells for anti human globulin procedures (igg detection) & neutral gel (igm detection) compatible with bio rad gel card, bio rad incubator 37 si and bio rad gel card centrifuge 12 sii.•concentration 3% reagent red blood cells comprise of human erythrocytes of group o cells,•should be able to identify all clinically significant antibodies against all clinically significant antibodies.•antigens of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg blood group system should be present on panel cells.•medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c 73 column agglutination antibody identification twenty cell panel consumable compatible for semi automated bio rad incubator37 si and centrifuge 12 •for antibody identification containing twenty cell panel of 3% reagent red blood cells for anti human globulin procedures (igg detection) & neutral gel (igm detection) compatible with bio rad gel card, bio rad incubator 37 si and bio rad gel card centrifuge 12 sii.•concentration 3% reagent red blood cells comprise of human erythrocytes of group o cells,•should be able to identify all clinically significant antibodies against all clinically significant antigens.•antigens of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg blood group system should be present on panel cells.•medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c 74 antibody screening three cell panel consumable based on solid phase red cell adherence technology •for antibody screening containing 3 cells panel i,ii,iii based on solid phase red cell adherence technology • should be able to screen all clinically significant antibodies against antigen system of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg . •medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c• all media, equipment and consumables for setting up and standardization should be provided free of cost. 75 antibody identification fourteen cell panel consumable based on solid phase red cell adherence technology •for antibody identification containing forteen cell panel of 3% reagent red blood cells for anti human globulin procedures based on solid phase red cell adherence technology•concentration 3% reagent red blood cells comprise of human erythrocytes of group o cells,•should be able to identify all clinically significant antibodies against all clinically significant antigens.•antigens of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg blood group system should be present on panel cells.•medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c •all media and consumables for setting up and standardization should be provided free of cost. 76 antibody identification twenty cell panel consumable based on solid phase red cell adherence technology •for antibody identification containing twenty cell panel of 3% reagent red blood cells for anti human globulin procedures based on solid phase red cell adherence technology•concentration 3% reagent red blood cells comprise of human erythrocytes of group o cells,•should be able to identify all clinically significant antibodies against all clinically significant antigens.•antigens of rh, kell, duffy, mns & s & pi, lutheran, kidd, lewis, xg blood group system should be present on panel cells.•medium reagent red blood cells suspended in isotonic medium (red cell preserving solution)•stability atleast six weeks (42 days)•storage 2 – 8° c •all media and consumables for setting up and standardization should be provided free of cost. 77 hbsag elisa test kits • should be third generation elisa kit.• the kit should be based on “sandwich†principle of enzyme linked immunosorbent assay (elisa) for the detection of hepatitis b surface antigen (hbsag) in human serum or plasma. • should detect all known subtypes like ayw1, ayw2, ayw3, ayw4, ayw5, ayr, adw2, adw4, adr and mutant strains.• should have monoclonal antibodies on solid phase & combination of monoclonal antibodies & polyclonal antibodies in the conjugate to enable best coverage of all the subtypes• reagents should be preferably colour coded • preferably colour change on addition of samples/reagents in the wells.• total incubation time should not be more than 2 hrs• sample volume should be small preferably not be more than 100ul• the assay should have reactive and non reactive controls with each kit. • sensitivity should be more than 99.9%• analytical sensitivity should be less than 60 picogram/ml.• specificity should be more than of 99.5%• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the assay should have a shelf life on minimum 9 months at the time of delivery.• the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transport at 20c 80c. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit size should be 96 wells per kit. 78 hiv elisa test kits • should be fourth generation elisa kit.• should detect both antibody (ab) of hiv 1 group m (all known hiv 1 subtypes a, b, c, d, e, f, g and h), hiv 1 group o and hiv 2 as well as p24 antigen (ag) against hiv 1 .• should be solid phase micro plate based on sandwich elisa with monoclonal abs against p24 ag and gp160 recombinant proteins on the solid phase.• should have gp36 and gp 41 peptides in the conjugate. • should have separate conjugates for both antigens and antibodies • reagents should preferably be colour coded with verification criteria for reagent addition proof.• should detect all the three classes of antibodies to hiv i.e. igm, igg and iga simultaneously providing highest early sero conversion sensitivity.• total incubation time should not be more than 2 hrs.• sample volume should be small preferably not be more than 100ul• the assay should have positive (anti hiv1, anti hiv2 and hiv p24 antigen) controls with each kit. • the assay should have negative (non reactive) control with each kit. • the assay should have sensitivity of more than 99.9%.• the analytical sensitivity of ag detection should be less than 150 pg/ml .• specificity should be more than of 99.5% for both antigens as well as antibodies without compromising the assay sensitivity.• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the assay should have a shelf life of minimum 9 months at the time of delivery.• the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transport at 20c 80c. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit size should be 96 wells per kit 79 hiv elisa for anti hiv 1 and 2 antibodies • 96 well elisa 3 rd generation •should detect both antibody (ab) of hiv 1 group m (all known hiv 1 subtypes a, b, c, d, e, f, g and h), hiv 1 group o and hiv 2. • should be solid phase micro plate based on sandwich elisa with monoclonal abs against p24 ag and gp160 recombinant proteins on the solid phase.• should have gp36 and gp 41 peptides in the conjugate. • should have separate conjugates for both antigens and antibodies • reagents should preferably be colour coded with verification criteria for reagent addition proof.• should detect all the three classes of antibodies to hiv i.e. igm, igg and iga simultaneously providing highest early sero conversion sensitivity.• total incubation time should not be more than 2 hrs.• sample volume should be small preferably not be more than 100ul• the assay should have positive (anti hiv1, anti hiv2 and hiv p24 antigen) controls with each kit. • the assay should have negative (non reactive) control with each kit. • the assay should have sensitivity of more than 99.9%.• the analytical sensitivity of ag detection should be less than 150 pg/ml .• specificity should be more than of 99.5% for both antigens as well as antibodies without compromising the assay sensitivity.• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the assay should have a shelf life of minimum 9 months at the time of delivery.• the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transport at 20c 80c. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit size should be 96 wells per kit • elisa reader based test• must detect both hiv 1 and 2 antibody.• negative predictive value 0.01 %• kit must be as per naco guidelines. 80 hcv elisa test kits fourth generation hcv elisa kit• should detect igg antibody against hcv. • should have wells coated with recombinant antigens: c22c, c 200(c 33c + c 100), ns3, ns4, ns5.• should have murine monoclonal anti igg with hr peroxidase enzyme conjugate and it should be ready to use. • the sero conversion sensitivity should be based on minimum 20 anti hcv sero conversion panel study, and it should have highest earlysero conversion sensitivity.• total incubation time should not be more than 2 hrs• sample volume should be small preferably not be more than 100ul• the assay should have reactive and non reactive controls with each kit.• sensitivity of the test should be more than 99.9%• specificity should be more than of 99.5% for ab detection without compromising the assay sensitivity.• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the assay should have a shelf life on minimum 9 months at the time of delivery.• the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transport at 20 c 80c. • the kit procured should have approval of the statutory authority in it country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit size should be 96 wells per kit• the kit should be coated with immunodominant regions of the virus:core, ns3, ns4, and ns5. 81 hcv elisa test • 96 well elisa 3rd generation • serum can be used as sample.• both sensitivity & specificity should be more than 99 %.• documented study should be provided along with tender for sensitivity & specificity claims. • should have shelf life of 1 – 2 years. • should be stored at room temperature or in refrigerator (2 – 8 c).• company should provide good manufacturing product (gmp)/ who certificate & iso 13485 certificate / fda approved along with tender. • kit should provide all accessories & positive and negative controls.• for elisa kit, 12 strips of 8 wells should be supplied• should have good consumer base in gujarat.• expiry should be 1 – 2 year from date of manufacturing.• it is preferable, if kit is approved by any apex govt. institute in india.• it is preferable, if kit has good rapport in commercial market since last 3 years.• detailed literature regarding kit should be provided along with tender.• the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• authority letter from manufacturer is mandatory.• for imported item, ce certificate is must. 82 hiv, hcv, hbsag combo elisa test kit • should be fourth generation elisa kit based on sandwich principle of enzyme linked immunosorbent assay (elisa).• should detect both antibody (ab) of hiv 1 group m (all known hiv 1 subtypes a, b, c, d, e, f, g and h), hiv 1 group o and hiv 2 as well as p24 antigen (ag) against hiv 1 ; should detect igg antibody against hcv and wells coated with recombinant antigens: c22c, c 200 (c 33c + c 100), ns3, ns4, ns5 ; should detection hepatitis b surface antigen (hbsag) in human serum or plasma and detect all known subtypes like ayw1, ayw2, ayw3, ayw4, ayw5, ayr, adw2, adw4, adr and mutant strains. •the assay should have sensitivity of more than 99.9% and specificity of 99.5%. •total incubation time should not be more than 2 hrs. • sample volume should be small preferably not be more than 100ul • the assay should have positive and negative controls with each kit. •adequate literature detailing the components, methodology, validity, criteria, performance characteristics, storage conditions and expiry date should be provided with each kit • the assay should have a shelf life on minimum 9 months at the time of deliver • the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transport at 20c 80c. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit size should be 96 wells per kit. •the kits should be supplied with compatible fully automatic elisa machine. the machine should have random access 4 plate elisa processor with non conductive cross contamination free disposable tips • 2 needle multi purpose lhs (liquid handling system) • process security through alarm system • up to 12 assays at a time • powerful operating software with integrated quality control • password protected user’s operation• lis – bidirectional interface to exchange information • positive identification of samples, microplates and reagents with monitoring of sample, and reagent pipetting including low volume, clot detection • 4 plates of 96 wells • 4 independent incubators. • 180 sample positions. • 24 reagent positions. • 36 control/standard position • 2 pre dilution positions • 4 × 108 tips positions. 83 hiv rapid test •the kit should be 4th generation immunochromatography, based on sandwich principle for qualitative detection of hiv antibodies.• the kit should be designed to detect: human specific igg and igm antibodies hiv 1 group m & group o;all known hiv1 subtypes a, b, c, d, e, f, g and h hiv 2• the kit should be able to detect antibodies to hiv 1 & 2 during early sero conversion period. evidence based sero conversion data should be provided. • samples can be used: serum, plasma (heparinated, edta),venous whole blood, capillary blood• the kit should have stability for 18 months at +4 to +30°c. • the kit should have positive and negative controls• the kit should be designed for near patient testing: minimum training required no centrifugation (if capillary or whole blood) time to result: 15 min (maximum 30 minutes for negative result).• sensitivity: serum & plasma: 99.5%.;whole blood: 99.9%.• specificity: serum & plasma: 99.5%.; whole blood: 99.5%.• preferably should be ce certified for hiv 1/2.• easy to use (no material required).• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• maintenance of cold chain during storage and transport at 20c – 80c.• the kit should have a shelf life of minimal 12 months at the time of delivery.• preferable pack size shall not be more than 50 tests wherein each device should be individually packed 84 hbsag rapid test kits • rapid, visual, qualitative test based on the association of monoclonaland polyclonal antibodies specific to hepatitis b virus.• a rapid test using immuno chromatography technology (ict or lateral flow) for the qualitative detection of hbsag.• the kit should detects all known hbsag subtypes and mutation monoclonal antibodies :adw2, adw4, adrq+, ayw1, ayw2, ayw3, ayw4, and ayr.• samples that can be used: serum plasma (heparinated, edta) venous whole blood capillary blood• the kit should have a stability of 18 months at 4 to 30°c.• the kit should be designed for near patient testing:• minimum training required• no centrifugation (if capillary or whole blood)• time to result: 15 minutes (maximum 30 minutes for negative result)• sensitivity: serum & plasma: 99.9%.;whole blood: 99.9%.• specificity: serum & plasma: 99.5%.;whole blood: 99.5%.• easy to use (no material required).• adequate literature detailing the components, methodology, validitycriteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have beeregistered and licensed in india by dcg (i)• maintenance of cold chain during storage and transport at 20c – 80c.• the kit should have a shelf life of minimal 12 months at the time of delivery.• preferable pack size shall not be more than 50 tests wherein eachdevice should be individually packed. 85 hcv rapid test kits 4th generation kit based on immunofiltration / chromatography•should be rapid, visual, sensitive and qualitative in vitro diagnostic kit for the detection of antibodies of hepatitis c virus in human serum and plasma.•should detect antibodies to putative core, ns3, ns4, and ns5 regions of hcv.•samples can be used:o serumo plasma (heparinated, edta)•the kit should have stability for 18 months at +4 to +30°c. • the kit should have positive and negative controls• the kit should be designed for near patient testing:•minimum training required•no centrifugation (if capillary or whole blood)• time to result: 15 min (maximum 30 minutes for negative result).• sensitivity: 100 %• specificity: 99.8%.• easy to use (no material required).• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• maintenance of cold chain during storage and transport at 20c – 80c.• the kit should have a shelf life of minimal 12 months at the time of delivery.• preferable pack size shall be not more than 50 tests wherein each device should be individually packed 86 rapid malaria antigen detection rapid visual antigen based test for detecting infection with plasmodium falciparum (hrp 2) and plasmodium vivax (pldh) of malaria parasite in human whole blood.• easy to run. total run time should not be more than 30 minutes• easy to interpret colour bands.• storage at +40c to +300c• sensitivity of the test should be 100%• specificity of the test should be 99.8%• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guidelines• the kit should have a shelf life of minimal 18 24 months at the time of delivery.• preferable pack size of 25 tests wherein each device should be individually packed 87 malaria elisa kit •malaria antigen elisa kit should have a principle of sandwich enzyme linked immunosorbent assay for the qualitative detection of the presence of plasmodium lactate dehydrogenase (pldh), an enzyme produced both in the sexual and asexual forms of parasite. and should have an excellent high level of sensitivity and specificity adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. •should be simple buffer assay rack for safety use•system configuration should be compatible with all common elisa equipments•stability : 12 months at 2~8? 88 tpha kits for syphilis detection • should be based on detection of antibodies to treponema pallidum in human serum or plasma.• should be based on the principle of haemagglutination using avian red cells.• should have positive and negative controls• the sensitivity should be > 99.8%• the specificity should be > 99.00%• the kit should have all accessories required for the test. adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit. • the kit should have a shelf life of minimal 18 24 months at the time of delivery.• preferable pack size of > 100 tests. • storage temperature for the kit should be +2 to +8oc 89 rpr for syphilis detection • should be bases on flocculation principle using non treponemal antigens.• qualitative determination of reagin antibodies in serum or plasma for sero diagnosis of syphilis.• should be calibrated to who reference serum. • should be suitable to use with either serum or plasma. • sensitivity should be > 70%• should be rapid preferably < 15 min• should have positive and negative controls• the kit should have all accessories required for the test such as cards, dropper, applicator.• the kit should have a shelf life of minimal 18 24 months at the time of delivery.• preferable pack size of > 100 tests. • storage temperature for the kit should be +2 to +8oc 90 syphilis elisa test kit • the kit should be based on “ sandwich†principle of enzyme linked immunosorbent assay(elisa) for the detection of igm and igg antibody against t. pallidum in human serum or plasma.• reagents should be preferably colour coded.• preferably colour change on addition of samples/reagents in the wells.• total incubation time should not be more than 2 hours.• sample volume should be small preferably not more than 100 µl.• the assay should have reactive and nonreactive controls with each kit.• sensitivity should be more than 99.9%.• specificity should be more than 99.5%.• adequate literature detailing the components, methodology, validity criteria, performance characteristics, storage conditions and expiry date should be provided with each kit.• the assay should have a shelf life of minimum 9 months at the time of delivery.• the manufacturer/authorized agent should ensure maintenance of cold chain during storage and transportation at 2 80 c.• the kit procured should have approval of the statutory authority in its country of origin. in case of imported kits it should have been registered and licensed in india by dcg (i) and as per naco guideline.• the kit size should be 96 wells per kit. 91 control sera for tti testing. • control sera (human base) for infectious diseases testing .• shelf life : minimum 2 year at 2–8oc• should have minimum 45 days open vial stability at 2–8oc• should be positive for anti hiv 1, anti hcv, hbsag, anti cmv.• should be compatible with all elisa kits and elisa machine. 92 single blood bag (350 ml) blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: single blood bag – 350 ml.should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpda label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 93 double blood bags(350ml) blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: • double bag primary bag 350 ml one satellite bag (300 ml)should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpda label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 94 double blood bag (450 ml) blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: • double bag primary bag 450 ml one satellite bag (300 ml)should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (63 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpda label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 95 double blood bags(350ml) blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: • double bag primary bag 350 ml one satellite bag (300 ml)should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml), 300ml transfer bag with 80ml additive solution & 100ml transfer bag pouch without transfusion port • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpda label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 96 double blood bag (450 ml) blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: • double bag primary bag 450 ml one satellite bag (300 ml)should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (63 ml), 300ml transfer bag with 80ml additive solution & 100ml transfer bag pouch without transfusion port • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpda label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 97 triple blood bag (350 ml) with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity : triple blood bag primary bag – 350 ml first satellite bag (300 ml) containing additive solution for 42 days red cell storage. second satellite bag (300 ml) for platelet storage for 5 days• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml)• clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand 98 triple blood bag (350 ml) without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: triple blood bag primary bag – 350 ml first satellite bag (300 ml) containing additive solution for 42 days red cell storage. second satellite bag (300 ml) for platelet storage for 5 days• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml)• additive solution (80 ml)• clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distor 99 triple blood bag (450 ml) with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: triple blood bag primary bag – 450 ml first satellite bag (300 ml) containing additive solution for 42 days red cell storage. second satellite bag (300 ml) for platelet storage for 5 days• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml)• clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand 100 triple blood bag (450 ml) without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: triple blood bag primary bag – 450 ml first satellite bag (300 ml) containing additive solution for 42 days red cell storage.second satellite bag (300 ml) for platelet storage for 5 days• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand 101 quadruple blood bag (350 ml) top and top with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (350 ml) with top and top first satellite bag – containing additive solution for 42 days red cell storage second satellite bag (300 ml) for platelet storage for 5 daysthird satellite bag (300 ml) fourth satellite bag (100ml)• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g 102 quadruple blood bag (350 ml) top and top without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (350 ml) with top and top first satellite bag – containing additive solution for 42 days red cell storage second satellite bag (300 ml) for platelet storage for 5 days third satellite bag (300 ml)fourth satellite bag (100ml)• sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperatu 103 quadruple blood bag (350 ml) top and bottom with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (350 ml) with top and bottom first satellite bag – containing additive solution for 42 days red cell storage second satellite bag (300 ml) for platelet storage for 5 days third satellite bag (300 ml) • sample pouch/diversion pouch for collection of first 15 to 20 ml blood should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml) • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity sh 104 quadruple blood bag (350 ml) top and bottom without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (350 ml) with top and bottom first satellite bag – containing additive solution for 42 days red cell storage, second satellite bag (300 ml) for platelet storage for 5 days third satellite bag (300 ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • cpda1 (49 ml) • additive solution (80 ml) primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temper 105 quadruple blood bag (450 ml) top and top with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (450 ml) with top and top. first satellite bag – containing additive solution for 42 days red cell storage, second satellite bag (300 ml) for platelet storage for 5 daysthird satellite bag (300 ml) fourth satellite bag (100ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temp 106 quadruple blood bag (450 ml) top and top without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag primary bag – (450 ml) with top and bottom or top and top. first satellite bag – containing additive solution for 42 days red cell storage, second satellite bag (300 ml) for platelet storage for 5 days , third satellite bag (300 ml), fourth satellite bag (100ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capa 107 quadruple blood bag (450 ml) top and bottom with sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag : primary bag – (450 ml) with top and bottom . first satellite bag – containing additive solution for 42 days red cell storage second satellite bag (300 ml) for platelet storage for 5 daysthird satellite bag (300 ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g 108 quadruple blood bag (450 ml) top and bottom without sample pouch blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: quadruple blood bag : primary bag – (450 ml) with top and bottom . first satellite bag – containing additive solution for 42 days red cell storage , second satellite bag (300 ml) for platelet storage for 5 daysthird satellite bag (300 ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000 109 penta blood bag (450 ml) with sample pouch with in line leukocyte reduction filter blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination. capacity: penta blood bag primary bag – (450 ml) with top and bottom or top and top. first satellite bag – containing additive solution for 42 days red cell storagesecond satellite bag (300 ml) for platelet storage for 5 days third satellite bag (300 ml)fourth satellite bag (300 ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity 110 penta blood bag (450 ml) without sample pouch with in line leukocyte reduction filter blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: penta blood bag primary bag – (450 ml) with top and bottom or top and top. first satellite bag – containing additive solution for 42 days red cell storagesecond satellite bag (300 ml) for platelet storage for 5 days third satellite bag (300 ml)fourth satellite bag (300 ml) should comply to iso 3826 standards for all the parameters & confirms to iso3826 should be printed on label. • sterilization process should be according to iso 17665 1 • should reduce moisture loss design and shapes:• flexible pre sterilized, pyrogen free , non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags). • slit on the both sides of the bags. tubing of bag:• flexible non kinking, non sticking ,transparent • leak proof. • the tubing should have same id number as that on the bag • the tube should have multiple printed id numbers with clear visibility. needle:• 16 gauge ultra thin walled and straight. • sharp regular margins and beveled tip.• rust proof. • tightly fixed with hub covered with sterile guard. • hermetically sealed external port: • tamper proof • shouldn’t be re capped • easily accessiblepackage: • protective dual packaging (individual & 4 layer aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle anticoagulant and preservative solution: • • cpd ( 63 ml) – primary bag only • additive solution (100 ml) – first satellite bag • clear & colourless • no discolouration on storage at room temperature• manufacturer to supply anticoagulant quality check certificate along with stability test report on cpd sagm label:• non peel off • heat sealed labels • remain attached between room temperature to 80c with a transparent adhesive • date of manufacturing, date of expiry and lot number must be mentioned on each bag, should have barcode printing and not stamping • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand 111 quintiple inline filter bags • quintuple in line redcell filter 450ml bags with sagm 4 pvc dehp bags and 1 pvc totm coated bag and lcrd filter for plasma, buffy coat derived paltelte cocnentrate and leuco depleted red cell concentrate preparation • soft housing lcrd filter offers a first step to move buffy coat method with short filtrationduration below 20 min and optimal leucoreduction • high componenet recovery filter >90%. • lcrd enables the filteration up to 24 hrs after collection at room temperature and up to 48 hrs after collection and storage at 1 ?c to 6 ?c • angled bevel 16 guage needle with silicon coating to reduce penetration force , • color making at the top of the hub indicating the bevel orientation and needle diameter , • molded needle hub with lining • same segment no in each tubing, • bactivam – pre donoation sampling pouch allows collection of 40ml of blood that may contain skin bacteria thus prevents contamination of complete blood unit and safety of receipients • secuvam – needle safety guard with unique locking mechanism to cover needle after blood collection ensuring safety of healthcare workers from needle stick injuries. irreversible lock with audio locking system 112 quadruple inline filter bags • quadruple in line redcell filter 450ml bags with sagm 4 pvc dehp bags and a lcrd filter for plasma, buffy coat and leuco depleted red cell concentrate preparation • soft housing lcrd filter offers a first step to move buffy coat method with short filtrationduration below 20 min and optimal leucoreduction • high componenet recovery filter >90%. • lcrd enables the filteration up to 24 hrs after collection at room temperature and up to 48 hrs after collection and storage at 1 ?c to 6 ?c • angled bevel 16 guage needle with silicon coating to reduce penetration force , • color making at the top of the hub indicating the bevel orientation and needle diameter , • molded needle hub with lining • same segment no in each tubing, • bactivam – pre donoation sampling pouch allows collection of 40ml of blood that may contain skin bacteria thus prevents contamination of complete blood unit and safety of receipients • secuvam – needle safety guard with unique locking mechanism to cover needle after blood collection ensuring safety of healthcare workers from needle stick injuries. irreversible lock with audio locking system 113 buffy coat pooling set • buffy coat pooling system comes with manifold 6 tubings for buffy pooling , dedicated tubing for additive solution bag , txp filter (optimal solution for leucocyte removal from platelet concentrate ) ,2 pvc dehp bags and 1pvc bthc(oxy pl) bag for platelet storage • train and octopus both buffy pooling method can be done • centrifuge compatable bags and filter • paltelet storage bag made of pvc bthc allows a better platlet viability due to its permiability • extremely high leucreduction preformace with a log reduction higher than 4 • validated upto 24hrs after the collection v) platelet storage volume 1800 ml • scd compatable tubings vii) screw on/off sampling site viii) steam sterilizationn used and comes with 2 years shelf life 114 paediatric blood bag blood collection bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.should comply to iso 3826 standards for all the parameters, iso 3826 test reports should be submitted. capacity : 100 ml design and shapes: • flexible pre sterilized • pyrogen free • non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all eaks proof seals (disposable bags). • slit on the both sides of the bagstubing of bag: • flexible non kinking • non sticking • transparent • leak proof • the tubing should have same id number as that on the bag. • the tube should have multiple printed id numberspackage: • protective dual packaging (individual & aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle label:• non peel off • heat sealed labels • remain attached between room temperature to 800c with a transparent adhesive• date of manufacturing, date of expiry and lot number must be mentioned on each bag • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 800c without breakage. 115 transfer bags (100 ml) capacity transfer bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: single blood bag – 100 mlshould comply to iso 3826 standards for all the parameters, design and shapes:• flexible pre sterilized• pyrogen free • non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags).• slit on the both sides of the bags tubing of bag:• flexible non kinking• non sticking • transparent • leak proof • the tubing should have same id number as that on the bag • the tube should have multiple printed id numberspackage: • protective dual packaging (individual & aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle label:• non peel off • heat sealed labels • remain attached between room temperature to 800c with a transparent adhesive• date of manufacturing, date of expiry and lot number must be mentioned on each bag • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 4c to 24c without becoming permanently distorted and should withstand temperature upto 80c without breakage. 116 transfer bags (300 ml) capacity transfer bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: single blood bag – 300 mlshould comply to iso 3826 standards for all the parameters,design and shapes:• flexible pre sterilized• pyrogen free • non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags).• slit on the both sides of the bags tubing of bag:• flexible non kinking• non sticking • transparent • leak proof • the tubing should have same id number as that on the bag • the tube should have multiple printed id numberspackage: • protective dual packaging (individual & aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle label:• non peel off • heat sealed labels • remain attached between room temperature to 800c with a transparent adhesive• date of manufacturing, date of expiry and lot number must be mentioned on each bag • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 800c without breakage. 117 transfer bags (600 ml) capacity transfer bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: single blood bag – 600 mlshould comply to iso 3826 standards for all the parameters,design and shapes:• flexible pre sterilized• pyrogen free • non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags).• slit on the both sides of the bags tubing of bag:• flexible non kinking• non sticking • transparent • leak proof • the tubing should have same id number as that on the bag • the tube should have multiple printed id numberspackage: • protective dual packaging (individual & aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle label:• non peel off • heat sealed labels • remain attached between room temperature to 800c with a transparent adhesive• date of manufacturing, date of expiry and lot number must be mentioned on each bag • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 800c without breakage. 118 transfer bags (1000 ml) capacity transfer bag made up of dehp plasticized pvc, collapsible, collapsible non vented sterile containers complete with collecting tube for completely closed system to avoid the chances of contamination.capacity: single blood bag – 1000 mlshould comply to iso 3826 standards for all the parameters, design and shapes:• flexible pre sterilized• pyrogen free • non toxic, non haemolytic, biocompatible material • no risk of contamination and air embolism (closed system) with all leaks proof seals (disposable bags).• slit on the both sides of the bags tubing of bag:• flexible non kinking• non sticking • transparent • leak proof • the tubing should have same id number as that on the bag • the tube should have multiple printed id numberspackage: • protective dual packaging (individual & aluminum) eliminating microbial contamination on surface maintaining the contents of the bag.• easy to handle label: • non peel off • heat sealed labels • remain attached between room temperature to 800c with a transparent adhesive• date of manufacturing, date of expiry and lot number must be mentioned on each bag • the expiry date should be at least 2 years from the date of supply of blood bags to the instituteresistance to distortion: filled to normal capacity shall withstand a acceleration of 5000g for 30 min at temperature 40c to 240c without becoming permanently distorted and should withstand temperature upto 800c without breakage. 119 apheresis kit for sdp single needle (fresenius) • for model com.tec , fresenius kabi .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure.• should able to perform procedure through single needle phlebotomy. 120 apheresis kit for sdp double needle (fresenius) • for model com.tec , fresenius kabi .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure.• should able to perform procedure through double needle phlebotomy. 121 apheresis kits for tpe (fresenius) • for model com.tec , fresenius kabi .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 122 apheresis kits for mnc collection (fresenius) • for model com.tec , fresenius kabi .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 123 apheresis kits for leucocytapheresis. (fresenius) • for model com.tec , fresenius kabi .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 124 apheresis kits for sdp single needle (fresenius) • for model amicus.• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure.• should able to perform procedure through single needle phlebotomy. 125 apheresis kits for sdp double needle (fresenius) • for model amicus.• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure.• should able to perform procedure through double needle phlebotomy. 126 apheresis kits for sdp (terumo bct) single needle • for model spectra optia , terumo bct .• disposable kit supplied with anticoagulant acd and normal saline withneedle set and other accessories required for procedure. 127 apheresis kits for sdp (terumo bct) double needle • for model spectra optia , terumo bct .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 128 apheresis kits for plasmapheresis (terumo bct) • for model spectra optia , terumo bct .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 129 apheresis kits for tpe and red cell exchange (terumo bct) • for model spectra optia , terumo bct .• disposable kit supplied with anticoagulant acd and normal saline withneedle set and other accessories required for procedure. 130 apheresis kits for mnc collection (terumo bct) • for model spectra optia , terumo bct .• disposable kit supplied with anticoagulant acd and normal saline with needle set and other accessories required for procedure. 131 red cell leukodepletion filters lab side •should provide 4 log reduction of leucocytes.•should be made of proven biocompatible material which is negatively charged.•if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required. •for laboratory type filter there should be a convenient system for air vent facility.•rbc losses should not be greater than 10%.•sterilization by ethylene oxide gas• should avoid cellular inactivation 132 red cell leukodepletion filters lab side •should provide 4 log reduction of leucocytes.•should be made of proven biocompatible material which is positively charged.•if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required. •for laboratory type filter there should be a convenient system to remove air from filtered blood with bypass line or air vent facility.•rbc losses should not be greater than 10%.•sterilization by ethylene oxide gas• should avoid cellular inactivation 133 red cell leukodepletion filters lab side with transfer bag •should provide 4 log reduction of leucocytes. with transfer bag with 600 ml capacity•should be made of proven biocompatible material which is neutral.•if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required. •for laboratory type filter there should be a convenient system for air vent facility.•rbc losses should not be greater than 10%.•sterilization by ethylene oxide gas• should avoid cellular inactivation 134 red cell leukodepletion filters lab side with transfer bag •should provide 4 log reduction of leucocytes. with transfer bag with 600 ml capacity•should be made of proven biocompatible material which is negatively charged.•if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required. •for laboratory type filter there should be a convenient system for air vent facility.•rbc losses should not be greater than 10%.•sterilization by ethylene oxide gas• should avoid cellular inactivation 135 red cell leukodepletion filters lab side with transfer bag •should provide 4 log reduction of leucocytes. with transfer bag with 600 ml capacity•should be made of proven biocompatible material which is positively charged.•if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required. •for laboratory type filter there should be a convenient system to remove air from filtered blood with bypass line or air vent facility.•rbc losses should not be greater than 10%.•sterilization by ethylene oxide gas• should avoid cellular inactivation 136 red cell leukodepletion filters lab side i) should have dockable labside redcell filter comes with leucolab lcg2b filter, 1pvc dehp transfer bag and pre filter 200micro meter ii) lcg2b enables the red cell concetrate filteration up to 24 hrs after collection at room temperature and up to 72 hours after collection and storage at 4 ?c iii) two layered filter system for up to 90% recovery of red cell iv) by pass system to maintain the sterility and recovery iv) sterilized by beta radiation v) performance as per aabb and european guidlines vi) three years self life 137 platelet leukodepletion filters lab side •should provide 4 log reduction of leucocytes.•should be made of proven biocompatible material which is neutral.• if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required.•for laboratory type filter there should be a convenient system for air vent facility.• platelet loss should be minimal.• sterilization by ethylene oxide gas• should avoid cellular inactivation 138 platelet leukodepletion filters lab side •should provide 4 log reduction of leucocytes.•should be made of proven biocompatible material which is negatively charged.• if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required.•for laboratory type filter there should be a convenient system for air vent facility.• platelet loss should be minimal.• sterilization by ethylene oxide gas• should avoid cellular inactivation 139 platelet leukodepletion filters lab side •should provide 4 log reduction of leucocytes.•should be made of proven biocompatible material which is positively charged.• if the filter requires priming, it should be suitable for easy and small volume priming. rinsing of the filter should not required.•for laboratory type filter there should be a convenient system for air vent facility.• platelet loss should be minimal.• sterilization by ethylene oxide gas• should avoid cellular inactivation 140 platelet leukodepletion filters lab side i) should have labside platelet filters txp filter (optimal solution for leucocyte removal from platelet concentrate ) ,1 pvc dehp bag and 1pvc bthc(oxy pl) bag for platelet storage ii) paltelet storage bag made of pvc bthc allows a better platlet viability due to its permiability iii) extremely high leucreduction preformace with a log reduction higher than 4 iv) validated upto 24hrs after the collection v) platelet storage volume 1800 ml vi) scd compatable tubings vii) screw on/off sampling site viii) steam sterilizationn used and comes with 2 years shelf life 141 standard blood transfusion set • standard blood transfusion sets should be made up of medical grade pvc, designed for transfusion of blood or blood component. • the plastic should be non toxic and pyrogen free. • it should have a moulded cylindrical drip chamber fitted with sharp plastic spike and a nylon filter with a pore size ranging from 170 260 microns.• the drip chamber containing the filter should be clear, transparent and have an adequate space for drop rate counting. the filter should be on top drip chamber for easy management• the plastic of the drip chamber and blood transfusion set tubing should have good elastic recoil to withstand manual or roller clamp compression.• there should be a roller type regulator for accurate control of flow of blood or blood component • the male port should be sturdy at least 1½ inches long with vertical slits for proper flow of blood. • female port should be able to fit snuggly with all the available venous access devices in the market. • there should be moulded bubble latex tube attached to the female port for extra medication • 18 g vein needle with protective cap. • it should be pre sterilized with ethylene oxide /gamma rays and ready for use. • it should accompany a sterility report. • all pvc items should be of certified medical grade only. • all the connections in the blood transfusion set should be leak proof.• standards:iso 10993;is 1135;usp class iv;ce 142 copper sulphate powder ( cuso4, 5 h2o) 250gm per pack ar of glaxo/e.merk/ranbaxy/unilab 143 ammonium hydroxide 500gm per pack ar glaxo/e.merk/ranbaxy/unilab 144 sulphuric acid h2so4 0.5 mol/l 1n 1 liter pack ar glaxo/e.merk/ranbaxy/unilab 145 ammonium oxalate powder 250 gm per pack glaxo/e.merk/ranbaxy/unilab 146 acid hydrochloride 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 147 dextrose powder 1 kg per pack latex agglutination ar glaxo/e.merk/ranbaxy/unilab 148 field stain a 500ml per pack ar glaxo/e.merk/ranbaxy/unilab 149 field stain b 500ml per pack ar glaxo/e.merk/ranbaxy/unilab 150 edta salt 250 gm per pack ar/ex/lobal/bdh/glaxo 151 gentian violet 100 gm /pack ar glaxo/e.merk/ranbaxy/unilab 152 giemsa stain 100ml bottle ar glaxo/e.merk/ranbaxy/unilab 153 giemsa stain 500ml bottle ar glaxo/e.merk/ranbaxy/unilab 154 glyserin ip 500 ml per pack ar glaxo/e.merk/ranbaxy/unilab 155 koh powder 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 156 leishman stain 100gm per pack ar glaxo/e.merk/ranbaxy/unilab 157 leishman stain 250 mg per pack ar glaxo/e.merk/ranbaxy/unilab 158 methylene blue staining reagent for reticulocytes 125 ml per pack glaxo/e.merk/ranbaxy/unilab 159 potassium permanganet crystal 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 160 potassium dihydrogen orthophosphate 500gm per pack ar glaxo/e.merk/ranbaxy/unilab 161 potassium ferrocyanide 100gm per pack ar glaxo/e.merk/ranbaxy/unilab 162 potassium ferrocyanide 250gm per pack ar glaxo/e.merk/ranbaxy/unilab 163 reticulin stain 100 gm per pack ar glaxo/e.merk/ranbaxy/unilab 164 sodium citrate 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 165 sodium citrate 1 kg per pack ar glaxo/e.merk/ranbaxy/unilab 166 sodium hydroxide 100gm per pack ar glaxo/e.merk/ranbaxy/unilab 167 sodium hydroxide 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 168 sodium carbonate 500gm per pack ar glaxo/e.merk/ranbaxy/unilab 169 sodium thiosulphate 500gm. per pack ar glaxo/e.merk/ranbaxy/unilab 170 sodium acetate 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 171 sodium dihydrogen orthophosphate 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 172 sodium ferricyanide 100gm per pack ar glaxo/e.merk/ranbaxy/unilab 173 sodium ferricyanide 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 174 sodium metabisulphate 100gm. per pack ar glaxo/e.merk/ranbaxy/unilab 175 phosphoric acid 250 ml per pack ar glaxo/e.merk/ranbaxy/unilab 176 phosphoric acid 1 ltr per pack ar glaxo/e.merk/ranbaxy/unilab 177 wright stain 1 ltr per pack ar glaxo/e.merk/ranbaxy/unilab 178 trisodium citrate ar 500gm per pack ar glaxo/e.merk/ranbaxy/unilab 179 papain powder 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 180 dtt(dithiothreitol) powder 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 181 l cysteine hydeochloride powder 5 gm/pack ar glaxo/e.merk/ranbaxy/unilab 182 imidazole powder 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 183 2 me(2 mercaptoetanol ) powder 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 184 phosphate buffer 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 185 dimethyl sulfoxide (dmso) 500 ml per pack ar glaxo/e.merk/ranbaxy/unilab 186 dimethyl sulfoxide (dmso) 20 ml per pack ar glaxo/e.merk/ranbaxy/unilab 187 polyethylene glycol 500 ml per pack ar glaxo/e.merk/ranbaxy/unilab 188 ficin powder 50 gm/pack ar glaxo/e.merk/ranbaxy/unilab 189 bovine thrombin powder 1 gm per pack 50 nih u/mg ar glaxo/e.merk/ranbaxy/unilab 190 glycerol powder 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 191 potassium hydrogen phosphate 500 gm per pack ar glaxo/e.merk/ranbaxy/unilab 192 double distilled water clear appearance. ph should be between 6 to 7. pack size 10 liter. 193 sodium hypochlorite solution 5% sodium hypochlorite solution.pack size : 5 lit. 194 thromboplastin reagent • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•liquid stable rabbit brain thromboplastin reagent with a shelf life of at least 18 months at 2 8°c. •the reagent must be stable for 7 days at rt and 2 days at 37°c. •the reagent must be available in the market for at least 10 years. •pack 5 ml/12 x 5ml •shelf life: 12 months at 2 8°c •pack 6 x 1m 195 cephaloplastin reagent reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•liquid stable rabbit brain cephaloplastin using ellagic acid as an activator with a shelf life of 18 months at 2 8°c. •the reagent must be stable for 7 days at rt and 2 days at 37°c. •shelf life: 12 months at 2 8°c •pack 6 x 1ml. 196 actin fsl • reagent should compatible with semiautomatic coagulometer sysmex model ca 50.• liquid purified soy and rabbit phosphatides in ellagic acid with added buffer, stabilizers and preservative.• can be used manually and on fully automated coagulation machine.• the reagent must be stable for 7 days at 2 to 80 c once opened.• shelf life: 12 months at 2 8°c 197 fibrinogen reagent • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•for quantitative estimation of fibrinogen. •the kit must include calibrator. •the reconstituted stability of thrombin reagent must be at least 2 weeks at 2 8°c. available in maximum 20 t packs. •shelf life: 12 months at 2 8°c 198 calcium chloride •reagent should compatible with semiautomatic coagulometer. sysmex model ca 50 and fully automated coagulation machine.•use for different coagulation assay.•cacl2 solution 0.025 mol/l.•pack size 10 x 15 ml.•shelf life: 12 months at 2 8°c. 199 owren’s kollar buffer • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•use for different coagulation assay.•ph should be 7.4•shelf life: 12 months at 2 8°c. 200 owren’s veronal buffer • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•use for different coagulation assay.•ph should be 7.4 • shelf life: 12 months at 2 8°c 201 imidazole buffer • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•use for different coagulation assay.•ph should be 7.4 • shelf life: 12 months at 2 8°c 202 coagulometer quality control reagents • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine. (lyocheck level 1, 2 and 3), should provide normal reference ranges for pt, aptt and fibrinogen 203 factor vii deficient plasma •reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•lyophilized human source plasma deficient in factor vii while having the other factors within normal limits. •the shelf life of the reagent must be at least 2 years. •the reconstituted stability of the reagent must be 1 month at 20°c. pack 5 x 1 ml •shelf life: 12 months at 2 8°c •pack 6 x 1ml. 204 factor viii deficient plasma •reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•lyophilized human source plasma deficient in factor viii while having the other factors within normal limits. •the shelf life of the reagent must be at least 2 years. •the reconstituted stability of the reagent must be 1 month at 20°c. •pack 5 x 1 ml •shelf life: 12 months at 2 8°c •pack 6 x 1ml. 205 factor ix deficient plasma • reagent should compatible with semiautomatic coagulometer sysmex model ca 50 and fully automated coagulation machine.•lyophilized human source plasma deficient in factor ix while having the other factors within normal limits. •the shelf life of the reagent must be at least 2 years. •the reconstituted stability of the reagent must be 1 month at 20°c. •pack 5 x 1 ml •shelf life: 12 months at 2 8°c •pack 6 x 1ml. 206 plasmatrol r •lyophilized preparation of human pool plasma with assayed values for pt/aptt/fibrinogen/factors ii, v, vii, viii, ix, x, xi and xii/protein c/protein s/antithrombin iii. •shelf life: 12 months at 2 8°c •pack 6 x 1ml. 207 cuvettes for ca 50 coagulometer cuvettes for semi auto coagulometer sysmex model ca 50 for coagulation test 208 pt reagent for il acl elite pro reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized preparation of rabbit thromboplastin and liquid preparation of buffer. •shelf life: 12 months at 2 8°c and 5 days after reconstitution of reagent at 40 c •pack : 5 x 8.5 ml reagent and 5 x 8.5 ml buffer 209 aptt reagent for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•aptt reagent with calcium chloride in lyophilized or liquid form.•shelf life: 12 months at 2 8°c and 30 days after opening of vial at 40 c•pack : 5 x 10 ml reagent and 5 x 10 ml buffer. 210 fibrinogen reagent for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized preparation of bovine thrombin. •shelf life: 12 months at 2 8°c.•pack : 10 x 2 ml reagent . 211 d dimer reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized preparation of latex reagent and d dimer calibrator and liquid preparation of reaction buffer.•shelf life: 12 months at 2 8°c and 30 days after reconstitution of reagent at 40 cpack : 4 x 3 ml reagent , 3 x 9 ml reaction buffer , 2 x 1 ml calibrator. 212 factor viii deficient plasma for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor viii while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •pack 10 x 1 ml •shelf life: 12 months at 2 8°c 213 factor vii deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor viii while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 214 factor ix deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor ix while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 215 factor ii deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor ii while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 216 factor v deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor v while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 217 factor x deficient plasma il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor x while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 218 factor xi deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor xi while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 219 factor xii deficient plasma for il acl elite pro • reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•lyophilized human source plasma deficient in factor xii while having the other factors within normal limits. •the reconstituted stability of the reagent must be 1 month at 20°c. •shelf life: 12 months at 2 8°c •pack 10 x 1ml. 220 vwf antigen reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• liquid latex reagent and liquid preparation of reaction buffer.•shelf life: 12 months at 2 8°c and 7 days after reconstitution of reagent at 40 cpack : reagent 2 x2 ml and substrate 4 x 4 ml 221 reagnet for vwf recof us fda approved test kits should be compitibale with il instruments; 2x2ml 222 vwf activity reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• liquid latex reagent and liquid preparation of reaction buffer.•shelf life: 12 months at 2 8°c and 7 days after reconstitution of reagent at 40 cpack : reagent 2 x4.5 ml and buffer 2 x 4.5 ml 223 aptt reagent for la test for il acl elite pro reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• reagent should be used for lupus anticoagulant assay.•shelf life: 12 months at 2 8°c and 7 days after reconstitution of reagent at 40 cpack : aptt reagent 5 x9 ml and calcium chloride 5 x 8 ml 224 reagent for drvvt screen and la screen for il acl elite pro reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• reagent should be used for lupus anticoagulant assay. •shelf life: 12 months at 2 8°c and 15 days after reconstitution of reagent at 40 c pack : drvtt screen 10 x2 ml and drvvt confirm 10 x 2 ml 225 reagent for drvvt confirm and la confirm for il acl elite pro reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• reagent should be used for lupus anticoagulant assay. •shelf life: 12 months at 2 8°c and 15 days after reconstitution of reagent at 40 c pack : drvtt scrren 10 x2 ml and drvvt confirm 10 x 2 ml 226 la positive control for il acl elite pro reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. pack : 1x10 ml 227 la negative control for il acl elite pro reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. pack : 1x10 ml 228 antithrombin reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• liquid fxa reagent and liquid substrate.•shelf life: 12 months at 2 8°c and 5 weeks after reconstitution of reagent at 40 cpack : reagent 2 x3ml and buffer 2 x 4 ml 229 protein c reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• lyophilized protein c activator and substrate and iquid diluents and working diluent.•shelf life: 12 months at 2 8°c and 90 days after reconstitution of reagent at 40 c pack : reagent 2 x2.5 ml and buffer 2 x 2.5 ml; diluent 1 x 8 ml. 230 free protein s reagent for il acl elite pro •reagents should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.• lyophilized recombinant tissue factor, ps deficient plasma and ps control plasma.•shelf life: 12 months at 2 8°c and 90 days after reconstitution of reagent at 40 cpack : reagent 3 x 3 ml; ps def plasma 5 x 1 ml; ps control plasma 2 x 1 ml. 231 rinse solution for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 232 reference emulsion solution for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 233 clean a for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 234 clean b for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 235 factor diluent for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 236 calibration plasma for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 237 normal control assayed for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 238 low abnormal control assayed for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 239 high abnormal control assayed for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.the shelf life of the reagent must be at least 1 year. 240 d dimer controls level 1 for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 241 d dimer controls level 2 for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 242 low fibrinogen control for il acl elite pro •reagent should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•the shelf life of the reagent must be at least 1 year. 243 rotors for il acl elite pro •should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•to perform different coagulation test. 244 cup for il acl elite pro •should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•to perform different coagulation test.•capacity : 0.5 ml 245 cup for il acl elite pro •should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•to perform different coagulation test.•capacity : 2 ml 246 clening solution clean a for il instrument; 1 x 500 ml 247 cleaning solution clean b for il instrument; 1 x 80 ml 248 cuvette for test cuvettes/ rotor for il instrument; 2400 test 249 cup for il acl elite pro •should compatible with fully automatic coagulometer of instrument and laboratory model acl elite pro.•to perform different coagulation test.•capacity : 4 ml 250 cell pack (diluent) for cell counter •for cell counter model sysmex kx 21•the shelf life of the reagent must be at least 1 year. 251 lyser (diluent) for cell counter •for cell counter model sysmex kx 21•the shelf life of the reagent must be at least 1 year. 252 cell clean for cell counter •for cell counter model sysmex kx 21•the shelf life of the reagent must be at least 1 year. 253 controls for cell counter •for cell counter model sysmex kx 21•the shelf life of the reagent must be at least 1 year. 254 calibrators for cell counter •for cell counter model sysmex kx 21•the shelf life of the reagent must be at least 1 year. 255 thermal paper for cell counter for cell counter model sysmex kx 21and to print cbc report from cell counter 256 cryovial to preserve the serum sample . 2ml vial 257 temperature recording chart for 2 60 c blood bag refrigerator helmer • for model hhb 120.• should be made up of good quality thermal paper and ink should not be spread out. • 7 days (weekly) temperature recording .• temperature range should be 500 to +20 0 c 258 temperature recording chart for 2 60c blood bag refrigerator haier • for model hxc 608 a.• 7 days (weekly) temperature recording .• should be made up of good quality thermal paper and ink should not be spread out. • temperature range should be 400 to +30 0 c 259 temperature recording chart for 2 60c blood bag refrigerator remi • for the model br300. • 7 days (weekly) temperature recording . • should be made up of good quality paper and ink should not be spread out. • temperature range should be 100 to +20 0 c 260 temperature recording chart for platelet incubator terumo penpol • for model pi200• 7 days (weekly) temperature recording .• should be made up of good quality paper and ink should not be spread out. • temperature range should be 0 to +40 0 c 261 temperature recording chart for 2 60 c refrigerator terumo penpol • for model bbr g600• 7 days (weekly) temperature recording .• should be made up of good quality paper and ink should not be spread out. • temperature range should be 0 to +40 0 c 262 temperature recording chart for 400 c refrigerator terumo penpol • for model df 40u• 7 days (weekly) temperature recording .• should be made up of good quality paper and ink should not be spread out. • temperature range should be 500 to +30 0c 263 temperature recording chart for 800 c refrigerator terumo penpol • for model df 80u • 7 days (weekly) temperature recording .• should be made up of good quality thermal paper and ink should not be spread out.• temperature range should be 1000 to +50 0 c 264 ink pen for temperature recording chart ink pen for temperature recording chart to record 7 days (weekly) temperature on chart . should be made up of good quality and ink should not be spread out. 265 thermel pen for temperature recording chart thermal pen for temperature recording chart to record 7 days (weekly) temperature on thermal chart . should be made up of good quality. 266 tips 2 200ul for dispensing samples/reagents in routine immunohematology tests 267 tips 100 1000 ul for dispensing samples/reagents in routine immunohematology tests 268 carbon biotips 300ul, for dispensing reagents in fully automatic elisa machine evolis 269 carbon biotips 1100ul, for dispensing reagents in fully automatic elisa machine evolis 270 disposable plastic test tubes • should made from good quality transparent colourless plastic.• size : 12 mm x 75 mm• without screw cap 271 disposable glass test tubes • should made from good quality transparent colourless glass.• size : 12 mm x 75 mm• without screw cap 272 glass slide • microscopic polished edge and lint free glass slides.• should made from transparent colourless glass.• should have refractive index (ne) 1.53 + 0.02.• size : 76 mm x 26 mm; thickness : 1.10 mm. 273 ph indicator strips range : 2 to 10.5. box of 10 strips graduation 1 ph, iso, sigma/ glaxo/siemens/beyer 274 ph indicator strips range : 5 to 8, graduation 0.5 ph box of 10 strips iso, sigma/ glaxo/siemens/beyer 275 ph indicator strips ph range 6.0 7.7 graduation 0.3 0.4 ph, iso, sigma/ glaxo/siemens/beyer 276 ph tablets use for measurement and calibration of ph meter with ph 4. 277 ph tablets use for measurement and calibration of ph meter with ph 7 278 ph tablets use for measurement and calibration of ph meter with ph 9.2 279 wafer wafer for tscd model sc 201(sterile tube connecting device) use for connecting tubings in sterile condition. 280 lancets for hb estimation and blood grouping by finger prick.should fit the lancet gun device.should have protective cap. 281 filter paper whatman / whatman type superquality.size 57 cm x 46 cm. 282 biological indicator • use for quality control of autoclaving.• should contain spores of bacillus stereothermophillus.• spores per unit should be 1.0 x 105 to 5 x 106• survival time limit for a suitable resistance should be 4.5 to 14 min.• indicator change the colour after autoclaving at 1210 c temperature for 30 min.• should packaged in a suitable primary overwrap package that does not adversely affect the performance of the indicator. 283 temperature indicator • use to monitor cold chain maintenance during transportation of blood and blood components. • response to temperature at or more than 90 c. • should have irreversible colour change in a window and simple to read.• response time to temperature should be not more than 2 hours.• should not require any activation to start the monitoring. accuracy ± 10 c.• self adhesive and easy to apply on blood bags.• no known toxicity of active material.• time temperature indicator technology used should be qualified by a recognized regulatory body. 284 temperature indicator • use to monitor cold chain maintenance during transportation of blood and blood components.• response to temperature at or more than 250 c. • should have irreversible colour change in a window and simple to read.• response time to temperature should be not more than 2 hours.• should not require any activation to start the monitoring. accuracy ± 10 c.• self adhesive and easy to apply on blood bags.• no known toxicity of active material.• time temperature indicator technology used should be qualified by a recognized regulatory body. 285 haemoglobin estimation test system for blood donor screening • haemoglobin estimation test system for blood donor screening. • should be based on broad spectrum photometric measurement of hb.• system should be light weight and easy to transport.• should measure hb of capillary whole blood.• digital display of result in gm/dl within 10 seconds with high accuracy and precision.• should be provided with reagent free disposable cuvette .• disposable cuvettes should not influenced by temperature and humidity.• should have built in self check before every measurement.• disposable cuvette should have long expiry (at least 12 months).• the system should have minimum 24 hours battery back up after full charging.• the equipments for measuring thehaemoglobin six in number should be provided with test system without any additional cost. the maintenence, repair and calibration will be the responsibility of vendor. 286 microcuvette for hb estimation. microcuvette for hb estimation for hemocue machine model hb 301.disposable microcuvette should have long expiry (at least 12 months).pack : 4 x 50 287 control for hemocue hb301 control for hemocue hb301 : high, low and normal control to verify hemocue hb 301. 288 antiseptic solution for phlebotomy • should be used for surgical cleaning of the arm(venipuncture site) of blood donor before collection of blood.• should be bactericidal, fungicidal and virucidal.• should be non allergic and non irritating.• should be supplied with plastic container for easy handling.• expiry : at least 12 months 289 disposable reagent troughs/reservoir • should be use for reagent reservoir e.g. buffer, conjugate, substrate during elisa testing.• should be made up of polypropylene/pvc with cylindrical shape and v shape bottom.• capacity : 20 ml.• size : height : 7.5 cm; diameter : 2.5 cm. 290 disposable reagent troughs/reservoir • should be use for reagent reservoir e.g. buffer, conjugate, substrate during elisa testing.• should be made up of polypropylene/pvc with rectangle shape and flat bottom.• capacity : 20 ml.• size : 9 x 6 x 2 cm.. 291 platelet additive solution 250ml •should be used for apheresis platelet concentrate or buffy coat platelet concentrate or random donor platelet in up to 80% platelet additive solution and 20% plasma to reduce plasma volume of platelet component to decrease adverse events e.g. trali and abo mismatch.•platelet quality, function, storage stability, morphology and cell integrity must be well maintained during processing and storage of platelet concentrate after adding platelet additive solution.•platelet product can be stored up to 5 days at 20 to 240 c in platelet incubator with agitator.•should be compatible with all available technologies for preparation of platelet components. (e.g. automated devices for whole blood and apheresis derived platelet.)•the container of solution should be made up of non pcv material e.g. polyolefin.•container should have connections for sterile connection and luer lock for easy connection to apheresis kits.•should have shelf life of 24 months.•the product should have been registered and licensed in india by dcg(i).•should be available in volume of 250 ml. 292 platelet additive solution 300ml • should be used for apheresis platelet concentrate or buffy coat platelet concentrate or random donor platelet in up to 80% platelet additive solution and 20% plasma to reduce plasma volume of platelet component to decrease adverse events e.g. trali and abo mismatch.•platelet quality, function, storage stability, morphology and cell integrity must be well maintained during processing and storage of platelet concentrate after adding platelet additive solution.•platelet product can be stored up to 5 days at 20 to 240 c in platelet incubator with agitator.•should be compatible with all available technologies for preparation of platelet components. (e.g. automated devices for whole blood and apheresis derived platelet.)•the container of solution should be made up of non pcv material e.g. polyolefin.•container should have connections for sterile connection and luer lock for easy connection to apheresis kits.•should have shelf life of 24 months.•the product should have been registered and licensed in india by dcg(i).•should be available in volume of 300 ml. 293 platelet additive solution 500ml • should be used for apheresis platelet concentrate or buffy coat platelet concentrate or random donor platelet in up to 80% platelet additive solution and 20% plasma to reduce plasma volume of platelet component to decrease adverse events e.g. trali and abo mismatch with polyolefin bag and two connectors (manual and apheresis) •platelet quality, function, storage stability, morphology and cell integrity must be well maintained during processing and storage of platelet concentrate after adding platelet additive solution.•platelet product can be stored up to 5 days at 20 to 240 c in platelet incubator with agitator.•should be compatible with all available technologies for preparation of platelet components. (e.g. automated devices for whole blood and apheresis derived platelet.)•the container of solution should be made up of non pvc material e.g. polyolefin.•container should have connections for sterile connection and luer lock for easy connection to apheresis kits.•should have shelf life of 24 months.•the product should have been registered and licensed in india by dcg(i).•should be available in volume of 500 ml. 294 dockcounter dockcounter for compodock fresenius model s 2 (sterile tube connecting device) use for connecting tubings of blood bags in sterile condition. 295 variant ii for hplc (bio rad) should compatible with variant ii for high performance liquid chromatography (hplc) (bio rad) including all reagents and accessories elusion buufer 1 2, whole blood primer, calibrator diluent set, cartridge, aliqote, wash diluent 296 controls for variant ii for hplc (bio rad) should compatible with variant ii for high performance liquid chromatography hplc (bio rad). cat # 553 (4 x 0.5 ml) lyphocheck a2 control ...
Due Date : August 24, 2022
Tender Value : ₹ Ref. Documents
