TENDER FOR PROCUREMENT OF LABORATORY KITS, ANTI SERA, BLOOD BAGS, VACUTAINER, ETC., ITEMS

TENDER NO : DMC(D-H&H)/CMS/11/2025-26

NOTE : THIS SHEET IS USED ONLY FOR CALCULATION OF EMD PURPOSE. DO NOT QUOTE/MENTION RATE HERE. PLEASE ATTACHED THIS SHEET WITH ONLINE TECHNICAL BID.

Item Serial Item Code Item Name Specification Del Days Quantity Unit Description EMD Rs. QUOTED ITEMS Y/N QUOTED MANUFACTURER CO.

1 23/001/0003/00/0/0/0 EOSIN 2% LIQUID ( READY TO USE & ISO CERTIFIED - AR) 100ML 30 25 BOTTLE 100.00

2 23/001/0007/00/0/0/0 HEMATOXYLENE (HARRIS) LIQUID (READY TO USE & ISO CERTI.) AR-100ML 30 60 BOTTLE 200.00

3 23/001/0009/00/0/0/0 GIEMSA STAIN SOLUTION(READY TOUSE PREFER WITH BUFER&ISO CERT-100ML 30 2000 BOTTLE 3800.00

4 23/001/0020/00/0/0/0 REAGENT STRIP FOR URINE ANALYSIS-MULTISTIX-BOTTLE OF 100 STRIP SHOULD INCLUDE PARAMETERS GLUCOSE, SPECIFIC GRAVITY, PH, PROTEIN, BLOOD, UROBILINOGEN,BILLIRUBIN AND KETONE BODIES. 30 225 BOTTLE 100.00

5 23/001/0021/00/0/0/0 KETODIASTIX STRIP FOR DETECT OF SUGAR,ACETONE IN URINE-BOTLE 50 STRIP 30 110 BOTTLE 100.00

6 23/001/0022/00/0/0/0 HAEM TEST (OCULT BLOOD TEST) 30 4000 TEST 200.00

7 23/001/0023/00/0/0/0 URISTIX STRIPS--BOTTLE OF 100 STRIP 30 1400 BOTTLE 900.00

8 23/001/0026/00/0/0/0 LEISHMAN STAIN SOLU(CYTOCHROMIC)READY TO USE WITH BUFER BSC CERT-500ML BSC CERTIFIED 30 110 BOTTLE 600.00

9 23/001/0030/00/0/0/0 22% BOVINE ALBUMIN VIAL OF 5 ML 1.FDA Approved (Fulfil DGHS criteria).2. No precipitate, particles or gel.3. >98% albumin, as determied by electrophoresis.4. No agglutination of unsensitized red cells; no hemolytic activity; no prozone phenomenon. 5. IgG anti-D should give a titer of 32-64 with red cell R1 cell.6. Pack Size - 05 ml vial 7. Shelf Life - Minimum 18 months. Additional information 8. company should provide the record of temprature maintainance during storage and transport at the time of delivery. 30 8 VIAL 100.00

10 23/001/0031/00/0/0/0 COOMB'S SERUM ( ANTI HUMAN SERUM) (POLY SPECIFIC) 5ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 120 VIAL 200.00

11 23/001/0041/00/0/0/0 NUTRIENT AGAR (BACTERIOLOGIAL MEDIA)--500GM 30 85 BOTTLE 1800.00

12 23/001/0042/00/0/0/0 MACCONKEY'S AGAR(BACTERIOLOGIALMEDIA)500GM(W/CV,NaCLAND 0.15%BILE SALT PEPTONE 20.0GM, SODIUM CLORIDE 5.0 GM, LACTOSE 10.0 GM,BILE SALTS 1.5 GM,NUTRAL RED 0.05GM, CRYSTAL VIOLET 0.001 GM, AGAR 15.0GM, PH 7.2+/- 0.2 30 95 BOTTLE 3100.00

13 23/001/0045/00/0/0/0 GLUCOSE PHOSPHATE BROTH (BACTERIOLOGIAL MEDIA) 500 GM 30 10 BOTTLE 500.00

14 23/001/0056/00/0/0/0 RETICULOCYTE COUNTING FLUID(READY TOUSE& ISO CERTI.) AR 25ML 30 40 BOTTLE 300.00

15 23/001/0061/00/0/0/0 CALCIUM CHLORIDE REAGENT FOR APTT--10ML 30 245 VIAL 300.00

16 23/001/0065/00/0/0/0 BLOOD GROUP SERA ANTI 'A' MONOCLONAL--10ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 1300 VIAL 900.00

17 23/001/0066/00/0/0/0 BLOOD GROUP SERA ANTI 'B' MONOCLONAL--10ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 1300 VIAL 900.00

18 23/001/0067/00/0/0/0 BLOOD GROUP SERA ANTI 'D' MONOCLONAL IgM--10ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 1300 VIAL 2000.00

19 23/001/0068/00/0/0/0 BLOOD GROUP SERA ANTI-D (POLYCLONAL IgM+IgG)--10ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 155 VIAL 300.00

20 23/001/0069/00/0/0/0 ANTI A1 (LECTIN)--5ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 30 VIAL 100.00

21 23/001/0070/00/0/0/0 ANTI H--5ML VIAL TO REFER SPECIFICATION IN TECHNICAL BID. 30 4 VIAL 100.00

22 23/001/0071/00/0/0/0 BLOOD GROUP SERA ANTI AB--10ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 36 VIAL 100.00

23 23/001/0116/00/0/0/0 VIRAL TRANSPORT MEDIUM 3ML VTM IN 15ML TUBE WITH 2 VISCOS SWABS 30 3000 NUMBER 200.00

24 23/001/0119/00/0/0/0 TCBS AGAR--100GM YEST EXTRACT 5.0 GM,SODIUM CITRATE 10.0 GM, SODIUM THIOSULPHATE 10.0 GM , SODIUM CHOLATE 3.0 GM, BILE # 5.0 GM,SUCROSE 20.0 GM ,SODIUM CLORIDE 10.0 GM , FERRIC CITRATE 1.0 GM, BROMO THYMOL BLUE 0.040 GM , THYMOL BLUE 0.040 GM, AGAR 15.0 GM , PH 8.8 +/- 0.2 30 25 BOTTLE 300.00

25 23/001/0122/00/0/0/0 ALKALINE PEPTONE WATER 100 GMS. PEPTIC DIGEST OF ANIMAL TISSUE 20.0 GM ,SODIUM CLORIDE 30.0 GM, PH 8.6 +/- 0.2 30 2 BOTTLE 100.00

26 23/001/0125/00/0/0/0 TRIPLE SUGAR IRON AGAR--100GM 30 35 BOTTLE 300.00

27 23/001/0135/00/0/0/0 CALCIUM KIT ARSENAZO-III METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID. 30 36000 MILILITER 700.00

28 23/001/0136/00/0/0/0 CHOLINESTRASE BUTIRYL THIOCHOLINE/PROPIONYL THIOCHOLINE SUBSTRATE SUBSTRATE, KINETIC KIT SHOULD BE ABLE TO ESTIMATE ACTIVITY OF CHOLINESTRASE IN SERUM. TO REFER SPECIFICATION IN TECHNICAL BID. 30 5500 MILILITER 1600.00

29 23/001/0139/00/0/0/0 HbsAg ELISA KIT BASE ON 3RD GEN.(MONOCLONAL ANTIBODIES) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. Sensitivity -: 100 %• Antigen sensitivity should be 0.05 ng/ml.• Specificity -: More than or equal to 98 %.• Assay time should not be more than 2 hours.• Detects all the known 11 subtypes of HBV and also mutant strains.• Shelf life -: minimum 9 months at the time of delivery. 30 24576 TEST 2100.00

30 23/001/0140/00/0/0/0 HCV ELISA KIT TO REFER SPECIFICATION IN TECHNICAL BID. 30 14016 TEST 1800.00

31 23/001/0141/00/0/0/0 HCV RAPID KIT STRIP TEST (IC) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. SENSITIVITY: 100 %, SPECIFICITY: MORE THAN 98%. 30 29000 TEST 4300.00

32 23/001/0156/00/0/0/0 TOTAL PROTEIN KIT BIURET METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID. 30 44000 MILILITER 400.00

33 23/001/0157/00/0/0/0 RPR TEST FOR SYPHILIS (CHARCOAL CARBON PARTICLE) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 165000 TEST 3200.00

34 23/001/0224/00/0/0/0 QUADRUPLE BLOOD BAG 450 ML WITH SAGM TO REFFER SPECIFICATION IN TECHNICAL BID. 30 520 NUMBER 1700.00

35 23/001/0229/00/0/0/0 DOUBLE BLOOD BAG 350ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 2400 NUMBER 3500.00

36 23/001/0249/00/0/0/0 DOUBLE BLOOD BAG 450ML WITH SAGM TO REFER SPECIFICATION IN TECHNICAL BID. 30 6600 NUMBER 13100.00

37 23/001/0252/00/0/0/0 TRANSFER BAG 300ML CAPA.,FDA, APROVED, QUALITY CERTI.(CE,ISO-9001-2000) 30 3000 NUMBER 2200.00

38 23/001/0267/00/0/0/0 PENTA BLOOD BAG Mother bag of the Penta blood bag should have 450ml capacity and is connected to four satellite transfer bags of 100ml capacity.Mother bag should be with 0.39mm thickness and the inner iameter of the transfer tube from mother bag should be with 2.95±0.05mm ID to provide easy flow of the blood. Needle should be 16G with triple bevel design to reduce penetration force and enable painless vein puncture Blood bags should have segment numbers in all tubes of the transfer bags.Blood Bags and its packing should be properly labeled with Batch. No., Date of Mfg., and Date of Expiry.Product labels should be barcoded as per ISBT-128.Secondary packing and shipping cartons should be barcoded as per GS1-128.3 units of bags is packed in an outer cover with sufficient barrier properties to prevent moisture loss during storage.Complies to ISO 3826 and quality of blood components stored as per Indian Drugs and Cosmetics Act. 30 108 NUMBER 500.00

39 23/001/0268/00/0/0/0 TRIPLE BLOOD BAG WITH SAGM 450ML TO REFER SPECIFICATION IN TECHNICAL BID. 30 3000 NUMBER 8400.00

40 23/001/0269/00/0/0/0 DOUBLE BLOOD BAG 450ML TO REFER SPECIFICATION IN TECHNICAL BID 30 3000 NUMBER 4500.00

41 23/001/0270/00/0/0/0 CPDA SINGLE BLOOD BAG 350ML TO REFER SPECIFICATION IN TECHNICAL BID 30 100 NUMBER 100.00

42 23/001/0406/00/0/0/0 SYPHILIS Ab RAPID TEST KIT ( DIP STRIP ) TO REFER SPECIFICATION IN TECHNICAL BID. 30 88000 TEST 8800.00

43 23/001/0407/00/0/0/0 RAPID MALARIA KIT TO REFER SPECIFICATION IN TECHNCAL BID. 30 515000 TEST 57200.00

44 23/001/0412/00/0/0/0 LEPTOSPIRA RAPID KIT (FOR IgM DETECTION) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 50 TEST 100.00

45 23/001/0610/00/0/0/0 TOP & BOTTOM QUADRUPLE BLOOD BAG WITH INTEGRATED FILTER FOR COMPONENT TO REFER SPECIFICATION IN TECHNICAL BID 30 1188 NUMBER 12000.00

46 23/001/0924/00/0/0/0 PARAFFIN WAX in generular(Pellets) form(MELTING POINT 58' - 60') 30 150 KILO GRAMME 1000.00

47 23/002/0005/00/0/0/0 PARAFFIN WAX (MELTING POINT 58'-60') 30 250000 GRAMME 1600.00

48 23/002/0024/00/0/0/0 COPPER SULPHATE ANALYTICAL GRADE--500GM 30 37 BOTTLE 200.00

49 23/002/0035/00/0/0/0 SGOT/AST. AST: IFCC KINETIC WITH PLP TO REFER SPECIFICATION IN TECHNCAL BID. 30 57000 MILILITER 1200.00

50 23/002/0036/00/0/0/0 SGPT/ALT. ALT: IFCC KINETIC WITH PLP TO REFER SPECIFICATION IN TECHNICAL BID. 30 52000 MILILITER 1100.00

51 23/002/0168/00/0/0/0 COOMBS SERUM IgG--5ML VIAL SHELF LIFE SHOULD MORE THAN 18 MONTHS 30 4 VIAL 100.00

52 23/002/0169/00/0/0/0 BLOOD GROUP SERA ANTI D MONOCLONAL (IgG)--10ML VIAL 30 10 VIAL 100.00

53 23/003/0001/00/0/0/0 LDL CHOLESTEROL BY DIRECT METHOD TO REFER SPECIFICATION IN TECHNCAL BID. 30 8500 MILILITER 1600.00

54 23/003/0003/00/0/0/0 S.AMYLASE TEST KIT CNP-G3 KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 7500 MILILITER 1100.00

55 23/003/0004/00/0/0/0 S.URIC ACID TEST KIT URICASE PEROXIDASE END POINT TO REFER SPECIFICATION IN TECHNICAL BID. 30 16500 MILILITER 900.00

56 23/003/0005/00/0/0/0 TRIGLYCERIDES ENZYMATIC,END POINT TO REFER SPECIFICATION IN TECHNICAL BID. 30 22000 MILILITER 1500.00

57 23/003/0006/00/0/0/0 S.BILIRUBIN TEST KIT TOTAL&DIRECT, JENDRASSIK&GROF'S METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID. 30 103000 MILILITER 1100.00

58 23/003/0007/00/0/0/0 S.CRETININE TEST KIT ALKALINE PICRATE FIX TIME KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 75000 MILILITER 400.00

59 23/003/0008/00/0/0/0 HDL-CHOLESTEROL DIRECT HOMOGENOUS METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 20500 MILILITER 3100.00

60 23/003/0009/00/0/0/0 S.PHOSPHEROUS TEST KIT MOLYBDATE AT 340nm WITHOUT REDUCING AGENT TO REFER SPECIFICATION IN TECHNICAL BID. 30 5300 MILILITER 200.00

61 23/003/0013/00/0/0/0 URINE PREGNANCY TEST KIT ( STRIP ) 30 160000 TEST 5400.00

62 23/003/0014/00/0/0/0 GLUCOSE TEST KIT ENZYMATIC GLUCOSE OXIDASE PEROXIDASE METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 55000 MILILITER 300.00

63 23/003/0016/00/0/0/0 A.S.O.TEST KIT RAPID SLIDE TEST,POSSITIVE & NEGATIVE CONTROL & NECESSARY ACCESSERIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 5000 TEST 400.00

64 23/003/0017/00/0/0/0 R.A. TEST KIT RAPID SLIDE AGGLUTINATION TEST METHOD WITH POSSITIVE & NEGATIVE CONTROLS & NECESSARY ASSECCERIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 9000 TEST 500.00

65 23/003/0018/00/0/0/0 C.R.P. TEST KIT LATEX AGGLUTINATION TEST WITH CONTROL & NECESSARY ACCESSRIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 35000 TEST 2000.00

66 23/003/0023/00/0/0/0 GLUCOSE 6 PHOSPHATE DEHYDROGENASE(1) SCREENING (G.6.P.D SINGLE TEST VIAL & TEST TO BE COUNTED T IN 11/2 TO 1 HOURS THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS. 30 13000 TEST 3800.00

67 23/003/0025/00/0/0/0 LACTATE DEHYDROGENASE KINETIC AT UV RANGE KIT SHOULD BE BASED ON LACTATE TO PYRUVATE CONVERSION. TO REFFER SPECIFICATION IN TECHNICAL BID. 30 9500 MILILITER 300.00

68 23/003/0030/00/0/0/0 FIBRINOGEN KIT (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION FOR FIBRINOGEN(2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP(5) CE MARK, ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHOULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FIBRINOGEN IN CASES OF DIC 30 40 TEST 100.00

69 23/003/0031/00/0/0/0 FIBRIN DEGRADATION PRODUCT KIT (FDP) (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION OF FIBRIN DEGRADATION PRODUCTS (2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP (5) CE MARK,ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FDP IN CASES OF DIC 30 2000 TEST 3900.00

70 23/003/0033/00/0/0/0 HIV IMMUNOCOMB RAPID TEST TO REFER SPECIFICATION IN TECHNICAL BID.1. Employs same principle as Enzyme Immuno Assay(EIA) whereby the immmobilised antigen-antibody complex is visuallised by means of chromogenic reaction 2.There should be coloured end point developed by a colloidal Gold Protein A Signal reagent 3. Each tooth of comb is spotted with a circular spot,one near the tip with an optimally standardised blend of HIV 1 & HIV 2 recombinant antigens and /or synthetic peptides (test spot),and the other spot ,a little above the first spot is spotted with control reagent (Control spot) 4. The immune comlpex should be directly visualised after incubation with the colloidal Gold -Protein A Signal reagent. 5. Built in control should be visualised seprately in the upper part of the tooth(Control area),where control reagent has been spotted, serving as the procedural control 6. Pink coloured spot/Dot should always appear at the control area with recommended test specimen irrespective of the presence or absence of HIV antibodies in the specimen 7. Test should have 100%Sensitivity as well 100% Specificity,too. 30 255000 TEST 33100.00

71 23/003/0034/00/0/0/0 ACTIVATED PARTIAL PROTHOMBIN TIME (APTT) KIT READY TO USE READY TO USE 30 2450 MILILITER 1700.00

72 23/003/0035/00/0/0/0 A.S.O. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. 30 500 TEST 200.00

73 23/003/0036/00/0/0/0 R.A. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. 30 2200 TEST 500.00

74 23/003/0037/00/0/0/0 C.R.P. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. 30 7500 TEST 1900.00

75 23/003/0038/00/0/0/0 RAPID PAP STAIN KIT OF 250 TEST (1) ONE KIT SHOULD STAIN ATLEAST 250 SMEARS. (2) STAIN SHOULD BE COMPLETED WITHIN 3 MIN.(3) IT SHOULD CONTAIN- NUCLEAR STAIN- CYTOPLASMIC STAIN- OG-65 SOLUTION- LIGHT GREEN SF EOSIN- BIO-FIX SPARY- DPX- XYLENE- WASH BUFFER (4) IT SHOULD GIVE COMPARABLE RESULT WITH USUAL PAP STAIN IT IS MUST FOR REPORTING OF GYNAC SMEAR, OTHER CYTOLOGY SMEAR AND MASS CYTOLOGY SCREENING CAMP. 30 100 KIT 1100.00

76 23/003/0040/00/0/0/0 BRAIN THROMBOPLASTIN (PROTHOMBINTIME TEST KIT) 30 4750 MILILITER 2400.00

77 23/003/0041/00/0/0/0 CSF PROTEIN/URINARY PROTEIN BY PYROGALLO RED DIE BINDING METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 3000 MILILITER 200.00

78 23/003/0042/00/0/0/0 WIDAL ANTIGEN SETS (SLIDE AGGLUTINATION ANTIGEN TEST) WIDAL AGGLUTINATION ANTIGENS O,H,AH,BH (4 AGX5ML) POSSITIVE CONTROL IS TO BE PROVIDED WITH ACCESSORIES 30 11500 MILILITER 900.00

79 23/003/0044/00/0/0/0 HBsAG RAPID KIT TO REFER SPECIFICATION IN TECHNCAL BID. 30 150000 TEST 10400.00

80 23/003/0047/00/0/0/0 BLOOD UREA UREASE, GLDH FIXED TIME KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID. 30 56500 MILILITER 1300.00

81 23/003/0048/00/0/0/0 ALKALINE PHOSPHATASE WITH PNPP SUBSTRATE WITH AMP BUFER TO REFER SPECIFICATION IN TECHNICAL BID. 30 41500 MILILITER 1100.00

82 23/003/0049/00/0/0/0 DENGUE ELISA NS 1 KIT, FOR DENGUE DETECTION OF NS1 ELISA Sensitivity -: should be 100%. Specificity -: 99 %. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. 30 11136 TEST 5000.00

83 23/003/0051/00/0/0/0 HAV IgM ELISA KIT, FOR HEPATITIS A VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 % 30 1152 TEST 500.00

84 23/003/0052/00/0/0/0 HEV IgM ELISA KIT, FOR HEPATITIS E VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 % 30 1152 TEST 500.00

85 23/003/0053/00/0/0/0 CHOLESTEROL ENZYMATIC, END POINT REFER TECHNICAL BID FOR SPECIFICATION. 30 17000 MILILITER 400.00

86 23/003/0054/00/0/0/0 CPK-MB IMMUNOINHIBITION UV METHOD WITH HUMAN SERUM BASED CONTROL ONLY REFER TECHNICAL BID FOR SPECIFICATION. 30 4000 MILILITER 1400.00

87 23/003/0055/00/0/0/0 CPK TOTAL. CPK: NAC ACTIVATED UV METHOD REFER TECHNICAL BID FOR SPECIFICATION. 30 7400 MILILITER 2200.00

88 23/003/0056/00/0/0/0 MEASLES IgM ELISA KIT, FOR MEASLES VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 % 30 192 TEST 200.00

89 23/003/0057/00/0/0/0 SERUM ALBUMIN BCG METHOD REFER TECHNICAL BID FOR SPECIFICATION. 30 46000 MILILITER 400.00

90 23/003/0058/00/0/0/0 ANTI Hbc IgM ELISA KIT Sensitivity -: should be 100%.Specificity -: 99 % 30 96 TEST 200.00

91 23/003/0059/00/0/0/0 TYPHOID IgM RAPID KIT 30 30000 TEST 4500.00

92 23/003/0060/00/0/0/0 HBSAG TRI-DOT KIT RAPID VISUAL SENSITIVE & QUALITATIVE IN VITRO DIAGNOSTIC TEST,SHOULD HAVE MINIMUM CHANCE OF CROSS REACTIVITY,SHOULD HAVE SUPERIOR SENSITIVITY OF TEST,PRINCIPLE -: ENZYME IMMUNOASSAY BASED ON ANTIGEN CAPTURE, OR 'SANDWICH' PRINCIPLE,USE FOR VISUAL, RAPID, SENSITIVE AND ACCURATE ONE STEP IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF HEPATITIS B SURFACE ANTIGEN IN HUMAN SERUM OR PLASMA,PACK SIZE -: 20 TO 50 TEST.DETECT ALL THE 11 SUBTYPE OF HBSAG.SENSITIVITY -: 100 %, SPECIFICITY -: MORE THAN 99 % ( AGAINST WHOLE HBSAG ANTIGEN ),SHELF LIFE -: MORE THAN ONE YEAR.SHOULD HAVE TWO TEST DOTS & ONE CONTROL DOT FOR VALIDATION, ISO / CE/ WHO /GMP CERTIFIED. Additional requirement:Company should provide the record for temprature maintainance during storage and transportation at the time of delivery of kit. 30 3600 TEST 600.00

93 23/003/0063/00/0/0/0 HBeAG DETECTION ELISA METHOD KIT Sensitivity -: should be 100%.Specificity -: 99 % 30 96 TEST 200.00

94 23/003/0065/00/0/0/0 MALARIA ELISA KIT REFER TECHNICAL BID FOR SPECIFICATION. 30 960 TEST 200.00

95 23/003/0068/00/0/0/0 DENGUE ELISA DETECTION OF IgM CAPUR ELISA QUALITATIVE DETECTION OF DENGUE VIRUS SPECIFIC IgM ANTIBODIES IN SERUM/PLASMA OR CsF FOR LABORATORY DIAGNOSIS OF THE DENGUE KIT SHOULD BE COMPATIBLE WITH FULLY AUTOMATIC ELISA READER WITH ADDITIONAL WASH-BUFFER ATLEAST ONE (1) BOTTLE WITH EACH KIT. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. Sensitivity -: should be 100%.Specificity -: 99 % 30 10080 TEST 4700.00

96 23/003/0069/00/0/0/0 DENGUE RAPID KIT (TO DETECT NS1 ANTIGEN, IgM, IgG ANTIBODIES SENSITIVITY SHOULD BE 100%, SPECIFICITY 99%. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION. 30 60000 TEST 36000.00

97 23/003/0094/00/0/0/0 HCV RAPID KIT 4TH GENRATION TO REFER SPECIFICATION IN TECHNICAL BID. 30 980 TEST 300.00

98 23/003/0098/00/0/0/0 TPHA ELISA KIT ( IgG + IgM ) REFER SPECIFICATION IN TECHNICAL BID. 30 2400 TEST 500.00

99 23/003/0101/00/0/0/0 SICKLING TEST (READY TO USE BASED ON QUALITATIVE SOLUBILITY TEST) 30 6000 TEST 900.00

100 23/003/0111/00/0/0/0 MANUAL RNA EXTRACTION KIT,FROM VTM SAMPLE,FOR RNA SPIN COLUMN BASE 30 1000 TEST 200.00

101 23/003/0112/00/0/0/0 COVID 19 RT-PCR KIT, ATLEAST 2 GENES,MULTIPLEXING FOR SCREENING 1- PACK SIZE 100 TESTS2- COMPATIBLE WITH QS5 AND INSTA 96 RT-PCR MACHINE3-CONFIRMATORY GENE ORF / RdRP GENE4- SCREENING GENE E / N GENE5- PROVIDE WITH TEMPERATURE RECORDER6 - REQUIRED REAGENTS AND CONTROL IN SUFFICIENT QUANTITY. 30 200 TEST 200.00

102 23/003/0114/00/0/0/0 RAPID ANTIGEN DETECTION TEST FOR COVID-19 KIT CONTAINS TYPE OF SWAB IS NASOPHRYANGEAL SWAB, OROPHRYANGEAL SWAB, NASAL SWAB, THROAT SWAB AND OTHER REQUIRED ACCESSORIES. KIT EVALUATED AND VALIDATED BY ICMR-NIV-PUNE OR ANY OTHER ICMR VALIDATION CENTER. 30 2000 TEST 100.00

103 23/003/0115/00/0/0/0 RNA EXTRACT KITAUTO COMPATIBLE WITH RNA EXT.MACHINE-LA1097INSTANXMAG96 30 480 TEST 300.00

104 23/003/0119/00/0/0/0 COVID 19 RTPCR KIT FOR 3 GENE SCREENING,INCLUDE ATLEAST 3 GENES ( S GENE IS REQUIRED IN 3 GENES) MULTIPLXING FOR SCREENING (E-GENE / S-GENE / N-GENE) & CONFIRMATORY GENES (ORF-GENE, RdRp-GENE) 30 500 TEST 300.00

105 23/003/0120/00/0/0/0 RPR TRUST Test Quantitative and Qualitative Seologic detection of Syphilis. Smooth negatives should be attained by the use of dye ( toludine red unheated serum).Sensitivity and specificity should be determined/evaluated by WHO/Gov authority. More than year.Should have minimum chance of False positive and False negative and minimum inderminate result( More than 95% Sensitivity and Specificity. Company should provide track record for temperature during storage and transport. 30 6000 TEST 200.00

106 23/003/0121/00/0/0/0 H1N1 Influenza PCR testing Kit Primers and 5' FAM labelled probe for Influenza A (H1N1) ,Influenza A and B and internal controls. A complete Kit with all required reagents must be supplied. 30 500 TEST 2900.00

107 23/003/0122/00/0/0/0 MPO- Myeloperoxidase Assay(Stain kit) kit Ready to use 30 1 TEST 300.00

108 23/004/0017/00/0/0/0 PETRIDISH 100MM PLA. AUTOCLAVABL-MADE FROM POLYSTYRENE/POLYPROPYLENE Made from Polystyrene Or Polypropylene material 30 110 NUMBER 100.00

109 23/004/0032/00/0/0/0 GLASS MUSEUM JAR WITH LID(COVER) BIG (30*20*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 20 NUMBER 500.00

110 23/004/0033/00/0/0/0 GLASS MUSEUM JAR WITH LID(COVER) BIG (25*15*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 20 NUMBER 200.00

111 23/004/0034/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 30 NUMBER 500.00

112 23/004/0035/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*15) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 20 NUMBER 400.00

113 23/004/0036/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*15*10) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 20 NUMBER 300.00

114 23/004/0037/00/0/0/0 GLASS MUSEUM JAR WITH LID SMALL (15*10*5) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 30 NUMBER 200.00

115 23/004/0038/00/0/0/0 GLASS MUSEUM JAR WITH LID VERY SMALL (10*5*5)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 30 NUMBER 100.00

116 23/004/0040/00/0/0/0 COVER GLASSES 22MM SQUARE (THIN NO.1)----BOX OF 20 PACKETS PACKING:1BOX CONTAIN 20 PACKETS OF 10 GRAMME EACH 30 250 BOX 2600.00

117 23/004/0041/00/0/0/0 COVER GLASSES 22*50MM (THIN NO.1)----BOX OF 20 PACKETS English Glass type: transparent, optically homogeneous, 0.13 to 0.17 mm thickess, pack size 1 BOX CONTAIN 20 PACKETS OF 10 GMS EACH 30 400 BOX 5600.00

118 23/004/0058/00/0/0/0 SABARAUD DEXTROSE AGAR MEDIUM 100 GM 30 10 BOTTLE 100.00

119 23/004/0059/00/0/0/0 BRAIN HEART INFUSION BROTH--500GM 30 30 BOTTLE 800.00

120 23/004/0127/00/0/0/0 PRINTER PAPER ROLL 57MM X 25 METER THERMAL PAPER,HIGH QUALITY,PLAIN PAPER 30 150 NUMBER 100.00

121 23/004/0131/00/0/0/0 RETRACTILE, SINGLE USE SAFETY LANCET FOR CAPILLARY BLOOD COLLECTION TO REFER SPECIFICATION IN TECHNICAL BID. 30 40000 NUMBER 1600.00

122 23/004/0132/00/0/0/0 VACCUMIZED TUBE WITH SPRAY DRIED K2 EDTA WITH PINK COLOR CAP TO REFER SPECIFICATION IN TECHNICAL BID. 30 27000 NUMBER 800.00

123 23/004/0212/00/0/0/0 PLAIN NONVACCUM TUBE(PLAIN PET TUBEWITH CLOTACTIVATOR&POLYEMER GEL5ML NON VACCUM BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 5ML FITTED WITH COLOURED CAP, MADE OF PET, WITH CLOT ACTIVATER ACCREDITED WITH STANDARD QUALITY CERTIFICATE 30 370000 NUMBER 9600.00

124 23/004/0213/00/0/0/0 EDTA NON VACCUM TUBE NON VACCUM BLOOD COLLECTION TUBE K2-EDTA, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE 30 350000 NUMBER 6200.00

125 23/004/0214/00/0/0/0 FLUORIDE NON VACCUM TUBE( PET TUBE WITH NA FLUORIDE 2ML CAP.) NON VACCUM BLOOD COLLECTION TUBE K2-EDTA & NA FLUORIDE 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE 30 120000 NUMBER 2000.00

126 23/004/0215/00/0/0/0 PT NON VACCUM TUBE ( PROTHROMBIN TIME TEST) NON VACCUM BLOOD COLLECTION TUBE WITH CITRATE, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, 3 ML BLOOD + 0.3ML TSC 3.2% ISO, ACCREDITED WITH STANDARD QUALITY CERTIFICATE 30 150000 NUMBER 4700.00

127 23/004/0216/00/0/0/0 PLAIN VACUTTE (PLAIN PET TUBE) WITH CLOT ACTIVATOR 5MLCAP VACCUM BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 5ML FITTED WITH RED COLOURED CAP,STERILE, MADE OF PET, WITH CLOT ACTIVATER ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE. 30 34000 NUMBER 1400.00

128 23/004/0217/00/0/0/0 PLAIN NON-VACUTTE (PLAIN PET TUBE) WITHOUT CLOT ACTIVATOR 4MLCAP BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 4ML FITTED WITH RED COLOURED CAP,STERILE, MADE OF PET, WITHOUT CLOT ACTIVATER . 30 20000 NUMBER 600.00

129 23/004/0218/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*5) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES 30 30 NUMBER 300.00

130 23/005/0101/00/0/0/0 HIV RAPID TEST KIT (IC) TO REFER SPECIFICATION IN TECHNICAL BID. Specifications: 1. Kit should be based on lateral flow immunoassay for the differentiation of HIV-1 and HIV- 2 antibodies(IgM,IgG,IgA) in human serum/plasma /whole blood.2. The test cassette should consist of;a)Conjugate pad containng recombinant HIV- 1 antigens(gp 41+120 ,p24)conjugated with colloidal gold (HIV -1 conjugate), recombinant HIV-2 antigen(gp36)conjugated with colloidal gold((HIV- 2 conjugate)b) A nitrocellulose membrane strip containing two test line(1 & 2) and a control line(C).Test line 1 is pre coated with HIV-1 antigen for the detection of antibodies to HIV- 1 test line.Test line 2 is pre coated with HIV-2 antigen for the detection of antibodies to HIV -2 test line. The C line is pre coated with a cotrol line (anti rabbit IgG)antibody.3. The test should contain an internal control (C line) which should exhibit colored line of the immunocomplex of the control antibodies regardless of color develpoment on test line. 4. Test should have 100% Sensitivity as well 100% Specificity,too. 30 16000 TEST 3500.00

131 23/006/0004/00/0/0/0 MUELLER HINTON AGAR--500GM 30 95 BOTTLE 2900.00

132 23/006/0053/00/0/0/0 HIV Ag+Ab DETECTION RAPID TEST KIT (4TH GENERATION ) REFER TECHNICAL BID FOR SPECIFICATION. 30 300 TEST 300.00

133 25/001/0007/00/0/0/0 GLASS SLIDE PRECLEANED WITH POLISH EDGE(75x25x1.35)MM-PKT OF 50 NUMBER 1. SIZE : 75 mm x 25 mm 2. Thickness 1.35 mm 3. PRECLEANED WITH POLISH EDGE 30 50000 PACKET 28500.00

TENDER No. DMC(D-H&H)/CMS/11/2025-26

PLEASE MENTION THE DETAILS OF SAMPLES SUBMITTED BY YOU IN THIS SHEET

SAMPLES MUST BE SUBMITTED TO CENTRAL MEDICAL STORE AT MAGOB, SURAT ONLY UP TO 24/03/2026. 18.00 HRS.

MUST BE MENTION TENDER ITEM SERIAL NUMBER ON EACH AND EVERY SAMPLE

Name of Tenderer :

Sr. No. Tender Item Sr. No. Name of Item (As per Tender) Name of Manufacturer Name of Brand Quantity of Sample Provided Batch No. Mfg. Dt. Exp. Dt.

Note: It is mandatory to fill up all details. If not applicalble then mention NA.

SIGN & STAMP TENDERER

LIST OF REQUIRED SAMPLE

TENDER NO : DMC(D-H&H)/CMS/11/2025-26

Sr. No Item Serial Item Code Item Name Specification

1 1 23/001/0003/00/0/0/0 EOSIN 2% LIQUID ( READY TO USE & ISO CERTIFIED - AR) 100ML

2 2 23/001/0007/00/0/0/0 HEMATOXYLENE (HARRIS) LIQUID (READY TO USE & ISO CERTI.) AR-100ML

3 3 23/001/0009/00/0/0/0 GIEMSA STAIN SOLUTION(READY TOUSE PREFER WITH BUFER&ISO CERT-100ML

4 4 23/001/0020/00/0/0/0 REAGENT STRIP FOR URINE ANALYSIS-MULTISTIX-BOTTLE OF 100 STRIP SHOULD INCLUDE PARAMETERS GLUCOSE, SPECIFIC GRAVITY, PH, PROTEIN, BLOOD, UROBILINOGEN,BILLIRUBIN AND KETONE BODIES.

5 5 23/001/0021/00/0/0/0 KETODIASTIX STRIP FOR DETECT OF SUGAR,ACETONE IN URINE-BOTLE 50 STRIP

6 6 23/001/0022/00/0/0/0 HAEM TEST (OCULT BLOOD TEST)

7 7 23/001/0023/00/0/0/0 URISTIX STRIPS--BOTTLE OF 100 STRIP

8 8 23/001/0026/00/0/0/0 LEISHMAN STAIN SOLU(CYTOCHROMIC)READY TO USE WITH BUFER BSC CERT-500ML BSC CERTIFIED

9 9 23/001/0030/00/0/0/0 22% BOVINE ALBUMIN VIAL OF 5 ML 1.FDA Approved (Fulfil DGHS criteria).2. No precipitate, particles or gel.3. >98% albumin, as determied by electrophoresis.4. No agglutination of unsensitized red cells; no hemolytic activity; no prozone phenomenon. 5. IgG anti-D should give a titer of 32-64 with red cell R1 cell.6. Pack Size - 05 ml vial 7. Shelf Life - Minimum 18 months. Additional information 8. company should provide the record of temprature maintainance during storage and transport at the time of delivery.

10 10 23/001/0031/00/0/0/0 COOMB'S SERUM ( ANTI HUMAN SERUM) (POLY SPECIFIC) 5ML TO REFER SPECIFICATION IN TECHNICAL BID.

11 11 23/001/0041/00/0/0/0 NUTRIENT AGAR (BACTERIOLOGIAL MEDIA)--500GM

12 12 23/001/0042/00/0/0/0 MACCONKEY'S AGAR(BACTERIOLOGIALMEDIA)500GM(W/CV,NaCLAND 0.15%BILE SALT PEPTONE 20.0GM, SODIUM CLORIDE 5.0 GM, LACTOSE 10.0 GM,BILE SALTS 1.5 GM,NUTRAL RED 0.05GM, CRYSTAL VIOLET 0.001 GM, AGAR 15.0GM, PH 7.2+/- 0.2

13 13 23/001/0045/00/0/0/0 GLUCOSE PHOSPHATE BROTH (BACTERIOLOGIAL MEDIA) 500 GM

14 14 23/001/0056/00/0/0/0 RETICULOCYTE COUNTING FLUID(READY TOUSE& ISO CERTI.) AR 25ML

15 15 23/001/0061/00/0/0/0 CALCIUM CHLORIDE REAGENT FOR APTT--10ML

16 16 23/001/0065/00/0/0/0 BLOOD GROUP SERA ANTI 'A' MONOCLONAL--10ML TO REFER SPECIFICATION IN TECHNICAL BID.

17 17 23/001/0066/00/0/0/0 BLOOD GROUP SERA ANTI 'B' MONOCLONAL--10ML TO REFER SPECIFICATION IN TECHNICAL BID.

18 18 23/001/0067/00/0/0/0 BLOOD GROUP SERA ANTI 'D' MONOCLONAL IgM--10ML TO REFER SPECIFICATION IN TECHNICAL BID.

19 19 23/001/0068/00/0/0/0 BLOOD GROUP SERA ANTI-D (POLYCLONAL IgM+IgG)--10ML TO REFER SPECIFICATION IN TECHNICAL BID.

20 20 23/001/0069/00/0/0/0 ANTI A1 (LECTIN)--5ML TO REFER SPECIFICATION IN TECHNICAL BID.

21 21 23/001/0070/00/0/0/0 ANTI H--5ML VIAL TO REFER SPECIFICATION IN TECHNICAL BID.

22 22 23/001/0071/00/0/0/0 BLOOD GROUP SERA ANTI AB--10ML TO REFER SPECIFICATION IN TECHNICAL BID.

23 23 23/001/0116/00/0/0/0 VIRAL TRANSPORT MEDIUM 3ML VTM IN 15ML TUBE WITH 2 VISCOS SWABS

24 24 23/001/0119/00/0/0/0 TCBS AGAR--100GM YEST EXTRACT 5.0 GM,SODIUM CITRATE 10.0 GM, SODIUM THIOSULPHATE 10.0 GM , SODIUM CHOLATE 3.0 GM, BILE # 5.0 GM,SUCROSE 20.0 GM ,SODIUM CLORIDE 10.0 GM , FERRIC CITRATE 1.0 GM, BROMO THYMOL BLUE 0.040 GM , THYMOL BLUE 0.040 GM, AGAR 15.0 GM , PH 8.8 +/- 0.2

25 25 23/001/0122/00/0/0/0 ALKALINE PEPTONE WATER 100 GMS. PEPTIC DIGEST OF ANIMAL TISSUE 20.0 GM ,SODIUM CLORIDE 30.0 GM, PH 8.6 +/- 0.2

26 26 23/001/0125/00/0/0/0 TRIPLE SUGAR IRON AGAR--100GM

27 27 23/001/0135/00/0/0/0 CALCIUM KIT ARSENAZO-III METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID.

28 28 23/001/0136/00/0/0/0 CHOLINESTRASE BUTIRYL THIOCHOLINE/PROPIONYL THIOCHOLINE SUBSTRATE SUBSTRATE, KINETIC KIT SHOULD BE ABLE TO ESTIMATE ACTIVITY OF CHOLINESTRASE IN SERUM. TO REFER SPECIFICATION IN TECHNICAL BID.

29 29 23/001/0139/00/0/0/0 HbsAg ELISA KIT BASE ON 3RD GEN.(MONOCLONAL ANTIBODIES) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. Sensitivity -: 100 %• Antigen sensitivity should be 0.05 ng/ml.• Specificity -: More than or equal to 98 %.• Assay time should not be more than 2 hours.• Detects all the known 11 subtypes of HBV and also mutant strains.• Shelf life -: minimum 9 months at the time of delivery.

30 30 23/001/0140/00/0/0/0 HCV ELISA KIT TO REFER SPECIFICATION IN TECHNICAL BID.

31 31 23/001/0141/00/0/0/0 HCV RAPID KIT STRIP TEST (IC) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. SENSITIVITY: 100 %, SPECIFICITY: MORE THAN 98%.

32 32 23/001/0156/00/0/0/0 TOTAL PROTEIN KIT BIURET METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID.

33 33 23/001/0157/00/0/0/0 RPR TEST FOR SYPHILIS (CHARCOAL CARBON PARTICLE) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

34 34 23/001/0224/00/0/0/0 QUADRUPLE BLOOD BAG 450 ML WITH SAGM TO REFFER SPECIFICATION IN TECHNICAL BID.

35 35 23/001/0229/00/0/0/0 DOUBLE BLOOD BAG 350ML TO REFER SPECIFICATION IN TECHNICAL BID.

36 36 23/001/0249/00/0/0/0 DOUBLE BLOOD BAG 450ML WITH SAGM TO REFER SPECIFICATION IN TECHNICAL BID.

37 37 23/001/0252/00/0/0/0 TRANSFER BAG 300ML CAPA.,FDA, APROVED, QUALITY CERTI.(CE,ISO-9001-2000)

38 38 23/001/0267/00/0/0/0 PENTA BLOOD BAG Mother bag of the Penta blood bag should have 450ml capacity and is connected to four satellite transfer bags of 100ml capacity.Mother bag should be with 0.39mm thickness and the inner iameter of the transfer tube from mother bag should be with 2.95±0.05mm ID to provide easy flow of the blood. Needle should be 16G with triple bevel design to reduce penetration force and enable painless vein puncture Blood bags should have segment numbers in all tubes of the transfer bags.Blood Bags and its packing should be properly labeled with Batch. No., Date of Mfg., and Date of Expiry.Product labels should be barcoded as per ISBT-128.Secondary packing and shipping cartons should be barcoded as per GS1-128.3 units of bags is packed in an outer cover with sufficient barrier properties to prevent moisture loss during storage.Complies to ISO 3826 and quality of blood components stored as per Indian Drugs and Cosmetics Act.

39 39 23/001/0268/00/0/0/0 TRIPLE BLOOD BAG WITH SAGM 450ML TO REFER SPECIFICATION IN TECHNICAL BID.

40 40 23/001/0269/00/0/0/0 DOUBLE BLOOD BAG 450ML TO REFER SPECIFICATION IN TECHNICAL BID

41 41 23/001/0270/00/0/0/0 CPDA SINGLE BLOOD BAG 350ML TO REFER SPECIFICATION IN TECHNICAL BID

42 42 23/001/0406/00/0/0/0 SYPHILIS Ab RAPID TEST KIT ( DIP STRIP ) TO REFER SPECIFICATION IN TECHNICAL BID.

43 43 23/001/0407/00/0/0/0 RAPID MALARIA KIT TO REFER SPECIFICATION IN TECHNCAL BID.

44 44 23/001/0412/00/0/0/0 LEPTOSPIRA RAPID KIT (FOR IgM DETECTION) ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

45 45 23/001/0610/00/0/0/0 TOP & BOTTOM QUADRUPLE BLOOD BAG WITH INTEGRATED FILTER FOR COMPONENT TO REFER SPECIFICATION IN TECHNICAL BID

46 46 23/001/0924/00/0/0/0 PARAFFIN WAX in generular(Pellets) form(MELTING POINT 58' - 60')

47 47 23/002/0005/00/0/0/0 PARAFFIN WAX (MELTING POINT 58'-60')

48 48 23/002/0024/00/0/0/0 COPPER SULPHATE ANALYTICAL GRADE--500GM

49 49 23/002/0035/00/0/0/0 SGOT/AST. AST: IFCC KINETIC WITH PLP TO REFER SPECIFICATION IN TECHNCAL BID.

50 50 23/002/0036/00/0/0/0 SGPT/ALT. ALT: IFCC KINETIC WITH PLP TO REFER SPECIFICATION IN TECHNICAL BID.

51 51 23/002/0168/00/0/0/0 COOMBS SERUM IgG--5ML VIAL SHELF LIFE SHOULD MORE THAN 18 MONTHS

52 52 23/002/0169/00/0/0/0 BLOOD GROUP SERA ANTI D MONOCLONAL (IgG)--10ML VIAL

53 53 23/003/0001/00/0/0/0 LDL CHOLESTEROL BY DIRECT METHOD TO REFER SPECIFICATION IN TECHNCAL BID.

54 54 23/003/0003/00/0/0/0 S.AMYLASE TEST KIT CNP-G3 KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

55 55 23/003/0004/00/0/0/0 S.URIC ACID TEST KIT URICASE PEROXIDASE END POINT TO REFER SPECIFICATION IN TECHNICAL BID.

56 56 23/003/0005/00/0/0/0 TRIGLYCERIDES ENZYMATIC,END POINT TO REFER SPECIFICATION IN TECHNICAL BID.

57 57 23/003/0006/00/0/0/0 S.BILIRUBIN TEST KIT TOTAL&DIRECT, JENDRASSIK&GROF'S METHOD END POINT TO REFER SPECIFICATION IN TECHNICAL BID.

58 58 23/003/0007/00/0/0/0 S.CRETININE TEST KIT ALKALINE PICRATE FIX TIME KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

59 59 23/003/0008/00/0/0/0 HDL-CHOLESTEROL DIRECT HOMOGENOUS METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

60 60 23/003/0009/00/0/0/0 S.PHOSPHEROUS TEST KIT MOLYBDATE AT 340nm WITHOUT REDUCING AGENT TO REFER SPECIFICATION IN TECHNICAL BID.

61 61 23/003/0013/00/0/0/0 URINE PREGNANCY TEST KIT ( STRIP )

62 62 23/003/0014/00/0/0/0 GLUCOSE TEST KIT ENZYMATIC GLUCOSE OXIDASE PEROXIDASE METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

63 63 23/003/0016/00/0/0/0 A.S.O.TEST KIT RAPID SLIDE TEST,POSSITIVE & NEGATIVE CONTROL & NECESSARY ACCESSERIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

64 64 23/003/0017/00/0/0/0 R.A. TEST KIT RAPID SLIDE AGGLUTINATION TEST METHOD WITH POSSITIVE & NEGATIVE CONTROLS & NECESSARY ASSECCERIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

65 65 23/003/0018/00/0/0/0 C.R.P. TEST KIT LATEX AGGLUTINATION TEST WITH CONTROL & NECESSARY ACCESSRIES. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

66 66 23/003/0023/00/0/0/0 GLUCOSE 6 PHOSPHATE DEHYDROGENASE(1) SCREENING (G.6.P.D SINGLE TEST VIAL & TEST TO BE COUNTED T IN 11/2 TO 1 HOURS THE REAGENTS CONTAINED IN THE KITS MUST BE AS PER NORMS ISO:13485 AND WITH TRACEABILITY CERTIFICATE AS PER NABL NORMS.

67 67 23/003/0025/00/0/0/0 LACTATE DEHYDROGENASE KINETIC AT UV RANGE KIT SHOULD BE BASED ON LACTATE TO PYRUVATE CONVERSION. TO REFFER SPECIFICATION IN TECHNICAL BID.

68 68 23/003/0030/00/0/0/0 FIBRINOGEN KIT (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION FOR FIBRINOGEN(2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP(5) CE MARK, ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHOULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FIBRINOGEN IN CASES OF DIC

69 69 23/003/0031/00/0/0/0 FIBRIN DEGRADATION PRODUCT KIT (FDP) (1) EASY & READY TO USE REAGENTS FOR QUANTITATIVE ESTIMATION OF FIBRIN DEGRADATION PRODUCTS (2) IDEALLY SUITABLE FOR BOTH MANUAL & AUTOMATED PROCESSING (3) EXCELLENT BATCH TO BATCH SENSITIVITY, SPECIFICITY, PRECISION & REPRODUCIBILITY (4) LONG STABILITY & SHELF LIFE IDEAL FOR LABORATORY SET UP (5) CE MARK,ISO 9001 & ISO 13485 CERTIFICATE IS REQUIRED (6) THE ASSAY OF SOLUTIONS SHULD BE ACCORDING TO ISO STANDARDS (7) KIT SHOULD CONTAIN CALIBRATOR (8) SHOULD BE AVAILABLE IN 20-25 TEST PACK (9) LONG STABILITY AT LEAST 1 MONTH AFTER RECONSTITUTION OF REAGENT (DATA SHOULD BE ATTACHED) USED FOR QUANTITATIVE ESTIMATION OF FDP IN CASES OF DIC

70 70 23/003/0033/00/0/0/0 HIV IMMUNOCOMB RAPID TEST TO REFER SPECIFICATION IN TECHNICAL BID.1. Employs same principle as Enzyme Immuno Assay(EIA) whereby the immmobilised antigen-antibody complex is visuallised by means of chromogenic reaction 2.There should be coloured end point developed by a colloidal Gold Protein A Signal reagent 3. Each tooth of comb is spotted with a circular spot,one near the tip with an optimally standardised blend of HIV 1 & HIV 2 recombinant antigens and /or synthetic peptides (test spot),and the other spot ,a little above the first spot is spotted with control reagent (Control spot) 4. The immune comlpex should be directly visualised after incubation with the colloidal Gold -Protein A Signal reagent. 5. Built in control should be visualised seprately in the upper part of the tooth(Control area),where control reagent has been spotted, serving as the procedural control 6. Pink coloured spot/Dot should always appear at the control area with recommended test specimen irrespective of the presence or absence of HIV antibodies in the specimen 7. Test should have 100%Sensitivity as well 100% Specificity,too.

71 71 23/003/0034/00/0/0/0 ACTIVATED PARTIAL PROTHOMBIN TIME (APTT) KIT READY TO USE READY TO USE

72 72 23/003/0035/00/0/0/0 A.S.O. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION.

73 73 23/003/0036/00/0/0/0 R.A. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION.

74 74 23/003/0037/00/0/0/0 C.R.P. TEST KIT (QUNTITATIVE / TURBIDOMETRY) WITH CALIBRATOR ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION.

75 75 23/003/0038/00/0/0/0 RAPID PAP STAIN KIT OF 250 TEST (1) ONE KIT SHOULD STAIN ATLEAST 250 SMEARS. (2) STAIN SHOULD BE COMPLETED WITHIN 3 MIN.(3) IT SHOULD CONTAIN- NUCLEAR STAIN- CYTOPLASMIC STAIN- OG-65 SOLUTION- LIGHT GREEN SF EOSIN- BIO-FIX SPARY- DPX- XYLENE- WASH BUFFER (4) IT SHOULD GIVE COMPARABLE RESULT WITH USUAL PAP STAIN IT IS MUST FOR REPORTING OF GYNAC SMEAR, OTHER CYTOLOGY SMEAR AND MASS CYTOLOGY SCREENING CAMP.

76 76 23/003/0040/00/0/0/0 BRAIN THROMBOPLASTIN (PROTHOMBINTIME TEST KIT)

77 77 23/003/0041/00/0/0/0 CSF PROTEIN/URINARY PROTEIN BY PYROGALLO RED DIE BINDING METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

78 78 23/003/0042/00/0/0/0 WIDAL ANTIGEN SETS (SLIDE AGGLUTINATION ANTIGEN TEST) WIDAL AGGLUTINATION ANTIGENS O,H,AH,BH (4 AGX5ML) POSSITIVE CONTROL IS TO BE PROVIDED WITH ACCESSORIES

79 79 23/003/0044/00/0/0/0 HBsAG RAPID KIT TO REFER SPECIFICATION IN TECHNCAL BID.

80 80 23/003/0047/00/0/0/0 BLOOD UREA UREASE, GLDH FIXED TIME KINETIC METHOD TO REFER SPECIFICATION IN TECHNICAL BID.

81 81 23/003/0048/00/0/0/0 ALKALINE PHOSPHATASE WITH PNPP SUBSTRATE WITH AMP BUFER TO REFER SPECIFICATION IN TECHNICAL BID.

82 82 23/003/0049/00/0/0/0 DENGUE ELISA NS 1 KIT, FOR DENGUE DETECTION OF NS1 ELISA Sensitivity -: should be 100%. Specificity -: 99 %. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION.

83 83 23/003/0051/00/0/0/0 HAV IgM ELISA KIT, FOR HEPATITIS A VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 %

84 84 23/003/0052/00/0/0/0 HEV IgM ELISA KIT, FOR HEPATITIS E VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 %

85 85 23/003/0053/00/0/0/0 CHOLESTEROL ENZYMATIC, END POINT REFER TECHNICAL BID FOR SPECIFICATION.

86 86 23/003/0054/00/0/0/0 CPK-MB IMMUNOINHIBITION UV METHOD WITH HUMAN SERUM BASED CONTROL ONLY REFER TECHNICAL BID FOR SPECIFICATION.

87 87 23/003/0055/00/0/0/0 CPK TOTAL. CPK: NAC ACTIVATED UV METHOD REFER TECHNICAL BID FOR SPECIFICATION.

88 88 23/003/0056/00/0/0/0 MEASLES IgM ELISA KIT, FOR MEASLES VIRUS TESTING Sensitivity -: should be 100%.Specificity -: 99 %

89 89 23/003/0057/00/0/0/0 SERUM ALBUMIN BCG METHOD REFER TECHNICAL BID FOR SPECIFICATION.

90 90 23/003/0058/00/0/0/0 ANTI Hbc IgM ELISA KIT Sensitivity -: should be 100%.Specificity -: 99 %

91 91 23/003/0059/00/0/0/0 TYPHOID IgM RAPID KIT

92 92 23/003/0060/00/0/0/0 HBSAG TRI-DOT KIT RAPID VISUAL SENSITIVE & QUALITATIVE IN VITRO DIAGNOSTIC TEST,SHOULD HAVE MINIMUM CHANCE OF CROSS REACTIVITY,SHOULD HAVE SUPERIOR SENSITIVITY OF TEST,PRINCIPLE -: ENZYME IMMUNOASSAY BASED ON ANTIGEN CAPTURE, OR 'SANDWICH' PRINCIPLE,USE FOR VISUAL, RAPID, SENSITIVE AND ACCURATE ONE STEP IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF HEPATITIS B SURFACE ANTIGEN IN HUMAN SERUM OR PLASMA,PACK SIZE -: 20 TO 50 TEST.DETECT ALL THE 11 SUBTYPE OF HBSAG.SENSITIVITY -: 100 %, SPECIFICITY -: MORE THAN 99 % ( AGAINST WHOLE HBSAG ANTIGEN ),SHELF LIFE -: MORE THAN ONE YEAR.SHOULD HAVE TWO TEST DOTS & ONE CONTROL DOT FOR VALIDATION, ISO / CE/ WHO /GMP CERTIFIED. Additional requirement:Company should provide the record for temprature maintainance during storage and transportation at the time of delivery of kit.

93 93 23/003/0063/00/0/0/0 HBeAG DETECTION ELISA METHOD KIT Sensitivity -: should be 100%.Specificity -: 99 %

94 94 23/003/0065/00/0/0/0 MALARIA ELISA KIT REFER TECHNICAL BID FOR SPECIFICATION.

95 95 23/003/0068/00/0/0/0 DENGUE ELISA DETECTION OF IgM CAPUR ELISA QUALITATIVE DETECTION OF DENGUE VIRUS SPECIFIC IgM ANTIBODIES IN SERUM/PLASMA OR CsF FOR LABORATORY DIAGNOSIS OF THE DENGUE KIT SHOULD BE COMPATIBLE WITH FULLY AUTOMATIC ELISA READER WITH ADDITIONAL WASH-BUFFER ATLEAST ONE (1) BOTTLE WITH EACH KIT. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPERATURE CONTROL DURING TRANSPORTATION. Sensitivity -: should be 100%.Specificity -: 99 %

96 96 23/003/0069/00/0/0/0 DENGUE RAPID KIT (TO DETECT NS1 ANTIGEN, IgM, IgG ANTIBODIES SENSITIVITY SHOULD BE 100%, SPECIFICITY 99%. ADDITIONAL REQUIREMENTS OF CERTIFICATION FOR TEMPRATURE CONTROL DURING TRANSPORTAION.

97 97 23/003/0094/00/0/0/0 HCV RAPID KIT 4TH GENRATION TO REFER SPECIFICATION IN TECHNICAL BID.

98 98 23/003/0098/00/0/0/0 TPHA ELISA KIT ( IgG + IgM ) REFER SPECIFICATION IN TECHNICAL BID.

99 99 23/003/0101/00/0/0/0 SICKLING TEST (READY TO USE BASED ON QUALITATIVE SOLUBILITY TEST)

100 100 23/003/0111/00/0/0/0 MANUAL RNA EXTRACTION KIT,FROM VTM SAMPLE,FOR RNA SPIN COLUMN BASE

101 101 23/003/0112/00/0/0/0 COVID 19 RT-PCR KIT, ATLEAST 2 GENES,MULTIPLEXING FOR SCREENING 1- PACK SIZE 100 TESTS2- COMPATIBLE WITH QS5 AND INSTA 96 RT-PCR MACHINE3-CONFIRMATORY GENE ORF / RdRP GENE4- SCREENING GENE E / N GENE5- PROVIDE WITH TEMPERATURE RECORDER6 - REQUIRED REAGENTS AND CONTROL IN SUFFICIENT QUANTITY.

102 102 23/003/0114/00/0/0/0 RAPID ANTIGEN DETECTION TEST FOR COVID-19 KIT CONTAINS TYPE OF SWAB IS NASOPHRYANGEAL SWAB, OROPHRYANGEAL SWAB, NASAL SWAB, THROAT SWAB AND OTHER REQUIRED ACCESSORIES. KIT EVALUATED AND VALIDATED BY ICMR-NIV-PUNE OR ANY OTHER ICMR VALIDATION CENTER.

103 103 23/003/0115/00/0/0/0 RNA EXTRACT KITAUTO COMPATIBLE WITH RNA EXT.MACHINE-LA1097INSTANXMAG96

104 104 23/003/0119/00/0/0/0 COVID 19 RTPCR KIT FOR 3 GENE SCREENING,INCLUDE ATLEAST 3 GENES ( S GENE IS REQUIRED IN 3 GENES) MULTIPLXING FOR SCREENING (E-GENE / S-GENE / N-GENE) & CONFIRMATORY GENES (ORF-GENE, RdRp-GENE)

105 105 23/003/0120/00/0/0/0 RPR TRUST Test Quantitative and Qualitative Seologic detection of Syphilis. Smooth negatives should be attained by the use of dye ( toludine red unheated serum).Sensitivity and specificity should be determined/evaluated by WHO/Gov authority. More than year.Should have minimum chance of False positive and False negative and minimum inderminate result( More than 95% Sensitivity and Specificity. Company should provide track record for temperature during storage and transport.

106 106 23/003/0121/00/0/0/0 H1N1 Influenza PCR testing Kit Primers and 5' FAM labelled probe for Influenza A (H1N1) ,Influenza A and B and internal controls. A complete Kit with all required reagents must be supplied.

107 107 23/003/0122/00/0/0/0 MPO- Myeloperoxidase Assay(Stain kit) kit Ready to use

108 108 23/004/0017/00/0/0/0 PETRIDISH 100MM PLA. AUTOCLAVABL-MADE FROM POLYSTYRENE/POLYPROPYLENE Made from Polystyrene Or Polypropylene material

109 109 23/004/0032/00/0/0/0 GLASS MUSEUM JAR WITH LID(COVER) BIG (30*20*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

110 110 23/004/0033/00/0/0/0 GLASS MUSEUM JAR WITH LID(COVER) BIG (25*15*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

111 111 23/004/0034/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*10)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

112 112 23/004/0035/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*15) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

113 113 23/004/0036/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*15*10) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

114 114 23/004/0037/00/0/0/0 GLASS MUSEUM JAR WITH LID SMALL (15*10*5) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

115 115 23/004/0038/00/0/0/0 GLASS MUSEUM JAR WITH LID VERY SMALL (10*5*5)CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

116 116 23/004/0040/00/0/0/0 COVER GLASSES 22MM SQUARE (THIN NO.1)----BOX OF 20 PACKETS PACKING:1BOX CONTAIN 20 PACKETS OF 10 GRAMME EACH

117 117 23/004/0041/00/0/0/0 COVER GLASSES 22*50MM (THIN NO.1)----BOX OF 20 PACKETS English Glass type: transparent, optically homogeneous, 0.13 to 0.17 mm thickess, pack size 1 BOX CONTAIN 20 PACKETS OF 10 GMS EACH

118 118 23/004/0058/00/0/0/0 SABARAUD DEXTROSE AGAR MEDIUM 100 GM

119 119 23/004/0059/00/0/0/0 BRAIN HEART INFUSION BROTH--500GM

120 120 23/004/0127/00/0/0/0 PRINTER PAPER ROLL 57MM X 25 METER THERMAL PAPER,HIGH QUALITY,PLAIN PAPER

121 121 23/004/0131/00/0/0/0 RETRACTILE, SINGLE USE SAFETY LANCET FOR CAPILLARY BLOOD COLLECTION TO REFER SPECIFICATION IN TECHNICAL BID.

122 122 23/004/0132/00/0/0/0 VACCUMIZED TUBE WITH SPRAY DRIED K2 EDTA WITH PINK COLOR CAP TO REFER SPECIFICATION IN TECHNICAL BID.

123 123 23/004/0212/00/0/0/0 PLAIN NONVACCUM TUBE(PLAIN PET TUBEWITH CLOTACTIVATOR&POLYEMER GEL5ML NON VACCUM BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 5ML FITTED WITH COLOURED CAP, MADE OF PET, WITH CLOT ACTIVATER ACCREDITED WITH STANDARD QUALITY CERTIFICATE

124 124 23/004/0213/00/0/0/0 EDTA NON VACCUM TUBE NON VACCUM BLOOD COLLECTION TUBE K2-EDTA, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE

125 125 23/004/0214/00/0/0/0 FLUORIDE NON VACCUM TUBE( PET TUBE WITH NA FLUORIDE 2ML CAP.) NON VACCUM BLOOD COLLECTION TUBE K2-EDTA & NA FLUORIDE 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, ACCREDITED WITH STANDARD QUALITY CERTIFICATE

126 126 23/004/0215/00/0/0/0 PT NON VACCUM TUBE ( PROTHROMBIN TIME TEST) NON VACCUM BLOOD COLLECTION TUBE WITH CITRATE, 13X75MM, 2-4ML FITTED WITH COLOURED CAP, MADE OF PET, 3 ML BLOOD + 0.3ML TSC 3.2% ISO, ACCREDITED WITH STANDARD QUALITY CERTIFICATE

127 127 23/004/0216/00/0/0/0 PLAIN VACUTTE (PLAIN PET TUBE) WITH CLOT ACTIVATOR 5MLCAP VACCUM BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 5ML FITTED WITH RED COLOURED CAP,STERILE, MADE OF PET, WITH CLOT ACTIVATER ACCREDITED WITH STANDARD QUALITY CERTIFICATE VACCUM MUST BE ADEQUATE TO DRAW THE MENTIONED VOLUME OF SAMPLE.

128 128 23/004/0217/00/0/0/0 PLAIN NON-VACUTTE (PLAIN PET TUBE) WITHOUT CLOT ACTIVATOR 4MLCAP BLOOD COLLECTION TUBE FOR SERUM, 13X75MM, 4ML FITTED WITH RED COLOURED CAP,STERILE, MADE OF PET, WITHOUT CLOT ACTIVATER .

129 129 23/004/0218/00/0/0/0 GLASS MUSEUM JAR WITH LID SQUARE (20*20*5) CM3 SHOULD BE MADE OF CLEAR TRANSPARENT GLASS WITH TIGHT FITTING LIDS. JAR SHOULD HAVE INSIDE RODS & MOUNTING PLATES

130 130 23/005/0101/00/0/0/0 HIV RAPID TEST KIT (IC) TO REFER SPECIFICATION IN TECHNICAL BID. Specifications: 1. Kit should be based on lateral flow immunoassay for the differentiation of HIV-1 and HIV- 2 antibodies(IgM,IgG,IgA) in human serum/plasma /whole blood.2. The test cassette should consist of;a)Conjugate pad containng recombinant HIV- 1 antigens(gp 41+120 ,p24)conjugated with colloidal gold (HIV -1 conjugate), recombinant HIV-2 antigen(gp36)conjugated with colloidal gold((HIV- 2 conjugate)b) A nitrocellulose membrane strip containing two test line(1 & 2) and a control line(C).Test line 1 is pre coated with HIV-1 antigen for the detection of antibodies to HIV- 1 test line.Test line 2 is pre coated with HIV-2 antigen for the detection of antibodies to HIV -2 test line. The C line is pre coated with a cotrol line (anti rabbit IgG)antibody.3. The test should contain an internal control (C line) which should exhibit colored line of the immunocomplex of the control antibodies regardless of color develpoment on test line. 4. Test should have 100% Sensitivity as well 100% Specificity,too.

131 131 23/006/0004/00/0/0/0 MUELLER HINTON AGAR--500GM

132 132 23/006/0053/00/0/0/0 HIV Ag+Ab DETECTION RAPID TEST KIT (4TH GENERATION ) REFER TECHNICAL BID FOR SPECIFICATION.

133 133 25/001/0007/00/0/0/0 GLASS SLIDE PRECLEANED WITH POLISH EDGE(75x25x1.35)MM-PKT OF 50 NUMBER 1. SIZE : 75 mm x 25 mm 2. Thickness 1.35 mm 3. PRECLEANED WITH POLISH EDGE