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Tender Corrigendum :
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| Tender Corrigendum | Technical Bid Corrigendum | | Tender Corrigendum Publication | Company Web Site - Internet | | Tender Corrigendum Document | Can be download by Subscribers | | Tender Corrigendum | Deadline has been changes from Sep 8 2025 12:00AM to Sep 18 2025 12:00AM
Date Amendment | | Tender Corrigendum Publication | Company Web Site - Internet | | Tender Corrigendum Document | Can be download by Subscribers | | Tender Corrigendum | Deadline has been changes from Aug 21 2025 12:00AM to Sep 8 2025 12:00AM
Date amendment | | Tender Corrigendum Publication | Company Web Site - Internet | | Tender Corrigendum Document | Can be download by Subscribers |
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Product Detail :
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Tender Invite for Biochemistry Reagents and Kits - Glucose Liquid stable, linearity 600 mg/dl & above with standard (as & when required) (Glucose oxidase/Hexokinase), Cholesterol linearity 1000 mg/dl with standard (as & when required) (cholesterol oxidase), Urea- Kinetic linearity 500 mg/dl with standard(as & when required) (Urease kinetic), Creatinine- with standard, linearity 20 mg/dl & above (Enzymatic/Jaffe modified), Phosphorus – Liquid stable ready to use, linearity 15 mg/ml & above with standard (as & when required) (U.V. end point using ammonium molybdate), Uric Acid- liquid stable with standard, (as & when required) linearity 20 mg/dl & above (Uricase peroxidase with no ascorbate oxidase), Triglyceride linearity 1000 mg/dl & above (GPO-PAD) with standard(as & when required), Calcium- liquid stable with standard linearity 20 mg/dl & above (Arsenzo III), Phospholipid – with standard linearity 500 mg/dl & above {CHO (Choline oxidize) /POD (presence of peroxide enzymatic – colorimetric)}, SGOT- Kinetic , linearity 500 U/L & above (IFCC without pyrdoxal phosphate method two reagent kit) (Liquid stable reagent), SGPT- Kinetic, linearity 500 U/L & above (IFCC without pyrdoxal phosphate method two reagent kit)(Liquid stable reagent), LDH- Liquid stable, linearity 1500 U/L & above (P?L method) IFCC, CPK- NAC – Liquid stable, linearity 1500 U/L & above (Creatinine kinase kinetic IFCC method), CPK MB – liquid stable, linearity 2000 U/L & above, kinetic (NADH Kinetic) with control & calibrator, Amylase – liquid stable, linearity 2000 U/L and above (Kinetic using CN PG3), Lipase- kinetic , linearity upto 300 U/L and above with calibrator and controls (Enzymatic colorimetric) , Alkaline Phosphatase- kinetic , linearity 1000 U/L (IFCC or AACC optimized method using AMP buffer), Total protein- Linearity 15 gm/dl & above (Biuret), Albumin- linearity 7 gm/dl & above (Bromocresol green), Iron liquid stable linearity = 850 µg/ (Ferrozine method), UIBC-liquid stable, linearity = 750 µg/dl (Ferrozine method) no manual step should be required outside analyzer., Acid Phosphatase – kinetic , linearity 80 U/L & above with calibrator and control (NaphthyI phosphate kinetic with penta anedise activation) , Bilirubin- biochromatic kit suitable for auto analyzer, linearity 20 mg/dl & above preferably single reagent for total and direct bilirubin with standard (as & when required) (Diazo with sulphanilic acid) , LDL Cholesterol- (Direct) suitable for auto analyzer , linearity 1000 mg/dl & above with calibrator & control. Calibrator should be traceable to internationally accepted norms., Gamma GT- Liquid stable , linearity 250 U/L & above (IFCC CY-glutamyl 3- Carboxy 4 nitroanilide), Quality control (Normal) human sera basedQuality control (Normal) human sera based ( as per tender Technical Specifications), Quality control (Abnormal) human sera based Quality control (Abnormal) human sera based ( as per tender Technical Specifications), "HbA1c- Kit suitable for auto analyzer with calibrator and control1. 1. Should be NGSP and IFCC approved. , 2. Should provide four level calibrator (0.5ml) with each kit and also two levels -L1 & L2 (low & high ) 0.5 ml each of control. , 3. Turbidometric inhibition immunoassay or Enzymatic, 4. Should be supplied with lysing solution (not less than 75ml/kit) and calibrator (not less than 4ml/kit), ", "Multi-analyte calibrator for calibrating biochemical parameters. Should be traceable to internationally accepted standards/norms., 1. Should be human sera based. , 2. Should have long stability , 3. Should have maximum number of parameters.", Total Lipids –with standard linearity up to 1500 mg/dl & above ready to use for auto analyzer, CSF Protein – linearity 250 mg/dl with calibrator. (2x3ml per kit.) , "CSF Protein quality control -5 ml , 1. Human based material , 2. True third party control providing unbiased , 3. performance assessment , 4. Assayed target values should be available , 4. Shelf life of 2 years from the date of manufacture , 5. Open vial stability of 30 days for all analytes when , stored at 20C 8oC, ", HDL cholesterol- (direct) clearance two reagent method suitable for auto analyzer linearity up to 150 mg/dl & above with calibrator and control. Calibrator should be traceable to internationally accepted norms. Control and calibrator volume approx. 3 ml per kit., "Blood Gas , Quality control material should be designed to meet the expanded test menus of today's blood gas analyzers. 1. Quality control should include pH, Blood Gas, Electrolytes and Metabolites. , 2. Quality control should be aqueous, clear matrix , 3. Quality control can be stored for up to 12 months at 20–25°C , 4. Quality control should be USFDA approved , 5. Quality control provider should offer peer group reports as and when required. , 6. Analytes , 1) Calcium(Ionized), 2) Chloride, 3) Glucose, 4) Lactate(Lactic Acid), 5) pCO2, 6) pH, 7) pO2, 8) Potassium, 9) Sodium, 10) TotalCO2, 11) HCO3", Quality control tri-lev
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Biochemistry Reagents and Kits #*. Biochemistry Reagents and Kits |