Tender 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)., jaipur-Rajasthan

Tender 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) IPOD (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 UIL and above with calibrator and controls (Enzymatic colorimetric) Alkaline Phosphatase-kinetic, linearity 1000 UIL (IFCC or AACC optimized method using AMP buffer) Total protein-Linearity 15 gm/dl & above (Biuret) Albumin-linearity 7 gm/dl & above (Bromocresol Iron liquid stable linearity ≥ 850 µg/ (Ferrozine 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 (Naphthyl 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 based Quality 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 controll 1. Should be NGSP and IFCC approved. 2. Should provide four level calibrator (0.5ml) with each kit and also two levels -L, & L. (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 4mlikit) 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 2°C 8°C 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 Blood Gas Quality control material should be designed to meet the expanded test menus of todays 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(lonized) 2) Chloride 3) Glucose 4) Lactate(Lactic Acid) 5) pCO₂ 6) pH 7) p0 8) Potassium 9) Sodium 10) TotalCO₂ 11) HCO, Quality control tri-level (as per tender Technical Specifications) Serum Magnesium 1. Method-Calmagide method 2. Linearity 5 mg/dl & above with control & calibrator 3. Liquid stable suitable for fully automated analyzer 4. With standard (as & when required) Third party control for CSF Protein. Third party control & calibrator for Acid Third party control & calibrator for CPK-MB

Sr No	CorrigendumDate	Corrigendum	CorrigendumType	NewSubmissionDate
1	06-08-2025	Date amendment	Date	08-09-2025
2	06-08-2025	Date Amendment Corrigendum	Date	03-09-2025
3	20-08-2025	Date Amendment	Date	18-09-2025
4	28-08-2025	Technical Bid Corrigendum	Technical Bid	18-09-2025

INR 5000 /-

INR 4 Crore /-

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