Tender For Biochemistry Reagents And Kits, Jaipur-Rajasthan

Tender For Biochemistry Reagents And Kits Glucose Liquid with standard, linearity 600 mg/dl & above (Glucose oxidase/ lexokinase) 2. Cholesterol with standard, linearity 1000 mg/dl (Cholesterol oxidase) 3. Urea Kinetic with standard, linearity 500 mg/dl (Urease Kinetic) Creatinine with standard, linearity 20 mg/dl & above (Enzymatic/Jaffe modified) 5. Phosphorus Liquid stable ready to use with standard, linearity 15 mg/ml & above (U.V. end point using ammonium molybdate) 6. Uric Acid with standard liquid stable standard, linearity 20 mg/dl & above (Uricase peroxidase with no ascorbate oxidize) 7. Triglyceride with standard, linearity 1000 mg/dl & above (GPO-PAD) 8. Calcium Liquid stable with standard linearity 20 mg/dl& above (Arsenzoe III) 9. Phospholipid with standard linearity 500 mg/dl & thove (CHO (Choline oxidize) peroxide enzymatic colorimetric) POD(presence of 10. SGOT Kinetic, linearity 500 U/l& above (IFCC without pyrdoxal phosphate method two reagent kit) (Liquid stable reagent) 11. SGPT Kinetic, linearity 500 U/l & above (IH-CC without pyrdoxal phosphate method two reagent kit) (Liquid stable reagent) 12. LDH Liquid stable, linearity 1500 u/l & above (P1. method) IFCC 13 CPK-NAC Liquid stable, linearity 1500 U/l & above (Creatinine kinase kinetic IFCC method)) CPK MB liquid stable, linearity 2000 U/l & above. 11. 12. Liquid stable, linearity 1500 u/l & above (P1. method) IFCC 13 CPK-NAC Liquid stable, linearity 1500 U/l & above (Creatinine kinase kinetic IFCC method)) 14. CPK MB liquid stable. linearity 2000 U/l & above. kinetic (NADH Kinetic) with control & Calibrator 15. Amylase Liquid stable, linearity 2000 U/l and above (Kinetic using CN PG3) 16. Lipase Kinetic, linearity 700 u/l, with standard and controls (Enzymatic colorimetric) 17. Alkaline Phosphatase Kinetic, linearity 1000 u/1 (H-СС or AACC optimized method using AMP buffer) 18. Fotal Protein Linearity 15 gm/dl & above(Biuret) Mbumin green) Linearity 7 gm/dl & above (Bromocresol 20. Iron IBC Liquid stable, linearity up to 600 mg/dl suitable for fully anto Analyzer Ferrozine method) 21. Acid Phosphates Kinetic, linearity 80 u/l & above (Naphthyl Phosphate Kinetic with pentaanedise activation) 22. Bilirubin Biochromatic kit suitable for Auto analyzer. linearity 20 mg/dl & above preferably single reagent for total and direct bilirubin (Diazo with sulphanilic acid) 2 23. DI Cholesterol (Direct) suitable For Auto Analyzer, linearity 1000 mg/dl & above with calibrator & control. Calibrator should be traceable to internationally accepted norms. 34. Gamma GT Liquid stable, linearity 250 u/l & above (IFCC CY glutamyl 3 Carboxy 4 Nitroanilide) Quality Control (Normal) | Human sera based 1. Assigned values should be available for major automated analyzers, making this control a highly efficient solution for laboratories that focus on routine tests. 2. Quality control should be aqueous, clear matrix 3 . Quality control should have 3 year shelf life at 2-8°C 4. Quality control can be stored for up to 12 month at 20-25°C 5. Should have open vial stability at least 25 to 30 days. 6. Quality control should be USFDA approved 25. 7. Quality control provider should offer peer group reports as and when required. 8. Company should have offer of QC Data management solutions & connectivity to support controls. 9. Company should offer inter laboratory program 10. Company should offer individual laboratory comparison report with Bias and Histogram Report 26. 3. Quality control should have 3 year shelf life at 2-8°C 4 Quality control can be stored for up to 12 month at 20-25 5. Should have open vial stability at least 25 to 30 days. 6. Quality control should be USFDA approved 7. Quality comel provider should offer peer group reports as and when required. 8. Company should have offer of QC Data managemem solutions & connectivity to support controls. 27 9. Company should offer inter laboratory program 10. Company should offer individual laboratory comparison report with Bias and Histogram Report 11. Company should offer affiliated laboratory comparison report. 17 Company should offer monthly evaluation report 13 Fraceable certificate to be enclosed 27. tibAle Kit suitable for Auto Analyzer with calibrator Should be NGSP and IFCC approved. 2. Quality control should be third party. 3. Torbidometric inhibition immunoassay or Enzymatic Multi-analyte Calibrator for calibrating biochemical sunetees should be traceable to internationally meerted standards/norms. 8 Should have long stability 1 Should have maximum mumber of biochemical parameters. 29. Lotal Lipids with standard linearity up to 1500 mg/dl & shove, ready to use for Auto Analyzer 334 SF Pristein Linearity up to 250 mg/dl with standard . and calibrator. Minimune of 2 vials per kit calibrator should be provided with each kit. (2 x 3 ml) US Patein quality control-5ml Human based material True third party control providing unbiased performance assessment Assayed target values available 4 Shelf life of 2 years from the date of manufacture Open vial stability of 30 days for all analytes when stored at 2°C to 8°C DL Cholesterol (Direct) clearance two reagent 32. method suitable for anto analyzer linearity up to 180 mg/dl with calibrator and control, Calibrator should be traceable to internationally accepted norins. Control and calibrator volume approx. 3 ml per kit.. Blood Gas Quality control material should be designed to meet the expanded test memax of todays blood gas analyzers. Quality control should include Ph.Blood Gas, Electrolytes and Metabolites. 2 Quality control should be aqueous.clear matrix 33. 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 wiren required. 1) Calcium(lonized) 2) Chloride 3) Glucose 4) Lactate(lactic Acid) 5) PCO 6) Ph 7) PO 8) Potassium 9) Sodium 10) TotalCO Quality Control Tri Level For routine monitoring of both accuracy and precision with assayed instrument specific target values. Including fertility, steroid-thyroid hormones, tumor marker, vitamins etc. Minimum Parameters Free T TS11 ESH Prolactin Testosterone Growth (NGH) Hormone Insulin Vitamin B THE PSA Vitamin D CA-125 Free T Anti TPO (Anti oxidase) 1.11 Beta HCG Cortisol PTH Hell Folate Alpha Female Protein (AFP) Total IgE *Anti CCP 1. Lyophilized human origin serum 2. Reconstituted stability of at 2°C to 8°C, at least 25 days at 20°C 3. Assigned values should be available for major automated analyzers,making this control a highly efficient solution for laboratories that focus on routine Jests. 4. Quality control should be USFDA approved 5.Quality control provider should offer peer group reports as and when required. Serun Magnesium 1) Method Calmagide Method 35. 2) Linearity 5 mg/dl& above with control & Calibrator 3) Liquid stable suitable for fully automated analyzer 34.

Sr No	CorrigendumDate	Corrignedum	CorrigendumType	NewSubmissionDate
1	10-09-2024		Amendment	27-09-2024
2	11-09-2024		Amendment	07-10-2024
3	23-08-2024		Amendment	17-09-2024
4	24-09-2024		Technical Specification	07-10-2024

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