Cleaning Solution Solution Intended For Cleaning Automatic And Semi-Automatic Biochemical Analyzers, Removing Residues That Remain In Pipes, Hoses And Continuous Flow Cuvettes After Using The Equipment. Containing: Carbonate Buffer, Stabilizer, Detergent And Preservative. Presentation: Bottle With 250 Ml., Systems Liquid To Be Used Together With The Cleaning Solution. Presentation: 250Ml, Kit For Calibrating Quantitative Methods In Biochemical Tests. Bottle With At Least 5 Ml Presentation: Cal 1X5 Ml, Kit Intended For Use As A Normal Precision Control Of Quantitative Methods In Biochemical Tests Bottle With At Least 5 Ml Presentation: Cal 1X5 Ml, Kit Intended For Use As A Pathological Control Precision Control Of Quantitative Methods In Biochemical Tests. Bottle With At Least 5 Ml Presentation: Cal 1X5 Ml, Kit Intended For The Determination Of Uric Acid In Serum, Urine And Synovial Fluid. Colorimetric Enzymatic Method – Trinder Reaction: End Point Presentation: R1 2X100 Ml+Sdt 1X4 Ml Linearity At Least 20 Mg/Dl, Kit Intended For The Determination Of The Enzymatic Activity Of Alpha-Amylase In Serum, Plasma (Heparin), Urine, Ascitic Fluid And Pleural Colorimetric Kinetic Method – Galg2 Reaction: Continuous Kinetic Presentation: R1:4X15ml Serum Linearity: At Least 1200 U/L Urine Linearity 2000 U/L, Kit For Determination Of Direct Bilirubin In Serum And Plasma (Heparin And Edta)Method Dca (Diazotted Dichloroaniline). Reaction: Final Pointpresentation: R1 1X80 + R2 2X12 Ml Linearity At Least 20 Mg/Dl, Kit Intended For The Determination Of Total Bilirubin In Serum And Plasma (Heparin And Edta) Dca Method (Diazotted Dichloroaniline). Reaction: End Point Presentation: R1 1X80 + R2 2X12 Ml Linearity At Least 50 Mg/Dl, Kit Intended For Quantitative Determination Of The Enzymatic Activity Of Creatine Kinase Subunit B (Ck-Mb) In Serum Uv Kinetic Method – Ifcc Reaction: Continuous Kinetic Presentation: R1 1X40 Ml + R2 1X10 Ml + Control 1X1 Ml Linearity At Least 600 U/L 550 U/L, Kit Intended For Quantitative Determination Of The Enzymatic Activity Of Total Creatine Kinase (Ck Nac) In Serum And Plasma Uv Kinetic Method – Ifcc Reaction: Thin Point Increasing Kinetic Presentation: R1 1X40 + R2 1X10 Linearity At Least 1000 U/L, Kit Determined For Determination Of Cholesterol In Serum Trinder Colorimetric Enzymatic Method Reaction: End Point Presentation: 1-R1 1X250 + Std 1X4 Linearity No Minimum 800 Mg/Dl, Kit Designed For The Determination Of Creatinine Present In Serum, Plasma And Urine Method: Enzymatic Pap Enzymatic Reaction End Point/Crescent Presentation:1- R1: 1X 40 Ml / R2: 1X 10 Ml Linearity At Minimum 80 Mg/Dl, Kit Intended For The Determination Of Alkaline Phosphatase Enzyme Activity In Serum And Plasma (Heparin) Using The Method Of The German Clinical Chemistry Association (Dgkc) Colorimetric Kinetic Method – Dgkc Continuous Kinetic Reaction Presentation: R1 2X40 Ml + R2 2X10 Ml Linearity At Minimum Of 700 U/L, Kit Intended For The Quantitative Determination Of Gt Range Enzymatic Activity In Serum Plasma (Edta) And Urinekinetic Colorimetric Method Continuous Increasing Kinetic Reaction Presentation: R1 2X40 Ml + R2 2X10 Ml Linearity At Minimum 250 U/L L 270 U/L, Kit For The Determination Of Glucose In Serum, Plasma Csf And Urine Enzymatic Method – God Reaction Final Point Presentation: 1-R1 1X250 Ml + Std 1X4 Ml Minimum Linearity Of Serum And Urine 800 Mg/Dl Csf Linearity 740 Mg/Dl
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