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Standard Human Plasma 10 X For 1 Ml. Reagent Designed For Calibration Of Various Clotting, Chromogenic And Immunological Tests. Ingredients: Plasma Is Produced From Citrated Plasma Obtained From Healthy Blood Donors, Stabilized With A Solution Of Hepes Buffer (12 G/L) And Lyophilized. Packaging 10X1 Ml. Stability After Opening: 4 Hours At +15 To +25 °C. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Control Plasma N 10 X For 1 Ml (Control Plasma N 10 X For 1 Ml). The Reagent Is Intended For Daily Intra-Laboratory Monitoring Of The Correct Determination Of The Parameters Of Coagulation, Anticoagulation And Fibrinolytic Systems. Composition: Lyophilized Pooled Plasma Of Selected Healthy Blood Donors, Stabilized With Hepes Buffer (12 G/L); Does Not Contain Preservatives. Packaging: 10X1 Ml. Stability After Opening: 4 Hours At +15 To +25 °C. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Wash Solution Ca Clean Ii 1 X 5000 Ml. Intended For Use As A Cleaning Solution For Fully Automatic Sysmex Blood Clotting Analyzers. Ingredients: Hydrochloric Acid 0.16%, Nonionic Surfactant 0.50%, Ph Acidic. Stability After Opening (Closed Bottle): At Temperatures From 5 To 35 °C – 2 Months. Packaging: 5000 Ml. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Actin Fs 10 X 10 Ml (Reagent For Determination Of Actin Fs 10 X 10 Ml). The Aptt Reagent Shows High Sensitivity To Deficiency Of Intrinsic Coagulation Factors (Viii, Ix, Xi And Xii). Composition: Purified Soy Phosphatides In 1.0 × 10–4 Ellagic Acid Solution With The Addition Of Buffer, Stabilizers And Preservatives. The Release Form Must Be Liquid, Ready For Use. After Printing The Reagent Stable For 7 Days At Temperatures From 2 To 15 °C. Do Not Freeze. Packaging: 10X10ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Control Plasma P 10 X For 1 Ml (Control Plasma P 10 X For 1 Ml). The Reagent Is Intended For Monitoring Coagulometer And Fibrinolysis Tests In Pathological Values. Composition: Lyophilized Pooled Plasma Of Selected Healthy Blood Donors, Stabilized With Hepes Buffer (12 G/L); Does Not Contain Preservatives. Packing: 10 X 1 Ml. Stability After Reconstitution At Temperatures From +15 To +25°C - 4 Hours. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Thrombin Reagent 100 I. U. 10 X For 5 Ml (Reagent For Determining Thrombin 100 I. U. 10 X Per 5 Ml). Reagent For Quantitative Determination Of Thrombin Time In Human Plasma. Composition: Thrombin (Diluted ~ 100 Iu/Ml), Stabilizer, Buffer. After Unsealing, The Reagent Is Stable For At Least 5 Days At Temperatures From 2 To 8°C; At Least 8 Hours At A Temperature Of 15 To 25°C. Packaging 10X5ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Washing Reagent Cn-Coagwasher (2L). Intended For Use As A Cleaning Solution For Fully Automatic Sysmex Blood Clotting Analyzers. Composition: Sodium Hypochlorite 1.0% (According To Active Chlorine Concentration). Stability After Opening (Closed Bottle): At Temperatures From 2 To 35 °C – 3 Months. Packaging: 1 × 2 L. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Berichrom At Iii 1 Kit (Reagent For Determining Berichrom At Iii 1 Set). Kit For Quantitative Determination Of The Functional Activity Of Antithrombin Iii In Automatic Analyzers. The Kit Should Include A Reagent Containing Freeze-Dried Thrombin, Heparin And Aprotinin. The Lyophilized Substrate Reagent Should Contain Tos-Gly-Pro-Arg-Anba-Ipa (4 Mmol/L); Buffer Solution: Tris (Hydroxymethyl)-Aminomethane (100 Mmol/L), Nacl (8.7 G/L), Ph 8.2 Sodium Azide (< 1 G/L) Acts As A Preservative. The Stability Of The Reagent After Opening At Temperatures From +2 °C To +8 °C Is At Least 2 Weeks. Measuring Range: From 0 To 140% Of Normal. Sensitivity Limit: 3.7% Of Normal. Coefficient Of Variation: From 1.3 To 2.7%. The Calibrator Of The Method Is Reference Plasma (Shp). Packing: 6X5ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Calcium Chloride 0.025 Mol/L 10 X 15 Ml. Calcium Chloride Solution Is Used As An Auxiliary Reagent For Various Coagulometer Analyses. Composition: Cacl2 Solution 0.025 Mol/L. Stability After Opening: 8 Weeks At +2 To +25 °C. Packaging: -10X15 Ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Innovin 10 X For 10 Ml 1000 (Reagent For Determination Of Innovin 10 X For 10 Ml 1000). The Reagent Is Used To Quantify Prothrombin Time. A Lyophilized Reagent Consisting Of Trackcombinant Human Tissue Factor And Synthetic Phospholipids (Thromboplastin), Calcium Ions, Heparin Neutralizing Agent, Buffers And Stabilizers (Bovine Serum Albumin). It Is Not Sensitive To Therapeutic Levels Of Heparin, Which, In Combination With Its High Sensitivity To Coagulation Factor Deficiencies, Makes It An Ideal Reagent For Monitoring Oral Anticoagulation Therapy. Packaging: 10X10ml. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Pt-Multi Calibrator (6 Levels) 6 X For 1 Ml (Pt-Multi Calibrator 6 X For 1 Ml). The Calibrator Kit Is Intended For Use As A Reagent For Hemostasis Studies. To Determine The Local Value Of Mich. Composition: Six Calibration Plasmas For Pv Calibration. Calibration Plasma Is Lyophilized And Calibrated. Stability After Reconstitution (Closed Vial): - At A Temperature Of 2-8 °C 8 Hours; - At A Temperature Of 15-25 °C 4 Hours; - At Temperatures ≤ −18 °C 4 Weeks. Packaging 6X1ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Ourena Buffer Veronal 10 X 15 Ml. Dilution Buffer For Hemostasis Studies, As Well As For Any Laboratory Test Using Isotonic Barbital Buffer With A Ph Level Of 7.35. Composition: Ourens Veronal Buffer: 2.84 X 10–2 M Sodium Barbital In 1.25 X 10–1 M Sodium Chloride, Ph 7.35 ± 0.1. The Release Form Must Be Liquid, Ready For Use. Packaging 10X15ml. After Unsealing, The Reagent Is Stable For 8 Weeks. At Temperatures From 2 To 8°C. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Reaction Cells For Cs 2100. Cells For Carrying Out Analytical Reactions And Recording By Optical Methods In The Visible And Ultraviolet Parts Of The Spectrum. Plastic Container 0.6 Ml With A Fixing Ring, Height 30 Mm, Diameter 8 Mm, Ring Diameter - 10 Mm. Packaging 3X1000 Pcs. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Thromboclotin 10 X For 10 Ml (Reagent For Determination Of Thromboclotin 10 X Per 10 Ml). Reagent For Determining Thrombin Time, Monitoring Fibrinolytic Therapy, Screening For Disorders Of Fibrin Formation, In Cases Of Severe Fibrinogen Deficiency On Semi-Automatic And Automatic Analyzers Of The Hemostasis System. Composition: Lyophilized Stabilized Bovine Thrombin (2.5 Iu/Ml). Reagent Stability After Opening At Temperatures From +2 ° C To +15 ° C For At Least 1 Week; At A Temperature From +15 °C To +22 °C For At Least 1 Day; At A Temperature Of -20°C For At Least 1 Month, If The Reagent Is Frozen After Opening. The Reconstituted Ampoule Contains Approximately 2.5 Nih Units Of Thrombin Per Ml. Accuracy: Coefficient Of Variation Within Test Series Is 1.3% And 1.9%, Respectively, And From Day To Day - 2.4% And 7.6%, Respectively. Packaging: 10X10 Ml. To Determine Compatibility With The Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Innovance D-Dimer Kit 1 Kit 300 (Large) (Reagent For Determining Innovance D-Dimer 1 Set 300 - Large. Set Of Reagents For Determining The Concentration Of D-Dimer. Composition: Reagent (Polystyrene Particles Coated With Monoclonal Antibodies To D-Dimer, Human Serum Albumin. Preservatives: Amphotericin B, Gentamicin); Buffered Saline Solution (Dextran, Imidazole. Preservative: Sodium Azide); Additive (Buffered Saline Solution, Heterophilic Blocking Agent. Preservative: Sodium Azide); Diluent (Buffered Saline Solution, Imidazole. Preservative: Sodium Azide); Calibrator (Human Blood Plasma, D-Dimer Preparation. Preservatives: Sodium Azide And 5-Chloro-2-Methyl-4-Isothiazol-3-One And 2-Methyl-4-Isothiazole-3-One). Once Unsealed, The Reagent Is Stable For 4 Weeks At Temperatures From 2 To 8°C. Packaging: 300 Tests. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of Calibration On Approved Reference Materials By The Manufacturer, Supplier Upon Delivery, The Kit Is Spectral Calibrated. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software., Innovance D-Dimer Control 2 X 5 X 1 Ml (Level Normal And Pathologic) Control Solutions Designed To Determine The Accuracy And Analytical Bias In The Normal And Pathological Range When Detecting D-Dimer Composition: D-Dimer, Based On Lyophilized Human Plasma. Preservatives: 5-Chloro-2-Methyl-Isothiazol-3-One And 2-Methyl-4-Isothiazol-3-One (< 1 Mg/L), Sodium Azide (< 1 G/L). Packaging 5X1 Ml Two Levels. After Printing, The Reagent Is Stable For 8 Hours At Temperatures From 15 To 25°C; 7 Days At Temperatures From 2 To 8°C; 4 Weeks - < -18°C. To Determine Compatibility With Oem Software Of Medical Equipment Available To The Customer, And Subsequent Validation Of The Calibration On Standard Samples Approved By The Manufacturer, The Supplier Performs Spectral Calibration Of The Kit Upon Delivery. The Supplied Kit Must Be Compatible With The Oem Version Of The Installed Software.
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