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The MUNICIPAL STATE ENTERPRISE WITH THE RIGHT OF ECONOMIC MANAGEMENT "CHILDREN'S CITY CLINICAL HOSPITAL NO. 2" OF THE PUBLIC HEALTH DEPARTMENT OF THE CITY OF ALMATY has issued a Tender notice for the procurement of a Laboratory Hemostasis Analyzer, Amt: 1981286.00 in the Kazakhstan. This Tender notice was published on 08 Jun 2026 and is scheduled to close on 10 Jun 2026, with an estimated Tender value of KZT 1981286.00. Interested bidders can access detailed Tender information, eligibility criteria, and complete bidding documents by referencing TOT Ref No. 142878509, while the tender notice number is 17141267-1 and Registering on the platform.
Procurement Summary
Country: Kazakhstan
Summary: Laboratory Hemostasis Analyzer, Amt: 1981286.00
Deadline: 10 Jun 2026
Posting Date: 08 Jun 2026
Other Information
Notice Type: Tender
TOT Ref.No.: 142878509
Document Ref. No.: 17141267-1
Competition: ICB
Financier: Self Financed
Purchaser Ownership: Public
Tender Value: KZT 1981286.00
Purchaser's Detail
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Email: Login to see tender_detailsLogin to see details Tender Details Lots: Reagent set - BIOPHEN™ Normal Control Plasma (Control plasma 1) The BIOPHEN™ Normal Control Plasma set is a set of normal citrated human plasma, lyophilized, intended for quality control of certain analyzes blood clotting factors. Composition: normal human citrated plasma, lyophilized. Control plasma contains stabilizing agents. Packaging: 12 x 1ml. Storage conditions: Reagents should be stored at 2-8°C in the original packaging box. Use before the expiration date indicated on the box. The stability of the reagent after dilution, without any contamination or evaporation, when stored unopened is: • For AT, PC; VII-X, plasminogen, FII, FVII, FIX, FX, FXI, FXII, FXIII, fibrinogen, aPCr (%FVL), lupus anticoagulant, PT/INR/%, aPTT, vWF:Ag, α2-AP and thrombin time: 24 hours at 2-8°C, 8 hours at room temperature (18-25°C), 2 months at -20°C or below. • For FVIII:C, FV and PS: 8 hours at 2-8°C, 4 hours at room temperature (18-25°C), 2 months at -20°C or below. To identify compatibility with the software of medical equipment available to the Customer and subsequent validation 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 version of the installed software... Documents
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