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Purchase of Medical Products in Accordance Tender - 142871165

The STATE UTILITY ENTERPRISE WITH THE RIGHT OF ECONOMIC MANAGEMENT "REGIONAL PERINATAL CENTER NO. 3" OF THE HEALTH DEPARTMENT OF THE TURKESTAN REGION has issued a Tender notice for the procurement of a Purchase of Medical Products in Accordance with Technical Specifications (Through Paid Services), Amt: 3621639.77 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 3621639.77. Interested bidders can access detailed Tender information, eligibility criteria, and complete bidding documents by referencing TOT Ref No. 142871165, while the tender notice number is 17140948-1 and Registering on the platform.

Procurement Summary

Country: Kazakhstan

Summary: Purchase of Medical Products in Accordance with Technical Specifications (Through Paid Services), Amt: 3621639.77

Deadline: 10 Jun 2026

Posting Date: 08 Jun 2026

Other Information

Notice Type: Tender

TOT Ref.No.: 142871165

Document Ref. No.: 17140948-1

Competition: ICB

Financier: Self Financed

Purchaser Ownership: Public

Tender Value: KZT 3621639.77

Purchaser's Detail

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Tender Details

Lots: KaryoMAX Colcemid solution in PBS, 10 ml. Technical characteristics: The reagent must be a ready-to-use liquid solution of N-desacetyl-N-methylocolchicine (Colcemid), intended to arrest mammalian cells in metaphase of the cell cycle with for the purpose of subsequent separation and analysis of chromosomes. The drug must be used in cytogenetic studies and must also be suitable for use in in vitro diagnostic procedures, clinical and translational studies. Active the substance must be dissolved in phosphate-buffered saline (PBS). The concentration of Colcemid™ must be at least 10 µg/ml. The mechanism of action of the reagent should be to inhibit the formation of the spindle during mitosis, causing metaphase cell cycle arrest. The drug should have a mechanism of action similar to colchicine, and should be characterized by lower toxicity to mammalian cells. The reagent must be in liquid form and must be sterile filtered. The pH value of the solution must be in the range of not less than 6.0 and not more than 8.0. The volume of the primary packaging must be at least 10 ml. The drug must belong to the KaryoMAX line and must be classified as a reagent for chromosome analysis. Supplier provides documents confirming the compliance of the supplied goods with the requirements established by technical regulations, provisions of standards or other documents in accordance with the legislation of the Republic...

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