Vietnam MOH registration 240001127/PCBA-HCM

Dilution solution for blood

VN: Dung dịch pha loãng huyết tương
Vietnam flagVietnam·Risk Class TTBYT Loại A·843 742·"Bio-Ksel" Sp. Z o.o.·Registered Jul 26, 2024
Registration details
Analysis ID
240001127/PCBA-HCM
Submission ID
000.00.19.H29-240605-0023
Product Type
843 742
Company information
Manufacturer Country
POLAND
Product Owner
“Bio-Ksel” Sp. Z o.o.
Technical details
Intended Use
Used for dilution of the tests (Clauss Fibrinogen test) and for calibration (calibration curve)
Dates and status
Registration Date
Jul 26, 2024
About this record

Access comprehensive regulatory information for Dilution solution for blood in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại A medical device is registered under number 240001127/PCBA-HCM and manufactured by "Bio-Ksel" Sp. Z o.o.. The authorized representative in Vietnam is CÔNG TY TNHH KHOA HỌC VÀ KỸ THUẬT OLYMPIC.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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