Quantitative uric acid test reagent
Vietnam·Risk Class TTBYT Loại B·UA2·Roche Diagnostics GmbH·Registered Aug 26, 2024- Analysis ID
- 240001937/PCBB-HCM
- Submission ID
- 000.00.19.H29-240822-0002
- Product Type
- UA2
- Product Code
- 03183807190
- Manufacturer
- Roche Diagnostics GmbH
- Authorized Representative
- CÔNG TY TNHH ROCHE VIỆT NAM
- Intended Use
- In vitro testing for quantifying uric acid in human serum, plasma, and urine on the cobas c and COBAS INTEGRA systems.
- Registration Date
- Aug 26, 2024
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Access comprehensive regulatory information for Quantitative uric acid test reagent in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240001937/PCBB-HCM and manufactured by Roche Diagnostics GmbH. The authorized representative in Vietnam is CÔNG TY TNHH ROCHE VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Biolabo S.A.S., DIALAB Production and Distribution of Chemical-Technical Products and Laboratory Instruments Gesellschaft m.b.H. (tên viết tắt: DIALAB hoặc DIALAB GmbH), Austria , and 5 recent registrations in the same category. 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.