Drug Test for Direct Bilirubin Quantification
- Analysis ID
- 240002203/PCBB-HCM
- Submission ID
- 000.00.19.H29-240923-0016
- Product Type
- BILD2
- Product Code
- 08056951190
- Manufacturer
- Roche Diagnostics GmbH
- Authorized Representative
- CÔNG TY TNHH ROCHE VIỆT NAM
- Intended Use
- In vitro testing for the quantitative detection of direct bilirubin in human serum and plasma on the cobas c systems
- Registration Date
- Sep 27, 2024
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Access comprehensive regulatory information for Drug Test for Direct Bilirubin Quantification in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại B medical device is registered under number 240002203/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, 2 companies making similar products including Roche Diagnostics (Suzhou) Ltd., Theo theo phụ lục, and 2 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.