Quantitative uric acid test reagent - Vietnam Registration 240001937/PCBB-HCM

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.