CRP Quantitative Test Card - Vietnam Registration 220002783/PCBB-BYT
Access comprehensive regulatory information for CRP Quantitative Test Card 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 220002783/PCBB-BYT and manufactured by SD Biosensor, Inc..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Getein Biotech, Inc, Nanjing Norman Biological techlonogy Co., Ltd, 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.
Device Details
Registration Details
220002783/PCBB-BYT
000.00.04.G18-220806-0004
STANDARD™ F CRP
Mã REF.: F-CRP /Mã Cat.: 10CRP10B
Technical Details
STANDARD™ F CRP is used in in vitro diagnosis to quantify CRP in human serum, plasma, and whole blood samples. The quantification of CRP provides information for the detection and assessment of infections, tissue damage, inflammatory disorders, and related diseases. The STANDARD™ F CRP Test Kit should be used in conjunction with the STANDARD™ F Analyzers, which are manufactured by SD BIOSENSOR.
Dates and Status
Aug 06, 2022