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β-HCG Quantitative Test Kit - Vietnam Registration 220002953/PCBB-HN

Access comprehensive regulatory information for β-HCG Quantitative Test Kit 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 220002953/PCBB-HN and manufactured by Lansion Biotechnology Co.,Ltd.

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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220002953/PCBB-HN
Registration Details
Vietnam MOH Registration: 220002953/PCBB-HN
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Device Details

β-HCG Quantitative Test Kit
VN: Thuốc thử xét nghiệm định lượng β-HCG
β-HCG Test Kit (Dry Fluorescence Immunoassay)
Risk Class TTBYT Loại B

Registration Details

220002953/PCBB-HN

000.00.19.H26-220908-0015

β-HCG Test Kit (Dry Fluorescence Immunoassay)

Company Information

Technical Details

The fluorescent dry blood spot immunoassay for in vitro diagnosis of β-HCG concentration in human serum and plasma.

Dates and Status

Sep 09, 2022