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hCG Qualitative Test Kit - Vietnam Registration 240002780/PCBB-HN

Access comprehensive regulatory information for hCG Qualitative Test Kit 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 240002780/PCBB-HN and manufactured by GeneSign Biotech (Xiamen) Co., Ltd. The authorized representative in Vietnam is CÔNG TY TNHH STV TECHNOLOGY.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Diagnosis F Biotech Co., Ltd, Acro Biotech Inc., and 4 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.

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240002780/PCBB-HN
Registration Details
Vietnam MOH Registration: 240002780/PCBB-HN
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Device Details

hCG Qualitative Test Kit
VN: Que thử/Khay thử xét nghiệm định tính hCG
Risk Class TBYT Loại B

Registration Details

240002780/PCBB-HN

000.00.19.H26-241014-0030

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

GeneSign Biotech (Xiamen) Co., Ltd

Technical Details

It is an immunofluorescence chromatography test, a rapid qualitative test to detect hCG hormone in urine samples, aimed at supporting early pregnancy detection.

Dates and Status

Oct 16, 2024