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Qualitative Antibody Test (IgG, IgM, IGA) for HIV-1 and HIV-2 - Vietnam Registration 2402919ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Qualitative Antibody Test (IgG, IgM, IGA) for HIV-1 and HIV-2 in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2402919ĐKLH/BYT-HTTB and manufactured by GenBody Inc.. The authorized representative in Vietnam is CÔNG TY TNHH ĐẦU TƯ THIẾT BỊ CÔNG NGHỆ NTN GLOBAL.

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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2402919ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402919ĐKLH/BYT-HTTB
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Device Details

Qualitative Antibody Test (IgG, IgM, IGA) for HIV-1 and HIV-2
VN: Khay thử xét nghiệm định tính kháng thể (IgG, IgM, IGA) kháng HIV-1 và HIV-2
Risk Class TTBYT Loại D

Registration Details

2402919ĐKLH/BYT-HTTB

000.00.04.G18-230727-0001

GenBody HIV 1/2

Theo phụ lục

Company Information

Theo theo phụ lục

GenBody Inc.

Technical Details

GenBody HIV 1/2 is an immuno-precipitation test for the rapid qualitative detection of all HIV-1 and HIV-2 antibodies (IgG, IgM, IgA) in plasma, serum, and whole blood of humans.

Dates and Status

Oct 22, 2024