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Quantitative and Qualitative Antibody Test Kit for Toxoplasma gondii - Vietnam Registration 2301802ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Quantitative and Qualitative Antibody Test Kit for Toxoplasma gondii in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại C medical device is registered under number 2301802ĐKLH/BYT-HTTB and manufactured by DRG Instruments GmbH.

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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2301802ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2301802ĐKLH/BYT-HTTB
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Device Details

Quantitative and Qualitative Antibody Test Kit for Toxoplasma gondii
VN: Bộ xét nghiệm định lượng và định tính kháng thể IgG kháng Toxoplasma gondii
Risk Class TTBYT Loại C

Registration Details

2301802ĐKLH/BYT-HTTB

000.00.04.G18-220504-0038

Toxoplasma gondii IgG

EIA-3519

Company Information

GERMANY

Technical Details

The DRG Toxoplasma gondii IgG ELISA provides materials to determine the quantitative and qualitative levels of IgG antibodies against Toxoplasma gondii in serum or plasma (EDTA, lithium heparin, or citrated plasma)

Dates and Status

Dec 30, 2023