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Myo Quantitative Testing Kit - Vietnam Registration 2403222ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Myo Quantitative Testing Kit 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 2403222ĐKLH/BYT-HTTB and manufactured by Getein Biotech, Inc.. The authorized representative in Vietnam is CÔNG TY TNHH STV TECHNOLOGY.

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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2403222ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2403222ĐKLH/BYT-HTTB
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Device Details

Myo Quantitative Testing Kit
VN: Bộ xét nghiệm định lượng Myo
Risk Class TTBYT Loại C

Registration Details

2403222ĐKLH/BYT-HTTB

000.00.04.G18-230428-0018

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

Getein Biotech, Inc.

Technical Details

MAGICL Myo (CLIA) is used to determine the quantitative in vitro Myoglobin in the serum, plasma, or whole blood of humans. It is primarily used clinically as a supportive diagnostic tool for myocardial infarction and other diseases, and it is a very sensitive indicator of acute myocardial infarction

Dates and Status

Nov 02, 2024