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Baynex Respiratory Fusion Viral Antigen Rapid Test Reagent - Taiwan Registration ab61079d2d7407e1306e335e5e3e0974

Access comprehensive regulatory information for Baynex Respiratory Fusion Viral Antigen Rapid Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ab61079d2d7407e1306e335e5e3e0974 and manufactured by BINAX, INC. The authorized representative in Taiwan is Dachen Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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ab61079d2d7407e1306e335e5e3e0974
Registration Details
Taiwan FDA Registration: ab61079d2d7407e1306e335e5e3e0974
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Device Details

Baynex Respiratory Fusion Viral Antigen Rapid Test Reagent
TW: ๆ‹œๅฅˆๅ…‹ๆ€ๅ‘ผๅธ้“่žๅˆ็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

ab61079d2d7407e1306e335e5e3e0974

DHA04400117303

Company Information

United States

Product Details

It is used in serum tests to identify antibodies to respiratory fusion cell viruses in serum.

C Immunology and microbiology

import

Dates and Status

Oct 24, 2005

Oct 24, 2010

Nov 06, 2012

Cancellation Information

Logged out

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