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Baynex Influenza 2-in-1 Viral Antigen Rapid Test Reagent - Taiwan Registration c0c850965733b38abe7fa0bcd41e2a2a

Access comprehensive regulatory information for Baynex Influenza 2-in-1 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 c0c850965733b38abe7fa0bcd41e2a2a 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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Registration Details
Taiwan FDA Registration: c0c850965733b38abe7fa0bcd41e2a2a
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Device Details

Baynex Influenza 2-in-1 Viral Antigen Rapid Test Reagent
TW: ๆ‹œๅฅˆๅ…‹ๆ€ๆต่กŒๆ€งๆ„Ÿๅ†’ไบŒๅˆไธ€ๅž‹็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

c0c850965733b38abe7fa0bcd41e2a2a

DHA04400117201

Company Information

United States

Product Details

It is used in serum tests to identify antibodies to cold viruses in serum.

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 24, 2005

Oct 24, 2010

Nov 06, 2012

Cancellation Information

Logged out

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