Baynex Influenza 2-in-1 Viral Antigen Rapid Diagnostic Test Card (Unsterilized) - Taiwan Registration 176e04456a28b0b60b6e7e1b44d8ddcc
Access comprehensive regulatory information for Baynex Influenza 2-in-1 Viral Antigen Rapid Diagnostic Test Card (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 176e04456a28b0b60b6e7e1b44d8ddcc and manufactured by Abbott Diagnostics Scarborough, Inc.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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.
Device Details
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
C Immunology and microbiology
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import
Dates and Status
Jul 18, 2012
Jul 18, 2022
Apr 12, 2024
Cancellation Information
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