"Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized) - Taiwan Registration d5de22d733848682829d7a136b7359f7
Access comprehensive regulatory information for "Mei Eliel" Baynex Staphylococcus aureus rapid diagnostic reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d5de22d733848682829d7a136b7359f7 and manufactured by ALERE SCARBOROUGH, INC.. The authorized representative in Taiwan is Ariel Health Inc.
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 "Staphylococcus aureus serum reagent (C.3700)" of the Measures for the Administration of Medical Devices.
C Immunology and microbiology
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import
Dates and Status
Apr 22, 2010
Apr 22, 2020
Jul 15, 2022
Cancellation Information
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