"Abbot" adenovirus antigen rapid test reagent (unsterilized) - Taiwan Registration 4d72344e11118606b70e0eafbc2a8cb0
Access comprehensive regulatory information for "Abbot" adenovirus antigen rapid test 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 4d72344e11118606b70e0eafbc2a8cb0 and manufactured by ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT. 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 "Adenovirus Serological Reagent (C.3020)".
C Immunology and microbiology
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import
Dates and Status
Jan 11, 2012
Jan 11, 2022
Apr 12, 2024
Cancellation Information
Logged out
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