"Meieliel" Precision Influenza A&B Virus Rapid Screening Test (Unsterilized) - Taiwan Registration fbda0e53832bc5ec51b32189170963ca
Access comprehensive regulatory information for "Meieliel" Precision Influenza A&B Virus Rapid Screening Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fbda0e53832bc5ec51b32189170963ca and manufactured by ALERE MEDICAL CO.,LTD CHIBA PLANT. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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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
Oct 26, 2011
Oct 26, 2021
Oct 12, 2023
Cancellation Information
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