Alere i Influenza A&B - Taiwan Registration 30bff5a3cea5b71721c72d2e2e4205cc
Access comprehensive regulatory information for Alere i Influenza A&B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30bff5a3cea5b71721c72d2e2e4205cc and manufactured by ALERE 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
Registration Details
30bff5a3cea5b71721c72d2e2e4205cc
Ministry of Health Medical Device Import No. 027999
DHA05602799903
Product Details
C Immunology and microbiology devices
C3980 Multi-standard nucleic acid test reagent for respiratory viruses
Imported from abroad
Dates and Status
Dec 16, 2015
Dec 16, 2020
Jul 15, 2022
Cancellation Information
Logged out
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