"GHope" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile) - Taiwan Registration c57e4f678de6776250a8752be8c5e3ba
Access comprehensive regulatory information for "GHope" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c57e4f678de6776250a8752be8c5e3ba and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..
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
c57e4f678de6776250a8752be8c5e3ba
Ministry of Health Medical Device Import No. 014243
DHA09401424302
Product Details
C Immunology and microbiology devices
C3330 Influenza virus serum reagent
Imported from abroad
Dates and Status
Jun 13, 2014
Jun 13, 2019
May 19, 2022
Cancellation Information
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