"GHope" Influenza A&B Virus Antigen Rapid Test (Non-Sterile) - Taiwan Registration d76504632b3790e08cff6972ed985ee4
Access comprehensive regulatory information for "GHope" 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 d76504632b3790e08cff6972ed985ee4 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
d76504632b3790e08cff6972ed985ee4
Ministry of Health Medical Device Import No. 015386
DHA09401538600
Product Details
C Immunology and microbiology devices
C3330 Influenza virus serum reagent
Imported from abroad
Dates and Status
Jun 26, 2015
Jun 26, 2020
May 19, 2022
Cancellation Information
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