"GHope" Adenovirus Antigen Rapid Diagnostic Kit (Non-Sterile) - Taiwan Registration 5846541fdb748dbaa03a27b7488acccb
Access comprehensive regulatory information for "GHope" Adenovirus Antigen Rapid Diagnostic Kit (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 5846541fdb748dbaa03a27b7488acccb 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
5846541fdb748dbaa03a27b7488acccb
Ministry of Health Medical Device Import No. 013879
DHA09401387900
Product Details
C Immunology and microbiology devices
C3020 adenovirus serum reagent
Imported from abroad
Dates and Status
Feb 25, 2014
Feb 25, 2019
May 19, 2022
Cancellation Information
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