"MIZUHO" INFLUENZA A/B RAPID TEST (Non-Sterile) - Taiwan Registration bdeddb5fae8a9a04a4abd12fa2a46926
Access comprehensive regulatory information for "MIZUHO" INFLUENZA A/B 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 bdeddb5fae8a9a04a4abd12fa2a46926 and manufactured by MIZUHO MEDY CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING 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
bdeddb5fae8a9a04a4abd12fa2a46926
Ministry of Health Medical Device Import No. 015864
DHA09401586400
Product Details
C Immunology and microbiology devices
C3330 Influenza virus serum reagent
Imported from abroad
Dates and Status
Nov 16, 2015
Nov 16, 2020
May 19, 2022
Cancellation Information
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