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"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.

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bdeddb5fae8a9a04a4abd12fa2a46926
Registration Details
Taiwan FDA Registration: bdeddb5fae8a9a04a4abd12fa2a46926
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Device Details

"MIZUHO" INFLUENZA A/B RAPID TEST (Non-Sterile)
TW: "็พŽๆ—ฅๅ’Œ" ๆตๆ„ŸA/Bๅž‹ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bdeddb5fae8a9a04a4abd12fa2a46926

Ministry of Health Medical Device Import No. 015864

DHA09401586400

Company Information

Japan

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

Logged out

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