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"Baiyou Jingya" Influenza Virus A+B Rapid Test Reagent (Unsterilized) - Taiwan Registration 95ab940986193d61ea302c0087ea2289

Access comprehensive regulatory information for "Baiyou Jingya" Influenza Virus A+B Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95ab940986193d61ea302c0087ea2289 and manufactured by BIOMERIEUX (SHANGHAI) BIOTECH CO., LTD.. The authorized representative in Taiwan is Hong Kong Commercial Mรฉrieux S.p.A. Taiwan Branch.

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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95ab940986193d61ea302c0087ea2289
Registration Details
Taiwan FDA Registration: 95ab940986193d61ea302c0087ea2289
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Device Details

"Baiyou Jingya" Influenza Virus A+B Rapid Test Reagent (Unsterilized)
TW: "็™พๅ„ช่€ๆž้›…" ๆตๆ„Ÿ็—…ๆฏ’A+Bๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

95ab940986193d61ea302c0087ea2289

DHA04600144908

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Aug 25, 2011

Aug 25, 2021

Sep 08, 2023

Cancellation Information

Logged out

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