"Core generation" influenza virus reagent (unsterilized) - Taiwan Registration c95786a496227cbc8aa78180bde11bef
Access comprehensive regulatory information for "Core generation" influenza virus 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 c95786a496227cbc8aa78180bde11bef and manufactured by Xintang Enterprise Co., Ltd. Taichung Factory. The authorized representative in Taiwan is GENPRONEX INC..
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
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 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
Domestic;; Contract manufacturing
Dates and Status
Oct 24, 2016
Oct 24, 2021
May 12, 2017
Cancellation Information
Logged out
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