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"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.

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c95786a496227cbc8aa78180bde11bef
Registration Details
Taiwan FDA Registration: c95786a496227cbc8aa78180bde11bef
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Device Details

"Core generation" influenza virus reagent (unsterilized)
TW: "่Šฏไธ–ไปฃ"ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c95786a496227cbc8aa78180bde11bef

Company Information

Taiwan, Province of China

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‘

Domestic;; Contract manufacturing

Dates and Status

Oct 24, 2016

Oct 24, 2021

May 12, 2017

Cancellation Information

Logged out

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