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Longteng influenza virus type A and B kit (unsterilized) - Taiwan Registration 87a7208d1323f7240dd8f944d0d4c829

Access comprehensive regulatory information for Longteng influenza virus type A and B kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87a7208d1323f7240dd8f944d0d4c829 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Longteng Biotechnology 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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87a7208d1323f7240dd8f944d0d4c829
Registration Details
Taiwan FDA Registration: 87a7208d1323f7240dd8f944d0d4c829
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Device Details

Longteng influenza virus type A and B kit (unsterilized)
TW: ้พ้จฐๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹ๅŠBๅž‹่ฉฆๅŠ‘็›’(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

87a7208d1323f7240dd8f944d0d4c829

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

Dates and Status

Aug 25, 2009

Aug 25, 2019

Jun 17, 2023

Cancellation Information

Logged out

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