Genisis influenza virus test reagent type A+B - Taiwan Registration eb8d6dadac71bcbcfdbff01f98baac66
Access comprehensive regulatory information for Genisis influenza virus test reagent type A+B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb8d6dadac71bcbcfdbff01f98baac66 and manufactured by HANGZHOU GENESIS BIODETECTION & BIOCONTROL CO., LTD. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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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
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Chinese goods;; input
Dates and Status
Aug 02, 2010
Aug 02, 2015
Aug 14, 2018
Cancellation Information
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