IF i-test Influenza A&B cassette (non-sterile) - Taiwan Registration dbe8266a692d63fdeaafef77d2e113b9
Access comprehensive regulatory information for IF i-test Influenza A&B cassette (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dbe8266a692d63fdeaafef77d2e113b9 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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Device Details
Registration Details
dbe8266a692d63fdeaafef77d2e113b9
Ministry of Health Medical Device Manufacturing No. 007116
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 devices
C3330 Influenza virus serum reagent
Produced in Taiwan, China
Dates and Status
Feb 12, 2018
Feb 12, 2023