IF i-test Influenza A&B (non-sterile) - Taiwan Registration 6212fce07fc2bb16499a6b9cc45f17e6
Access comprehensive regulatory information for IF i-test Influenza A&B (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 6212fce07fc2bb16499a6b9cc45f17e6 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
6212fce07fc2bb16499a6b9cc45f17e6
Ministry of Health Medical Device Manufacturing No. 006972
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
Oct 17, 2017
Oct 17, 2022