"Response Biomedical" Flu A/B Rapid Test (Non-sterile) - Taiwan Registration 544c4ca8f1bee73db9a4280c004b7f5d
Access comprehensive regulatory information for "Response Biomedical" Flu A/B Rapid Test (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 544c4ca8f1bee73db9a4280c004b7f5d and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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Device Details
Registration Details
544c4ca8f1bee73db9a4280c004b7f5d
Ministry of Health Medical Device Import No. 016043
DHA09401604301
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
Imported from abroad
Dates and Status
Jan 05, 2016
Jan 05, 2021

