"Siloam" Influenza A&B Test (Non-sterile) - Taiwan Registration f17546d024bae39030cb6e5f152cc42a
Access comprehensive regulatory information for "Siloam" Influenza A&B 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 f17546d024bae39030cb6e5f152cc42a and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..
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Device Details
Registration Details
f17546d024bae39030cb6e5f152cc42a
Ministry of Health Medical Device Import No. 016985
DHA09401698501
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
Sep 09, 2016
Sep 09, 2021

