"bioMerieux" VITEK MS Mould Kit (Non-Sterile) - Taiwan Registration a1d2c91bba0e80b2b9a4d4b0b7508603
Access comprehensive regulatory information for "bioMerieux" VITEK MS Mould Kit (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 a1d2c91bba0e80b2b9a4d4b0b7508603 and manufactured by BIOMERIEUX SA. The authorized representative in Taiwan is Hong Kong Commercial Mรฉrieux S.p.A. Taiwan Branch.
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Device Details
Registration Details
a1d2c91bba0e80b2b9a4d4b0b7508603
Ministry of Health Medical Device Import No. 017592
DHA09401759200
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
C Immunology and microbiology devices
C2660 Microbial identification and assay equipment
Imported from abroad
Dates and Status
Mar 13, 2017
Mar 13, 2027