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“Bio-Rad” Disks for Antibiotic Susceptibility Testing_Fusidic Acid - Taiwan Registration d212db0c8d394464ad33a1b767192e17

Access comprehensive regulatory information for “Bio-Rad” Disks for Antibiotic Susceptibility Testing_Fusidic Acid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d212db0c8d394464ad33a1b767192e17 and manufactured by BIO-RAD. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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d212db0c8d394464ad33a1b767192e17
Registration Details
Taiwan FDA Registration: d212db0c8d394464ad33a1b767192e17
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Device Details

“Bio-Rad” Disks for Antibiotic Susceptibility Testing_Fusidic Acid
TW: 伯瑞抗生素感受性試驗紙錠-褐黴素
Risk Class 2
MD

Registration Details

d212db0c8d394464ad33a1b767192e17

Ministry of Health Medical Device Import No. 027545

DHA05602754503

Company Information

France

Product Details

These ingot are used to semi-quantitatively assess the in vitro drug susceptibility performance of fast-growing bacteria and several uncontrollable strains against the antimicrobial Fusidic Acid by the agar diffusion method.

C Immunology and microbiology devices

C1620 Antimicrobial susceptibility test tray

Imported from abroad

Dates and Status

Aug 11, 2015

Aug 11, 2025