Taiwan FDA registration d212db0c8d394464ad33a1b767192e17
“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
Taiwan·Risk Class 2·MD·BIO-RAD·Registered Aug 11, 2015 – Aug 11, 2025ExpiredRegistration details
- Analysis ID
- d212db0c8d394464ad33a1b767192e17
- License Form
- Ministry of Health Medical Device Import No. 027545
- Customs Code
- DHA05602754503
Company information
- Manufacturer
- BIO-RAD
- Manufacturer Country
- France
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1620 Antimicrobial susceptibility test tray
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 11, 2015
- Expiry Date
- Aug 11, 2025
About this record
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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