Taiwan FDA registration ea0eff80a9c5514530f916b6266b7a53
“Bio-Rad” Disks for Antibiotic Susceptibility Testing_Aztreonam
TW: “伯瑞” 抗生素感受性試驗紙錠-氮烯內醯胺
Taiwan·Risk Class 2·MD·BIO-RAD·Registered Jul 23, 2015 – Jul 23, 2025ExpiredRegistration details
- Analysis ID
- ea0eff80a9c5514530f916b6266b7a53
- License Form
- Ministry of Health Medical Device Import No. 027526
- Customs Code
- DHA05602752602
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 systems are used to semi-quantitatively assess the in vitro drug susceptibility of fast-growing bacteria and several difficult-to-control strains to nitrogenenolam antimicrobials by agar diffusion.
- 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
- Jul 23, 2015
- Expiry Date
- Jul 23, 2025
About this record
Access comprehensive regulatory information for “Bio-Rad” Disks for Antibiotic Susceptibility Testing_Aztreonam in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea0eff80a9c5514530f916b6266b7a53 and manufactured by BIO-RAD. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices