Taiwan FDA registration 2fef5d4ba07cb1fce55f59eca590aaf0
VITEK 2 System Gram Negative AST for Flomoxef
TW: 微鐵克2革蘭氏陰性菌藥敏卡抗生素-氟氧頭孢
Taiwan·Risk Class 2·MD·BIOMERIEUX, INC.·Registered Jun 21, 2016 – Jun 21, 2026ExpiredRegistration details
- Analysis ID
- 2fef5d4ba07cb1fce55f59eca590aaf0
- License Form
- Ministry of Health Medical Device Import No. 028450
- Customs Code
- DHA05602845000
Company information
- Manufacturer
- BIOMERIEUX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- Combined with Microtek 2 automatic microbial analyzer, the susceptibility of clinically important gram-negative bacteria to Flomoxef antibiotics was determined.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C1645 Automatic Short Incubation Period Antibiotic Susceptibility Testing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 21, 2016
- Expiry Date
- Jun 21, 2026
About this record
Access comprehensive regulatory information for VITEK 2 System Gram Negative AST for Flomoxef in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fef5d4ba07cb1fce55f59eca590aaf0 and manufactured by BIOMERIEUX, INC.. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.
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