Taiwan FDA registration aa7f0f793851ae04776849930d525584
BD TB Identification Test (Unsterilized)
TW: BD 結核菌群鑑定測試 (未滅菌)
Taiwan·Risk Class 1·BECTON DICKINSON AND COMPANY·Registered Sep 20, 2022 – Sep 20, 2027ActiveRegistration details
- Analysis ID
- aa7f0f793851ae04776849930d525584
- Customs Code
- DHA09402290107
Company information
- Manufacturer
- BECTON DICKINSON AND COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, Mycobacterium tuberculosis immunofluorescent reagent (C.3370) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3370 結核桿菌免疫螢光試劑
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Sep 20, 2022
- Expiry Date
- Sep 20, 2027
About this record
Access comprehensive regulatory information for BD TB Identification Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa7f0f793851ae04776849930d525584 and manufactured by BECTON DICKINSON AND COMPANY. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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