Taiwan FDA registration 11537340cb273a3dad15a9baf0d4c98b
"Biti" Mycobacterium tuberculosis test agent (unsterilized)
TW: “必帝”結核桿菌測試劑(未滅菌)
Taiwan·Risk Class 1·BECTON, DICKINSON AND COMPANY·Registered Sep 05, 2008 – Sep 05, 2018CancelledRegistration details
- Analysis ID
- 11537340cb273a3dad15a9baf0d4c98b
- Customs Code
- DHA04400704702
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 first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
- 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
- import
Dates and status
- Registration Date
- Sep 05, 2008
- Expiry Date
- Sep 05, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Biti" Mycobacterium tuberculosis test agent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 11537340cb273a3dad15a9baf0d4c98b 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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