Taiwan FDA registration 55bf589c44d63cc9d85fb75dd4d07fb0
"Braun" Vivida infusion tube group
TW: "柏朗" 維視達輸注管組
Taiwan·Risk Class 2·B.BRAUN MELSUNGEN AG·Registered Aug 19, 2003 – Aug 19, 2018CancelledRegistration details
- Analysis ID
- 55bf589c44d63cc9d85fb75dd4d07fb0
- Customs Code
- DHA00601037002
Company information
- Manufacturer
- B.BRAUN MELSUNGEN AG
- Manufacturer Country
- Germany
- Authorized Representative
- NOVARTIS (TAIWAN) CO., LTD.
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Aug 19, 2003
- Expiry Date
- Aug 19, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Braun" Vivida infusion tube group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55bf589c44d63cc9d85fb75dd4d07fb0 and manufactured by B.BRAUN MELSUNGEN AG. The authorized representative in Taiwan is NOVARTIS (TAIWAN) CO., LTD..
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