Taiwan FDA registration a27e6f0e176946b26af88e1d5a7220b3
"Braun" temporary vena cava filter
TW: “柏朗”暫時性腔靜脈過濾器
Taiwan·Risk Class 2·B.BRAUN MEDICAL·Registered Feb 13, 2008 – Feb 13, 2018CancelledRegistration details
- Analysis ID
- a27e6f0e176946b26af88e1d5a7220b3
- Customs Code
- DHA00601859501
Company information
- Manufacturer
- B.BRAUN MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3375 Cardiovascular vascular spillers
- Import Information
- import
Dates and status
- Registration Date
- Feb 13, 2008
- Expiry Date
- Feb 13, 2018
- Cancellation Date
- Nov 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Braun" temporary vena cava filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a27e6f0e176946b26af88e1d5a7220b3 and manufactured by B.BRAUN MEDICAL. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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