Taiwan FDA registration 1dc7359e5f22f701ac1964f48f9d9303
"Fuji" Serbronchial atresia catheter
TW: “富士”塞爾布朗支氣管閉鎖導管
Taiwan·Risk Class 2·Fuji Systems Corporation, Shirakawa Plant·Registered Jan 09, 2013 – Jan 09, 2018CancelledRegistration details
- Analysis ID
- 1dc7359e5f22f701ac1964f48f9d9303
- Customs Code
- DHA00602439005
Company information
- Manufacturer
- Fuji Systems Corporation, Shirakawa Plant
- Manufacturer Country
- Japan
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5740 Gas pipe/bronchi divergence gas line
- Import Information
- import
Dates and status
- Registration Date
- Jan 09, 2013
- Expiry Date
- Jan 09, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fuji" Serbronchial atresia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1dc7359e5f22f701ac1964f48f9d9303 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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