Taiwan FDA registration f32e5183dc2ec4cc0293e9fb49f8b3fd
"Fusch" bronchial atresia catheter
TW: “富世”支氣管閉鎖導管
Taiwan·Risk Class 2·Fuji Systems Corporation, Shirakawa Plant·Registered Feb 21, 2013 – Feb 21, 2023ExpiredRegistration details
- Analysis ID
- f32e5183dc2ec4cc0293e9fb49f8b3fd
- Customs Code
- DHA00602447704
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
- Feb 21, 2013
- Expiry Date
- Feb 21, 2023
About this record
Access comprehensive regulatory information for "Fusch" bronchial 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 f32e5183dc2ec4cc0293e9fb49f8b3fd and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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