Taiwan FDA registration a53ed01ad08b65cc43db51cbc2c54567
"Bo Yilai" stereotactic treatment planning system
TW: “博醫來”立體定位治療計畫系統
Taiwan·Risk Class 2·BRAINLAB AG·Registered Mar 15, 2007 – Mar 15, 2017CancelledRegistration details
- Analysis ID
- a53ed01ad08b65cc43db51cbc2c54567
- Customs Code
- DHA00601793902
Company information
- Manufacturer
- BRAINLAB AG
- Manufacturer Country
- Germany
- Authorized Representative
- BARRY TEC ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.5050 Medical Charged Particle Radiotherapy System
- Import Information
- import
Dates and status
- Registration Date
- Mar 15, 2007
- Expiry Date
- Mar 15, 2017
- 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 "Bo Yilai" stereotactic treatment planning system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a53ed01ad08b65cc43db51cbc2c54567 and manufactured by BRAINLAB AG. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..
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