Taiwan FDA registration d2ac3f4f3f02ee2f459db06523c134e6
“B. Braun” Aesculap TSPACE XP Interbody Fusion System
TW: “柏朗”雅氏椎間盤融合系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Apr 25, 2018 – Apr 25, 2028ActiveRegistration details
- Analysis ID
- d2ac3f4f3f02ee2f459db06523c134e6
- License Form
- Ministry of Health Medical Device Import No. 031055
- Customs Code
- DHA05603105501
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- 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)
- N Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 25, 2018
- Expiry Date
- Apr 25, 2028
About this record
Access comprehensive regulatory information for “B. Braun” Aesculap TSPACE XP Interbody Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2ac3f4f3f02ee2f459db06523c134e6 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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