Taiwan FDA registration ed7784c0bd3f1e18ff90752155659bae
“B. Braun” Aesculap CeSPACE XP Anterior Cervical Interbody Fusion System
TW: “柏朗”雅氏頸椎前路椎間融合系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Aug 16, 2017 – Aug 16, 2027ActiveRegistration details
- Analysis ID
- ed7784c0bd3f1e18ff90752155659bae
- License Form
- Ministry of Health Medical Device Import No. 030113
- Customs Code
- DHA05603011300
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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 16, 2017
- Expiry Date
- Aug 16, 2027
About this record
Access comprehensive regulatory information for “B. Braun” Aesculap CeSPACE XP Anterior Cervical 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 ed7784c0bd3f1e18ff90752155659bae and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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