Taiwan FDA registration e72087eb69e6629dab29f97478836f63
“B. Braun” Aesculap PROSPACE XP Posterior Interbody Fusion System
TW: “柏朗”雅氏後路椎間盤融合系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered May 12, 2019 – May 12, 2024ExpiredRegistration details
- Analysis ID
- e72087eb69e6629dab29f97478836f63
- License Form
- Ministry of Health Medical Device Import No. 032544
- Customs Code
- DHA05603254408
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
- May 12, 2019
- Expiry Date
- May 12, 2024
About this record
Access comprehensive regulatory information for “B. Braun” Aesculap PROSPACE XP Posterior 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 e72087eb69e6629dab29f97478836f63 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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