Taiwan FDA registration 05bd4dc4d83a3a2cdf85889182a46606
“Aesculap” 3D Interbody Fusion System
TW: “雅氏” 3D椎體間融合系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Aug 08, 2022 – Aug 08, 2027ActiveRegistration details
- Analysis ID
- 05bd4dc4d83a3a2cdf85889182a46606
- License Form
- Ministry of Health Medical Device Import No. 035733
- Customs Code
- DHA05603573300
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 08, 2022
- Expiry Date
- Aug 08, 2027
About this record
Access comprehensive regulatory information for “Aesculap” 3D 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 05bd4dc4d83a3a2cdf85889182a46606 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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