Taiwan FDA registration c7de9b4bf85928ab9e74f859d195a06e
"Medtronic" Siddy percutaneous spinal fixation system
TW: “美敦力”思迪經皮脊椎固定系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Feb 06, 2009 – Feb 06, 2029ActiveRegistration details
- Analysis ID
- c7de9b4bf85928ab9e74f859d195a06e
- Customs Code
- DHA00601964202
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK MANUFACTURING
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3070 椎弓螺釘系統
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2009
- Expiry Date
- Feb 06, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Siddy percutaneous spinal fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c7de9b4bf85928ab9e74f859d195a06e and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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