Taiwan FDA registration d9683a08731b38ed1897f6e9b22ba35f
"Medtronic" spinal fixation system
TW: “美敦力”脊椎固定系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Jan 10, 2008 – Jan 10, 2023ExpiredRegistration details
- Analysis ID
- d9683a08731b38ed1897f6e9b22ba35f
- Customs Code
- DHA00601853901
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.3050 椎弓板間之脊椎矯正固定物
- Import Information
- import
Dates and status
- Registration Date
- Jan 10, 2008
- Expiry Date
- Jan 10, 2023
About this record
Access comprehensive regulatory information for "Medtronic" 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 d9683a08731b38ed1897f6e9b22ba35f and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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