Taiwan FDA registration 073e9573a5f8813a26630869ba53cb8d
“Medtronic” RIALTO SI Fusion System
TW: “美敦力”里亞托薦髂關節融合系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Aug 30, 2018 – Aug 30, 2028ActiveRegistration details
- Analysis ID
- 073e9573a5f8813a26630869ba53cb8d
- License Form
- Ministry of Health Medical Device Import No. 031577
- Customs Code
- DHA05603157705
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 Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 30, 2018
- Expiry Date
- Aug 30, 2028
About this record
Access comprehensive regulatory information for “Medtronic” RIALTO SI 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 073e9573a5f8813a26630869ba53cb8d and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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