Taiwan FDA registration 53d178e2874fb2727d3ac455ae8b9ba8
“Medtronic” ARTiC-L 3D Ti Spinal System with TiONIC Technology
TW: “美敦力”亞堤克3D脊椎系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Jul 10, 2019 – Jul 10, 2024ExpiredRegistration details
- Analysis ID
- 53d178e2874fb2727d3ac455ae8b9ba8
- License Form
- Ministry of Health Medical Device Import No. 032733
- Customs Code
- DHA05603273301
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC.
- 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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 10, 2019
- Expiry Date
- Jul 10, 2024
About this record
Access comprehensive regulatory information for “Medtronic” ARTiC-L 3D Ti Spinal System with TiONIC Technology in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 53d178e2874fb2727d3ac455ae8b9ba8 and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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