Taiwan FDA registration fa3930d84a2e67a227ccc94253d89cb9
“Medtronic” Prestige LP Cervical Disc System
TW: “美敦力”貝堤頸椎椎間盤系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Sep 16, 2013 – Sep 16, 2023ExpiredRegistration details
- Analysis ID
- fa3930d84a2e67a227ccc94253d89cb9
- License Form
- Ministry of Health Medical Device Import No. 025419
- Customs Code
- DHA05602541901
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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 16, 2013
- Expiry Date
- Sep 16, 2023
About this record
Access comprehensive regulatory information for “Medtronic” Prestige LP Cervical Disc System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa3930d84a2e67a227ccc94253d89cb9 and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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