Taiwan FDA registration 8874ae4d2b425f1b0a125ee242f48af1
“Medtronic” PIVOX Oblique Lateral Spinal System
TW: “美敦力”派維斯斜側位脊椎系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Jun 28, 2019 – Jun 28, 2024ExpiredRegistration details
- Analysis ID
- 8874ae4d2b425f1b0a125ee242f48af1
- License Form
- Ministry of Health Medical Device Import No. 032723
- Customs Code
- DHA05603272308
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
- Jun 28, 2019
- Expiry Date
- Jun 28, 2024
About this record
Access comprehensive regulatory information for “Medtronic” PIVOX Oblique Lateral Spinal System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8874ae4d2b425f1b0a125ee242f48af1 and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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