Taiwan FDA registration 92902ee5de0b3b8e5109f474e4c115c7
“Medtronic” Vertex Reconstruction System
TW: “美敦力”脊椎重建系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Jul 14, 2014 – Jul 14, 2019CancelledRegistration details
- Analysis ID
- 92902ee5de0b3b8e5109f474e4c115c7
- License Form
- Ministry of Health Medical Device Import No. 026339
- Customs Code
- DHA05602633908
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK MANUFACTURING
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 14, 2014
- Expiry Date
- Jul 14, 2019
- Cancellation Date
- Jul 10, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Medtronic” Vertex Reconstruction System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92902ee5de0b3b8e5109f474e4c115c7 and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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