Taiwan FDA registration e81283c368a4300c622be08c5c8912cd
"Medtronic" median bone plate fixation system
TW: “美敦力”正中置物骨板固定系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Mar 24, 2009 – Mar 24, 2029ActiveRegistration details
- Analysis ID
- e81283c368a4300c622be08c5c8912cd
- Customs Code
- DHA00601997105
Company information
- Manufacturer
- MEDTRONIC SOFAMOR DANEK MANUFACTURING
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- The Medtronic median placement laminoplasty system is used in laminoplasty of the lower cervical and upper thoracic spine (C3 to T3) to support bone grafts used to perform laminoplasty to prevent the graft material from being squeezed out or invaded to spinal nerves.
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2009
- Expiry Date
- Mar 24, 2029
About this record
Access comprehensive regulatory information for "Medtronic" median bone plate fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e81283c368a4300c622be08c5c8912cd and manufactured by MEDTRONIC SOFAMOR DANEK MANUFACTURING. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices