Taiwan FDA registration d5e3e32e82a4f7967575ef8ed1d1c561
“Medtronic” ELEVATE Spinal System
TW: “美敦力”艾樂斐特脊椎系統
Taiwan·Risk Class 2·MD·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered May 30, 2018 – May 30, 2028ActiveRegistration details
- Analysis ID
- d5e3e32e82a4f7967575ef8ed1d1c561
- License Form
- Ministry of Health Medical Device Import No. 030978
- Customs Code
- DHA05603097805
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
- May 30, 2018
- Expiry Date
- May 30, 2028
About this record
Access comprehensive regulatory information for “Medtronic” ELEVATE 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 d5e3e32e82a4f7967575ef8ed1d1c561 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