Taiwan FDA registration be4fd4426959e1c0caa541e940a9af9b
"Medtronic" can open the interbody fusion system
TW: “美敦力”開立扶可撐開椎間融合系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK USA, INC.;; MEDTRONIC SOFAMOR DANEK MANUFACTURING·Registered Aug 21, 2024 – Aug 21, 2029ActiveRegistration details
- Analysis ID
- be4fd4426959e1c0caa541e940a9af9b
- Customs Code
- DHA05603737306
Company information
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2024
- Expiry Date
- Aug 21, 2029
About this record
Access comprehensive regulatory information for "Medtronic" can open the interbody fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be4fd4426959e1c0caa541e940a9af9b and manufactured by MEDTRONIC SOFAMOR DANEK USA, INC.;; 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