Taiwan FDA registration e4c8553d01239617f2ec8d07163c858f
"Medtronic" Keneng titanium-coated intervertebral fusion system
TW: “美敦力”科能鈦塗層椎間融合系統
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Jan 29, 2019 – Jan 29, 2029ActiveRegistration details
- Analysis ID
- e4c8553d01239617f2ec8d07163c858f
- Customs Code
- DHA05603223100
Company information
- Manufacturer Country
- United States;;Germany
- 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 Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- import
Dates and status
- Registration Date
- Jan 29, 2019
- Expiry Date
- Jan 29, 2029
About this record
Access comprehensive regulatory information for "Medtronic" Keneng titanium-coated intervertebral 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 e4c8553d01239617f2ec8d07163c858f and manufactured by MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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