Taiwan FDA registration 7c41aceebd6d9682f616db292b6f7684

"Medtronic" Keneng spine system device

TW: “美敦力”科能脊椎系統裝置

Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Jan 10, 2013 – Jan 10, 2028Active

Registration details

Analysis ID: 7c41aceebd6d9682f616db292b6f7684
Customs Code: DHA00602443208

Company information

Manufacturer: MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.
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 10, 2013
Expiry Date: Jan 10, 2028

About this record

Access comprehensive regulatory information for "Medtronic" Keneng spine system device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7c41aceebd6d9682f616db292b6f7684 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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