Taiwan FDA registration 54c7cb62578c2ad2970ae82764c3708d

"Medtronic" Creedy Spine System

TW: “美敦力”克萊迪脊椎系統

Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Nov 04, 2013 – Nov 04, 2028Active

Registration details

Analysis ID: 54c7cb62578c2ad2970ae82764c3708d
Customs Code: DHA05602551803

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: Nov 04, 2013
Expiry Date: Nov 04, 2028

About this record

Access comprehensive regulatory information for "Medtronic" Creedy Spine System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54c7cb62578c2ad2970ae82764c3708d 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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