Taiwan FDA registration d65deb7ada0ad06eeccdbd4ae0307b5d

"Medtronic" Kerrison spinal system

TW: “美敦力”克里森脊椎系統

Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Dec 02, 2011 – Dec 02, 2026Active

Registration details

Analysis ID: d65deb7ada0ad06eeccdbd4ae0307b5d
Customs Code: DHA00602304509

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: Dec 02, 2011
Expiry Date: Dec 02, 2026

About this record

Access comprehensive regulatory information for "Medtronic" Kerrison 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 d65deb7ada0ad06eeccdbd4ae0307b5d 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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