Taiwan FDA registration 22ab6cf50558907cc1ea57565d0e8d65

"Medtronic" recommends a neurostimulator (patient) program controller

TW: “美敦力” 薦神經刺激器(病患)程控儀

Taiwan·Risk Class 3·MEDTRONIC NEUROMODULATION;; Medtronic Inc.·Registered Apr 25, 2013 – Apr 25, 2023Expired

Registration details

Analysis ID: 22ab6cf50558907cc1ea57565d0e8d65
Customs Code: DHA00602466505

Company information

Manufacturer: MEDTRONIC NEUROMODULATION;; Medtronic Inc.
Manufacturer Country: United States
Authorized Representative: MEDTRONIC (TAIWAN) LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5270 植入式電子排尿自制裝置
Import Information: import

Dates and status

Registration Date: Apr 25, 2013
Expiry Date: Apr 25, 2023

About this record

Access comprehensive regulatory information for "Medtronic" recommends a neurostimulator (patient) program controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 22ab6cf50558907cc1ea57565d0e8d65 and manufactured by MEDTRONIC NEUROMODULATION;; Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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