Taiwan FDA registration a76045d7504f8b57ddc4c674c9d8740b

"Medtronic" Cooper MRI implantable cardiac rectifier defibrillator

TW: “美敦力”庫柏磁振造影植入式心臟整流去顫器

Taiwan·Risk Class 3·Medtronic Inc.;; MEDTRONIC EUROPE SARL·Registered Feb 22, 2021 – Feb 22, 2026Expired

Registration details

Analysis ID: a76045d7504f8b57ddc4c674c9d8740b
Customs Code: DHA05603433601

Company information

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

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.3610 Pulsator of implantable cardiac rhythm apparatus
Import Information: import

Dates and status

Registration Date: Feb 22, 2021
Expiry Date: Feb 22, 2026

About this record

Access comprehensive regulatory information for "Medtronic" Cooper MRI implantable cardiac rectifier defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a76045d7504f8b57ddc4c674c9d8740b and manufactured by Medtronic Inc.;; MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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