Taiwan FDA registration 58803c16cde9dc9f42feb000e76bdc26

"Medtronic" Vihia MRI implantable cardiac rectifier defibrillator

TW: “美敦力”維希亞磁振造影植入式心臟整流去顫器

Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Aug 30, 2017 – Aug 30, 2027Active

Registration details

Analysis ID: 58803c16cde9dc9f42feb000e76bdc26
Customs Code: DHA05603016605

Company information

Manufacturer: Medtronic Inc.; Medtronic Europe Sàrl
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: Aug 30, 2017
Expiry Date: Aug 30, 2027

About this record

Access comprehensive regulatory information for "Medtronic" Vihia 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 58803c16cde9dc9f42feb000e76bdc26 and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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