Taiwan FDA registration 14a38717331d8242c7ac6244f87b39ae

"Medtronic" Brightstar MRI implantable cardiac resynchronization rhythmometer

TW: “美敦力” 博視達磁振造影植入式心臟再同步節律器

Taiwan·Risk Class 3·Medtronic Inc.; Medtronic Europe Sàrl·Registered Mar 15, 2018 – Mar 15, 2028Active

Registration details

Analysis ID: 14a38717331d8242c7ac6244f87b39ae
Customs Code: DHA05603076106

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: Mar 15, 2018
Expiry Date: Mar 15, 2028

About this record

Access comprehensive regulatory information for "Medtronic" Brightstar MRI implantable cardiac resynchronization rhythmometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 14a38717331d8242c7ac6244f87b39ae and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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