Taiwan FDA registration a67aff833ffbb0aed71114e11f031bd5

"Medtronic" Ampere MRI implantable cardiac rectifier defibrillator

TW: “美敦力”安培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 May 12, 2017 – May 12, 2027Active

Registration details

Analysis ID: a67aff833ffbb0aed71114e11f031bd5
Customs Code: DHA05602975409

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: May 12, 2017
Expiry Date: May 12, 2027

About this record

Access comprehensive regulatory information for "Medtronic" Ampere 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 a67aff833ffbb0aed71114e11f031bd5 and manufactured by Medtronic Inc.; Medtronic Europe Sàrl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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