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"Medtronic" Ampere MRI implantable cardiac rectifier defibrillator - Taiwan Registration a67aff833ffbb0aed71114e11f031bd5

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 Sร rl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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a67aff833ffbb0aed71114e11f031bd5
Registration Details
Taiwan FDA Registration: a67aff833ffbb0aed71114e11f031bd5
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Device Details

"Medtronic" Ampere MRI implantable cardiac rectifier defibrillator
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๅฎ‰ๅŸนไบž็ฃๆŒฏ้€ ๅฝฑๆคๅ…ฅๅผๅฟƒ่‡Ÿๆ•ดๆตๅŽป้กซๅ™จ
Risk Class 3

Registration Details

a67aff833ffbb0aed71114e11f031bd5

DHA05602975409

Company Information

United States;;Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.3610 Pulsator of implantable cardiac rhythm apparatus

import

Dates and Status

May 12, 2017

May 12, 2027