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"Medtronic" Vidor implantable cardiac defibrillator - Taiwan Registration adbf88d55b8eefa12a74059448ca54d2

Access comprehensive regulatory information for "Medtronic" Vidor implantable cardiac defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number adbf88d55b8eefa12a74059448ca54d2 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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Registration Details
Taiwan FDA Registration: adbf88d55b8eefa12a74059448ca54d2
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Device Details

"Medtronic" Vidor implantable cardiac defibrillator
TW: โ€œ็พŽๆ•ฆๅŠ›โ€็ถญๅคšๆคๅ…ฅๅผๅฟƒ่‡ŸๅŽป้กซๅ™จ
Risk Class 3
Cancelled

Registration Details

adbf88d55b8eefa12a74059448ca54d2

DHA00601846804

Company Information

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

Nov 29, 2007

Nov 29, 2017

Dec 13, 2019

Cancellation Information

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