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Medtronic "Botdo Eti Implantable Cardiac Rectifier Defibrillator - Taiwan Registration 854c80f065c42e9f9a310a7288a179e8

Access comprehensive regulatory information for Medtronic "Botdo Eti 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 854c80f065c42e9f9a310a7288a179e8 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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854c80f065c42e9f9a310a7288a179e8
Registration Details
Taiwan FDA Registration: 854c80f065c42e9f9a310a7288a179e8
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Device Details

Medtronic "Botdo Eti Implantable Cardiac Rectifier Defibrillator
TW: ็พŽๆ•ฆๅŠ›โ€ๅš็‰นๅคš่‰พ็ทนๆคๅ…ฅๅผๅฟƒ่‡Ÿๆ•ดๆตๅŽป้กซๅ™จ
Risk Class 3
Cancelled

Registration Details

854c80f065c42e9f9a310a7288a179e8

DHA00602233105

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

Jun 03, 2011

Jun 03, 2021

Sep 26, 2020

Cancellation Information

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