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"Medtronic" Maxmond implantable cardiac defibrillator - Taiwan Registration cbf9fe556164e3e46774dd3f0fed0fe2

Access comprehensive regulatory information for "Medtronic" Maxmond 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 cbf9fe556164e3e46774dd3f0fed0fe2 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC EUROPE SARL, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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Registration Details
Taiwan FDA Registration: cbf9fe556164e3e46774dd3f0fed0fe2
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Device Details

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

Registration Details

cbf9fe556164e3e46774dd3f0fed0fe2

DHA00601980909

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

Apr 28, 2009

Apr 28, 2019

Jun 16, 2022

Cancellation Information

Logged out

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