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"Medtronic" Vihia MRI implantable cardiac rectifier defibrillator - Taiwan Registration 58803c16cde9dc9f42feb000e76bdc26

Access comprehensive regulatory information for "Medtronic" Vihia 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 58803c16cde9dc9f42feb000e76bdc26 and manufactured by Medtronic Inc.; Medtronic Europe Sร rl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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58803c16cde9dc9f42feb000e76bdc26
Registration Details
Taiwan FDA Registration: 58803c16cde9dc9f42feb000e76bdc26
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Device Details

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

Registration Details

58803c16cde9dc9f42feb000e76bdc26

DHA05603016605

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

Aug 30, 2017

Aug 30, 2027