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"Medtronic" Avitha MRI implantable cardiac rhythmometer - Taiwan Registration 974d4d2a987d6af19b5697809a11aecb

Access comprehensive regulatory information for "Medtronic" Avitha MRI implantable cardiac rhythmometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 974d4d2a987d6af19b5697809a11aecb and manufactured by Medtronic Inc.; Medtronic Europe Sร rl. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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974d4d2a987d6af19b5697809a11aecb
Registration Details
Taiwan FDA Registration: 974d4d2a987d6af19b5697809a11aecb
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Device Details

"Medtronic" Avitha MRI implantable cardiac rhythmometer
TW: โ€œ็พŽๆ•ฆๅŠ›โ€่‰พ็ถญ่ŽŽ็ฃๆŒฏ้€ ๅฝฑๆคๅ…ฅๅผๅฟƒ่‡Ÿ็ฏ€ๅพ‹ๅ™จ
Risk Class 3

Registration Details

974d4d2a987d6af19b5697809a11aecb

DHA00602311800

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

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Nov 25, 2011

Nov 25, 2026