"Medtronic" Botdo Eti implantable cardiac rectifier defibrillator - Taiwan Registration 3141696a374b29ad908cc74ec8df1e83
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 2 medical device is registered under number 3141696a374b29ad908cc74ec8df1e83 and manufactured by MEDTRONIC EUROPE SARL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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Device Details
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
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". input
Dates and Status
Apr 29, 2011
Apr 29, 2021
Sep 26, 2020
Cancellation Information
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