"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..
This page provides complete technical specifications, regulatory compliance details. 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.
Device Details
Registration Details
974d4d2a987d6af19b5697809a11aecb
DHA00602311800
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

