"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..
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
58803c16cde9dc9f42feb000e76bdc26
DHA05603016605
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

