“BIOTRONIK” Rivacor Implantable Defibrillators with a conditional intended use in a MRI environment - Taiwan Registration 4c4392f690e67279cc6d4caf816d8afa
Access comprehensive regulatory information for “BIOTRONIK” Rivacor Implantable Defibrillators with a conditional intended use in a MRI environment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4c4392f690e67279cc6d4caf816d8afa and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.
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
4c4392f690e67279cc6d4caf816d8afa
Ministry of Health Medical Device Import No. 032797
DHA05603279701
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular devices
E3610 Pulse generator for implantable heart rhythm apparatus
Imported from abroad
Dates and Status
Aug 20, 2019
Aug 20, 2024

