Pure Global

“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.

Free Database
Powered by Pure Global AI
89,000+ Devices
4c4392f690e67279cc6d4caf816d8afa
Registration Details
Taiwan FDA Registration: 4c4392f690e67279cc6d4caf816d8afa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“BIOTRONIK” Rivacor Implantable Defibrillators with a conditional intended use in a MRI environment
TW: “百多力”雷安可磁振造影植入式心臟去顫器
Risk Class 3
MD

Registration Details

4c4392f690e67279cc6d4caf816d8afa

Ministry of Health Medical Device Import No. 032797

DHA05603279701

Company Information

Germany

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