Pure Global

“BIOTRONIK” Intica Implantable Defibrillator with a conditional intended use in a MRI environment - Taiwan Registration 10c66eb514a96f27518c1b04390ae5ed

Access comprehensive regulatory information for “BIOTRONIK” Intica Implantable Defibrillator 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 10c66eb514a96f27518c1b04390ae5ed 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
10c66eb514a96f27518c1b04390ae5ed
Registration Details
Taiwan FDA Registration: 10c66eb514a96f27518c1b04390ae5ed
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

10c66eb514a96f27518c1b04390ae5ed

Ministry of Health Medical Device Import No. 030619

DHA05603061903

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

Dec 15, 2017

Dec 15, 2022