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“BIOTRONIK” Intica Neo Implantable Defibrillators with a conditional intended use in a MRI environment - Taiwan Registration 6ac91973d3b198d0d3e3d0a973b00866

Access comprehensive regulatory information for “BIOTRONIK” Intica Neo 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 6ac91973d3b198d0d3e3d0a973b00866 and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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6ac91973d3b198d0d3e3d0a973b00866
Registration Details
Taiwan FDA Registration: 6ac91973d3b198d0d3e3d0a973b00866
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Device Details

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

Registration Details

6ac91973d3b198d0d3e3d0a973b00866

Ministry of Health Medical Device Import No. 032798

DHA05603279800

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