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"BIOTRONIK" Enticos 4 Implantable Cardiac Pacemakers with a conditional intended use in a MRI environment。 - Taiwan Registration d1fe0ec80229e7accc57944e21e54e4d

Access comprehensive regulatory information for "BIOTRONIK" Enticos 4 Implantable Cardiac Pacemakers 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 d1fe0ec80229e7accc57944e21e54e4d and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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d1fe0ec80229e7accc57944e21e54e4d
Registration Details
Taiwan FDA Registration: d1fe0ec80229e7accc57944e21e54e4d
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Device Details

"BIOTRONIK" Enticos 4 Implantable Cardiac Pacemakers with a conditional intended use in a MRI environment。
TW: “百多力”艾緹可磁振造影植入式心律調節器。
Risk Class 3
MD

Registration Details

d1fe0ec80229e7accc57944e21e54e4d

Ministry of Health Medical Device Import No. 030000

DHA05603000000

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 07, 2017

Aug 07, 2027