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“BIOTRONIK” Protego ProMRI SD Implantable Defibrillator Leads Incl. Accessories with a conditional intended use in a MRI environment - Taiwan Registration 7b2abb157257b7415b591ec9ae7bcea4

Access comprehensive regulatory information for “BIOTRONIK” Protego ProMRI SD Implantable Defibrillator Leads Incl. Accessories 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 7b2abb157257b7415b591ec9ae7bcea4 and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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7b2abb157257b7415b591ec9ae7bcea4
Registration Details
Taiwan FDA Registration: 7b2abb157257b7415b591ec9ae7bcea4
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Device Details

“BIOTRONIK” Protego ProMRI SD Implantable Defibrillator Leads Incl. Accessories with a conditional intended use in a MRI environment
TW: “百多力”保心護心內除顫器磁振造影植入式四極主動導線(包括附件)
Risk Class 3
MD

Registration Details

7b2abb157257b7415b591ec9ae7bcea4

Ministry of Health Medical Device Import No. 026377

DHA05602637703

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E3680 Permanent or temporary heart rhythm regulator electrode for cardiovascular use

Imported from abroad

Dates and Status

Jun 27, 2014

Jun 27, 2024