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“BIOTRONIK” Protego ProMRI S Implantable Defibrillator Leads incl. Accessories with a Conditional Intended use in a MRI environment. - Taiwan Registration 50286ecb36a9a6de91890b19e461b070

Access comprehensive regulatory information for “BIOTRONIK” Protego ProMRI S 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 50286ecb36a9a6de91890b19e461b070 and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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50286ecb36a9a6de91890b19e461b070
Registration Details
Taiwan FDA Registration: 50286ecb36a9a6de91890b19e461b070
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Device Details

“BIOTRONIK” Protego ProMRI S 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三極主動導線(包括附件)
Risk Class 3
MD

Registration Details

50286ecb36a9a6de91890b19e461b070

Ministry of Health Medical Device Import No. 026938

DHA05602693804

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

Jan 14, 2015

Jan 14, 2025