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“Biotronik” Lumax Implantable Defibrillator Systems with a conditional intended use in a MRI environment - Taiwan Registration 5eee462b697c96d2f98f341dc19d8b81

Access comprehensive regulatory information for “Biotronik” Lumax Implantable Defibrillator Systems 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 5eee462b697c96d2f98f341dc19d8b81 and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

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5eee462b697c96d2f98f341dc19d8b81
Registration Details
Taiwan FDA Registration: 5eee462b697c96d2f98f341dc19d8b81
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Device Details

“Biotronik” Lumax Implantable Defibrillator Systems with a conditional intended use in a MRI environment
TW: “百多力” 路麥斯核磁共振植入式心臟去顫器
Risk Class 3
MD
Cancelled

Registration Details

5eee462b697c96d2f98f341dc19d8b81

Ministry of Health Medical Device Import No. 025456

DHA05602545607

Company Information

Germany

Product Details

E Cardiovascular devices

E3610 Pulse generator for implantable heart rhythm apparatus

Imported from abroad

Dates and Status

Nov 12, 2013

Nov 12, 2018

Jun 16, 2022

Cancellation Information

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