“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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Device Details
Registration Details
5eee462b697c96d2f98f341dc19d8b81
Ministry of Health Medical Device Import No. 025456
DHA05602545607
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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