“BIOTRONIK” Itrevia 5 Implantable Defibrillators with a conditional intended use in a MRI environment incl. Accessories - Taiwan Registration f0fca46fe81520e2c796dc327af20df7

Access comprehensive regulatory information for “BIOTRONIK” Itrevia 5 Implantable Defibrillators with a conditional intended use in a MRI environment incl. Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f0fca46fe81520e2c796dc327af20df7 and manufactured by BIOTRONIK SE & CO. KG. The authorized representative in Taiwan is BIOTRONIK TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.