EEG Monitor - ANVISA Registration 80145119019

Access comprehensive regulatory information for EEG Monitor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80145119019 and manufactured by FRESENIUS KABI AG. The registration is held by FRESENIUS KABI BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including DANMETER A/S, CADWELL INDUSTRIES, INC., and 2 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.