Software - ANVISA Registration 80022060047

Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80022060047 and manufactured by FUJIFILM CORPORATION, MEDICAL SYSTEMS RESEARCH & DEVELOPMENT CENTER. The registration is held by FUJIFILM DO BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., CARDIO SISTEMAS COMERCIAL E INDUSTRIAL LTDA, and 5 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.