Software - ANVISA Registration 81285510003

Access comprehensive regulatory information for Software in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81285510003 and manufactured by GENOME DIAGNOSTICS B.V. (GENDX). The registration is held by PENSABIO INSTRUMENTOS DE BIOTECNOLOGIA LTDA with validity until Feb 10, 2035.

This page provides complete technical specifications for 2 related devices, 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.