Clinical data interface software for medical equipment - ANVISA Registration 80914690022

Access comprehensive regulatory information for Clinical data interface software for medical equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80914690022 and manufactured by manufacturer not specified. The registration is held by Nihon Kohden Brasil Importação, Exportação e Comércio de Equipamentos Médicos LTDA with validity until Nov 30, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including MICROMED BIOTECNOLOGIA S.A., NEOLIFE WIZARD, S.A., 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.