Clinical data interface software for medical equipment - ANVISA Registration 82999420001

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 II medical device is registered under ANVISA number 82999420001 and manufactured by NEOLIFE WIZARD, S.A.. The registration is held by DIRECTHEALTH TECNOLOGIA EM SISTEMAS E SERVICOS 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 MICROMED BIOTECNOLOGIA S.A., SPINEGUARD, 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.