Clinical data interface software for medical equipment - ANVISA Registration 80134860290

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 80134860290 and manufactured by DIAGNOSTIC GRIFOLS, S.A.. The registration is held by GRIFOLS 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., 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.