Clinical data interface software for medical equipment - ANVISA Registration 10307270015

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 10307270015 and manufactured by MICROMED BIOTECNOLOGIA S.A.. The registration is held by MICROMED BIOTECNOLOGIA S.A. 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 NEOLIFE WIZARD, 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.