Clinical data interface software for medical equipment - ANVISA Registration 10216710397

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 10216710397 and manufactured by PHILIPS MEDIZIN SYSTEME BOBLINGEN GMBH. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Apr 12, 2031.

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