Device For Sleep Apnea Syndrome Test - ANVISA Registration 80193710008

Access comprehensive regulatory information for Device For Sleep Apnea Syndrome Test in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80193710008 and manufactured by M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP. The registration is held by M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including SERDIA ELETRONICA INDUSTRIAL S.A., Icelera indústria e comércio de equipamentos médicos ltda me, and 2 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.