Device For Sleep Apnea Syndrome Test - ANVISA Registration 80475810004

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 80475810004 and manufactured by SERDIA ELETRONICA INDUSTRIAL S.A.. The registration is held by SERDIA ELETRONICA INDUSTRIAL S.A. 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 Icelera indústria e comércio de equipamentos médicos ltda me, M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP, 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.