Humidifier - ANVISA Registration 80825800003

Access comprehensive regulatory information for Humidifier in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80825800003 and manufactured by SALTER LABS DE MEXICO S.A. DE C.V.. The registration is held by RESPIROX COMÉRCIO DE OXIGÊNIO LTDA - EPP with validity until currently active (VIGENTE).

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 5 companies making the same product including PULMODYNE, INC, FISHER & PAYKEL HEALTHCARE LIMITED, 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.