Humidifier - ANVISA Registration 10432309021

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 10432309021 and manufactured by UNITEC INDUSTRIA E COMERCIO DE APARELHOS HOSPITALARES LTDA. The registration is held by UNITEC INDUSTRIA E COMERCIO DE APARELHOS HOSPITALARES LTDA 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 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.