Humidifier - ANVISA Registration 80113019018

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 80113019018 and manufactured by VADI MEDICAL TECHNOLOGY CO., LTD. The registration is held by RESPIRATORY CARE HOSPITALAR 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.