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 similar products found using AI-powered semantic search, 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.

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80113019018
Registration Details
ANVISA Registration Number: 80113019018
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Câmara de umidificação Vadi de uso único
Risk Class II

Registration Details

80113019018

25351339675202120

02126465000119

Company Information

Taiwan
PT: TAIWAN

Dates and Status

Apr 29, 2021

VIGENTE

09/18/2025 19:00:01