Respiratory Flow Sensor - ANVISA Registration 80181930056

Access comprehensive regulatory information for Respiratory Flow Sensor in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80181930056 and manufactured by DYMEDIX DIAGNOSTICS, INC. The registration is held by Ger-Ar Comércio de Produtos Médicos 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 EMSA EQUIPAMENTOS MÉDICOS LTDA, NEW COMPANY SERVIÇOS HOSPITALARES LTDA-ME, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
80181930056
Registration Details
ANVISA Registration Number: 80181930056
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

SENSOR DE FLUXO DE AR TRIPLEPLAY DYMEDIX - REUTILIZÁVEL
Risk Class II

Registration Details

80181930056

25351419100201780

04696139000172

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Nov 20, 2017

VIGENTE

09/18/2025 19:00:01