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Respiratory Flow Sensor - ANVISA Registration 80181930057

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 80181930057 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 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.

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80181930057
Registration Details
ANVISA Registration Number: 80181930057
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Device Details

SENSOR DE FLUXO DE AR TRIPLEPLAY DYMEDIX - DESCARTÁVEL.
Risk Class II

Registration Details

80181930057

25351419112201750

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