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Patient Monitoring System - ANVISA Registration 81721489004

Access comprehensive regulatory information for Patient Monitoring System in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81721489004 and manufactured by MGC DIAGNOSTICS CORPORATION. The registration is held by JRMEDIC -COMERCIO E ASSISTÊNCIA TÉCNICA 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 MGC DIAGNOSTICS CORPORATION, HILL-ROM CLINICAL WORKFLOW SOLUTIONS, 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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81721489004
Registration Details
ANVISA Registration Number: 81721489004
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Device Details

Resmon PRO V3 - Dispositivo de Monitoração da Função Respiratória
Risk Class II

Registration Details

81721489004

25351963720202081

03329477000103

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 01, 2020

VIGENTE

09/18/2025 19:00:01