Patient Monitoring System - ANVISA Registration 81944280013

Access comprehensive regulatory information for Patient Monitoring System in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81944280013 and manufactured by manufacturer not specified. The registration is held by MASIMO IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS LTDA with validity until Dec 02, 2034.

This page provides complete technical specifications for 2 related devices, 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.