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 similar products found using AI-powered semantic search, 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
81944280013
25351414025202413
08172593000185
Company Information
Dates and Status
Dec 02, 2024
02/12/2034
09/18/2025 19:00:01
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10405410044
Oct 25, 2021
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Not specified
10405410044
Oct 25, 2021
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81721489004
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