Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

Sensors - ANVISA Registration 81944289005

Access comprehensive regulatory information for Sensors in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81944289005 and manufactured by MASIMO CORPORATION. The registration is held by MASIMO IMPORTAÇÃO E DISTRIBUIÇÃO 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 QINHUANGDAO KAPUNUOMAITE MEDICAL EQUIPMENT S AND T CO. LTD., S.L.P. LTD. SCIENTIFIC LABORATORY PRODUCTS, 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 Competitors
5 Recent Registrations
81944289005
Registration Details
ANVISA Registration Number: 81944289005
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

RD SedLine para EEG
Risk Class II

Registration Details

81944289005

25351377536202447

08172593000185

Company Information

MASIMO CORPORATION
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 09, 2024

VIGENTE

09/18/2025 19:00:01