Device For Sleep Apnea Syndrome Test - ANVISA Registration 80884619004
Access comprehensive regulatory information for Device For Sleep Apnea Syndrome Test in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80884619004 and manufactured by Icelera indústria e comércio de equipamentos médicos ltda me. The registration is held by Icelera indústria e comércio de equipamentos médicos ltda me with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including SERDIA ELETRONICA INDUSTRIAL S.A., M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP, and 2 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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🇧🇷 Brazil Regulatory Expert
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Registration Details
80884619004
25351375576202454
07729919000160
Company Information
Dates and Status
Sep 16, 2024
VIGENTE
09/18/2025 19:00:01
Device For Sleep Apnea Syndrome Test
OXISTAR
SERDIA ELETRONICA INDUSTRIAL S.A.
80475810004
May 07, 2018
Device For Sleep Apnea Syndrome Test
MAXXISNORE - SENSOR DE RONCO PARA PSG
M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP
80193710008
Dec 07, 2010
Sleep Monitoring System
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80047309156
Oct 08, 2020
Sleep Monitoring System
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Sleep Monitoring System
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MEDITRON ELETROMEDICINA LTDA
10380630005
Apr 24, 2006
Dispositivo P/Teste da Sindrome Apneia do Sono
OXISTAR
SERDIA ELETRONICA INDUSTRIAL S.A.
80475810004
May 07, 2018
Dispositivo P/Teste da Sindrome Apneia do Sono
MAXXISNORE - SENSOR DE RONCO PARA PSG
M. F. EQUIPAMENTOS MÉDICOS LTDA - EPP
80193710008
Dec 07, 2010