Ear impression material - ANVISA Registration 80943570003
Access comprehensive regulatory information for Ear impression material in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80943570003 and manufactured by BECON MEDICAL, LTD. The registration is held by MDS HOSPITALAR 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 DREVE-OTOPLASTIK GMBH, BECON MEDICAL, LTD, 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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Registration Details
80943570003
25351601404202107
16541292000100
Company Information
Dates and Status
Jun 17, 2021
VIGENTE
09/18/2025 19:00:01
Instrument Kit
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Instrument Kit
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DEPUY (IRELAND)
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Jun 08, 2015
Instrument Kit
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DEPUY INTERNATIONAL LTD
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Jun 08, 2015
Material de moldagem auricular
Material de Moldagem Auricular
DREVE-OTOPLASTIK GMBH
80179150081
Dec 26, 2019
Material de moldagem auricular
Material de Moldagem Auricular
DREVE-OTOPLASTIK GMBH
80179150082
Dec 26, 2019
Material de moldagem auricular
EarWell
BECON MEDICAL, LTD
80748430006
Sep 28, 2015
Material de moldagem auricular
Otoform AK
DREVE-OTOPLASTIK GMBH
80872830007
May 25, 2015
Material de moldagem auricular
MASSA DE PRÉ-MOLDAGEM AURICULAR
DREVE-OTOPLASTIK GMBH
10356330031
Dec 26, 2011