Ear impression material - ANVISA Registration 80748430006
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 80748430006 and manufactured by BECON MEDICAL, LTD. The registration is held by DUNNIA ASSESSORIA EMPRESARIAL LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 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.
Device Details
Registration Details
80748430006
25351460308201540
05889049000160
Company Information
Dates and Status
Sep 28, 2015
VIGENTE
09/18/2025 19:00:01
Material de moldagem auricular
Kit EarWell
BECON MEDICAL, LTD
80943570003
Jun 17, 2021
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
Otoform AK
DREVE-OTOPLASTIK GMBH
80872830007
May 25, 2015
Material de moldagem auricular
MASSA DE PRร-MOLDAGEM AURICULAR
DREVE-OTOPLASTIK GMBH
10356330031
Dec 26, 2011

