Ear impression material - ANVISA Registration 80179150081
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 80179150081 and manufactured by DREVE-OTOPLASTIK GMBH. The registration is held by STARKEY DO BRASIL 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
80179150081
25351720019201935
04216059000172
Company Information
Dates and Status
Dec 26, 2019
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
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 PRร-MOLDAGEM AURICULAR
DREVE-OTOPLASTIK GMBH
10356330031
Dec 26, 2011

