Otoacoustic Emission Equipment - ANVISA Registration 10356020095

Access comprehensive regulatory information for Otoacoustic Emission Equipment in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10356020095 and manufactured by DIAGNOSTIC GROUP LLC - DBA MAICO DIAGNOSTICS. The registration is held by CENTRO AUDITIVO TELEX LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including DIAGNOSTIC GROUP LLC - DBA GRASON-STADLER, INTERACOUSTICS A/S, 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.