Retinometer - ANVISA Registration 10243869014

Access comprehensive regulatory information for Retinometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10243869014 and manufactured by HEINE OPTOTECHNIK GMBH & CO. KG. The registration is held by EFE IMPORTACAO & DISTRIBUICAO LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.