Retinoscope - ANVISA Registration 80891620081

Access comprehensive regulatory information for Retinoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80891620081 and manufactured by KEELER LTD.. The registration is held by Halma Saúde e Ótica do Brasil Importação Exportação e Distribuição Ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including WELCH ALLYN INC., CARL ZEISS MEDITEC INC. (DUBLIN-US), 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.