Retinoscope - ANVISA Registration 80170800015

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 80170800015 and manufactured by TAKAGI SEIKO CO., LTD. The registration is held by OPTIVISION COMÉRCIO, IMPORTAÇÃO E EXPORTAÇÃO - LTDA - EPP 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., KEELER 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.