Retinograph - ANVISA Registration 80625080021

Access comprehensive regulatory information for Retinograph in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80625080021 and manufactured by NIDEK CO., LTD (MAEHAMA). The registration is held by NIDEK EYECARE DO BRASIL COMERCIO DE INSTRUMENTOS OPTICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SHANGHAI MEDIWORKS PRECISION INSTRUMENT CO., LTD. (SANLU ROAD), CENTERVUE S.P.A., 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.