Pupillometer - ANVISA Registration 80625080037

Access comprehensive regulatory information for Pupillometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80625080037 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 companies making the same product including TAIZHOU WENBANG TECHNOLOGY DEVELOPMENT CO, .LTD., KFF S.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.