Retinograph - ANVISA Registration 80192010071

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 80192010071 and manufactured by CENTERVUE S.P.A.. The registration is held by ADAPT PRODUTOS OFTALMOLÓGICOS 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 SHANGHAI MEDIWORKS PRECISION INSTRUMENT CO., LTD. (SANLU ROAD), NIDEK CO., LTD (MAEHAMA), 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.