Retinograph - ANVISA Registration 80170809007

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 80170809007 and manufactured by SHANGHAI MEDIWORKS PRECISION INSTRUMENT CO., LTD. (SANLU ROAD). 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 CENTERVUE S.P.A., 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.