Retinoscope - ANVISA Registration 80548419006

Access comprehensive regulatory information for Retinoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80548419006 and manufactured by Plusoptix Gmbh. The registration is held by PROJETOS OPTICOS COMERCIAL LTDA - ME 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.