Retinoscope - ANVISA Registration 10332030108

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 10332030108 and manufactured by CARL ZEISS MEDITEC INC. (DUBLIN-US). The registration is held by CARL ZEISS DO BRASIL 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 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.