Retinoscope - ANVISA Registration 80070219007

Access comprehensive regulatory information for Retinoscope in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80070219007 and manufactured by ZUMAX MEDICAL CO, LTD.. The registration is held by COMERCIO DE MATERIAIS MEDICOS HOSPITALARES MACROSUL 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.