Solution For Ophthalmic Use - ANVISA Registration 80164790023

Access comprehensive regulatory information for Solution For Ophthalmic Use in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80164790023 and manufactured by EUROFARMA LABORATÓRIOS S.A.. The registration is held by EUROFARMA LABORATORIOS S.A. with validity until Jun 17, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including ALCON LABORATORIES, INC, LEBON PRODUTOS QUÍMICOS E FARMACÊUTICOS LTDA, 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.