DEVICE FOR LACRIMAL OSMOLARITY ASSESSMENT - ANVISA Registration 80628810009

Access comprehensive regulatory information for DEVICE FOR LACRIMAL OSMOLARITY ASSESSMENT in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80628810009 and manufactured by QUIDEL CORPORATION. The registration is held by GEDAT INDUSTRIA E COMERCIO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 2 companies making the same product including TRUKERA MEDICAL, I-MED PHARMA INC., and 3 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.