DEVICE FOR LACRIMAL OSMOLARITY ASSESSMENT - ANVISA Registration 81770680000

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 81770680000 and manufactured by I-MED PHARMA INC.. The registration is held by DRYCOM COMÉRCIO, IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS E HOSPITALARES 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, QUIDEL CORPORATION, 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.