Intense Pulsed Light for dry eye therapy - ANVISA Registration 81770680002

Access comprehensive regulatory information for Intense Pulsed Light for dry eye therapy in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81770680002 and manufactured by E-SWIN. 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 DEKA M.E.L.A S.R.L., ESPANSIONE MARKETING SPA, and 2 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.