Intense Pulsed Light for dry eye therapy - ANVISA Registration 81341749009

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 81341749009 and manufactured by DEKA M.E.L.A S.R.L.. The registration is held by OCULUS BRASIL COMERCIO IMPORTACAO EXPORTACAO E SERVICOS DE EQUIPAMENTOS 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 E-SWIN, 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.