Intense Pulsed Light for dry eye therapy - ANVISA Registration 10161029006

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 10161029006 and manufactured by ESPANSIONE MARKETING SPA. The registration is held by MEDIPHACOS INDÚSTRIAS MÉDICAS S/A 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., E-SWIN, 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.