Multiple Use Device in Aesthetics - ANVISA Registration 10245239022

Access comprehensive regulatory information for Multiple Use Device in Aesthetics in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10245239022 and manufactured by KLD BIOSISTEMAS EQUIPAMENTOS ELETRONICOS LTDA. The registration is held by KLD BIOSISTEMAS EQUIPAMENTOS ELETRONICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including LMG LASERS - COMERCIO, IMPORTACAO E EXPORTACAO LTDA, BIOSET INDÚSTRIA DE TECNOLOGIA ELETRÔNICA LTDA, and 5 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.