Multiple Use Device in Aesthetics - ANVISA Registration 80571459011

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 80571459011 and manufactured by BEIJING ADSS DEVELOPMENT CO., LTD.. The registration is held by FISMATEK INDÚSTRIA E COMÉRCIO LTDA - ME 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, KLD BIOSISTEMAS EQUIPAMENTOS ELETRONICOS 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.