Multiple Use Device in Aesthetics - ANVISA Registration 80485739012

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 80485739012 and manufactured by JIANGSU LENGFENG MEDICAL PRODUCTS CO.,LTD.. The registration is held by BELLE ARTI INDUSTRIA E COMERCIO 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, 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.