Multiple Use Laser System in Aesthetics - ANVISA Registration 80571450002

Access comprehensive regulatory information for Multiple Use Laser System in Aesthetics in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80571450002 and manufactured by manufacturer not specified. The registration is held by FISMATEK INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Jun 09, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including DEKA M.E.L.A SRL, LUTRONIC CORPORATION, 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.