DEVICE FOR DIAGNOSIS - ANVISA Registration 80380269007

Access comprehensive regulatory information for DEVICE FOR DIAGNOSIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80380269007 and manufactured by SPECLIPSE, INC.. The registration is held by MEDSYSTEMS COMERCIO, IMPORTACAO E EXPORTACAO LTDA - EPP 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 MADHU INSTRUMENTS PVT. LTD, LEEDSAY S/A, 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.