SURGICAL/CLINICAL PLANNING SOFTWARE - ANVISA Registration 80263050131

Access comprehensive regulatory information for SURGICAL/CLINICAL PLANNING SOFTWARE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80263050131 and manufactured by GLOBUS MEDICAL, INC. The registration is held by GLOBUS MEDICAL BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BRAINLAB AG, CARL ZEISS MEDITEC AG, 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.