SURGICAL/CLINICAL PLANNING SOFTWARE - ANVISA Registration 80042070059

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 III medical device is registered under ANVISA number 80042070059 and manufactured by BRAINLAB AG. The registration is held by BRAINLAB LTDA with validity until Oct 13, 2030.

This page provides complete technical specifications for 2 related devices, 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.