SURGICAL/CLINICAL PLANNING SOFTWARE - ANVISA Registration 10332030140

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 10332030140 and manufactured by CARL ZEISS MEDITEC AG. The registration is held by CARL ZEISS DO BRASIL 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 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.