Biopsy Device - ANVISA Registration 80199950043

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80199950043 and manufactured by VIGEO SRL. The registration is held by MM Diagnostika Comercial Ltda - EPP 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 STERYLAB S.R.L., Zamar D.O.O., 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.