Applicators - ANVISA Registration 80136999044

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80136999044 and manufactured by AESCULAP AG. The registration is held by LABORATORIOS B. BRAUN S/A 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 FAGA MEDICAL INDUSTRIA DE EQUIPAMENTOS E INSTRUMENTOS MEDICO-HOSPITALARES LTDA ME, Baxter Healthcare 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.