Applicators - ANVISA Registration 80320680101

Access comprehensive regulatory information for Applicators in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80320680101 and manufactured by AEGIS LIFESCIENCES PVT. LTD.. The registration is held by DANIALEX TEC - MATERIAL MEDICO HOSPITALAR LTDA ME 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 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.