Applicators - ANVISA Registration 80153820022

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 80153820022 and manufactured by GUANGZHOU EKAI ELECTRONIC TECHNOLOGY CO. LTD. The registration is held by TG MED COMERCIO IMPORTACAO, EXPORTACAO, FABRICACAO E DISTRIBUICAO DE PRODUTOS MEDICOS 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 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.