INFUSION DEVICE - ANVISA Registration 80686360225

Access comprehensive regulatory information for INFUSION 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 80686360225 and manufactured by MORIA S.A.. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA 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 SMITHS MEDICAL ASD, INC. (MINNEAPOLIS), UNOMEDICAL A/S, 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.