GLUTATHIONE PEROXIDASE - ANVISA Registration 80464810821

Access comprehensive regulatory information for GLUTATHIONE PEROXIDASE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810821 and manufactured by LUMIQUICK DIAGNOSTICS, INC.. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including RANDOX LABORATORIES LTD., RANDOX LABORATORIES LTD., and 4 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.