ELECTROLYTES - ANVISA Registration 80298970094

Access comprehensive regulatory information for ELECTROLYTES in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80298970094 and manufactured by PHOENIX DIAGNOSTICS INC. The registration is held by MEDMAX COMÉRCIO DE EQUIPAMENTOS MÉDICOS E SIMILARES 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 CARETIUM MEDICAL INSTRUMENTS CO.,LIMITED, ROCHE DIAGNOSTICS GMBH, 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.