Monitoring Kit - ANVISA Registration 81210770041

Access comprehensive regulatory information for Monitoring Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81210770041 and manufactured by NEURO TECNOLOGIA DA AMERICA LATINA IMPORTAÇÃO E EXPORTAÇÃO LTDA. The registration is held by NEURO TECNOLOGIA DA AMERICA LATINA IMPORTAÇÃO E EXPORTAÇÃO 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 EDWARDS LIFESCIENCES LLC (IRVINE, CA), SPES MEDICA S.R.L, 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.