IMMUNOGLOBULIN E - ANVISA Registration 10402200059

Access comprehensive regulatory information for IMMUNOGLOBULIN E in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10402200059 and manufactured by BIOCHECK, INC.. The registration is held by INTERTECK INTERNACIONAL 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 PHADIA AB, SHENZHEN DYMIND BIOTECHNOLOGY CO., LTD, 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.