IMMUNOGLOBULIN G SUBCLASS (IgG1/IgG2/IgG3/IgG4) - ANVISA Registration 80105220277

Access comprehensive regulatory information for IMMUNOGLOBULIN G SUBCLASS (IgG1/IgG2/IgG3/IgG4) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80105220277 and manufactured by AESKU DIAGNOSTICS GMBH & CO. KG. The registration is held by KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS 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 THE BINDING SITE GROUP LTD, GOLD STANDARD DIAGNOSTICS KASSEL 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.