TOXOPLASMA GONDII - ANVISA Registration 80047580228

Access comprehensive regulatory information for TOXOPLASMA GONDII in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80047580228 and manufactured by MBIOLOG DIAGNOSTICOS LTDA. The registration is held by MBIOLOG DIAGNÓSTICOS LTDA with validity until Jul 14, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ABBOTT GMBH, 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.