TOXOPLASMA GONDII - ANVISA Registration 80474870108

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 80474870108 and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. The registration is held by BIOSUL PRODUTOS DIAGNOSTICOS LTDA - ME with validity until Aug 30, 2032.

This page provides complete technical specifications for 2 related devices, 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.