SCHISTOSOMA SP - ANVISA Registration 80780040024

Access comprehensive regulatory information for SCHISTOSOMA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80780040024 and manufactured by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ. The registration is held by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ with validity until May 19, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including EUROIMMUN AG, NOVATEC IMMUNDIAGNOSTICA 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.