BORDETELLA PERTUSSIS - ANVISA Registration 10259610122

Access comprehensive regulatory information for BORDETELLA PERTUSSIS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10259610122 and manufactured by DIASORIN MOLECULAR LLC. The registration is held by MEDIVAX INDÚSTRIA E COMÉRCIO LTDA with validity until Oct 17, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including DIASORIN ITALIA S.P.A., EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG, 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.