BORDETELLA PERTUSSIS - ANVISA Registration 80416660142

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 80416660142 and manufactured by manufacturer not specified. The registration is held by SEBIA IMPORTAÇÕES COMERCIALIZAÇÃO E DISTRIBUIÇÃO DE APARELHOS E REATIVOS PARA DIAGNÓSTICO IN VITRO LTDA. with validity until Aug 31, 2035.

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