BORDETELLA PERTUSSIS - ANVISA Registration 80867150205

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 80867150205 and manufactured by USTAR BIOTECHNOLOGIES (HANGZHOU) LTD. The registration is held by BIOMOLECULAR TECHNOLOGY COMÉRCIO, IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO DE MATERIAIS MÉDICOS E LABORATORIAIS LTDA - EPP with validity until Dec 09, 2034.

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.