BORDETELLA PERTUSSIS - ANVISA Registration 82444370014

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 82444370014 and manufactured by manufacturer not specified. The registration is held by Enzytec Biotecnologia Ltda. with validity until Dec 03, 2033.

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.