INFLUENZA B VIRUS - ANVISA Registration 81905510060

Access comprehensive regulatory information for INFLUENZA B VIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81905510060 and manufactured by manufacturer not specified. The registration is held by GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDA with validity until Mar 10, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including R-BIOPHARM 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.