HUMAN ASTROVIRUS - ANVISA Registration 80826840123

Access comprehensive regulatory information for HUMAN ASTROVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80826840123 and manufactured by R-BIOPHARM AG. The registration is held by SERION BRASIL IMPORTAÇÃO E DISTRIBUIÇÃO DE PRODUTOS DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA, and 1 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.