HEPATITIS A VIRUS (HAV) - ANVISA Registration 80345000021

Access comprehensive regulatory information for HEPATITIS A VIRUS (HAV) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80345000021 and manufactured by DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.. The registration is held by GOYAZES BIOTECNOLOGIA LTDA with validity until Jan 07, 2028.

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 ABBOTT GMBH, ROCHE DIAGNOSTICS 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.