ZIKA - ANVISA Registration 80524900063

Access comprehensive regulatory information for ZIKA in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80524900063 and manufactured by BEIJING GENESE BIOTECH, INC.. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Dec 04, 2027.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including Eco Diagnostica Ltda, VIRCELL S.L., 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.