DENGUE - ANVISA Registration 80785070202

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80785070202 and manufactured by Vida Biotecnologia Ltda - ME. The registration is held by Vida Biotecnologia Ltda - ME with validity until May 22, 2033.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including Eco Diagnostica Ltda, HANGZHOU ALLTEST BIOTECH CO. LTD, 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.