DENGUE - ANVISA Registration 82533950047

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 82533950047 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD. The registration is held by MR SAUDE LTDA with validity until Nov 27, 2033.

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 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.