DENGUE - ANVISA Registration 82206010007

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 82206010007 and manufactured by GUANGZHOU WONDFO BIOTECH CO. LTD. The registration is held by EBD BIOTECH IMPORTACAO E COMERCIO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Jan 02, 2033.

This page provides complete technical specifications for 2 related devices, 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.