DENGUE - ANVISA Registration 10350840483

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 10350840483 and manufactured by manufacturer not specified. The registration is held by BIOSYS LTDA with validity until Aug 04, 2035.

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.