KETONE - ANVISA Registration 80074330022

Access comprehensive regulatory information for KETONE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80074330022 and manufactured by TAIDOC TECHNOLOGY CORPORATION. The registration is held by GLOBO REAGENTES E EQUIPAMENTOS P/ LABORATORIOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ABBOTT DIABETES CARE LTD., TAIDOC TECHNOLOGY CORPORATION, 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.