KETONE - ANVISA Registration 80115310298

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 80115310298 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The registration is held by KOVALENT DO BRASIL 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 TAIDOC TECHNOLOGY CORPORATION, ABBOTT DIABETES CARE 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.