SELF-TEST FOR KETONE BODIES - ANVISA Registration 81692610295

Access comprehensive regulatory information for SELF-TEST FOR KETONE BODIES in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81692610295 and manufactured by manufacturer not specified. The registration is held by VYTTRA DIAGNOSTICOS S.A. with validity until Aug 26, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including APEX BIOTECHNOLOGY 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.