Self-test instrument for glucose and ketone bodies - ANVISA Registration 80146501882

Access comprehensive regulatory information for Self-test instrument for glucose and 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 80146501882 and manufactured by manufacturer not specified. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Jul 07, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 2 companies making the same product including ABBOTT DIABETES CARE LTD, APEX BIOTECHNOLOGY CORPORATION, and 4 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.