SELF-TEST FOR KETONE BODIES - ANVISA Registration 80146501875

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 80146501875 and manufactured by manufacturer not specified. The registration is held by ABBOTT LABORATORIOS DO BRASIL LTDA with validity until Feb 03, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 2 companies making the same product including APEX BIOTECHNOLOGY CORPORATION, VIVACHEK BIOTECH (HANGZHOU) 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.