SELF-TEST FOR KETONE BODIES - ANVISA Registration 80117581193

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 80117581193 and manufactured by APEX BIOTECHNOLOGY CORPORATION. The registration is held by EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA with validity until Dec 02, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 3 companies making the same product including VIVACHEK BIOTECH (HANGZHOU) CO., LTD., APEX BIOTECHNOLOGY 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.