Self-test instrument for glucose - ANVISA Registration 80867150002

Access comprehensive regulatory information for Self-test instrument for glucose in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80867150002 and manufactured by HMD BIOMEDICAL INC.. The registration is held by BIOMOLECULAR TECHNOLOGY COMÉRCIO, IMPORTAÇÃO, EXPORTAÇÃO E DISTRIBUIÇÃO DE MATERIAIS MÉDICOS E LABORATORIAIS LTDA - EPP with validity until Aug 11, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including OK BIOTECH CO., LTD., TIANJIN EMPECS MEDICAL DEVICE 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.