Self-test instrument for glucose - ANVISA Registration 80770430015

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 80770430015 and manufactured by M.I. TECH CO., LTD. The registration is held by DMAX - DISTRIBUIDORA DE MEDICAMENTOS E MATERIAL HOSPITALAR LTDA - EPP with validity until Jan 04, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.