Self-test instrument for glucose - ANVISA Registration 80102512237

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 80102512237 and manufactured by TIANJIN EMPECS MEDICAL DEVICE CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jun 24, 2029.

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.