Guide Wire - ANVISA Registration 81403789002

Access comprehensive regulatory information for Guide Wire in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81403789002 and manufactured by ACE MEDICAL DEVICES PVT. LTD. (EAST AVENUE). The registration is held by ARQUIMED DISTRIBUIDORA E REPRESENTACAO DE PRODUTOS MEDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details. 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.