GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 80076809020

Access comprehensive regulatory information for GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80076809020 and manufactured by BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED. The registration is held by ARTMÉDICA - PRODUTOS MÉDICOS E HOSPITALARES 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.