GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 80073119004

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 80073119004 and manufactured by MEDI-GLOBE GMBH. The registration is held by MEDI-GLOBE BRASIL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, 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.