GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 81506640019

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 I medical device is registered under ANVISA number 81506640019 and manufactured by BIÇAKCILAR TIBBI CIHAZLAR SANAYI A.S.. The registration is held by ONCORMED PRODUTOS PARA SAÚDE LTDA - ME with validity until currently active (VIGENTE).

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