Electrode Removal Device - ANVISA Registration 10216719033

Access comprehensive regulatory information for Electrode Removal Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10216719033 and manufactured by PHILIPS IMAGE GUIDED THERAPY CORPORATION. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including SPECTRANETICS CORPORATION, and 1 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.