SHOCK WAVE EQUIPMENT FOR THERAPY - ANVISA Registration 82155249003

Access comprehensive regulatory information for SHOCK WAVE EQUIPMENT FOR THERAPY in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82155249003 and manufactured by LIKAMED GMBH. The registration is held by KTR GROUP IMPORTACAO E EXPORTACAO LTDA 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 DORNIER MEDTECH GMBH, RICHARD WOLF GMBH, 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.