SHOCK WAVE EQUIPMENT FOR THERAPY - ANVISA Registration 80102512137

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 80102512137 and manufactured by DORNIER MEDTECH GMBH. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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.