Device typeDermatological extracorporeal shock wave therapy system: An assembly of devices designed to provide spark-gap-generated extracorporeal shock wave therapy (ESWT) intended to treat acute and chronic conditions of the skin and subcutaneous soft tissues (e.g., arterial, venous, diabetic or pressure ulcers; burns; postoperative or traumatic wounds; cellulite). It typically consists of a generator that supplies the high voltage energy; and a hand-held, fluid-filled, shock wave applicator that produces spark-gap (electrohydraulic) energy delivered non-invasively to the area of the skin in contact with the applicator. Treatment parameters are intended to be input manually or from a pre-programmed radio-frequency identification (RFID) card.
FDA categoryExtracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers
Device ID04260484571267
Catalog number1000024
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information
Weight21 Kilogram
Depth459 Millimeter
Width400 Millimeter
Height218 Millimeter