BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    BALLOON UTERINE STENT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NEUROPROBES

    FDA 510(k)
    FDA Class 2 ·Neurology

    Integra DigiFuse Cannulated Intramedullary Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BASIX COMPAK INFLATION SYRINGE KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DTL·March 14, 2011

    EON MINI

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL NEUROMODULATION·Product code GZB·May 15, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 7, 2011