BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    VIBRATRON II, VIBRATION SENSITIVITY TESTER

    FDA 510(k)
    FDA Class 1 ·Neurology

    ECG Acquisition Systems

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPINEASSIST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 10, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 11, 2010

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·December 10, 2012