BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    OXYLOG 2000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MODIFICATION TO ARM BLOOD PRESSURE MONITOR, MODELS KP-6821, KP-6822

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Rapid Therapy System

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·January 9, 2013

    OUTBACK RE-ENTRY CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS·Product code DQY·December 10, 2010

    ACCU-CHEK ® TENDER INFUSION SET

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FPA·July 18, 2014