BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    RUBELLA IGM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    INTEGRA CAMINO ICP MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    PURITAN-BENNETT 840 VENTILATIOR SYSTEM WITH VOLUME VENTILATION PLUS OPTION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    ELEVATE PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·January 10, 2013

    M2A-MAGNUM PF CUP 58ODX52ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 9, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 9, 2016

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 12, 2016