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

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    Filters FDA Adverse Event ×

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 17, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 26, 2012

    ALLEGRETTO WAVE EYE-Q EXCIMER LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 17, 2015

    PEDICLE SCREW PERCUTANOUS TOWER ENH. JPN

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·December 12, 2018

    MIS PEDICLE SCREW PERCUTANOUS TOWER ENH. JPN

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·August 30, 2019