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

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    Filters FDA Adverse Event ×

    POSSIS SUTURELESS MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·POSSIS MEDICAL, INC.·Product code LWS·November 17, 1995

    AXON DIGITAL PREAMPLIFIER

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code GWF·March 1, 2013

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·July 21, 2014

    ELECTRIC MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 3, 2011