BEUDAMED
    4 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LUMA ARCH

    FDA Adverse Event
    Injury ·LUMALITE, INC.·Product code EEG·July 6, 2004

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 15, 2013

    SCREWDRIVER BLADE, T7, AO

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code LXH·January 28, 2011

    SEQUOIA

    FDA Adverse Event
    Injury ·ABBOTT SPINE, INC.·Product code KWP·February 26, 2008