BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPINALPAK(R) STIMULATOR ELECTRODES

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·March 14, 2017

    SPINALPAK(R) STIMULATOR ELECTRODES

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·March 14, 2017

    SPINALPAK(R) STIMULATOR ELECTRODES

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·March 14, 2017

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 4, 2014

    MEDEX LOGICAL PRESSURE MONITORING KIT

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code DRS·November 14, 2012

    ADVANTAGE SERIES 29

    FDA Adverse Event
    Malfunction ·STRYKER CORP. MEDICAL DIVISION·Product code FPO·September 27, 2010