BEUDAMED
    6 results · 21ms · 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

    530G INSULIN PUMP

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·June 4, 2014

    ALTRX +4 10D 36IDX52OD

    FDA Adverse Event
    Injury ·Product code LPH·November 29, 2012

    ACCOLADE STEM INSERTER

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·September 27, 2010