BEUDAMED
    6 results · 27ms · 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

    DUAL TRIGGER ROTARY

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·June 5, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·October 1, 2010

    PARADYM

    FDA Adverse Event
    Injury ·SORIN CRM S.R.L.·Product code MRM·November 23, 2012