BEUDAMED
    7 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

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 9, 2014

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·December 3, 2012

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 5, 2010

    LOGIC CR TIB INSERT SLOPE++, SZ 5, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 17, 2023