BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 23, 2023

    PULSE GEN MODEL 105

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·May 20, 2014

    ENDEAVOR RESOLUTE RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·November 7, 2012

    3005075853-2010-04826

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·August 24, 2010