BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VERTE-STACK K030736, K041197

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019

    BD INSYTE AUTOG BC

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 2, 2024

    LIFESCAN

    FDA Adverse Event
    Injury ·LIFESCAN·Product code NBW·January 27, 2017

    GORE VIABAHN ENDOSPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·March 27, 2013

    ENDO STITCH SURGIDAC 2/0 48 GRN DLU SU

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL·Product code KOG·March 22, 2011

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Death ·PHYSIO-CONTROL, INC.·Product code MKJ·April 17, 2008