BEUDAMED
    14 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EMPTY CONTAINER

    FDA Adverse Event
    Malfunction ·HOSPIRA·Product code KPE·February 8, 2017

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 23, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 23, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 22, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 23, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 22, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 23, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 22, 2011

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 22, 2011

    CHEMFORT

    FDA Adverse Event
    Malfunction ·SIMPLIVIA HEALTHCARE LTD.·Product code ONB·February 2, 2026

    LIGACLIP 20/20 MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·LACEY MANUFACTURING CO.·Product code GDO·April 6, 1999

    32MM STANDARD FEMORAL HEAD

    FDA Adverse Event
    Injury ·Product code KWY·September 2, 1997

    CYBERONICS NEUROCYBERNETIC PROSTHESIS

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·February 23, 2001

    STYLE 15 SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·April 24, 2020