BEUDAMED
    7 results · 38ms · Sources: EU EUDAMED, US FDA

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    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·May 3, 2023

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 6, 2019

    ECHOTIP CELIAC PLEXUS NEUROLYSIS NEEDLE

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code BSP·November 21, 2019

    APPLICAT OUT SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code LXH·April 2, 2013

    TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 4

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code DQX·March 25, 2011

    ACCU-CHEK RAPID D INFUSION SET

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code FPA·April 14, 2008

    ECHOTIP ULTRA CELIAC PLEXUS NEUROLYSIS NEEDLE

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·July 5, 2023