BEUDAMED
    5 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SILVERSPEED HYDROPHILIC GUIDEWIRE

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code DQX·April 24, 2014

    IACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·September 28, 2012

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 20, 2010

    BD ALARIS¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022