BEUDAMED
    3 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 2, 2014

    RESOLUTION HEMOSTASIS CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·October 25, 2010

    PINN.SECTOR ACET.CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·December 20, 2012