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

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    Filters FDA Adverse Event ×

    PRESSURE WIRE CERTUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL S.C., INC, US DIVISION·Product code DQX·November 5, 2012

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 9, 2014

    SIEMENS BRAND NAME: ARTISTE MV

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·September 1, 2010