BEUDAMED
    3 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 10, 2021

    CLINITEK STATUS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code KQO·June 25, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 4, 2010