BEUDAMED
    4 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 31, 2013

    ENDURON NEUT 52OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 31, 2011

    MAXGUARD BLOOD COLLECTION DEVICE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FMH·June 27, 2014