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

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    Filters FDA Adverse Event ×

    HEARTSINE SAMARITAN 300P AND PAK PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 6, 2014

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 13, 2010

    UNKNOWN DEPUY ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 19, 2012