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

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    Filters FDA Adverse Event ×

    FR3, REFURB ECG AED - US ENGLISH

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 12, 2014

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·January 10, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 25, 2008