BEUDAMED
    3 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEFINIUM 8000

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code KPR·March 21, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·October 31, 2012

    IMMULITE 2000

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJQ·August 12, 2010