BEUDAMED
    219 results · 47ms · Sources: EU EUDAMED, US FDA

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    CELLTRACKS AUTOPREP SYSTEM

    FDA Adverse Event
    Other ·VERIDEX, LLC·Product code GKH·March 11, 2009

    COULTER AC-T DIFF 2 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Other ·BECKMAN COULTER, INC.·Product code GKH·October 14, 2003

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    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code GKH·August 13, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·August 13, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    ORTHO SUMMIT PROCESSOR

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code GKH·July 24, 2003

    2250051-2003-00340

    FDA Adverse Event
    Malfunction ·Product code GKH·July 24, 2003

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    FDA Adverse Event
    Malfunction ·*·Product code GKH·September 16, 2003

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    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code GKH·August 13, 2003

    *

    FDA Adverse Event
    Malfunction ·*·Product code GKH·September 16, 2003

    *

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code GKH·August 13, 2003

    *

    FDA Adverse Event
    Malfunction ·*·Product code GKH·July 24, 2003

    *

    FDA Adverse Event
    Malfunction ·*·Product code GKH·July 24, 2003

    2250051-2003-00336

    FDA Adverse Event
    Malfunction ·Product code GKH·July 24, 2003

    *

    FDA Adverse Event
    Malfunction ·*·Product code GKH·July 24, 2003