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

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    CYTOPREP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    URIC ACID REAGENT

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

    QV-9000 UNIVERSAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNCHRON CX4/CX5 CLINICAL CHEMISTRY ANALYZER REAGE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    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