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

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    RADKOR, XG-515

    FDA 510(k)
    FDA Class 1 ·Radiology

    URIC ACID REAGENT

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

    Spectra Optia Apheresis System

    FDA 510(k)
    FDA Unclassified ·Unknown

    MODIFICATION TO SECURACATH, MODEL: SPK01

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 7, 2014

    ULTRA-COAT MICRO EJECT KERRISON 40D UP 8 2MM

    FDA Adverse Event
    Malfunction ·Product code MDM·October 15, 2010

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·December 18, 2012