BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    RINN PROTECTIVE X-RAY APRON AND PROTECTIVE COLLAR

    FDA 510(k)
    FDA Class 1 ·Radiology

    SMARTDRIVE WHEELCHAIR POWER-ASSIST

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD SAF-T PRN LUER ACTIVATED VALVE, MODEL 385100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    1319681-2017-00049

    FDA Adverse Event
    Malfunction ·June 27, 2017

    SCD COMFORT THIGH LENGTH MED

    FDA Adverse Event
    Other ·COVIDIEN·Product code JOW·January 8, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 12, 2010

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·July 3, 2014

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 31, 2019

    Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 13, 2020

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 8, 2022

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 7, 2018