BEUDAMED
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    Filters FDA Adverse Event ×

    CRE(TM) BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·Product code KOG·April 26, 2018

    CRE(TM) BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·Product code KOG·October 26, 2017

    B1005, ACUCISE ENDOPYELOTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code EYB·April 17, 2017

    UNKNOWN

    FDA Adverse Event
    Injury ·CONMED CORPORATION·Product code KOG·September 7, 2011

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·November 8, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·November 21, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·December 13, 2016

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·November 22, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·October 18, 2016

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·November 10, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·December 5, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·November 23, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·December 15, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·November 21, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·December 22, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·October 3, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·October 7, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·November 29, 2016

    ENDO STITCH* 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KOG·October 11, 2016

    CAPTIVATOR¿ ENDOSCOPIC MUCOSAL RESECTION DEVICE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KOG·November 17, 2016