BEUDAMED
    9 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VIDEO GUIDED CATHETER

    FDA Adverse Event
    Other ·MYELOTEC, INC.·Product code HRX·February 15, 2011

    ARTHROSCOPE

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·October 31, 2014

    VIDEO GUIDED CATHETER

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·December 7, 2012

    2017 NAVICATH KIT

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·December 30, 2013

    MYELOTEC SPINAL ENDOSCOPY ACCESS KIT

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC.·Product code HRX·June 11, 2013

    UNK

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·July 11, 2012

    2010 VIDEO GUIDED CATHETER

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC·Product code HRX·April 13, 2017

    2017 NAVICATH KIT

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC·Product code HRX·April 13, 2017

    MYELOTEC NAVICATH STEERABLE EPIDURAL CATHETER

    FDA Adverse Event
    Other ·MYELOTEC, INC.·Product code BSO·January 11, 2008