BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ENDOTRACHEAL TUBE 7.5 MM EMG FLEX

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code BTR·July 28, 2010

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·December 16, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·January 22, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 10, 2014

    ENDOTRACH TUBE 8229306J NIM EMG 6MM

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code ETN·March 6, 2013

    ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·May 10, 2013

    ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·March 11, 2013

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 26, 2013

    ENDOTRACH TUBE 8229980 5PK 8MM EMG FLEX

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·February 11, 2013

    NIM® EMG - ENDOTRACHEAL TUBE - NIM FLEX¿

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·October 18, 2021

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·August 28, 2013

    UNSPECIFIED BD VACUTAINER BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 11, 2021