BEUDAMED
    12 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MAINFRAME 8253001 NIM RESPONSE 3.0

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·November 7, 2013

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·June 3, 2015

    MAINFRAME 8253001 NIM RESPONSE 3.0

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

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 6, 2014

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 15, 2012

    PROVISC IBC

    FDA Adverse Event
    Malfunction ·ALCON - BELGIUM/S.A. ALCON-COUVREUR N.V.·Product code LZP·September 10, 2010

    NIM® 3.0 MAINFRAME

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code ETN·January 14, 2015

    ENDOTRACH TUBE 8229507 CONTACT EMG 7MM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ETN·January 7, 2014

    NIM® EMG ELECTRODE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GXZ·January 27, 2017

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code ETN·July 1, 2016

    NIM® EMG - ENDOTRACHEAL TUBE - TRIVANTAGE®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·December 8, 2016

    NIM® EMG ELECTRODE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GXZ·February 13, 2017