BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LOBSTER CLAMP, RADIOLUCENT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 11, 2022

    HOLDING SLEEVE, 2.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 27, 2021

    LOBSTER CLAMP, RADIOLUCENT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 28, 2022

    LOBSTER CLAMP, RADIOLUCENT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 27, 2021

    LOBSTER CLAMP, RADIOLUCENT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·July 5, 2022

    HOLDING SLEEVE, 2.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·January 4, 2022

    LOBSTER CLAMP, RADIOLUCENT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·January 4, 2022

    DURALENS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·May 4, 2016

    CONTEGRA PULMONARY VALVED CONDUIT

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·June 12, 2014

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·December 12, 2012

    PHOENIX TIBIAL NAIL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HSB·October 15, 2010