BEUDAMED
    6 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

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    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS·Product code HBE·November 20, 2024

    3.0MM CARBIDE MATCH HEAD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·January 10, 2018

    3.0MM CARBIDE MATCH HEAD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HBE·January 10, 2018

    HUDSON ET TUBE, CF, 4.0MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code JOH·April 1, 2014

    PLEXUR M

    FDA Adverse Event
    Injury ·OSTEOTECH, INC.·Product code MBP·November 1, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 23, 2010