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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LWJ·June 2, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·November 24, 2012

    EXETER 2.5 I M PLUG 10MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·June 15, 2015

    MENTOR SMOOTH ROUND SPECTRUM

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·January 14, 2019