BEUDAMED
    6 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Death ·THORATEC CORP.·Product code DSQ·May 23, 2014

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·November 30, 2012

    DEPUY PINNACLE SECTOR II CUP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY·Product code KWA·September 28, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 8, 2021

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·December 8, 2021