BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EGIA ULTRA UNIVERSAL SHORT STAPLER

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SUR·Product code GDW·April 18, 2012

    ENDO GIA ROTICULATOR* 60-3.5 SULU

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·October 10, 2014

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·September 19, 2016

    ENDO GIA* II 45-2.5 DLU

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAG·October 9, 2014

    ENDO GIA ROTICULATOR* 60-4.8 SULU

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·November 25, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE·Product code ITI·April 29, 2013

    RESOLUTION HEMOSTASIS CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·May 10, 2011

    CAPIO SUTURE DEVICE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code MFJ·July 29, 2008

    TRUSTEEL

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·December 12, 2024

    EGIA 45 ARTICULATING MED/THICK SULU

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·December 9, 2015