BEUDAMED
    9 results · 26ms · 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 ×

    FOOTSWITCH 1895420 XPS MULTIFUNCTIONAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·January 31, 2013

    FOOTSWITCH 1895420 XPS MULTIFUNCTIONAL

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ERL·April 9, 2009

    FOOTSWITCH 1895420 XPS MULTIFUNCTION

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ERL·November 21, 2012

    FOOTSWITCH 1895420 XPS MULTIFUNCTION

    FDA Adverse Event
    Malfunction ·XOMED MFG JACKSONVILLE·Product code ERL·December 28, 2012

    FOOTSWITCH 1895420 XPS MULTIFUNCTIONAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·September 22, 2009

    FOOTSWITCH 1895420 XPS MULTIFUNCTIONAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC·Product code ERL·November 2, 2012

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·Product code OYC·June 25, 2014

    4 FR SINGLE LUMEN GROSHONG NXT CLEARVUE BASIC KIT

    FDA Adverse Event
    Injury ·C. R. BARD INC. (BASD)·Product code LJS·November 4, 2010

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 3, 2013