BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN V. MUELLER DEVICE

    FDA Adverse Event
    Injury ·CAREFUSION·Product code GEI·March 23, 2015

    SWITCH-BLADE CVD METZ SCISSORS TIP 10/EA

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code GEI·October 21, 2014

    SWITCH-BLADE CLICKFIT REUSE HAND 5MM45CM

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code GEI·June 7, 2016

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITJ·June 25, 2014

    ASR ACETABULAR IMPLANT 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 5, 2010

    FENESTRATED BIPOLAR FORCEPS

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 3, 2013

    SWITCH-BLADE CLICKFIT REUSE HNDL 5MM36CM

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code GEI·October 5, 2011