BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INNOVA 4100

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011

    INNOVA 4100

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011

    PINNACLE 300 ACET CUP 56MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·April 11, 2013

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 16, 2011

    VITROS CHEMISTRY PRODUCTS VALP REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LEG·May 20, 2008

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2017

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X40 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL (MDR)·Product code HSB·May 11, 2015

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X45 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL (MDR)·Product code HSB·May 11, 2015

    LOCKING SCREW, FULLY THREADED T2 TIBIA Ø5X40 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL (MDR)·Product code HSB·May 11, 2015