BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    PEDIFRAG 4.0MM CANNULATED CANCELLOUS SCREW, T15 HEX, FULL THREAD, 20MM

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·February 16, 2020

    UNKNOWN ORTHOPEDIATRICS SCREW

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·February 16, 2020

    ORTHOPEDIATRICS 3.5MM CORTEX SCREW

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·February 16, 2020

    ORTHOPEDIATRICS 3.5 CORTEX SCREW

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·February 16, 2020

    3.5MM SELF TAPPING CORTICAL SCREW WITH T15 HEXALOBE, SIZE 22MM

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·March 20, 2020

    3.5MM LOCKING CORTICAL SCREW WITH T15 HEXALOBE, SIZE 26MM

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·March 20, 2020

    ORTHOPEDIATRICS 130 DEGREE LOCKING CANNULATED INFANT BLADE 25MM X 0MM X 3-HOLE

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, CORP·Product code HRS·February 10, 2018

    UNKNOWN ORTHOPEDIATRICS PEDILOC TIBIA SCREW

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·August 8, 2018

    ORTHOPEDIATRICS 3.5MM LOCKING CORTICAL SCREW, T15 HEX, SIZE 20MM

    FDA Adverse Event
    Malfunction ·ORTHOPEDIATRICS, INC·Product code HWC·August 2, 2018

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·November 25, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 12, 2014

    CADD ADMINISTRATION SETS WITH FLOW STOP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·December 20, 2022

    CADD ADMINISTRATION SET WITH FLOW STOP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FPA·December 13, 2022