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

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    Filters FDA Adverse Event ×

    LOCKING END CAP 5 MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·March 27, 2014

    11.0MM TI HELICAL BLADE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·April 24, 2014

    ASR ACETABULAR IMPLANT 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 3, 2012

    VERIFLEX LIBERTE' CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC IRELAND LTD.·Product code MAF·July 25, 2010

    LOCKING END CAP 5 MM

    FDA Adverse Event
    Death ·ORTHOFIX SRL·Product code HSB·March 27, 2014

    LOCKING END CAP 5 MM

    FDA Adverse Event
    Injury ·ORTHOFIX SRL·Product code HSB·October 6, 2022

    LOCKING END CAP 5 MM

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HSB·March 27, 2014

    LOCKING END CAP 5 MM

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code HSB·March 18, 2019