BEUDAMED
    4 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K042172

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·September 2, 2022

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·November 30, 2010

    ALTRX +4 10D 36IDX62OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 4, 2013

    ACTIVA

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code MHY·July 17, 2014