BEUDAMED
    3 results · 24ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    HUDSON ET TUBE, CUFFED, SPIRAL -FLEX 7.5

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·May 16, 2014

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    POSEY BED

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code OYS·November 20, 2012