BEUDAMED
    3 results · 18ms · 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 ×

    ALARIS PUMP MODULE ADMIN SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·June 4, 2014

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    MAXAN IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·November 22, 2010