BEUDAMED
    3 results · 28ms · 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 ×

    LEAD MODEL 302

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·June 6, 2014

    MALLINCKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code BTR·November 27, 2012

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNKNOWN SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·September 3, 2010