BEUDAMED
    3 results · 29ms · 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 ×

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2014

    FAST-CATH HEMO. INT., 8.5F, SWARTZ SL1, TRANS.

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DYB·November 2, 2012

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·August 27, 2010