BEUDAMED
    3 results · 23ms · 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 ×

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 18, 2014

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code MMH·October 3, 2012

    FOGARTY ARTERIAL EMBOLECTOMY CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES PR·Product code DXE·July 27, 2010