BEUDAMED
    3 results · 27ms · 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 ×

    PROXIMATE** LINEAR CUTTER RELOAD

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 30, 2014

    ENDURANT II STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·November 20, 2012

    SILICONE ULTRAVIOLET-ABSORING POSTERIOR CHAMBER 3 PC FOLADABLE INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·September 15, 2010