BEUDAMED
    5 results · 21ms · 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 ×

    1043565-2003-00001

    FDA Adverse Event
    Death ·Product code ---·May 13, 2003

    IBP ELB INT. ULNA LRG RGT LNG STM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·June 24, 2016

    LAPAROSCOPIC TISSUE MORCLTR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code HET·April 9, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 28, 2011

    FINELINE II

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008