BEUDAMED
    3 results · 26ms · 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 ×

    11/13 S-ROM 44MM M SPEC+9

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code LPH·January 25, 2013

    TRIA PLUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION·Product code HAW·November 18, 2010

    TECNIS CL

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code HQL·July 11, 2014