BEUDAMED
    8 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 ×

    LOCKING SCREW VARIAX FULL THREAD 3.5MM / L10MM

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code HRS·July 8, 2015

    LOCKING SCREW VARIAX FULL THREAD 3.5MM / L18MM

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code HRS·July 8, 2015

    ARROW ARTERIAL CATH KIT: 20GA X 5" (12 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·June 8, 2017

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Malfunction ·AV-REDWOOD CITY·Product code MGB·November 22, 2010

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 1, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·November 30, 2012

    ARROW ARTERIAL CATH KIT: 20GA X 5" (12 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·June 8, 2017

    ARROW ARTERIAL CATH KIT: 20GA X 5" (12 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQX·June 8, 2017