BEUDAMED
    4 results · 38ms · 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 ×

    LIBERTY POSTERIOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·February 11, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 22, 2010

    QUICKSITE LV

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code OJX·January 9, 2013

    ADVANCE(R) TOT COND FEMORAL NON-POROUS

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JWH·July 1, 2014