BEUDAMED
    3 results · 19ms · 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 ×

    TRIDENT X3 ELEVATED RIM 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·June 16, 2014

    MARQUIS VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·October 19, 2010

    5MMX45CM 22MM DIRECT DRIVE DISPOSABLE GRASPER

    FDA Adverse Event
    APPLIED MEDICAL·Product code GCJ·December 12, 2012