BEUDAMED
    15 results · 33ms · Sources: EU EUDAMED, US FDA

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    Luminoah FLOW™ Enteral Nutrition System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CEPH, MODEL 4900

    FDA 510(k)
    FDA Class 2 ·Dental

    Ventix Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    VENTAK PRIZM HE VR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    3002 SECURE II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·August 10, 2011

    UNKNOWN DEPUY ACETABULAR CUP

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KXA·July 30, 2013

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    EXTRACTION SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·February 16, 2017

    EXTRACTION SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HXX·February 16, 2017

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017

    SCRDRIVERSHAFT F/LOCKCAP F/URS

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·February 16, 2017