BEUDAMED
    170 results · 12ms · Sources: EU EUDAMED, US FDA

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    HiSpeed FX/I (2200997 with Gantry mo. #2201000)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997 with Gantry mo. #2249696)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997 with Gantry mo. #2200997)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2201000)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2249696)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2201000)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2200997)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2200997)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997 with Gantry mo. #2201000-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997 with Gantry mo. #2200997-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997 with Gantry mo. #2249696-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2249696)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2201000-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2200997-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2201000-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2201000-2 with Gantry mo. #2249696-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2200997-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    HiSpeed FX/I (2200997-2 with Gantry mo. #2249696-2)

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code JAK·February 1, 2010

    Stackhouse FreedomAire Lens/Hood; a sterile disposable protective head garment for use with the FreedomAire Surgical Helmet System, providing a clear plastic bubble lens and protective head hood to connect to the surgical helmet; individually packaged hoods, 12 per case; Manufactured for Viasys MedSystems, Wheeling, IL 60090

    FDA Recall
    Terminated ·VIASYS Med Systems·Product code FXY·September 13, 2005

    Stackhouse Lens/Hood, Mark III Universal; a sterile disposable protective head garment for use with the Stackhouse Mark III Helmet, providing a clear plastic bubble lens and protective head hood to connect to the surgical helmet; individually packaged hoods, 12 per case; Manufactured for Viasys MedSystems, Wheeling, IL 60090

    FDA Recall
    Terminated ·VIASYS Med Systems·Product code FXY·September 13, 2005