Device Recall Skytron Ergon 2 Skyboom

  • Modèle / numéro de série
    Model Number(s): H8-010-50-FC2-LH and H8-010-50-FC2-RH. VESA plates distributed from 09/26/08 to 04/30/13.
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US including WI, TX, FL, NC, MD, OH, AZ, CA, UT, MT, OK, HI, CO, WY, MO, NJ, IL, NY, MA, IA, DE, PA, MI, IN, and WV and Internationally to Canada, and Japan.
  • Description du dispositif
    Ergon 2 Articulating Equipment Boom Monitor Brackets || mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment pendant / booms
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Skytron, Div. The KMW Group, Inc, 5085 Corporate Exchange Blvd Se, Grand Rapids MI 49512-5515
  • Société-mère du fabricant (2017)
  • Source
    USFDA