Device Recall AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS

  • Modèle / numéro de série
    Model Numbers: 3111668, 3111676, 8890407, 8890415, and 10093902
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, and WY.
  • Description du dispositif
    AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS || System, X-Ray, Fluoroscopic, image-intensified; solid state x-ray imager (flat panel/digital imager)
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355
  • Société-mère du fabricant (2017)
  • Source
    USFDA