Devices

Device Recall iGUIDE Software 2.2

  • Modelo / Serial
    Scope; iGUIDE 2.2.0, iGUIDE 2.2.1
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution in the states of AK, CT, GA, KY, LA, MA, MD, MN, NC, NM, OH, OK, OR, PA, SC, SD, TN, TX, VA, WA and countries of Hawaii Australia, Austria, Belgium, Denmark, France, Germany, Hong Kong, India, Indonesia, Ireland, Italy, Japan, Netherlands, New Zealand, Poland, Slovenia, Spain, Sweden, Switzerland, United Kingdom, & Vietnam.
  • Descripción del producto
    iGUIDE Software 2.2 || Product Usage: || Control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.
  • Manufacturer
    Elekta, Inc.
  • 1 Event

Fabricante

Elekta, Inc.
  • Dirección del fabricante
    Elekta, Inc., 400 Perimeter Center Ter NE Ste 50, Atlanta GA 30346-1227
  • Empresa matriz del fabricante (2017)
    Elekta AB
  • Source
    USFDA