Elekta ERGO

  • Model / Serial
    Version 1.7.3 and higher
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - US Nationwide in the states of: VA, CA, TX, MO, NY, WA, NM, MA, FL, CT, OK, SC, MS, NY, GA, NC and the countries of: AUSTRALIA, BANGLADESH, BRAZIL, BULGARIA, CANADA, COLOMBIA, CZECH REPUBLIC, ECUADOR, FRANCE, GERMANY, GREECE, HONG KONG, INDIA, IRELAND, ITALY, JAPAN, JORDAN, MALAYSIA, MEXICO, NETHERLANDS, NEW ZEALAND, PERU, PHILIPPINES, PORTUGAL, RUSSIA, SAUDI ARABIA, SINGAPORE, SOUTH KOREA, SPAIN, TAIWAN, THAILAND, TURKEY, VENEZUELA, and VIETNAM
  • Product Description
    Elekta ERGO++ || Product Usage: || ERGO is often used for stereotactic treatments.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Elekta Inc, 13723 Riverport Dr Ste 100, Maryland Heights MO 63043-4819
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
  • Product Description
    Elekta ERGO++ RTP Software, IMPAC Inc
  • Manufacturer