Device Recall Theratron 1000

  • Model / Serial
    Model Theratron 1000
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The products were shipped to medical facilities in FL and KS. The product was also shipped to Kuwait, Spain, Honduras, Romania, France, Grrece, Bangladesh, Germany, Nepal, Canada, England, Thailand, Phillippines, Mexico, Columbia, India, Switzerland, Syria, Trinidad & Tobago, Ireland, Turkey, Algeria, Portugal, Poland, Iran, China, Cuba, Belgium, Hungary, Egypt, Italy, Vietnam, Sri Lanka, and Costa Rica.
  • Product Description
    Theratron 1000 Cobalt Radiotherapy
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    MDS Canada Inc. DBA MDS Nordion, 447 March Road, Kanata Canada
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Model Theratron 1000E
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The products were shipped to medical facilities in FL and KS. The product was also shipped to Kuwait, Spain, Honduras, Romania, France, Grrece, Bangladesh, Germany, Nepal, Canada, England, Thailand, Phillippines, Mexico, Columbia, India, Switzerland, Syria, Trinidad & Tobago, Ireland, Turkey, Algeria, Portugal, Poland, Iran, China, Cuba, Belgium, Hungary, Egypt, Italy, Vietnam, Sri Lanka, and Costa Rica.
  • Product Description
    Theratron 1000E Cobalt Radiotherapy
  • Manufacturer