Device Recall Interplant

  • 모델명 / 제조번호(시리얼번호)
    Interplant Release 3.4.0
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution -- USA (nationwide) including states of: CA, KS, KY, MA, MD, ME, MO, NC, NE, NY, OH, PA, TX and VA and countries of: Australia, Brazil, Chile, China, Germany and Japan.
  • 제품 설명
    Interplant Radiation Treatment Planning System, Interplant Release 3.4.0 || Used when planning and performing prostate brachytherapy implant procedure. It provides ultrasound probe alignment and radioactive seed implantation.
  • Manufacturer
  • 1 Event

제조사

  • 제조사 주소
    Computerized Medical Systems Inc, 13723 Riverport Drive, Suite 100, Maryland Heights MO 63043
  • 제조사 모회사 (2017)
  • Source
    USFDA