X-ray Generator, X-ray Generator Set (1) Model KXO-50R, (2) Model KXO-50F, Model KXO-80N 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Toshiba America Medical Systems Inc 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 사례 ID
    676
  • 날짜
    2001-10-26
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.
  • 데이터 추가 비고
    BRASIL-03.10.2002 / Letter from the company Toshiba Medical do Brasil Ltda, C-0340RX.2002, dated 27.03.2002, informs that the corrections are already being carried out with customers with the X-ray generator, model KXO 50- F. In addition, it covers not only the referenced model, but also the KXO-30R, KXO-30F, KXO-50N and KXO-80N models. -------------------------------------------------- ---------------------- On July 29, 2002, C-084RX.2002, the company Toshiba Medical do Brasil Ltda, announces the closure of the adequacy procedures of generators. Circuit Modification as instructed by Toshiba Corporation, Medical Sistems Division (Field Modification Instruction FMI - XR863) to conform to international standard CFR1020.31.
  • 원인
    The above x-ray controls / generators did not meet the 21 cfr 1020.31 (a) (2) requirements since uninterrupted exposure may occur as a result of tube bending. the manufacturer initiated a correction by letter dated july 19, 2001.
  • 조치
    Verify receipt of letter and safety instructions from Toshiba America Medical Systems x-ray generator dated July 19, 2001. Identify all affected products in your inventory. Follow the instructions for safety use of the x-ray generators. For more information, contact your legal representative.

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