ARTIS ANGIOGRAPHY EQUIPMENT Technical Name: Angiography Equipment ANVISA Registration Number: 10345162023 Hazard Class: III Model Affected: Artis zee ceiling Serial Numbers Affected: 17582 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Siemens Healthcare Diagnósticos S.A; Siemens Healthcare GmbH 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
    2241
  • 날짜
    2017-03-20
  • 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
    Siemens recommends the use of sterilized covers to protect the wireless radar drive pedal from all types of contamination. Since it is already standard practice in many installations, this approach is an effective way to prevent the wireless radius trigger pedal from coming into contact with liquids. When cleaning or disinfecting the radiation trigger pedal, use cloths that are moist but not dripping. You should avoid immersing the wireless radiation trigger pedal into liquids until corrective action has been taken. If the wireless radiation trigger pedal stops working, the radiation delivery for acquisition of images continues to be possible via the manual radiation trigger pedal. Normal emergency procedures should be implemented in case of system failure. Ensure that these processes are prepared in advance until our countermeasures have been implemented. There is no need to re-examine any patients. This is a possible hardware defect that has no influence on the treatment of patients. ### UPDATED ON 10/26/2017, the company presented the completion report of the field action proving the sending of the security warning to the client with evidence of science and all actions completed.
  • 원인
    Siemens healthcare diagnostics informs its customers about a potential safety quality issue that affects the use of the wireless radar foot pedal in an artis system. slack in the wireless radar trigger pedal may result in fluid entering the interior. these liquids may include disinfecting or cleaning agents but also body fluids, and may, in rare instances, result in failure of the wireless radiation drive pedal. only the wireless radiation trigger pedals that have been shipped with artis systems after january 1, 2005 are affected.
  • 조치
    Field Action Code AX063 / 16 / S triggered under the responsibility of the company Siemens Healthcare Diagnósticos SA Company will send letter to the client.

Manufacturer