Events

Angiography equipment, risk class III: AXIOM ARTIS FC, registration 10234230075, lots / series: 10151, 10279, 10312, 10320, 10379, 10409, 10481, 10501, 10513, 10520, 10526, 10533./// AXIOM ARTIS FA , registration: 10234230093, lots / series: 25062; 25179; 25282; 25329; 25330; 25379; 25418; 25447; 25452. /// Angiography equipment models: AXIOM ARTIS dFA; AXIOM ARTIS dFC, registration 10234230096, batches / series: 35117; 35318; 35396; 35485; 35622; 35729; 35748; 35751; 35817; 35862; 35872; 35883; 35884; 35885; 35910; 35913; 35936; 35949; 50138./// Angiography equipment Artis models ARTIS ZEE CEILING, ARTIS ZEE FLOOR AND ARTIS ZEEGO, registry 1023420190, lots / series: 135297; 135329; 135758; 135785; 135816; 135825; 135835; 135848; 135869; 135941; 135969; 135980; 135984; 135991; 136056; 136060; 136067; 136068; 136098; 136115; 136119; 136136; 136144; 136199; 136213; 136214; 136215; 136276; 136282; 136283; 136284; 136285; 136288; 136301; 136320; 136355; 136363; 136369; 136373; 136419; 136421; 136424; 136425; 136440; 136443; 136457; 136492; 136580; 136908; 136918; 136926; 136933; 136936; 136944; 136947; 136977; 136995; 137020; 137026; 137033; 137042; 137045; 137074; 137083; 137088; 137089; 137094; 137098; 137099; 137100; 137102; 137105; 137120; 137143; 137158; 137159; 137160; 137161; 137162; 137164; 137182; 137246; 146646; 147531; 147551; 147582; 147600; 147602; 147617; 147619; 147637; 147650; 147706; 147708; 147744; 160143; 160343; 160360; 160415; 160457; 160467; 160836. 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Siemens Ltda.; SIEMENS AG. 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
    1653
  • 날짜
    2015-07-24
  • 사례 국가
    Brazil
  • 사례 출처
    ANVISA
  • 사례 출처 URL
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • 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
    The holder informs that the problem involves a failure of the equipment having no influence on the treatment of patients.
  • 원인
    In case the table is near its maximum extension at the end of the head and there is a large amount of liquid on the table surface, the liquid may infiltrate the table through the existing fault and cause contamination of the electronic components. in the event of contamination, table movements may not occur.
  • 조치
    The holding company will do the sealing in the failure of the top cover of the table column. This will ensure protection against ingress of liquids. The company will contact customers to schedule a visit to carry out corrective action.

Device

Angiography equipment, risk class III: AXIOM ARTIS FC, registration 10234230075, lots / series: 1...

Manufacturer

Siemens Ltda.; SIEMENS AG.