RM Magnetom apparatus, Open model, Impact and Vision, registration 10234230012, series: 7449; 5709; 9190; 15024; 15517 /// RM Magnetom Symphony Equipment, registration 10234230057, series: 13131; 13286; 13424; 13564; 22202; 22379; 22388; 22389; 22448; 22460; 22583; 22744; 23207; 23286; 37503. /// Equipment of RM Magnetom Sonata, registration 10234230089, series: 21120; 21179; 21271 /// Equipment of RM Magnetom Spectra, registration 10345161996 (original registration 10234230182), series: 73002; 73003 /// Magnetom Avanto, registration 10345162003 (original registration: 10234230095), series: 57140; 57206; 57241; 59081. /// Magnetom Essenza, registration 10345162004 (original registration 10234230155), series: 64132; 71310; 71326; 71330; 71338; 71341; 71343; 71347; 71349; 71350; 71355; 71357; 71358; 71359; 71361; 71362; 71365; 71366; 71381; 71384. /// Equipment of RM Magnetom Prisma, registration 10345162015 (original registration 10234230203), series: 67047; 67051. /// Equipment of RM Magnetom Aera, registration 10345162032 (original registration 10234230175), series: 41904; 41909; 41986; 42031; 53501; 53502. /// Magnetom Harmony Equipment, registration 10234230056. 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Siemens Healthcare Diagnósticos S.A; Siemens AG; Siemens Shenzhen Magnetic Resonance Ltd.; Siemens Healthcare Diagnósticos S.A 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
    1782
  • 날짜
    2015-12-23
  • 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
    Suppressor lines in magnetic resonance systems serve to vent helium gas in case of dissipation. In the event of installation failure, the helium gas would be blown into the magnet room or other areas. This could lead to a displacement of the local oxygen gas, cause cold burns and / or pose a risk to users, patients and others.
  • 원인
    Siemens healthcare comes across the letter mr047 / 15 / s to alert its customers in brazil about the possibility that the suppressor lines of some superconducting magnets have not been installed properly.
  • 조치
    The field action code MR047 / 15 / S initiated by Siemens addresses the sending of a Risk Letter III to the Customer (situation in which there is a low probability that the use or exposure to a health product may have adverse health consequences ). Recommendation to Users and Patients: Proprietary MRI customers must follow one of the steps below, depending on who performed the MRI suppression facility. The guideline is for customers to have the equipment inspected for installation to assess the existence of the problem. 1) If Siemens has been contracted to install the suppressor line, contact the local Siemens organization for appropriate action. 2) If a third party has been contracted to install the suppressor line, it is recommended that they be contacted and requested to inspect the suppressor line in order to ensure that it has been installed in accordance with the system owner's manual and in accordance with requirements in the design document of the Siemens suppressor line. Notwithstanding, and alternately, Siemens makes itself available to offer users the possibility of requesting an inspection of the installation, after which it will be informed of the result and any identified deficiencies that need to be resolved. Finally, it is important to note that it is important to follow all the guidelines mentioned in the system owner's manual, including ensuring that there is an on-site emergency plan in the event of helium gas dissipation to the magnet room or adjoining rooms.