Acuson Sequoia C512 / C256 / 512 # Series Affected Series Acuson Sequoia C512 / C256 / 512 # Product Name: Acuson Sequoia C512 / C256 / 512 # Product Name: ACUSON SEQUOIA ULTRASONIC SYSTEM # : 40507963, 41008034, 41008038, 41608093 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Siemens Ltda.; Siemens Medical Solutions USA, 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
    1427
  • 날짜
    2014-09-15
  • 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
    Recommendations to users: "To avoid the potential risk of this problem, Siemens recommends: - Perform the leak test for the transesophageal transducer before each use (this test may indicate cracks, cuts, tears, perforations and protuberances in the joint material , and thus avoid possible risk to the patient and / or operator) - Use only Siemens approved cleaning and disinfection solutions - Carefully follow manufacturer's instructions - Use commercially available transducer guides designed specifically for TEE applications. Follow the instructions provided by the manufacturer of the transducer guide - When storing the transesophageal transducer, take extreme care to keep the transducer tip vertically - Never move the transducer end by hand Always use the flexible controls Recommended steps are provided in the existing user's manual of the ultrasound system. s have been instructed to share the information contained in the letter with all employees in your organization who need to know about this problem and to file the letter with the Operator's Manual. "
  • 원인
    Siemens has identified the possibility of deterioration of the material covering the articulation section of the transesophageal transducer v5ms.
  • 조치
    The base installed in the system will be corrected. Code: US024 / 14 / S (LETTER TO THE CLIENT IN ANNEX)

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