Patient Data Manager and Origin Data Management 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Brainlab 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
  • 날짜
    2015-09-29
  • 사례 출판 날짜
    2015-09-29
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 Hong Kong.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: brainlab patient data manager and origin data management the medicines and healthcare products regulatory agency (mhra), united kingdom posted a medical device safety alert concerning patient data manager and origin data management manufactured by brainlab. the affected devices are identified as follows: content manager (versions 2.0.0, 2.0.1, 2.0.2, 2.0.3, 2.1.0); patient browser (versions 4.0.0, 4.0.1, 4.0.2, 4.0.3, 4.1.0) and dicom viewer (versions 2.0.0, 2.0.1, 2.0.2, 2.0.3, 2.1.0). according to the alert, when users actively deselect a fused reference dataset in content manager (the default setting is “selected”), a contained point, object or trajectory may appear shifted and/or distorted in the subsequently used brainlab navigation or planning software. if a reference dataset is deselected and the error occurs, the magnitude of shift or distortion varies, depending on the differences between the two datasets. therefore, for some cases, the shift or distortion will be clearly visible when the plan is used in a brainlab planning or navigation system. however, a shift could also be non-obvious. if a shift or distortion occurred and was not detected during review of the data, the deviation of the information displayed in the brainlab planning or navigation software could mislead the user regarding clinical decisions. this could ultimately lead to ineffective treatment, serious injury or even death of the patient. for details, please refer to the mhra website:https://www.Gov.Uk/government/publications/safety-information-from-manufacturers-field-safety-notices/field-safety-notices-21-to-25-september-2015 if you are in possession of the affected products, please contact your supplier for necessary actions posted on 29 september 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Brainlab Patient Data Manager and Origin Data Management
  • Manufacturer

Manufacturer