Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0 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
    2015-12-01
  • 사례 출판 날짜
    2015-12-01
  • 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 brain metastases v1.0.0 and adaptive hybrid surgery analysis v1.0.0 the therapeutic goods administration (tga) of australia has posted a medical device safety alert concerning the brainlab brain metastases v1.0.0 and adaptive hybrid surgery analysis v1.0.0 manufactured by brainlab. under very specific circumstances, there is the potential for large objects with fine resolution to be displayed cropped when imported from smartbrush into brainlab brain metastases v1.0.0 or adaptive hybrid surgery analysis v1.0.0. for the brain metastases v1.0.0, if the cropped object is not recognised by the user before the plan is used for treatment and the deviation exceeds clinically acceptable limits, this could result in ineffective radiation treatment, serious patient injury, or even death of the patient. structures that are cropped in brain metastases are also cropped in the exported dicom rt structure set files. for the adaptive hybrid surgery analysis v1.0.0, if determination regarding the potential for radiotherapy is made, the incorrect information displayed can have an effect on clinical decisions. if the determination is done during surgery this could even, in a worst case scenario, mislead the user in regards to assessing the extent of resection during this surgery. the manufacturer will provide a software update with this issue solved. in the interim, users are advised to implement the workarounds instruction provided by the manufacturer. for details, please refer to the tga website:http://apps.Tga.Gov.Au/prod/sara/arn-detail.Aspx?k=rc-2015-rn-01164-1 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 1 december 2015.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Brainlab Brain Metastases v1.0.0 and Adaptive Hybrid Surgery Analysis v1.0.0
  • Manufacturer

Manufacturer