translation missing: ko.activerecord.attributes.event.titles.recall_field_safety_notice

Saudi Food & Drug Authority에 따르면, 해당 translation missing: ko.activerecord.attributes.event.types.recall_field_safety_notice 는 Saudi Arabia 에서 GE Healthcare 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

현장 안전성 서한은 의료기기 제조사 또는 제조사 대리인이 시중에 유통되고 있는 자사 의료기기 제품에 대하여 취할 수 있는 조치를 알리는 소통방식입니다. 주요 대상층은 보건의료업계 종사자와 의료기기 사용자들입니다. 여기에는 회수(recall) 조치와 경고도 포함될 수 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall / Field Safety Notice
  • 사례 ID
    mdprc 057 04 12 000
  • 사례 시작날짜
    2012-04-17
  • 사례 국가
  • 사례 출처
    SFDA
  • 사례 출처 URL
  • 비고 / 경고
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug Authority, 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 recall data from the U.S. and Saudi Arabia.
  • 데이터 추가 비고
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • 원인
    When using the fmri protocol in ready view, the ready view application may incorrectly sort the phases of the fmri native data set. this happens when the fmri data was acquired using the brainwave rt acquisition scheme on the mr console. no adverse event has been reported related to this issue. this affects the analysis of the image set made by the correlation algorithm used in the fmri protocol. as a result, activated pixels identified as having a high correlation with a reference pattern may not be correctly identified.

Device

  • 모델명 / 제조번호(시리얼번호)
    READY View version 10.3.67 is affected; PR# 7130256 to AFSSAPS (reference 201205472)
  • 제품 설명
    Workstation software, analyzing fMRI images
  • Manufacturer

Manufacturer