MEDUMAT Transport Ventilator 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Weinmann Emergency Medical Technology GmbH & Co. KG 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
    2013-10-22
  • 사례 출판 날짜
    2013-10-22
  • 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: weinmann medumat transport ventilator the medicines and healthcare regulatory agency (mhra), united kingdom has posted a field safety notice concerning medumat transport ventilator (with and without co2 measurement) manufactured by weinmann emergency medical technology gmbh & co. kg. all the serial numbers are affected. according to the manufacturer, in some cases medumat transport ventilators have failed as a result of a device-internal fault. there is the potential risk of this fault recurring sporadically in future too. furthermore, according to the manufacturer, in the interaction of the internal structural components and sensors for internal device monitoring, device internal occurrences of this kind may coincide unfavourably, resulting in an undefined operating state and the device displaying a "device malfunction" for safety reasons. the manufacturer has developed new device software version 2.35. moreover, affected users are advised to take the following necessary actions: all medumat transport devices must be verifiably updated with the new xc firmware version 2.35 and embedded pc version 2.35. affected users can continue to use their medumat transport devices until the update has been installed. users are reminded to observe the recommendations and the addition to the instructions for use as mentioned in this field safety notice. for details, please visit the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con323827 if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 22 october 2013.

Device