Amplimat 5-Field Chamber 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Philips Medical Systems 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
    2012-10-19
  • 사례 출판 날짜
    2012-10-19
  • 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: philips amplimat 5-field chamber medical device manufacturer, philips medical systems, has issued a medical device safety alert concerning all units of digitaldiagnost, essenta dr, essenta dr compact, buckydiagnost, easydiagnost eleva and traumadiagnost using the 5-field amplimat chamber, serial numbers from 11320067 to 11321695 and from 11322000 to 11322231. if direct radiation hits an amplimat field (selected or unselected), the amplimat signal amplifier can enter an undefined state, and one or more of the following automated exposure control (aec) exposures (using the amplimat) can be overexposed. as a result, the generator does not switch off the exposure when the intended dose is reached; however, it does switch off when the backup shutoff condition is reached. if the pre-programmed apr/epx settings are used, the overexposure is small and the image generated is usable for diagnostic purposes. if the operator overrides the pre-programmed settings, the image generated may be unusable (i.E. not correctly exposed) and more radiation may be administered than intended. the manufacturer advised the affected users to take the following actions: use the pre-programmed apr/epx settings for aec technique exposures. if overriding the apr/epx settings, monitor the exposure time. if the exposure time is longer than expected, abort the exposure. the decision if a retake is required or not should be based on the expected benefit in relation to the radiation risk. the manufacturer will instruct field service engineer to remove the affected amplimat chamber for devices with serial numbers from 11320067 to 11321695 and from 11322000 to 11322231, and install a new one. according to the local supplier, the affected devices were distributed in hong kong. if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 19 october 2012.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Philips Amplimat 5-Field Chamber
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH