Doyen-Collin Mouth Gag 120mm 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Aesculap AG 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
    2018-02-14
  • 사례 출판 날짜
    2018-02-14
  • 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: aesculap ag doyen-collin mouth gag 120mm medical device manufacturer, aesculap ag, has issued a medical device safety alert concerning its doyen-collin mouth gag 120mm [om040r; production period from february 2016 to october 2017]. an affected product om040r can be clearly identified by two options: identification on the basis of the labelled production date (from 02 16 to 10 17 inclusively), identification on the basis of the labelled encoding (from 000330 to 000449 inclusively). the manufacturer received knowledge about the possibility that the plastic sleeves of a doyen-collin mouth gag 120mm - om040r could stick together after reprocessing. according to the manufacturer, the used plastic sleeves of the instrument do not meet the valid specification. instead of the specified material silicone, the material pvc was used for the manufacturing of the sleeves. this could render affected instruments unusable after reprocessing. the results of investigation revealed that there is no increased risk expected for patients who have been treated with the affected product. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 14 february 2018.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Aesculap AG Doyen-Collin Mouth Gag 120mm
  • Manufacturer

Manufacturer