Events

unkown device 의 리콜

L’Agence nationale de sécurité du médicament et des produits de santé (ANSM)에 따르면, 해당 리콜 는 France 에서 N/A 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 날짜
    2004-03-31
  • 사례 국가
    France
  • 사례 출처
    ANSM
  • 사례 출처 URL
    https://ansm.sante.fr/S-informer/Informations-de-securite-Retraits-de-lots-et-de-produits/retrait-de-plusieurs-lots-de-dispositifs-medicaux-de-differents-fabricants
  • 비고 / 경고
    French data is current through early September 2018. All of the data comes from L’Agence nationale de sécurité du médicament et des produits de santé (ANSM), 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 France.
  • 데이터 추가 비고
  • 조치
    Afssaps has asked 25 manufacturers to withdraw from the market, batches of medical devices sterilized with ethylene oxide by ESTER, for which sterility can not be guaranteed. This animal health measure (09/03/2004) (87 KB) follows an inspection conducted in early 2004 by Afssaps with ESTER, a sterilization subcontractor. The various manufacturers (see list below) attached: format pdf (31/03/2004) (118 ko) - excel format (31/03/2004) (111 ko)) directly informed their customers (end-users) .. Information / Recommendation (31/03 / 2004) (98 ko) of materiovigilance was sent to all the directors of health establishments, local correspondents of materiovigilance and hospital pharmacists.

Device

unkown device
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    medical_device
  • Manufacturer
    N/A

Manufacturer

N/A
  • Source
    LAANSM