Events

LPS FLEX PRECOAT FEMORAL A-L 에 대한 현장 안전성 서한

Turkey Drugs and Medical Devices Agency (Titck)에 따르면, 해당 현장 안전성 서한 는 Turkey 에서 Zimmer Inc. 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
    Field Safety Notice
  • 사례 ID
    2016/169 & ZFA 2015-180
  • 날짜
    2016-02-22
  • 사례 국가
    Turkey
  • 사례 출처
    TDMDAT
  • 사례 출처 URL
    https://web.archive.org/web/20170817145621/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-169%20SGB.pdf
  • 비고 / 경고
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • 데이터 추가 비고

Device

LPS FLEX PRECOAT FEMORAL A-L
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Class III
  • Manufacturer
    Zimmer Inc.

Manufacturer

Zimmer Inc.
  • 제조사 모회사 (2017)
    Zimmer Biomet Holdings
  • 제조사 의견
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    TDMDAT