St Jude Medical CRMD

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 44 건

  • 모델명 / 제조번호(시리얼번호)
    All lots with a manufacturing date of May 30, 2006 or earlier
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • 제품 설명
    CPS Aim, Models 410140, 410141, 410142, 410144, 410145, 410146, 410147, & 410148
  • 모델명 / 제조번호(시리얼번호)
    All lots with a manufacturing date of May 30, 2006 or earlier
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • 제품 설명
    CPS Implant Kit, Model 410190
  • 모델명 / 제조번호(시리얼번호)
    All lots with a manufacturing date of May 30, 2006 or earlier
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • 제품 설명
    CPS Valve Bypass Tool (VBT), Model 410192
  • 모델명 / 제조번호(시리얼번호)
    All lots with a manufacturing date of May 30, 2006 or earlier
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • 제품 설명
    CPS Slitter, Model 410191
  • 모델명 / 제조번호(시리얼번호)
    All lots with a manufacturing date of May 30, 2006 or earlier
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Hospitals/Medical Centers in AZ, CA, MS, NY, & PA
  • 제품 설명
    CPS Direct SL, Models 410110, 410111, 410112, 410113, 410114, 410115, 410116, 410120, 410121, 410122, 410123, 410124, 410125, & 410126
하나 더 39 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 2 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • 제조사 의견
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    SMPA