Becton, Dickinson & Company

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 5 건

  • 모델명 / 제조번호(시리얼번호)
    443376
  • 제품 설명
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • 모델명 / 제조번호(시리얼번호)
    443710
  • 제품 설명
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • 모델명 / 제조번호(시리얼번호)
    221606, 221607 | 4042455, 4067180, 4087204, 4127564
  • 제품 설명
    IVD: Culture medium, transport

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 22 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • 제조사 의견
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
  • 제조사 모회사 (2017)
  • 제조사 의견
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
하나 더 17 건 더