Philips Medical Systems Nederland BV

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 20 건

  • 모델명 / 제조번호(시리얼번호)
    Model: OmniDiagnost Eleva and OmniDiagnost Classic, Affected:
  • 모델명 / 제조번호(시리얼번호)
    Model: Intera 1.5T and Achieva 1.5T., Affected:
  • 모델명 / 제조번호(시리얼번호)
    Model: MultiDiagnost Eleva 708032, MultiDiagnost Eleva with Flat Detector 708034, MultiDiagnost Eleva with Flat Detector 708038, Affected:
  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected: Philips Allura Xper R9 systems and Azurion R1.1 systems
  • 모델명 / 제조번호(시리얼번호)
    Model: , Affected: Allura Xper and Allura CV20 Releases 3 to 8.1 with an installed Laird chiller, Allura Xper Release 8.2: only configurations FD10, FD10/10, FD20/10, FD20/20 have a Laird chiller
하나 더 15 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 12 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • Source
    AEMPSVFOI
  • 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
  • 제조사 모회사 (2017)
  • Source
    MHSIDCCCDMIS
하나 더 7 건 더