Philips Medical Systems Nederland BV

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 5 건

  • 모델명 / 제조번호(시리얼번호)
    Model Number: 722026; 722027; 722028; 722029; 722033; 722034; 722035; 722038; 722039; 722058; 722059 with release R8.2 (Allura Xper) or R1.0 (UNIQ)
  • 제품 설명
    Medical devices for diagnostics and radiation therapy
  • 모델명 / 제조번호(시리얼번호)
    Model Number: 708032, 708033, 708034, 708036, 708037, 708038
  • 제품 설명
    Medical devices for diagnostics and radiation therapy
  • 모델명 / 제조번호(시리얼번호)
    Model Number: 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029, 722031, 722033, 722034, 722035, 722038, 722039, 722058 and 722400.
  • 제품 설명
    Medical devices for diagnostics and radiation therapy
  • 모델명 / 제조번호(시리얼번호)
    Model Number: 722010, 722011, 722012, 722013, 722022, 722023, 722024, 722025
  • 제품 설명
    Medical devices for diagnostics and radiation therapy
  • 모델명 / 제조번호(시리얼번호)
    Catalog Number: See UAL Model Number: 722010, 722011, 722012, 722013, 722022, 722023, 722024, 722025 and all other eventual model numbers mentioned on the Unit Affected List.
  • 제품 설명
    Medical devices for diagnostics and radiation therapy

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

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 모회사 (2017)
  • Source
    NZMMDSA
  • 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
하나 더 7 건 더