Philips Medical Systems Nederland BV

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 9 건

  • 모델명 / 제조번호(시리얼번호)
    722001, 722002, 722003, 722010, 722026, 722005, 722011, 722027, 722006, 722012, 722028, 722008, 722013, 722015, 722023, 722035, 722020, 722029, 722038, 722039, 722058, 722059 | See UAL
  • 제품 설명
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • 모델명 / 제조번호(시리얼번호)
    722063 (Azurion 3 M12), 722064 (Azurion 3 M15), 722065 (Allura R9 7 M12), 722066 (Allura R9 7 M20), 722078 (Azurion 7 M12), 722079 (Azurion 7 M20) | Allura Xper R9 and Azurion R 1.1
  • 제품 설명
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • 모델명 / 제조번호(시리얼번호)
    see letter
  • 제품 설명
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • 모델명 / 제조번호(시리얼번호)
    72247, 722043, 722001, 722002, 722003, 722005, 722006, 722008 | 989000070011, 989000070122, 989000070123, 989000070124, 989000070125, 989000070126 or 989000070321
  • 제품 설명
    MD: Stationary general-purpose fluoroscopic x-ray system, analogue
  • 모델명 / 제조번호(시리얼번호)
    881005 | see FSN | IntelliSpace Portal V.6.5
  • 제품 설명
    MD: Food tray, single-use
하나 더 4 건 더

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