Maquet Cardiopulmonary GmbH

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 5 건

  • 모델명 / 제조번호(시리얼번호)
    Model Number: viz FSN Batch Number: All Lot numbers for the affected timeframe: • for non-coated Arterial Cannulae (Class IIa) the shelf life is defined for 3 years, therefore the affected timeframe is March 2015 up to now • for all coated Arterial Cannulae (Class III) the shelf life is defined for 2 years, therefore the affected timeframe is March 2016 up to now
  • 제품 설명
    Medical devices for single use
  • 모델명 / 제조번호(시리얼번호)
    Model Number: 70101.0892; 70101.0895; 70101.0896; 70102.8717; 70101.7239; 70102.2333; 70102.2336; 70102.8718; 70103.4642; 70103.4653;70103.4371 Serial Number: All
  • 제품 설명
    Electromechanical medical devices
  • 모델명 / 제조번호(시리얼번호)
    Model Number: HCU40 Serial Number: all serial numbers
  • 제품 설명
    Electromechanical medical devices
  • 모델명 / 제조번호(시리얼번호)
    Model Number: HU35 Serial Number: Všechna čísla
  • 제품 설명
    Electromechanical medical devices
  • 모델명 / 제조번호(시리얼번호)
    Model Number: HU35, HCU20, HCU30, HCU40 Serial Number: All Serial Numbers
  • 제품 설명
    Electromechanical medical devices

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 15 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 10 건 더