CARDIOSAVE Hybrid Intra-Aortic Balloon Pump


  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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.
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12 devices with a similar name

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  • Model / Serial
    Model Number: 0998-00-0800-XX and 0998-UC-0800-XX (excluding 0998-00-0800-83, 0998-UC-0800-83 & 0998-00-0800-75)
  • Product Classification
  • Product Description
    Medical devices for single use
  • Manufacturer
  • Model / Serial
  • Product Description
    Maquet: Cardiosave Hybrid intra-aortic balloon pump
  • Manufacturer
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