Maquet Cardiopulmonary GmbH

5 devices in the database

  • Model / Serial
    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
  • Product Description
    Medical devices for single use
  • Model / Serial
    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
  • Product Description
    Electromechanical medical devices
  • Model / Serial
    Model Number: HCU40 Serial Number: all serial numbers
  • Product Description
    Electromechanical medical devices
  • Model / Serial
    Model Number: HU35 Serial Number: Všechna čísla
  • Product Description
    Electromechanical medical devices
  • Model / Serial
    Model Number: HU35, HCU20, HCU30, HCU40 Serial Number: All Serial Numbers
  • Product Description
    Electromechanical medical devices

15 manufacturers with a similar name

Learn more about the data here

  • 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.
  • Source
    IGJ
  • 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.
  • Source
    IGJ
  • Manufacturer Parent Company (2017)
  • Source
    AMPMDRS
10 more