Maquet Cardiopulmonary GmbH

5 dispositivos en la base de datos

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

15 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
  • Empresa matriz del fabricante (2017)
  • Source
    BAM
  • Empresa matriz del fabricante (2017)
  • Source
    AMPMDRS
  • Empresa matriz del fabricante (2017)
  • Source
    SMPA
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