Maquet Critical Care Ab

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Description

3 dispositivos en la base de datos

  • Modelo / Serial
    SERVO-I, SERVO-S, SERVO-N, SERVO-U, SERVO-AIR
  • Descripción del producto
    Performs controlled ventilation, assisted and combined in an invasive and non-invasive way in adult, pediatric and neonatal patients who need respiratory volumes of 2ml to 4000ml of tidal volume.
  • Modelo / Serial
    FLOW-i, specific serial
  • Descripción del producto
    Intended for the administration of anesthesia while controlling the complete ventilation of patients with no ability to breathe, as well as in the support of patients with limited ability to breathe.
  • Modelo / Serial
    FLOW-i, serials before 2753
  • Clasificación del producto
  • Descripción del producto
    Intended for the administration of anesthesia while controlling the complete ventilation of patients with no ability to breathe, as well as in the support of patients with limited ability to breathe.

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Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Source
    NIDFSINVIMA
  • Empresa matriz del fabricante (2017)
  • Source
    NZMMDSA
  • Empresa matriz del fabricante (2017)
  • Source
    MSHM
  • Empresa matriz del fabricante (2017)
  • Source
    AEMPSVFOI
  • 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
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