Maquet Critical Care Ab

3 dispositifs dans la base de données

  • Modèle / numéro de série
    SERVO-I, SERVO-S, SERVO-N, SERVO-U, SERVO-AIR
  • Description du dispositif
    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.
  • Modèle / numéro de série
    FLOW-i, specific serial
  • Description du dispositif
    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.
  • Modèle / numéro de série
    FLOW-i, serials before 2753
  • Classification du dispositif
  • Description du dispositif
    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.

23 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Source
    NIDFSINVIMA
  • Société-mère du fabricant (2017)
  • Source
    NZMMDSA
  • Société-mère du fabricant (2017)
  • Source
    MSHM
  • Société-mère du fabricant (2017)
  • Source
    AEMPSVFOI
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    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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