Enterprise Imaging for Radiology

Fabricant

  • 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

4 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    -Enterprise Imaging for Radiology 8.0.0, 8.0.0 SP1 & 8.0.0 SP2. -Enterprise Imaging for Radiology 8.0.1, 8.0.1 SP1, 8.0.1 SP2, 8.0.1 SP3, 8.0.1 SP4, 8.0.1 SP5 & 8.0.1 SP6. -Enterprise Imaging for Radiology 8.1, 8.1 SP1 & 8.1 SP2.
  • Description du dispositif
    Radiology
  • Manufacturer
  • Modèle / numéro de série
    • Enterprise Imaging for Radiology 8.0.0, 8.0.0 SP1 & 8.0.0 SP2. • Enterprise Imaging for Radiology 8.0.1, 8.0.1 SP1, 8.0.1 SP2, 8.0.1 SP3, 8.0.1 SP4, 8.0.1 SP5 & 8.0.1 SP6. • Enterprise Imaging for Radiology 8.1, 8.1 SP1 & 8.1 SP2.
  • Description du dispositif
    Unified imaging platform
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    Agfa Healthcare: Enterprise Imaging for Radiology
  • Manufacturer
  • Modèle / numéro de série
  • Manufacturer