Device Recall Philips Intellispace Portal

  • Modèle / numéro de série
    Software release 4.0.0
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- US, including states of IN and TX, and countries of Australia, Austria, Czech, Denmark, France, Germany, Indonesia, Netherlands, Poland, Spain, and Switzerland.
  • Description du dispositif
    Philips Intellispace Portal, Release 4.0.0. || For storing, processing and management of electronic information/data || Model: 881001. || Indicated for use as a diagnostic device.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Philips Medical Systems Nederlands, Veenpluis 4-6, Best Netherlands
  • Société-mère du fabricant (2017)
  • Source
    USFDA