Device Recall Philips eCareManager System

  • Modèle / numéro de série
    v3.7, v3.7.1, v3.8
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution (USA) including states of MA, MO, WI, AR, AZ, PA, SD, VA, and IN.
  • Description du dispositif
    Philips eCareManager System, Model 865325, software versions 3.7, 3.7.1 and 3.8. || Product Usage: The Philips eCareManager System software is intended for use in data collection, storage, and clinical information management with independent bedside devices and ancillary systems that are connected either directly or through networks. The eCareManager system provides patient information and surveillance of monitored patients at the point of care location and at a remote, supplementary care location through wide area networking technology and dedicated phone lines and is solely intended for use in a hospital environment. It is not intended to be used in a home environment.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Visicu, Inc., 217 E Redwood St Ste 1900, Baltimore MD 21202-3315
  • Société-mère du fabricant (2017)
  • Source
    USFDA