Device Recall eCare Coordinator

  • Modèle / numéro de série
    453564506091  eCareCoordinator
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution-US Nationwide
  • Description du dispositif
    eCare Coordinator || Product Usage: is software intended for use in data aggregation, patient interaction facilitation, storage and clinical information management with independent physiological devices and ancillary systems that are connected either directly or through networks. The software is intended to provide patient information from the patient location through networking technology to a remote care team. eCare Coordinator does not send any real time alarms and is not intended to provide automated treatment decisions. This software is an informational tool only and is not to be used as a substitute for professional judgment of healthcare providers in diagnosing and treating patients.
  • Manufacturer
  • 1 Event

Fabricant

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

Un dispositif médical avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    453564506091 eCareCoordinator 1.3
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US Distribution -- to the stated of FL, MA, MI, MS, PA, and KS.
  • Description du dispositif
    eCareCoordinator allows the customer to schedule patient tasks (i.e., take weight measurement, take blood pressure). || For medical use by professional medical staff.
  • Manufacturer