Device Recall ED PulseCheck

  • Modèle / numéro de série
    Software Versions 5.2 and 5.3
  • Classification du dispositif
  • Classe de dispositif
    Unclassified
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution, including the states of: AK, AR, AZ, CA, CO, DC, DE, FL, GA, ID, IN, MA, MD, MO, NH, NJ, OH, OR, SC, TN, WA, and WV.
  • Description du dispositif
    Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Picis Inc., 100 Quannapowitt Parkway, Suite 405, Wakefield MA 01880
  • Société-mère du fabricant (2017)
  • Source
    USFDA