Device Recall ED PulseCheck

  • Modelo / Serial
    Software Versions 5.2 and 5.3
  • Clasificación del producto
  • Clase de dispositivo
    Unclassified
  • ¿Implante?
    No
  • Distribución
    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.
  • Descripción del producto
    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

Fabricante

  • Dirección del fabricante
    Picis Inc., 100 Quannapowitt Parkway, Suite 405, Wakefield MA 01880
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA