Devices

Device Recall Agfa IMPAX Cardiovascular

  • Modelo / Serial
    Versions CV 12.2 SU3, CV 12.2 SU4, CV 12.2 SU5 and CV 12.2 SU6
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution to NJ, NC, OH, PA, SC, TN, TX, and WI
  • Descripción del producto
    IMPAX Cardiovascular || The IMPAX CV Reporting module consists of a database and graphical user interface (GUI) that allows users to document procedure and clinical findings as structured data, with representation in printed or electronic formats
  • Manufacturer
    AGFA Healthcare Corp.
  • 1 Event

Fabricante

AGFA Healthcare Corp.
  • Dirección del fabricante
    AGFA Healthcare Corp., 10 S Academy St, Greenville SC 29601-2632
  • Empresa matriz del fabricante (2017)
    Agfa-Gevaert NV
  • Source
    USFDA

Dispositivo con un nombre similar

Más información acerca de la data acá

Device Recall Agfa IMPAX CardioVascular Suite Results Management
  • Modelo / Serial
    Software Versions: 2.04.17, 2.04.19 and 2.04.20.
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide to five hospitals in DC, NY, OH, TN, and VA.
  • Descripción del producto
    Agfa IMPAX CardioVascular Suite Results Management Nuclear Reporting Module, Outbound Report, Model/Catalog No.: L7W1P, Software Versions: 2.04.17, 2.04.19 and 2.04.20, AGFA HealthCare, Westerly, RI
  • Manufacturer
    AGFA Corp.