Devices

Device Recall Regius

Fabricante

Konica Minolta Medical Imaging USA, Inc.
  • Dirección del fabricante
    Konica Minolta Medical Imaging USA, Inc., 411 Newark Pompton Tpke, Wayne NJ 07470-6657
  • Source
    USFDA

2 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Regius
  • Modelo / Serial
    All serial numbers.
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    These units have been distributed to hospitals and clinics nationwide.
  • Descripción del producto
    Regius-IM. The Regius Image Manager for Centralized workflow and improved image quality software.
  • Manufacturer
    Konica Medical Imaging, Inc.
Device Recall REGIUS IM, RIM
  • Modelo / Serial
    58 units distributed between June 2003 and January 2006. Software version prior to January 31, 2006.
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The units were distributed to hospitals nationwide through the firm''s sales force and resellers. There are no government accounts.
  • Descripción del producto
    REGIUS Image Manager (AKA REGIUS IM, RIM). Catalogue Number 5900554. Centralized CR Image Quality Control. Patient throughput optimization via offloaded processing from various CR readers. Technologist review and audit. Key processing for specialized exams, totally automated processing for hands off operation. Centralized workflow device for dispersed readers environments. HIS/RIS patient status updates. Demographic Correction.
  • Manufacturer
    Konica Minolta Medical Imaging USA, Inc.