Devices

Device Recall Fujifilm

  • Modelo / Serial
    will be entered.
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Nationwide Distribution
  • Descripción del producto
    Fujifilm Endoscope || Models || ED-250XL5 || ED-250XT5 || ED-450XT5 || ED-450XL5 || Product Usage: || This product is a medical endoscope for the duodenum and upper GI tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach and duodenum. This product is not used for any other purposes.
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
  • 1 Event

Fabricante

Fujifilm Medical Systems U.S.A., Inc.
  • Dirección del fabricante
    Fujifilm Medical Systems U.S.A., Inc., 10 Highpoint Dr, Wayne NJ 07470-7431
  • Empresa matriz del fabricante (2017)
    FUJIFILM Holdings Corp.
  • Source
    USFDA

16 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Fujifilm
  • Modelo / Serial
    2500.0312.00 and 2500.0312.01
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide US and Canada
  • Descripción del producto
    Fujifilm Processor EPX 2500 High Definition Endoscopy; (Sales Brochure). || For use in endoscopic procedures. Used to observe, record and capture images.
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
Device Recall Fujifilm Aspire HD, Full Field Digital, System
  • Modelo / Serial
    Serial Number: 26320119
  • Clasificación del producto
    Radiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed in HI.
  • Descripción del producto
    Aspire HD, Full Field Digital, System, x-Ray, Mammographic; || Model: FOR MS-1000. || A mammography system used for screening and diagnosis of breast cancer.
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
Device Recall Fujifilm Medical Systems
  • Modelo / Serial
    Software Versions: Synapse Cardiovascular v4.0.8 Synapse Cardiovascular v4.0.8 SR1
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution including PR and the states of IL, IN, FL, GA, MD, MI, MO, MS, NC, NY, OR, and PA, PR and the country of Canada.
  • Descripción del producto
    Fujifilm Synapse Cardiovascular I ProSolv CardioVascular || Synapse Cardiovascular v4.0.8 || Synapse Cardiovascular v4.0.8 SR1 || Intended Use: || Picture Archiving and Communication System || Computer, Diagnostic, Programmable
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
Device Recall Fujifilm
  • Modelo / Serial
    Part Numbers: 202B1230408A, 202B1230408B, 202B1230408C, 202B1230408D and 202B1230408E
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide US and Canada
  • Descripción del producto
    Fujinon/Fujifilm Processor EPX 2500 Operation Manual. For use in endoscopic procedures.
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
Device Recall FujiFilm
  • Modelo / Serial
    ED-530XT - Part #202B1237697D; ED-250XT5 and ED-250XL5 - Part #202B1260196A; ED-450XT5 - Part #202B1260211A and ED-450XL5 - Part #202B1237681
  • Clasificación del producto
    Gastroenterology-Urology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Distributed in the US and Canada.
  • Descripción del producto
    Fujifilm Medical Endoscope for the duodenum and upper G.I. tract. ED-530XT, ED-250XT5, ED-250XL5, ED-450XT5, and ED-450XL5 Endoscope Operation Manuals.
  • Manufacturer
    Fujifilm Medical Systems U.S.A., Inc.
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