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Fujifilm Medical Systems USA Inc.

Division of Fujifilm Holdings Corp.
www.fujifilmusa.com

Latest From Fujifilm Medical Systems USA Inc.

US FDA Says Custom Ultrasonics Device May Be Used To Disinfect Certain Duodenoscopes

Custom Ultrasonics' System 83 Plus automated endoscope reprocessors may now be used to disinfect specific models of Olympus and Pentax duodenoscopes, FDA says.

Regulation Recalls

FDA Warning Letters For Olympus, Fujifilm, Pentax: Duodenoscope-Makers Fail To Meet Agency's Post-Market Surveillance Study Order

US FDA sent the letters to

FDA Enforcement

New Duodenoscope Protocols Released

US FDA, CDC and medical groups joined forces to develop safer handling standards for the endoscope equipment, which has been tied to infection outbreaks.

Regulation Safety

Easier-To-Clean Duodenoscope Gets US FDA Clearance

The device from Pentax features a disposable distal cap, thus cutting the risk of infection transmission between patients. An earlier Pentax duodenoscope model was the subject of an infection-related safety alert in January.

Safety Approvals
See All

Company Information

  • Industry
  • Medical Devices
    • Diagnostic Imaging Equipment & Supplies
      • Digital Imaging
      • X-ray
  • Therapeutic Areas
  • Non-Specific
  • Alias(es)
  • Ownership
  • Private
  • Headquarters
  • Worldwide
    • North America
      • USA
  • Parent & Subsidiaries
  • Fujifilm Holdings Corp.
  • Senior Management
  • Naohiro Fujitani, Pres. & CEO
    Yujiro Nagasawa, VP, Fin. & Bus. Ops.
  • Contact Info
  • Fujifilm Medical Systems USA Inc.
    Phone: (203) 324-2000
    419 West Ave.
    Stamford, CT 06902
    USA
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