Olympus Announces Market Launch of EVIS X1 Endoscopy System

Olympus Corporation, a global medical technology company committed to making people’s lives healthier, safer and more fulfilling, announced today the market launch of its next-generation EVIS X1™ endoscopy system, which will be on display and demonstrated Oct. 22-24 during the American College of Gastroenterology (ACG) annual meeting in Vancouver, Canada.

Richard Reynolds, President of the Medical Systems Group for Olympus America, Inc.

“Olympus is thrilled to bring our most advanced endoscopy system to GI practitioners in the U.S. The remarkable new technologies for visualizing the GI tract are designed to help physicians see more and do more to help their patients.”

The EVIS X1 endoscopy system received clearance earlier this year along with two compatible endoscopes: the GIF-1100 gastrointestinal videoscope indicated for use within the upper digestive tract and the CF-HQ1100DL/I colonovideoscope indicated for use within the lower digestive tract. The ErgoGrip control section of these endoscopes is 10% lighter than Olympus’ previous generation, and they are designed to increase user comfort and scope handling and to accommodate users with small hands.1

Features of the EVIS X1™ endoscopy system include:

  • Texture and Color Enhancement Imaging (TXI™) technology is designed to increase the visibility of lesions and polyps by enhancing image color and texture during endoscopic screening. 2
  • Red Dichromatic Imaging (RDI™) technology is designed to enhance the visibility of deep blood vessels and bleeding points.
  • Brightness Adjustment Imaging with Maintenance of Contrast (BAI-MAC™) technology is designed to correct the brightness levels in dark areas of the endoscopic image, while maintaining the brightness of lighter areas, to increase the total distance view.3
  • Narrow Band Imaging™ (NBI™) technology continues to be featured in the EVIS X1 endoscopy system. NBI technology enhances visual observation of mucosal and vascular patterns by utilizing specific blue and green wavelengths absorbed by hemoglobin.
  • Streamline procedures: The touch panel on the CV-1500 video system center allows the user to initiate all procedures and settings and control image data from one device.4
  • MyCV mode: MyCV mode allows a physician to personalize imaging configurations and turn multiple functions off and on with a single scope button.

TXI, RDI, BAI-MAC and NBI technologies are not intended to replace histopathological sampling as a means of diagnosis. These are adjunctive tools for endoscopic examination that can be used to supplement Olympus white light imaging.

Olympus® GI endoscopy systems are used by physicians to help them to diagnose, treat, and observe diseases and disorders of the upper and lower GI tract such as acid reflux, ulcers, Crohn’s disease, Celiac disease, and colorectal cancer (CRC). An endoscope is commonly used during a screening colonoscopy, when a gastroenterologist examines the lining of the colon and may remove any potentially cancerous growths, known as polyps. The addition of new imaging technologies in the EVIS X1 endoscopy system may help physicians to visualize these abnormalities.

CRC represents the third most common cancer diagnosis for men and women with an estimated 153,000 cases diagnosed annually, according to the American Cancer Society.5 CRC is a preventable and treatable disease, however, with a 5-year survival rate of up to 91%, if caught at a localized stage.6

For more information, visit the EVIS X1 endoscopy system page. For a demonstration, visit the Olympus booth #911 at ACG. Live demonstrations of the new imaging technologies will be offered during ACG 5 p.m. Oct. 22 and 11 a.m. Oct. 23-24. Visit the Olympus website for information on the entire gastroenterology portfolio.

As a leading medical technology company, Olympus uses innovative capabilities in medical technology, therapeutic intervention, and precision manufacturing to help healthcare professionals deliver diagnostic, therapeutic, and minimally invasive procedures to improve clinical outcomes, reduce overall costs, and enhance the quality of life for patients. Olympus’ portfolio includes endoscopes, laparoscopes, and video imaging systems, as well as surgical energy devices, system integration solutions, medical services, and a wide range of endotherapy instruments. For more information, visit medical.olympusamerica.com.

1 Data on file with Olympus (DC00482729, DC00600786, DC00031984, DC00482747, DC00482867, DC00600794, DC00481878, DC00031984 and DC00841888).
2 Data on file with Olympus (D00489968).
3 Data on file with Olympus (DC00436067).
4 Data on file with Olympus (DC00460933).
5 American Cancer Society, “Key Statistics for Colorectal Cancer.” Rev. January 2023.
6 American Cancer Society, “Survival Rates for Colorectal Cancer.” Rev. March 2023.

Hot this week

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”

Avery Dennison Medical Introduces Ipdated SilFoam Lite: Sustainability, MDR Certification & Performance Improvements

The newly enhanced SilFoam Lite delivers superior efficiency and reliability, bringing improved fluid handling capabilities and improved tack. These improvements make the product ideal for customers seeking quality, high-performance solutions in wound care notes Avery Dennison Medical.

Voluntary Recall Notifying Medtronic Insulin Pump Users of Potential Risks of Shortened Pump Battery Life

Medtronic plc voluntarily issued a field action starting on July 31, 2024, notifying global customers of its MiniMed™ 600 series or 700 series insulin pumps to follow their pump's built-in alerts and alarms for battery status and to contact Medtronic if they observe changes in the battery life of their pump