ACUTE NEED FOR NEW TECHNOLOGY

  • Current tools struggle with today’s level of endoscope complexity and contamination.
  • Channel cleaning and drying failure rates point to a critical need for new innovation.2,3

Note: The Venturi Clean + Dry Endoscope Channel Cleaning + Drying System are medical devices registered with the United States Food and Drug Administration (FDA) and are intended for sale within the United States only.

Venturi® Clean+DryTM Select Benefits

(  Hover over button to reveal benefit )

Clean Channels

Advanced physics creates unmatched channel cleaning results

Easy to Implement

Human Factors Validated:
Rapid, easy implementation with existing staff techniques

Patient Safety

Fastest way to satisfy infection prevention requirements

Space Saving

No capital expense and no additional real estate/no construction

Dry Channels

Advanced physics dries all channels in minutes

Evidence

Comprehensive validation

Universal Compatibility

Works seamlessly
with leading endoscope 
manufacturers

Operational Efficiency

Accelerates turnaround time, increasing workflow productivity

Want to Know More About
Venturi®
Clean+DryTM?

Exclusive Access Log-In

If you are already registered, you may log in here:

Not registered yet?

For exclusive access, please register first:

Note: Information submitted for Registered Exclusive Access will be governed by GI Scientific’s Privacy Statement which can be reviewed on the Privacy and Legal pages of this website. Exclusive Access is provided at the sole discretion of GI Scientific, LLC.

Register to Access

For exclusive access, please register first:

Note: Information submitted for Registered Exclusive Access will be governed by GI Scientific’s Privacy Statement which can be reviewed on the Privacy and Legal pages of this website. Exclusive Access is provided at the sole discretion of GI Scientific, LLC.

Exclusive Access Log In

If you are already registered, you may log in here:

SOURCES:

  1. “1 in 4 patients exposed to endoscope contamination” is a calculation based on overall flexible endoscopy procedure data (260 million, iData Research, 2024) and published endoscope clean and dry failure rates (3, 4).
  2. Terune, Chad. “Study: Nearly Three-quarters of Commonly Used Medical Scopes Tainted by Bacteria.” American Journal of Infection Control, Apr. 2018, www.fiercehealthcare.com/hospitals-health-systems/study-nearly-three-quarters-commonly-used-medical-scopes-tainted-by.
  3. Ofstead CL, Heymann OL, Quick MR, et al. “Residual moisture and waterborne pathogens inside flexible endoscopes: Evidence from a multi-site study of endoscope drying effectiveness.” Am J Infect Control 2018; https://doi.org/10.1016/j.ajic.2018.03.002
  4. (2025, January 10). Endoscopy Room Incidents Shine Spotlight on Safety, Once Again. Gastroenterology & Endoscopy News. Dr. Klaus Mergener, Affliate Professor of Medicine, University of Washington. Retrieved January 23, 2025, from https://www.gastroendonews.com/Endoscopy-Reprocessing-Infection-Control-and-Operations/Article/12-24/Scope-Safety-Endoscopy-Incidents/75909?ses=ogst AND Rutala WA, Weber DJ. Gastrointestinal Endoscopes: A Need to Shift From Disinfection to Sterilization? JAMA. 2014;312(14):1405–1406. doi:10.1001/jama.2014.12559
  5. (2025, January 10). Endoscopy Room Incidents Shine Spotlight on Safety, Once Again. Gastroenterology & Endoscopy News. Lawrence Muscarella, PhD. Retrieved January 23, 2025, from https://www.gastroendonews.com/Endoscopy-Reprocessing-Infection-Control-and-Operations/Article/12-24/Scope-Safety-Endoscopy-Incidents/75909?ses=ogst