Greater Control of channel cleaning
Remove inconsistencies and produce repeatable results
CORIS is an automated endoscope channel cleaner that empowers reprocessing staff to take greater control over scope turnaround time and demand management by removing the inconsistencies in the manual cleaning workflow. The system uses multiple sensors and an algorithm to accurately control a validated cleaning cycle that ensures consistent and repeatable cleaning results.
Simplicity of Operation
Ease of use and hands-off time helps make cleaning endoscope channels simpler
CORIS enables staff to quickly connect an endoscope, start a cleaning cycle and leverage the time they are not brushing and flushing to focus on other tasks or endoscopes, potentially improving their workflow and throughput.
CORIS UI animation with connection steps
Features At-A-Glance
CORIS is equipped with both RFID and Barcode readers to scan endoscopes and streamline the selection of adaptors and accessories.
Based on the endoscope being cleaned (as determined by the RFID/Barcode) CORIS selects the appropriate cleaning cycle and provides the expected duration to the user.
Dedicated adaptors equipped with RFID technology identify the correct adaptor for the scope being cleaned. The colour coded connectors have been designed to be easy to connect but firm enough to prevent disconnection and leakage while the physical cleaning agent is delivered.
The system constantly monitors for cycle status and alerts users via visual and audible alarms when action is required.
At the end of each cleaning cycle users will be presented with the pass/fail information to confirm.
1. Moshkanbaryans L, Shah V, Tan LY, et al. Comparison of two endoscope channel cleaning approaches to remove cyclic build-up biofilm. J Hosp Infect. 2024;150:91-95. doi:10.1016/j.jhin.2024.05.014
2. Roberts CG. The role of biofilms in reprocessing medical devices. Am J Infect Control. 2013 May;41(5 Suppl):S77-80. doi: 10.1016/j.ajic.2012.12.008.
3. Kovaleva J Infectious complications in gastrointestinal endoscopy and their prevention. Best Pract Res Clin Gastroenterol. 2016 Oct;30(5):689-704.
4. Ren-Pei et al. Correlation between the growth of bacterial biofilm in flexible endoscopes and endoscope reprocessing methods. Am J Infect Control. 2014 Nov;42(11):1203-6.
5. Ribeiro MM, Graziano KU, Olson N, França R, Alfa MJ. The polytetrafluoroethylene (PTFE) channel model of cyclic-buildup biofilm and traditional biofilm: The impact of friction, and detergent on cleaning and subsequent high-level disinfection. Infect Control Hosp Epidemiol. 2020; 41(2):172-180.
6. Qiu L, Zhou Z, Liu Q, Ni Y, Zhao F, Cheng H. Investigating the failure of repeated standard cleaning and disinfection of a Pseudomonas aeruginosa-infected pancreatic and biliary endoscope. Am J Infect Control 2015;43:e43–e46
7. Simulated Use Testing Data on File
8. CL528
9. Ofstead, C. L., Hopkins, K. M., Smart, A. G. & Brewer, M. K. Droplet dispersal in decontamination areas of instrument reprocessing suites. Am J Infect Control 50, 126–132 (2022).
10. Data on file – CL536
11. Data on file - CL535
* CTS = Combination Test Soil and cATS = Artificial Test soil with 20% coagulated blood.
** ISO 15883-5:2021. Washer-disinfectors - Part 5: Performance requirements and test method criteria for demonstrating cleaning efficacy. International Organization for Standardization; 2021. AAMI ST98:2022. Cleaning and Sterilization of Medical Devices. Association for the Advancement of Medical Instrumentation; 2022.
