Olympus OER-Pro Automated Endoscope Reprocessor Manufactured in 2019

Olympus OER-Pro Automated Endoscope Reprocessor Manufactured in 2019

• Model:OER-Pro
• S/N: 2934789
• Date of Manufacture: 2019-12-11
• Disinfectant compatibility: Supports two dedicated Olympus-validated high-level disinfectants — Acecide-C (peracetic acid based) and ALDAHOL 1.8 (glutaraldehyde based)
• Water supply requirements: Flow ≥ 17 L/min, Pressure 0.1-0.5 MPa, Temperature Max 28 °C, Water Hardness up to 400 ppm
• Dimensions: 18" W × 37-1/2" H × 30" D
• Weight: appx. ~265 lbs.
• Documentation, Operating Manual, Tubing Included
• Warranty: 90 Day

Unlock faster, safer, and more efficient endoscope reprocessing with the Olympus OER-Pro Automated Endoscope Reprocessor. Designed by the same expert engineers who create Olympus endoscopes, this all-in-one system delivers high-level disinfection specifically validated for Olympus flexible scopes and accessories. With its compact footprint — only 18 inches wide — it fits seamlessly into tight procedure-room environments while maintaining the throughput needed for high-volume endoscopy units.

Time is critical in endoscopy workflows, and the OER-Pro rises to the challenge: it can process two flexible endoscopes simultaneously in as little as 26 minutes when paired with the peracetic acid-based Acecide-C disinfectant. By automating 7 of 11 manual cleaning steps, including ultrasonic cleaning, channel flushing, alcohol drying, and leak testing, the system dramatically reduces operator burden and variability, while enhancing infection-prevention quality and documentation.

Built-in RFID tracking records operator ID, scope serial/model numbers, cycle times and results — streamlining traceability and regulatory compliance with minimal added effort. Combined with the flexibility to use two validated disinfectant chemistries (Acecide-C or ALDAHOL 1.8), the OER-Pro offers a future-proof investment for GI, pulmonary and multispecialty endoscopy departments seeking best-in-class reprocessing performance and workflow optimization.

This medical equipment item is being sold in its current condition, with only a basic assessment performed. It powers up and successfully completes its self-check or boot process, indicating that it is operational to that extent. However, no further testing beyond this initial check has been conducted.