The EW 1 S Series of automatic endoscope reprocessors is designed for low-temperature washing and high-level disinfection/liquid sterilization of endoscopes. Its capacity differs depending on the scopes to reprocess: one flexible or rigid endoscope, up to three broncho/cystoscopes.
The device is compatible with the One-Time Connection System (OCS) technology – a single connection system shared among pre-washing, washing/disinfection, and drying/storage devices. In this model, the OCS connector is automatically coupled through a pneumatic piston located on the top of the washing chamber.
Available as single door or double door pass-through versions, it can also perform thermal self-disinfection. An RFID system for endoscopes and operators’ recognition enables a touchless cycle activation.
Service accessibility from the front for a smaller footprint and easier maintenance even in pass-through installations.
Treatment of one standard flexible endoscope, up to two video bronchoscopes/cystoscopes, and up to three fiber bronchoscopes/cystoscopes. Rigid endoscopes can also be reprocessed.
Smaller footprint on a bigger chamber and washing cart dimensions in comparison with EW 1 S Series.
Process chemicals, their lot number, and expiry date are identified via RFID – a critical safety application to make sure that only validated chemicals will be used in order to comply with ISO 15833-4 requirements.
Doors open automatically via a foot pedal or RFID sensor. Hands-free endoscope loading and unloading operations ensure higher operator safety.
Service accessibility from the front allows for easier maintainance activities and a reduced footprint.
Faster endoscope and operator recognition through barcode/RFID reader options. Cycle details can be printed by the built-in thermal printer or alternatively registered in the optional traceability software.
Steelco-branded endoscope reprocessors are designed to comply with the European EN ISO 15883-1/4/5 and EN ISO 14937 guidelines on performance, EN ISO 14971, EN 61010-1/2-040, EN IEC 61326-1, EN 62366 guidelines on safety, and EN 62304 guidelines on software design. They are classified CE0051 legacy medical devices (Directive 93/42/EEC, MDD).
Single and Double Door Version
Overall Dimensions WxDxH
650 x 587 x 1850 mm
25.59 x 23.11 x 72.83 in