ED 250 Series
Vertical Storage with Traceability - up to 18 Flexible Endoscopes
This Series of drying cabinets with vertical storage protects reprocessed endoscopic instruments from the risk of contamination before reuse. It ensures adequate drying and storage of endoscopes by blowing filtered air through endoscope channels and on their external surfaces. Endoscopes are connected to the drying circuit through specific CPC connectors.
The ED 250 Series is available in different storage configurations: with a single cabinet or a side-by-side double cabinet module, in both single- and double-door versions. The former version allows the drying and storage of up to 9 endoscopes, the latter of up to 18 endoscopes. Barcode/RFID systems and printer for logging scopes in and out to ensure full tracking are available upon request.
Microbiological Integrity
Microorganisms can grow to an unsafe amount within a few hours. Our range of drying cabinets protects reprocessed endoscopes from the risk of contamination by drying them thoroughly and by maintaining microbiological integrity up to 720 hours.
Independently validated.
Complete Endoscope Reprocessing Traceability
Our whole range of endoscope reprocessing devices is compatible with SD Ares, the traceability software specially developed for the endoscope reprocessing process. SD Ares software is designed to meet the endoscopy room’s operational requirements by promptly tracking scopes and providing information to maintain safety, efficiency, and high production.
Features
Configurable
The ED 250 Series is available with different storage configurations: with a single cabinet or a side-by-side double cabinet module, with single or double interlocked doors.
Flexible Solution
Drying and storage of up to 9 endoscopes in the single-cabinet version or up to 18 endoscopes in the double-cabinet one.
Safe
Convenient guides ensure correct endoscope hanging, thus avoiding damage and providing correct airflow around and through endoscopes.
Ergonomic
The sliding holder design allows easy access from either side of the cabinet in a compact footprint.
Optimal Drying
High-quality air drying circuit for a homogeneous heat distribution inside the storage chamber. Maximum safety with HEPA H14 filter.
Full Traceability
Faster endoscope and operator recognition through the barcode / RFID reader option. Cycle details can be printed by the built-in thermal printer or alternatively registered in the optional SD Ares traceability software.
Configurations
ED 250 Single Cabinet
Simultaneous drying and storage of up to 9 endoscopes. Technical compartment on the right side of the device.
Single Door Version
Overall dimensions WxDxH
968 x 810 x 2270 mm
38.11 x 31.89 x 89.37 in
Double Door Version
Overall dimensions WxDxH
968 x 845 x 2270 mm
38.11 x 33.27 x 89.37 in
ED 250 Double Cabinet
Simultaneous drying and storage of up to 18 endoscopes. Double cabinet in a unique frame structure sharing the technical compartment in the middle. It allows for space optimization and workflow maximization.
Single Door Version
Overall dimensions WxDxH
1705 x 810 x 2270 mm
67.13 x 31.89 x 89.37 in
Double Door Version
Overall dimensions WxDxH
1705 x 845 x 2270 mm
67.13 x 33.27 x 89.37 in
Solutions
Endoscope Reprocessing
The safest patient care and infection prevention for endoscopy and CSSDs departments, regardless of their size and application focus. With one of the broadest portfolios for endoscope reprocessing, SteelcoBelimed covers the entire workflow of endoscope reprocessing from pre-cleaning to storage.
Services
Digitalization in Healthcare
The future is smart. Smart systems in CSSDs work flawlessly, informing you well in advance when an error occurs or a repair is needed. Plan your operations with more precision than ever, consequently reducing costs and improve efficiency.
Digitalization also helps track and trace instruments and sets, so to be sure they have been correctly reprocessed inside your CSSD or outside in big reprocessing centers.
Steelco-branded drying cabinets are designed to comply with the European EN 16442 guidelines on performance, EN ISO 14971, EN 61010-1/2-010, EN IEC 61326-1 and EN 62366 guidelines on safety, and EN 62304 guidelines on software design. They are classified CE medical devices (Regulation 2017/745/EU, MDR).
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