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2 Cubic Feet Ethylene Oxide Sterilizer

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2 Cubic Feet Ethylene Oxide Sterilizer
2 Cubic Feet Ethylene Oxide Sterilizer | Compact EO Gas Sterilizer for Hospitals & OEMs `

2 Cubic Feet Ethylene Oxide Sterilizer

The 2 cubic feet Ethylene Oxide (EO) sterilizer is a compact, high-efficiency chamber engineered for hospitals, clinics, laboratories, and OEM pilot lines that need validated low-temperature sterilization without the footprint of large industrial systems. Despite its small size, the 2 cu ft chamber supports deep EO penetration through breathable packaging and complex geometries such as lumens, narrow channels, and mixed-material assemblies. Typical users deploy it for endoscopy accessories, catheter kits, sensor cables, power-tool components, and small, electronics-bearing surgical instruments that are not compatible with steam or high-moisture methods.

Built around ISO 11135 principles, the unit offers repeatable pre-conditioning, controlled EO exposure, and reliable post-cycle aeration. Automated parameter control and event logging improve compliance, while cartridge-based dosing options available on many models simplify gas handling and reduce operator interaction. For facilities scaling from trial to routine use, the 2 cu ft platform provides a predictable path to larger capacities, keeping validation and workflow concepts consistent.


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Working Principle and Process Flow for 2 cu ft EO Chambers

Devices are first cleaned, dried, and packaged in EO-compatible pouches or wraps. Inside the 2 cu ft chamber, pre-conditioning brings the load to target temperature and humidity so that EO can interact effectively with microorganisms. During exposure, EO gas diffuses through porous packaging, along channels and interfaces, and into hard-to-reach surfaces to disrupt cellular metabolism and reproduction. The load then undergoes aeration to reduce residual gas to acceptable levels before release. Throughout the cycle, sensors track temperature, humidity, pressure, and time; operators confirm performance using chemical and biological indicators at defined frequencies.

Because the internal volume is modest, smaller batches turn around quickly and utility consumption is comparatively lower. Controlled load patterns, validated packaging, and documented parameters keep outcomes consistent from cycle to cycle, making the 2 cu ft size ideal for departmental CSSD work, R&D builds, and specialty contract sterilization runs.


Variants and Configurations

  • Hospital/CSSD 2 cu ft Units with preset cycles for common device families and auto documentation.
  • Cartridge-Dosed Chambers enabling precise EO delivery and simplified handling for small batches.
  • 2 cu ft Chambers with Integrated Aeration to streamline throughput and reduce room requirements.
  • OEM/Pilot Configurations tailored for validation lots, engineering builds, and new product introduction.

Key Features and Specifications

  • Chamber Volume: approximately 2 cubic feet suitable for small trays, pouches, and accessory sets.
  • Low-Temperature Operation protecting plastics, elastomers, adhesives, optics, and electronics.
  • Validated Cycles aligned with ISO 11135 concepts, compatible with biological indicator programs.
  • Parameter Monitoring with data logging for temperature, humidity, pressure, and exposure time.
  • Safety Architecture including interlocks, gas detection readiness, and door-lock mechanisms.
  • Terminal Sterilization in breathable packaging to maintain sterility until point of use.

Typical Applications of a 2 cu ft EO Sterilizer

  • Endoscopy valves, light cables, biopsy accessories, and flexible scope components compatible with EO.
  • Catheters, tubing sets, connectors, and small patient-contact devices requiring low temperature processing.
  • Electronics-bearing surgical tools, battery modules, sensors, and delicate cable assemblies.
  • R&D and pilot OEM lots for single-use device components and implant packaging trials.

Benefits of the 2 cu ft Format

  • Compact Footprint for hospitals and labs with limited space, while maintaining validated performance.
  • Fast Turnaround on small batches supporting urgent case needs and engineering evaluations.
  • Material Preservation thanks to gentle temperature and controlled humidity compared with steam.
  • Traceable Compliance via routine BI/CI use and automatic cycle record storage.

Manufacturers and Support Options

Qualified suppliers provide site assessment, installation, IQ/OQ/PQ support, and preventive maintenance tailored to 2 cu ft chambers. Training for operators and supervisors covers load preparation, indicator use, aeration practices, and safety procedures. Facilities often pair the sterilizer with dedicated storage and labeling standards so that sterile inventory remains organized and audit-ready.


Maintenance and Safety Tips

  • Use only EO-compatible packaging and avoid over-packing; follow validated load patterns for the 2 cu ft volume.
  • Verify dryness of lumened devices to optimize EO diffusion and reduce residuals.
  • Place biological indicators in worst-case locations per your validation map and trend results over time.
  • Calibrate sensors at defined intervals and review cycle reports for parameter drifts.
  • Ensure adequate ventilation and PPE; conduct periodic safety drills for EO handling and alarm response.


FAQs – 2 Cubic Feet Ethylene Oxide Sterilizer

1. What types of loads fit best in a 2 cu ft chamber? +
Pouched sets, small trays, cable assemblies, catheters, and endoscopic accessories are ideal. Follow your validated load matrix for density and orientation.
2. Can I achieve terminal sterilization with a 2 cu ft unit? +
Yes. EO permeates breathable packaging, enabling terminal sterilization and sterile shelf life when packaging and cycles are validated appropriately.
3. How do I manage residual EO safely on small batches? +
Use defined aeration times and conditions, verify with residual testing when required, and release loads only after meeting acceptance criteria.
4. Are cartridge-based systems suitable for 2 cu ft chambers? +
Cartridge dosing is common in this size and supports precise EO delivery with simplified handling. Follow the manufacturer’s IFU and safety procedures.
5. Which standards should I reference during validation and routine use? +
Align your process with ISO 11135 concepts, use biological and chemical indicators routinely, and maintain complete cycle and maintenance records for audits.

Contact Details

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