STERIS System 1 Overview
The STERIS System 1 is a state-of-the-art automated processor dedicated to ensuring effective and standardized sterile processing of medical devices. Engineered with a microcomputer control system, it maintains crucial process parameters within an environmentally sealed chamber, creating optimal conditions for sterilization. The device is specifically designed to adhere to the safe temperature limits recommended by most manufacturers, thereby protecting heat-sensitive instruments throughout the processing cycle.
Key Features
Upon completion of each sterilization cycle, the STERIS System 1 generates a comprehensive printout, delivering vital documentation of the process and load information.
The system accommodates a diverse range of devices and procedure-specific sets thanks to its specialized processing trays and containers. These are meticulously crafted to position devices correctly, ensuring a continuous exchange of sterilant and rinse on all exposed surfaces, including internal structures and lumens. Moreover, the design helps to safeguard sensitive devices from potential environmental contamination during transportation to the sterile field.
Specifications
Space and Weight Requirements:
Electrical Requirements:
- 120 VAC nominal, 60 Hz, 15A
- 230 VAC nominal, 50 Hz, 7 A delayed fuse
- 120 Volt, 20 amp., 60 Hz dedicated circuit (hospital grade)
- 230 Volt, 10 amp, 50 Hz dedicated circuit with FI safety switch (2-5 mA)
Water Requirements:
- Pressure: 40 - 50 psig (2.8 - 3.5 bar)
- Flow Rate: 4 gpm (15 Lpm) at 40 psig (2.8 bar)
- Temperature: 110 - 118°F (43 - 48°C), preferred at 115 - 118°F (46 - 48°C)
- Supply Line Size: 1/2" 1.0 minimum
- Connection: 3/4" male hose connector
- Quality: Potable/tap water
- Drain: 1 1/4" 1.0 (minimum) non-backpressuring drain
- Water usage: Approximately 13.3 gal (50 L) per sterile processing cycle
Environmental Requirements:
- Room Temperature: 60 - 90°F (15.5 - 32°C)
- Humidity: 10 - 90% relative, non-condensing
Conclusion
The STERIS System 1 stands out as an essential tool for any healthcare facility committed to delivering high standards of sterile processing. Its efficient design and comprehensive documentation capabilities elevate the assurance of safety and effectiveness in medical device sterilization.