STERIS - System 1
DESCRIPTION
System 1 Sterile Processing System[b]This item has been discontinued in the US for sale or use[/b] The Steris System 1 Processor is an automated, microcomputer controlled device which maintains the process parameters necessary to ensure standardized and effective sterile processing. The entire STERIS PROCESS takes place within the environmentally sealed chamber of the Processor. Processing temperatures do not exceed the safe temperature limits that most manufacturers recommend to ensure protection of heat sensitive devices. Upon completion of each cycle, a comprehensive printout is produced to document the process and load information. Various processing trays and containers permit the Processor to accommodate a wide variety of devices and procedure specific sets. The specialized trays and containers are designed to enable the operator to fix devices in the appropriate position for sterile processing, ensure a continuous exchange of sterilant and rinse on exposed surfaces of the devices (including internal structures and lumens), and protect certain types of devices from environmental contamination during transportation to sterile field following sterile processing.
FORUMSView All (1)
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FEATURES
[list] [*] For rapid, safe, standardized low temperature sterile processing of immersible surgical and diagnostic devices [*] The SYSTEM 1 Processor is an automated, tabletop, microcomputer-controlled device which maintains the process parameters necessary to ensure standardized and effective sterile processing. [/list]
FDA AlertsView All
Steris System 1 Processor: Extended Transition Period
Steris System 1 Processor: 6 Month Extension for Healthcare Facilities To Transition to Legally-Marketed Alternatives. FDA has extended the transition period to February 2, 2012. All healthcare facilities must be transitioned from Steris