OFERTA
VHP® VICTORY™ BIODECONTAMINATION UNIT

Marka : STERIS

The VHP VICTORY Biodecontamination Unit is designed for mobile Biodecontamination* of clean, dry, sealed Enclosures† with volumes from 1000 - 20,000 ft3 (28 - 566 m3) using STERIS’s VHP® Process Technology, featuring SmartPhase™ (US Patent No. 8007717) software and Vaprox® Hydrogen Peroxide Sterilant.

* In this document, when referring to the use of VHP® Biodecontamination Systems with Vaprox Hydrogen Peroxide Sterilant in the United States, the term Biodecontamination is defined as sterilization of exposed porous and non-porous surfaces in a precleaned, dry, sealed Enclosure. Any reference to Biodecontamination pertaining to the use of this equipment in the United States does not, and is not intended to convey, additional claims of effectiveness beyond those contained in the Environmental Protection Agency (EPA) registered labeling of Vaprox Hydrogen Peroxide Sterilant (EPA Reg. No. 58779-4).

DESCRIPTION
The VICTORY Biodecontamination Unit uses high sterilant output, shortened cycle times and ease of operation to establish a new standard for Enclosure Biodecontamination. Biodecontamination Unit is equipped with four factoryprogrammed cycles:
• Dryerless Cycle (12 Log Reduction)
• Dryerless Cycle (6 Log Reduction)
• Concentration Control 400 PPM (Minimum 40% Saturation)
• Concentration Control 250 PPM (Minimum 40% Saturation).
Operator uses a Programmable Logic Controller (PLC) touch screen to select a factory-programmed cycle and SmartPhase software automatically runs selected Biodecontamination Cycle. Utilizing internal tri-scale sensor (measures temperature, percent relative humidity and hydrogen peroxide vapor concentration) inputs, SmartPhase software adjusts Sterilant injection rates to Enclosure conditions to achieve bioburden control targets while eliminating need for Dehumidification Phase and Conditioning Phase found in most traditional processes and limits possibility of condensation. With 5 to 35g/min of Sterilant injection, Biodecontamination Unit is capable of Biodecontaminating single Enclosures of up to 20,000 ft3 (566 m3) and multiple units are capable of Biodecontaminating Enclosures up to 175,000 ft3 (5,000 m3) at one time. The Biodecontamination Unit can operate inside Enclosure and can operate as a standalone unit or up to 10 Biodecontamination Units can be networked via Ethernet. Biodecontamination Units can be operated via the integrated B&R PLC control or over Ethernet connection using windows-based software‡. For larger Enclosures, up to three TS1000™ Tri-Scale Sensors can be linked to a VICTORY Biodecontamination Unit. These additional sensors boost cycle efficiency and effectiveness ensuring Sterilant is adequately distributed. A separate AR1200™Aerator is available for catalyzing Sterilant for applications not utilizing a facility-supplied buildingmanagement air handling system. Up to two AR1200 Aerators can be linked to a VICTORY Biodecontamination Unit. The VICTORY Biodecontamination Unit is multi-lingual (English,
French, Spanish, Italian and German) and available in either 120 or 230 Vac, single phase, electrical service. To minimize exposure to liquid hydrogen peroxide during handling, the system uses specially designed 0.25 gal (950 mL) disposable cartridges or bulk containers containing approximately 5 gal (19 L) of Vaprox Hydrogen Peroxide Sterilant.
The STERIS Biodecontamination Unit is only to be operated by Trained and Certified Applicators who have successfully completed both the STERIS Training and Certification Course for Applicators of Vaprox Hydrogen Peroxide Sterilant and the VICTORY Biodecontamination System Operator Course. Certification must be active and in force for all Applicators of Vaprox Hydrogen Peroxide Sterilant.

STANDARDS
The VHP VICTORY Biodecontamination Unit meets the applicable requirements of the following standards:
• Underwriters Laboratories (UL): UL61010-1 Second Edition as certified by Intertek Testing Services NA Inc.
• Canadian Standards Association (CSA): Standard C22.2 No. 61010-1 Second Edition.
• Ingress Protection Rating (IP) 21 as certified by Intertek Testing Services NA Inc.
• Governing Directives for Affixing the CE Mark:
» EMC Directive (2004/108/EC, 92/31/EEC, 93/68/EEC) as certified by Intertek Testing Services NA Inc.
» Low Voltage Directive (2006/95/EC, 93/68/EEC) as certified by Intertek Testing Services NA Inc.

CYCLE DESCRIPTION (Typical)
The VICTORY Biodecontamination Unit uses STERIS’s VHP® process technology. This process uses hydrogen peroxide vapor as a broad-spectrum antimicrobial without condensation of active ingredient onto surfaces. This non-condensation feature provides additional benefit of a wide range of material compatibility. In practice, an aqueous solution of 35% H2O2 (Vaprox Hydrogen Peroxide Sterilant) vapor is atomized and a high velocity air stream disperses it throughout the Enclosure. NOTE: Refer to Vaprox Hydrogen Peroxide Sterilant package insert for additional information and Application instructions. SmartPhase software technology automatically runs the selected Biodecontamination Cycle. Basic description of example Biodecontamination Cycles: 
After selecting and starting chosen Cycle at B&R Control, a two-minute countdown allows Trained and Certified Applicator to safely exit and seal Enclosure prior to Cycle start. Once time has elapsed, blower initializes and diffuser begins to heat. After diffuser reaches setpoint, injection pump primes and SmartPhase software controls Cycle as follows:

1. Dryerless Cycle – (Dryerless Cycle 12 Log Reduction or Dryerless Cycle 6 Log Reduction) Primary Cycle of VICTORY Biodecontamination Unit. Bioburden log reduction is calculated in real time once Sterilant concentration equals or is greater than 50 ppm. Biodecontamination Phase is completed when
programmed bioburden log reduction value (usually 1012) is achieved. Cycle advances to Aeration Phase.
During Aeration Phase, Sterilant concentration is reduced to less than or equal to one ppm. At one ppm, Biodecontamination Cycle completes and datalog is output to USB memory stick.

2. Concentration Control Cycle – (Concentration Control 400 ppm or Concentration Control 250 ppm) Cycle for special applications. Condition phase rapidly increases Enclosure Sterilant concentration to concentration setpoint. Biodecontamination Phase follows. Biodecontamination Phase is completed when setpoint time at Sterilant setpoint concentration is achieved. Cycle advances to Aeration Phase.
During Aeration Phase, Sterilant concentration is reduced to less than or equal to one ppm. At one ppm, Biodecontamination Cycle completes and datalog is output to USB memory stick.

NOTE: For Cycles with relative humidity (RH) greater than 50%,
a dryer may be recommended to improve Cycle time.

ACCESSORIES:
AR1200 Aerator – Portable, high capacity, Sterilant
catalyzation unit designed to shorten Biodecontamination
Cycles in Enclosures. AR1200 Aerator delivers 1200 cfm
(2039 cmh) aeration.
TS1000 Tri-Scale Sensor – Sensing unit boosts Cycle
efficiency and effectiveness of Enclosure Biodecontamination by
ensuring Sterilant is adequately distributed. TS1000 Sensor
measures Enclosure H2O2 concentration, RH% and
temperature.
RealVNC Software – VNC1 Client Software enabling remote
operation of a single or multiple Biodecontamination Units via
Ethernet.




Pliki do porania:
Steris_VHP VICTORY 1.pdf
Steris_VHP VICTORY 2.pdf
VHP 1 PL.pdf
VHP 2 PL.pdf

 
 
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© IACOBUS SP. Z O.O. 2016