| Extended Duty/Enhanced
Design |
| The standard in low temperature sterilization
that you've depended on for the past fifteen years
is now even more efficient. VHP 1000ED offers extended
duty to maximize production efficiency and enhanced
design for improved, more robust operation
|
|
|
For low temperature sterilization of isolators,
workstations, filling lines, rooms, etc. in
research, biological safety, and production
applications |
|
Select from new control options; expanded
feature touch-screen control which can be interfaced
with a PLC, or Siemens, or Allen-Bradley PLC
|
| |
Unit is mobile for multiple site low temperature
sterilization |
|
| The
VHP cycle operates in a closed-loop configuration
where the enclosure is subjected to four phases: |
| |
Dehumidification - Reduction of relative
humidity |
| |
Condition - Rapid increase to desired hydrogen
peroxide vapor concentration |
|
Biodecontamination* - Maintenance of desired
hydrogen peroxide vapor concentration |
|
Aeration - Rapid reduction of hydrogen peroxide
vapor |
|
Cycle
times vary with initial temperature and humidity; enclosure
type, size and configuration; and load.
The process is fully automated. All cycle parameters
are monitored and recorded for process validation. |
| Products
Available for Equipment Operation/Validation |
|
Vaprox® 35% Hydrogen Peroxide
Sterilant
Formulated to provide optimum equipment performance
Cartridge is specially designed for fast,
easy installation
|
|
VHP Chemical Indicators retain color change
for proof of exposure |
| |
Spordex® VHP Biological Indicators
ensure reliable process validation |
|
| VHP
Training, Technical Support and Service |
|
|
Full operator training is provided either
on-site or at a STERIS training facility. |
|
Application Engineers are available to assist
with custom cycle development and validation. |
|
|
Field Service Engineers are available to
assist with IQ/OQ, calibration, start-up, and
preventative maintenance. |
|
*When
using VHP equipment with Vaprox Hydrogen Peroxide
Sterilant in the United States, the term biodecontamination
referred to in this document is defined as sterilization
of exposed porous and non-porous surfaces in a pre-cleaned,
dry, sealed enclosure. Any reference to biodecontamination
as it relates to the use of this equipment in the
United States does not impart additional claims of
effectiveness beyond that approved in the EPA-registered
labeling of Vaprox Hydrogen Peroxide Sterilant. |
|
