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English
1. INTRODUCTION
This manual should be used for initial set up of the system and for reference purposes.
1.1 GENERAL INFORMATION
This system is a high quality, affordable mattress system, suitable for the treatment and prevention of
pressure ulcers. This product has been tested and successfully approved for the following standards:
EN 60601-1
EN 60601-1-2
EN 55011 Class B
IEC61000-3-2
IEC 61000-3-3
EMC Warning Statement
This equipment has been tested and found to comply with the limits for medical devices to the EN
60601-1-2:2007. These limits are designed to provide reasonable protection against harmful
interference in a typical medical installation. This equipment generates uses and can radiate radio
frequency energy and, if not installed and used in accordance with the instructions, may cause harmful
interference to other devices in the vicinity. However, there is no guarantee that
occur in a particular installation. If this equipment does cause harmful interference to other devices,
which can be determined by turning the equipment off and on, the user is encouraged to try to correct
the interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit different from that to which the other device(s)
are connected.
Consult the manufacturer or field service technician for help.
1.2 INTENDED USE
This product is intended:
to help and reduce the incidence of pressure ulcers while optimizing patient comfort.
for long term home care of patients suffering from pressure ulcers.
for pain management as prescribed by a physician.
The product can only be operated by personnels who are qualified to perform general nursing
procedures and has received adequate training in knowledge of prevention and treatment of pressure
ulcer.
NOTE: This equipment is not suitable for use in the presence of flammable anesthetic
mixture with air or with pure oxygen or nitrous oxide.
interference will not
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