Introduction; Modes Of Operation; Indications For Use; Intended Use - SPAN PressureGuard PROTOCOL Owner's Manual

OVERVIEW: The system consists of a two-part microclimate management (often called "low air loss") system
of cover and coverlet, a foam shell, air cylinder inflation system, and a control-unit. The foam shell has a high-
density foam topper, a patented Safety Edge™ contoured foam bolster on the perimeter of the mattress for
added patient stability and positioning, and graduated Heel Slope™ feature designed to further reduce
pressures on vulnerable heels. The air-cylinder inflation system is housed within the foam shell, and consists
of air-cylinders oriented lengthwise within the mattress. The control unit connects to the mattress at the
patient's foot-end.
MODES OF OPERATION:. The Protocol provides the choice of two powered therapy modes of operation,
FLOAT or ALTERNATING.
WARNING – This product is not intended for use as a non‐powered support surface. Except
during emergency power interruption (see page 13) and during occasional patient transport
(see page 14), patients should be on the surface only when control unit is connected,
plugged in to wall outlet, and powered ON.
INDICATIONS FOR USE: The PressureGuard Protocol provides powered prevention and treatment of
pressure injuries through immersion and envelopment. Therapies provided include alternating pressure,
powered flotation, and microclimate management (management of excess moisture and heat). The system
may be indicated for use as a preventative tool against further complications associated with critically ill
patients or immobility. PressureGuard Protocol should always be used as part of a comprehensive medically
supervised care plan that includes appropriate repositioning, nutrition, and any necessary topical therapies
or incontinence management.
INTENDED USE: A pressure management system used for the prevention and treatment of pressure injuries.
Contraindication: The PressureGuard Protocol™ is not for use by those with unstable spinal
cords. Patient injury could occur.
WARNING ‐ To reduce the risk of burns, electrocution, fire or injury to persons: READ ALL
INSTRUCTIONS BEFORE USING THIS UNIT.
1. Always unplug this unit immediately after using.
2. Do not operate near water.
3. Do not place or store product where it can fall or be pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water. Unplug immediately.
6. Use this unit only for its intended use as described in the operating instructions.
7. Never operate this product if it has a damaged cord or plug, if it is not working properly, if it has been
dropped or damaged, or dropped into water. Return the unit to Span-America Medical Systems, Inc. for
examination and repair.
8. Keep the cord away from heated surfaces.
9. Never drop or insert any object into any opening or hose.
10. Do not use outdoors.

INTRODUCTION

PressureGuard
CONSTRUCTION AND DESIGN FEATURES
5
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Protocol™
P10452 R6 CO# 2648