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User-Service Manual
Joerns® Support Surface
FlapCair
To avoid injury, read user’s manual before using.
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Joerns® Support Surface
FlapCair Model
Important Precautions
Important Notice: The equipment must be installed
and operated in the manner for which it was intended.
Facility staff/user is responsible for reading and
understanding the product user manual and contacting
Joerns Healthcare if anything in this manual is unclear.
Joerns will not be held responsible for any injuries
resulting from failure to comply with the instructions
and precautions in this manual.
Warning: Joerns Healthcare’s specialty support
surfaces are designed as mattress replacement
systems. The risk of entrapment may occur when
the equipment is placed on bed frames that leave
gaps of even a few inches between the mattress and
the headboard, footboard, and bed or side rails. The
equipment is NOT to be used when such gaps are
present.
Facility staff/user is responsible for ensuring that all
mattresses properly t the bed frames. Joerns is not
responsible for the placement of its equipment on bed
frames that leave gaps between the mattress and
the headboard, footboard or bed or side rails which
present a risk of harm to patients.
Warning: An optimal bed system assessment should
be conducted on each patient by a qualied clinician
or medical provider to ensure maximum safety of
the patient. The assessment should be conducted
within the context of and in compliance with the state
and federal guidelines related to the use of restraints
and bed system entrapment guidance, including
the Clinical Guidance for the Assessment and
Implementation of Side Rails published by the Hospital
Bed Safety Workgroup of the U.S. Food and Drug
Administration. Further information can be obtained at
the following web address: http://www.fda.gov/cdrh/
beds/.
When using the mattress system, always ensure that
the patient is positioned properly within the connes
of the bed. Do not let any extremities protrude over
the side or between the bed rails when the mattress is
being used.
Danger: Explosion Hazard: Do not use in the
presence of ammable anesthetics. Do not use in
the presence of smoking materials or open ame.
Air owing through the air mattress will support
combustion.
Danger: To reduce the risk of shock, adhere to the
following instructions. Failure to do so could result in
personal injury or equipment damage.
• Immediately after using the FlapCair, unplug it
from its power source.
• Do not place or store the product where it can fall
or be pulled into a tub or sink.
• Do not place or drop the product into water or
other liquid.
• Do not remove the back of the control unit. Refer
servicing to Joerns Healthcare.
Warning: To reduce the risk of burns, shock, re, or
personal injury, adhere to the following instructions.
Failure to do so could result in personal injury or
equipment damage.
1. Use this product only for its intended purpose as
described in this manual. Only use attachments
and/or accessories that are recommended by
the manufacturer.
2. If this product has a damaged power cord or
plug, is not working properly, has been dropped
or damaged, or has been dropped into water, do
not operate it. For examination and repair, return
the product to Joerns.
3. Keep the control unit and power cord away from
heated surfaces, e.g. space heaters.
4. Never block the air openings of the product. Do
not place the control unit on a surface, such as a
bed or couch, where the air opening and/or lter
compartment, located on the back of the control
unit, may be blocked. Keep the air openings free
of lint and hair.
5. Never drop or insert any object into any opening
or hose.
6. Do not spill food or liquids onto the control
unit. If a spillage does occur, turn off the unit,
disconnect it from its power supply and allow at
least 24 hours for drying.
7. Do not use the product outdoors, or where
aerosol-spray products are used.
8. Plug this product only into a properly grounded
outlet. Refer to “Grounding Instructions”.
9. Ensure nothing is placed on the power cord and
ensure it is not located where it can be stepped
on or tripped over.
10. Do not attempt to service the control unit. Please
call Joerns Healthcare for any service requests.
11. The therapy pad (top cover) of this product is
not air permeable and may present a
suffocation risk. It is the responsibility of the
caregiver to ensure that the patient can use
this product safely.
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Joerns® Support Surface
FlapCair Model
Save These Instructions for Future
Reference
Bed System Entrapment Information
Although essential in the practice of long-term care,
bedside rails, in recent years, have also been a
subject of regulatory review and evolution in design
and use.
That focus includes not only the challenge of
achieving an appropriate balance between resident
security and unnecessary restraint, but also the
additional safety issue of entrapment.
The U.S. Food and Drug Administration (FDA),
working with our company and other industry
representatives has addressed the potential danger
of entrapment with new safety guidelines for medical
beds. These guidelines recommend dimensional
limits for critical gaps and spaces between bed
system components.
Entrapment zones involve the relationship of
components often directly assembled by the
healthcare facility rather than the manufacturer.
Therefore, compliance is the responsibility of the
facility.
Creating a Safer Care Environment
While the guidelines apply to all healthcare settings,
(hospitals, nursing homes and at home), long-term
care facilities have particular exposure since serious
entrapment events typically involve frail, elderly or
dementia patients.
For More Information
To learn more about compliance options with Joerns
products, visit our website at www.joerns.com, or
contact our Customer Care reps at 800-826-0270 and
ask for free informational publications.
To learn more about entrapment zones, assessment
methods and guidelines concerning entrapment,
contact Joerns Healthcare at 800-826-0270 or
consult the FDA website: http://www.fda.gov/
MedicalDevices/ProductsandMedicalProcedures/
GeneralHospitalDevicesandSupplies/HospitalBeds/
default.htm.
As the leading manufacturer of long-term care beds
and a frontrunner in addressing this critical issue,
Joerns Healthcare can offer you the expertise,
assistance and products to bring your facility into
compliance.
Joerns® Compliance Solutions
Matching the right bed components in order to meet
regulatory guidelines can be complex.
That is why Joerns offers a wide array of compliance
options. We assist customers in selecting compliant
accessories recommended for their specic bed
model.
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Joerns® Support Surface
FlapCair Model
Table of Contents
Important Precautions ............................................................................................................................... 2
Introduction ................................................................................................................................................. 5
Moisture Control
Shear and Friction Reduction
Indications for use ...................................................................................................................................... 5-6
Spinal Cord Injury
Pressure Relief
Pain Management
Features....................................................................................................................................................... 6
Therapy Control Unit Features
Therapy Mattress System Features
Therapy Pads
Grounding Instructions .............................................................................................................................. 7
Setup ............................................................................................................................................................ 7-8
To Create Super Flotation Zones
Operation ..................................................................................................................................................... 8
Patient Comfort Controls and Monitoring
Additional Features .................................................................................................................................... 9-10
CPR
Transport
Power Failure
CairRails
Optional Accessories
Troubleshooting .........................................................................................................................................10
Therapy Surface Not Inating
Unable to Change Therapy Mode or Adjust Comfort Control
Nursing Procedures ................................................................................................................................... 10-11
Recommended Linen
Changing the Therapy Pad
Patient Positioning and Comfort
Incontinence
Safety Information ...................................................................................................................................... 11
Patient Migration
Traction
Skin Care
Bed Height
Cleaning ...................................................................................................................................................... 11-12
Control Unit
General Cleaning
Disinfecting
Therapy Pad
Steam Cleaning
Filter Cleaning
Maintenance ................................................................................................................................................ 12
Storage and Care ........................................................................................................................................ 12-13
Control Unit
Support Surface
System Specications ............................................................................................................................... 13
Weight
Dimensions
Electrical Specications
Environmental Conditions
Agency Approvals
Call for Assistance ..................................................................................................................................... 13
Warranty ...................................................................................................................................................... 14
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Joerns® Support Surface
FlapCair Model
Introduction
The FlapCair, provided by Joerns Healthcare, is a
unique therapy system that provides pressure relief
by combining low air loss with pulsation. Low air loss
therapy has been demonstrated to reduce the risk of
pressure ulcers as well as being a valuable aid in the
treatment of pressure ulcers. The pulsation feature
may provide additional patient comfort and enhance
the function of the lymphatic system.
The FlapCair mattress replacement system is suitable
for the care and prevention of all stages of pressure
ulcers, for patients who have been assessed to be
at risk from the complications of immobility, and for
patients with healing grafts and ap sites. Our unique
cellular system allows caregivers to provide super
otation zones to provide extra relief to these sites.
Joerns FlapCair is the rst true low air loss mattress to
take pressure relief to the next level with 160 individual
therapy cells instead of the industry standard of 20.
More air cells mean a more exible surface area to
evenly distribute the patient’s weight. The patient’s
weight is evenly distributed over a substantial surface
area resulting in low average interface pressures.
The caregiver has the exibility to provide additional
pressure reduction on any part of the patient’s body by
simply closing off the air supply to any of the 160 cells-
thereby “oating” the wound or surgical site. FlapCair
is truly customizable to meet the needs of your patient.
Warning: The risk of entrapment can arise when
equipment is placed on bed frames that leave gaps
of even a few inches between the mattress and the
headboard, footboard, and bed or side rails. The
equipment is NOT to be used when such gaps are
present. See “Important Precautions” section of this
manual.
The FlapCair is quiet, comfortable and simple enough
for single caregiver installation, featuring rapid ination
in just ve minutes or less. The user-friendly controls
allow for easy adjustment of patient comfort.
Additionally, low friction and low shear materials,
together with average interface pressures well below
capillary closure levels, means that the FlapCair meets
the comfort and clinical requirements of your patients
up to 350 lbs.
Moisture Control
Patients are at risk for skin maceration if excess
moisture is permitted to accumulate beneath the
patient. This may be due to perspiration, incontinence
or wound drainage.
On the FlapCair, moisture is controlled via the specially
treated breathable, uid-proof, urethane coated nylon
therapy pad. The moisture vapor permeable fabric
of the therapy pad allows a sufcient amount of air
to circulate beneath the pad and wick away excess
moisture.
Shear and Friction Reduction
Shearing occurs when the skin is stationary in relation
to the support surface, while the underlying tissues
and vessels are stretched and damaged. When a
patient’s skin rubs against another surface, the result
is friction. The top surface of the FlapCair therapy pad
is constructed from a very smooth nylon fabric with low
friction and low shear properties to protect the patient’s
skin from these damaging forces.
Indications for Use
Note: The selection of a pressure-relieving surface
needs to be based on each individual patient’s clinical
condition, diagnosis and/or co-morbidities. The choice
and use of a support surface is one factor in a holistic
program of wound care
and treatment.
Spinal Cord Injury
The FlapCair is not recommended for use by patients
with unstable spinal fractures. Advice should be
obtained from the appropriate physician before using
the FlapCair system for these patients.
Pressure Relief
Pressure Ulcers Flaps
Grafts Rehabilitation
Neurology Dermatology
Burns Amputations
Pain Management
We have ensured that the FlapCair addresses the
four key areas in the treatment of compromised skin:
pressure relief, moisture control, and reduction in both
friction and shearing forces.
AIDS Arthritis
Oncology
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Joerns® Support Surface
FlapCair Model
The FlapCair provides distribution of weight over a
wide surface area, which relieves pressure against
bony prominences and provides a soft, gentle therapy
surface to lie on. For patients experiencing severe
pain and discomfort due to pressure and/or positioning
limitations, consider the FlapCair as an adjunct to pain
management interventions.
Note: Pressure relief and pain management are
conditions and diagnoses for which the FlapCair may
be indicated. Occasionally, there are orthopedic and
neurological patients that require body positioning to
be maintained in specic alignment. The use of the
FlapCair for these patients should be considered on
an individual basis and discussed with the attending
physician.
Features
The FlapCair is comprised of two components:
• Therapy control unit
• Therapy mattress system
Therapy Control Unit Features
• True low air loss
• Three modes of operation – Autorm, Pulsate and
Therapy
• Autormmode provides maximum air
ination designed to assist both patients
and caregivers during patient transfer and
treatment.
• Pulsate mode oscillates the air throughout the
mattress every 30 seconds provides increased
patient comfort.
• Therapy mode provides eight comfort control
settings to maximize patient compliance and
promote healing.
• Patient position sensor optimizes support for seated
occupants (Fowler boost)
• Closed loop pressure sensor control system
eliminates concerns of changes in mattress interface
pressure due to ambient temperature and pressure
changes.
• Quick disconnect hose feature allows for rapid
attach and CPR deate at the control unit.
• Compact lightweight control unit is quiet, robust and
powerful, with a reusable air lter and integrated
carrying handle for portability.
• Crisp, easy to read graphics for intuitive set up and
therapy control.
• Automatic panel lock out to avoid unwanted or
accidental adjustments.
• Specially designed enclosure for low noise
and durability.
• Integrated swing out hanging brackets for xing to
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most bed types.
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Therapy Mattress System Features
• 160 individual therapy cells help to evenly distribute
the patient’s weight and maximize pressure relief.
Modular cell design mattress for ease of cleaning,
re-assembly and cost effective service.
• Six-inch deep therapy cells are constructed of highly
durable, polyurethane lm to provide adequate
support and prevent bottoming out for most patients
within weight limit.
• Customizable pressure relief- caregiver can close
off individual cells to reduce the pressure on specic
areas of the patient’s body that are a concern
(wounds or surgical sites) thereby “oating” the
wound or surgical site.
• Lower two-inch therapy support cell provides
additional therapeutic support and remains inated
for up to 12 hours in the event of a power failure.
• Integrated low-pressure heel section provides lower
interface pressures for high-risk patients.
• Lower mattress therapy enclosure is constructed
from 100% heavy weight 1680 Denier nylon with
1.5 oz Urethane coating and incorporates bed
attachment loops for stability.
• Maximum weight capacity of 350 lbs.
• Anti-kink, easy clean air supply hose set.
Therapy Pads
Many healthcare facilities are facing the challenge of
infection control. Joerns’s quilted therapy covers are
treated with an antimicrobial to protect the therapy pad
itself from the growth of mold, mildew and bacteria.
Key features and benets:
• Treated with a highly effective bacteriostat agent
to inhibit the growth of bacterial and fungus.
• Constructed from a very smooth nylon fabric with
low friction and low shear properties to protect
the patient’s skin from damaging friction/shearing
forces.
• Breathable, moisture vapor permeable fabric
allows air to circulate beneath the pad and wicks
away excess moisture. This keeps your patient dry
and helps to prevent skin maceration.
• Two-way stretch therapy pad is designed for
optimal comfort, moisture vapor transfer, stain
resistance and ease of laundering.
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Joerns® Support Surface
FlapCair Model
Grounding Instructions
Warning: Use a properly grounded, three-prong,
120V AC outlet for this product. Failure to use a
grounded outlet could result in personal injury or
damage to equipment or house wiring, including risk
of re. A qualied electrician should be contacted to
correct the wiring and ensure a properly grounded
outlet.
Before installing this product, have the electrical
system checked to make sure the electrical circuits
and the electrical service are properly grounded.
Having a three-prong outlet does not necessarily
mean it is grounded. Sometimes two-prong outlets
are replaced with a three-prong type even though
there is no ground wire.
There is always a chance of a loose connection
or poor installation of a ground wire that causes
the loss of proper ground at the outlet. Inadequate
grounding at electrical outlets can occur even if there
is a ground wire. Wires can become loose over time
at the connection to the outlet.
Note: To install new wires on a circuit requires a
qualied electrician.
How to Determine if Your Outlet has the
Proper Grounding
Most hardware stores sell circuit testers (Figure
1) that can be used to test an outlet for proper
grounding. The tester plugs into an outlet and by
observing the indicator lights you can determine if
the outlet is properly grounded. For a higher level
of assurance, an electrician should be requested
to thoroughly test the electrical system with more
reliable equipment.
If repair or replacement of the cord or plug is
necessary, please contact Joerns for assistance.
Setup
Warning: For important precautions please see
page two.
Caution: Do not place the control unit on the oor.
Position the power cord to keep personnel from
tripping over it.
• If the therapy pad is not already on the mattress,
place it on the mattress. Attach the zippered cover to
the mattress surround.
• Hang the control unit on the foot of the bed facing
away from the bed. Attach the
hose connector marked CPR to the
control unit.
• Plug in the control unit and the
yellow Standby light will illuminate.
Press the Power button. The control
unit will start and the green light will
illuminate. Keep the control unit ON
while the patient is on the mattress.
• Fully inate the mattress by
selecting Autorm. When the
mattress is fully inated, select
the Therapy mode, and place the
patient on
the mattress.
• Select the appropriate Comfort Adjust level to
prevent bottoming out (i.e., providing greater than
one inch of air between the patient’s sacral area/
buttocks and the lower safety mattress) as outlined
below:
1. Begin by placing the head of the bed in the
appropriate position based on the patient’s
clinical condition.
2. Select the highest or most rm Comfort Adjust
setting.
3. Hand Check: Place a hand with three (3) ngers
(if head of bed at 30° or higher) or four (4)
ngers (if head of bed lower than 30°) stacked
vertically beneath the cells of the mattress and
above the safety mattress directly between the
lowest point of the patient’s sacral area/buttocks.
The
smallest nger should be resting on the safety
mattress.
4. Sequentially reduce the Comfort Adjust setting
to the rmness level where the height of the
three (3) or four (4) ngers can slide with
minimal resistance between the patient’s sacral
area/buttocks and the lower safety mattress.
This is the proper Comfort Adjust setting for the
patient to assure proper ination of the air cells
and prevent bottoming out of the mattress.
5. Document the patient’s Comfort Adjust setting
for future reference, and re-evaluate with the
Hand Check as the patient’s condition warrants.
• The CairRails risk management side air bolsters
can be inated or deated as required. Locate
the turn valve on the hose assembly between the
mattress and the control unit. Next, inate/deate the
CairRails by moving the turn valve to the up (inate)
or down (deate) position.
Figure 1
• Remove the existing mattress from the bed.
• Unroll the mattress with the hose connection at the
foot end of the bed and the therapy cells facing
up. Secure the ten (10) straps on the mattress
securely to the movable part of the bed frame.
Note: When inating or deating CairRails it is
recommended that the support surface be in Autorm
mode.
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Joerns® Support Surface
FlapCair Model
To Create Super Flotation Zones
The cells can be decreased in height or diameter to
reduce the pressure in the desired area. To reduce
the height compress the cell and clasp strap around
material as detailed below. To reduce the diameter,
which results in a shorter cell, place the strap around
the outside of the cell and tighten as desired
(Figures 2-4).
Cell fixation method:
• Determine cells that need to be closed off.
• Locate the straps stored in the foot section of the
mattress by footboard.
• Using the strap to secure cell in position desired.
• Position the patient on the surface, ensuring
that the wound site is placed over the super otation
zone.
• Ensure the strap buckle is positioned under the air
cell away from the patient.
Figure 2
Note: Patients that are mobile will need to be
monitored to ensure they remain in the correct position
to oat the wound.
Operation
Warning: For important precautions please see page
two.
Caution: The patient’s head should be positioned in
the center of the top section of the mattress. When
using the mattress system always ensure that the
patient is positioned properly within the connes of the
bed. Do not let any extremities protrude over the side
or between the bed rails when the mattress is being
used.
Patient Comfort Controls and Monitoring (Figure 5)
Power Switch
The power switch is used to turn the power on and off.
Standby
The unit starts up in Standby. Press the Power button
to inate the mattress. When the Standby light is
on, it may also indicate that there has been a power
interruption and the therapy control unit is ready to be
turned back on. Press the Power button and reset the
preferred mode of therapy and comfort level.
Figure 3
Eliminate cell by securing vertically
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Figure 4
Reduce cell by securing around cell
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Position Sensor
Patient Position Sensor (Fowler boost) will be
illuminated when the head of the bead is elevated by
more than 30 degrees.
Modes
Autorm
Autormmode provides maximum air ination
designed to assist both patients and caregivers
during patient transfer and treatment. The unit
will automatically return to the mode it was in
prior to Autorm(either Pulsate or Therapy) in
approximately 12 minutes.
Therapy Modes: Therapy and Alternating
• Pulsate: Pulsate will slightly decrease the pressure
in all cushions every 30 seconds, which some
patients nd comfortable.
• Therapy: The unit starts in the Therapy mode,
which is the standard low air loss therapy.
Comfort Adjust
The Comfort Adjust function is located on the right
side of the control panel. The FlapCair can be
customized to meet individual patient needs within a
therapeutic window. See “Setup” section for further
information. This function will not work in Autorm
mode.
Lockout
This feature is to prevent any unauthorized
changes to the patient settings. To unlock and make
adjustments to the settings press both up and down
comfort arrows at the same time to disengage the
Lockout function. The Lockout function will return in
approximately ve minutes.
Note: The unit is designed to lock out all the
adjustment controls after the patient has been
positioned correctly. In approximately ve minutes
after the last button push the power on light begins
to ash indicating Lockout is enabled.
Additional Features
Warning: A possible re hazard exists. This
product is suitable for use with oxygen administering
equipment of the nasal, mask, or half bed-length,
tent-type only. To prevent personal injury or
equipment damage, ensure that the oxygen tent
does not extend below the mattress.
Joerns® Support Surface
FlapCair Model
Figure 5
CPR
The hose connection at the control unit is marked
CPR. Disconnect the hose from the control unit.
Deation times will vary based on patient weight and
prole. To resume therapy, reattach the hose to the
control unit.
Transport
To transport the patient in bed, turn the control unit
off. Unplug the power cord from the outlet. Do not
disconnect the hose connection at the control unit.
The lower support cell will prevent the patient from
bottoming out for up to 12 hours.
Power Failure
The FlapCair control unit has an advanced power
failure notication alarm and Comfort Adjust setting
memory capability. Upon power failure the control unit
will ash a red Alarm light on the keypad and sound an
audible signal every two (2) seconds for up to twenty
(20) minutes. The power interruption feature keeps the
current settings in memory based on the frequency of
use and level of battery charge. The Alarm Reset will
turn off audible and visual alarm.
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Joerns® Support Surface
FlapCair Model
Power Interruption (Brown out)
In the event of a brief power interruption, up to twenty
(20) minutes, the Flapcair control unit will automatically
restart and reset to the previous Comfort Adjust
settings. The power interruption feature keeps the
current settings in memory based on the frequency of
use and level of battery charge.
Power Loss
In the event of a power failure in excess of twenty
(20) minutes, the control unit’s stand by light will be
illuminated after power restoration. Press the Power
button and reset the preferred mode and comfort level
as described in the “Operation” section.
Safety cell
In the event of a power failure, the lower support
cells should remain inated for up to 12 hours as
long as the control unit remains connected. In case
of an extended power failure, transfer the patient to a
hospital mattress or other surface.
CairRails
Integrated CairRails risk management air bolsters offer
a bilateral side bolster solution designed to address
healthcare’s growing concerns of liability in relation
to patient falls and entrapment. CairRails are being
recognized by some of the nations leading healthcare
systems for improving their patient safety and risk
management programs.
CairRails are recommended for patients requiring
additional support during patient care and transfer.
CairRails can help reduce costs while ensuring optimal
clinical outcomes and increasing patient safety.
Note: When inating CairRails, it is recommended that
the control unit be in Autormmode to achieve optimal
results.
Features and Benets
• A bilateral side air bolster solution which can
enhance your facilities entrapment/risk management
program.
• Easy to engage Ready Valve for instant ination and
deation.
• Transfer friendly-deate for ease of assisted transfer
or when bolsters are not required.
• Unique contoured design allows ease of ingress/
egress, while providing additional protection, comfort
and supports patient compliance.
• Designed to t on most key Joerns therapeutic
support surfaces.
• Promotes maximum independence by allowing
caregiver to decide when added protection is
required.
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Note: CairRails are meant to provide a documentable
and functional intervention for the risk management
issues of falls and entrapment but in no way guarantee
the prevention of falls or entrapment occurrences.
Optional Accessories
• Additional therapy pads – available for purchase
Troubleshooting
Therapy Surface is Not Inflating
• Ensure the hose connection from the therapy
mattress system (mattress) to the control unit is
securely connected.
• Ensure that the control unit is plugged into
an AC outlet.
• Ensure that the power is not on Standby. If on
Standby, press the Power button.
• Ensure that all air cells are connected to the internal
mattress manifold.
Unable to Change Therapy Mode or Adjust
Comfort Control
Make sure the Lockout function is disabled. To
disable, press the up and down Comfort Adjust arrows
simultaneously.
Nursing Procedures
Recommended Linen
Special linens are not necessary for the FlapCair.
There is no need for a bottom sheet as the therapy
pad should be covering the therapy cells at all times.
The patient should never be lying directly on the
therapy cells. Upon the patient specic needs the
following linens may be utilized:
• Draw or slide sheet to aid in positioning and to
further minimize friction and shearing.
• Incontinence barrier pad for patients incontinent of
urine and/or stool, and patients with heavily draining
wounds.
• Add top sheet, blanket and/or bedspread as needed
for patient comfort.
• Keep the amount of padding between the patient
and bed to a minimum for optimum performance.
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Joerns® Support Surface
FlapCair Model
Changing the Therapy Pad
• Place the therapy pad over the therapy cells, tting
the corner of the cushions into the corner of the
therapy pad. (Similar to a tted sheet.)
• Zip the therapy pad along each side of the mattress
tub.
Patient Positioning and Comfort
General Repositioning
Patients should be turned and repositioned per
individual turning schedule or per facility policy. It may
be helpful to activate the Autorm mode to achieve
a rm surface for repositioning purposes. The unit
will automatically return to the mode it was in prior
to Autormin approximately 12 minutes or you can
manually return to therapy mode once patient has
been repositioned.
Unless counter indicated, it is desirable to keep
the head of the bed in the low position to provide
optimal pressure relief and minimize the risk of
shearing injuries.
If using super otation zones, always ensure wound
site is placed appropriately to ensure maximum
pressure relief.
Safety Information
Patient Migration
Specialty bed products are designed to reduce/
relieve pressure and the shearing/friction forces on
the patient’s skin. The risk of gradual movement and/
or sinking into hazardous positions of entrapment and/
or inadvertent bed exit may be increased due to the
nature of these products.
Traction
With any traction or unstable fractures, maintain
physician-directed angle of articulation and guard
against risks of patient migration or inadvertent
deation of patient surface.
Skin Care
Monitor skin conditions regularly, particularly in areas
where incontinence and drainage occur or collect,
and consider adjunct or alternative therapies for high
acuity patients. Early intervention may be essential to
preventing serious skin breakdown.
Bed Height
Elevating Patient into Sitting Position
The special properties of the FlapCair, therapy pad
reduce the opportunity for shear and friction that may
occur when raising the head of other beds. As with any
surface, sliding can be expected, therefore patients
should be repositioned after elevation. The knee gatch
or foot of the bed may be elevated rst, to help prevent
the patient from sliding when the head of the bed is
elevated.
Incontinence
Moisture against the skin surface leads to maceration,
or softening of the tissues. To prevent maceration, we
recommend you use an incontinence barrier pad to
absorb the excess moisture.
In the event of incontinence or excess drainage on the
therapy pad, you should wipe off the excess uid from
the bed surface.
To minimize the risks of falls or injury the patient
surface should always be in the lowest practical
position when the patient is unattended. Make sure
areas under and around the frame are clear of objects,
persons and parts of body before adjusting height.
Cleaning
Warning: Unplug the control unit from its power
source. Failure to do so could result in personal injury
or equipment damage.
Warning: Do not expose the unit to excessive
moisture that would allow for liquid pooling. Personal
injury or equipment damage could occur.
Caution: Do not use harsh cleansers/detergents, such
as scouring pads and heavy-duty grease removers, or
solvents, such as acetone. Equipment damage could
occur.
Control Unit
Wipe off dust. If necessary, clean the housing exterior
with a disinfectant solution or a mild detergent and a
damp cloth. Then wipe dry.
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Joerns® Support Surface
FlapCair Model
General Cleaning
If there is no visible soilage with possible body uids,
we recommend that you clean the mattress system
with a mild detergent and warm water. If disinfection
is desired, you may use a combination cleanser/
disinfectant as explained in “Disinfecting” section.
• Patient care equipment that does not come in
contact with mucous membranes or non-contact skin
requires low-level disinfection. Wiping surfaces with
a properly prepared detergent or disinfectant carries
out low level disinfecting.
• Processing of dirty patient care equipment should
take place in a designated area away from clean or
sterile supplies and food preparation areas.
• Detergent/disinfectants should not be mixed with
other germicides or detergents. Using the proper
dilution insures the most effective killing power of the
disinfectant.
• Wash hands often and well, including after removal
of gloves.
• Patient care equipment that is used in isolation
areas should be disinfected in accordance with
all internal policies and procedures regarding such
equipment.
Disinfecting
When there is visible soilage and between patients,
we recommend that you disinfect the unit and mattress
with a tuberculocidal disinfectant. Disinfectant should
be registered with the Environmental Protection
Agency (EPA).
• Use rubber gloves and eye protection.
• Prepare detergent/disinfectant (registered by EPA
as hospital disinfectant) solution according to
instructions on label for correct use-dilution.
• With support surface deated, thoroughly wipe down
entire mattress, as air cells will lie at. Be sure to
reach all areas underneath and in-between air cells.
Allow to air dry.
• If dust or other soiling has accumulated along
air hoses, remove using swabs moistened with
detergent/disinfectant as necessary. Allow all
components to air dry. Wrap mattress in plastic and
return to storage area.
• Thoroughly wipe down outside of control unit and
allow to air dry. Cover with plastic and return to
storage area.
• Remove gloves and dispose; wash hands.
Therapy Pad
The therapy pad can be wiped down with a
disinfectant solution or a mild detergent with a
damp cloth. If heavily soiled, the therapy pad can
be laundered in a washer and dryer with warm
water (no more than 120º Fahrenheit). A non-bleach
detergent should be used sparingly. Wipe dry or
allow to air dry.
Steam Cleaning
Do not use any steam cleaning device on the unit.
Excessive moisture can damage mechanisms in
this unit.
Filter Cleaning
Check the air lter on the rear of the unit regularly
for buildup of dust/dirt. If buildup is visible turn off the
control unit and disconnect the power cord from the
wall outlet. Remove the lter by grasping the lter
pulling outward. Replace with the second supplied
lter. Ensure the replaced lter covers the entire lter
region.
Hand-wash the removed lter in warm soapy water
and allow to air dry. When dry, store the lter in a
safe place for the next lter maintenance.
Maintenance
Warning: Only facility-authorized personnel
trained by Joerns should perform preventative
maintenance. Preventative maintenance performed
by unauthorized personnel could result in personal
injury or equipment damage. Any maintenance done
without Joerns’s authorization will invalidate any
warranties on this product.
Storage and Care
When the product is not in use, properly store the
power cord. Failure to do so could result in personal
injury.
Note: Clean the FlapCair as described in the
previous section prior to storage.
Control Unit
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The power cord may be wrapped around the unit for
convenience. Wrap the unit in a plastic bag for dust
resistance then store the unit in an area appropriate
for an electronic medical device.
Page 13
Joerns® Support Surface
FlapCair Model
Support Surface
Gently roll up the support surface, expelling any
residual air, for temporary storage. The mattress
should be wrapped in plastic and/or a clean bag
for storage.
System Specifications
Weight:
Control Unit:...........................10 lbs (4.5 kg)
Mattress: ................................29.5 lbs (13.4 kg)
Maximum Weight Capacity: ...350 lbs (159 kg)
Dimensions:
Control Unit
7.25" (18 cm) W x 11.5" (29 cm) H x 5.5" (14 cm) D
Mattress:
36" (91 cm) W x 80" (203 cm) L x 8" (20 cm) D
Electrical Specifications:
Environmental Conditions:
Operating Conditions:
Ambient temperature: +10°C to +40°C
Relative humidity: 30% to 75% non-condensing
Storage And Shipping Conditions:
Ambient temperature: 10ºC to +40ºC
Relative humidity: 10% to 100%
Agency Approvals:
• UL Classied Medical Equipment No. 60601-1 Can/
CSA C22.2 No.601.1
UL Classication refers to the power unit only, not the
complete mattress replacement system.
Call for Assistance
If you have any questions or require service on a
Joerns product, please call Joerns Healthcare at
800.826.0270.
USA
120V AC, 60 Hz, 5A
* Mattress weight capacity only; total weight must not
exceed bed frame manufacturers’ specied load
capacity.
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Page 14
Joerns Healthcare Warranty Program
for Joerns® FlapCair Support Surface
Joerns Healthcare warrants the FlapCair mattress
to be sold free from defects in workmanship and
materials, under normal and proper use, for a period
of two (2) years on the mattress, and one (1) year on
the cover and electromechanical mattress components
(compressors, valves, printed circuit boards, hoses,
and couplers). Damages arising from improper use will
not be covered by this warranty.
Improper use is dened as, but not limited to, those
caused by:
• Burns
• Use of improper chemical agents
• Needle punctures, cuts, or abrasions
• Excessive loads
• Staining
• Negligent or excessive usage
• Improper maintenance, handling and/or cleaning
• Failure to use in the manner indicated in the
FlapCair user manual
Any modication, repair or alteration done to the
FlapCair that was not authorized in writing by Joerns
Healthcare will void this warranty.
Parts
Joerns’s FlapCair contain various parts that wear from
normal use. Joerns Healthcare’s obligation under this
warranty is limited to supplying replacement parts,
servicing or replacing, at its option, any product which
is found by Joerns to be defective. When requested
by Joerns, parts must be returned for inspection at the
customer’s expense. Credit will be issued only after
inspection.
Service
Most service requests can be handled by the facility
Maintenance Department with assistance from the
Joerns Healthcare Product Service Department.
Most parts requested can be shipped next day air at
the customer’s expense.
Should a technician be required, one will be provided
by Joerns Healthcare, at our discretion. Only the
Joerns Healthcare Product Service Department can
dispatch authorized technicians.
Damage caused by use in unsuitable environmental
conditions, abuse or failure to maintain the product in
accordance with user and service instructions is not
covered.
This warranty is extended to the original purchaser of
the equipment.
Manufactured by:
Joerns Healthcare, LLC
2100 Design Rd. Ste 100
Arlington, TX 76014
Post Acute, Acute, HomeCare
2430 Whitehall Park Dr. Ste 100
Charlotte, NC 28273
(P) 800.826.0270
(F) 800.457.8827
www.joerns.com • email: info@joerns.com © 2013 Joerns Healthcare • 6110066 RevD • 13-2631
VA/Government
19748 Dearborn Street
Chatsworth, CA 91311
(P) 800.966.6662
(F) 800.232.9796
Canadian Ofce
1000 Clarke Rd. Ste 6
London, ON Canada N5V 3A9
(P) 866.546.1151
(F) 519.451.8662
United Kingdom and
Other Countries
+44 (0)844 811 1156
+44 (0)844 811 1157
Netherlands
+31 (0)30 6363700
+31 (0)30 6363799
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