Joerns JHI-DFAPL3680NZ DermaFloat APL Therapy System User Manual

User-Service Manual
Joerns® Support Surface
DermaFloat® APL
To avoid injury, read the user’s manual before using it.

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’ 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 head panel, foot panel, 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 fit the bed frames. Joerns is not
responsible for the placement of its equipment on bed frames that leave gaps between the mattress and the head panel, foot panel or bed or side rails which present a risk of harm to residents.
Warning: An optimal bed system assessment should be conducted on each resident by a qualified clinician or medical provider to ensure maximum safety of the resident. 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/MedicalDevices/ProductsandMedicalProcedures/GeneralHospitalDevicesandSupplies/HospitalBeds/default.htm.When using the mattress system, always ensure that the resident is positioned properly within the confines 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 flammable anesthetics. Do not use in the presence of smoking materials or open flame. Air flowing 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 DermaFloat ® APL, 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.
Warning: To reduce the risk of burns, shock, fire, 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 filter 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 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 resident can use this product safely.

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.
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 specific bed model.

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.

Introduction

The DermaFloat®  APL, provided by Joerns Healthcare, is a unique therapy system that provides pressure redistribution by alternating pressure between adjacent  A-B) air cells. The alternating pressure in the therapy cells automatically alternates on a regular basis to maximize wound healing. Alternating pressure can aid the healing process by increasing circulation to the resident’s wounds.
The DermaFloat APL also offers low air loss therapy through an integrated air delivery system beneath the therapy pad. Alternating pressure and low air loss therapy have been demonstrated to be valuable aids in the treatment of those identified as being at risk of developing pressure ulcers.
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 head panel, foot panel, and bed or side rails. The equipment is NOT to be used when such gaps are present. See the “Important Precautions” section of this manual.
The DermaFloat APL mattress replacement system is suitable for both the treatment of existing pressure ulcers Stage I through Stage IV, as well as for
those who have been assessed at risk from the complications of immobility. The DermaFloat APL is quiet, comfortable, and simple enough for single
caregiver installation, featuring rapid inflation in just 15 minutes or less. The user-friendly controls allow for easy adjustment of resident comfort.
Additionally, low friction and low shear materials, together with average interface pressures well below capillary closure levels, means that the DermaFloat APL meets the comfort and clinical requirements of your residents up to 350 lbs.
We have ensured that the DermaFloat APL addresses the four key areas in the treatment of compromised skin: pressure redistribution, moisture control, and reduction in both friction and shearing forces.

Moisture Control

Residents are at risk for skin maceration if excess moisture is permitted to accumulate beneath the resident. This may be due to perspiration, incontinence, or wound drainage.
On the DermaFloat APL, moisture is controlled via the specially treated breathable, fluid-proof, urethane-coated nylon therapy pad. The moisture vapor permeable fabric of the therapy pad allows a sufficient amount of air to circulate beneath the pad and wicks 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 resident’s skin rubs against another surface, the result is friction. The top surface of the DermaFloat APL therapy pad is constructed from a very smooth nylon fabric with low friction and low shear properties to protect the resident’s skin from these damaging forces.

Indications for Use

Note: The selection of a pressure-redistributing surface needs to be based on each individual resident’s clinical condition, diagnosis, and/or comorbidities. The choice and use of a support surface is one factor in a holistic program of wound care and treatment.

Spinal Cord Injury

The DermaFloat APL is not recommended for use by residents with unstable spinal fractures. Advice should be obtained from the appropriate physician before using the DermaFloat APL system for these residents.

Pressure Redistribution

Pain Management

AIDS Arthritis: Oncology

The DermaFloat® APL provides distribution of weight over a wide surface area, which redistributes pressure against bony prominences and provides a soft, gentle therapy surface to lie on. For residents experiencing severe pain and discomfort due to pressure and/or positioning limitations, consider the DermaFloat APL as an adjunct to pain management interventions.
Note: Pressure redistribution and pain management are conditions and diagnoses for which the DermaFloat APL may be indicated. Occasionally, there are orthopedic and neurological residents that require body positioning to be maintained in a specific alignment. The use of the DermaFloat APL for these residents should be considered on an individual basis and discussed with the attending physician.

Features

The DermaFloat APL is comprised of two components:

• Therapy control unit
• Therapy mattress system

Therapy Control Unit Features

• Eight comfort control settings to maximize resident compliance and promote healing.
• Three modes of operation – Auto firm, Therapy (static), and Alternating.
• Auto firm mode provides maximum air inflation designed to assist both residents and caregivers during resident transfer and treatment.
• Choice of three alternating cycle times: 5, 10, and 15 minutes.
• Eight therapeutic comfort control settings to maximize resident compliance and promote healing.
• The quick disconnect hose feature allows for rapid attach and CPR deflates at the control unit.
• Automatic panel lockout to avoid unwanted or accidental adjustments.
• Resident position sensor optimizes support for seated residents.
• The compact lightweight control unit is quiet, robust, and powerful, with a reusable air filter and integrated carrying handle for portability.
• Crisp, easy-to-read graphics for intuitive setup and therapy control.
• A closed-loop pressure sensor control system eliminates concerns of changes in mattress interface pressure due to ambient temperature and pressure changes.
• Audible and visual power fail alarms.
• Forty liters per minute pump.
• Specially designed enclosure for low noise and durability.
• Integrated swing-out hanging brackets for fixing to most bed types.
• Suitable for special needs residents in specific clinical specialties.

Therapy Mattress System Features

• Twenty individual therapy cells help to evenly distribute the resident’s weight and maximize pressure redistribution. Modular cell design mattress for ease of cleaning, re-assembly, and cost-effective service.
• Integrated low air loss delivery system below the therapy cover.
• Eight-inch deep therapy cells are constructed of highly durable, polyurethane-coated nylon to provide adequate support and prevent bottoming out for most residents within the weight limit. (Lower safety mattress not required)
• The lower mattress therapy enclosure is constructed from 100% heavyweight 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.
• Quick CPR deflation.

Therapy Pads
Many healthcare facilities are facing the challenge of infection control. Joerns’ quilted therapy pads are treated with an antimicrobial to protect the therapy pad itself from the growth of mold, mildew, and odor-causing bacteria.

Key features and benefits:

• 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 resident’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 resident dry and helps to prevent skin maceration. A two-way stretch therapy pad is designed for optimal comfort, moisture vapor transfer, stain resistance, and ease of laundering.

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 the risk of fire. A qualified 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 rounding 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 qualified 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.

SetupAdditional Features

Warning: For important precautions, see page two
Caution: Do not place the control unit on the floor. Position the power cord to keep personnel from tripping over it.

• 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.
• If the therapy pad is not already on the mattress, place it on the mattress. Attach the elastic straps to the mattress buckles around each corner of the mattress. Attach the six (6) additional straps to the movable part of the bed frame.
• Hang the control unit on the foot of the bed facing away from the bed. Attach the hoses to the control unit.
• Plugin 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 resident is on the mattress.
• Fully inflate the mattress by selecting Autofirm. When the mattress is fully inflated, select the Therapy mode, and place the resident on the mattress.
• Select the appropriate Comfort Adjust level to prevent bottoming out (i.e., providing greater than one inch of air between the resident’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 resident’s clinical condition.
2. Select the highest or most firm Comfort Adjust setting.
3.  Hand Check: Place a hand with three (3) fingers (if the head of the bed at 30° or higher) or four (4) fingers (if the head of the bed is lower than 30°) stacked vertically beneath the cells of the mattress and above the safety mattress directly between the lowest point of the resident’s sacral area/ buttocks. The smallest finger should be resting on the safety mattress.
4. Sequentially reduce the Comfort Adjust setting to the firmness level where the height of the three (3) or four (4) fingers can slide with minimal resistance between the resident’s sacral area/buttocks and the lower safety mattress. This is the proper Comfort Adjust setting for the resident to assure proper inflation of the air cells and prevent bottoming out of the mattress.
5. Document the resident’s Comfort Adjust the setting for future reference and re-evaluate with the Hand Check as the resident’s condition warrants.
   • The CairRails risk management side air bolsters can be inflated or deflated as required. Locate the turn valve on the hose assembly between the mattress and the control unit. Next, inflate/deflate the CairRails by moving the turn valve to the up (inflate) or down (deflate) position.

Note: When inflating or deflating CairRails it is recommended that the support surface is in Autofirm mode.

Operation

Warning: For important precautions, see page two.
Caution: The resident’s head should be positioned in the center of the top section of the mattress. When using the mattress system always ensure that the resident is positioned properly within the confines of the bed. Do not let any extremities protrude over the side or between the bed rails when the mattress is being used.
Resident Comfort Controls and Monitoring (Figure 2)
Power
The Power button is used to turn the power on and off.
Standby
The unit starts up in Standby. Press the Power button to inflate 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.
Modes
Autofirm
Autofirm mode provides maximum air inflation designed to assist both residents and caregivers during resident transfer and treatment. The unit will automatically return to the mode it was in prior to Autofirm (either Therapy or Alternating) in approximately 12 minutes.
Therapy Modes: Therapy and Alternating

• Therapy: The unit starts in the Therapy mode, which is the standard low air loss therapy.
• Alternating: The air cylinders are inflated and deflated in an A-B-A-B pattern; that ensures the resident is always supported.

Cycle Times
The Cycle Times function is located in the center of the control panel. Select the frequency of the alternation of the therapy cells in 5, 10 or 15 minutes
cycles. For more aggressive therapy, choose the five-minute option.
Comfort Adjust
The Comfort Adjust function is located on the right side of the control panel. The DermaFloat® APL can be customized to meet individual resident needs within a therapeutic window. See the “Setup” section for more information. This function will not work in Autofirm mode.
Lockout
This feature is to prevent any unauthorized changes to the resident 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 five minutes.
Note: The unit is designed to lock out all the adjustment controls after the resident has been positioned correctly. In approximately five minutes after the last button push the power on light begins to flash indicating Lockout is enabled.

Additional Features

Warning: A possible fire 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.
CPR
Disconnect the hose from the control unit. Deflation times will vary based on resident weight and profile. To resume therapy, reattach the hose to the control unit.
Transport
To transport the resident in bed, turn the control unit off. Unplug the power cord from the outlet. Transport can be done with the unit plugged into the mattress.
Power Failure
The DermaFloat® APL control unit has an advanced power failure notification alarm and Comfort Adjust setting memory capability. Upon power failure, the control unit will flash 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 the audible and visual alarms.
Power Interruption (Brownout)
In the event of a brief power interruption, up to twenty (20) minutes, the DermaFloat APL 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 standby 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.
Therapy cells
In the event of a power failure, the therapy support cells should remain inflated for up to 12 hours as long as the control unit remains connected. In case of an extended power failure, transfer the resident 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 resident falls and entrapment. CairRails are being recognized by some of the nations leading healthcare systems for improving their resident safety and risk management programs.
CairRails are recommended for residents requiring additional support during resident care and transfer. CairRails can help reduce costs while ensuring optimal clinical outcomes and increasing resident safety.
Note: When inflating CairRails, it is recommended that the control unit be in Autofirm mode to achieve optimal results.
Features and Benefits

•  A bilateral side air bolster solution that can enhance your facility’s entrapment/risk management program.
• Easy to engage Ready Valve for instant inflation and deflation.
• Transfer friendly-deflate for ease of assisted transfer or when boosters are not required.
• Unique contoured design allows ease of ingress/ egress, provides additional protection, and comfort and supports resident compliance.
• Designed to fit on most key Joerns therapeutic support surfaces.
• Promotes maximum independence by allowing caregivers to decide when added protection is required.

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
• Quick inflation pump

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 DermaFloat® APL. There is no need for a bottom sheet as the therapy pad should be covering the therapy cells at all times. The resident should never be lying directly on the therapy cells. Depending on the specific needs of the resident, the following lines may be utilized:

• Draw or slide sheet to aid in positioning and to further minimize friction and shearing.
• Incontinence barrier pad for residents incontinent of urine and/or stool, and residents with heavily draining wounds.
• Add top sheet, blanket, and/or bedspread as needed for resident comfort.
• Keep the amount of padding between the resident and bed to a minimum for optimum performance.

Changing the Therapy Pad

• Place the therapy pad over the therapy cells, fitting the corner of the cushions into the corner of the therapy pad. (Similar to a fitted sheet)
• Attach the therapy pad to the mattress tub using the straps provided.

Resident Positioning and Comfort
General Repositioning
Residents should be turned and repositioned per individual turning schedule or per facility policy. It may be helpful to activate the Autofirm mode to achieve a firm surface for repositioning purposes. The unit will automatically return to the mode it was in prior to Autofirm in approximately 12 minutes or you can manually return to therapy mode once the resident has been repositioned.
Unless counter-indicated, it is desirable to keep the head of the bed in the low position to provide optimal pressure redistribution and minimize the risk of shearing injuries.
Elevating Resident into Sitting Position
The special properties of the DermaFloat APL, 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, residents should be repositioned after elevation. The knee gatch or foot of the bed may be elevated first, to help prevent the resident 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 fluid from the bed surface.

Safety Information

Resident Migration
Specialty bed products are designed to reduce/redistribute pressure and the shearing/friction forces on the resident’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 the physician-directed angle of articulation and guard against risks of resident migration or inadvertent
deflation of resident 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 residents. Early intervention may be essential to preventing serious skin breakdown.
Bed Height
To minimize the risks of falls or injury the resident’s surface should always be in the lowest practical position when the resident is unattended. Make sure areas under and around the frame are clear of objects, persons, and parts of the body before adjusting the 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.
Cautio n: 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.
General Cleaning
If there is no visible spoilage with possible body fluids, we recommend that you clean the mattress system with a mild detergent and warm water. If disinfection is desired, you may use a combination cleaner/ disinfectant as explained in the “Disinfecting” section.

• Resident 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 resident 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 ensures the most effective killing power of the disinfectant.
• Wash hands often and well, including after the removal of gloves.
• Resident 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 spoilage and between residents, we recommend that you disinfect the unit and mattress with a tuberculocidal disinfectant. Disinfectants 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 the label for correct use-dilution.
• With support surface deflated, thoroughly wipe down the entire mattress, as air cells will lie flat. Be sure to reach all areas underneath and in-between air cells. Allow airing to dry.
• If dust or other soiling has accumulated along with air hoses, remove using swabs moistened with detergent/disinfectant as necessary. Allow all components to air dry. Wrap mattress in plastic and return to the storage area.
• Thoroughly wipe down outside of control unit and allow to air dry. Cover with plastic and return to the storage area.
• Remove gloves and dispose of; 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 filter on the rear of the unit regularly for the buildup of dust/dirt. If buildup is visible turn off the control unit and disconnects the power cord from the wall outlet. Remove the filter by grasping the filter pulling outward. Replace with the second supplied filter. Ensure the replaced filter covers the entire filter region.
Hand-wash the removed filter in warm soapy water and allow it to air dry. When dry, store the filter in a safe place for the next filter 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 DermaFloat® APL as described in the previous section prior to storage.
Control Unit
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.
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: …………………………………………. 22 lbs (10 kg)
Maximum Weight Capacity*: ………….. 350 lbs (159 kg)
Dimensions:
Control Unit
7.5″ (19 cm) W x 12.25″ (31 cm) H x 5.5″ (14 cm) D
Mattress:
35″ (89 cm) W x 80″ (203 cm) L x 8″ (20 cm) D
Electrical Specifications:
USA
120V AC, 60 Hz, 0.6A
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%
Control Unit Agency Approvals:

• UL Classified Medical Equipment UL 60601-1 Can/CSA C22.2 No. 601.1

Joerns Healthcare Warranty Program
for Joerns® DermaFloat® APL Support Surfaces

Joerns Healthcare warrants the DermaFloat APL 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 defined 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 DermaFloat APL user manual

Any modification, repair, or alteration done to the DermaFloat APL that was not authorized in writing by Joerns will void this warranty.
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.

Parts

Joerns’ DermaFloat APL contains various parts that wear from normal use. Joerns’ 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 Product Service Department.
Most parts requested can be shipped the next day air at the customer’s expense.
Should a technician be required, one will be provided by Joerns, at our discretion. Only the Joerns Product Service Department can dispatch authorized
technicians.

References

• U.S. Food and Drug Administration

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