Stryker XPRT 2950 Series Manual

2012/06 B.0 2950-109-005 REV B www.stryker.com
REF
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For Parts or Technical Assistance:
Service technique et pièces de rechange :
Für Ersatzteile oder technische Hilfe:
Voor onderdelen of technische bijstand:
Para solicitar asistencia técnica o piezas:
Para encomendar peças ou solicitar assistência técnica:
USA/États-Unis/USA/VS/EE. UU/EUA: 1-800-327-0770
XPRT™ 2950
Operations/Maintenance Manual
Integrated with FL27 (2155/2156)
Intégré avec FL27 (2155/2156)
Integriert in Modell FL27 (2155/2156)
Geïntegreerd met FL27 (2155/2156)
Integración con FL27 (2155/2156)
Integrado com o FL27 (2155/2156)
Therapeutic Support Surface
Surface de soutien thérapeutique
Therapeutische Auflagefläche
Therapeutisch steunoppervlak
Superficie de apoyo terapéutico
Superfície de suporte terapêutico
Manuel d’utilisation et d’entretien
Bedienungs- und Wartungshandbuch
Gebruiks-/onderhoudshandleiding
Manual de uso y mantenimiento
Manual de funcionamento/manutenção

EASTERN EUROPE
Stryker SA - Export Business
Grand-Rue 90
P.O. Box 1567
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
AUSTRALIA
Stryker Australia
8 Herbert Street
St Leonards NSW 2065
Australia
Phone: [phone]
Fax: [phone]
AUSTRIA
Stryker GmbH
Euro Plaza, Gebäude G
Am Euro Platz 2
1120 Wien
Austria
Phone: [phone]
Fax: [phone]
BELGIUM
NV Stryker SA
Ikaros Business Park- Fase III
Ikaroslaan 12
1930 Zaventem, Brussels
Belgium
Phone: [phone]
Fax: [phone]
DENMARK
Stryker Denmark
Filial of Stryker AB
Postbox 772
1532 Copenhagen
Denmark
Phone: [phone]
Fax: [phone]
NORWAY
Stryker Norway
Norsk Fillial
Nedre Vollgate 3
0158 Oslo
Norway
Phone: [phone]
Fax: [phone]
POLAND
Stryker Polska Sp. ZO.O
Kolejowa 5/7
01-217 Warsawa
Poland
Phone: [phone]
Fax: [phone]
PORTUGAL
Stryker Portugal Produtos
Medicos, LTDA.
Avenida Marechal Gomes
da Costa, 35
1800-255 Lisboa
Portugal
Phone: [phone]
Fax: [phone]
ROMANIA
Stryker Osteonics Romania S.R.L.
19, Leonida Str.
District 2
7000 Bucharest
Romania
Phone: [phone]
Fax: [phone]
SOUTH AFRICA
Stryker Osteonis PTY. LTD.
3 Susan Street
Strydom Park
Johannesburg, 2194 - South Africa
Mailing Address:
P.O. Box 48039
2129 Roosevelt Park
Johannesburg, South Africa
Phone: [phone]
Fax: [phone]
SPAIN
Stryker Iberia SL
c/Sepulveda n17
28108 Alcobendas
Madrid
Spain
Phone: [phone]
Phone: [phone]
Fax: [phone]
SWEDEN
Stryker AB/Scandinavia
Box 50425
SE-204 14 Malmo
Sweden
Phone: [phone]
Fax: [phone]
UK/IRELAND
Stryker UK Limited
Stryker House
Hambridge Road
Newbury, Berkshire
RG14 5EG, England
Phone: [phone]
Phone: [phone]
Fax: [phone]
FINLAND
Stryker AB, Finland
PO 80 Makelankatu 2
00501 Helsinki
Finland
Phone: [phone]
Fax: [phone]
FRANCE
Stryker France S.A.S.
ZAC - Avenue de Satolas Green
69330 Pusignan
France
Phone: [phone]
Fax: [phone]
GERMANY
Stryker Howmedica GmbH
Dr. Homer Stryker Platz 1
47228 Duisburg
Germany
Phone: [phone]
Fax: [phone]
GREECE
Stryker Hellas EPE
455 Messogion ave
153 43 Agia Paraskevi
Athens, Greece
Phone: [phone]
Fax: [phone]
ITALY
Stryker Italia SrL
Via Ghisalba 15B
00188 Roma
Italy
Phone: [phone]
Fax: [phone]
MIDDLE EAST / NORTH AFRICA
Stryker Osteonics SA
Twin Towers
11th Floor, Suite 1101 & 1102
P.O. Box 41446
Baniyas Road
Dubai, Deira, UAE
Phone: [phone]
Fax: [phone]
NEDERLANDS
Stryker Nederlands BV
(P.O. Box 13, 4180 BA Waardenburg)
4181 CD Waardenburg
The Nederlands
Phone: [phone]
Fax: [phone]
EUROPE HEADQUARTERS
Stryker SA
Cite-Centre, Grand-Rue 90
P.O. Box 1568
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
International Addresses

www.stryker.com 2950-109-005 REV B 1-1
English
Table of Contents
Symbols and Definitions ....................................................................1-3
Warning/Caution/Note Definition ...........................................................1-4
Introduction .............................................................................1-5
Intended Use of Manual .................................................................1-5
Brief product description and intended use statement ...........................................1-5
Product Illustration .....................................................................1-6
Specifications ........................................................................1-7
Contact Information ....................................................................1-8
Product Serial Number Location/Identification.................................................1-8
Summary of Safety Precautions ..............................................................1-9
Contraindications .....................................................................1-11
Setup Procedures........................................................................1-12
Installing the Support Surface ...........................................................1-12
Powering Up the Support Surface.........................................................1-14
Controller Backlighting .................................................................1-14
Siderail Position......................................................................1-14
Therapy Modes .........................................................................1-15
XPRT™ Clinical Functions ..............................................................1-15
Low Air Loss (LAL) ...................................................................1-15
Sloped Heel Section ..................................................................1-15
Operation Guide.........................................................................1-16
Rotation Therapy .....................................................................1-16
To Prepare for Rotation Therapy..........................................................1-16
To Start Rotation Therapy ..............................................................1-17
To Adjust the Active Therapy Parameters ...................................................1-18
To Stop Rotation Therapy...............................................................1-18
Percussion Therapy ...................................................................1-19
To Start Percussion Therapy ............................................................1-19
To Adjust the Active Therapy Parameters ...................................................1-2 0
To Stop Percussion Therapy.............................................................1-20
Vibration Therapy ....................................................................1-21
To Start Vibration Therapy ..............................................................1-21
To Adjust the Active Therapy Parameters ...................................................1-2 2
To Stop Vibration Therapy ..............................................................1-22
To Start Max Inflate ...................................................................1-23
To Stop Max Inflate ...................................................................1-24
To Adjust Support Surface Firmness.......................................................1-25
Patient Positioning ....................................................................1-25
To Start Turn Assist ...................................................................1-26
To Stop Turn Assist ...................................................................1-27
To Lock All Functions..................................................................1-28
To Unlock All Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-28
Advanced Settings ....................................................................1-29
To Change the Displayed Language .......................................................1-29

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Table of Contents
To Reset Therapy History ...............................................................1-30
To Reset Parameters To Default..........................................................1-31
To View Therapy History ...............................................................1-3 2
CPR Activation.......................................................................1-33
Transferring a Patient to the XPRT™ Therapeutic Support surface ................................1-34
Transferring a Patient From the XPRT™ Therapeutic Support Surface..............................1-34
Transporting a Patient on the Bed ........................................................1-34
Nursing Care ...........................................................................1-35
Skin Care Guidelines ..................................................................1-35
Bathing a Patient .....................................................................1-35
Bed Pan Placement ...................................................................1-36
Bed Pan Removal ....................................................................1-36
Incontinence / Drainage ................................................................1-36
Preventative Maintenance Checklist ..........................................................1-37
Cleaning...............................................................................1-38
Support Surface Cleaning ..............................................................1-38
Foot Box Cleaning ....................................................................1-38
Troubleshooting Guide ....................................................................1-39
Quick Reference Replacement Parts List ......................................................1-43
Service Information.......................................................................1-44
Top Cover Replacement................................................................1-44
Foot Box Power Board Replacement.......................................................1-44
Foot Box Transformer Replacement .......................................................1-44
Foot Box Pump Replacement ............................................................1-45
Head Box CPU Board Replacement .......................................................1-47
Head Box Diaphragm and Slip Disc Replacement .............................................1-47
Head Box Stepper Motor / Rotary Valve Assembly ............................................1-48
Cell Assembly Replacement Kit ..........................................................1-49
Installation of New Cell Assembly .........................................................1-51
To Access the Service Screen ...........................................................1-54
Service Screen Functions ..............................................................1-56
Service Codes.......................................................................1-58
Alarms / Errors ......................................................................1-65
Recycling Passports ......................................................................1-66
EMC Information.........................................................................1-68
XPRT™ Therapeutic Support Surface......................................................1-68
Warranty ..............................................................................1-72
Limited Warranty .....................................................................1-72
To Obtain Parts and Service ............................................................1-72
Return Authorization...................................................................1-72
Damaged Merchandise ................................................................1-72
International Warranty Clause............................................................1-72
Patent Information ....................................................................1-72

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English
Symbols and Definitions
Warning/Caution, consult accompanying documentation
Safe Working Load
~Alternating Current
Type BF Equipment: equipment providing a particular degree of protection against electric shock,
particularly regarding allowable leakage current and reliability of the protective earth connection.
Class 1 Equipment: equipment in which protection against electric shock does not rely on BASIC
INSULATION only, but which includes an additional safety precaution in that means are provided
for the connection of the EQUIPMENT to the protective earth conductor in the fixed wiring of the
installation in such a way that ACCESSIBLE METAL PARTS cannot become live in the event of a
failure of the BASIC INSULATION.
Mode of Operation: Continuous
IPX4 Protection from liquid splash
Dangerous Voltage
Protective Earth Terminal
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock,
Fire, Mechanical and Other Specified Hazards Only in Accordance with IEC60601-1(ed.2),
IEC60601-1(ed.2); am1, IEC60601-1(ed.2); am2
In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment, this
symbol indicates that the product must not be disposed of as unsorted municipal waste, but should
be collected separately. Refer to your local distributor for return and/or collection systems available
in your country.
Consult Instructions for Use
Model Number Manufacturer
Damp Wipe Only 10% Chlorinated Bleach
Do Not Tumble Dry Do Not Iron
Do Not Dry-Clean Allow to Completely Air Dry

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English
Symbols and Definitions
WARNING/CAUTION/NOTE DEFINITION
The words WARNING, CAUTION and NOTE carry special meanings and should be carefully reviewed.
WARNING
Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CAUTION
Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the
user or patient or damage to the equipment or other property. This includes special care necessary for the safe and
effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or
misuse.
NOTE
Provides special information to make maintenance easier or important instructions clearer.

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Introduction
INTENDED USE OF MANUAL
This manual is designed to assist with the operation and the maintenance of the Stryker Medical 2950 XPRT™
therapeutic support surface. Carefully read thoroughly before using or beginning maintenance on the XPRT. To ensure
safe operation of this equipment, it is recommended that methods and procedures be established for educating and
training staff on the safe operation of the XPRT therapeutic support surface.
BRIEF PRODUCT DESCRIPTION AND INTENDED USE STATEMENT
INTENDED MEDICAL INDICATION:
The XPRT™ support surface is intended to assist with the treatment of pulmonary complications associated with
immobility of human patients in acute care. XPRT is intended to assist in the prevention and treatment of pressure
ulcers associated with immobile, critically ill or injured human patients. XPRT is intended to assist in the therapies of
percussion, vibration, and continuous lateral rotation therapy (CLRT). XPRT offers turn assist and pressure redistribution.
XPRT also offers a powered low air loss feature to provide a flow of air and a breathable cover to assist in maintaining
the micro-climate of the skin. The XPRT support surface is a powered support surface replacement system that is
integrated with the Stryker InTouch™ bed.
INTENDED PATIENT POPULATION:
The XPRT support surface is intended for patients with existing pressure ulcers or patients at risk of developing
pressure ulcers. Please refer to the operations manual for environmental requirements. The patient must not exceed
safe working load specified by the frame and accessories.
XPRT IS NOT INTENDED TO BE USED ON:
• Patients with unstable fractures
• Patients with unstable spinal cord injuries
• Patients in skeletal traction
• Stroke victim
CLRT, TURN ASSIST, ROTATION, PERCUSSION AND VIBRATION ARE NOT INTENDED TO BE USED ON:
• Patients with significant hemoptysis
• Patients for whom a head down position is contraindicated (e.g. head injury)
• Patients with bleeding disorders
• Patients with rib fractures
• Patients with a predisposition to pathologic fractures
• Patients for whom the techniques cause increased dyspnea or wheezing
• Patients who are hemodynamically unstable
PERCUSSION/VIBRATION THERAPY IS NOT INTENDED TO BE USED ON:
• Patients with rib fractures
• Patients experiencing persistent intracranial hypertension
• Patients exhibiting bronchospasms
• During post-operative periods following cardiac surgery
INTENDED USER PROFILE:
The XPRT™ therapeutic support surface is for patient use in acute care settings, to include critical care, step down,
progressive care, med/surg, sub acute care, and post anesthesia care unit (PACU) or other locations in a professional
health care facility as prescribed by a healthcare professional. XPRT is not intended to be used in a home health care
environment. The typical operator for XPRT would be healthcare professionals.
INTENDED CONDITION OF USE AND EXPECTED LIFE:
XPRT is not suitable for use in the presence of flammable anesthetic mixture with air rich in oxygen or nitrous oxide.
XPRT is designed for a five (5) year expected life for the product and three (3) year life for the covers, under normal
use, conditions, and with appropriate periodic maintenance as described in the maintenance manual for each device.

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Foot End
Head Box
Foot Box
CPR Plug
Head End
PRODUCT ILLUSTRATION
Introduction

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Introduction
Model 2950-200-002 Dartex Cover
Dimensions Support surface 84" x 35" x 8.5" 213.4 cm x 88.9 cm x 21.6 cm
Weight Complete system 115 lbs 52.2 kg
Safety working load 500 lbs 226.8 kg
Power Cord 3 feet, 16 AWG cord with hospital grade plug for use with accessory
outlet on FL27 InTouch bed frame
Over Current Protection 3 fuses - (2) Fuses 5 x 20 mm., 6.3A Slo-blo, 250 VAC, (1) Fuse (F1)
1/4 x 1 1/4 in., 7A Slo-blo, 250 VAC
Voltage 120 VAC +5% -10% VAC, 2.5A 50/60 Hz
Operating Ambient Temperature Range 60°F - 85°F 16°C - 30°C
Storage Temperature If the product is stored at temperatures below 60°F or above 85°F,
the product must be allowed to stabilize for two hours within the
specified operating temperature range before use.
Output Flow Rate 12.5 LPM (0.4 SCFM) minimum @ 30 mmHg
Current Leakage 300 µA Maximum
Classification Class I, grounded equipment
Class II, FDA and Health Canada
Type BF equipment
Continuous operation - Not suitable for use in the presence of
flammable anesthetic mixture with air or with oxygen or nitrous
oxide. Suitable for continuous duty.
IPX4, Splash Proof
Medical equipment: Classified with respect to electric shock,
mechanical hazards only, in accordance with IEC60601-1 CAN/CSA
C22.2 No. 601.1.-M90
Electromagnetic compatibility, meets IEC60601-1-2 (CISPR 11
classified as Class A, Group 1 ISM equipment)
SPECIFICATIONS

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Introduction
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at: [phone] or [phone].
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
Please have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical
Support. Include the serial number in all written communication.
PRODUCT SERIAL NUMBER LOCATION/IDENTIFICATION
The serial number (A) is located on the label located on the front of the foot box and again at (B) on the head box of
the support surface as shown in Figure 1.
Figure 1
A
B

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English
Before operating or servicing the XPRT™ Therapeutic Support Surface it is important to read and understand all
information in this manual. Carefully read and strictly follow the safety guidelines listed in this section. The warnings and
cautions are repeated throughout the manual, where applicable. To ensure safe operation, methods and procedures
must be established for educating and training staff on the safe operation of therapy support surfaces. U.S. Federal
law restricts this device to be sold by or on the order of a physician.
WARNING
• Explosion risk. Do not use in the presence of flammable mixture with air or with oxygen or nitrous oxide.
• Do not plug into the power source until assembly is complete.
• Electrical shock risk. Refer all servicing to qualified personnel.
• The support surface is equipped with a hospital grade plug for protection against shock hazard. It must be plugged
directly into the FL27 InTouch three-prong receptacle. Grounding reliability can be achieved only when a hospital
grade receptacle is used.
• Medical electrical equipment requires special precautions regarding EMC and needs to be installed and put into
service according to the EMC information provided within this manual to prevent equipment malfunction.
• Portable and mobile RF communication equipment can affect Medical Electrical Equipment.
• Risk of injury. Use of XPRT therapeutic support surface for stroke victims should be only under physician’s order.
• It is the caregiver’s responsibility to monitor the patient’s condition at regular intervals to ensure patient safety.
• Consult physician if redness or skin breakdown occurs.
• Failure to position the patient along the support surface center line before starting rotation therapy could result in
patient injury. Check patient frequently to assure proper positioning and support surface inflation.
• Rotation angle settings approximate the degrees of rotation achieved by a 165 pound patient with an 18 inch
shoulder width. The actual amount of rotation achieved is dependent on patient size, patient weight and shoulder
width. Monitor the patient for at least one complete cycle to verify the unit achieves the desired angle.
• Ensure that any and all tubing and wiring connected to the patient is long enough, stabilized, and secure to assure
safe and unrestricted lateral rotation/elevation of the patient. Be sure to monitor the patient frequently.
• To avoid possible injury, when using rotation or pulmonary therapy, take care not to extubate intubated patients.
• Always secure the support surface straps to the bed frame to prevent the support surface from sliding and causing
patient injury.
• To ensure patient safety, always raise the bed siderails before beginning therapy.
• Do not leave the patient unattended during Turn Assist. Serious injury could result.
• Deflate the XPRT™ therapeutic support surface or use Max Inflate to inflate it completely before beginning CPR.
• Disinfect the support surface between patients. Failure to properly disinfect could result in cross-contamination
and infection.
• Unplug the support surface power cord before cleaning the support surface. Failure to unplug the unit could cause
equipment damage or personal injury.
• Do not immerse the support surface or foot box in cleaning or disinfectant solutions. Do not allow liquid to pool
on the support surface or foot box. Immersion or liquid pooling could cause malfunction resulting in equipment
damage or patient injury.
• Do not attach the power cord to any moving parts of the bed frame.
• Ensure the power cord is routed to the side of the bed and not out the foot end of the bed. If routed improperly,
the power cord may become pinched and could cause electrical shock.
• Allow the foot box to completely dry before placing the support surface over it. Excess moisture could cause
equipment malfunction resulting in equipment damage or patient injury.
• To reduce risk of patient or user injury and equipment damage, do not exceed the safe working load of the hospital
bed frame when supporting both the patient and XPRT™ therapeutic support surface.
• The service screen and its functions are for use by authorized service personnel only otherwise equipment
malfunction could result.
• Do not perform the Diagnostic Test with a patient on the support surface to ensure patient safety.
• Do not perform Burn In function in the field, this function is for ‘manufacturing’ purposes only.
• To avoid possible injury and to assure proper operation when using the XPRT™ therapeutic support surface on a
bed frame equipped with scales or bed exit follow manufacturer’s instructions for use of these options.
Summary of Safety Precautions

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WARNING (CONTINUED)
Summary of Safety Precautions
• To avoid possible injury do not zero bed scales or weigh patient with Percussion,
Vibration, Rotation or Turn Assist active. Patient motion and position resulting from
the support surface may adversely affect scale system performance.
• To avoid possible injury confirm proper scale system operation following support surface installation. For best
results, secure the XPRT™ therapeutic support surface power cord to prevent damage to the cord and interference
with the bed frame and the scale system.
• Max Inflate should not be used as a firmness setting and is only intended for a short duration of up to 30 minutes.
• To avoid possible injury do not initialize “Arm” bed exit with Percussion, Vibration, Rotation or Turn Assist active. The
patient motion and position resulting from the support surface may adversely affect bed exit system performance.
CAUTION
• Do not drop the head section of the support surface back onto the bed frame. Abruptly dropping the support
surface head section could damage the controls and cause equipment malfunction.
• The XPRT™ therapeutic support surface should not be used adjacent to or stacked with other equipment to avoid
malfunction (excluding on a bed). If adjacent or stacked use is necessary, the XPRT™ therapeutic support surface
should be observed to verify normal operation in the configuration in which it will be used.
• To avoid possible patient injury, do not use the side handles to transport the patient.
• Follow all applicable safety rules and protocols concerning patient and caregiver safety.
• To prevent pulling, removal or breakage, stabilize and secure all patient lines and tubing before starting rotation
and monitor them frequently.
• Monitor the patient’s skin condition regularly to ensure skin integrity.
• Patients with body weight or size near the recommended limits should be monitored more frequently to verify
desired results are being achieved.
• The bed’s caster brakes should always be locked except during transport to prevent unintentional movement.
• The bed should always be in the lowest position when the patient is unattended to minimize fall consequences.
• Do not iron, dry-clean, or tumble dry the XPRT™ therapeutic support surface, as this will cause malfunction and
damage the product.
• The support surface cover must be completely dry before storing, adding linens or placing a patient on the surface.
Failure to remove excess disinfectant could cause degradation of the cover material.
• Avoid contact of sharp objects with the support surface. Punctures, cuts and tears in the cover could result
in contamination of the cushions, prevent proper air pressure control and compromise therapy and safety.
• Avoid over exposure to alcohol or hydrogen peroxide. Swelling of the cover material will result.
• If fluids spill on any part of the controller or foot box, immediately unplug the power cord. Remove the patient from
the support surface and clean up the fluid. Fluids can cause corrosion of components and may cause the support
surface to operate erratically or may make some functions completely inoperable. Do not put the support surface
back into service until it is completely dry and has been thoroughly tested for safe operation.

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English
Summary of Safety Precautions
CONTRAINDICATIONS
Stryker Medical promotes the clinical assessment of each patient’s condition and appropriate therapy administration
by the caregiver.
Air support therapy is not recommended for patients with unstable fractures, unstable spinal cord injuries or those in
skeletal traction.
Use of powered support surface systems for stroke victims should be used only under physician’s order.
Percussion/Vibration Therapy is contraindicated in the presence of: multiple rib fractures, persistent intracranial
hypertension, bronchospasms and during post-operative periods following cardiac surgery.
Additional contraindications for Rotation, Percussion and Vibration therapies include, but are not limited to:
• Patients with spinal cord injury
• Patients in skeletal traction
• Patients with significant hemoptysis
• Patients for whom a head down position is contraindicated (e.g., those with a head injury)
• Patients with bleeding disorders
• Patients with rib fractures, or predisposition to pathologic fractures
• Patients for whom the techniques cause increased dyspnea or wheezing
• Patients who are hemodynamically unstable
• Patients with rib fractures

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English
Setup Procedures
INSTALLING THE SUPPORT SURFACE
WARNING
• Do not plug into the power source until assembly
is complete.
• Explosion risk. Do not use in the presence of
flammable mixture with air or with oxygen or nitrous
oxide.
1. Place support surface over bed litter with printed
logo at foot end of bed.
2. Fold back foot end section of support surface.
3. Place foot box on foot end of bed litter.
CAUTION
• The XPRT™ therapeutic support surface should not
be used adjacent to or stacked with other equipment
to avoid malfunction (excluding on a bed). If
adjacent or stacked use is necessary, the XPRT™
therapeutic support surface should be observed to
verify normal operation in the configuration in which
it will be used.
• Avoid contact of sharp objects with the support
surface. Punctures, cuts and tears in the cover
could result in contamination of the cushions,
prevent proper air pressure control and compromise
therapy and safety.
4. Connect the two (2) color coded connectors on
the foot box to the corresponding color coded
connectors on the support surface. Connect
black connection on foot box to cable adapter
2950-001-180 and then connect the other end of
the black connector to the bed (left side of litter at
foot end behind the accessory outlet).
5. Turn the locking collars clockwise to secure the
connections.
6. Connect the air line from the support surface
to the corresponding fitting on the foot box.
7. Fasten the two (2) retaining clips to the 2 “D”
Rings on foot box.
To support surface
Interface at Foot End Left
on Foot Frame of Bed.
To Power Source Outlet on Bed Frame.
“D” Ring
Retaining
Strap

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English
(a)
(b)
(c)
Setup Procedures
8. Lower the foot section of support surface over
the foot box. Attach the support surface to the
bed frame using the support surface tie-downs.
9. Apply linens utilizing the “D” rings for the flat
sheet.
10. To secure linens (a), to support surface (b), thread
four corners through “D” Rings (c) attached to
support surface as shown in the diagram to the
right.
11. To ensure proper therapy, do not pull linens
taut. The linens should remain loose and
wrinkly on the surface of the support surface.
12. Plug the power cord for the support surface
into the FL27 InTouch foot end outlet.
WARNING
• The support surface is equipped with a
hospital grade plug for protection against
shock hazard. It must be plugged directly into
the FL27 InTouch three-prong receptacle.
Grounding reliability can be achieved only
when a hospital grade receptacle is used.
• Do not attach the power cord to any moving parts
of the bed frame.
• To avoid possible injury confirm proper scale
system operation following support surface
installation. For best results, secure the XPRT™
therapeutic support surface power cord to prevent
damage to the cord and interference with the bed
frame and the scale system.
• Ensure the power cord is routed to the side of
the bed and not out the foot end of the bed (refer
to figures on the right). If routed improperly, the
power cord may become pinched and could cause
electrical shock.
Note: After the support surface power cord is
plugged into a power source, if the cable adapter
2950-001-180 is disconnected or the FL27 InTouch
controller is not responding, the support surface will
beep to alert the user.
INSTALLING THE SUPPORT SURFACE (CONTINUED)
Tie-downs “D” Ring
Tie-downs
Tie-downs

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Setup Procedures
Ensure the power cord for the support surface is plugged
into the FL27 InTouch foot end outlet.
WARNING
The support surface is equipped with a hospital grade plug
for protection against shock hazard. It must be plugged
directly into the FL27 InTouch three-prong receptacle.
Grounding reliability can be achieved only when a hospital
grade receptacle is used.
Select the SUPPORT SURFACES button on the FL27
InTouch control panel.
1. Select whether to reset tracking of the current
therapy history.
a) To reset the current therapy history
select the “Ok” button.
b) To continue to store the current therapy history
in memory, select the “Cancel” button.
2. Confirm whether to delete history or continue to
store in memory.
a) To reset the current therapy history, select the
“Ok” button.
b) To continue to store the current therapy history
in memory, select the “Cancel” button.
CONTROLLER BACKLIGHTING
The controller display backlighting will come on during
initial power up. After a period of non-use, the backlighting
goes into standby mode. When the display is in standby,
the support surface continues to function normally. A single
touch anywhere on the screen will turn the backlighting on.
The Status screen indicates which therapies (if any) are
currently active and the amount of therapy time remaining.
Each therapy has a status indicator showing ON, OFF or
PAUSED.
SIDERAIL POSITION
The position of the siderails determines the functionality
of the XPRT™.All the therapies including Max Inflate,
Firmness and Turn Assist, will function if the siderails are
unlocked, except for the rotation therapy. If a siderail
is unlocked during the rotation therapy, this therapy will
automatically stop. If two therapies are simultaneously
executed and a siderail is unlocked during these therapies,
they will automatically stop.
POWERING UP THE SUPPORT SURFACE

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XPRT™ CLINICAL FUNCTIONS
Note:
• All references to right and left on the touch screen and throughout the manual refer to the right and left of a patient
lying face up on the support surface.
• Refer to “Contraindications” on page 1-11 prior to starting therapy.
XPRT™ is a Therapeutic Support Surface that provides patients with continuous pressure redistribution for patients.
This encompasses a safe working load of 500 pounds. The XPRT™ therapeutic support surface features selectable
rotation, percussion, vibration, turn assist and automatic low-air-loss. The touch screen controller is easy to use, offers
12 and 24 hour therapy history, and can be displayed in multi-lingual languages.
XPRT™ is a pressure redistributing therapeutic support surface that assists with pulmonary management.
LOW AIR LOSS (LAL)
XPRT™ provides continuous flow of air through the multi-zoned support surface. LAL assists with skin management of
microclimate at the interface of skin and support surface.
SLOPED HEEL SECTION
The sloped heel section reduces the tissue interface
pressure on the heels by providing support to the calves
and redistributing the heel pressure.
Therapy Modes

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Operation Guide
ROTATION THERAPY
WARNING
• Always secure the support surface straps to the bed frame to prevent the support surface from sliding and to prevent
patient injury.
• Risk of injury. Use of XPRT therapeutic support surface for stroke victims should be only under physician’s order.
• Rotation angle settings approximate the degrees of rotation achieved by a 165 pound patient with an 18 inch
shoulder width. The actual amount of rotation achieved is dependent on patient size, patient weight and shoulder
width. Monitor the patient for at least one complete cycle to verify the unit achieves the desired angle.
• Ensure that any and all tubing and wiring connected to the patient is long enough, stabilized, and secure to assure
safe and unrestricted lateral rotation/elevation of the patient. Be sure to monitor the patient frequently.
• To avoid possible injury, when using rotation or pulmonary therapy, take care not to extubate intubated patients.
• To ensure patient safety, always raise the bed siderails before beginning therapy.
• To avoid possible injury and to assure proper operation when using the XPRT™ therapeutic support surface on a
bed frame equipped with scales or bed exit follow manufacturer’s instructions for use of these options.
• To avoid possible injury do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn
Assist active. Patient motion and position resulting from the support surface may adversely affect scale system
performance.
• To avoid possible injury do not initialize “Arm” bed exit with Percussion, Vibration, Rotation or Turn Assist active. The
patient motion and position resulting from the support surface may adversely affect bed exit system performance.
CAUTION
• To prevent pulling, removal or breakage, stabilize and secure all patient lines and tubing before starting rotation
and monitor them frequently.
• Patients with body weight or size near the recommended limits should be monitored more frequently to verify
desired results are being achieved.
• The bed’s caster brakes should always be locked except during transport to prevent unintentional movement.
TO PREPARE FOR ROTATION THERAPY
PATIENT POSITIONING
1. Position the patient along the center line of the
support surface.
WARNING
Failure to position the patient along the support surface
center line before starting therapy could result in patient
injury. Check patient frequently to ensure proper positioning
and support surface inflation.
2. Align the patient’s shoulders with the graphic
indicator on the side of the support surface.
BED POSITIONING
1. Raise the bed siderails.
2. Lower the bed height to the lowest practical position.
3. Lower the head section to flat or as low as possible.