Fuse Rating for Beds with the 100V~ or 120V~ Electric System
Potential Equalization
Protective Earth Terminal
Protection from liquid splash
Type B Applied Part
Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire,
and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1: 2005 and CAN/CSA-C22.2
No. 60601-1:08.
In accordance with European Directive 2012/19/EU 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.
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Non-ionizing radiation; i.e. RF transmitter (Wi-Fi)
International Warranty Clause...........................................................249
82141-2 09 -002 REV Hwww.stryker.com
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
This provides special information to make maintenance easier or important instructions clearer.
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Return To Table of Contents
Introduction
This manual assists you with the operation or maintenance of the Stryker Model FL27 (2131/2141) InTouch® Critical
Care bed. Read this manual thoroughly before operating or maintaining this product. Set methods and procedures to
educate and train your staff on the safe operation or maintenance of this product.
WARNING
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described
in this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
Notes
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current
product information available at the time of printing. There may be minor discrepancies between your product and
this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1–800–327-0770.
PRODUCT DESCRIPTION
InTouch is an AC-powered, adjustable hospital bed designed to position human patients for procedures, therapy, and
recovery in a healthcare environment, and transport patients between bays and procedural rooms. InTo u c h measures
and displays patient weight. The scale output is not intended to be used to determine diagnosis or treatment. The nurse
call allows patients to alert an operator when the patient requires assistance. There is a 30-degree head of bed (HOB)
button that puts the patient at a 30-degree angle that is calculated relative to the base to assist in ventilator-associated
pneumonia (VAP) prevention. When the Chaperone bed exit system is active, it monitors a chosen zone, and alerts the
operator of a deliberate or non-deliberate bed exit. The bed has 39 prerecorded clinical phrases in 24 languages and
a sound feature that offers various environmental and musical selections.
INTENDED USE: INTOUCH CRITICAL CARE BED
InTouch is intended for use by patients in an acute care setting. The safe working load (the sum of the patient, the
mattress, and accessory weight) for InTouch is 550 lb (249 kg).
InTouch is intended to support a human patient. The frame can come in contact with human skin, but a patient should
never be on the frame without a support surface in use.
InTouch is intended for use in acute care. These settings may include critical care, step down, progressive care, med/
surg, sub-acute care, and post anesthesia care unit (PACU), or other locations, as prescribed. Intended operators are
healthcare professionals (nurses, nurse aids, doctors) that can use all bed operations (such as bed motion functions,
nurse call, siderail communications, bed exit, therapy options), patient and bystander that can use bed motion functions,
nurse call and siderail communications, and trained professionals for installation, service, and calibration.
The product is intended for use in a healthcare environment, including hospitals, surgery centers, long term acute care
centers, and rehabilitation centers.
The product is compatible with 35 in. x 84 in. support surfaces, the facility nurse call system, standard med/surg
equipment, and the facility infrastructure. InTo u c h is intended for use with a 6 in. to 8.5 in. support surface. You may
use a support surface or overlay greater than 6 in. that offers therapeutic value with added patient supervision.
The Chaperone bed exit system is intended only to aid in the detection of a patient exiting the unit. It is not intended
to replace patient monitoring protocol.
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102141-209-0 02 RE V Hwww.stryker.com
Introduction
INTENDED USE – iBED® WIRELESS WITH iBED AWARENESS
The intended use for the iBed® Wireless (with iBed® Awareness) is to assist clinical staff to monitor bed parameters
on specific Stryker beds. The desired bed parameters will be set by clinicians at the bedside. The iBed® Wireless
software is intended to be used only with specifically enabled Stryker beds that have been verified and validated with
the iBed® Wireless software, and is not intended to provide bed status information for non-Stryker beds. The iBed®
Wireless software is not intended to communicate any patient status information, nor to permanently store any type
of data. The iBed® Wireless with iBed® Awareness System is not intended to provide automated treatment decisions
or as a substitute for professional healthcare judgment. The iBed® Wireless with iBed® Awareness System is not a
replacement or substitute for vital signs monitoring or alert equipment. All patient medical diagnosis and treatment are
to be performed under direct supervision and oversight of an appropriate health care professional.
EXPECTED SERVICE LIFE
InTouch has a 10 year expected service life under normal use conditions and with appropriate periodic maintenance.
CONTRAINDICATIONS
InTouch is not intended to:
• be used without a support surface
• use the scale output to determine diagnosis or treatment
• be used with an oxygen tent
• support more than one individual at a time
• be used with patients that are 35 in. or less
• be used with patients that weigh 50 lb or less
• be used on patient less than two years old
• be used in a home healthcare environment
• be used in the presence of flammable anesthetics
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SPECIFICATIONS
Safe Working Load
Introduction
Note: Safe Working Load indicates the
sum of the patient, mattress and accessory
weight.
Bed Weight750 lbs340.2 kg
Overall Bed Length90 in.228,6 cm
Overall Bed
Width
BaseUnderbed Clearance5 in. 12,7 cm
LitterPatient Surface
Bed Lift
System
Scale SystemCapacity550 lbs249 kg
CPR SystemSpeed to level bed from any position
Zoom®
motorized
drive (Model
2141) (option)
Siderails Up42 in. 106,7 cm
Siderails Down40 in.102,9 cm
• Width
• Length
• Length (with Optional Bed
Extender)
Seat Section
• Depth
Foot Section
• Length
• Angle
Fowler Section
• Length
• Width
• Angle
Gatch Section
• Length
• Width
• Angle
Cardiac Chair
• Standard Cardiac Chair Position
• Enhanced Cardiac Chair Position
Height (high) to top of litter33 in. 83,8 cm
Height (low) to top of litter16 in. 40,6 cm
Trendelenburg/Reverse Trendelenburg12° (± 2°)
Bed Lift Time35 seconds maximum from lowest to highest position
Accuracy:
• For weight from 100 lb to 550 lb
• For weight from 100 lb to 550 lb
• For weight under 100 lb
• For weight under 100 lb
• Fowler
• Foot and Seat
Speed
• Forward
• Backwards
550 lbs249 kg
35 in.
84 in.
90 in.
18.5 in. 47 cm
29 in.
0° to 50° (± 5°)
36 in.
34 in. to 35 in.
0° to 70°
(0°-40° and 50°-70° ± 3°)
(40°-50° ± 5°)
120 ± 10% Vac, 50/60Hz - Two 250V, 10A Fuses
120V~, 50-60Hz, 4.0A (9.8A with 120V Optional Auxiliary
Outlet) - Two 250V, 10A Fuses
Recommended Support Surface Size35” x 84” x 6”88,9 cm x 213,4 cm x 15,2 cm
• With Bed Extender DM64196
(PositionPRO® and Isolibrium™) (35” x 6” x 4”)
• With Bed Extender DM64197 (XPRT™) (35” x 6” x 5.5”)35” x 90” x 5.5”88,9 cm x 228,6 cm x 13,9 cm
Recommended Air Mattress Size35” x 84” x 6” - 8.5”
• With Bed Extender DM64196
(PositionPRO® and Isolibrium™) (35” x 6” x 4”)
• With Bed Extender DM64197 (XPRT™) (35” x 6” x 5.5”)35” x 90” x 5.5”88,9 cm x 228,6 cm x 13,9 cm
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35” x 90” x 4”88,9 cm x 228,6 cm x 10,1 cm
88,9 cm x 213,4 cm x
15,2 cm - 21,6 cm
35” x 90” x 4”88,9 cm x 228,6 cm x 10,1 cm
Return To Table of Contents
50 °F
(1
104 °F
-40 °F
(-40 °C)
158 °F
30%
75%
10
95%
7
1060 hPa
500 hP
1060 hPa
64 °F
(1
77 °F
Introduction
ENVIRONMENTAL CONDITIONS
Environmental ConditionsOperationStorage and Transportation
Ambient Temperature
(40 °C)
(70 °C)
0 °C)
Relative Humidity
(Non-Condensing)
%
Atmospheric Pressure
00 hPa
a
(25 °C)
Scale Accuracy
8 °C)
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
Stryker reserves the right to change specifications without notice.
Return To Table of Contents
142141-209- 002 REV Hwww.stryker.com
PRODUCT ILLUSTRATION
ST
Introduction
B
O
N
P
H
G
J
I
R
A
D
L
K
E
F
U
A110V outlet (optional)LManual backup brake
BBrake control panel (outside siderail)MMattress retainer
CCasterNNurse call (inside siderail) (optional)
DCPR release pedalOMotion control panel (outside siderail)
EFoley bag hooksPPendant holder
FFootboardQRoller bumpers
GFootboard control panelRSiderail release levers
HHeadboardSSiderails
IHead end control panel (optional)TSupport surface (optional)
JInTouch touch screenUZoom drive system (model 2141) (optional)
KIsolated foley bag hooks
C
M
Q
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Introduction
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, Michigan 49002
USA
To view your operations or maintenance manual online, see https://techweb.stryker.com/.
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.
SERIAL NUMBER LOCATION
You can find the serial number plate behind the patient right siderail near the foot end of the product.
A
SPECIFICATION LABEL LOCATION
You can find the specification label behind the head end cover on the patient right side of the product.
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162141-209 -002 RE V Hwww.stryker.com
Summary of Safety Precautions
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described
in this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
• Always allow the product to reach room temperature before conducting any setup or testing functional operations
to prevent permanent product damage.
• Always operate the product when all operators are clear of the mechanisms.
• Always plug the product directly into a properly grounded, three-prong receptacle. You can only achieve grounding
reliability when you use a hospital-grade receptacle. This product is equipped with a hospital-grade plug for
protection against electric shock hazard.
• Always properly handle the power cord to avoid the risk of entanglement, damage to the power cord, or potential
shock hazards. If the power cord is damaged, immediately remove the product from service and contact the
appropriate maintenance personnel.
• Do not attach the power cord to any moving parts of InTouch.
• Always unplug the power cord, turn the battery switch to the OFF (O) position, press the N/Brake Off button, and
call maintenance if unanticipated motion occurs.
• Always unplug the product power cord from the wall when using oxygen administering equipment. Possible fire
hazard exists when this product is used with oxygen administering equipment other than nasal, mask type, or half
bed-length tent type.
• The optional iBed® Wireless function is only intended to provide remote information of product status and parameter
conditions. It is not intended to replace patient monitoring protocol.
• The line of sight between an iBed Locator and the head end of bed must be free of obstruction at all times. Any
interference could interrupt communication between the iBed Locator and the IR module.
• You must use an iBed® Wireless compatible footboard with an iBed® Wireless compatible product. You will lose
iBed® Wireless functionality if you use an older version of the footboard.
• You must verify all iBed® Wireless functionality after installation. Verify that the iBed locator communicates the
product’s positions, and that iBed® Wireless communicates with the wireless access point. Failure to do may result
in the loss of information or the transmission of incorrect information.
• You must install the iBed Locators more than 71” apart from one another in the same room (such as in a
semiprivate room with more than one product). Failure to do may result in the product transmitting information to
the incorrect iBed Locator.
• Do not use iBed® Wireless to replace the existing nurse call system. iBed® Wireless products are only intended
to transmit product information. They are not intended to transmit nurse call information.
• Always correctly associate or map the iBed Locator to the room or location to provide accurate location information.
Failure to properly map the iBed Locator to the room or location may result in the product transmitting incorrect
information.
• If you move an iBed Locator after it has been installed and mapped, you must remap to the new room or location
in which it is moved to. You must also remap the iBed Locator if you change the room or location information after
initial installation.
• Always wash your hands after handling a battery. Battery posts, terminals and related accessories contain lead
and lead compounds, chemicals known to the State of California to cause cancer and birth defects or other
reproductive harm. Properly dispose of batteries when required.
• Power save mode activates after one hour on battery power with no motion release switch activation. Bed exit,
scale, and product motion stops operating when the product enters the power save mode.
• Always keep feet clear from the area above the base cover or below the base cover when lowering the product or
when applying the brakes or releasing the brakes.
• Always apply the brakes when a patient is getting in the product or out of the product to avoid instability.
• Always apply the brakes when the patient is unattended.
• Do not apply the electronic brake to slow or stop the product while it is in motion.
• Always keep the product in a low, horizontal position with the siderails fully raised and locked when transporting a
patient.
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Summary of Safety Precautions
WARNING (CONTINUED)
• Do not use the Zoom motorized drive when the batteries become discharged. Press N/Brake Off to place the drive
wheel in neutral and push the product manually. Recharge the batteries before using the Zoom motorized drive
again to avoid the risk of battery damage and the drive wheel getting stuck in the down position.
• Use caution while maneuvering the product with the drive wheel activated. Always make sure that there are no
obstacles near the product while the Zoom motorized drive is activated. Injury to the patient, user or bystanders or
damage to the frame or surrounding equipment could occur if you collide with an obstacle.
• Make sure that the brakes are completely released before attempting to move the product. Attempting to move the
product with the brakes applied could result in injury to the patient or operator.
• Do not attempt to move the product manually when you activate the Zoom motorized drive. Always place the drive
wheel into the neutral position and release the brakes before attempting to move the product manually.
• Always make sure that all persons and equipment are away from the area below and around the product before
you activate the CPR release. The CPR release is for emergency use only.
• Always determine the proper use of the restraint straps and restraint strap locations. Improperly adjusted restraint
straps can cause serious injury to a patient. Stryker is not responsible for the type or use of restraint straps on
any of Stryker’s products.
• Only use hospital-grade electric equipment consuming 5A or less with the auxiliary power outlet (optional). The
use of standard electric equipment may bring the current leakage to a level unacceptable for hospital equipment.
• Always keep the siderails in the fully raised position and the sleep surface horizontal in its lowest position unless
the patient’s medical condition dictates otherwise.
• Do not use siderails, with or without their padded covers, as restraint devices to keep patient from exiting the
product. Siderails are designed to keep a patient from inadvertently rolling off the product. It is the responsibility
of the attending medical personnel to determine the degree of restraint necessary to ensure a patient’s safety.
Failure to use the siderails properly could result in serious patient injury.
• Always keep the siderails outside of the oxygen tent.
• The scale system is intended to assist in the monitoring of the patient’s weight variation. Under no circumstances
should its reading be used as sole reference for medical treatment.
• Bed exit is intended only to aid in the detection of a patient exiting the product. It is not intended to replace patient
• onitoring protocol.
• Bed exit is not designed to be used with patients weighing less than 50 lb (23 kg).
• Do not use extension cords with support surfaces. Support surfaces are only intended to be powered by InTouch
with the power cord supplied.
• Do not route cables between the support surface and InTouch.
• Always make sure that all of the patient’s limbs are within the raised and locked siderails when the support surface
is articulating to avoid the risk of patient injury.
• Always center the patient on the support surface. Align the patient’s head toward the headboard before starting
functions. Check the patient frequently to make sure that you maintain the proper positioning.
• Always make sure that the tubing and wiring that is connected to the patient is long enough, stable, and secure
during Lateral Rotation or Turn Assist.
• Always raise all of the InTouch bed siderails before starting Turn Assist or Lateral Rotation functions.
• Do not exceed the safe working load of the Isolibrium support surface. Excess weight could cause unpredictable
safety and performance of this system.
• Always use extra caution when reading radiology images taken of a patient on a support surface because internal
components can cause artifacts and distort readings.
• Do not extubate or intubate patients during Lateral Rotation or Turn Assist. The functions could interfere with the
performance of the ancillary devices.
• Do not zero the bed scales or weigh the patient with Lateral Rotation or Turn Assist active. Motion from the support
surface functions may adversely affect the scale system performance.
• Do not arm bed exit with Lateral Rotation or Turn Assist active. The patient motion and position that results from
the support surface may adversely affect bed exit system performance.
• Do not leave the patient unattended during Turn Assist.
• Always deflate the Isolibrium support surface before beginning CPR.
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182141-209 -002 RE V Hwww.stryker.com
Summary of Safety Precautions
WARNING (CONTINUED)
• Always lock the control panel when the patient is unattended, or when a patient’s condition requires greater safety
measures for their condition.
• Do not use iBed® Awareness as a lock indicator for siderails. iBed® Awareness is only intended to detect the
position of the siderails. It is not intended to replace patient monitoring protocol.
• The iBed® Awareness LED light bars are only intended to monitor the product status and parameter conditions. It
is not intended to replace patient monitoring protocol.
• You must physically verify that the siderails are locked before arming iBed® Awareness.
• Always securely set the footboard connector on the optional bed extender into the footboard connector slot at the
foot end of the product.
• Do not pinch the power cord or cables when installing the optional bed extender.
• Do not sit on the optional bed extender. This may cause the product to flip.
• Do not allow the optional line management clip to interfere with a mechanical or electronic mechanism of the
product.
• Do not pinch tubes inside the clip.
• Do not clean the clip with a liquid solution.
• Always adjust the scale or bed exit system if an option is added while the scale or bed exit system is armed.
• Do not place objects that exceed 40 lb (18 kg) onto the optional monitor tray.
• Do not exceed the 150 lb (68 kg) load capacity for the tray support pole.
• Do not clean, service, or perform maintenance while the product is in use.
• Always unplug the power cord and turn the battery switch to the OFF (O) position before cleaning, servicing, or
performing maintenance.
• Always immediately unplug the power cord from the wall outlet when large spills occur near the circuit boards,
cables, and motors. Remove the patient from the product, clean up the fluid, and have service personnel completely
inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product.
Do not return the product to service until it is completely dry and has been thoroughly tested for safe operation.
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Summary of Safety Precautions
CAUTION
• Always plug the product into a wall outlet (regulated AC power source) when not in use to maintain a sufficient
battery charge and to maximize product performance while operating on battery power.
• Always immediately replace batteries that have corrosion at the terminals, display cracking, have expanded or
bulging sides, or no longer can maintain a full charge.
• Always use only Stryker authorized batteries when replacing the batteries. Use of non-Stryker batteries may lead
to unpredictable system performance.
• Upon a Battery Low alarm (Battery Low LED on Footboard and audible beep), stop using the Zoom motorized drive
and recharge the batteries immediately. Ignoring the Battery Low alarms may cause your batteries to degrade
quicker than normal and may decrease battery life.
• Always clean Velcro® after each use. Saturate Velcro with disinfectant and allow disinfectant to evaporate.
Appropriate disinfectant for nylon Velcro should be determined by the hospital.
• Do not move footboards from one product to another. Individual products may have different options. Mixing
footboards could result in unpredictable operation of the product.
• Do not use the siderails to move the product. Move the product using the integrated handles in the headboard and
footboard.
• Do not use pencils, pen caps, pen tips, or other pointed objects to tap the touch screen display. Using excessive
pressure may damage the footboard control panel and the touch screen display.
• Always use extra supervision when using a mattress or support surface thicker than six in. (15,4 cm).
• Do not allow sharp objects to come into contact with the support surface that could puncture, tear, or cut the cover.
• Make sure that you set the desired product parameters before enabling iBed® Awareness.
• Do not use accessories that cover the footboard and outside siderail LED light bars.
• Do not turn off the iBed® Awareness alarm. You will lose access to the event manager that displays the compromised
parameter condition.
• Do not hang IV bags that exceed 22 lb (10 kg) onto the IV pole.
• Always make sure that the IV pole is at a low height to pass safely through door openings.
• Do not use the IV pole as a push/pull device.
• Always make sure that the clip is stable when installed.
• Do not inset tubes that are larger than 0.75 in. into the line management clip.
• Always sterilize the clip after each use.
• Always make sure that the clip is stable when installed.
• Always unplug the product before cleaning or servicing.
• Always unplug the product, set the brakes, and place blocks under the litter frame for support when working under
the product.
• Always make sure that you wipe each product with clean water and thoroughly dry each product after cleaning.
Some cleaning products are corrosive in nature and may cause damage to the product if you use them improperly.
If you do not properly rinse and dry the product, a corrosive residue may be left on the surface of the product that
could cause premature corrosion of critical components. Failure to follow these cleaning instructions may void
your warranty.
• Do not steam clean, pressure wash, ultrasonically clean, or immerse any part of the product in water. Exposure to
water may damage the internal electric parts. These methods of cleaning are not recommended and may void this
product’s warranty.
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202141-209-0 02 RE V Hwww.stryker.com
Static Discharge Precautions
PROTECTING AGAINST ELECTROSTATIC DISCHARGE (ESD)
CAUTION
• Always use ESD protective equipment before opening antistatic bags and servicing electronic parts.
• Do not place unprotected circuit boards on the floor.
• All electronic service parts will be shipped in static shielding bags. Do not open the bags until you have completed
steps 2 and 3 of the Static Protection Procedure.
Note: Always ship back circuit boards to Stryker in the same antistatic bags that the new boards were
originally shipped in.
The electronic circuits in the product are completely protected from static electricity damage when factory assembled.
Always use adequate static protection when servicing the electronic systems of the product. All service personnel must
use static protection whenever they are touching wires.
Static Antistatic Protection Equipment Includes:
• 1 antistatic wrist strap
• 1 grounding plug
• 1 test lead with a banana plug on one end and an alligator clip on the other end
Static Protection Procedure
1. Unplug the power cord from the power source.
2. Insert the grounding plug into a properly grounded hospital grade wall receptacle. Plug the banana plug of the
test lead into the receptacle on the grounding plug. Connect the alligator clip on the other end of the test lead to
a ground point on the bed.
3. Place the static control wrist strap on your wrist. Connect the alligator clip at the other end of the wrist strap cord
to a ground point on the bed.
BED
GROUNDING DIAGRAM
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Setup
To unpack your product, see the unpacking instructions that are attached to the product inside of the shipping crate.
WARNING
• Always allow the product to reach room temperature before conducting any setup or testing functional operations
to prevent permanent product damage.
• Always operate the product when all operators are clear of the mechanisms.
• Always properly handle the power cord to avoid the risk of entanglement, damage to the power cord, or potential
shock hazards. If the power cord is damaged, immediately remove the product from service and contact the
appropriate maintenance personnel.
• Do not attach the power cord to any moving parts of InTouch.
• Always unplug the power cord, turn the battery switch to the OFF (O) position, press the N/Brake Off button, and
call maintenance if unanticipated motion occurs.
CAUTION
Always plug the product directly into a properly grounded, three-prong receptacle. You can only achieve grounding
reliability when you use a hospital-grade receptacle. This product is equipped with a hospital-grade plug for protection
against electric shock hazard.
To turn on the product:
1. Plug the power cord into a properly grounded, hospital-grade wall outlet.
2. Turn the battery switch to the ON (|) position.
Before placing the product into service, make sure that these components are working properly:
1. Visually inspect the product for any signs of shipping damage.
2. Flip down and depress the manual brake pedal and make sure that the neutral, drive, and brake functions of the
manual brake pedal hold.
3. Press BRAKE on each control panel and make sure that the neutral, drive, and brake functions of the electronic
brake hold.
4. Test the Zoom drive system (Model 2141).
5. Raise and lower the siderails to make sure that they move smoothly and lock securely in the full up position.
6. Press each button on the head end control panel (optional), motion control panel, brake control panel, footboard
control panel, and patient control pendant (optional) to make sure that each function operates properly.
7. Make sure that the footboard operates properly.
8. Make sure that the scale system operates properly.
9. Make sure that the bed exit system operates properly.
10. Make sure that the CPR release pedal operates properly.
11. Make sure that the support surface operates properly (optional).
12. Make sure that optional accessories are installed and operate as described.
WARNING
Always unplug the product power cord from the wall when using oxygen administering equipment. Possible fire hazard
exists when this product is used with oxygen administering equipment other than nasal, mask type, or half bed-length
tent type.
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222141-209-0 02 RE V Hwww.stryker.com
Installation
INSTALLING THE XPRT THERAPY SUPPORT SURFACE (OPTIONAL)
To install the XPRT support surface option onto InTouch, see the installation instructions in the XPRT support surface
operations manual.
INSTALLING THE POSITIONPRO SUPPORT SURFACE (OPTIONAL)
To install the PositionPRO support surface option onto InTouch, see the installation instructions in the PositionPRO
support surface operations manual.
INSTALLING THE ISOLIBRIUM SUPPORT SURFACE (OPTIONAL)
To install the Isolibrium support surface option onto InTouch, see the installation instructions in the Isolibrium support
surface operations manual.
INSTALLING IBED WIRELESS (120V NORTH AMERICAN ONLY) (OPTIONAL)
WARNING
• The optional iBed® Wireless function is only intended to provide remote information of product status and parameter
conditions. It is not intended to replace patient monitoring protocol.
• The line of sight between an iBed Locator and the head end of bed must be free of obstruction at all times. Any
interference could interrupt communication between the iBed Locator and the IR module.
• You must use an iBed® Wireless compatible footboard with an iBed® Wireless compatible product. You will lose
iBed® Wireless functionality if you use an older version of the footboard.
• You must verify all iBed® Wireless functionality after installation. Verify that the iBed locator communicates the
product’s positions, and that iBed® Wireless communicates with the wireless access point. Failure to do may result
in the loss of information or the transmission of incorrect information.
• You must install the iBed Locators more than 71” apart from one another in the same room (such as in a semiprivate room with more than one product). Failure to do may result in the product transmitting information to the
incorrect iBed Locator.
• Do not use iBed® Wireless to replace the existing nurse call system. iBed® Wireless products are only intended to
transmit product information. They are not intended to transmit nurse call information.
You must install the iBed Locator on the wall at the head end of the bed. The iBed Locator communicates with the IR
Module that is installed onto the product.
To mount the iBed Locator, see the installation instructions that were included with your iBed Locator Installation kit.
After you install the iBed Locator, you must configure the wireless connection settings for the iBed Server application.
To configure the iBed Server application, see the installation and configuration instructions in the iBed Server
Installation/Configuration manual.
WARNING
• Always correctly associate or map the iBed Locator to the room or location to provide accurate location information.
Failure to properly map the iBed Locator to the room or location yields incorrect remote information.
• If you move an iBed Locator after it has been installed and mapped, you must remap to the new room or location
in which it is moved to. You must also remap the iBed Locator if you change the room or location information after
initial installation.
If you have any problems during the iBed Wireless installation process, contact Stryker Technical Support at
1–800–327−0770.
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Return To Table of Contents
Maintenance Menu Guide
The Maintenance Menu is accessed through the Touch Screen and contains additional features of the product. This
menu provides an interface to the user and/or service personnel in order to provide the ability to control and access
maintenance features.
ACCESSING THE CONFIGURATION SCREEN
WARNING
Please ensure patient is not in the bed prior to starting bed calibration. In calibration mode, the software does not control
the interferences between the mechanical parts of the bed. Mechanical damage could occur without supervision. Only
qualified personnel should perform the calibration.
Note
Verify that the bed is on a level surface which does not have any slopes or inclines prior to entering into the calibration
mode.
1. Unseat and reseat the footboard and wait until the main control screen is displayed.
2. Push and hold the Main Menu button located in the upper right corner of the footboard control panel
(see Figure 1 below). Continue pressing on the Main Menu button while executing steps 3-5.
3. Push and hold the Brake button for 5 seconds and then release.
4. Push the HOB 30o+ button once and release.
5. Push the Drive button once and release.
6. Release the Main Menu button and you will be taken into the Configuration Screen shown in Figure 2.
HOB
Brake
Main Menu
Drive
Figure 1: Footboard Control Panel
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Figure 2: Configuration Screen
Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN
The following items A, B, and C are configuration buttons
available and displayed on the Configuration screen
(Figure 3).
A. Bed Calibration
B. Full Diagnostic (see page 36)
C. Touch Screen Calibration (see page 37)
D. Optional Wi-Fi Configuration (see page 38)
The following items D and E are configuration options
available but are not displayed on the Configuration
screen To access these configuration options, follow the
procedures identified on page listed below.
E. Bed Options Configuration (see page 39)
F. Serial Number Configuration (see page 40)
Figure 3: Configuration Screen Menu Items
A. Bed Calibration
Note: During calibration, if the backlight shuts off touch the screen to continue.
1. Connect the bed to an A/C outlet.
2. Place the mattress onto the frame.
3. Press the Bed Calibration button on the Configuration Screen (refer to Figure 3).
4. After pressing the Bed Calibration button, Figure 4 will be displayed. Press “NEXT” to continue with
calibration.
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Figure 4: Bed Calibration - WARNING
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
5. After pressing Next to continue calibration,
Figure 5 will appear.
Figure 5: Bed Calibration - Step #1 of 6
6. Place the Litter surface to a flat position by
pressing simultaneously the Foot Up, Fowler Down and Gatch Down buttons as shown in
Figure 6.
7. Lower the bed to the lowest position. Press
the Bed Height Down (Head Lift Down) and
Reverse Trendelenburg (Foot Lift Down)
buttons simultaneously as shown in Figure 7.
Foot Up
QDF27-2237
Fowler Down
Gatch Down
Figure 6: HE Siderail Control Panel - (Right Side Shown)
Reverse Trendelenburg
(Foot Lift Down)
Bed Height
Down
(Head Lift
Down)
QDF27-2237
Figure 7: HE Siderail Control Panel - (Right Side Shown)
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
Bed Calibration
Do Not
8. Press the Next button when done. The “Do Not
Touch Bed
Touch Bed” screen will appear as shown in Figure
8.
Cancel
Figure 8
9. When step 1 of the calibration procedure has completed, step 2 of the calibration procedure will begin and
Figure 9 will be displayed.
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Figure 9: Bed Calibration - Step 2
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
10. Raise the bed height to 20 inches measuring
from the top of the seat section to the floor.
Press the Bed Height Up (Head Lift Up) and
Trendelenburg (Foot Lift Up) buttons as
shown in Figure 10.
11. Standing on either side of the bed at the fowler
section, raise the foot siderail and then position
the digital level/inclinometer on the bottom of
the litter below the mattress retainer (refer to
Figure 11). Using the digital level/inclinometer,
verify the bed is level (0.0 +/- 0.1).
Bed Height Up
(Head Lift Up)
Trendelenburg
(Foot Lift Up)
Figure 10: Head Siderail Control Panel
(Right Side Shown)
QDF27-2237
Note: Cycle power on the digital level/
inclinometer prior to placing it on the
bottom of the litter frame and do not zero/
calibrate the digital level/inclinometer.
12. Press the Next button when done. The “Do
Not Touch Bed” screen will appear as shown
in Figure 12.
Placement
on Litter
Figure 11: Inclinometer placement
Bed Calibration
Do Not
Touch Bed
Cancel
Figure 12: Do Not Touch Bed Screen
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
13. When step 2 of the calibration procedure has completed, step 3 of the calibration procedure will begin and
Figure 13 as shown below will appear on the screen.
Figure 13: Bed Calibration - Step 3
14. Place the bed at +12 degrees Trendelenburg by pressing
the Trendelenburg (Foot Lift Up) button as shown in
Figure 14. Verify +12 degrees +/- 0.1 with the inclinometer
you previously placed on the litter frame in step 11.
Trendelenburg
(Foot Lift Up)
QDF27-2237
Figure 14: Head Siderail Control Panel
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Return To Table of Contents
Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
15. Press the Next button when done.
16. The “Do Not Touch Bed” screen will appear as
shown in Figure 15.
Bed Calibration
Do Not
Touch Bed
Cancel
Figure 15: Do Not Touch Bed Screen
17. When step 3 of the calibration procedure has completed, step 4 of the calibration procedure will begin and
Figure 16 will be displayed as shown below.
Figure 16: Bed Calibration - Step 4
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
18. Level the bed back out to zero degrees by pushing
the Reverse Trendelenburg button until the litter
is level while referencing the inclinometer. Note:
Confirm inclinometer reads zero degrees.
19. Place the bed at -12 degrees Reverse Trendelenburg
by pressing the Bed Height Up (Head Lift Up) button
as shown in Figure 17 below. Verify -12 degrees +/-
0.1 with the inclinometer you previously placed on the
bottom of the litter frame in step 11.
Bed Height Up
(Head Lift Up)
QDF27-2237
Figure 17: Head Siderail Control Panel -
(Right Side Shown)
20. Press the Next button when done.
21. The “Do Not Touch Bed” screen will appear as
shown in Figure 18.
Bed Calibration
Do Not
Touch Bed
Cancel
Figure 18: Do Not Touch Bed Screen
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
22. When step 4 of the calibration procedure has completed, step 5 of the calibration procedure will begin and
Figure 19 will appear on the screen as shown below.
Figure 19: Bed Calibration - Step 5
23. Place the bed at the highest height by pressing
simultaneously the Trendelenburg(Foot Lift Up)
button and Bed Height Up (Head Lift Up) button as
shown in Figure 20.
Trendelenburg
(Foot Lift Up)
Bed Height Up
(Head Lift Up)
QDF27-2237
Figure 20: Head Siderail Control Panel -
(Right Side Shown)
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
Gatch Up
24. Press the Fowler Up button until the Fowler reaches
the highest height, next press the Gatch Up button
until the Gatch reaches its highest height, lastly
press the Foot Up button until the foot section
reaches its highest height (refer to Figure 21
below). The foot section should be at a flat position.
25. Press the Next button when done.
Fowler Up
Figure 21: Head Siderail Control Panel -
(Right Side Shown)
Bed Calibration
Foot Up
QDF27-2237
26. The “Do Not Touch Bed” screen will appear as
shown in Figure 22.
Do Not
Touch Bed
Cancel
Figure 22: Do Not Touch Bed Screen
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
27. When step 5 of the calibration procedure has completed, step 6 of the calibration procedure will begin and
Figure 23 will be displayed as shown below.
Figure 23: Bed Calibration - Step 6
28. Place the bed at the highest height by pressing
simultaneously the Trendelenburg(Foot Lift Up)
button and Bed Height Up (Head Lift Up) button (see
Figure 24).
29. Place the Fowler and Gatch section of the bed at the
highest height by first pressing the Fowler Up button
then the Gatch Up button (See Figure 24).
30. Place the foot at the lowest position by pushing the
Foot Down button until limit is met (see Figure 24) .
CAUTION: The Gatch must be raised to the highest
height prior to running the Foot Down or damage
could occur.
Bed Height Up
(Head Lift Up)
Fowler Up
Trendelenburg
(Foot Lift Up)
Gatch Up
Figure 24: Calibration Complete
Foot Down
QDF27-2237
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
A. Bed Calibration (Continued)
31. When the calibration procedure is completed, Figure 25 will be displayed as shown below.
32. Press the Close button to exit the Calibration Procedure Menu.
33. Level the litter flat using the CPR pedal. Verify all display readings are zero degrees while the bed is at
33” (84 cm) (highest height). Lower the bed to 16” (41 cm) (lowest height) and verify the display readings
maintain a constant reading of zero degrees with no fluctuations. When the bed reaches it lowest height at
16”, verify the display readings are still at zero degrees.
Note: If readings are not all zero, you will need to recalibrate the bed by repeating steps 1-30.
Figure 25: Calibration Complete
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN
(CONTINUED)
B. Full Diagnostic
1. From the Configuration Screen, press the
Full Diagnostic button. Figure 26 will appear.
2. The following menu items may be selected
by pressing their button.
a. BOARDS (Figure 27a)
Provides information on the switch
boards and the touch screen’s
software version.
b. ERROR CODES (Figure 27b)
Provides information on errors which
the CPU board has identified.
c. INPUT STATES (F igure 2 7c)
Provides information on the status of
all switches and jumpers on the bed.
d. MOTORS (Figu r e 27d)
Provides information on what a motor is doing when a function button is pushed.
Note: This requires assistance to press the buttons on the head siderails or at the head end control.
e. BUTTONS PRESSED (Figu r e 27e)
Provides information on when the CPU has detected a button being pressed.
Note: This requires assistance to press the buttons on the head siderails or at the head end control.
f. SIGNAL VALUES (Figure 27f)
Provides information on CPU voltages, load cell values, and angle sensor values.
Figure 26: Full Diagnostic Screen
Boards Connected
Nurse A.0 A.1
Nurse (SRH) A.1
Nurse (SRL) A.1
Nurse (SRR) A.1
Power board B.37
Room Interface A.1
TouchScreen D.3
Figure 27a: Board
Motors
Gatch - Reverse
Hilo Foot - Forward
Foot - Forward
Figure 27d: Motor
Close
Close
Figure 27c: Input StatesFigure 27b: Error Codes
Buttons Pressed
Nurse SRR - Trend
Footboard - Hob
Nurse Head - Leg up
Close
Figure 27e: Pressed ButtonsFigure 27f: Signal Values
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
C. Touch Screen Calibration
Ensure patient is not present on the bed before performing the Touch Screen Calibration.
1. From the Configuration Screen, press the Touch Screen Calibration button. Figure 28 will appear.
NOTE: If the touch screen will not respond, you will need to push the HOB 300+, Brake and Drive buttons
on the footboard at the same time (this will enable you to get directly into the touch screen calibration).
CAUTION: When pushing the buttons above the fowler, brakes, or drive, actuators may activate.
2. Carefully press and briefly hold a stylus or your finger on the center of the cross hair shown on the screen.
3. Repeat as the target moves around the screen. There will be five different locations to press: center, lower
right, upper right, upper left, and lower left.
4. When the last cross hair has been touched, Figure 29 displays ‘New calibration settings have been measured’.
5. Tap the screen to register saved data.
6. If you do not want to save the new data, wait for 30 seconds to cancel saved data and keep the current setting.
NOTE: The TOUCH SCREEN CALIBRATION SCREEN is a validation of the touch screen’s calibration. When the
user presses anywhere on the screen, the coordinates x and y are displayed on the lower part of the screen.
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
D. Optional Wi-Fi Configuration
CAUTION
These settings should only be modified by trained personnel. Changing these settings may disable the wireless feature.
These settings should only be changed or updated with the aid of the hospital’s IT department or the appropriate
maintenance personnel.
1. From the Configuration Screen, tap Wi-Fi Configuration to configure wireless settings for the bed.
2. Tap Wi-Fi OFF to toggle the wireless network connection on.
3. Tap the appropriate tab, and then tap the pencil icon to configure the network settings (Figure 30 - Figure 33).
4. Tap Save to save the network settings.
5. After saving the configured network settings, a power cycle notification appears.
6. Unplug the power cord from the wall outlet.
7. Turn the battery switch to the OFF (O) position.
8. Plug the power cord into the wall outlet.
9. Turn the battery switch to the ON (|) position.
Note: After you cycle power, InTouch reboots to the Patient Information screen.
Figure 30: Network Parameters
Figure 32: Security
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Figure 31: User Authentication
Figure 33: Advanced
Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
E. Bed Options Configuration
Access the configuration screen as shown on page 24. Once in the configuration screen, follow the steps below to
access the options screen or the serial number screen.
To access the Bed Options screen:
1. Press and hold the HOB 30 button and the BRAKE button at the same time for 5 seconds, then release both
buttons. The Bed Options screen (Figure 34) will be displayed.
NOTE: When the European Community message window displays, push the Close button to close out
of the message. That is not applicable in this configuration.
Figure 34: Bed Options screen
2. Select all of the options shown on the Bed Options screen that apply to the bed configuration then, press Continue.
NOTE: In Figure 34, the options selected are iBed, iAudio, iDoc and Wi-Fi. All of the options selected will turn
green.
3. After pressing Continue in step 2, a confirmation screen
as shown in Figure 35 will be displayed verifying the
options you selected.
a. If the options on the confirmation screen do not
match the options on the bed, press the Back
button.
b. If the options on the confirmation screen match the
options on the bed, press the OK button.
4. After pressing the OK button, the options will be saved
and the screen will return to the configuration screen.
Press the Close button to close the configuration
screen.
5. After pressing the Close button, a cycle power screen
(Figure 38) will be displayed stating to cycle power on
the bed.
6. To cycle power on the bed, turn the battery disconnect
switch to OFF (O) then unplug the power cord from the
wall outlet. Plug the power cord back into the wall outlet
then turn the battery disconnect switch back ON (|).
7. Test bed functionality prior to returning the bed into service.
Figure 35: Bed Options Confirmation Screen
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Maintenance Menu Guide
INTOUCH CONFIGURATION SCREEN (CONTINUED)
F. Serial Number Configuration
To access the Serial Number screen:
1. Press and hold the HOB 30 button and the Vascular Position button at the same time for 5 seconds then release
both buttons. The Bed Configuration - Serial Number screen (Figure 36) will be displayed.
Pencil icon
Press to edit
Figure 36: Bed Configuration Serial Number Screen
2. Enter or confirm the serial number of the bed (Figure 36).
a. To enter the serial number:
i. Press the pencil button located to the right of the serial
number field. The Edit screen will be displayed.
ii. Enter the serial number of the bed in the serial number
field, then press the OK button. You will be returned to
the serial number main screen as shown in Figure 36.
iii. Press the Continue button and proceed to step 3.
b. To confirm the serial number:
i. Review the serial number displayed in the serial number
field.
ii. If serial number is correct, press the Back button and
proceed to step 6.
iii. If the serial number is incorrect, press the pencil icon
button to open the Edit screen then enter the correct
serial number.
iv. Press the OK button and you will be returned to the
serial number main screen.
v. Press the Continue button and proceed to step 3.
3. After pressing the Continue button, the serial number will be
saved and the serial number confirmation screen (Figure 37) will
be displayed. Press the OK button.
4. After pressing the OK button, a cycle power screen (Figure 38)
will be displayed stating to cycle power on the bed.
5. To cycle power on the bed, turn the battery disconnect switch to
OFF (O) then unplug the power cord from the wall outlet. Plug
the power cord back into the wall outlet then turn the battery
disconnect switch back ON (|).
6. Test bed functionality prior to returning the bed into service.
Figure 37: Serial Number
Confirmation Screen
Figure 38: Cycle Power Screen
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Maintenance Menu Guide
AB
ACCESSING THE ISOLIBRIUM DIAGNOSTIC MENU
WARNING
• Electrical shock risk. Refer all servicing to qualified personnel.
• Do not perform diagnostic test with a patient or other weight on the support surface.
CAUTION
Do not touch the support surface while performing diagnostics test. Failure to do so could lead to inaccurate diagnostic
results.
Note: Make sure that you plug the support surface power
cord into the InTouch auxiliary mattress outlet (A) and the
integration cable to the mattress connector (B) (Figure
39).
The service display and its functions are for use by
authorized service personnel only to avoid the risk of
equipment malfunction. The entry to this menu is through a
key combination in the Support Surface menu.
To access the diagnostic menu:
Figure 39: InTouch auxiliary mattress outlet and
integration cable
1. Unplug the InTouch bed and turn the battery switch to off and wait one minute.
2. Turn the battery switch to on and plug the InTouch bed into a wall outlet.
3. Tap Support Surfaces.
4. Enter the following key combination within 5 minutes of the support surface connection (Figure 40):
a. Lock (A) (lock is activated)
b. Low Air Loss (B) (press and hold for a minimum of 5 seconds)
c. Therapy History (C) (press and hold for a minimum of 5 seconds)
B
Figure 40: Diagnostic Entry Combination
5. If you have entered into the diagnostic menu and need to exit, tap X (Figu r e 41).
A
C
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Figure 41: Diagnostic Main Screen Sample
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Maintenance Menu Guide
REVIEWING ACTIVE ISOLIBRIUM ERRORS
Note: For Isolibrium error codes, see the Isolibrium operations/maintenance manual.
To enter the Active Errors screen, tap the Active Errors tabon the Service Diagnostic screen (Figure 42).
Figure 42: Active Errors
A list of the active errors are displayed (Figure 42). A maximum of five active errors are displayed simultaneously, and
are ordered by priority.
REVIEWING AND CLEARING ISOLIBRIUM ERROR HISTORY
To enter the Error History screen, tap the Error History tab on the Diagnostic Screen (Figure 43).
Figure 43: Diagnostic Screen
The error list is ordered from the oldest entry to the newest, with a maximum of 10 errors.
To clear the Error History screen, tap Clear Error History on the Diagnostic screen (Figure 43).
Notes
• Always tap Clear Error History after troubleshooting is complete
• If you clear the error history while there is an active error, the active error does not show in the Error History tab
until the active error is fixed.
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Maintenance Menu Guide
VIEWING ADVANCED SIGNAL VALUES FOR ISOLIBRIUM
The Advanced Signal Values screen displays the complete list of signal values of the support surface. The screen
displays the actual and goal pressure values. For other non-pressure signals, only the actual values are displayed.
To enter the Advanced Signal Values screen, tap Advanced Signal Values on the Diagnostics screen (Figure 44).
Figure 44: Diagnostic Main Screen - Sample
To exit the Advanced Signal Values screen, tap Back to return to the Diagnostics screen (Figure 45).
Figure 45: Advanced Signal Values
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Maintenance Menu Guide
RUNNING A DIAGNOSTIC TEST FOR ISOLIBRIUM
WARNING
Do not perform diagnostic test with a patient or other weight on the support surface.
CAUTION
Do not touch the support surface while performing diagnostics test. Failure to do so could lead to inaccurate diagnostic
results.
Notes
• The results of the test will not be displayed until all tests have been completed.
• No results will be displayed if the tests are canceled.
• Other diagnostic functions are disabled while the diagnostic test is running.
The diagnostic test runs seven tests at one time on the support surface and take approximately 45 minutes to complete.
They include the following:
• Seat Left
• Seat Right
• Back Left
• Back Right
• Turn Left
• Turn Right
• Low Air Loss
To run diagnostics, tap start on the lower portion of the Diagnostics screen (Figure 46).
Figure 46: Diagnostic Main Screen - Sample
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Maintenance Menu Guide
RUNNING A DIAGNOSTIC TEST FOR ISOLIBRIUM (CONTINUED)
Note: Diagnostics running (Figure 47) appears to indicate that the diagnostic test is in progress.
To cancel diagnostics, tap stop on the lower portion of the Diagnostics screen (Figure 47).
Figure 47: Diagnostic Main Screen - Sample
When the test is complete, the results of each test section is indicated by a red cross when there is a failure or a green
check mark when successful (Figure 48).
Note: When a failure is first detected, all following pressure tests will be marked as a failure.
Figure 48: Diagnostic Test Result - Sample
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Cleaning
WARNING
• Do not clean, service, or perform maintenance while the product is in use.
• Always unplug the power cord and turn the battery switch to the OFF (O) position before cleaning, servicing, or
performing maintenance.
• Always immediately unplug the power cord from the wall outlet when large spills occur near the circuit boards,
cables, and motors. Remove the patient from the product, clean up the fluid, and have service personnel completely
inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product.
Do not return the product to service until it is completely dry and has been thoroughly tested for safe operation.
CAUTION
• Always unplug the product before cleaning or servicing.
• Always unplug the product, set the brakes, and place blocks under the litter frame for support when working under
the product.
The recommended cleaners for this product’s surfaces include the following:
Quaternary Cleaners (active ingredients - ammonium chloride)
Phenolic Cleaners (active ingredient - o-phenylphenol)
Chlorinated Bleach Solution (5.25% - less than 1 part bleach to 100 parts water)
Hand wash all surfaces of the product with warm water and mild detergent. Dry thoroughly.
Avoid oversaturation and make sure the product does not stay wet longer than the chemical manufacturer’s guidelines
for proper disinfecting.
CAUTION
• Always make sure that you wipe each product with clean water and thoroughly dry each product after cleaning.
Some cleaning products are corrosive in nature and may cause damage to the product if you use them improperly.
If you do not properly rinse and dry the product, a corrosive residue may be left on the surface of the product that
could cause premature corrosion of critical components. Failure to follow these cleaning instructions may void
your warranty.
• Do not steam clean, pressure wash, ultrasonically clean, or immerse any part of the product in water. Exposure
to water may damage the internal electric parts. These methods of cleaning are not recommended and may void
this product’s warranty.
• Always clean Velcro® after each use. Saturate Velcro with disinfectant and allow the disinfectant to evaporate.
Appropriate disinfectant for nylon Velcro should be determined by hospital protocol.
CLEANING A SUPPORT SURFACE
To clean and disinfect a support surface, see the cleaning and disinfecting instructions in the support surface operations
manual.
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Preventive Maintenance
At a minimum, check all items listed during annual preventive maintenance for all Stryker Medical products. You may
need to perform preventive maintenance checks more frequently based on your level of product usage.
Remove product from service before performing preventive maintenance. Preventive maintenance should only be
performed by trained or certified personnel.
Notes
• Clean and disinfect the exterior of the support surface before inspection, if applicable.
• For Isolibrium preventive maintenance items, see the Isolibrium operations/maintenance manual.
All welds and all fasteners are secure
Tubing or sheet metal for bends or breaks
Casters are free of debris
Casters are secure and swivel properly
Casters lock securely by depressing the brake pedal
Manual and electric brakes apply and release properly
Brake Not Set LED on the footboard and head end siderails when brakes are not engaged
Locking steer caster engages and disengages properly (model 2131)
Steer caster latches properly
Fowler operates properly
Litter up/down operates properly
Trend operates properly
IV pole is intact and operating properly (optional)
Support surface cover after each use
Support surface cover for rips or cracks
Headboard, footboard, and siderail panels for cracks or splits
All covers are not damaged and are not producing sharp edges
Night light operating properly
CPR release operating properly
All siderail motion functionality
Siderails move, latch, and stow properly
Siderail switches working properly (iBed Awareness option)
iBed Awareness light bars on footboard and siderails are working properly (iBed Awareness option)
All functions on head end siderails working properly (including LEDs)
All functions on footboard working properly (buttons, touch screen display, and LEDs)
Touch screen is accurately calibrated
Product is accurately calibrated
Scale and bed exit system operating properly
Drive wheel to make sure it is operating properly (model 2141 — Zoom option)
Motion release switches working properly (model 2141 — Zoom option)
Head end Zoom handle functionality operates properly (2141 model only)
Batteries for replacement (every two years) (use only QDF9188 for battery replacement)
Batteries for corrosion at the terminals, cracking, expanded or bulging at the sides, or can no longer maintain a
full charge
Nurse call functionality (optional)
Lubricate where required
Pendant for any physical damage
Power cord not frayed
Cables not worn or pinched
All electrical connections tight
All grounds secure to the frame
Ground impedance not more than 100 mΩ (milliohms)
Current leakage not more than 300 μA (microamps)
Ground chains are clean, intact, and have at least two links touching the floor
Enclosure is free from wear, tear, stresses and mechanical damage
No rust or corrosion of parts
Labels for legibility, proper adherence, and integrity
iBed Wireless Module and IR Module are intact and footboard icons are displaying (iBed Wireless option)
Return To Table of Contents
482141-209-0 02 RE V Hwww.stryker.com
Quick Reference Replacement Parts
These parts are currently available for purchase. Call Stryker Customer Service: 1–800–327–0770 for availability and
pricing.
Board, Footboard, Function Section/LED’sQDF75-0010
Board, Siderail, Outside (Bed Motion)QDF27-1099
Board, Wi-Fi27-2775
Fuse, 8Amp CeramicQDF2120
Fuse, 10Amp, Main PowerQDF8078
Fuse, 25Amp CartridgeQDF2119
Load CellQD F 2 7-1372
Motor, Drive (2141 Zoom® Only)QD F 2 7-14 4 5
Motor, Drive Actuator (2141 Zoom® Only)27-2593
Position Sensor, Brake/Brake Off/DriveQDF27-2024
Power Cord27-2782
Speaker, Right SiderailQDF27-2216
Speaker, Left SiderailQDF27-2175
Touch Screen, Footboard27-2757
Transformer (120VAC)QDF27-2038
www.stryker.com2141-209-0 02 RE V H49
Return To Table of Contents
Quick Reference Replacement Parts
Part NamePart Number
Other Components
Caster (2141 Model - all four casters) (2131 Model - both head end casters)RD27-1970
Caster, Steer (2131 Model Only - both foot end casters)RD27-19 7 1
Headboard Assembly27-25 8 3 K
Footboard Assembly without iBed27-2285K
Footboard Assembly with iBed and iAudio27-2824K
Footboard Assembly with iBed and Wi-Fi27-2827K
Footboard Assembly with iBed, without iAudio27-2826 K
Return To Table of Contents
502141-209-0 02 RE V Hwww.stryker.com
Troubleshooting
Notes:
• See the Bed Circuit Boards section for an outline of InTouch PCBs and voltage test points.
• For Isolibrium troubleshooting, see the Isolibrium operations/maintenance manual.
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Power to Bed.
(On wall voltage 120VAC)
COUNTRY VOLTAGE (CV) TABLE
VO LTAG EFUSE
100V10A
110V10A
120V10A
1.Verify the bed is plugged into a functional wall outlet.
A. Check your country voltage option at wall outlet.
I. If your country voltage option is present, go to step 2.
II. If 1your country voltage option is not present, contact
hospital maintenance staff and try another outlet.
2.Verify the Bed main power fuses are good, located in drawer where
power cord plugs into the bed.
A. Check for continuity of each 10A fuse.
I. If each fuse (see CV Table) is good, go to step 3.
II. If either fuse (see CV Table) does not have continuity,
replace the fuse.
200V10A
220V10A
230V10A
240V10A
3.Verify there is power at the transformer connection (J11) on the
CPU/Power board at the foot end.
A. Check for 24VAC at J11 between the blue and red wires.
I. If 24VAC is present, go to step 4.
II. If 24VAC is not present, check the 25 Amp fuse in the fuse
holder on the red wire from the transformer. If bad, replace
the fuse.
III. If 24VAC is not present, check the power cable quick
connection going to the transformer for (see CV Table)
VAC. If no voltage, follow the cable and repair or replace
the damaged component.
IV. If (see CV Table) VAC is present, replace the transformer
assembly.
4.A. Check for 30VAC at J11 between the yellow and orange wires
for the transformer.
I. If 30VAC is present, go to step 5.
II. If 30VAC is not present, check the power cable quick
connection going to the transformer for (see CV Table)
VAC. If no voltage, follow the cable and repair or replace
the damaged component.
III. If (see CV Table) VAC is present, replace the transformer
assembly.
5.A. Check fuse F1 on the CPU/Power board.
I. If fuse is good, replace CPU/Power board.
II. If fuse does not have continuity, replace the fuse (littelfuse
215008.P).
www.stryker.com2141-209-0 02 RE V H51
Return To Table of Contents
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Bed Up Motion.
No Bed Down Motion.
FOOT
HEAD
FOOT
Troubleshooting
1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the trend button.
I. If the foot lift motor runs up, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the litter angle
sensor and recalibrate.
II. If the foot lift motor does not run up, check for 24VDC at
connector J6 while pressing the trend button. Black lead
to pin 1, red lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power board.
1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the bed up button.
I. If the head lift motor runs up, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the litter angle
sensor and recalibrate.
II. If the head lift motor does not run up, check for 24VDC at
connector J4 while pressing the trend button. Black lead
to pin 1, red lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power board.
1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the reverse trend button.
I. If the foot lift motor runs down, recalibrate the bed (refer
to the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the litter angle
sensor and recalibrate.
II. If the foot lift motor does not run down, check for 24VDC
at connector J6 while pressing the reverse trend button.
Red lead to pin 1, black lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power board.
HEAD
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522141-209 -002 REV Hwww.stryker.com
1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the bed down button.
I. If the head lift motor runs down, recalibrate the bed (refer
to the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the litter angle
sensor and recalibrate.
II. If the head lift motor does not run down, check for 24VDC
at connector J4 while pressing the trend button. Red lead
to pin 1, black lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power board.
Troubleshooting
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Fowler Up Motion.1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the fowler up button.
I. If the fowler motor runs up, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the fowler angle
sensor and recalibrate.
II. If the fowler motor does not run up, check for 24VDC at
connector J5 while pressing the fowler up button. Black
lead to pin 1, red lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
No Fowler Down Motion.1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the fowler down button.
I. If the fowler motor runs down, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the fowler angle
sensor and recalibrate.
II. If the fowler motor does not run down, check for 24VDC
at connector J5 while pressing the fowler down button.
Red lead to pin 1, black lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
No Gatch Up Motion.1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the gatch up button.
I. If the gatch motor runs up, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the gatch angle
sensor and recalibrate.
II. If the gatch motor does not run up, check for 24VDC at
connector J3 while pressing the gatch up button. Red
lead to pin 1, black lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
www.stryker.com2141-209-0 02 RE V H53
Return To Table of Contents
Troubleshooting
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Gatch Down Motion.1.Go to the Bed Calibration menu.
A. Using one of the head siderails, push the gatch down button.
I. If the gatch motor runs down, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the gatch angle
sensor and recalibrate.
II. If the gatch motor does not run down, check for 24VDC
at connector J3 while pressing the gatch down button.
Black lead to pin 1, red lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
No Foot Up Motion.1.Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the foot up button.
I. If the foot motor runs up, recalibrate the bed (refer to the
Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the foot angle
sensor and recalibrate.
II. If the foot motor does not run up, check for 24VDC at
connector J1 while pressing the foot up button. Red lead
to pin 1, black lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
No Foot Down Motion.1.2.Ensure there is no debris in the foot end traction sockets. If debris
exists, remove it and press the foot down button. If the foot motor
still does not run down, proceed to step 2.
Put the bed into the Bed Calibration menu.
A. Using one of the head siderails, push the foot down button.
I. If the foot motor runs down, recalibrate the bed (refer to
the Bed Calibration procedures located on page 25).
a. If recalibration does not work, replace the foot angle
sensor and recalibrate.
II. If the foot motor does not run down, check for 24VDC at
connector J1 while pressing the foot down button. Black
lead to pin 1, red lead to pin 2.
a. If voltage is present, replace the motor.
b. If voltage is not present, replace the CPU/Power
board.
Return To Table of Contents
542141-209 -002 RE V Hwww.stryker.com
Troubleshooting
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Trendelenburg Motion.1.Check the touch screen trend angle display for accuracy of the level
of the litter.
I. If not accurate, recalibrate the bed (refer to the Bed
Calibration procedures located on page 25).
a. If recalibration does not work, replace the trend angle
sensor and recalibrate.
b. If replacement of the trend angle sensor did not
resolve
the problem, replace the CPU/Power board.
No Reverse Trendelenburg Motion.1.Check the touch screen trend angle display for accuracy of the level
of the litter.
I. If not accurate, recalibrate the bed (refer to the Bed
Calibration procedures located on page 25).
a. If recalibration does not work, replace the trend angle
sensor and recalibrate.
b. If replacement of the trend angle sensor did not
resolve
the problem, replace the CPU/Power board.
No Cardiac Chair Motion.1.Check the touch screen fowler and foot section angle display for
accuracy of the angle of the fowler and foot section.
I. If not accurate, recalibrate the bed (refer to the Bed
Calibration procedures located on page 25).
a. If recalibration does not work, replace the fowler or
foot
section angle sensor depending on the one which was
not accurate, then recalibrate.
b. If replacement of the fowler or foot section angle
sensor did not resolve the problem, replace the CPU/
HOB 30
Power board.
0.
1.Check the touch screen fowler angle display for accuracy of the
angle of the fowler.
I. If not accurate, recalibrate the bed (refer to the Bed
Calibration procedures located on page 25).
a. If recalibration does not work, replace the fowler angle
sensor and recalibrate.
b. If replacement of the fowler angle sensor did not
resolve the problem, replace the CPU/Power board.
www.stryker.com2141-209-0 02 RE V H55
Return To Table of Contents
Troubleshooting
BED TROUBLESHOOTING
Problem / FailureRecommended Action
No Vascular Motion.1.Check the touch screen fowler, gatch, foot, and trend/rev. trend
display for accuracy of the angle of all.
I. If not accurate, recalibrate the bed (refer to the Bed
Calibration procedures located on page 25).
a. If recalibration does not work, replace the angle
sensor of the section that is not accurate and then
recalibrate the bed (refer to the Bed Calibration
procedures located on page 25).
b. If replacement of the fowler angle sensor did not
resolve the problem, replace the CPU/Power board.
No Electric Brake Motion.1.Verify the Brake Not Set LED is flashing and the Brake Set LED is
O F F.
I. If the Brake Set LED is ON, check manual brake position.
a. If manual brake pedal is in the brake position, the bed
should not move and is okay; go to step 2.
b. If manual brake is not in the brake position, check the
switch on the patients left side in the middle below the
base hood.
2.If the brake motor does not run down when the brake button is
pushed, check for 24VDC at connector J7 while pressing the brake
button. Black lead to pin 1, red lead to pin 2.
Return To Table of Contents
562141-209-0 02 RE V Hwww.stryker.com
Troubleshooting
SCALE TROUBLESHOOTING
When the Scale system is unable to correctly weigh the patient weight due to a problem with the electronics, Figure 49
appears. It also appears when there is a problem with the Trendelenberg angle sensor. Because of this, the value for
the weight and the angle cannot be displayed.
When the weight exceeds 550 lbs., Figure 50 appears. If the weight is less than 2 lbs., the screen displays “0 lb.”
Figure 49
When the Trendelenburg or Reverse Trendelenburg angle is above 120 or below -120, Figure 51 appears.
When the scale system is unstable due to a problem with scale electronics or excessive patient movement, the weight
reading is orange (Figure 52).
Figure 51
Figure 50
Figure 52
www.stryker.com2141-209-0 02 RE V H57
Return To Table of Contents
Error Codes
ERROR HANDLING
• There are two different CAN networks; each of the networks is divided into two connectors.
• A safe error without command can be obtained when a bad connection is carried out on the Power Sensor Board
when the control panel is defective (there is no message sent on the network when a button is pressed) or when
the network is defective (short-circuit between the signals, open circuit or defective network circuit).
• A command error without safe is obtained when a bad connection is done on the Power Sensor board, when the
control panel is defective (a message is sent over the network but not the safe signal) or when the safe signal is
defective (short-circuit panel or open circuit or safe circuit on the Power Sensor board is broken).
• These errors can be present when a button is pressed, or at any time, and will thus cause the Call Maintenance
LED to light up.
• There is a LED on the Power Sensor Board (DS2 SAFE) which is active when there is at least one safe signal
which is active. There are also four LEDs on the Power Sensor board, which shows the activity of the network.
Every time a message is sent on the network, the LEDs will flash. If the network is defective, the LEDs will remain
on or remain off. If there is nothing connected to the network, the LEDs will remain on or off.
• A safe error can be obtained if a command button is pressed without having the Power Sensor Board receiving a
safe signal or if a safe signal is received by the Power Sensor board without having any command button pressed.
• The control panel for the weighing scale of the Power Sensor board can also send errors to the micro-controller
which will display them. An error of the weighing scale control panel will light on the Call Maintenance LED.
ERROR MESSAGES
Touch Screen Error Messages Name Definition
Atd Invalid ValuesDigital to analog converter is damaged (Replace the Control Board).
Brake pot bad rangeVerify if potentiometer is still in place.
Brake unable to elec ctlVerify wiring to Brake motor and limit switch for manual engage.
Brake pot Disconnected or shortVerify wiring to potentiometer and replace potentiometer.
Ensure potentiometer is still in place.
Brake motor time outVerify wiring to brake motor.
Calibration ErrorPrevious calibration step performed incorrectly, redo calibration procedure.
Cmd WO safe from nurse SRRRight siderail outside board has a network communication error (Check
network connections, dip-switch configuration of board or if a button is
stuck).
Cmd WO safe from nurse SRLLeft siderail outside board has a network communication error (Check
network connections, dip-switch configuration of board or if a button is
stuck).
Cmd WO safe from nurse SRHHead end board has a network communication error (Check network
connections).
Cmd WO safe from pat pend ROptional pendant control has a network communication error (Check
network connections).
Cmd WO safe from pat pend LOptional pendant control has a network communication error (Check
network connections).
Cmd WO safe from pat pend HOptional pendant control has a network communication error (Check
network connections).
Cmd WO safe from TSTouch screen has a network communication error (Check network
connections).
Return To Table of Contents
582141-209-0 02 REV Hwww.stryker.com
Error Codes
Touch Screen Error Messages Name Definition
Cmd WO safe from roomCommunication board has a network communication error (Check network
connections).
Cmd WO safe from roomCommunication board has a network communication error (Check network
connections).
GPIO Failure InitInitialization of the PCA9555 (GPIO expansion chip) failed (Replace control
board).
GPIO Failure ReadReading from the PCA9555 (GPIO expansion chip) failed (Replace control
board).
GPIO Failure WriteWriting to the PCA9555 (GPIO expansion chip) failed (Replace control
board).
Limit switch head side rail rightVerify wiring to limit switch and replace limit switch.
Limit switch head side rail leftVerify wiring to limit switch and replace limit switch.
Limit switch foot side rail rightVerify wiring to limit switch and replace limit switch.
Limit switch foot side rail leftVerify wiring to limit switch and replace limit switch.
Foot Right Load cell over rangeFoot Right load cell or cabling is damaged (Replace load cell).
Head Right cell over rangeHead Right load cell or cabling is damaged (Replace load cell).
Foot Left Load cell over rangeFoot Left load cell or cabling is damaged (Replace load cell).
Head Left Load cell over rangeHead Left load cell or cabling is damaged (Replace load cell).
Motor Brake OverheatBrake motor has ran too long (Leave motor stationary for 54 minutes).
Motor Brake OverloadBrake motor is drawing too many AMPS (remove restriction or replace
motor).
Motor Foot OverheatFoot motor has ran too long (Leave motor stationary for 54 minutes).
Motor Foot OverloadFoot motor is drawing too many AMPS (remove restriction or replace motor).
Motor Gatch OverheatGatch motor has ran too long (Leave motor stationary for 54 minutes).
Motor Gatch OverloadGatch motor is drawing too many AMPS (remove restriction or replace
motor).
Motor Head OverheatFowler motor has ran too long (Leave motor stationary for 54 minutes).
Motor Head OverloadFowler motor is drawing too many AMPS (remove restriction or replace
motor).
Motor HL Foot OverheatFoot lift motor has ran too long (Leave motor stationary for 54 minutes).
Motor HL Foot OverloadFoot lift motor is drawing too many AMPS (remove restriction or replace
motor).
Motor HL Head OverheatHead lift motor has ran too long (Leave motor stationary for 54 minutes).
Motor HL Head OverloadHead lift motor is drawing too many AMPS (remove restriction or replace
motor).
Motor Zoom® OverheatZoom® motor has ran too long (Leave motor stationary for 54 minutes).
Motor Zoom® OverloadZoom® motor is drawing too many AMPS (remove restriction or replace
motor).
No ErrorAngle sensor failure or calibration issue.
One Motor Drive ShortShort on drive motor detected.
Safe WO Cmd from A1Network A1 has a wiring issue (Check cabling).
Safe WO Cmd from A2Network A2 has a wiring issue (Check cabling).
Safe WO Cmd from B1Network B1 has a wiring issue (Check cabling).
Safe WO Cmd from B2Network B2 has a wiring issue (Check cabling).
Scale ADC ErrorScale chip not calibrated. DC Control Board needs to be replaced.
www.stryker.com2141-209-0 02 RE V H59
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Error Codes
Touch Screen Error Messages Name Definition
Scale Chip FailureControl board is bad (Replace Control Board).
Tilt base over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Tilt Error BaseAngle sensor is damaged (Replace sensor).
Tilt Error FootAngle sensor is damaged (Replace sensor).
Tilt Error GatchAngle sensor is damaged (Replace sensor).
Tilt Error HeadAngle sensor is damaged (Replace sensor).
Tilt Error HiLo FootAngle sensor is damaged (Replace sensor).
Tilt Error TrendAngle sensor is damaged (Replace sensor).
Tilt foot over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Tilt gatch over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Tilt head over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Tilt hiLo foot over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Tilt trend over rangeVerify if tilt sensor is still in place. Inspect for a damaged or improperly
assembled tilt sensor or recalibrate bed.
Zoom® time out for switchVerify wiring to Zoom® motor.
Wi-Fi / IR Communication ErrorDefinition
Wireless Adapter FailureUnable to detect or communicate with Wi-Fi radio. Check assembly or
cabling of Wi-Fi card in footboard or replace Wi-Fi card or footboard.
DHCP Error: Unable to obtain IP
Address
Unable to connect to networkBed is not able to connect to the wireless network. Check wireless network
Internal Communication ErrorInternal software failure. Software corruption may have occurred. Re-upload
Wi-Fi Settings corruptedReconfigure Wi-Fi settings in bed.
Bed Serial Number not availableConfigure bed serial number.
Left IR Module not detectedUnable to detect IR module. Check cabling or replace the IR module.
Right IR Module not detectedUnable to detect IR module. Check cabling or replace the IR module.
IR Interface Board not detectedUnable to detect the Room interface board. Check cabling or replace the
IR Crosstalk detectedCrosstalk detected with iBed Locator Wall module. Verify placement of IR
Isolibrium Error CodeDefinition
0100Sensor Board communication failure
0101Sensor Board EEPROM corruption
0102Sensor Board not calibrated
0200GUI CANopen Heartbeat Lost
0400EEPROM corruption
0500Ambient temperature sensor failure
0501Ambient temperature out of range
0600Pressure sensor failure
0601Seat Left pressure sensor failure
Bed is not able to connect to the wireless network. Check wireless network
settings and Wi-Fi configuration of bed.
settings and Wi-Fi configuration of bed.
software or replace footboard.
Room interface board.
modules on bed or wall modules.
Return To Table of Contents
602141-2 09 -002 REV Hwww.stryker.com
Error Codes
Isolibrium Error CodeDefinition
0602Seat Right pressure sensor failure
0603Back Left pressure sensor failure
0604Back Right pressure sensor failure
0605Turn Left pressure sensor failure
0606Turn Right pressure sensor failure
0700Mattress zone overpressure
0701Seat Left zone overpressure
0702Seat Right zone overpressure
0703Back Left zone overpressure
0704Back Right zone overpressure
0800Turn bladder overpressure
0801Turn Left bladder overpressure
0802Turn Right bladder overpressure
0900Compressor current not detected
1000Fan current not detected
1001Fan 1 current not detected
1002Fan 2 current not detected
110 0Valve not detected
110 1Seat Left inflate valve not detected
110 2Seat Left deflate valve not detected
110 3Seat Right inflate valve not detected
110 4Seat Right deflate valve not detected
110 5Back Left inflate valve not detected
110 6Back Left deflate valve not detected
110 7Back Right inflate valve not detected
110 8Back Right deflate valve not detected
110 9Turn Left inflate valve not detected
1110Turn Left deflate valve not detected
1111Turn Right inflate valve not detected
1112Turn Right deflate valve not detected
1113Intake valve not detected
1114Exhaust valve not detected
120 0Compressor current when OFF
1300Fan current when OFF
1301Fan 1 current when OFF
1302Fan 2 current when OFF
1400Valve current when OFF
1401Seat Left inflate valve current when OFF
1402Seat Left deflate valve current when OFF
1403Seat Right inflate valve current when OFF
1404Seat Right deflate valve current when OFF
1405Back Left inflate valve current when OFF
1406Back Left deflate valve current when OFF
1407Back Right inflate valve current when OFF
1408Back Right deflate valve current when OFF
www.stryker.com2141-209-0 02 RE V H61
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Error Codes
Isolibrium Error CodeDefinition
1409Turn Left inflate valve current when OFF
1410Turn Left deflate valve current when OFF
1411Turn Right inflate valve current when OFF
1412Turn Right deflate valve current when OFF
1413Intake valve current when OFF
1414Exhaust valve current when OFF
150 0Mattress leak
1501Seat Left zone leak
150 2Seat Right zone leak
150 3Back Left zone leak
150 4Back Right zone leak
150 5Turn Left bladder leak
150 6Turn Right bladder leak
160 0Mattress deflate timeout
1601Seat Left deflate timeout
160 2Seat Right deflate timeout
160 3Back Left deflate timeout
160 4Back Right deflate timeout
160 5Turn Left deflate timeout
160 6Turn Right deflate timeout
170 0Reference voltage hardware failure
180 0Weight input out of range
1900HOB angle out of range for Lateral Rotation
1901HOB angle out of range for Turn Assist
Return To Table of Contents
622141-209 -002 RE V Hwww.stryker.com
CPU/Power Board - QDF75-0440
Sanity
Error
Charge
5VDC
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Return To Table of Contents
CPU/Power Board - QDF75-0440
FUSE SPECIFICATION
LocationDescriptionAmp
F130VAC from transformer for the battery charger and the
5VDC / 12VDC supply
F224 VDC from batteries for power supply 40 Amp - 142.6185.5402
F324 VAC from transformer for power supply40 Amp - 142.6185.5402
OPTION 2 COM
READ LIGHT
ROOM LIGHT
SPEAKER HIGH
POT WIPER
RADIO COM
N_CALL INTERLOCK
AUDIO TRANSFERT AUDIO TRANSFERT +
INTERLOCK +
INTERLOCK SPARE
OPTION 3 COM
POT LOW COM
POT HI COM
NURSE ANSWER LIGHT
OPTION 1 NO/NC
OPTION 1 COM
NURSE CALL LIGHT
OPTION 2 NO/NC
OPTION 3 NO/NC
OPTION 3A NO/NC
OPTION 2A COM
OPTION 2A NO/NC
N_CALL +
N_CALL NO/NC
ROOM/READ LIGHT COM
NURSE CALL LIGHT
NURSE ANSWER LIGHT
PRIORITY NO/NC
PRIORITY COM
OPTION 3A COM
TV COM (TV -)
TV+
SPEAKER LOW COM
AUDIO SHIELD
RADIO NO/NC
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
PORT DB-37
J20
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
CIRCUIT ASSEMBLY
"ROOM CONTROL INTERFACE"
ALL MODELS PRIOR TO 3.1
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6
5
4
3
2
NOT USED
1
14
13
12
11
10
9
8
7
6
NOT USED
5
4
3
2
1
Pillow Speaker Nurse Call
J9
and Speaker
J2
Left Side Pillow Speaker
39
GH
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Bed Electrical Diagram
IIBED STATUS ON
READ LIGHT
ROOM LIGHT
SPEAKER HIGH
POT WIPER
BED EXIT STATUS
N_CALL INTERLOCK
TRANSFERT -
AUDIO
AUDIO TRANSFERT +
INTERLOCK +
INTERLOCK IBED FOWLER 30 ALERTING
OPTION 3 COM
POT LOW COM
POT HI COM
NURSE ANSWER LIGHT
IIBED ALERTING
IBED SIDERAIL ALERTING
NURSE CALL LIGHT
CH DOWN NO
OPTION 3 NO/NC
OPTION 3A NO/NC
BRAKE STATUS ON
OPTION 2A NO/NC
N_CALL +
N_CALL NO/NC
ROOM/READ LIGHT COM
NURSE CALL LIGHT
NURSE ANSWER LIGHT
PRIORITY NO/NC
PRIORITY COM
IIBED LOW HGT ALERTING
TV COM (TV -)
TV+
SPEAKER LOW COM
AUDIO SHIELD
AWARENESS COMMON
1
2
3
4
5
5
6
7
8
9
10
11
12
13
14
15
16
17
18
PORT DB-37
J20
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
INTOUCH 3.1 ALL MODELS
INCLUDING WI-FI/IR OPTION
(2131/2141)
77
IR MODULE
(OPTIONAL)
77
IR MODULE
(OPTIONAL)
IR - TX
+5V
GND
IR-RX
FEED BACK
IR - TX
+5V
GND
IR-RX
FEED BACK
1
2
3
4
IR CONNECTOR
5
1
IR CONNECTOR
2
3
4
5
J2
ROOM CONTROL INTERFACE ASSEMBLY
39
J5
GH
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802141-209- 0 02 REV Hwww.stryker.com
Bed Electrical Diagram
ALL MODELS
SMART_TV_ON_OFF
DB_TV+
SMART_TV_CH_DOWN
DB_TV SMART_TV_CH_UP / CLOCK
SMART_TV_CC_SLEEP / DATA
SMART_TV_RADIO_MUTE
"SMART TV BOARD"
52
GND
GND
GND
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
Smart TV
J6
CIRCUIT ASSEMBLY
"ROOM CONTROL INTERFACE"
39
www.stryker.com2141-209-0 02 RE V H81
H
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Bed Electrical Diagram
Bed Electrical Diagram - 27-1136 Rev R (Reference Only)
Item Part No. Part Name Qty.
1 QDF5095 Sound Alarm 1
2 QDF75-0440 DC Power Control 1
3 QDF27-1185 Number 3 Harness 1
4 QDF27-2229 Footboard Brake Cable 1
5 QDF27-2181 Number 2 Harness 1
6 QDF27-2182 Base Structure Extension 1
7 QDF27-1381 Battery Switch Cable 2
8 QDF9188 12V, 17.9 Ah Battery 2
9 QDF27-1208 Limit Switch Siderail Cable 2
10 QDF27-1430 CSI 1109 Board 1
11 QDF27-1097 Brake / Neutral / Drive Board 3
12 QDF27-2196 Speaker 2
13 QDF27-1429 Nurse Call Board 2
14 QDF75-0230 Zoom® Control Board 1
15 QDF9136 Load Cell Handle 1
16 QDF9130 Right Handle 1
17 QDF9131 Left Handle 1
18 QDF8066 Power Cord 2
19 QDF2087 Toggle Switch 1
20 QDF8078 10A Fuse 2
22 QDF27-1607 I.V. Pole and Bed Extender Cable 1
23 QDF27-1682 Nurse Call Board Cable 2
24 QDF8024 120V Auxiliary Outlet 1
25 QDF27-2024 Linear Position Sensor 1
26 QDF9025 Breaker 1
27 QDF27-2214 Footboard Control Board Cable 1
28 QDF27-2038 Toroid Power Supply 1
29 QDF27-1646 Battery Cable 2
30 QDF9004 Micro-Switch 2
31 QDF27-2232 Footboard Cable 1
32 QDF27-1834 Footboard LBS Cable 2
33 QDF27-1841 100V Adapter 1
35 QDF27-1372 Load Cell 4
36 QDF21-1151 CAN Head Control Board 3
37 QDF21-2895 12” Network Cable 2
39 QDF75-0270 CAN Room Interface Board w/o GEN III 1
40 QDF27-1521 Siderail Limit Switch 2
41 QDF27-2213 Number 1 Harness Wire 1
42 QDF27-2230 Touch Screen Cable 2
43 QDF75-0290 Touch Screen Board 1
44 QDF27-2049 Multivoltage Power Supply 1
45 QDF75-0140 Angle Sensor 6
46 QDF27-1156 Brake Board Cable 2
47 QDF27-2025 12V 3 LEDs Night Light 1
48 QDF27-2432 Serial Interface Connector Cable 1
49 QDF27-2212 Head Siderail Cable 2
52 QDF2060 Smart TV Board 1
53 QDF21-2901 SIP-N-PUFF Cable 2
54 QDF27-1099 Siderail & Head Nurse Control Board 3
55 QDF75-0010 Menu Touch Screen Board 1
56 QDF9573 XPRT™ Mattress Plug -
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822141-209 -002 REV Hwww.stryker.com
Bed Electrical Diagram
Bed Electrical Diagram - 27-1136 Rev R (Reference Only) (Continued)
Item Part No. Part Name Qty.
57 QDF27-1842 200V Adaptor 1
58 QDF27-1843 220V Adaptor 1
59 QDF27-1102 Patient Pendant Control 2
60 – Patient Pendant Connector 1
61 QDF27-1525 Patient Pendant Cable 2
62 27-2848 Inlet Filter Assembly 1
63 QDF9575 Schurter #4303.2901 1
64 QDF27-1840 240V Adaptor 1
65 QDF27-2253 LBS Cable 1
66 QDF27-1562 Local Bed Status Board 2
67 QDF9571 Medical Filter 1
68 QDF27-1524 Filter and Receptacle Connector 1
69 QDF27-1681 Interior Siderail Cable 2
70 QDF27-1526 Speaker 4
72 QDF27-2231 USB Cable 1
73 QDF27-1976 Auxiliary Plug + Mattress Cable 1
74 QDF27-2542 Zoom® Interface Board Harness 1
75 QDF75-0240 Zoom® Interface Board 1
76 QDF27-2658 230V Transformer 1
77 QDF75-0310 IR Module 2
78 QDF75-0630 Wi-Fi Board 1
79 QDF27-2573 USB Y Cable to Interface Board 1
80 QDF27-2594 Brake Card to Interface Cable 1
www.stryker.com2141-209-0 02 RE V H83
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Service Information
BED LIFT ACTUATOR (HEAD) REMOVAL AND REPLACEMENT - (BASE)
Tools Required:
• Needle-Nose Pliers
• Diagonal Pliers
• Jack (if needed)
• 2 x 4 (20” recommended)
Step #8:
Locate Jack Stand between
floor and underside of Foot
Frame.
Floor
Procedure:
1. Plug bed into wall outlet.
2. Raise the head end siderails to the full up position and set the brakes using one of the brake control locations or
by using the manual brake pedal.
3. Remove head end base cover by pulling up and out.
4. Remove center base cover by pulling up and out.
5. Using diagonal pliers, cut the zip tie securing the actuator cable to the base frame.
6. Using Needle-nose pliers, remove the rue clips from the clevis pins securing the actuator.
CAUTION
Do not remove the clevis pins.
7. If the bed will lower down, run it all the way down so the litter is supported by the base litter stop.
8. If the bed will not lower all the way down; using a jack and a 2 x 4, take tension off of the actuator
clevis pins by placing the jack and 2 x 4 between the bottom of the right side of the litter and the floor
and jack up just enough to take the litter weight off of the base frame (reference picture above).
CAUTION
Make sure that prior to jacking, the 2 x 4 is perpendicular to the floor.
9. Using the bed up/down controls, tap the up or down button to remove
tension on the clevis pins and remove clevis pins.
10. Unplug the cable quick connect and remove the actuator.
11. Reverse the steps to install the new actuator.
12. Test all bed functionality prior to putting bed back in service.
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Service Information
BED LIFT ACTUATOR (FOOT) REMOVAL AND REPLACEMENT - (BASE)
Tools Required:
• Needle-Nose Pliers
• Diagonal Pliers
Procedure:
1. Plug bed into wall outlet.
2. Raise head end siderails to full up position and ensure brakes are activated.
3. Remove head end base cover by pulling up and out.
4. Remove center base cover by pulling up and out.
5. Using diagonal pliers, cut the zip tie securing the actuator cable to the base frame.
6. Using Needle-nose pliers, remove the rue clips from the clevis pins securing the actuator.
CAUTION
Do not remove the clevis pins.
7. Lower the bed all of the way down so the litter is supported by the base litter stops.
8. Using the bed up/down controls, tap the up or down button to remove tension on the clevis pins and remove clevis
pins.
9. Unplug the cable quick connect and remove the actuator.
10. Reverse the steps to install the new actuator.
11. Test all bed functionality prior to putting bed back in service.
www.stryker.com2141-209-0 02 RE V H85
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Service Information
FOWLER ACTUATOR REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Diagonal Pliers
• Regular Screwdriver
• Phillips Screwdriver #2
• 3/8” Combination Wrench
Procedure:
1. Plug bed into wall outlet.
2. Raise bed to the full up position.
3. Raise the head end siderails to the full up position and set the brakes using one of the brake control locations or
by using the manual brake pedal.
4. Working from the right side of the bed, step on the CPR pedal to lower the fowler all the way down.
5. Raise the gatch to the full up position.
6. Remove the three center base hoods (head, center, foot), then remove the right base hood.
7. Using Needle-nose pliers, remove the two rue clips from the clevis pins holding the actuator.
8. Using diagonal pliers, cut the zip ties securing the CPR cable to the actuator and the litter frame. Also cut the zip
ties securing the actuator cable to the wire harness.
9. Unplug the actuator from the quick connect.
10. Holding the actuator with one hand remove the clevis pins from the actuator and carefully lower the actuator down.
11. Using a Phillips screwdriver and a 3/8” combination wrench, remove the CPR cable retaining screw from the right
CPR pedal.
12. Using a regular screwdriver, loosen the CPR cable retainer on the actuator just enough so it will move.
13. Slide the gray cable retainer lock towards the CPR cable retainer and unclip the CPR cable from the red actuator
release activator.
14. Remove actuator.
15. Reverse these steps to reinstall.
16. When re-adjusting the cable retainer lock set,
set it to 1.00 +/- 0.06 as shown (right). When
the actuator is back in place, use needle-nose
pliers to reattach the spring to the center of
the clevis pin.
17. Test all bed functionality prior to putting bed
back into service.
1.00 ±0.06
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862141-209-0 02 REV Hwww.stryker.com
Service Information
GATCH ACTUATOR REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Needle-Nose Pliers
Procedure:
1. Plug bed into wall outlet.
2. Set the brakes using one of the brake control locations or by using the manual brake pedal.
3. Remove the mattress and set aside.
4. Raise bed to the full up position.
5. If the actuator will run, lower the gatch down to take the tension off of the actuator mounting pins. If the actuator
will not run, support the gatch section to take tension off of the actuator mounting pins.
6. Unplug the actuator cable from the quick connect near the actuator.
7. Using Needle-nose pliers, remove the two rue clips from the clevis pins holding the actuator in place.
8. Holding the actuator with one hand, remove the clevis pins securing the actuator to the bed then remove the
ac tuato r.
9. Reverse these steps to reinstall
Note: If new actuator shaft does not line up with mounting holes, mount the base of the actuator then plug the
actuator in and run it electrically in or out until lined up.
10. Test all bed functionality prior to putting bed back in service.
www.stryker.com2141-209-0 02 RE V H87
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Service Information
FOOT ACTUATOR REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Needle-Nose pliers
Electrical Cover
• Diagonal Pliers
• Phillips Screwdriver #2
• Jack Stand
Head
Foot
A
B
Step #4:
Locate Jack Stand between floor
and underside of Foot Frame.
Floor
Procedure:
1. Plug bed into wall outlet.
2. Set the brakes by using one of the brake control locations or the manual brake pedal.
3. Remove the mattress and set aside.
4. Using a jack stand, support the foot section by lowering the bed height down enough to take the tension off the
actuator mounting pins (reference drawing above).
5. Using diagonal pliers, cut the zip ties securing the actuator cable to the bed.
6. Remove the mattress assembly or fold back to expose the foot section.
7. Using a Phillips screwdriver, remove the two screws (reference drawing above, item A and B) securing the
electrical cover from the foot section and remove the cover.
Note: Use caution as the cover is large and heavy.
8. Unplug the actuator from J1 and feed cable down to actuator.
9. Using needle-nose pliers, remove the two rue clips from the clevis pins holding the actuator in place.
10. Holding the actuator with one hand, remove the clevis pins securing the actuator to the bed then remove the
ac tuato r.
11. Reverse these steps to reinstall.
Note: If new motor shaft does not line up with mounting holes, mount the base of the actuator then plug the
actuator in and run it electrically in or out until lined up.
12. Test all bed functionality prior to putting bed back in service.
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882141-209- 0 02 REV Hwww.stryker.com
Service Information
ZOOM® DRIVE ACTUATOR REMOVAL AND REPLACEMENT (2141 MODEL ONLY) - (BASE)
Tools Required:
• Needle-Nose Pliers
• Pry Bar or 2 x 4
• Diagonal Pliers
Procedure:
1. Plug bed into wall outlet.
2. Position the bed height in the middle range.
3. Remove the center base cover then remove the Zoom® drive actuator cover and set aside.
4. Using Needle-nose pliers, remove the two rue clips from the clevis pins securing the actuator to the base frame.
5. Using diagonal pliers, cut the zip ties securing the actuator cable and then unplug the actuator from the quick
connect.
6. Using a pry bar or a 2 x 4, pry upward on the Zoom® drive actuator frame and push the actuator clevis pins out.
7. Remove actuator.
8. Reverse steps to install new actuator.
9. Test all bed functionality prior to putting bed back into service.
www.stryker.com2141-209-0 02 RE V H89
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Service Information
CPU / POWER BOARD REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Phillips Screwdriver #2
• ESD System
• 3/8” Nutdriver
Procedure:
1. Plug bed into wall outlet.
2. Set the brakes using one of the brake control locations
or by using the manual brake pedal.
3. Raise the bed to the full upright position.
4. Remove the mattress assembly or fold back to expose
the foot section.
5. Using a Phillips screwdriver, remove the two screws
(reference drawing, item A and B) securing the
electrical cover and remove the cover.
Note: Use caution as the cover is large and heavy.
6. Unplug the bed from the wall outlet and turn battery
switch OFF. The bed should now have no power.
7. Using an ESD system, properly ground yourself.
8. Unplug all cable connections from the CPU/Power
board.
9. Using a 3/8” nutdriver and a Phillips screwdriver, unscrew
the four screws (C) securing the metal CPU/Power
board mounting plate to the electrical tray (reference
drawing above).
10. Remove CPU/Power board and discard.
11. Reverse steps 9-4 to install the new CPU/Power board
(QDF75-0440).
12. Plug bed back into wall outlet and turn the battery switch
back ON.
13. Configure bed options (refer to the Bed Options
Configuration procedure on page 39).
14. Configure the bed serial number (refer to the Serial
Number Configuration procedure on page 40).
15. Recalibrate the bed by referring to the Bed Calibration
procedure on page 25.
16. Test all bed functionality prior to putting the bed back
into service.
CPU/Power board
Electrical Cover
A
B
C
C
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902141-209 -002 REV Hwww.stryker.com
Service Information
Rue Clip
LOAD CELL (HEAD END) REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Phillips Screwdriver #2
• Needle-Nose Pliers
• 3/8” Drive Ratchet
• 1/2” Socket
• 1/2” Combination Wrench
Screw
Wire Cover
Upper Frame
Flat Washer
Clevis Pin
Figure 1
Screw
Screw
Head Frame Cover
Screw
Screw
Figure 2
Head Frame
Screw
Screw
Procedure: (procedure the same for left and right sides)
1. Plug bed into wall outlet.
2. Raise bed and fowler to full up position, gatch down and foot up.
3. Raise head end siderails.
4. Using a Phillips screwdriver, remove the two screws securing the wire cover to the head frame (Figure 1).
5. Using a Phillips screwdriver, remove the six screws from the head frame cover, lift up on the cover and lay it on
the litter (Figure 2)
6. Unscrew the load cell connection and feed the connection back towards the cell.
7. Using Needle-nose pliers, remove the rue clip and the flat washer.
8. Using one hand, grab the upper frame cross bar to remove tension on the litter then push the clevis pin out.
9. Using a ratchet with a 1/2” socket and a 1/2 combination wrench, remove the two bolts securing the load cell then
remove the load cell.
10. Reverse procedures to install the new load cell.
CAUTION
Ensure cables do not get pinched when securing the head end frame cover together.
11. Recalibrate the bed (refer to Bed Calibration procedures on page 25).
12. Test all bed functionality prior to putting bed back into service.
www.stryker.com2141-209-0 02 RE V H91
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Service Information
LOAD CELL (FOOT END) REMOVAL AND REPLACEMENT - (LITTER)
Tools Required:
• Phillips Screwdriver #2
• Needle-Nose Pliers
• 1/2” Combination Wrench
• 3/8” Ratchet
• 1/2” Shallow Well Socket
• Diagonal Pliers
• Jack
• 2 x 4 (20” recommended)
Procedure: (procedure the same for left and right sides)
1. Plug bed into wall outlet.
2. Raise bed to around 24” (reference the footboard display) and gatch to full up position.
3. Remove the mattress assembly.
4. Using a 1/2” combination wrench, remove the four bolts securing the gatch section cover and remove by lifting up
on the foot end and then pushing backwards on the cover.
5. Raise the foot end siderails up.
6. Using needle-nose pliers, remove the rue clip and flat washer.
7. Remove the foot end base cover.
8. Using a Phillips screwdriver, remove the four screws securing the foley bag bracket.
9. Using a jack and 2 x 4, take the tension off of the load cells and remove the clevis pins from both foot end load
cells.
10. Unscrew load cell cable connector.
11. Using diagonal pliers, cut the two cable ties securing the main wire harness and the siderail cable located just
behind the load cell.
12. Using a ratchet and 1/2” socket, remove the two nuts and bolts securing the load cell to the litter frame.
13. Remove the load cell by pulling back and upward towards the middle of the bed while feeding the cable through
the litter frame.
14. Reverse procedures to install the new load cell.
CAUTION
Do not pinch the cable when installing the load cell.
15. Recalibrate the bed (refer to Bed Calibration procedures on page 25).
16. Test all bed functionality prior to putting bed back into service.
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922141-209 -002 REV Hwww.stryker.com
Service Information
DISPLAY REMOVAL AND REPLACEMENT - (FOOTBOARD)
Tools Required:
• Phillips Screwdriver #2
• Stubby Phillips Screwdriver #2
• Small Slotted Screwdriver
• Utility Knife
• ESD System
Rear Footboard Back Label
Screws
Display
Procedure:
Note: ESD protection is required for this procedure.
1. Remove the footboard assembly and place onto a nearby work surface, face down.
2. Using a small slotted screwdriver or a utility knife, remove the rear footboard label.
Note: This label will need to be replaced with a new label (QDF27-2756).
3. Using a Phillips screwdriver, remove the six screws securing the footboard display panel to the footboard.
4. Pivot the display panel up.
5. Using a stubby Phillips screwdriver, remove the two screws from the bottom of the display panel.
6. Hold the display panel and footboard assembly together and flip the footboard assembly over, with the display
panel facing up.
7. Carefully remove the display panel from the footboard assembly. Rotate over to display the circuit boards.
8. Disconnect the two ribbon cables from J3 and J7 by pulling outward on the locking tabs, then pulling the ribbon
cable.
9. Disconnect the menu board cable from connector J6.
10. Using a Phillips screwdriver, remove the two screws that secure the Wi-Fi board to the LCD interface board.
11. Using a Phillips screwdriver, remove the two screws that secure the LCD interface board to the display housing.
12. Remove the two spacer shims between the LCD interface board and the display housing.
13. Carefully remove the LCD interface board from the display.
Note: The components are secured together with double-sided foam tape. Slight upward force will be
necessary to separate.
14. Using a small slotted screwdriver, separate the locking tabs from the display and remove the display.
15. Reverse the procedure to install the new display.
16. Recalibrate the touch screen, by referencing the Touch Screen Calibration procedure on page 25.
17. Test all bed functionality before returning the bed to service.
www.stryker.com2141-209-0 02 RE V H93
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Service Information
BRAKE CONTROL BOARD REMOVAL AND REPLACEMENT - (FOOTBOARD)
Tools Required:
• Phillips Screwdriver #2
• Stubby Phillips Screwdriver #2
• Small Slotted Screwdriver
• Utility Knife
• ESD System
Rear Footboard Back Label
Screws
Brake Control Board
Procedure:
Note: ESD protection is required for this procedure.
1. Remove the footboard assembly and place onto a nearby work surface, face down.
2. Using a small slotted screwdriver or a utility knife, remove the rear footboard label.
Note: This label will need to be replaced with a new label (QDF27-2756).
3. Using a Phillips screwdriver, remove the six screws securing the footboard display panel to the footboard.
4. Pivot the display panel up.
5. Using a stubby Phillips screwdriver, remove the two screws from the bottom of the display panel.
6. Hold the display panel and footboard assembly together and flip the footboard assembly over, with the display
panel facing up.
7. Carefully remove the display panel from the footboard assembly. Rotate over to display the circuit boards.
8. Using a Phillips screwdriver, remove the two screws that secure the Wi-Fi antenna P-clamps to the brake control
board.
9. Using a Phillips screwdriver, remove the remaining four screws that secure the brake control board to the footboard
display housing.
10. Disconnect the brake control cable from the brake control board.
11. Remove the brake control board.
12. Reverse the procedure to install the new brake control board.
13. Test all bed functionality before returning the bed to service.
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942141-209 -002 REV Hwww.stryker.com
Service Information
FUNCTION SELECTION/LED BOARD REMOVAL AND REPLACEMENT - (FOOTBOARD)
Tools Required:
• Phillips Screwdriver #2
• Stubby Phillips Screwdriver #2
• Small Slotted Screwdriver
• Utility Knife
• ESD System
Rear Footboard Back Label
Screws
Function Selection/LED Board
Procedure:
1. Plug the bed into a wall outlet.
2. Raise the bed to the full up position and level.
3. Unplug the bed and turn the battery disconnect “OFF” (0).
4. Using a small slotted screwdriver or a utility knife, remove the rear footboard label.
Note: This label will need to be replaced with a new label (QDF27-2756).
5. Using a Phillips screwdriver, remove the six screws from the top of the control panel which the label was covering.
6. Raise the display up and using a stubby Phillips screwdriver, remove the three screws on the bottom.
7. Remove the display housing and unplug the two cables from the function control board and set the display
assembly on a bench to work on.
8. Using a Phillips screwdriver, remove the four screws securing the function selection/LED board.
9. Unplug the cable going to the function selection/LED board.
10. Reverse the procedures to install the new function selection/LED board.
11. Test all bed functionality prior to putting the bed back into service.
www.stryker.com2141-209-0 02 RE V H95
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Service Information
TOUCH SCREEN REMOVAL AND REPLACEMENT - (FOOTBOARD)
Tools Required:
• Phillips Screwdriver #2
• Stubby Phillips Screwdriver #2
Rear Footboard Back Label
Screws
• Small Slotted Screwdriver
• Utility Knife
• ESD System
Display
Tou c h
Screen
Procedure:
Note: ESD protection is required for this procedure.
1. Remove the footboard assembly and place onto a nearby work surface, face down.
2. Using a small slotted screwdriver or a utility knife, remove the rear footboard label.
Note: This label will need to be replaced with a new label (QDF27-2756).
3. Using a Phillips screwdriver, remove the six screws securing the footboard display panel to the footboard.
4. Pivot the display panel up.
5. Using a stubby Phillips screwdriver, remove the two screws from the bottom of the display panel.
6. Hold the display panel and footboard assembly together and flip the footboard assembly over, with the display
panel facing up.
7. Carefully remove the display panel from the footboard assembly and rotate over to display the circuit boards.
8. Disconnect the two ribbon cables from J3 and J7 by pulling outward on the locking tabs, then pulling the ribbon
cable.
9. Disconnect the menu board cable from connector J6.
10. Using a Phillips screwdriver, remove the two screws that secure the Wi-Fi board to the LCD interface board.
11. Using a Phillips screwdriver, remove the two screws that secure the LCD interface board to the display housing.
12. Remove the two spacer shims between the LCD interface board and the display housing.
13. Carefully remove the LCD interface board from the display.
Note: The components are secured together with double-sided foam tape. Slight upward force will be
necessary to separate.
14. Using a small slotted screwdriver, separate the locking tabs from the display and remove the display.
15. Using a small slotted screwdriver or utility knife, remove the foot control overlay label.
Note: This overlay label will need to be replaced with a new overlay label (QDF27-2188-ENG) and patent
pending label (QE71-1094-ENG).
16. Carefully separate the touch screen from the display housing.
17. Reverse the procedure to install the new touch screen.
18. Recalibrate the touch screen, by referencing the Touch Screen Calibration procedure on page 25.
19. Test all bed functionality before returning the bed to service.
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962141-2 09 -002 REV Hwww.stryker.com
Service Information
BATTERY REMOVAL AND REPLACEMENT - (FOOTBOARD)
Tools Required:
• Phillips Screwdriver #2
• Stubby Phillips Screwdriver #2
• Small Slotted screwdriver
• Utility Knife
• ESD System
Procedure:
1. Plug the bed into a wall outlet.
2. Raise the bed to the full up position and level.
3. Unplug the bed and turn the battery disconnect switch to the “OFF” (0) position.
4. Using a small slotted screwdriver or a utility knife, remove the rear footboard label.
Note: This label will need to be replaced with a new label (QDF27-2756).
5. Using a Phillips screwdriver remove the six screws from the top of the control panel which the label was covering.
6. Raise the display up and using a stubby Phillips screwdriver, remove the three screws on the bottom.
7. Remove the display housing and unplug the two cables from the function control board and set the display
assembly on a bench to work on.
8. Remove the battery and replace with new battery (see figure below).
9. Reverse the above steps to reassemble.
10. Referencing the operation manual complete the Time / Date Setup procedure.