Type B Equipment: equipment providing a particular degree of protection against electric shock,
particularly regarding allowable leakage current and reliability of the protective earth connection.
Class 1 Equipment: equipment in which protection against electric shock does not rely on BASIC
INSULATION only, but which includes an additional safety precaution in that means are provided
for the connection of the EQUIPMENT to the protective earth conductor in the fixed wiring of the
installation in such a way that ACCESSIBLE METAL PARTS cannot become live in the event of a
failure of the BASIC INSULATION.
Mode of Operation: Continuous
Protection from liquid splash
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock, Fire,
Mechanical and Other Specified Hazards Only in Accordance with UL 60601−1, First Edition (2003)
and CAN/CSA C22.2 No. 601.1−M90 with updates 1 and 2 and IEC 60601-1 (1998) with Amendment
1 (1991) and Amendment 2 (1995).
In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment,
this symbol indicates that the product must not be disposed of as unsorted municipal waste, but
should be collected separately. Refer to your local distributor for return and/or collection systems
available in your country.
Non-ionizing radiation; i.e. RF transmitter (WiFi)
This icon means the iBed Locator is connected.
X
This icon means the iBed Locator is not connected.
This icon means the Network is connected.
This icon means the Network is not connected.
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Symbols and Definitions
WARNING/CAUTION/NOTE DEFINITION
The words Warning, Caution and Note carry special meanings and should be carefully reviewed.
WARNING
Alerts the reader about a situation, which if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CAUTION
Alerts the reader of a potentially hazardous situation, which if not avoided, may result in minor or moderate injury to
the user or patient or damage to the equipment or other property. This includes special care necessary for the safe
and effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use
or misuse.
Note
This provides special information to make maintenance easier or important instructions clearer.
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Introduction
This manual is designed to assist you with the operations of the S3™ MedSurg Bed, Model 3002 Patriot™ Series. Read
it thoroughly before using the equipment.
INTENDED USE – STRYKER S3™
This device is an AC-powered adjustable hospital bed intended for medical purposes that consists of a bed with a
built-in motor and remote controls that can be operated by the patient to adjust the height and surface contour of the
bed. The device includes movable and latchable siderails.
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.
SPECIFICATIONS
Safe Working Load
Note: Safe Working Load indicates the sum of the
patient, mattress, and accessory weight.
Bed Weight570 lbs259 kg
Scale System Capacity (optional equipment). Loads weighing up to
Scale System Accuracy (optional equipment) ± 2 pounds at 0° - ± 10° Trendelenburg for patients
weighing 100 pounds or less
± 2% of the total patient weight at 0° - ± 10°
Trendelenburg for patients weighing greater than
100 pounds
Overall Length/
Width
Patient Sleep Surface - Standard Bed84” x 35”213.4 cm x 88.9 cm
Bed Height to Top of Seat
Litter - 6” Casters
Litter Platform
to Top of
Siderail
Space Between Siderails (Full Up)2-1/4”5.72 cm
Knee Gatch Angle0° to 45°
Fowler Angle0° to 60°
Trendelenburg/Reverse Trendelenburg+12° to -10° ± 1°
Electrical Requirements - all electrical requirements meet
UL 2601 specifications.
Standard Bed Siderails Up93” x 41-1/2” 236.2 cm x 105.41 cm
Siderails Down93” x 39-1/2” 236.2 cm x 100.3 cm
Standard16” to 30” ±0.540.6 cm to 76.2 cm
Full UpHead End Siderail15”38.1 cm
Full UpFoot End Siderail15 -1/2”39.37 cm
115VAC, 60Hz, 8A
500 lbs227 kg
500 lbs227 kg
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Introduction
Wireless Radio (iBed® Wireless Option)802.11 b/g, 2.4 GHz
The above stated mattress specifications assist in ensuring the product conforms to HBSW and IEC specifications.
ENVIRONMENTAL CONDITIONS
Environmental ConditionsOperationStorage and Transportation
0
F
104
0
C)
Ambient Temperature
50 0F
(10
0
C)
(40
-22 0F
(-30
0
C)
75%
Relative Humidity
(Non-Condensing)
30%
10%
1060 hPa
Atmospheric Pressure
700 hPa
500 hPa
Stryker reserves the right to change specifications without notice.
Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.
140
(60
95%
1060 hPa
0
F
0
C)
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PRODUCT ILLUSTRATION
Introduction
Control Panel
Steer
Pedal
(no t
shown)
Nurse
Siderail Release
Headboard
Handle
Brake
Pedal
Patient
Control Panel
Siderail
Footboard
Control Panel
Caster
Footboard
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Introduction
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at (800) 327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, Michigan 49002
USA
Please have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical
Support. Include the serial number in all written communication.
SERIAL NUMBER LOCATION
The serial number is located at the head end of the
bed just below the headboard and above the power
cord where it comes out from the frame.
Head End of Bed
A
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Summary of Safety Precautions
Before operating the S3™ MedSurg Bed, Model 3002 Patriot™ Series, it is important to read and understand all
information in this manual. Carefully read and strictly follow the safety guidelines listed on this page. It is important
that all users have been trained and educated on the inherent hazards associated with the usage of electric beds.
WARNING
• Powered bed mechanisms can cause serious injury. Operate bed only with persons clear of mechanisms.
• Danger: Explosion hazard. Do not use in the presence of flammable anesthetics.
• Always apply the caster brakes when a patient is getting on or off the bed.
• Always keep the caster brakes applied when a patient is on the bed (except during transport). After the brake
pedal is applied, push on the bed to ensure the brakes are locked. Serious injury could result if the bed moves
while a patient is getting in or out of bed.
• Ensure the brakes are completely released prior to moving the unit. Attempting to move the unit with the brakes
actuated could result in injury to the user and/or patient.
• Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal
is activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when
the steer pedal is activated may cause injury to the user.
• The S3™ MedSurg Bed, Model 3002 Patriot™ Series is not intended for use with patients less than two years of
age.
• Serious injury can result if caution is not used when operating the unit. Operate the unit only when all persons are
clear of the electrical and mechanical systems.
• To help reduce the number and severity of falls by patients, always leave the bed in the lowest position when the
patient is unattended.
• When attaching equipment to the frame, ensure it will not impede normal frame operation. For example: hooks
on hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, foley bags
must not rest on brake pedal, etc. Use only a Stryker supplied interface cable. Use of any other cable may cause
the bed to function improperly, which may result in patient or user injury.
• The S3™ MedSurg Bed, Model 3002 Patriot™ Series is equipped with a hospital grade plug for protection against
electric shock hazard. It must be plugged directly into a properly grounded three prong receptacle. Grounding
reliability can be achieved only when a hospital grade receptacle is used.
• When raising the siderails, listen for the “click”. When raising the siderail, the first click will indicate you can return
to the intermediate position, the second click indicates the full up position. Once in position, move the siderail
from side to side to ensure it is locked into position. Siderails are not intended to be a patient restraint device. It
is the responsibility of attending medical personnel to determine the degree of restraint and the siderail positioning
to ensure a patient will remain safely in bed.
• The 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. The bed exit system signals when a patient is about to exit. Adding or
subtracting objects from the frame after zeroing the weigh system may cause a reduction in the sensitivity of the
bed exit system.
• Before servicing or cleaning the bed, always unplug the bed power cord from the wall socket and push the battery
power on/off switch to the “OFF” position (if applicable). When working under a bed in the high position, always
place blocks under the litter frame and apply the brakes to prevent injury in case the Bed Down switch is accidently
pressed.
• To avoid pinching your fingers, place the I.V. pole in the upright position before using the drive handle.
• When using any mattress and/or mattress overlay that increases the overall height greater than 6,” extra caution
and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.
• When a Patient’s condition (such as disorientation due to medication or clinical condition) could lead to patient
entrapment, the mattress support platform should be left in the flat position while the patient is unattended (except
when required otherwise my medical staff for special or particular circumstances).
• Trendelenburg is not easily achievable when mains voltage has been interrupted.
• Medical electrical equipment (i.e. Optional Scale System) requires special precautions regarding EMC and needs
to be installed and put into service according to the EMC information provided on page 70 to prevent equipment
malfunction.
• Portable and mobile RF communication equipment can affect Medical Electrical Equipment (i.e. Optional Scale
System).
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Summary of Safety Precautions
WARNING CONTINUED
• To avoid malfunction, the Optional Scale System should not be used adjacent to or stacked with other equipment.
If adjacent or stacked use is necessary, the Optional Scale System should be observed to verify normal operation
in the configuration in which it will be used.
To avoid possible injury and to assure proper operation when using model number 2750, 2920, 2950 or 2981 mattress:
• Confirm proper scale system operation following mattress installation. For best results, secure the therapy mattress
power cord to prevent damage to the cord or interference with the bed frame and the scale system.
• Do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn Assist active. Patient motion
and position resulting from the dynamic therapy mattress may adversely affect scale system performance.
• Do no initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and
position resulting from the dynamic therapy mattress may adversely affect bed exit system performance.
• When using an XPRT (2950), Position PRO (2920), Impression (2981) or Symmetric Aire (2750) mattress, extra
caution and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.
CAUTION
• Unplug bed during service or cleaning.
• When large spills occur in the area of the circuit boards, 120 volt cables and motors, immediately unplug the bed
power cord from the wall socket. Remove the patient from the bed and clean up the fluid. Have maintenance completely check the bed. Fluids can affect the operational capabilities of any electrical product. DO NOT put the bed
back into service until it is completely dry and has been thoroughly tested for safe operation.
• Preventative maintenance should be performed at a minimum of annually to ensure all bed features are functioning
properly. Close attention should be gi ven to safety features including, but not limited to, safety side latching mechanisms,
frayed electrical cords and components, all electrical controls returning to the off or neutral position when released,
caster braking systems, no controls or cabling entangled in bed mechanisms, leakage current 300 μA (microamps)
maximum, scale and bed exit systems calibrated properly, and the siderail gas spring not leaking oil.
• Because individual beds may have different options, footboards should not be moved from one bed to another.
Mixing footboards could result in unpredictable bed operation.
• The lockout buttons on the footboard lock the Fowler, Gatch and Bed Up/Down functions and prevent motion of the
bed. It is the responsibility of attending medical personnel to determine whether these functions should be locked
and to use the buttons accordingly.
• The maximum safe working load for each I.V. pole is 40 pounds.
• I.V. Poles should not be used as a bed push/pull device.
• Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse
Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the
potential for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full
down position to prevent the interference from causing the scale system to weigh inaccurately.
• The use of a mattress overlay may reduce the effectiveness of the siderail.
• The cleanliness and integrity of both ground chains must be maintained to minimize static build up and discharge.
• Do not add or remove weight when the bed exit system is armed.
• There is a possible fire hazard when using half bed length type oxygen administering equipment. Ensure the
siderails are outside of the tent.
• There is a possible fire hazard when used with oxygen administering equipment of other than the nasal or mask
type. Lock the control at foot of bed when using oxygen administering equipment.
• The weight of the foley bags placed on isolated bag hooks should not exceed five pounds.
• The weight of pumps placed on footboard pump holder should not exceed 45 pounds.
• The safe working load of the defibrillator tray is 40 lbs.
• The safe working load of the oxygen holder is 45 lbs.
• Bed may be equipped with an integrated scale intended to weigh the patient in bed. If the scale output is being
used to determine diagnosis and treatment, please consult with a medical professional and/or additional weight
references.
• Scale accuracy specifications do not apply for patients under 20 lbs.
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Summary of Safety Precautions
IBED® AWARENESS OPTION
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the iBed® Awareness option.
WARNING
• The optional iBed® Awareness system only indicates the siderail position, it does NOT indicate if the siderail is
locked. It is the caregiver’s responsibility to ensure that the siderails are locked after every move and also before
leaving a patient in the room.
• The optional iBed® Awareness system indicator lights are only an aid to the caregiver, and in no way replace the
caregiver’s responsibility of checking on patients. Caregivers should not rely on the lights to perform their duties.
• Before arming the optional iBed® Awareness system, the nurse must physically verify that the siderails are locked.
CAUTION
• If the optional iBed® Awareness system is being used, ensure the bed is in the desirable state (iBed® Awareness
ON and with the light green) before leaving the room.
• If the optional iBed
Awareness as the display information to troubleshoot the bed will get lost.
• If the optional iBed® Awareness system is being used, use of accessories that cover the center and side alert lights
at the footboard are not recommended.
®
Awareness system is being used and the iBed® Awareness is alerting, do not turn off iBed®
iBED® WIRELESS OPTION
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the iBed® Wireless option.
WARNING
• The optional iBed® Wireless function provides remote information of bedside information to aid the caregiver. In
no way does this option replace the caregiver’s responsibility of checking on patients. Caregivers should not rely
only on the remote information to perform their duties.
• The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate
location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote
information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be remapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the
room / location information is changed after initial installation.
• Line of sight between iBed Locator and the head end of bed must be free of obstruction at all times. Any line
of sight interference could impede communication and cause the room / location information not to be available.
• iBed® Wireless compatible footboard must be used for all iBed® Wireless beds. Some iBed® Wireless functionality
will be lost if an older version of the footboard is used.
• iBed
• iBed Locators must be installed more than 71” apart from one another in the same room, such as in a semi-private
®
Wireless functionality shall be verified after installation. Failure to do may result loss of remote information
or wrong remote information. At a minimum, verify iBed locator communication with bed in all bed positions, and
iBed® Wireless communication with the wireless access point.
room with more than one bed. Failure to do so could result in a bed communicating with the other adjacent iBed
Locator, thus providing incorrect bed location information.
CAUTION
• Wireless bed only transmits bed information and not nurse call information. The wireless bed is not intended to
replace the existing nurse call system.
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Summary of Safety Precautions
115V OPTION
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the 115V option.
• Only use equipment with the following electrical specs: 115VAC; 10A; 60Hz. Maximum total load drawn by
equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not
exceed 100 μA (microamps). Grounding continuity should be checked periodically.
• To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or
receptacle.
• Do not use the optional 115V outlet for life sustaining equipment.
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Setup Procedures
To prevent permanent damage to this unit, the unit must reach room temperature prior to conducting any setup
and/or unit operations.
It is important that the S3™ MedSurg Bed, Model 3002 Patriot™ Series is working properly before it is put into service.
The following list will help ensure that each part of the bed is tested.
WARNING
• The S3™ MedSurg Bed, Model 3002 Patriot™ Series is equipped with a hospital grade plug for protection against
electric shock hazard. It must be plugged directly into a properly grounded three prong receptacle. Grounding
reliability can be achieved only when a hospital grade receptacle is used.
• Use only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly
which may result in patient or user injury.
1. Plug the bed into a properly grounded, hospital grade wall receptacle and ensure the LED light at the foot
end of the bed comes on.
2. Plug the optional interface cable into the 37-pin connector under the litter frame at the head end of the bed, into
the “Patient Station”, “Head Wall”, “Docker Station” or equivalent (whichever applies). Test the interface cable to
verify it is functioning properly.
3. Ensure the siderails raise, lower, lock in the up position, lock in the intermediate position when lowered and store
smoothly (page 19).
4. Ensure that all four casters lock when the brake pedal is engaged (page 17).
5. Raise the fowler (head of bed) up to approximately 600. Squeeze the CPR release handle and ensure the back
will drop with minimal effort.
Note
Ensure that the “Brake” LED located on the outside of the head end siderails and on the footboard control panel
blink when the brakes are not engaged.
6. Perform each function on the footboard control panel to ensure that each function is working properly (page 27).
7. Perform each function on both head end siderails to ensure that each is working properly (page 22).
8. Activate the motion stop system to ensure it is functioning properly; press and hold the BED DOWN key. As the
bed lowers, push up on the motion interrupt pan under the bed and ensure the downward motion stops. Release
the pan and allow the downward motion to continue.
Note
The bed’s upward motion or other functions are not disrupted by the motion stop system.
9. If the bed is equipped with the Nurse Call option, verify it is functioning properly prior to patient use.
If any problems are found during bed setup, contact Stryker Technical Support at (800) 327−0770.
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Setup Procedures
iBED® WIRELESS OPTION
In order for your bed to be capable of receiving a wireless connection the iBed Locator needs to be installed on the
wall at the head end of the bed. The iBed Locator communicates with the IR Module installed in your bed. For detailed
instructions on mounting the 5212 iBed Locator refer to the instruction sheet (part number 5212-009-101) packaged
with your optional 5212 iBed Locator Installation kit.
If any problems are found during the iBed Locator Installation, contact Stryker Technical Support at (800) 327−0770.
WARNING
• The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate
location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote
information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be remapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the
room / location information is changed after initial installation.
The wireless connection settings need to be loaded before the device will communicate with the iBed Server application.
Reference the iBed Server Installation and Configuration Manual (5212-009-001).
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Base Operation Guide
BRAKE PEDAL OPERATION
WARNING
Always apply the caster brakes when a patient is getting on or off the bed. Push the bed sideways to ensure the brakes
are securely locked. Always engage the brakes unless the bed is being moved. Injury could result if the bed moves
while a patient is getting on or off the bed.
To activate the brakes, push down once on one of the pedals
located at the midpoint of the bed on both sides (identified by
the label at right). The pedal will remain in the lowered position,
indicating the brakes are engaged. To disengage the brakes,
push down once and the pedal will return to the upper position.
Note
The LED lights located on the outside of the head end siderails and on the foot end control panel will blink when the
brakes are not engaged only if the bed is plugged into a wall socket or is running on battery power (page 22 & page
30). The brakes will still operate properly when the bed is not plugged in.
STEER PEDAL OPERATION
When the bed is moved, the steer caster helps guide the bed along a straight line and helps the bed pivot around
corners.
To activate the steer caster, move the pedal located at the head
end of the bed to your right as shown on the label.
Note
For proper “tracking” of the steer caster, push the bed approximately 10 feet to allow the wheels to face the direction of
travel before engaging the steer pedal. If this is not done, proper “tracking” will not occur and the bed will be difficult
to steer.
WARNING
Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal is
activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when the
steer pedal is activated may cause injury to the user.
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Litter Operation Guide
CPR EMERGENCY RELEASE
When quick access to the patient is needed, and the Fowler (head of bed) is raised, squeeze one of the two release
handles (marked by the red CPR label) and the fowler can quickly be guided down to a flat position.
Note
The handle can be released at any time to stop the Fowler from lowering.
FOOT PROP USAGE
The foot prop causes the foot end of the Knee Gatch to rise
when the Gatch button is used to raise the Gatch. To lower
the foot end of the Gatch, release the prop by grasping the
end of the Knee Gatch, lifting upward and swinging the prop
(A) toward the head end of the bed which will disengage the
prop stop.
Head End
WARNING
To avoid injury while cleaning or servicing under the foot
section, secure the foot section with string or bungee cords or
hold it up out of the way.
Lift up Knee Gatch
Foot End
A
FRACTURE FRAME USAGE
A standard fracture frame can be mounted on the bed using the I.V. sockets located on all four corners of the bed. I.V.
poles can be used in conjunction with a fracture frame if the I.V. pole adaptor sockets are purchased.
WARNING
Use only retractable traction or fracture frames. Failure to use a retractable frame may result in injury to the patient
and/or damage to the equipment.
FOLEY BAG HOOKS USAGE
The standard foley bag hooks are found at four locations (on each side of the bed); below the seat (middle) section
and at the extreme foot end of the frame. Optional isolated foley bag hooks can be purchased and are located at the
foot end of the bed under the frame. The patient weight reading on the scale system is not affected when the optional
isolated foley bag hooks are used.
Patient Restraint Strap Locations
The bed has 10 locations for installing patient restraint straps on the litter top, five on each side of the bed.
WARNING
Improperly adjusted restraint straps can cause serious injury to a patient. The clinician must use her/his judgement
to determine proper use of restraint straps and restraint strap locations. 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.)
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Litter Operation Guide
POSITIONING SIDERAILS
• The siderails can be locked at two heights (intermediate & full up).
• The siderails can slide in towards the bed when not in use. To remove the rail from the tucked position, grasp the
top of the rail and pull outward.
• To raise head end siderail to full height position, grasp the rail and swing it upward until it locks in place (two clicks
are heard).
Note: When the siderail is being raised, it does not lock in the intermediate position unless it is
brought back after the first click.
• To lower the siderail and lock in intermediate position, pull outward on the siderail release handle (A) and rotate
the siderail down toward the head end of the bed until it locks at the intermediate position.
• To lower the siderail in its full down position, pull outward on the release handle (A) and rotate the siderail
downward toward the head end of the bed until it is completely lowered.
• To raise and lower the foot end siderail, the same procedures are required as for the head end siderail, however,
the siderail swings toward the foot end of the bed.
WARNING
• Be sure the siderail is locked securely into position.
• Siderails in a full up or intermediate position are
not intended to keep patients from exiting the
bed. They are designed to keep a patient from
inadvertently rolling off the bed. Proper restraint
methods should be utilized to ensure the patient
remains in the bed.
• The intermediate position is only intended to assist
patients and users when getting in or out of the bed
in addition to assisting in positioning themselves in
the bed.
• The Intermediate position should not be used in
place of the full up position.
• The siderails are not intended to be used as a push
device.
A
To disengage the rail, pull outward on release handle (A) and swing the rail down to the desired height (intermediate
or full down). When storing siderails, ensure they are at a full down position.
CONTROL PANEL LIGHTS
The bed is equipped with lights to illuminate the head end siderail control panel and the red nurse call switches.
Both can be activated at the footboard control panel. Five settings are available for the control panel lights: Off, Low
Intensity, Medium Intensity, High Intensity and Nurse Call Only.
To change the control panel light settings, press the “Menu” button on the footboard. Scroll down through the menu
items and select “Backlight” then press “Enter”. Select the desired setting by highlighting it and then pressing “Enter”.
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Litter Operation Guide
OPERATING I.V. POLES
WARNING
To avoid pinching your fingers, place the I.V. pole in the upright position
before using the drive handle.
To use the “Removable” I.V. pole:
1. Install the pole at any of the four receptacles on the bed top (located
on all four corners of the frame).
2. To raise the height of the pole, turn knob (A) counterclockwise and
pull up on the telescoping portion (B) of the pole and raise it to the
desired height.
3. Turn knob (A) clockwise to tighten the telescoping portion in place.
CAUTION
The maximum safe working load for each I.V. pole is 40 pounds.
To use the 2-Stage Permanently Attached I.V. pole:
Note
The 2-stage permanently attached I.V. pole is an option and may have been
installed at either the head, foot or both ends of the bed. The choice was made
at the time the unit was purchased.
1. Lift and pivot the pole from the storage position and push down until it
rests in the receptacle.
2. To raise the height of the pole, pull up on the telescoping portion (A) until
it locks into place at its fully raised position.
3. Rotate the I.V. hangers (B) to desired position and hang I.V. bags.
4. To lower the I.V. pole turn the latch (C) clockwise until section (A) lowers.
A
C
B
CAUTION
The maximum safe working load for each I.V. pole is 40 pounds.
Return To Table of Contents
20300 6-109 -101 REV Awww.stryker.com
Litter Operation Guide
NIGHT LIGHT USAGE
The bed is equipped with two night lights to illuminate the floor area
around the bed. There is a switch under the litter thigh section on the
patient’s left side that turns both lights on and off.
WARNING
Service only by qualified personnel. Refer to the maintenance
manual. Verify the power cord is unplugged before servicing.
NURSE CALL BACKUP BATTERY (OPTIONAL)
• To prevent a low battery condition when the bed is not
plugged in, position the cord out switch at the head end
of the bed to the off position. The switch is identified by
the label shown below. If the switch is not positioned as
shown below and the bed power cord and pendant cord are
unplugged, the life of the backup battery will be significantly
reduced.
• If the Nurse Call battery needs to be replaced, a message will appear on the footboard display. The battery is
located on the patient’s left side at the head end of the bed. No tools are required to replace the battery. Unplug
the bed power cord from the wall socket and remove the battery from its housing to replace.
1/4” NURSE CALL PORT (OPTIONAL)
• The optional ¼” nurse call port is only designed to function with nurse call cords that have a ¼” TS connector.
• Fully insert the attached dummy plug into the port whenever a nurse call cord is not inserted into the port.
• If a continuous nurse call signal is observed, ensure that the dummy plug or a compatible nurse call cord is fully
inserted into the port.
USING THE 115 VOLT OUTLET (OPTIONAL)
• The 115V outlet has its own power cord that must be plugged into a properly grounded hospital grade three prong
wall receptacle different from the wall receptacle the bed power cord is plugged into.
• If the equipment plugged into the bed outlet is not receiving power, check the 10A circuit breakers located on the
litter frame under the head section. Reset, if necessary.
WARNING
• Only use equipment with the following electrical specs: 115VAC; 10A; 60Hz. Maximum total load drawn by
equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not
exceed 100 μA (microamps). Grounding continuity should be checked periodically.
• To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or
receptacle.
• Do not use the optional 115V outlet for life sustaining equipment.
CPR BOARD USAGE (OPTIONAL EQUIPMENT)
If the bed is equipped with the optional CPR board, it is stored on the bed’s headboard. To remove it, pull it away from
the headboard using both hands and lift it out of storage position.
www.stryker.com30 06 -109-101 REV A21
Return To Table of Contents
Siderail Operation Guide
NURSE CONTROL FUNCTIONS (OUTSIDE SIDERAIL)
3
6
8
1
7
9245
LEFT OUTER SIDERAIL SHOWN
(Right Outer Siderail same as the Left)
ButtonButton NameButton Function
Brake LED
1
Cardiac Chair
2
Bed/Litter UpPress to raise the Bed/Litter.
3
Bed/Litter DownPress to lower the Bed/Litter.
4
Nurse CallPush to activate Nurse Call.
5
Knee Gatch UpPress to raise the Knee Gatch.
6
Knee Gatch DownPress to lower the Knee Gatch.
7
Fowler UpPress to raise the Fowler.
8
Fowler DownPress to lower the Fowler.
9
LED flashes when Brakes are not engaged.
LED is “Off” when brakes are engaged.
Press to activate the Cardiac Chair function.
• The Knee will raise.
• The back will raise to approximately 60
• The bed will tilt to approximately −100 reverse
Trendelenburg (foot end down).
0
Note: The intent of the nurse call light on the siderails is to ensure the patient immediately knows which button to push
to contact the nurse station. Turning the light off may compromise this ability, especially in a darkened room.
Return To Table of Contents
22300 6-109 -101 REV Awww.stryker.com
Siderail Operation Guide
PATIENT CONTROL FUNCTIONS WITHOUT OPTIONAL SMART TV (INSIDE SIDERAIL)
1
8
9
12
2
3
5
6
7
LEFT INSIDE SIDERAIL SHOWN
(Right Inside Siderail same as the Left with exception of the Nurse Call and Nurse
Answer LED. LED 7 and 8 will change positions on the right inner siderail )
10
114
ButtonButton NameButton Function
TV / RadioPress to turn TV or radio on and to select a channel.
1
Room LightPress to turn the room light On/Off.
2
Bed Overhead LightPress to turn the bed overhead light On/Off.
3
TV/Radio Volume DownPress to decrease volume; TV or Radio.
4
TV/Radio Volume UpPress to increase volume; TV or Radio.
5
Press to activate Nurse Call.
10
11
12
Nurse Call
6
Nurse Call LED
7
Nurse Call Answer LEDIlluminates green when answered by Nurse.
8
Fowler UpPress to raise the Fowler.
9
Fowler DownPress to lower the Fowler.
Knee Gatch DownPress to lower the Knee Gatch.
Knee Gatch UpPress to raise the Knee Gatch.
Note: Yellow LED will light when button is pushed.
Green LED will light with Nurse Station acknowledgment.
Illuminates amber when nurse call has been pressed by
patient.
www.stryker.com30 06 -109-101 REV A23
Return To Table of Contents
Siderail Operation Guide
PATIENT CONTROL FUNCTIONS WITH OPTIONAL SMART TV (INSIDE SIDERAIL)
1
8
9
12
2
3
56
10
1147
LEFT INSIDE SIDERAIL SHOWN
(Right Inside Siderail same as the Left)
ButtonButton NameButton Function
TV On/OffPress to turn TV on or off.
1
Room LightPress to turn the room light On/Off.
2
Bed Overhead LightPress to turn the bed overhead light On/Off.
3
TV/ Volume DownPress to decrease TV volume.
4
TV/ Volume UpPress to increase TV volume.
5
Press to activate Nurse Call.
10
11
Nurse Call
6
Nurse Call LED
7
Nurse Call Answer LEDIlluminates green when answered by Nurse.
8
Fowler UpPress to raise the Fowler.
9
Fowler DownPress to lower the Fowler.
Knee Gatch DownPress to lower the Knee Gatch.
Note: Yellow LED will light when button is pushed.
Green LED will light with Nurse Station acknowledgment.
Illuminates amber when nurse call has been pressed by
patient.
12
Return To Table of Contents
243006-10 9-101 RE V Awww.stryker.com
Knee Gatch UpPress to raise the Knee Gatch.
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