Operations
Manual
Medical
Secure II Med-Surg Bed
Model 3002
For parts or technical
assistance call
800 327 0770 (option 2)
Table of Contents
Introduction
Specifications 2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Warning / Caution / Note Definition 3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Safety Tips And Guidelines 4−6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Set−Up Procedures 7, 8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Bed Symbols 9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Bed Illustration 10. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Base
Brake Pedal Operation 11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Steer Pedal Operation 11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Litter
CPR Emergency Release Usage 12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Foot Prop Usage 12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Fracture Frame Usage 12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Foley Bag Hooks 12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Patient Restraint Strap Locations 12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Night Light Usage 13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Nurse Call Back−Up Battery 13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Optional 110V Outlet 13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
CPR Board Usage 13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
IV Poles 14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Siderails
Positioning Siderails 15. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Control Panel Lights 15. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Siderail Function Guide 16, 17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Foot Board
Foot Board Control Panel Guide 18. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Function Lockout System Usage 19. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Foot Board LED Display Panel Guide 19. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Bed Exit System Usage 20
Scale System Operation Guide 23−30. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Optional Pendant Operation 31. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Zoom Option Operation
Drive Wheel Operation 32, 33. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Head End Control Panel Operation 34. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Battery Charging and Operation 35. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Cleaning 36. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Preventative Maintenance Checklist 37. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Limited Warranty
Obtaining Parts and Service 38. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Extended Warranty Coverage 38. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Return Authorization 39. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Freight Damage Claims 39. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
−22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction
INTRODUCTION
This manual is designed to assist you with the operation of the Model 3002 Secure II Bed. Read it thoroughly
before using the equipment.
SPECIFICATIONS
Safe Working Load 500 pounds (227 kilograms)
Scale System Capacity (optional equipment) Loads weighing up to 500 pounds (227 kilograms)
Scale System Accuracy
(optional equipment)
Overall Bed Length/Width − Standard Bed
(inside the US and Canada)
Overall Bed Length/Width − Standard Bed
(outside the US and Canada)
Overall Bed Length/Width − Short Bed
Overall Bed Length/Width − Zoom Bed
Overall Bed Length/Width − Zoom Short Bed
Patient Sleep Surface − Standard Bed 84” x 35” − 213 cm. x 89 cm.
Patient Sleep Surface − Short Beds 76” x 35” − 193 cm. x 89 cm.
Bed Height to Top of Seat Litter − 6” Casters
(Add 2 inches if the bed has 8” casters.)
Litter Platform to Top of Siderail (Full Up)
Outside the US & Canada:
Space Between Siderails (Full Up)
Outside the US & Canada:
$ 2 pounds at 0 − $ 10 Trend for patients weighing 100
pounds or less
$2% of total patient weight at 0 − $ 10 Trend for patients
weighing greater than 100 pounds
93” x 42.5” (siderails up) − 40” (siderails down)
236 cm. x 108 cm. (siderails up) − 101.6 cm. (siderails down)
93” x 42.5” (siderails up) − 36” (siderails down)
236 cm. x 108 cm. (siderails up) − 92 cm. (siderails down)
85” x 42.5” (siderails up) − 36” (siderails down)
216 cm. x 108 cm. (siderails up) − 92 cm. (siderails down)
95” x 42.5” (siderails up) − 40” (siderails down)
241 cm. x 108 cm. (siderails up) − 101.6 cm. (siderails down)
87” x 42.5” (siderails up) − 36” (siderails down)
221 cm. x 108 cm. (siderails up) − 92 cm. (siderails down)
16” to 30” $0.5 / 41 cm. to 76 cm.
Beds with Zoom Option −19.75” x 30” − 50 cm. x 76 cm.
Short Beds with Zoom Option −20.5” x 30” − 52 cm. x 76 cm.
15.75” Head End Siderail, 15.25” Foot End Siderail
15” Head End Siderail, 14” Foot End Siderail
9.75”
8” − 9.125”
Knee Gatch Angle 0 to 40
Fowler Angle 0 to 60
Trendelenburg/Reverse Trendelenburg −12 to +12 $1
−10 to +10 $1 − Beds with Zoom Option
−8 to +8 $1 − Short Beds
Electrical Requirements − all electrical requirements meet UL 2601 specifications.
Outlet Option 125 VAC, 60 Hz, 10.0 Amp (not available with Zoom option)
115 VAC, 60 Hz, 7.0 Amp.
Optional: 230 VAC, 50/60 Hz, 4.0 Amp.
MATTRESS SPECIFICATIONS
Thickness 6”
Width >= 35”
Length >= 84”
ILD 80
Stryker reserves the right to change specifications without notice.
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2
Introduction
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 important instructions clearer.
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3
Safety Tips and Guidelines
SAFETY TIPS AND GUIDELINES
Before operating the Secure Bed, 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
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 attempting to move 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 Secure II Bed 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, etc.
Use only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improp-
erly which may result in patient or user injury.
The Secure II is equipped with a hospital grade plug for protection against 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 using the manual override shaft to manually actuate bed functions, always unplug the bed power
cord from the wall socket to avoid injury in the event of a sudden return of power to the bed.
When raising the siderails, listen for the ”click” that indicates the siderail has locked in the up position.
Pull firmly on the siderail 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.
Always unplug the bed power cord from the wall socket and push the battery power on/off switch to the
“OFF” position before servicing or cleaning the bed. When working under the bed with the 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.
The CPR emergency release on the Short Bed frame may require assistance to lower the back when the
Back is in the highest position. Attempting to lower the Back in this position without assistance may result
in injury to the operator.
Only use equipment with the following electrical specs: 110 VAC; 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 100uA. Grounding continuity should be checked periodically.
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4
Safety Tips and Guidelines
SAFETY TIPS AND GUIDELINES (CONTINUED)
WARNING
To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction
box or receptacle.
Do not use the optional 110V outlet for life sustaining equipment.
To avoid pinching your fingers, place the IV 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.
To avoid possible injury and to assure proper operation when using a powered mattress replacement system
such as XPRT:
Confirm proper scale system operation following mattress installation. For best results, secure the thera-
py 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. Pa-
tient 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 Therapy Mattress extra caution and/or operator supervision is required to help re-
duce the likelihood of a patient fall occurring.
CAUTION
When large spills occur in the area of the circuit boards, 110 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 given to safety features including, but not limited to:
safety side latching mechanisms, frayed electrical cords and components, all electrical controls return
to off or neutral position when released, caster braking systems, no controls or cabling entangled in bed
mechanisms, leakage current 100 microamps maximum, scale and bed exit systems calibrated properly.
Because individual beds may have different options, foot boards should not be moved from one bed to
another. Mixing foot boards could result in unpredictable bed operation.
The lockout buttons on the foot board 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 weight of the IV bags should not exceed 40 pounds.
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.
When attaching equipment to the frame, ensure it will not impede normal operation. For example: hooks
on hanging equipment must not actuate control buttons, equipment must not hide the nurse call button,
etc.
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5
Safety Tips and Guidelines
CAUTION CONT’D
The use of a mattress overlay may reduce the effectiveness of the siderail.
IV Poles should not be used as a bed push/pull device.
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.
SAFETY TIPS AND GUIDELINES (ZOOMr OPTION)
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units
equipped with the Zoom option.
WARNING
The 3002 Patient Transport Frame is intended for use by trained hospital personnel only. Failure to prop-
erly train personnel could result in injury.
USE CAUTION while maneuvering the unit with the drive wheel activated. Always ensure there are no
obstacles near the unit while the drive wheel is activated. Injury to the patient, user or bystanders or damage to the frame or surrounding equipment could occur if the unit collides with an obstacle.
Use caution when transporting the unit down halls, through doors, in and out of elevators, etc. Damage
to the siderails or other parts of the unit could occur if the unit comes in contact with walls or door frames.
Put the drive wheel in the neutral position and release the brakes before pushing the unit manually. Do
not attempt to push the unit manually with the drive wheel engaged. The unit will be difficult to push and
injury could result.
If unanticipated motion occurs, unplug the power cord from the wall socket, push the battery power on/off
switch to the ”OFF” position (the LED will not be illuminated) and actuate the drive wheel pedal to the
neutral position.
The power save mode is activated after one hour on battery power with no motion release switch activa-
tion. Functions including Bed Exit, scale and motion will cease to operate when the unit enters the power
save mode. Injury to the patient could occur if proper patient monitoring protocol is not observed.
Always unplug the power cord and push the battery power on/off switch to the “OFF” position before ser-
vice or cleaning. When working under the frame, always place blocks under the litter frame to prevent
injury in case the Bed Down switch is accidently activated.
Due to the weight the battery adds to the bed (approximately 50 pounds), additional force is required to
move the bed. Caution should be used when transporting this bed. Additional assistance should be used
when necessary. Failure to use caution while transporting this bed may result in injury to the user.
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. Wash hands after
handling.
Do not modify the 3002 Patient Transport Frame. Modifying the unit can cause unpredictable operation
resulting in injury to the patient or operator. Modifying the unit will also void its warranty.
CAUTION
To avoid damage while transporting the bed, verify the I.V. pole is at a low enough height to allow it to
safely pass through door openings and under light fixtures.
The battery tray assembly weighs 50 pounds. Take care when removing the two hex head screws secur-
ing it to the base frame or personal injury could result.
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6
Set−Up Procedures
SET−UP PROCEDURES
It is important that the Secure II Bed is working properly before it is put into service. The following list will
help ensure that each part of the bed is tested.
Plug the bed into a properly grounded, hospital grade wall receptacle and ensure the ”Power” LED light
at the foot end of the bed comes on.
WARNING
The Secure II is equipped with a hospital grade plug for protection against 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.
Plug the optional interface cable into the 37 pin connector under the litter frame at the head end of the
bed, and into the ”Patient Station”, ”Head Wall”, ”Docker Station”, or equivalent (whichever applies). Test
the interface cable to verify it is functioning properly.
WARNING
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.
Ensure the siderails raise, lower and store smoothly and lock in the up position and in the intermediate
position when lowered (page 15).
Ensure that all four casters lock when the brake pedal is engaged (page 11).
Raise the Back up to approximately 60. Squeeze the CPR release handle and ensure the Back will drop
with minimal effort.
NOTE
Ensure that the ”Brake Not Set” LEDs located on the outside of the head end siderails and on the foot board
control panel come on when the brakes are disengaged.
Run through each function on the foot board control panel to ensure that each function is working properly
(page 18−23).
Run through each function on both head end siderails to ensure that each is working properly (page 15
− 17).
Activate the motion stop system to ensure it is functioning properly: press and hold down the BED DOWN
key. As the bed lowers, lift up on the motion interrupt pan (reference illustration on page 10) 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.
If the bed is equipped with the Nurse Call option, verify it is functioning properly prior to patient use.
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7
Set−Up Procedures
SET−UP PROCEDURES (ZOOMr OPTION)
If your bed is equipped with the Zoom drive wheel option, run through the set−up procedures on page 7
and continue with the procedures listed below.
Plug the power cord into a properly grounded, hospital grade wall receptacle. The 12 volt batteries that
provide power to the drive wheel and back−up power to the unit functions will charge whenever the power
cord is plugged into the wall socket. The batteries require approximately 10 hours of charging time before
the bed is put into service.
Unplug the power cord from the wall socket. Push the battery power switch located on the lower left cor-
ner of the head end to the “ON” position. Again, verify each function on the foot board and siderails is
operating properly.
With the battery power switch in the “ON” position and the brakes engaged, ensure the “Release Brakes”
LED on the head end control panel is illuminated.
With the battery power switch in the “ON” position and the drive wheel in the neutral position (not touching
the floor), ensure the “Engage Drive Wheel” LED on the head end control panel is illuminated.
Run through the operation of the drive wheel (see page 32 & 33) to ensure it is operating properly.
If any problems are found during bed set−up, contact Stryker Customer Service at 800−327−0770.
Damaged Merchandise
ICC Regulations require that claims for damaged merchandise must be made with the carrier within fifteen
(15) days of receipt of merchandise. DO NOT ACCEPT DAMAGED SHIPMENTS UNLESS SUCH DAMAGE
IS NOTED ON THE DELIVERY RECEIPT AT THE TIME OF RECEIPT. Stryker Customer Service must be
notified immediately. Stryker will aid the customer in filing a freight claim with the appropriate carrier for damages incurred. Claim will be limited in amount to the actual replacement cost. In the event that this information
is not received by Stryker within the fifteen (15) day period following the delivery of the merchandise, or the
damage was not noted on the delivery receipt at the time of receipt, the customer will be responsible for payment of the original invoice in full.
Claims for any short shipment must be made within thirty (30) days of invoice.
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8
Symbols
Warning, Refer to Service/Maintenance Manual
~
Alternating Current
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
IPX4: Protection from liquid splash
Dangerous Voltage Symbol
Protective Earth Terminal
Potential Equalization Symbol
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
Safe Working Load Symbol
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.
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9
Footboard
Control
Panel
Bed Illustration
PATIENT’S
RIGHT
HEAD END
CPR Release
Handle
PATIENT’S
Steer
Pedal
LEFT
I.V. and
Fracture Frame
Mount
FOOT END
Brake Pedal
I.V. and
Fracture Frame
Mount (Behind Foot Board)
Siderail Release
Handle
Foley Bag Hooks
(Standard)
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10
Base Operation Guide
BRAKE PEDAL OPERATION
WARNING
Always apply the caster brakes when a patient is getting on or off the bed. Push on the bed 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
There are LED lights on the outside of the head end siderails and on the foot end control panel that will blink
when the brakes are not engaged only if the bed is plugged into a wall socket (see pages 17 & 19). The brakes
will still operate properly when the bed is not plugged in.
STEER PEDAL OPERATION (BEDS WITHOUT THE ZOOM DRIVE WHEEL OPTION)
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 left 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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11
Litter Operation Guide
CPR EMERGENCY RELEASE
When quick access to the patient is needed, and the Fowler is raised, squeeze one of the two red release
handles (see illustration, page 10) and the Fowler can be quickly guided down to a flat position.
NOTE
The handle can be released at any time to stop the Fowler from lowering.
A
FOOT PROP USAGE
To prop the foot end of the Knee Gatch up, grasp
the end of the Knee Gatch and lift upward, allowing
the foot prop (A) to engage at the desired height.
To release the prop, swing the prop (A) toward the
head end of the bed to disengage the hinge and
lower the foot 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.
FOOT END
FRACTURE FRAME USAGE
A standard fracture frame can be mounted on the bed using the IV sockets located on all four corners of the
bed. IV poles can be used in conjunction with a fracture frame if IV 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 two locations on both sides of the frame: under the frame below
the seat section and at the extreme foot end of the frame. The optional isolated Foley bag hooks are located
at the foot end of the bed on top of the lift header. The patient weight reading on the scale system will not
be affected when the optional isolated Foley bag hooks are used.
PATIENT RESTRAINT STRAP LOCATIONS
The bed has 12 locations for installing patient restraint straps on the litter top, 6 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. (Ap-
propriate disinfectant for nylon Velcro should be determined by the hospital.)
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12
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.
NOTE
The night lights have a sensor so the lights will turn off,
even when the switch is on, if the light in the room is bright
enough so a night light is not necessary.
NURSE CALL BACK−UP BATTERY (Optional Equipment)
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 back−up battery will be significantly reduced.
If the power light (located on the foot board) is flashing, the Nurse Call battery needs to be replaced. 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 replace the battery.
USING THE 110 VOLT OUTLET (Optional Equipment)
The 110V outlet has its own power cord that must be plugged into a properly grounded 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 circuit breakers located on the
litter frame under the head section. Reset, if necessary.
WARNING
Only use equipment with the following electrical specs: 110 VAC; 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 100uA. 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 110V 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 head board. To remove it,
pull it away from the head board and lift it out of storage position. If the CPR board option was not purchased, the head board can also be removed and used as an emergency CPR board.
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13
OPERATING IV POLES
C
B
Litter Operation Guide
A
To use the 2−Stage Permanently Attached IV pole:
NOTE
The 2−stage permanently attached IV pole is an option and may have been
installed at either the head, foot or both ends. 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 IV hangers (B) to desired position and hang IV bags.
4. To lower the IV pole turn the latch (C) clockwise until section (A) lowers.
CAUTION
The weight of the IV bags should not exceed 40 pounds.
WARNING
To avoid pinching your fingers, place the IV pole in the upright position before using the drive handle .
To use the ”Removable” IV 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 weight of the IV bags should not exceed 40 pounds.
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14
Siderail Operation Guide
POSITIONING SIDERAILS
NOTE
The siderails can be locked at two heights (intermediate & full up). The foot end siderails on a Short Bed do
not have an intermediate position.
The siderails can slide to the side of the bed when not in use. To remove the rail from the tucked position,
grasp the top of the rail and pull outward.
To engage the head end siderail, grasp the rail and swing it upward to full height. When the siderail is being
raised, it does not lock in the intermediate position. To lower the siderail, push in the yellow release handle
(A) and rotate the siderail until it locks in the intermediate position. To lower the siderail fully, push in thel yellow
release handle (A) again and rotate the siderail until it is completely lowered.
To engage the foot end siderail, the same procedure is 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 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 bed.
The siderails are not intended to be
used as a push device.
A
To disengage the rail, push in the yellow release handle (A) and swing the rail down to the desired height.
Store the siderails slid.
SIDERAIL 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 foot board control panel. Three settings are available for the control
panel lights: low, medium and high intensity. When all lights are off, push the siderail control light button at
the foot board once to turn on both the control lights and the nurse call light at the siderail. Push again to
change from low to medium setting, and a third time to change to the high setting. The nurse call light intensity
is not affected. Pushing the button a fourth time will turn off the siderail control panel lights and pushing it
a fifth time will turn off the red nurse call light as well (see control panel guide page 18).
NOTE
The purpose of the red nurse call light on the siderails is to ensure the patient immediately knows which button
to push to contact the nurse station. Turning the red light off may compromise this ability, especially in a darkened room.
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15
Siderail Operation Guide
INSIDE SIDERAIL FUNCTION GUIDE
(Patient’s Right Rail)
1. Push to raise Knee Gatch.
2. Push to lower Knee Gatch.
3. Push to raise Fowler.
4. Push to lower Fowler.
(Patient’s Left Rail)
1. Push to raise Fowler.
2. Push to lower Fowler.
3. Push to raise Knee Gatch.
4. Push to lower Knee Gatch.
1. Push to activate Nurse Call.
NOTE
Yellow LED will light when button is pushed. Red LED will light with
Nurse Station acknowledgment.
This panel is optional equipment.
1. Push to turn TV or radio on and to select a channel.
2. Push to increase volume.
3. Push to decrease volume.
This panel is optional equipment.
1. Push to turn the room light on.
2. Push to turn the bed overhead light on.
This panel is optional equipment.
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1. Push to change the TV channel up.
2. Push to change the TV channel down.
3. Push to mute TV volume. Push again to turn the sound back on.
4. Push to display closed captioning. Push again to turn off closed captioning.
This panel is optional equipment.
16
Siderail Operation Guide
OUTSIDE SIDERAIL FUNCTION GUIDE
(Patient’s Right Rail)
1. Push to raise Fowler.
2. Push to lower Fowler.
3. Push to raise Knee Gatch.
4. Push to lower Knee Gatch.
This panel is optional equipment.
(Patient’s Left Rail)
1. Push to raise Knee Gatch.
2. Push to lower Knee Gatch.
3. Push to raise Fowler.
4. Push to lower Fowler.
This panel is optional equipment.
1. Push to raise bed height.
2. Push to lower bed height.
Push to activate Nurse Call.
This panel is optional equipment.
LED will blink when the brakes are not set.
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Push to activate the Cardiac Chair function. The Knee will raise, the
Back will raise or lower to approximately 52 and the bed will tilt to
approximately −12 (−10 if it’s a Short Bed) reverse Trendelenburg
(foot end down). Release the button to stop bed movement: hold the
button until movement stops to complete the function.
This panel is optional equipment.
17
Foot Board Operation Guide
FOOT BOARD CONTROL PANEL GUIDE
1. Push repeatedly for low, medium and high settings for the siderail control panel lights. Pushing a fourth
and fifth time will turn off the siderail lights and the red nurse call light respectively (see page 15).
NOTE
The intent of the red nurse call light on the siderails is to ensure the patient immediately knows which button
to push to contact the nurse station. Turning the red light off may compromise this ability, especially in a darkened room.
2. Push to lock out all bed motions. The MOTION lock icon and the “BED MOTION LOCKED” LED will light.
Push again to unlock.
3. Push to lock out Back Rest controls at both siderails. The HEAD lock icon will light. Push again to unlock.
4. Push to lock out Knee Gatch controls at both siderails. The KNEE lock icon will light. Push again to unlock.
5. Push to lock out bed height movement at both siderails. The UP/DOWN lock icon will light. Push again
to unlock.
6. Push to raise bed height.
7. Push to lower bed height.
8. Push to lower head end/raise foot end of bed (Trendelenburg position).
9. Push to lower foot end/raise head end of bed (Reverse Trendelenburg position).
CAUTION
Because individual beds may have different options, foot boards should not be moved from one bed to another. Mixing foot boards could result in unpredictable bed operation.
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18
Foot Board Operation Guide
FOOT BOARD CONTROL PANEL GUIDE (CONTINUED)
1. Push to raise Fowler.
2. Push to raise Knee Gatch.
3. Push to lower Fowler.
4. Push to lower Knee Gatch.
This panel is optional equipment.
LED DISPLAY PANEL GUIDE
The LED Display Panel is located at the foot end of the bed, under the Control Panel.
”POWER” − will light when the bed is plugged into the wall receptacle. Will blink if the 9V Nurse Call battery
needs to be replaced.
”BED MOTION LOCKED” − will light when the Bed Motion Lock has been activated.
”BRAKE NOT SET” − will blink when the brakes have not been set.
”BED EXIT ON” − will light when the Bed Exit function has been activated (optional equipment).
FUNCTION LOCKOUT SYSTEM USAGE
1. To lock out the bed movement functions on the siderails and prevent the patient from changing the position-
ing of the bed, push the ”HEAD”, ”KNEE” and/or ”UP/DOWN” switches in the ”Siderail Control Lockouts”
module on the foot board control panel.
NOTE
The foot board controls for these motions are not affected by the lockout switches.
The ”padlock” symbol on the control panel will be lighted when that function is locked out.
2. To lock out the entire bed motion for all switches on the bed (siderails and foot board), push the ”ON/OFF”
switch in the ”Bed Motion Lock” module on the foot board control panel.
CAUTION
The lockout buttons on the foot board 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.
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19
Foot Board Operation Guide
CHAPERONEr BED EXIT (OPTIONAL EQUIPMENT)
For beds with a scale system:
NOTE
If the weigh system is in use, it will switch to ”off” when the “ARM” key is pressed.
1. Before putting the patient on the bed, the weigh system must be zeroed for the Bed Exit System to function properly (see page 25 for instructions on zeroing the weigh system).
2. Put the patient on the bed and push the “ARM” key to activate the Bed Exit function. The ”ARMED” light
will come on.
3. To deactivate Bed Exit, push the ”DISARM” key. The ”ARMED” and ”BED EXIT ON” lights will turn off.
For beds without a scale system:
1. Before putting the patient on the bed, press and hold the ”ARM” and the ”DISARM” keys together until
the ”ARMED” light begins to flash.
2. Release the ”ARM” and the ”DISARM” keys and do not touch the bed until the ”ARMED” light stops flashing.
3. Put the patient on the bed and push the ”ARM” key to activate the Bed Exit function. The ”ARMED” light
will come on.
4. To deactivate Bed Exit, push ”DISARM”. The ”ARMED” and ”BED EXIT ON” lights will turn off.
WARNING
The Bed Exit System is intended only to aid in the detection of a patient exiting the bed. It is NOT intended
to replace patient monitoring protocol. It signals when a patient is about to exit. Adding or subtracting objects
from the bed after arming the bed exit system may cause a reduction in the sensitivity of the bed exit system.
To avoid possible injury and to assure proper operation when using a powered mattress replacement system
such as XPRT, do not initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn−Assist active.
The patient motion and position resulting from a dynamic therapy mattress may adversely affect bed exit system performance.
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20
Foot Board Operation Guide
CHAPERONEr BED EXIT WITH ZONE CONTROL (OPTIONAL EQUIPMENT)
For beds with a scale system:
NOTE
If the weigh system is in use, it will switch to ”off” when Bed Exit is armed.
1. Before putting the patient on the bed, the weigh system must be zeroed for the Bed Exit System to function properly (see page 25 for instructions on zeroing the weigh system).
2. Put the patient on the bed and push and release the ”ARM/DISARM” key (top light will come on).
3. The Bed Exit system with Zone Control will automatically select the first zone. To change the zone, push
and hold the “SELECT ZONE” key until the light indicating the desired zone comes on.
4. To deactivate Bed Exit, push the ”ARM/DISARM” key. The selected zone light and ”BED EXIT ON” lights
will turn off.
For beds without a scale system:
1. Before putting the patient on the bed, press and hold the ”ARM/DISARM” and the ”SELECT ZONE” keys
together for 5 seconds. The top light will begin to flash.
2. Release the ”ARM/DISARM” and the ”SELECT ZONE” keys and do not touch the bed until the top light
stops flashing.
3. Put the patient on the bed and push and release the ”ARM/DISARM” key (top light will come on).
4. The Bed Exit system with Zone Control will automatically select the first zone. To change the zone, push
and hold the “SELECT ZONE” key until the light indicating the desired zone comes on.
5. To deactivate Bed Exit, push the ”ARM/DISARM” key. The selected zone light and ”BED EXIT ON” light
will turn off.
WARNING
To avoid possible injury and to assure proper operation when using a powered mattress replacement system
such as XPRT, do not initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn−Assist active.
The patient motion and position resulting from a dynamic therapy mattress may adversely affect bed exit system performance.
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Foot Board Operation Guide
CHAPERONEr BED EXIT WITH ZONE CONTROL (CONTINUED)
CHAPERONEr ZONE SETTINGS
The first zone (top indicator light) is the traditional Bed Exit zone. The patient can move around the bed freely
but cannot fully exit the bed or the alarm will sound.
The second zone (middle indicator light) is more restrictive than the first zone. When the zone is selected,
the bed measures the location of the patient’s center of gravity. If the patient’s center of gravity moves from
the original location more than 6.5 inches to either side or 13 inches toward the head or foot, an alarm will
sound.
The third zone (bottom indicator light) is the most restrictive zone. When the zone is selected, the bed measures the location of the patient’s center of gravity. If the patient’s center of gravity moves from the original
location more than 1 inch to either side or 1 inch toward the head or foot, an alarm will sound.
NOTE
All zone dimensions are ± .5 inches.
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22
Scale System Operation Guide
SCALE SYSTEM CONTROL PANEL GUIDE
This panel is optional equipment.
1. LCD − displays patient weight. Trendelenburg angle is displayed when the scale is not active.
2. Press to zero bed (see page 25). Also press to scroll while Menu Mode is active.
3. Press to enter and exit the Menu Mode.
4. Press when adding or removing equipment to the bed (see page 26).
5. Press to turn scale system on and off. Also press to scroll while Menu Mode is active.
6. Press to change weight from pounds to kilograms or back (see page 27). Also press while using the Menu
Mode.
NOTE
If weight is displayed, SCALE ON/OFF must be pressed to turn off the scale before the Trend. or Fowler angle
will display.
CAUTION
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.
WARNING
To avoid possible injury and to assure proper operation when using a powered mattress replacement system
such as XPRT:
Confirm proper scale system operation following mattress installation. For best results, secure the mat-
tress power cord to prevent damage to the cord and 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.
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23
Scale System Operation Guide
SCALE SYSTEM CONTROL PANEL GUIDE (CONTINUED)
For more detailed operating instructions, see the following:
1. Preparing The Bed For Patient Stay/Zeroing the Bed − page 25
2. Activating the Scale System and Displaying Patient Weight − page 25
3. Adding or Removing Items During a Patient’s Stay − page 26
4. Converting the Patient’s Weight − page 27
5. Displaying the Weight Log − page 28
6. Viewing Patient Weight In Gain/Loss Mode − page 29
7. Changing the Numerical Value Of Displayed Weight − page 30
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24
Scale System Operation Guide
PREPARING THE BED FOR PATIENT STAY/ZEROING THE SCALE SYSTEM
NOTE
Do not zero the bed while a patient is in bed. If this should occur, remove the patient and zero the bed again.
If Bed Exit is armed, it must be disarmed before the scales can be zeroed.
Prepare the bed for the patient’s stay by adding/removing linens, pillows, etc.
Press and release The scale monitor will read:
“LET GO FOR SCALE”
“WEIGHING”
“XXX.X LB”
Press and hold The scale monitor will read:
“HOLD TO ZERO WT.”
“RELEASE TO ZERO”
Release The scale monitor will now read:
“DO NOT TOUCH BED”
“0.0 LB”
The bed is now ready for the patient.
NOTE
If there is a problem with a load cell or another component of the scale system, the system will try to zero
for 30 seconds, and the scale monitor will read:
“UNABLE TO ZERO”
“TRY AGAIN”
If the problem continues, after 3 attempts at zeroing, the scale system will lock and the scale monitor will read:
“Scale Sys. Error”
“Call for service”
Unplug the bed power cord from the wall socket and plug it back in. If the problem continues, call a service
technician.
ACTIVATING THE SCALE SYSTEM AND DISPLAYING PATIENT WEIGHT
Press and release The scale monitor will read:
“LET GO FOR SCALE”
“WEIGHING”
“XXX.X LB”
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25
Scale System Operation Guide
ADDING OR REMOVING ITEMS DURING A PATIENT’S STAY
If it is necessary to add or remove items (monitors, pumps, etc.) during the patient’s stay, press and re-
lease to activate the scale system. After the scale monitor reads: “XXX.X LB”, press and hold
The scale monitor will read:
“HOLD TO START”
“RELEASE TO START”
Release The scale monitor will read:
“DO NOT TOUCH BED”
“ADD/REMOVE EQUIP.”
Add or remove the equipment and press The scale monitor will read:
“RELEASE TO FIN.”
Release The scale monitor will read:
“DO NOT TOUCH BED”
“XXX.X LB”
The weight displayed will be that of the patient only.
If the CHANGE EQUIPMENT function is started but not finished, after approximately 45 seconds the
monitor will read:
“HIT CH. EQ. TO END”
Press The scale monitor will read:
“RELEASE TO FIN.”
Release The scale monitor will read:
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“DO NOT TOUCH BED”
“XXX.X LB”
26
Scale System Operation Guide
CONVERTING THE PATIENT’S WEIGHT
Press and release The scale monitor will read:
”WEIGHT NOW KGS”
”XXX.X KG”
Repeat the procedure to return to pounds. The display will read:
”WEIGHT NOW LBS”
”XXX.X LB”
If the unit of measurement has been locked, the display will read:
“UNITS ARE LOCKED”
A service technician must be called to unlock the unit of measurement.
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27
Scale System Operation Guide
DISPLAYING THE WEIGHT LOG
To display a list of the previous 10 weight readings, press to activate the scale system. The scale
monitor will read:
“LET GO FOR SCALE”
“XXX.X LB”
Press to enter the Menu Mode. The scale monitor will read:
“ FOR OPTIONS”
Press or to scroll through the menu options. The scale monitor will read:
“SHOW WEIGHT LOG”
“PUSH ENTER”
Press The scale monitor will read:
“ WEIGHT LOG”
Press or to scroll through the weight log. The scale monitor will read:
“1. 0.0 LB”
A weight reading is logged each time the button is pressed and the bed is in the scale mode for
at least 15 seconds.
The first weight reading displayed (1.) is the most recent. If the change in the patient’s weight since the
last reading was taken is less than .2 pounds, the log will not update. Zeroing the scale system clears
the weight log.
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28
Scale System Operation Guide
VIEWING PATIENT WEIGHT IN GAIN/LOSS MODE
To view the patient’s weight and to begin totaling the amount of weight the patient has gained or lost, press
to activate the scale system. The scale monitor will read:
“LET GO FOR SCALE”
Press to enter the Menu Mode. The scale monitor will read:
“ FOR OPTIONS”
Press or to scroll through the menu options. The scale monitor will read:
“START GAIN/LOSS”
“PUSH ENTER”
Press The scale monitor will read:
“DO NOT TOUCH BED”
“XXX.X LB G XX.X”
To exit Gain/Loss mode, press to enter the Menu Mode. The scale monitor will read:
“ FOR OPTIONS”
Press to to scroll through the menu options. The scale monitor will read:
“QUIT GAIN/LOSS”
“PUSH ENTER”
Press The scale monitor will read:
“XXX.X LB“
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29
Scale System Operation Guide
CHANGING THE NUMERICAL VALUE OF DISPLAYED WEIGHT
To decrease the numerical value of the displayed weight, press to activate the scale system.
The scale monitor will read:
“LET GO FOR SCALE”
“XXX.X LB”
Press to enter the Menu Mode. The scale monitor will read:
“ FOR OPTIONS”
Press or to scroll through the menu options. The scale monitor will read:
“CHNG. PTNT. WGT.”
“PUSH ENTER”
Press The scale monitor will read:
“HOLD TO INC.
TO DEC.”
Press to decrease the displayed weight or to increase the displayed weight.
Once the desired weight is displayed, press The scale monitor will read:
“XXX.X LB”
NOTE
If one of the load cells is malfunctioning or overloaded, the scale monitor will read:
“Scale Sys. Error”
“Call for service”
Call a service technician.
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30
Optional Pendant Operation
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31
Zoomr Option Operation Guide
DRIVE WHEEL OPERATION
1. Unplug the power cord from the wall socket and
secure the cord sufficiently to prevent entanglement while the unit is in motion. The drive wheel
will not operate if the power cord is plugged into the
wall socket.
2. Activate the power to the drive wheel by placing
the battery power switch located at the left side of
the head end of the litter in the “ON” position. The
LED will illuminate.
3. Engage the drive wheel by rotating the pedal located at the head end to the left as shown on the
label. To place the drive wheel in the neutral position, rotate the pedal to the right.
4. Release the brakes. The drive system will not
function while the brakes are engaged. The “Release Brakes” LED on the head end control panel
will be illuminated if the brakes are engaged while
the battery power switch is on.
WARNING
USE CAUTION while maneuvering the unit with the drive wheel activated. Always ensure there are no obstacles near the unit while the drive wheel is activated. Injury to the patient, user or bystanders or damage
to the unit or surrounding equipment could occur if the unit collides with an obstacle.
Use caution when transporting the unit down halls, through doors, in and out of elevators, etc. Damage to
the siderails or other parts of the unit could occur if the unit comes in contact with walls or door frames.
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32
Zoomr Option Operation Guide
DRIVE WHEEL OPERATION (CONTINUED)
5. Grasp the drive handle at the two raised grip areas. Squeeze either of the motion release switches (A)
located under the handle to enable the movement of the drive wheel. Either or both switches will enable
movement but both switches must be released to stop movement.
A
6. While continuing to squeeze the switch(es), push the handle away from you or pull the handle toward you
to initiate motion in that direction. The forward speed will increase proportionally to the distance the drive
handle is moved. I.E. the farther forward the drive handle is pushed, the faster the unit will move. To
stop motion, remove your hands from the switches and the handle.
NOTE
The drive wheel does not pivot. The unit cannot be moved directly sideways with the drive wheel engaged.
With the drive wheel pedal in the neutral position and the unit’s brakes released, the unit can be moved in
any direction including sideways.
Driving a Zoom−equipped unit over liquids or slick surfaces could decrease the traction of the drive wheel.
WARNING
Put the drive wheel in the neutral position and release the brakes before pushing the unit manually. Do not
attempt to push the unit manually with the drive wheel engaged. The unit will be difficult to push and injury
could result.
CAUTION
When attaching equipment to the frame, ensure it will not impede normal operation. For example: hooks on
hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, etc.
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33
Zoomr Option Operation Guide
HEAD END CONTROL PANEL OPERATION
UP
DOWN
7
ENGAGE DRIVE WHEEL
9
1. Press and hold to raise the litter.
2. Press and hold to lower the litter
3. Press to raise the Knee section.
4. Press to lower the Knee section.
1
2
3
KNEE BACK
4
8
PLUG BED IN TO CHARGE
5
6
RELEASE BRAKES
5. Press to raise the Back section.
6. Press to lower the Back section.
7. The “Engage Drive Wheel” LED will be illuminated whenever the battery power switch is on and the drive
wheel pedal is in the neutral position. The light will go off when the drive wheel is in the drive position.
8. The “Release Brakes” LED will be illuminated whenever the bed’s brakes are engaged while the battery
power switch is on. The light will go off when the brakes are disengaged.
9. The “Plug Bed In To Charge” LED will be illuminated while the battery power switch is on if the battery
level is low. Plug the bed power cord into the wall socket to charge the batteries.
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34
Zoomr Option Operation Guide
BATTERY CHARGING AND OPERATION
NOTE
The bed may be equipped with a battery back−up option without the Zoom drive wheel.
1. The unit has two 12 volt batteries to provide power to the drive wheel and back−up power to the unit func-
tions if the power cord is unplugged from the wall socket. Neither the unit functions nor the drive wheel
will operate properly if the batteries are not sufficiently charged. The batteries require approximately 10
hours of charging time when they are fully discharged.
2. The batteries are charging whenever the power cord is plugged into a properly grounded, hospital grade
wall socket. When the unit is stationary, the power cord should be plugged into a wall socket whenever
possible.
NOTE
The battery will operate under slightly decreased power until it has run through 10−15 cycles of usage and
recharging.
3. The “Plug Bed In To Charge” LED on the Head End Control Panel will be illuminated while the battery pow-
er switch is on if the battery level is low (see page 34). Plug the power cord into a wall socket to charge
the batteries.
4. After one hour on battery power with no motion release switch activation, the unit will enter power save
mode and none of the unit’s powered functions will operate. Squeeze either of the motion release switches
located under the drive handle to enable the unit functions.
NOTE
The three LED’s on the Head End Control Panel may still be illuminated when the unit is in power save mode.
The Battery Power LED located at the left side of the head end of the unit will be illuminated when the unit
is in power save mode.
WARNING
The power save mode is activated after one hour on battery power with no motion release switch activation.
Functions including Bed Exit, scale and motion will cease to operate when the unit enters the power save
mode. Injury to the patient could occur if proper patient monitoring protocol is not observed.
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35
Cleaning
Hand wash all surfaces of the bed with warm water and mild detergent. DRY THOROUGHLY. Do not steam
clean or hose off the Secure II Bed. Do not immerse any part of the bed. Some of the internal parts of the
bed are electric and may be damaged by exposure to water.
Suggested cleaners for bed surfaces:
Quaternary Cleaners (active ingredient − ammonium chloride)
Phenolic Cleaners (active ingredient − o−phenyl phenyl)
Chlorinated Bleach Solution (5.25% − less than 1 part bleach to 100 parts water)
Avoid over−saturation and ensure the product does not stay wet longer than the chemical manufacturer’s
guidelines for proper disinfecting.
CAUTION
SOME CLEANING PRODUCTS ARE CORROSIVE IN NATURE AND MAY CAUSE DAMAGE TO THE
PRODUCT IF USED IMPROPERLY. If the products described above are used to clean Stryker patient care
equipment, measures must be taken to insure the beds are wiped with clean water and thoroughly dried following cleaning. Failure to properly rinse and dry the beds will leave a corrosive residue on the surface of
the bed, possibly causing premature corrosion of critical components. Failure to follow the above directions
when using these types of cleaners may void this product’s warranty.
For mattress cleaning instructions, please see the tag on the mattress, or contact the mattress manufacturer.
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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36
Preventative Maintenance
CHECKLIST
All fasteners secure (reference all assembly prints)
Engage brake pedal and push on the bed to ensure all casters lock securely
”Brake Not Set” LED (on foot board) blinks when brakes are not engaged
Locking steer caster engages and disengages properly
Siderails move, latch and stow properly
CPR release working properly
Optional foot prop intact and working properly
I.V. pole working properly
Foley bag hooks intact
Optional CPR board not cracked or damaged and stores properly
No cracks or splits in head and foot boards
No rips or cracks in mattress cover
All functions on head end siderails working properly (including LED’s)
All functions on footboard working properly (including LED’s)
Scale and Bed Exit system calibrated properly
Motion Interrupt switches working properly
Night light working properly
Power cord not frayed
No cables worn or pinched
All electrical connections tight
All grounds secure to the frame
Ground impedance not more than 100 milliohms
Current leakage not more than 300 microamps
Apply grease to litter grease points
Engage drive wheel and ensure it is operating properly (Zoom option)
Motion release switches working properly (Zoom option)
Confirm Head End Control Panel functionality (Zoom option)
Confirm battery powered functionality (Zoom option)
Ensure ground chains are clean, intact, and have at least two links touching the floor.
Bed Serial No.
Completed By:_________________________________ Date:_____________
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37
Warranty
Limited Warranty:
Stryker Medical Division, a division of Stryker Corporation, warrants to the original purchaser that its products
should be free from defects in material and workmanship for a period of one (1) year after date of delivery.
Stryker’s obligation under this warranty is expressly limited to supplying replacement parts and labor for, or
replacing, at its option, any product which is, in the sole discretion of Stryker, found to be defective. Stryker
warrants to the original purchaser that the frame and welds on its beds will be free from structural defects
for as long as the original purchaser owns the bed. If requested by Stryker, products or parts for which a
warranty claim is made shall be returned prepaid to Stryker’s factory. Any improper use or any alteration or
repair by others in such manner as in Stryker’s judgement affects the product materially and adversely shall
void this warranty. Any repair of Stryker products using parts not provided or authorized by Stryker shall void
this warranty. No employee or representative of Stryker is authorized to change this warranty in any way.
Stryker Medical beds are designed for a 15 year expected life under normal use conditions and appropriate
periodic maintenance as described in the maintenance manual for each device.
This statement constitutes Stryker’s entire warranty with respect to the aforesaid equipment. STRYKER
MAKES NO OTHER WARRANTY OR REPRESENTATION, EITHER EXPRESSED OR IMPLIED, EXCEPT
AS SET FORTH HEREIN. THERE IS NO WARRANTY OF MERCHANTABILITY AND THERE ARE NO
WARRANTIES OF FITNESS FOR ANY PARTICULAR PURPOSE. IN NO EVENT SHALL STRYKER BE
LIABLE HEREUNDER FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES ARISING FROM OR IN ANY
MANNER RELATED TO SALES OR USE OF ANY SUCH EQUIPMENT.
To Obtain Parts and Service:
Stryker products are supported by a nationwide network of dedicated Stryker Field Service Representatives.
These representatives are factory trained, available locally, and carry a substantial spare parts inventory to
minimize repair time. Simply call your local representative, or call Stryker Customer Service at (800)
327−0770.
Service Contract Coverage:
Stryker has developed a comprehensive program of service contract options designed to keep your equipment operating at peak performance at the same time it eliminates unexpected costs. We recommend that
these programs be activated before the expiration of the new product warranty to eliminate the potential of
additional equipment upgrade charges.
A SERVICE CONTRACT HELPS TO:
Ensure equipment reliability
Stabilize maintenance budgets
Diminish downtime
Establish documentation for JCAHO
Increase product life
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Enhance trade−in value
Address risk management and safety
38
Warranty
Stryker offers the following service contract programs:
SPECIFICATIONS GOLD SILVER PM* ONLY
Annually scheduled preventative maintenance X X
All parts,** labor, and travel X X
Unlimited emergency service calls X X
Priority one contact; two hour phone response X X X
Most repairs will be completed within 3 business days X X
JCAHO documentation X X X
On−site log book w/ preventative maintenance & emergency service records X
Factory−trained Stryker Service Technicians X X X
Stryker authorized parts X X X
End of year summary X
Stryker will perform all service during regular business hours (9−5) X X X
* Replacement parts and labor for products under PM contract will be discounted.
** Does not include any disposable items, I.V. poles (except for Stryker HD permanent poles), mattresses, or damage re-
sulting from abuse.
Stryker Medical also offers personalized service contracts.
Pricing is determined by age, location, model and condition of product.
For more information on our service contracts,
please call your local representative or call (800) 327−0770 (option #2).
Return Authorization:
Merchandise cannot be returned without approval from the Stryker Customer Service Department. An authorization number will be provided which must be printed on the returned merchandise. Stryker reserves the
right to charge shipping and restocking fees on returned items.
SPECIAL, MODIFIED, OR DISCONTINUED ITEMS NOT SUBJECT TO RETURN.
Damaged Merchandise:
ICC Regulations require that claims for damaged merchandise must be made with the carrier within fifteen
(15) days of receipt of merchandise. DO NOT ACCEPT DAMAGED SHIPMENTS UNLESS SUCH DAMAGE
IS NOTED ON THE DELIVERY RECEIPT AT THE TIME OF RECEIPT. Upon prompt notification, Stryker
will file a freight claim with the appropriate carrier for damages incurred. Claim will be limited in amount to
the actual replacement cost. In the event that this information is not received by Stryker within the fifteen
(15) day period following the delivery of the merchandise, or the damage was not noted on the delivery receipt
at the time of receipt, the customer will be responsible for payment of the original invoice in full.
Claims for any short shipment must be made within thirty (30) days of invoice.
International Warranty Clause:
This warranty reflects U.S. domestic policy. Warranty outside the U.S. may vary by country. Please contact
your local Stryker Medical representative for additional information.
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39
European Representative
Stryker EMEA RA/QA Director
Stryker France
ZAC Satolas Green Pusignan
Av. De Satolas Green
69881 MEYZIEU Cedex
France
3800 E. Centre Ave., Portage, MI 49002
(800) 327−0770
www.stryker.com
JH 1/06 3002−209−001 REV D
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