Safe Working Load indicates the sum of the patient, mattress, and accessory weight
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.
Manufacturer
Do not store oxygen bottle
Do not push/pull
IPX6
Alternating Current
Direct 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.
Dangerous Voltage
Protective Earth Terminal
Protection from Liquid Jet
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Symbols and Definitions
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric
Shock, Fire, Mechanical and Other Specified Hazards Only in Accordance with UL
87VL
MEDICAL
ELECTR ICAL
EQUIPMENT
UL 60601-1
CAN/CSA C 22.2
N0. 601.1
*IEC 60601-
2-32:1994
WARNING/CAUTION/NOTE DEFINITION
The words WARNING, CAUTION and NOTE carry special meanings and should be carefully reviewed.
60601-1 First Edition (2003) and CAN/CSA C22.2 No. 601.1.
*For Prime-X Option, Associated Equipment of X-Ray Equipment IEC 60601-2-32:1994
Non-Ionizing Radiation
WARNING
Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CAUTION
Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the
user or patient or damage to the equipment or other property. This includes special care necessary for the safe and
effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or
misuse.
NOTE
Provides special information to make maintenance easier or important instructions clearer.
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Introduction
This manual is designed to assist you with the operation of Stryker Model 1115 Prime Series Stretcher. Read this
manual thoroughly before using the equipment or beginning maintenance on it. To ensure safe operation of this
equipment, it is recommended that methods and procedures be established for educating and training staff on the safe
operation of this stretcher.
PRODUCT DESCRIPTION
The Stryker Model 1115 Prime Series Stretcher with Big Wheel® decreases start-up force by 50 percent and steering
effort by 60 percent.
INTENDED USE OF PRODUCT
The Stryker Model 1115 Prime Series Stretcher is a wheeled device which consists of a platform mounted on a wheeled
frame that is designed to support patients in a horizontal position. The device has siderails and has the option available
to support the temporary or permanent placement of I.V. poles. A stretcher provides the caregiver a method of
transporting patients within a healthcare facility. The device has a two Big Wheels which reduces the required start-up
force to move the stretcher. Some stretchers may also be used for minor procedures and short-term stay (treatment
and recovery).
INTENDED USE OF PRODUCT - PRIME X OPTION
The Prime X option provides a platform for the short-term outpatient clinical evaluation and treatment of human patients
and additionally may be used for minor procedures and short-term outpatient stay (treatment and recovery). The Prime
X option provides an articulating radiographic patient support surface and a platform below the patient support surface
for X-Ray cassette placement to allow the capture of clinical X-Rays (AP Full Body, optional Full Body Lateral, and
optional Upright Chest) when used in conjunction with a medical X-Ray system. The Prime X option is a wheeled device
consisting of a platform mounted on a wheeled frame that is designed to transport patients in a horizontal position
within the interior of a healthcare facility by health professionals and/or trained representatives of the user facility. The
device has siderails and optional supports for fluid infusion equipment.
The Prime X option is intended to be used to transport patients to and from all departments within the interior of a
healthcare facility. The use of the Prime X option as a short-term outpatient clinical evaluation, treatment, minor
procedure, and short-term outpatient recovery platform may include use in, but not limited to, the Emergency Department
(ED), including the Trauma area, and Post-Anesthesia Care Unit (PACU). The Prime X option is not intended to be used
for long-term inpatient treatment and recovery. See the specification table in the operations manual of the device for
the intended environmental conditions.
The Prime X option has a safe working load up to 700 pounds (318 kg) and is intended to be used with all patients,
including those mildly to critically ill. The stretcher may also be used to transport deceased patients within an enclosed
healthcare facility.
The Prime X option has an optional scale system intended to measure and display weight in pounds or kilograms of
patients weighing 50 to 700 pounds (22.7 to 318 kg) and patients not exceeding the height of 75.25 inches (191 cm).
See the specification table for accuracy claims.
The Prime X option has an expected life of 10 years under normal use, conditions, and with appropriate periodic
maintenance as described in the maintenance manual for each device.
The Prime X option is not recommended for use with a Stryker Pioneer mattress or a mattress with a thickness
greater than four inches and is not compatible for use with a C-Arm. The Prime X option is intended for use in all
establishments other than home healthcare, domestic, and those directly connected to the public low voltage power
supply network that supplies buildings used for domestic purposes.
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IntroductionIntroduction
INTENDED USE OF PRODUCT - PRIME X OPTION (CONTINUED)
The Prime X option has the following options available: three-sided brake/steer pedal controls, three-sided and foursided hydraulic lift controls, powered lift controls, dual siderail latch assembly, slider board assembly, pump bar, I.V.
pole(s), restraint straps, defibrillator tray, defibrillator tray/foot extender, footboard/chartholder, serving tray, serving tray
holder/footboard, siderail pads, upright oxygen bottle holder, and I.V. caddy and may include other options as described
in the operations manual.
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SPECIFICATIONS
IntroductionIntroduction
26” Width30” Width Option
Safe Working Load
Note: Safe Working
Load indicates the sum
of the patient, mattress,
34” (± 1”)86.4 cm 38” (± 1”)96.5 cm38” (± 1”)96.5 cm
30.25”
(± .5”)
20.75” /
34” (± 1”)
+17°/-17° (± 3 °)
2.5”
nominal
1.75”
under the
hydraulic
jacks and
fifth wheel
1” under
the Big
Wheel
Not applicable
76.8 cm
52.7 cm /
86.4 cm
6.4 cm
4.5 cm
2.5 cm
30.5”
(± .5”)
20.75” /
34” (± 1”)
2.5”
nominal
1.75”
under the
hydraulic
jacks and
fifth wheel
1” under
the Big
Wheel
77.5 cm
52.7 cm /
86.4 cm
6.4 cm
4.5 cm
2.5 cm
Prime X Option
30” Width
30.5”
(± .5”)
23.25” /
36.5” (± 1”)
2.5”
nominal
1.75”
under the
hydraulic
jacks and
fifth wheel
1” under
the Big
Wheel
Maximum Value
Allowed is 1.7 mm Al
77.5 cm
59.1 cm /
92.7 cm
6.4 cm
4.5 cm
2.5 cm
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IntroductionIntroduction
SPECIFICATIONS (CONTINUED)
Electric OptionsOptional Electric LitterOptional Electric Lift
Electrical Requirements
Duty Cycle
Optional Scale System Non-Electric LitterOptional Electric Lift
Bat tery Type
Battery Voltage
Optional Scale SystemOptional Electric LitterOptional Electric Lift
Bat tery Type
Battery Voltage
Optional Scale System with
Chaperone (Stretcher Exit)
Bat tery Type
Battery Voltage
120V~, 60Hz, 10 A120V~, 60Hz, 10 A
Continuous operation with intermittent loading is 1
min ON/20 min OFF
4 x AA Battery (4 X 1.5V ) Alkaline Type (LR6)
6.0V6.0V
1 x Rechargeable Lithium Ion
Battery Pack (0058-135-000)
10.8V , 2.4Ah
Optional Electric LitterOptional Electric Lift
1 x Rechargeable Lithium Ion
Battery Pack (0058-134-000)
10.8V , 4.8Ah
Continuous operation
with intermittent loading
is 1 min ON/20 min OFF
4 x AA Battery (4 X 1.5V
) Alkaline Type (LR6)
Not applicable
Not applicable
Not applicable
Not applicable
Stryker reserves the right to change specifications without notice.
Note: Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or
nitrous oxide.
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SPECIFICATIONS (CONTINUED)
Environmental ConditionsOperationStorage and Transportation
IntroductionIntroduction
Temperature
0
50 F
0
(10 C)
0
100 F
0
(38 C)
75%
0
-4 F
0
(-20 C)
140 F
0
(60 C)
95%
0
Relative Humidity
30%
106 0 h Pa
10%
106 0 h Pa
Atmospheric Pressure
700 hPa
500 hPa
Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.
SPECIFICATIONS - OPTIONAL SCALE SYSTEM (NON-ELECTRIC LITTER/ELECTRIC LITTER OPTION)
Optional Scale System Weight Operating Range50 lb (22.7 kg) to 700 lb (318 kg)
Optional Scale System Accuracy
±3 lb (1.3 kg) for weights less than 100 lb (45 kg) and ±3% for
weights greater than or equal to 100 lb (45 kg) *
Environmental ConditionsOperationStorage and Transportation
Temperature
0
61 F
0
(16 C)
0
79 F
0
(26 C)
75%
0
-4 F
0
(-20 C)
0
140 F
0
(60 C)
95%
Relative Humidity
30%
106 0 h Pa
10%
106 0 h Pa
Atmospheric Pressure
700 hPa
500 hPa
* To meet this accuracy claim, the patient surface must be in the flat position (fowler and gatch down) and the
stretcher cannot exceed 5 degrees of Trendelenburg/reverse Trendelenburg.
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IntroductionIntroduction
PRODUCT ILLUSTRATION - ELECTRIC LITTER OPTION
Optional
Pop Up Push
Handle
Siderail
Push Pedal
Uni-Lower
Pedal
Brake/Steer
Control Pedal
Option
Integrated
Bumpers
Casters with
Integrated
Wheel Covers
Optional Siderail
Patient Controls
Gatch Release
Brake/Steer
Control Pedal
Optional
Handle
Siderail
Release
Siderail
Optional Patient
Control Lockout
Optional
Scale
System
Optional
Pump Rack
Optional Foot
End Nursing
Controls
Figure 1: Electric Litter Option
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IntroductionIntroduction
PRODUCT ILLUSTRATION - PRIME X OPTION
Optional
Pop Up Push
Handle
Cassette Tray
Patient
Surface with
Clear View
Technology
Pump Pedal
Uni-Lower
Pedal
Control Pedal
Brake/Steer
Option
Casters with
Integrated
Wheel Covers
Figure 2: Prime X Option
Integrated
Bumpers
Siderail
Release
Siderail
Brake/Steer
Control Pedal
Optional
Scale System
Optional
Pump Rack
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Introduction
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at: (800) 327-0770 or (269) 324-6500.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
Please have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical
Support. Include the serial number in all written communication.
SERIAL NUMBER LOCATION
A
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Figure 3: Serial Number Loction
Summary of Safety Precautions
Carefully read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
See the maintenance manual for additional information.
WARNING
• This stretcher 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.
• Always apply the brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure that the
brakes are securely locked. Always engage the brakes unless the stretcher is being moved. Injury could result if
the stretcher moves while a patient is getting on or off the stretcher.
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height
in a raised position could increase the chance of patient falls and injury.
• Make sure that the brakes are completely released before attempting to move the unit. Attempting to move the unit
with the brakes engaged could result in injury to the user and/or patient.
• After raising the siderails, pull firmly on the siderail to ensure that it is securely locked into the up position. Siderails
are not intended to serve as a patient restraint device to keep patients from exiting the unit. Siderails are intended
to keep a patient from inadvertently rolling off the unit. It is the responsibility of the attending medical personnel
to determine the degree of restraint necessary to ensure that a patient will remain in place. Failure to utilize the
siderails properly could result in patient injury.
• When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the siderail
spindles or injury could occur.
• Powered stretcher mechanisms can cause serious injury. Operate stretcher only with persons clear of mechanisms.
• Operation of the fowler is a manual procedure. Use caution when raising the fowler while a patient is on the
stretcher. Use proper lifting techniques and get additional assistance, if necessary. Failure to use proper lifting
techniques could cause injury to the operator.
• Keep hands/fingers clear of the area around the fowler release handle and the fowler frame when lowering the
fowler. Injury could result if care is not taken when lowering the fowler.
• To avoid the risk of injury, ensure that the gatch prop rod is fully raised and securely placed into position.
• Use caution when operating the gatch while a patient is on the stretcher. Powered stretcher mechanisms can
cause serious injury. Operate stretcher only with persons clear of mechanisms.
• Use caution when operating the recovery chair while a patient is on the stretcher. Powered stretcher mechanisms
can cause serious injury. Operate stretcher only with persons clear of mechanisms.
• To avoid patient injury or equipment damage, all lines from any equipment stored on the pump rack must be
diverted away from the gatch handles.
• To avoid patient injury or equipment damage, do not lift the stretcher by the pump rack.
• To avoid equipment damage, remove any equipment from the pump rack that may be in the way before lowering
the litter.
• To avoid equipment damage while transporting the stretcher, verify that any equipment on the pump rack can
safely pass through door openings and under light fixtures.
• When using the Prime X option in conjunction with devices that generate X-radiation, the generating devices may
produce residual, stray, and/or scattered radiation. Users should refer to local, state, and federal use guidelines
as well as appropriate facility protocols for safety before use. Special attention should be given when performing
X-Rays with the stretcher’s fowler in the upright position and also when performing X-Rays using a lateral cassette.
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Summary of Safety Precautions
WARNING (CONTINUED)
• The Prime X option is not recommended for use with a Stryker Pioneer mattress or a mattress with a thickness
greater than four inches and is not compatible for use with a C-Arm.
• To avoid the risk of injury to the patient or user or damage to the I.V. pole while transporting the stretcher, make
sure that the I.V. caddy is securely tightened on the I.V. pole.
• To avoid the risk of patient injury or equipment damage, do not sit on the foot support.
• Physical restraints, even if properly secured, may result in serious harm to patients and caregivers. The use of
restraint straps may potentially cause entanglement, entrapment, physical injury, and/or death. Caution must be
used in affixing restraint straps to avoid potential injury to both patients and caregivers.
• Restraint straps and/or devices must be attached only at the identified attachment points of the unit. Failure to do
so may result in patient or caregiver injury. Do not attach restraints straps to the siderail.
• This unit accommodates the use of ankle, chest, wrist, and body restraints. The use of restraint straps is regulated
by state and federal restrictions. Users, caregivers, and/or practitioners should refer to the applicable state and
federal restrictions and the appropriate facility protocols before using any restraint strap and/or device.
• If your unit is equipped with the optional electric lift/litter, unplug the power cord from the power outlet before
transporting or cleaning the unit. To unplug, grasp the mold near the outlet and pull the cord in a direction parallel
to the floor (not at an angle).
• This device does not offer any protection against X-Ray radiation.
• Do not steam clean the unit.
• Medical electrical equipment (such as the optional scale system or optional electric lift/litter) requires special
precautions regarding EMC and needs to be installed and put into service according to the EMC information
provided on page 64 to prevent equipment malfunction.
• Portable and mobile RF communication equipment can affect Medical Electrical Equipment (such as the optional
scale system or optional electric lift/litter).
• To avoid malfunction, the optional scale system or optional electric lift/litter should not be used adjacent to or
stacked with other equipment. If adjacent or stacked use is necessary, the optional scale system or optional
electric lift/litter should be observed to verify normal operation in the configuration in which it will be used.
• When using any mattress thicker than 2.5 inches or when using a mattress overlay with the Prime X option, extra
caution and operator supervision is recommended to reduce the risk of patient falls due to lesser siderail coverage.
CAUTION
• This stretcher is not intended for pediatric use or for patients under 50 lb. This stretcher is intended for use by
trained hospital personnel only.
• Do not modify this stretcher. Modifying the unit can cause unpredictable operation resulting in injury to the patient
or operator. Modifying the unit will also void its warranty.
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
• To avoid injury or damage to the equipment, do not allow the siderail to lower on its own.
• The weight capacity of the gatch is 200 lb. Do not sit or stand on the gatch. Injury or damage to the equipment
could occur.
• To achieve recovery chair position, your stretcher must be equipped with the lift assist backrest and gatch options.
• The weight capacity of the base hood is 60 lb. Do not sit or stand on the base hood. Injury or damage to the
equipment could occur.
• Do not step on the base hood.
• Do not engage the steer pedal when the Big Wheel is resting on a threshold or other raised area. The force
required to engage the Big Wheel will be higher than normal, possibly causing damage.
• Do not use the cutout for the oxygen bottle holder on the base hood for the storage of oxygen bottles or patient
belongings.
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Summary of Safety Precautions
CAUTION (CONTINUED)
• The weight capacity of the pump rack is 40 lb.
• Do not use the pump rack as a push/pull device, because equipment damage could occur.
• To avoid damage, do not put items weighing more than 30 lb on the defibrillator tray.
• To avoid risk of patient or operator injury, ensure that all devices placed on the defibrillator tray are securely
strapped to the tray.
• Do not use the defibrillator tray as a push/pull device, because equipment damage could occur.
• If the stretcher is equipped with the optional foot end I.V. pole, the I.V. pole must be in the raised position when the
foot extension/defibrillator tray is installed. If the I.V. pole is not raised, the foot extension will not function properly
and injury could occur.
• The push handles were designed for use while transporting the stretcher. Avoid using other parts of the stretcher
as push/pull devices because damage could occur.
• To avoid damage, do not put items weighing more than 30 lb on the foot extender/defibrillator tray.
• Do not use the foot extension/defibrillator tray as a push/pull device, because equipment damage could occur.
• Do not use the footboard/chartholder as a push/pull device because equipment damage could occur.
• Always store the I.V. caddy when not in use to avoid damaging it when the unit is moved.
• To avoid the risk of equipment damage, do not use the foot support to store patient belongings or other items.
• To avoid injury to the operator, ensure that the operator’s fingers are clear of the mechanism when positioning the
foot support.
• Foot supports should be in the stored position when moving. The stretcher should be in brake position when foot
supports are in use.
• To avoid the risk of damage to the equipment, do not use the foot support as a push/pull device.
• To avoid injury to the patient or operator, ensure foot supports are tightened securely prior to use.
• If the stretcher is equipped with the scale system option, the scale should not be utilized while the foot supports
are in use because inaccurate readings may occur.
• If the stretcher is equipped with the chaperone option, the chaperone option should not be utilized while the foot
supports are in use because false readings may occur.
• To avoid damage to the removable I.V. pole, the weight of the I.V. bags should not exceed 40 lb.
• To avoid damage, the safe working load of the two-stage permanently attached I.V. pole is 40 lb.
• To avoid damage while transporting the stretcher, verify that the I.V. pole is at a low enough height to allow it to
safely pass through door openings and under light fixtures.
• Do not use the I.V. pole as a push/pull device because equipment damage could occur.
• To avoid damage, the weight of the I.V. bags should not exceed 12 lb while the weight of any one item attached to
each stage of the three-stage permanently attached I.V. pole should not exceed 9.3 lb.
• To avoid damage, do not put items weighing more than 40 lb in the upright oxygen bottle holder.
• Do not use the upright oxygen bottle holder as a push/pull device because equipment damage could occur.
• To avoid damage, do not put items weighing more than 30 lb on the serving tray.
• To avoid risk of user injury or damage to the equipment, ensure that the Upright X-Ray Cassette Holder is installed
correctly, following the instructions below.
• To avoid risk of user injury or damage to the equipment, ensure that the Lateral X-Ray Cassette Holder is installed
correctly, following the instructions below.
• Do not use the serving tray holder/footboard as a push/pull device because equipment damage could occur.
• Before returning the unit to service after cleaning, ensure that the unit is functioning properly by verifying that all
labels are intact, raise/lower the stretcher height, brake/steer pedal locks properly in both positions, latch/unlatch
the siderails, and raise/lower the fowler and gatch.
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Summary of Safety Precautions
• Some cleaning products are corrosive in nature and may cause damage to the product if used improperly. If the
products suggested above are used to clean Stryker patient handling equipment, measures must be taken to ensure
that the stretcher is wiped with a damp cloth soaked in clean water and thoroughly dried following cleaning. Failure
to properly rinse and dry the stretcher will leave a corrosive residue on the surface of the stretcher, possibly causing
premature corrosion of critical components. Failure to follow the directions provided in the Cleaning section of this
manual (page 60) when using these types of cleaners may void this product’s warranty.
NOTE
• Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous
oxide.
• The bottom of the brake pads should be cleaned regularly to prevent wax or floor remnant buildup.
• Clean the base hood storage area regularly.
• In lieu of specific requirments from IEC 60601-1 and IEC 60601-2-32:1994, equivalent means of safety were used
on the Prime-X series of products regarding accessory overloading, applied parts, and indications to the operator.
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Summary of Safety Precautions
PINCH POINTS - PRIME X OPTION
Figure 4: Pinch Points - Prime X Option
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Setup Procedures
If this unit is equipped with the optional electric lift/litter, the unit must reach room temperature prior to conducting
any setup and/or unit operations to prevent permanent damage to the unit.
Make sure that the unit is working properly before it is put into service. The following list will ensure that each part of
the unit is checked.
Stretcher checklist:
1. Depress the pedal at either end of the stretcher fully to set the four wheel brakes and verify that all of the four
casters are locked (page 21).
2. Raise and lower the hydraulic lift system (page 22 or page 23).
3. Raise the unit completely and activate the Trendelenburg function. Ensure that the head end lowers to the full
down position (page 25).
4. Raise the unit completely and activate the reverse Trendelenburg function. Ensure the foot end lowers to the full
down position (page 25).
5. Run through the operation of the Big Wheel to ensure that it is operating properly (page 26).
6. Ensure that the siderails raise and lower smoothly and lock securely in the full up position (page 27).
7. Raise and lower the fowler (head end) (page 31).
8. Raise and lower the gatch (foot end) (page 33).
If equipped with the optional electric lift/litter:
1. Check all items on the stretcher checklist above.
2. Plug the unit into a properly grounded, hospital grade wall receptacle and ensure that the LED lights illuminate on
the lockout keypad.
3. Raise and lower the hydraulic lift system (page 24).
4. Perform each function on the patient siderail controls to ensure that they are working properly (page 28).
5. Perform each function on the foot end nursing controls to ensure that they are working properly (page 29).
6. Raise and lower the fowler (head end) (page 32).
7. Raise and lower the gatch (foot end) (page 34).
If equipped with the optional scale - electric litter option (with or without chaperone option):
1. Check all items on the stretcher checklist above.
2. Plug the power cord into a properly grounded, hospital grade wall receptacle to charge the batteries.
Note: To charge the battery, see “Charging the Optional Scale System Battery Pack - Electric Litter Option (Not
Available With Prime X Option)” on page 43or “Charging the Optional Scale System Battery Pack - Electric
Litter Option with Chaperone (Not Available With Prime X Option)” on page 45.
WARNING
This stretcher 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.
CAUTION
• Do not modify this stretcher. Modifying the unit can cause unpredictable operation resulting in injury to the patient
or operator. Modifying the unit will also void its warranty.
• This stretcher is not intended for pediatric use or for patients under 50 lb. This stretcher is intended for use by
trained hospital personnel only.
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Operation Guide
APPLYING THE BRAKE SYSTEM
For user convenience, a brake/steer control pedal is located on both ends of the stretcher as shown in Figure 5.
WARNING
Always apply the brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure that the brakes
are securely locked. Always engage the brakes unless the stretcher is being moved. Injury could result if the stretcher
moves while a patient is getting on or off the stretcher.
To e ngage the brakes on the head end, push down on the brake (red) side of pedal (A).
To engage the brakes on the foot end, push down on the brake (red) side of pedal (B).
To release the brakes on the head end, push down on the steer (green) side of pedal (A).
To release the brakes on the foot end, push down on the steer (green) side of pedal (B).
Note: Your stretcher may be equipped with optional side control brake and steer functions (C) in addition to the
standard head end (A) and foot end (B) controls. The side control brakes operate the same as the head end and foot
end brakes.
B
C
C
Figure 5: Brake System
Note: The bottom of the brake pads should be cleaned regularly to prevent wax or floor remnant buildup.
A
Head End
A
B
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Steer/Brake functions (head end)
Brake/Steer functions (foot end)
Figure 6: Steer/Brake Functions
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Operation Guide
OPERATING THE BASE CONTROLS - SIDE CONTROL HYDRAULICS
To operate the base controls, see Figure 7 to locate which pedals are used for what operation.
CAUTION
To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
To raise the litter height, pump pedal (A) repeatedly until the desired height is achieved.
To lower both ends of the litter together, depress the center of pedal (B).
To lower only the head end of the litter, depress the side of pedal (B) closest to the head end of the stretcher.
To lower only the foot end of the litter, depress the side of pedal (B) closest to the foot end of the stretcher.
WARNING
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height in
a raised position could increase the chance of patient falls and injury.
BA
B
Figure 7: Stretcher Base Controls - Side Control
A
Head End
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221115 -10 9 - 0 01 R EV Dwww.stryker.com
A
B
Figure 8: Side Base Control Label
Operation Guide
OPERATING THE BASE CONTROLS - OPTIONAL THREE-SIDED AND FOUR-SIDED CONTROL
HYDRAULICS
To operate the base controls, see Figure 9 to locate which pedals are used for what operation.
CAUTION
To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
To raise the litter height, pump pedal (A) repeatedly until the desired height is achieved.
To lower both ends of the litter together, depress pedal (B) and pedal (D) together using the same foot or depress in
the center of pedal (C).
To lower the foot end of the litter, depress pedal (B) or the side of pedal (C) closest to the foot end.
To lower the head end of the litter, depress pedal (D) or the side of pedal (C) closest to the head end.
WARNING
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height in
a raised position could increase the chance of patient falls and injury.
B
D
A
C
C
Figure 9: Stretcher Base Controls - Optional Three-Sided and Four-Sided Control
A
A
A
A
C
C
A
B
D
Head End
kg
Figure 10 : Side Base Three-Sided or Four-Sided Control Label
www.stryker.com1115 -10 9 - 0 01 R EV D23
Figure 11:
Label A
B
D
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Operation Guide
RAISING AND LOWERING THE LITTER HEIGHT - OPTIONAL ELECTRIC LIFT
Ensure that the power cord is plugged into a properly grounded, hospital grade wall outlet before using the optional
electric lift.
CAUTION
To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
To raise the litter height electrically, depress pedal (A) (see Figure 7 on page 22 or Figure 9 on page 23). The
litter will begin to raise. Hold the pedal down until the desired litter height is achieved. Release the pedal at any time
to stop the litter motion.
To lower the litter height manually, see the “Operating the Base Controls - Side Control Hydraulics” information on
page 22 or “Operating the Base Controls - Optional Three-Sided or Four-Sided Hydraulic Controls information” on
page 23. The litter height does not lower electrically.
WARNING
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height in
a raised position could increase the chance of patient falls and injury.
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241115 -10 9 - 0 01 R EV Dwww.stryker.com
Operation Guide
ADJUSTING TRENDELENBURG/REVERSE TRENDELENBURG POSITIONS - SIDE CONTROL
HYDRAULICS
Litter height must first be raised in order to achieve a Trendelenburg or reverse Trendelenburg position.
CAUTION
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
For Trendelenburg positioning (head down), depress the side of pedal (B) closest to the head end (see Figure 7 on
page 22).
For reverse Trendelenburg positioning (foot down), depress the side of pedal (B) closest to the foot end (see Figure
7 on page 22).
To lower the stretcher from reverse Trendelenburg position, depress pedal (A) once to raise the foot end of the
stretcher, and then depress pedal (B) (see Figure 7 on page 22).
Note: The higher the litter is before pedal (B) is activated, the greater the Trendelenburg or reverse Trendelenburg
angle will be. (Maximum Trendelenburg angle is +17°. Maximum reverse Trendelenburg angle is -17°.)
ADJUSTING TRENDELENBURG/REVERSE TRENDELENBURG POSITIONS - OPTIONAL THREE-SIDED
OR FOUR-SIDED CONTROL HYDRAULICS
Litter height must first be raised in order to achieve a Trendelenburg or reverse Trendelenburg position.
CAUTION
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
For Trendelenburg positioning (head down) (see Figure 8 on page 23):
• Depress pedal (D) at the foot end of the unit or
• Depress the side of pedal (C), located on the patient left or patient right side, closest to the head end of the unit.
For reverse Trendelenburg positioning (foot down) (see Figure 8 on page 23):
• Depress pedal (B) at the foot end of the unit or
• Depress the side of pedal (C), located on the patient left or patient right side, closest to the foot end of the unit.
To lower the stretcher from reverse Trendelenburg position, depress pedal (A) once to raise the foot end of the
stretcher, and then depress pedal (C) or (D) (see Figure 8 on page 23).
Note: The higher the litter is before pedal (B), (C), or (D) is activated, the greater the Trendelenburg or reverse
Trendelenburg angle will be. (Maximum Trendelenburg angle is +17°. Maximum reverse Trendelenburg angle is -17°.)
www.stryker.com1115 -10 9 - 0 01 R EV D25
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Operation Guide
OPERATING THE BIG WHEEL®
WARNING
• Make sure that the brakes are completely released before attempting to move the unit. Attempting to move the unit
with the brakes engaged could result in injury to the user and/or patient.
• If your unit is equipped with the optional electric lift/litter, unplug the power cord from the power outlet before
transporting or cleaning the unit. To unplug, grasp the mold near the outlet and pull the cord in a direction parallel
to the floor (not at an angle).
When the brake/steer pedal (A) is in the neutral or brake position, the Big Wheel (B) is elevated approximately 3/4”
and the stretcher rests on the four casters as shown in Figure 12. See page 21 for pedal operations.
A
B
Steer/Brake Label
Figure 12: Neutral or Brake Position
Note: The two Big Wheels (B) do not pivot. The stretcher cannot be moved directly sideways with the Big Wheel (B)
activated.
With the pedal (A) in the neutral position, the stretcher can be moved in any direction including sideways as shown
in Figure 12. See page 21 for pedal operations.
When the brake/steer pedal (A) is in the steer position, the foot end casters are elevated approximately 1/4” and the
stretcher rests on the two head end casters and the two Big Wheels (B) as shown in Figure 13. This provides increased
mobility and ease of steering the stretcher. See page 21 for pedal operations.
A
B
CAUTION
Do not engage the steer pedal when the Big Wheel is resting on a threshold or other raised area. The force required to
engage the Big Wheel will be higher than normal, possibly causing damage.
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261115 -10 9 - 0 01 R EV Dwww.stryker.com
Steer/Brake Label
Figure 13: Steer Position
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