Stryker M Series User manual

2006/xx XXXX-XXX-XXX REV X www.stryker.com
For Parts or Technical Assistance:
USA: 1-800-327-0770 (option 2)
Canada: 1-888-233-6888
Mode d’emploi
Bedienungsanleitung
Manuale d’uso
Bedieningshandleiding
M-Series Stretcher Model 1025 (SM304)
Chariot série M Modèle 1025 (SM304)
Stretcher der M-Serie Modell 1025 (SM304)
Barella serie M Modello 1025 (SM304)
M-reeks verpleegbed Model 1025 (SM304)
2009/02 1025-009-005 REV B www.stryker.com
Operations Manual
For Parts or Technical Assistance:
USA: 1-800-327-0770 (option 2)
Assistance technique et pièces de rechange:
États-Unis : 1-800-327-0770 (option 2)
Für Ersatzteile oder technische Hilfe:
USA: 1-800-327-0770 (Option 2)
Per parti o assistenza tecnica: USA:
1-800-327-0770 (opzione 2)
Voor onderdelen of technische bijstand:
VS: 1-800-327-0770 (optie 2)

EASTERN EUROPE
Stryker SA - Export Business
Grand-Rue 90
P.O. Box 1567
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
AUSTRIA
Stryker-Howmedica Osterreich GmbH
Millenium Tower
Handelskai 94-96
120 Wien
Austria
Phone: [phone]
Fax: [phone]
BELGIUM
NV Stryker SA
Ikaros Business Park- Fase III
Ikaroslaan 12
1930 Zaventem, Brussels
Belgium
Phone: [phone]
Fax: [phone]
DENMARK
Stryker Denmark
Filial of Stryker AB
Postbox 772
1532 Copenhagen
Denmark
Phone: [phone]
Fax: [phone]
ENGLAND
Stryker UK Limited
Stryker House
Hambridge Road
Newbury, Berkshire
RG14 5EG, England
Phone: [phone]
Phone: [phone]
Fax: [phone]
POLAND
Stryker Polska Sp. ZO.O
Kolejowa 5/7
01-217 Warsawa
Poland
Phone: [phone]
Fax: [phone]
PORTUGAL
Stryker Portugal Produtos
Medicos, LTDA.
Avenida Marechal Gomes
da Costa, 35
1800-255 Lisboa
Portugal
Phone: [phone]
Fax: [phone]
ROMANIA
Stryker Osteonics Romania S.R.L.
19, Leonida Str.
District 2
7000 Bucharest
Romania
Phone: [phone]
Fax: [phone]
SOUTH AFRICA
Stryker Osteonis PTY. LTD.
3 Susan Street
Strydom Park
Johannesburg, 2194 - South Africa
Mailing Address:
P.O. Box 48039
2129 Roosevelt Park
Johannesburg, South Africa
Phone: [phone]
Fax: [phone]
SPAIN
Stryker Howmedica Iberica S.L.U.
Manual Tovar, 35
28034 Madrid
Spain
Phone: [phone]
Phone: [phone]
Fax: [phone]
SWEDEN
Stryker AB/Scandinavia
Box 50425
SE-204 14 Malmo
Sweden
Phone: [phone]
Fax: [phone]
FINLAND
Stryker AB, Finland
PO 80 Makelankatu 2
00501 Helsinki
Finland
Phone: [phone]
Fax: [phone]
FRANCE
Stryker France SA
ZAC - Avenue de Satolas Green
69330 Pusignan
France
Phone: [phone]
Fax: [phone]
GERMANY
Stryker Howmedica GmbH
Dr. Homer Stryker Platz 1
47228 Duisburg
Germany
Phone: [phone]
Fax: [phone]
GREECE
Stryker Hellas EPE
455 Messogion ave
153 43 Agia Paraskevi
Athens, Greece
Phone: [phone]
Fax: [phone]
ITALY
Stryker Italia SrL
Via Ghisalba 15B
00188 Roma
Italy
Phone: [phone]
Fax: [phone]
MIDDLE EAST / NORTH AFRICA
Stryker Osteonics SA
Twin Towers
11th Floor, Suite 1101 & 1102
P.O. Box 41446
Baniyas Road
Dubai, Deira, UAE
Phone: [phone]
Fax: [phone]
NEDERLANDS
Stryker Nederlands BV
(P.O. Box 13, 4180 BA Waardenburg)
4181 CD Waardenburg
The Nederlands
Phone: [phone]
Fax: [phone]
NORWAY
Stryker Norway
Norsk Fillial
Nedre Vollgate 3
0158 Oslo
Norway
Phone: [phone]
Fax: [phone]
EUROPE HEADQUARTERS
Stryker SA
Cite-Centre, Grand-Rue 90
P.O. Box 1568
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
International Addresses
1025-009-005 REV B www.stryker.com

Table of Contents
Introduction..............................................................................1-3
IntendedUse.........................................................................1-3
ProductDescription ....................................................................1-3
Specifications ........................................................................1-3
Specifications(OptionalScaleSystem)......................................................1-5
Warning/Caution/NoteDefinition.........................................................1-6
Symbols................................................................................1-7
SummaryofSafetyPrecautions...............................................................1-8
SetupProcedures........................................................................1-10
StretcherOperation.......................................................................1-11
OperatingtheBaseControls.............................................................1-11
RaisingandLoweringtheLitterHeight......................................................1-12
Adjusting Trendelenburg / Reverse Trendelenburg Positions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-12
ApplyingtheBrakeSystem..............................................................1-13
BatteryChargingandOperation..........................................................1-13
TransportingtheStretcherUsingtheDriveWheel .............................................1-14
OperatingtheGlideaway™Siderails .......................................................1-16
OperatingthePneumaticFowler..........................................................1-17
OperatingtheOptionalKneeGatch........................................................1-18
Operating the Optional 2-Stage Permanently Attached I.V. Pole. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-19
Operating the Optional 3-Stage Permanently Attached I.V. Pole. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-20
Operating the Optional Foot Extension/Defibrillator Tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-21
OperatingtheOptionalServingTray .......................................................1-22
OperatingtheOptionalScaleSystem ......................................................1-23
UsingtheOptionalScaleSystemBatteries ..................................................1-24
Cleaning...............................................................................1-25
RecommendedCleaningMethod..........................................................1-25
RecommendedDisinfectants.............................................................1-25
RinseOffCorrosiveCleaners............................................................1-25
SpecialInstructions ...................................................................1-26
RemovalofIodineStains ...............................................................1-26
PreventativeMaintenance..................................................................1-27
Checklist...........................................................................1-27
Warranty...............................................................................1-29
LimitedWarranty .....................................................................1-29
ToObtainPartsandService.............................................................1-29
ServiceContractCoverage..............................................................1-29
ServiceContractPrograms..............................................................1-30
ReturnAuthorization...................................................................1-30
DamagedMerchandise.................................................................1-30
InternationalWarrantyClause............................................................1-30
RecyclingPassport.......................................................................1-31
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Introduction
Return To Table of Contents
INTENDED USE
This manual is designed to assist you with the maintenance of Stryker Model 1025 M-Series Stretcher with ZOOM®.
Carefully 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 1025 M-Series Stretcher with ZOOM® product is a general purpose patient transport and treatment
stretcher.
SPECIFICATIONS
Safe Working Load
Note: Safe Working Load
indicates the sum of the patient,
mattress, and accessory weight.
700 pounds 318 kg
Weight of Product
26” Stretcher 415 lbs (standard configuration)
465 lbs (all options/accessories)
188 kg
211 kg
30” Stretcher 435 lbs (standard configuration)
485 lbs (all options/accessories)
197 kg
220 kg
Overall Stretcher Length 85” (± .5”) 215.9 cm (± 1.27 cm)
Overall Stretcher Width (Siderails Up) 34.5” & 37” (± .5”) 87.6 cm & 93.98 cm (± 1.27 cm)
Overall Stretcher Width (Siderails Down) 26.5” & 30.75” (± .5”) 67.3 cm & 78.11 cm (± 1.27 cm)
Minimum / Maximum Stretcher Height 23” / 34” (± .5”) 58 cm / 86 cm (± 1.27 cm)
Fowler Angle 0° to 90° (± 3°)
Knee Gatch Angle 0° to 40° (± 1°)
Trendelenburg / Reverse Trendelenburg +15° to -15°
Electrical 115 VAC, 60 Hz, 3.0 Amp
Optional: 230 VAC, 50/60 Hz, 3.0 Amp
Battery Voltage 24 V, 31 Ah
Water Protection IPX5
Mode of Operation Continuous
Electromagnetic Compatibility: Product conforms to EN 60601-1-2:1993 - Class A
Ambient Temperature in Charge Mode Not to exceed 82.4°F 28°C

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Introduction
Return To Table of Contents
Introduction
Environmental Conditions Operation Storage and Transportation
Temperature
Relative Humidity 30%
75% 75%
10%
Atmospheric Pressure 700 hPa
1060 hPa
500 hPa
1060 hPa
** The 1040F (400C) maximum operating temperature only applies when the stretcher is not charging. 820F (280C) is
the maximum temperature while the stretcher is charging.
Note
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous
oxide.
Stryker reserves the right to change specifications without notice.
Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.
SPECIFICATIONS (CONTINUED)
10 0C
40 0C
(50 0F)
(104 0F)
-20 0C
40 0C
(-4 0F)
(104 0F)

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Return To Table of Contents
SPECIFICATIONS (OPTIONAL SCALE SYSTEM)
Optional Scale System Weight Operating Range 0 lbs to maximum capacity of the stretcher
Optional Scale System Accuracy
Between 10° Trend & 10° reverse Trend*
±2 lbs. (0.9 kg) of weights below 100 lbs (45.04 kg).
±2% of weights above 100 lbs (45.04 kg).
Environmental Conditions Operation Storage and Transportation
Temperature
Relative Humidity 30%
75% 75%
10%
Atmospheric Pressure 700 hPa
1060 hPa
500 hPa
1060 hPa
* Scale does not meet accuracy claims at Trend angles outside the specified range.
Internally Powered
Mode of Operation: Continuous
IPX5
Electromagnetic Compatibility: Product conforms to EN 60601-1-2:1993 - Class B
Type: 4 x AA Battery (4 x 1.5VDC)
Voltage: 6.0VDC
IntroductionIntroduction
-20 0C
40 0C
(-4 0F)
(104 0F)
16 0C
26 0C
(61 0F)
(79 0F)

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

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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 2601-1, Second Edition and
CAN / CSA C22.2 No. 601.1-M90.
Location not suitable for oxygen bottle storage/placement
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.
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.
Internally powered.
~
Safe Working Load Symbol
Symbols
Return To Table of Contents
Warning, consult accompanying documentation
Alternating Current
87VL
MEDICAL
EQUIPMENT
UL 2601-1
UL60601-1
CAN/CSA
C22.2 NO.
601.1
OPTIONAL SCALE SYSTEM
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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Before operating this stretcher, it is important to read and understand all information in this manual. Carefully read and
strictly follow the warnings and cautions listed on these pages.
Service only by qualified personnel. See the maintenance manual for additional information.
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.
• Always apply the caster brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure 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.
• 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.
• Do not attempt to push the unit manually with the drive wheel engaged and the “On/Drive - Off/Manual” switch in
the On position. The unit will be difficult to push and injury could result.
• When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the siderail
spindles or injury could occur.
• Keep hands/fingers clear of the area around the fowler release handles and the fowler frame when lowering. Injury
could result if care is not taken when lowering the fowler.
• 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.
• If the stretcher is equipped with the optional foot end push handles, use caution while the foot extension/defibrillator
tray is installed to avoid pinching your fingers.
• 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.
• If unanticipated motion occurs, unplug the power cord from the power source and rotate the “On/Drive - Off/ Manual”
switch to the Off position.
• Leave the stretcher litter in the lowest position when the patient is unattended. Leaving the litter in a raised position
could increase the chance of patient falls and injury.
• After raising the siderails, pull firmly on the siderail to ensure 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 designed 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 a patient will remain in place. Failure to utilize the siderails
properly could result in patient injury.
• Possible fire hazard when oxygen administering equipment of other than the nasal mask or 1/2 bed length tent type
is used. Oxygen tent should not extend below mattress support level.
• Possible fire and/or explosion hazard when used with oxygen tents, hyperbaric chambers, anesthesia, or other
combustible gases.
Summary of Safety Precautions
Return To Table of Contents

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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 pounds. This stretcher is intended for use by
trained hospital personnel only.
• The Model 1025 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. Be sure to move any equipment that may be in the way before raising or
lowering the litter height.
• Be sure to remove any equipment that may be in the way before lowering the stretcher.
• Remove the batteries if the equipment is placed in storage or will remain idle for an extended period of time. Each
battery weighs 25 pounds. To avoid personal injury, use caution when removing the two batteries.
• 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. Properly
dispose of batteries when required.
• Do not engage the pedal when the drive wheel is resting on a threshold or other raised area. The force required to
engage the drive wheel will be higher than normal, possibly causing damage.
• To avoid injury or damage to the equipment. Do not allow the siderail to lower on its own.
• The weight capacity of the knee gatch is 200 pounds. Do not sit or stand on the gatch. Injury or damage to the
equipment could occur.
• To avoid damage, the weight of the I.V. bags should not exceed 40 pounds.
• To avoid damage, do not put items weighing more than 30 pounds on the serving tray.
• Always unplug the power cord and rotate the “On/Drive - Off/Manual” switch to the Off position before service or
cleaning.
• If large fluid spills occur in the area of the Circuit boards or motors, immediately unplug the power cord from the
power source and rotate the “On/Drive - Off/Manual” switch to the Off position. Remove the patient from the unit
and clean up the fluid. Have maintenance completely check the unit. Fluids can short out controls and may cause
the unit to operate erratically or make some functions completely inoperable. Component failure caused by fluids
could even cause the unit to operate unpredictably and could cause injury to the patient. Do not put the unit back
into service until it is completely dry and has been thoroughly tested for safe operation.
• The cutout for the oxygen bottle holder may not be used for storage of oxygen bottles or patient belongings.
• The hood may not be used for stepping.
Note
Clean hood storage area regularly.
The bottom of the brake rings should be cleaned regularly to prevent wax and/or floor remnant buildup.
Summary of Safety Precautions
Return To Table of Contents

www.stryker.com 1025-009-005 REV B 1-9
It is important that the Model 1025 Stretcher is working properly before it is put into service. The following list will help
ensure that each part of the unit is checked.
• Plug the power cord into a properly grounded, hospital grade wall receptacle. The 12 volt batteries that provide power
to the drive wheel and backup power to the unit functions will charge whenever the power cord is plugged into the
power source. The batteries require approximately 6 hours of charging time before the stretcher is put into service
• Depress the pedal at either end of the stretcher fully to set the four wheel brakes and verify all four casters are
locked.
• Ensure the siderails raise and lower smoothly and lock securely in the full up position.
• Run through the operation of the drive wheel (see “Transporting the Stretcher Using the Drive Wheel” on page 1-13
and “Operating the Glideaway Siderails” on page 1-15) to ensure it is operating properly
CAUTION
The Model 1025 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.
Return To Table of Contents
Setup Procedures

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D
CA
AB
B
HEAD ENDFOOT END
Pump pedal (A) to raise the litter.
Depress in the center of pedal (B) to lower both ends of the stretcher
together.
Depress the side of pedal (B) closest to the foot end of the stretcher
to lower the foot end.
Depress the side of pedal (B) closest to the head end of the stretcher
to lower the head end.
Pedal (C) - Brake and Steer functions (foot end).
Pedal (D) - Brake and Steer functions (head end).
OPERATING THE BASE CONTROLS
To operate the base controls, see Figure 1 to locate which pedals are used for what operation. Pedal (A) raises the
litter. Pedal (B) lowers the stretcher ends. Pedal (C) operates the brake and steer function for the foot end and pedal
(D) operate the brake and steer functions for the head end.
Return To Table of Contents
Stretcher Operation
Figure 1 - Stretcher Base Controls
A
B
C
D

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RAISING AND LOWERING THE LITTER HEIGHT
CAUTION
Move 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 (see Figure 1 on page 1-10).
To lower both ends of the litter together, depress the center of pedal (B) (see Figure 1 on page 1-10).
To lower only the head end of the litter, depress the side of pedal (B) closest to the head end (see Figure 1 on page
1-10).
To lower only the foot end of the litter, depress the side of pedal (B) closest to the foot end (see Figure 1 on page
1-10).
Note
The base may be equipped with optional variable descent controls. With variable descent controls, the farther you press
down on the pedal, the faster the litter will lower.
WARNING
Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause the litter
surface to tip up, possible causing patient injury.
Leave the stretcher litter in the lowest position when the patient is left unattended. Leaving the litter in a raised positon
could increase the chance of patient falls and injury.
ADJUSTING TRENDELENBURG / REVERSE TRENDELENBURG POSITIONS
Note
Litter height must be raised first in order to achieve a Trendelenburg or reverse Trendelenburg position.
CAUTION
Remove any equipment that may be in the way before lowering the stretcher.
For Trendelenburg positioning (head down), depress the side of pedal (B) closest to the head end of the stretcher (see
Figure 1 on page 1-10).
For Reverse Trendelenburg positioning (foot down), depress the side of pedal (B) closest to the foot end (see Figure
1 on page 1-10).
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 +15°. Maximum reverse Trendelenburg angle is -15°).
Stretcher Operation
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BATTERY CHARGING AND OPERATION
The unit has two 12 volt batteries to provide power to the drive wheel. The drive wheel will not operate properly if the
batteries are not sufficiently charged. The batteries require approximately 6 hours of charging time when they are fully
discharged.
The batteries are charging whenever the power cord is plugged into a properly grounded, hospital grade power source.
When the unit is stationary, the power cord should be plugged into a power source whenever possible.
There is a battery power gauge at the head end of the litter (see Figure 2). The 7 LED’s illuminate individually to indicate
the level of battery power available. As the batteries are charging, the LED’s will flash in succession until all are flashing
(at 1 second intervals) to indicate the batteries are fully charged.
CAUTION
Remove the batteries if the equipment is placed in storage or will remain idle for an extended period of time. Each
battery weighs 25 pounds. To avoid personal injury, use caution when removing the two batteries.
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. Properly dispose
of batteries when required.
No
Charge
Fully
Charged
BATTERY POWER GAUGE
Return To Table of Contents
Stretcher Operation
APPLYING THE BRAKE SYSTEM
Note
For user convenience, the brake/steer pedal is located on both the head end and foot end of the stretcher.
WARNING
Always apply the caster brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure 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 engage the brakes on the head (non-control) end, push fully down on the left side of pedal (D) (see Figure 1 on
page 1-10).
To engage the brakes on the foot (control) end, push fully down on the right side of pedal (C) (see Figure 1 on page
1-10).
Figure 2 - Battery Power Gauge

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TRANSPORTING THE STRETCHER USING THE DRIVE WHEEL
WARNING
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.
Ensure that the brakes are completely released before
attempting to move the unit. Attempting to move the unit
with the brakes actuated could result in injury to the patient
or operator.
To transport the strecher using the drive wheel:
1. Unplug the power cord from the power source and
secure the cord on the storage bracket to prevent
entanglement while the unit is in motion. The drive
function will not operate if the power cord is plugged
into the power source.
2. Engage the drive wheel by rotating the pedal in the
proper direction as shown on the Head End or Foot
End Pedal Directional label. To place the drive wheel
in the neutral position, rotate the pedal until it is level.
CAUTION
Do not engage the pedal when the drive wheel is resting
on a threshold or other raised area. The force required to
engage the drive wheel will be higher than normal, possibly
causing damage.
3. Put the “On/Drive - Off/Manual” switch in the On
position. There are two LED’s on the drive handle
that indicate whether the unit is ready for driving.
• If the green LED is on, the unit is ready.
• If the amber LED is on, the unit is not ready. If
the unit is not ready for driving, verify that the:
• Pedal is in the brake or neutral position.
• Power cord is plugged in the power source.
• Power switch is in the “Off/Manual”
position.
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.
If unanticipated motion occurs, unplug the power source
and rotate the “On/Drive - Off/Manual” switch to the Off
position.
Head End Pedal
Directional Label
Foot End Pedal
Directional Label
On/Drive - Off/Manual Switch Label
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Stretcher Operation
Figure 3 - Pedal and Switch

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TRANSPORTING THE STRETCHER USING THE DRIVE WHEEL (CONTINUED)
4. Grasp the drive handles at the two raised grip areas. Squeeze either of the motion release switches (A) located
under the handles to enable the movement of the drive wheel as shown in Figure 4 and in the Drive Wheel Pedal
and Drive Handle Reference label. Either or both switches will enable movement but both switches must be released
to stop movement.
5. While continuing to squeeze the switch(es), push the handles away from you or pull the handles toward you to
initiate motion in that direction. The speed of the drive wheel will increase proportionally to the amount of force
applied to the drive handles. When the desired speed is reached, the stretcher will maintain speed and direction
with no extra push force. To accelerate, push or pull the handles again until the desired speed is reached. Relax the
force to a “neutral” position to maintain speed.
6. To slow down the motion of the stretcher, push or pull the handles in the opposite direction the stretcher is currently
moving.
7. To stop motion, remove your hands from the switches
and the handles.
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.
To transport the stretcher without using the drive wheel,
put the pedal in the neutral position and put the “On/ Drive
- Off/Manual” switch in the Off position. This allows the
stretcher to be maneuvered with the assistance of the
Big Wheel®but without power assistance from the ZOOM®drive wheel.
WARNING
Do not attempt to push the unit manually with the drive wheel engaged and the “On/Drive - Off/Manual” switch in the
On position. The unit will be difficult to push and injury could result.
CAUTION
Always unplug the power cord and rotate the “On/Drive - Off/Manual” switch to the Off position before service or
cleaning.
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Stretcher Operation
A
STORED POSITION
Figure 4 - Drive Handles with Motion Release Switches
Figure 5 - Drive Handles - Stored Position
Drive Wheel Pedal and Drive Handle Reference Label

www.stryker.com 1025-009-005 REV B 1-15
OPERATING THE GLIDEAWAY™ SIDERAILS
Note
Raising and lowering the siderails safely is a two-handed operation. Use one hand to hold and position the siderail and
the other hand to operate the siderail latch.
WARNING
When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the siderail spindles
or injury could occur.
To raise the siderails: Pull up on the siderail (A) and raise it to the full up position until the latch (B) engages as shown
in Figure 6.
To lower the siderails: Pull up on the latch (B) and guide the siderail to the full down position as shown in Figure 6.
The latches (B) are colored yellow for easy identification.
CAUTION
To avoid injury or damage to the equipment. Do not allow the siderail to lower on its own.
Note
There is a dual siderail latch option available with latches on both ends of the stretcher.
WARNING
After raising the siderails, pull firmly on the siderail to ensure 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 designed 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 a patient will remain in place. Failure to utilize the siderails properly could result
in patient injury..
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Stretcher Operation
A
B
B
Figure 6 - Siderails

1-16 1025-009-005 REV B www.stryker.com
OPERATING THE PNEUMATIC FOWLER
Squeeze either or both of the yellow fowler handles (A) for pneumatic assist in lifting the fowler to the desired height as
shown in Figure 7. Remove hand(s) from handle when the desired height is achieved.
The optional drop seat fowler uses the weight of the patient for additional assistance with lifting the fowler. It also helps
keep the patient from sliding toward the foot end of the stretcher when the fowler is raised.
WARNING
Keep hands/fingers clear of the area around the fowler release handles and the fowler frame when lowering. Injury could
result if care is not taken when lowering the fowler.
A
A
Stretcher Operation
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Figure 7 - Pneumatic Fowler