Stryker 1025, Zoom, SM304 Operation Manual
M-Series Stretcher
Model 1025 (SM304)
Operations Manual
For Parts or Technical Assistance:
USA: 1-800-327-0770 (option 2)
2009/01 1025-009-001 REV E www.stryker.com
Table of Contents
Introduction...............................................................................4
Intended Use ..........................................................................4
Product Description .....................................................................4
Specifications .........................................................................4
Specifications (Optional Scale System).......................................................6
Warning / Caution / Note Definition ..........................................................7
Symbols .................................................................................8
Summary of Safety Precautions................................................................9
Setup Procedures .........................................................................11
Stretcher Operation........................................................................12
Operating the Base Controls ..............................................................12
Raising and Lowering the Litter Height....................................................... 13
Adjusting Trendelenburg / Reverse Trendelenburg Positions .......................................13
Battery Charging and Operation ...........................................................14
Applying the Brake System ...............................................................14
Transporting the Stretcher Using the Drive Wheel ..............................................15
Operating the Glideaway™ Siderails ........................................................ 17
Operating the Pneumatic Fowler ...........................................................18
Operating the Optional Knee Gatch.........................................................19
Operating the Optional 2-Stage Permanently Attached I.V. Pole.....................................20
Operating the Optional 3-Stage Permanently Attached I.V. Pole.....................................21
Operating the Optional Foot Extension/Defibrillator Tray ..........................................22
Operating the Optional Serving Tray ........................................................23
Operating the Optional Scale System .......................................................24
Using the Optional Scale System Batteries ...................................................25
Cleaning................................................................................26
Recommended Cleaning Method...........................................................26
Recommended Disinfectants..............................................................26
Rinse Off Corrosive Cleaners .............................................................26
Special Instructions ....................................................................27
Removal of Iodine Stains ................................................................27
Preventative Maintenance ...................................................................28
Checklist ............................................................................28
Warranty................................................................................30
Limited Warranty ......................................................................30
To Obtain Parts and Service ..............................................................30
Service Contract Coverage ...............................................................30
Service Contract Programs ...............................................................31
Return Authorization....................................................................31
Damaged Merchandise..................................................................31
International Warranty Clause .............................................................31
Recycling Passport ........................................................................32
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Introduction
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
stretcher.
®
product is a general purpose patient transport and treatment
SPECIFICATIONS
Safe Working Load
Note: Safe Working Load
indicates the sum of the patient,
mattress, and accessory weight.
26” Stretcher
Weight of Product
30” Stretcher
Overall Stretcher Length 85” (± .5”) 215.9 cm (± 1.27 cm)
Overall Stretcher Width (Siderails Up) 34.5” & 37” (± .5”) 87.63 cm & 93.98 cm (± 1.27 cm)
Overall Stretcher Width (Siderails Down) 26.5” & 30.75” (± .5”) 67.31 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°)
415 lbs (standard configuration)
465 lbs (all options/accessories)
435 lbs (standard configuration)
485 lbs (all options/accessories)
700 pounds 318 kg
188 kg
211 kg
197 kg
220 kg
Knee Gatch Angle 0° to 40° (± 1°)
Trendelenburg / Reverse Trendelenburg +15° to -15°
Electrical 115 VAC, 60 Hz, 3.0 Amp
Battery Voltage
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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24 VDC, 31 Ah
SPECIFICATIONS (CONTINUED)
Environmental Conditions Operation Storage and Transportation
Introduction
Introduction
Temperature
10 0C
(50
0
C
40
(104 0F)
0
F)
-20 0C
0
(-4
F)
75%
0
C
40
(104 0F)
75%
Relative Humidity
30%
1060 hPa
10%
1060 hPa
Atmospheric Pressure
700 hPa
500 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.
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IntroductionIntroduction
SPECIFICATIONS (OPTIONAL SCALE SYSTEM)
Optional Scale System Weight Operating Range 0 lbs to maximum capacity of the stretcher
Between 10° Trend & 10° reverse Trend*
Optional Scale System Accuracy
Environmental Conditions Operation Storage and Transportation
±2 lbs. (0.9 kg) of weights below 100 lbs (45.04 kg).
±2% of weights above 100 lbs (45.04 kg).
0
C
26
Temperature
16 0C
(61
0
F)
(79 0F)
75%
Relative Humidity
30%
1060 hPa
Atmospheric Pressure
700 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)
-20 0C
0
(-4
10%
500 hPa
F)
0
C
40
(104 0F)
75%
1060 hPa
Voltage: 6.0VDC
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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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~
Symbols
Warning, consult accompanying documentation
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.
Internally powered.
Dangerous Voltage Symbol
Protective Earth Terminal
Potential Equalization Symbol
Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock, Fire,
87VL
MEDICAL
EQUIPMENT
UL 2601-1
Mechanical and Other Specified Hazards Only in Accordance with UL 2601-1, Second Edition and
CAN / CSA C22.2 No. 601.1-M90.
Safe Working Load Symbol
Location not suitable for oxygen bottle storage/placement
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.
OPTIONAL SCALE SYSTEM
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
UL60601-1
CAN/CSA
C22.2 NO.
601.1
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CAN/CSA C22.2 No. 601.1.
Summary of Safety Precautions
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.
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Summary of Safety Precautions
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.
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Setup Procedures
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 15
and “Operating the Glideaway Siderails” on page 17 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.
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D
C
A
AB
B
HEAD ENDFOOT END
Stretcher Operation
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.
Figure 1 - Stretcher Base Controls
A
B
C
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).
D
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Pedal (D) - Brake and Steer functions (head end).
Stretcher Operation
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 12).
To lower both ends of the litter together, depress the center of pedal (B) (see Figure 1 on page 12).
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
12).
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
12).
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 position
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 12).
For Reverse Trendelenburg positioning (foot down), depress the side of pedal (B) closest to the foot end (see Figure
1 on page 12).
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°).
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