Stryker 1115 User manual

2017/12 B.2 1115-309-001 REV B www.stryker.com
Operations Manual
Prime Series® Stretcher
Big Wheel®
1115

sample text

www.stryker.com 1115-309-001 REV B
Symbols
Refer to instruction manual/booklet
Operating instructions/Consult instructions for use
General warning
Caution
Warning; crushing of hands
Warning; non-ionizing radiation
No pushing
Do not store the oxygen bottle
Do not lubricate
Catalogue number
Serial number
Batch code
For US Patents see www.stryker.com/patents
CE mark
EC REP
Manufacturer
Date of manufacture
Safe working load
Maximum patient weight

1115-309-001 REV B www.stryker.com
Symbols
Mass of equipment with safe working load
Direct current
~
Alternating current
Dangerous voltage
Protective earth ground
IPX6 Protection from powerful water jets
Type B applied part
Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric
Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1: 2005
and CAN/CSA-C22.2 No. 60601-1:08. *For Prime X option, Associated Equipment of X-ray
Equipment IEC 60601-2-54
In accordance with European Directive 2012/19/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. Contact your local distributor for disposal
information.
Lubricate
Lift here
U.S.A.
English text below this symbol is intended for USA audiences only
CANADA
English text below this symbol is intended for Canada audiences only
Top view
Bottom view
Head end

www.stryker.com 1115-309-001 REV B
Symbols
Foot end
Patient foot end, left

sample text

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Table of Contents
Warning/Caution/Note Definition ..................................................................................................................4
Summary of safety precautions....................................................................................................................5
Pinch points .......................................................................................................................................8
Introduction..............................................................................................................................................9
Product Description .............................................................................................................................9
Indications for use...............................................................................................................................9
Expected service life.......................................................................................................................... 10
Contraindications .............................................................................................................................. 10
Specifications................................................................................................................................... 10
Product illustration - Prime base........................................................................................................... 13
Product illustration - Prime litter ........................................................................................................... 14
Position adjustment button identification................................................................................................. 15
Scale button identification................................................................................................................... 15
Applied parts - electric litter option........................................................................................................ 17
Applied parts - Prime X option.............................................................................................................. 18
Contact information ........................................................................................................................... 18
Serial number location ....................................................................................................................... 19
Date of manufacture.......................................................................................................................... 19
Setup.................................................................................................................................................... 20
Operation .............................................................................................................................................. 21
Applying and releasing the brakes ........................................................................................................21
Prime base controls........................................................................................................................... 21
Raising the non-electric litter ............................................................................................................... 21
Lowering the non-electric litter ............................................................................................................. 22
Raising the electric litter option ............................................................................................................ 22
Lowering the electric litter option .......................................................................................................... 23
Positioning the product in Trendelenburg................................................................................................ 23
Positioning the product in Reverse Trendelenburg.................................................................................... 23
Transporting a patient without the Big Wheel........................................................................................... 24
Transporting a patient with the Big Wheel............................................................................................... 25
Positioning or stowing the head end push handles option........................................................................... 25
Raising the siderail ............................................................................................................................ 26
Lowering the siderail .......................................................................................................................... 27
Positioning the product with the siderail patient control panel - electric litter - not available with Prime X
option .......................................................................................................................................... 27
Operator control panel - electric litter option - not available with Prime X option ............................................. 27
Locking and unlocking the patient control panel lockout - electric litter option - not available with Prime X
option .......................................................................................................................................... 28
Raising or lowering the Fowler backrest - non-electric litter........................................................................ 28
Raising or lowering the Fowler backrest - electric litter.............................................................................. 28
Raising or lowering the gatch - non-electric litter - not available with Prime X option........................................ 29
Raising or lowering the gatch - electric litter option - not available with Prime X option..................................... 29
Positioning the recovery chair - not available with Prime X option ................................................................ 30

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Table of Contents
Storing objects in the base hood...........................................................................................................31
Hanging devices with the pump rack option............................................................................................. 31
Extending or retracting the power cord with the retractable cord reel option - electric lift option or electric litter
option .......................................................................................................................................... 31
Scale system option........................................................................................................................... 32
Replacing the batteries for the scale system option - non-electric litter......................................................... 33
Charging the scale system battery pack option - electric litter option or electric litter option with Chaperone
option - not available with Prime X option ............................................................................................33
Arming or disarming the Chaperone option ............................................................................................. 33
Setting the Chaperone option alert pattern.............................................................................................. 34
Setting the Chaperone option alert volume ............................................................................................. 34
Accessories ........................................................................................................................................... 35
Attaching the defibrillator tray .............................................................................................................. 36
Converting the defibrillator tray/foot extender to a defibrillator tray .............................................................. 37
Converting the defibrillator tray/foot extender to a foot extender ................................................................. 38
Attaching the footboard/chart holder ..................................................................................................... 38
Attaching the IV caddy........................................................................................................................ 38
Positioning or stowing the foot supports - not available with Prime X option ................................................... 39
Positioning the two-stage permanently attached IV pole option ................................................................... 41
Positioning the three-stage permanently attached IV pole option ................................................................. 42
Attaching and positioning the removable IV pole ...................................................................................... 43
Attaching the upright oxygen bottle holder .............................................................................................. 43
Extending or stowing the serving tray holder/footboard.............................................................................. 44
Attaching the siderail pads .................................................................................................................. 44
Locating the patient restraint strap tie-ins ............................................................................................... 44
Positioning the upright X-ray cassette holder - Prime X option .................................................................... 45
Positioning the lateral X-ray cassette holder - Prime X option ..................................................................... 46
Inserting or removing X-ray cassettes - Prime X option.............................................................................. 47
Cleaning................................................................................................................................................ 49
Cleaning the product.......................................................................................................................... 49
Cleaning the product using a cart washer............................................................................................... 49
Cleaning the mattress ........................................................................................................................ 50
Remove iodine.................................................................................................................................. 51
Special instructions ........................................................................................................................... 51
Disinfecting............................................................................................................................................ 52
Disinfecting the product...................................................................................................................... 52
Disinfecting the mattress .................................................................................................................... 52
Preventive maintenance ........................................................................................................................... 54
EMC information ..................................................................................................................................... 55
Warranty ............................................................................................................................................... 59
Warranty exclusion and damage limitations ............................................................................................ 59
To obtain parts and service ................................................................................................................. 59
Return authorization........................................................................................................................... 59

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Table of Contents
Damaged product.............................................................................................................................. 59
International warranty clause ............................................................................................................... 59

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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 product 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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Summary of safety precautions
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
• Always allow the product to reach room temperature before setting up the product or testing functional operations.
Permanent product damage may occur.
• Always operate the product when all operators are clear of the mechanisms.
• Always use care when handling the power cord. Entanglement, damage to the power cord, or potential shock
hazards may occur. If the power cord is damaged, immediately remove the product from service and contact the
appropriate maintenance personnel.
• Always plug the product directly into a grounded, hospital grade wall outlet. You can only achieve grounding
reliability when you use a hospital grade outlet. This product is equipped with a hospital grade plug to protect
against electric shock hazard.
• Always apply the brakes when a patient is getting on the product or off the product or when the product is not
moving. Injury could result if the product moves while a patient is getting on the product or off the product.
• Always position the patient in the center of the product.
• Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended
on the product. Do not leave the product at a higher height.
• Always remove any devices that may be in the way before you raise or lower the litter.
• Do not sit on the end of the product. The product may tip.
• Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
• Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option.
• Always keep the patient’s limbs away from the siderail spindles when you raise or lower the siderail.
• Do not allow the siderails to lower on their own.
• Always keep hands and fingers clear of the Fowler backrest release handles and the Fowler backrest frame when
you lower the Fowler backrest.
• Always use caution when you raise a pneumatic Fowler backrest while a patient is on the product. Use proper lifting
techniques and get help, if necessary.
• Always keep hands and fingers clear of the foot end push handles when you lower the gatch.
• Always keep device lines on the pump rack away from the gatch handles.
• Always make sure that devices on the pump rack can pass safely through door openings.
• Do not lift the product by the pump rack.
• Always unplug the power cord from the wall outlet before you transport or clean the product.
• Always use the retractable cord reel to store the power cord inside the base when you transport the product.
• Do not use the scale system option or electric lift option or electric litter option adjacent to or stacked with other
devices. If adjacent or stacked use is necessary, the scale system option or electric lift option or electric litter
option should be observed to make sure that all devices are operating normally in the configuration in which they
will be used.
• Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray. Always strap down all devices that
you place on the defibrillator tray.
• Always use caution if the defibrillator tray/foot extender, footboard/chart holder, or upright oxygen bottle holder is
attached to avoid pinching your fingers when you position the foot end push handle option.
• Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray/foot extender. Always strap down all
devices that you place on the defibrillator tray.
• Always secure the IV pole to the IV caddy when you transport the product.
• Always store the IV caddy when not in use to avoid product damage.

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Summary of safety precautions
WARNING (CONTINUED)
• Do not sit on the foot supports. This may cause the product to tip.
• Always clear your fingers from the mechanisms when you operate the foot supports.
• Always stow the foot supports when you transport a patient with the product.
• Always tighten the foot supports before you use the foot supports.
• Do not operate the scale system with the foot supports. Inaccurate readings may occur.
• Do not operate the Chaperone option with the foot supports. Inaccurate readings may occur.
• Do not use the IV pole as a push/pull device. Product damage may occur.
• Do not place objects that exceed 40 lb (18 kg) in the upright oxygen bottle holder.
• Do not place objects that exceed 30 lb (14 kg) on the serving tray.
• Always use caution when you attach restraint straps. Patient or operator injury may occur. Physical restraints, even
if secured, may result in serious harm to patients and operators, including entanglement, entrapment, physical injury,
or death.
• Always attach restraint straps or devices only at the identified attachment points of the product. Failure to do so
may result in patient or operator injury. Do not attach restraint straps to the siderail.
• Always refer to the applicable state and federal restrictions and regulations and the appropriate facility protocols
before you use any restraint strap or device.
• Always take protective measures when you use the upright or lateral X-ray cassette holder. The X-ray cassette
holder does not protect against radiation.
• Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use Prime X
option with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered
radiation.
• Always follow the Positioning the upright X-ray cassette holder - Prime X option instructions to insert the X-ray
cassette.
• Always follow the Positioning the lateral X-ray cassette holder - Prime X option instructions to insert the X-ray
cassette.
• Do not immerse the mattress in cleaning or disinfectant solutions. Excess moisture could cause product
malfunction that results in product damage or patient injury.
• Do not allow fluid to pool on the mattress. Fluids can cause corrosion of components and may cause the safety and
performance of this product to become unpredictable.
• Always inspect mattress covers for tears, punctures, excessive wear, and misaligned zippers every time you clean
the covers. Remove and replace a damaged mattress immediately to prevent cross-contamination.
• Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may
void this product’s warranty.
• Always disinfect the mattress between patients. Failure to do so could result in cross-contamination and infection.
CAUTION
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in
this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
• Do not use the hydraulics on the base to raise the product with a patient lift under the product.
• Do not apply the steer pedal when the Big Wheel is resting on a threshold or other raised area. The force required
to apply the Big Wheel will be higher than normal which may cause product damage.

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Summary of safety precautions
CAUTION (CONTINUED)
• The weight capacity of the gatch is 200 lb (90.7 kg).
• Always make sure that the gatch prop rod is secure before use.
• Do not sit or stand on the gatch.
• Always use caution when you attempt to lower the gatch while the product is unpowered. Gravity may cause a rapid
drop of the gatch.
• Do not place objects that exceed 60 lb (27 kg) in the base hood.
• Do not sit, step, or stand on the base hood.
• The weight capacity of the pump rack is 40 lb (18 kg).
• Do not use the pump rack as a push/pull device.
• Do not use the scale for pediatric use or for patients under 50 lb.
• Always raise the IV pole before you attach the defibrillator tray/foot extender to the product. If you do not raise the
IV pole, the foot extender will not operate.
• Do not use abrasive cleaners to clean the display enclosure for the scale system option. Do not allow cleaning
solutions or other fluids to pool on the display unit. Dry all surfaces after spills or cleaning.
• The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could
result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper
operation.
• The emissions characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11
class A). If it is used in a residential environment, for which CISPR 11 class B is normally required, this equipment
might not offer adequate protection to radio frequency communication services. The user might need to take
mitigation measures, such as relocating or reorienting the equipment.
• Portable RF communications equipment, including peripherals such as antenna cables and external antennas,
should be used no closer than 12 inches (30 cm) to any part of the Prime stretcher, including cables specified by
the manufacturer.
• Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the products. If
such use is necessary, carefully observe stacked or adjacent equipment to make sure that they are operating
properly.

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Summary of safety precautions
Pinch points
Figure 1: Prime X option

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Introduction
This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating
or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or
maintenance of this product.
CAUTION
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in
this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
Notes
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current
product information available at the time of printing. There may be minor discrepancies between your product and
this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770.
Product Description
The Stryker Model 1115 Prime Series®stretcher with Big Wheel®is a wheeled device which consists of a platform
mounted on a wheeled frame that is designed to support patients in a horizontal position. A stretcher provides the
operator with a method of transporting patients within the interior of a healthcare facility by health professionals or
trained representatives of the facility. The Stryker Model 1115 Prime Series stretcher with Big Wheel decreases start-
up force by 50 percent and steering effort by 60 percent.
Indications for use
The Prime Series stretcher with Big Wheel has two big wheels to reduce the startup force required to move the
stretcher.
The Prime Series stretcher may be used as a short-term outpatient clinical evaluation, treatment, minor procedure, and
short-term outpatient recovery platform. The stretcher may include use in, but is not limited to:
• Emergency department (ED)
• Trauma area
• Post-anesthesia care unit (PACU)
The Prime Series stretcher may be used for minor procedures and short-term stay (treatment and recovery). See the
specifications table for the intended environmental conditions.
The Prime Series stretcher is not for use for long-term inpatient treatment and recovery.
The Prime Series stretcher has a safe working load up to 700 lb (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 Series stretcher has siderails and has the option available to support the temporary or permanent placement
of IV poles, along with various other options and accessories to assist with the transport of the patient.
Prime X®option provides an articulating radiographic patient support surface and a platform below the patient support
surface for X-ray cassette placement. Prime X option is intended to allow the capture of clinical X-rays (AP full body,
optional full body lateral, and optional upright chest) when used with a medical X-ray system.

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Introduction
Expected service life
Prime Series stretchers and Prime Series stretchers with Prime X option have a 10 year expected service life under
normal use conditions and with appropriate periodic maintenance.
Contraindications
Do not use Prime X option with a mattress with a thickness greater than 4 in.
Do not use a C-Arm with Prime X option. Prime X option is not compatible with a C-Arm.
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.
Specifications
Prime
26 in. Width
Prime
30 in. Width
Prime Series HT Packs
Prime X Option
30 in. Width
Safe working load
indicates the sum of the patient,
mattress and accessory weight
700 lb 318 kg 700 lb 318 kg 700 lb 318 kg
Maximum patient weight
675 lb 306 kg 675 lb 306 kg 675 lb 306 kg
Overall length 85 in. (± 0.5
in.) 215.9 cm 85 in. (± 0.5 in.) 215.9 cm 85 in. (± 0.5 in.) 215.9 cm
Overall length (litter extension
option)
89.9 in. (±
.75 in.) 228.3 cm 89.9 in. (± .75 in.) 228.3 cm NA NA
Overall width (siderails up) 34 in. (± 1
in.) 86.4 cm 38 in. (± 1 in.) 96.5 cm 38 in. (± 1 in.) 96.5 cm
Overall width (siderails down) 30.25 in. (±
0.5 in.) 76.8 cm 30.5 in (± 0.5 in.) 77.5 cm 30.5 in. (± 0.5 in.) 77.5 cm
Minimum height 20.75 in. 52.7 cm 20.75 in. 52.7 cm 23.25 in. 59.1 cm
Maximum height 34 in. (± 1
in.) 86.4 cm 34 in. (± 1 in.) 86.4 cm 36.5 in. (± 1 in.) 92.7 cm
Fowler backrest angle 0° to 90° (± 5°)
Gatch height 5.5 in. (14 cm) minimum Not applicable
Trendelenburg/Reverse
Trendelenburg +17° to -17° (± 3°)
Minimum clearance 2.5 in.
nominal 6.4 cm 2.5 in. nominal 6.4 cm 2.5 in. nominal 6.4 cm

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Introduction
Specifications (Continued)
Prime
26 in. Width
Prime
30 in. Width
Prime Series HT Packs
Prime X Option
30 in. Width
1.75 in.
under the
hydraulic
jacks
4.5 cm
1.75 in.
under the
hydraulic
jacks
4.5 cm
1.75 in.
under the
hydraulic
jacks
4.5 cm
1 in. under
the Big
Wheel
2.5 cm
1 in. under
the Big
Wheel
2.5 cm
1 in. under
the Big
Wheel
2.5 cm
Attenuation equivalent
(aluminum equivalence) Not applicable Maximum value allowed is
1.7 mm Al
Optional scale system weight
operating range 50 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) *
* To meet the scale accuracy claim, the patient surface must be in the flat position (Fowler backrest and gatch down),
in the highest position, and the product cannot exceed 5 degrees of Trendelenburg/Reverse Trendelenburg.
Electric options Optional electric litter (available on
Prime only)
Optional electric lift (available on
Prime and Prime X)
Electrical requirements 120 VAC, 60Hz, 10 A
240 VAC, 50 to 60 Hz, 5 A
120 VAC, 60Hz, 10 A
240 VAC, 50 to 60 Hz, 5 A
Duty cycle Continuous operation with
intermittent loading is 1 min. ON and
20 min. OFF
Continuous operation with
intermittent loading is 1 min. ON and
20 min. OFF
Scale system option Non-electric litter (available on
Prime and Prime X option)
Optional electric lift (available on
Prime and Prime X option)
Battery type 4 x AA Battery (4 X 1.5 VDC) Alkaline
Type (LR6)
4 x AA Battery (4 X 1.5 VDC) Alkaline
Type (LR6)
Battery voltage 6.0 VDC 6.0 VDC
Scale system option Optional electric litter (available on
Prime only) Optional electric lift
Battery type 1 x Rechargeable Lithium Ion Battery
Pack (0058-135-000) Not applicable
Battery voltage 10.8 VDC, 2.4Ah Not applicable

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Introduction
Specifications (Continued)
Optional scale system with
Chaperone® (stretcher exit)
Optional electric litter (available on
Prime only) Optional electric lift
Battery type 1 x Rechargeable Lithium Ion Battery
Pack (0058-134-000) Not applicable
Battery voltage 10.8 VDC, 4.8 Ah Not applicable
Stryker reserves the right to change specifications without notice.
Note: This product is not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or
nitrous oxide.
ID Name
IEC 60601-1 Medical electrical equipment - Part 1: General
requirements for basic safety and essential performance
IEC 60601-1-2
Medical electrical equipment - Part 1-2: General
requirements for basic safety and essential performance -
Collateral standard: Electromagnetic compatibility -
Requirements and tests
IEC 60601-1-3
Medical electrical equipment - Part 1-3: General
requirements for basic safety and essential performance -
Collateral Standard: Radiation protection in diagnostic X-
ray equipment
IEC 60601-2-52
Medical electrical equipment - Part 2-52: Particular
requirements for the basic safety and essential
performance of medical beds
IEC 60601-2-54
Medical electrical equipment - Part 2-54: Particular
requirements for the basic safety and essential
performance of X-ray equipment for radiography and
radioscopy
Environmental conditions Operation Storage and transportation
Temperature
100 °F
(38 °C)
50 °F
(10 °C)
140 °F
(60 °C)
-4 °F
(-20 °C)
Relative humidity
75%
30%
95%
10%
Atmospheric pressure
1060 hPa
700 hPa
1060 hPa
500 hPa
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.

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Introduction
Specifications (Continued)
Optional Scale system (Non-electric litter or electric litter option)
Environmental conditions Operation Storage and transportation
Temperature
79 °F
(26 °C)
61 °F
(16 °C)
140 °F
(60 °C)
-4 °F
(-20 °C)
Relative humidity
75%
30%
95%
10%
Atmospheric pressure
1060 hPa
700 hPa
1060 hPa
500 hPa
Product illustration - Prime base
A
B
C
D
E
F
GH
C
C
D
E
F
G
Figure 2: Prime base
ABase hood storage ECasters with integrated wheel covers
BBig Wheel FHydraulic release pedal
CBrake steer control pedal GPump pedal
DBumpers, integrated HUni-lower pedal

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Introduction
Product illustration - Prime litter
B
C
D
G
H
I
K
LMN
O
P
F
A
J
F
E
D
Figure 3: Prime litter
ACassette tray IPatient control lockout option
BDrop seat Fowler backrest with Lift Assist® JPatient surface with Clearview Technology®
(Prime X option)
CBackSmart™foot end operator controls option KBackSmart pop-up push handles option
D Fowler backrest release handle L Pump rack
EGatch pump handle option MBackSmart scale system option
FGatch release handle option NBackSmart siderail, Glideaway