Stryker Prime 1115 User manual

PPrriimmee SSeerriieess®® SSttrreettcchheerr
OOppeerraattiioonnss MMaannuuaall
1115
Big Wheel®
EN
1115-309-001 Rev C.2 2019/09

SSyymmbboollss
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
Lot (batch) code

Serial number
 
For US Patents see www.stryker.com/patents
CE mark
Authorized representative in the European Community
European medical device
Manufacturer
Safe working load
Maximum patient weight
Mass of equipment with safe working load
1115-309-001 Rev C.2 EN

Direct current
~
Alternating current
Dangerous voltage
Protective earth ground
IIPPXX66 Protection from powerful water jets
Type B applied part
87VL
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 PPrriimmee XX option, Associated Equipment of X-ray Equipment IEC
60601-2-54
In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic
Equipment (WEEE) as amended, this symbol indicates that the product should be collected
separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor
for disposal information. Ensure infected equipment is decontaminated prior to recycling.
Lubricate
Lift here
EN 1115-309-001 Rev C.2

TTaabbllee ooff CCoonntteennttss
Warning/Caution/Note Definition ..............................................................................................................................3
Summary of safety precautions ................................................................................................................................3
Pinch points .......................................................................................................................................................6
Introduction ...............................................................................................................................................................7
Product description .................................................................................................................................................7
Indications for use...................................................................................................................................................7
Clinical benefits ......................................................................................................................................................7
Expected service life ...............................................................................................................................................8
Disposal/recycle .....................................................................................................................................................8
Contraindications....................................................................................................................................................8
Specifications .........................................................................................................................................................8
Product illustration - Prime.....................................................................................................................................11
Product illustration - Prime X option........................................................................................................................12
Applied parts - electric litter option..........................................................................................................................13
Applied parts - Prime X option................................................................................................................................13
Contact information...............................................................................................................................................14
Serial number location...........................................................................................................................................14
Date of manufacture..............................................................................................................................................14
Setup.......................................................................................................................................................................15
Operation ................................................................................................................................................................16
Applying and releasing the brakes..........................................................................................................................16
Prime base controls ..............................................................................................................................................16
Raising the non-electric litter..................................................................................................................................16
Lowering the non-electric litter ...............................................................................................................................17
Raising the electric litter option...............................................................................................................................17
Lowering the electric litter option ............................................................................................................................17
Positioning the product in Trendelenburg ................................................................................................................18
Positioning the product in Reverse Trendelenburg...................................................................................................18
Transporting a patient ...........................................................................................................................................18
Transporting a patient without Big Wheel ................................................................................................................19
Transporting a patient with Big Wheel.....................................................................................................................19
Positioning or stowing the head end push handles option.........................................................................................20
Raising the siderail................................................................................................................................................21
Lowering the siderail .............................................................................................................................................21
Positioning the product with the siderail patient control panel - electric litter option- Prime only....................................22
Operator control panel - electric litter option - Prime only..........................................................................................23
Locking and unlocking the patient control panel lockout - electric litter option - Prime only...........................................23
Raising or lowering the Fowler backrest - non-electric litter.......................................................................................24
Raising or lowering the Fowler backrest - electric litter option ...................................................................................25
Raising or lowering the Gatch - non-electric litter - Prime only...................................................................................26
Raising or lowering the Gatch - electric litter option - Prime only................................................................................26
Positioning the recovery chair - Prime only..............................................................................................................26
Storing objects in the base hood.............................................................................................................................27
Hanging devices with the pump rack option.............................................................................................................27
Extending or retracting the power cord with the retractable cord reel option - electric lift option or electric litter
option...................................................................................................................................................................28
Scale system option ..............................................................................................................................................28
Scale icon/button identification ..........................................................................................................................29
Weighing a patient............................................................................................................................................29
Locking the scale unit of measure......................................................................................................................30
Arming or disarming the Chaperone option.........................................................................................................30
Setting the Chaperone option alert pattern .........................................................................................................30
Setting the Chaperone option alert volume .........................................................................................................31
Charging the scale system battery pack option - electric litter option or electric litter option with Chaperone option -
Prime only .......................................................................................................................................................31
1115-309-001 Rev C.2 1 EN

Replacing the batteries for the scale system option - non-electric litter .................................................................. 31
Accessories and parts ...........................................................................................................................................32
Attaching the defibrillator tray ............................................................................................................................35
Converting the defibrillator tray/foot extender to a defibrillator tray........................................................................35
Converting the defibrillator tray/foot extender to a foot extender ...........................................................................36
Attaching the footboard/chart holder ..................................................................................................................36
Attaching the IV caddy ......................................................................................................................................37
Positioning or stowing the foot supports - Prime only ...........................................................................................37
Positioning the two-stage permanently attached IV pole ......................................................................................38
Positioning the three-stage permanently attached IV pole....................................................................................39
Attaching and positioning the removable IV pole .................................................................................................40
Attaching the upright oxygen bottle holder ..........................................................................................................41
Extending or stowing the serving tray holder/footboard........................................................................................41
Attaching the siderail pads ................................................................................................................................42
Locating the patient restraint strap tie-ins ...........................................................................................................42
Positioning the upright X-ray cassette holder - Prime X option..............................................................................42
Positioning the lateral X-ray cassette holder - Prime X option...............................................................................43
Inserting or removing X-ray cassettes - Prime X option........................................................................................44
Cleaning and disinfecting with wipes......................................................................................................................46
Cleaning..................................................................................................................................................................47
Cleaning the product .............................................................................................................................................47
Cleaning the product using a cart washer................................................................................................................47
Cleaning the mattress ...........................................................................................................................................48
Remove iodine.................................................................................................................................................49
Special instructions ..........................................................................................................................................49
Disinfecting .............................................................................................................................................................50
Disinfecting the product .........................................................................................................................................50
Disinfecting the mattress .......................................................................................................................................50
Preventive maintenance .........................................................................................................................................52
EMC information .....................................................................................................................................................54
1070-110-260 / 1070-110-265 / 1070-110-360 / 1070-110-365 / 1070-110-270 / 1070-110-370 .........................57
1070-117-600 / 1070-117-300................................................................................................................................58
1070-237-020 .........................................................................................................................................................59
1008-010-302 .........................................................................................................................................................60
1008-011-320 / 1008-011-330................................................................................................................................61
1008-015-020 .........................................................................................................................................................62
1070-010-100 .........................................................................................................................................................63
1070-010-100 .........................................................................................................................................................64
1070-010-200 .........................................................................................................................................................65
1070-010-200 .........................................................................................................................................................66
1018-015-305 .........................................................................................................................................................67
1018-015-405 .........................................................................................................................................................68
EN 2 1115-309-001 Rev C.2

WWaarrnniinngg//CCaauuttiioonn//NNoottee DDeeffiinniittiioonn
The words WWAARRNNIINNGG,CCAAUUTTIIOONN, and NNOOTTEE carry special meanings and should be carefully reviewed.
WWAARRNNIINNGG
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.
CCAAUUTTIIOONN
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.
NNoottee -- Provides special information to make maintenance easier or important instructions clearer.
SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WWAARRNNIINNGG
• Always allow the product to reach room temperature before you set up the product or test 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. 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.
• Do not transport the product laterally on inclines greater than 5.7 degrees (10% grade) to avoid product tipping.
• Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with PPrriimmee XX option.
• Always lock the siderails in the full up position with the sleep surface flat and in the lowest position when you transport a
patient.
• 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 the 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.
1115-309-001 Rev C.2 3 EN

• 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.
• 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 CChhaappeerroonnee 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 PPrriimmee XX
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 use caution when you take X-rays with the Fowler backrest in the upright position or when you use a lateral
cassette.
• Always follow the
Positioning the lateral X-ray cassette holder - Prime X option instructions to insert the X-ray cassette.
• Do not clean, service, or perform maintenance while the product is in use.
• 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 to prevent cross-contamination.
• Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may void
the product’s warranty.
• Do not steam clean, hose off, or ultrasonically clean the product. Use of these methods of cleaning is not recommended
and may void the product’s warranty.
• Always disinfect the mattress between patients. Failure to do so could result in cross-contamination and infection.
CCAAUUTTIIOONN
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this
manual.
EN 4 1115-309-001 Rev C.2

• 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 BBiigg WWhheeeell is resting on a threshold or other raised area. The force required to apply
BBiigg WWhheeeell will be higher than normal which may cause product damage.
• 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. Product damage may occur.
• Do not use the scale for pediatric use or for patients under 50 lb.
• Do not use the scale system reading as a reference for medical treatment.
• 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 the IV pole as a push/pull device. Product damage may occur.
• Do not hang IV bags that exceed 40 lb (18 kg) on the IV pole.
• Always make sure that the IV pole is at a low height to pass through door openings when you transport a patient.
• 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 PPrriimmee stretcher, including cables specified by the
manufacturer.
• Avoid stacking or placing other 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.
1115-309-001 Rev C.2 5 EN

PPiinncchh ppooiinnttss
FFiigguurree 11 –– PPrriimmee XX ooppttiioonn
EN 6 1115-309-001 Rev C.2

IInnttrroodduuccttiioonn
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.
CCAAUUTTIIOONN
• 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.
NNoottee
• 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.
PPrroodduucctt ddeessccrriippttiioonn
The Stryker Model 1115 PPrriimmee SSeerriieess® stretcher with BBiigg WWhheeeell® is a wheeled device which consists of a platform
mounted on a wheeled frame 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 PPrriimmee SSeerriieess stretcher with BBiigg WWhheeeell decreases start-up force by 50 percent and
steering effort by 60 percent.
IInnddiiccaattiioonnss ffoorr uussee
The PPrriimmee SSeerriieess stretcher with BBiigg WWhheeeell has two big wheels to reduce the startup force required to move the stretcher.
The PPrriimmee SSeerriieess 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 PPrriimmee SSeerriieess stretcher may be used for minor procedures and short-term stay (treatment and recovery). See the
specifications table for the intended environmental conditions.
The PPrriimmee SSeerriieess stretcher is not for use for long-term inpatient treatment and recovery.
The PPrriimmee SSeerriieess 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 PPrriimmee XX® option provides an articulating radiographic patient support surface and a platform below the patient support
surface for X-ray cassette placement. PPrriimmee XX 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.
CClliinniiccaall bbeenneeffiittss
Patient transport, facilitate treatment, and diagnostic
1115-309-001 Rev C.2 7 EN

EExxppeecctteedd sseerrvviiccee lliiffee
The PPrriimmee SSeerriieess stretcher and the PPrriimmee SSeerriieess stretcher with PPrriimmee XX option have a 10 year expected service life
under normal use conditions and with appropriate periodic maintenance.
DDiissppoossaall//rreeccyyccllee
Always follow the current local recommendations and/or regulations governing environmental protection and the risks
associated with recycling or disposing of the equipment at the end of its useful life.
CCoonnttrraaiinnddiiccaattiioonnss
The PPrriimmee XX option is not recommended for use with a mattress with a thickness greater than four inches.
The PPrriimmee XX option is not compatible for use with a C-Arm.
The PPrriimmee XX 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.
SSppeecciiffiiccaattiioonnss
PPrriimmee SSeerriieess 2266 iinn.. wwiiddtthh
PPrriimmee SSeerriieess 3300 iinn.. wwiiddtthh
PPrriimmee SSeerriieess HHTT PPaacckkss
PPrriimmee XX ooppttiioonn 3300 iinn..
wwiiddtthh
NNoottee -- 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
EN 8 1115-309-001 Rev C.2

PPrriimmee SSeerriieess 2266 iinn.. wwiiddtthh
PPrriimmee SSeerriieess 3300 iinn.. wwiiddtthh
PPrriimmee SSeerriieess HHTT PPaacckkss
PPrriimmee XX ooppttiioonn 3300 iinn..
wwiiddtthh
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
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
BBiigg WWhheeeell 2.5 cm 1 in. under BBiigg WWhheeeell 2.5 cm 1 in. under BBiigg WWhheeeell 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 system accuracy claim, the patient surface must be in the flat position (Fowler backrest and Gatch
down) and the product cannot exceed 5 degrees of Trendelenburg/Reverse Trendelenburg.
EElleeccttrriicc ooppttiioonnss OOppttiioonnaall eelleeccttrriicc lliitttteerr ((aavvaaiillaabbllee oonn
PPrriimmee oonnllyy))
OOppttiioonnaall eelleeccttrriicc lliifftt ((aavvaaiillaabbllee oonn
PPrriimmee aanndd PPrriimmee XX ooppttiioonn))
Electrical requirements 120 VAC, 60Hz, 10A
240 VAC, 50/60 Hz, 5A
120 VAC, 60Hz, 10A
240 VAC, 50/60 Hz, 5A
Duty cycle Continuous operation with intermittent
loading is 1 min. ON/20 min. OFF
Continuous operation with intermittent
loading is 1 min. ON/20 min. OFF
OOppttiioonnaall ssccaallee ssyysstteemm NNoonn--eelleeccttrriicc lliitttteerr ((aavvaaiillaabbllee oonn
PPrriimmee aanndd PPrriimmee XX ooppttiioonn))
OOppttiioonnaall eelleeccttrriicc lliifftt ((aavvaaiillaabbllee oonn
PPrriimmee aanndd PPrriimmee XX ooppttiioonn))
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
OOppttiioonnaall ssccaallee ssyysstteemm OOppttiioonnaall eelleeccttrriicc lliitttteerr ((aavvaaiillaabbllee oonn
PPrriimmee oonnllyy)) OOppttiioonnaall eelleeccttrriicc lliifftt
Battery type 1 x rechargeable lithium ion battery
pack (0058-135-000) Not applicable
Battery voltage 10.8 VDC, 2.4Ah Not applicable
OOppttiioonnaall ssccaallee ssyysstteemm wwiitthh
CChhaappeerroonnee®® ((ssttrreettcchheerr eexxiitt))
OOppttiioonnaall eelleeccttrriicc lliitttteerr ((aavvaaiillaabbllee oonn
PPrriimmee oonnllyy)) OOppttiioonnaall eelleeccttrriicc lliifftt
Battery type 1 x rechargeable lithium ion battery
pack (0058-134-000) Not applicable
Battery voltage 10.8 VDC, 4.8Ah Not applicable
1115-309-001 Rev C.2 9 EN

Stryker reserves the right to change specifications without notice.
NNoottee -- This product is not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or
nitrous oxide.
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn
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
NNoottee -- The optional scale system (non-electric litter/electric litter option) operation temperature range is 61 °F (16 °C) to 79
°F (26 °C).
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
In accordance with the European REACH regulation and other environmental regulatory requirements, the components that
contain declarable substances are listed.
DDeessccrriippttiioonn NNuummbbeerr SSuubbssttaannccee ooff vveerryy hhiigghh ccoonncceerrnn ((SSVVHHCC))
cchheemmiiccaall nnaammee
26” three-stage IV pole assembly 0785-035-200 bis(2-ethklhexyl) phthatlate (DEHP)
Two-stage IV pole assembly 0785-035-101 bis(2-ethklhexyl) phthatlate (DEHP)
30” three-stage IV pole assembly 0785-035-300 bis(2-ethklhexyl) phthatlate (DEHP)
30” two-stage IV pole assembly 0785-035-401 bis(2-ethklhexyl) phthatlate (DEHP)
EN 10 1115-309-001 Rev C.2

PPrroodduucctt iilllluussttrraattiioonn -- PPrriimmee
C
D
EFGHIK
LMNO
P
Q
J
A
BC
D
D
E
FFiigguurree 22 –– PPrriimmee
AIV pole J Siderail latch
BBBaacckkSSmmaarrtt® pop up push handle, optional KHydraulic release pedal
CBBaacckkSSmmaarrtt siderail L Gatch release handle
DBrake/steer pedal MBBaacckkSSmmaarrtt foot end operator control
panel, optional
EPump pedal NPump rack, optional
FUni-lower pedal OBBaacckkSSmmaarrtt scale system, optional
GBBiigg WWhheeeell PPatient control panel lockout, optional
HBumper, integrated QSiderail patient control panel, optional
ICaster with integrated wheel cover
1115-309-001 Rev C.2 11 EN

PPrroodduucctt iilllluussttrraattiioonn -- PPrriimmee XX ooppttiioonn
C
D
E
F
GH
I
KLM
J
A
B
B
E
F
F
G
FFiigguurree 33 –– PPrriimmee XX ooppttiioonn
ABBaacckkSSmmaarrtt® pop up push handle, optional HUni-lower pedal
BIV pole IBumper, integrated
CCassette tray JCaster with integrated wheel cover
DPatient surface with CClleeaarrvviieeww
TTeecchhnnoollooggyy® deck K Siderail latch
EBBaacckkSSmmaarrtt siderail L Pump rack, optional
FBrake/steer control pedal MBBaacckkSSmmaarrtt scale system, optional
GPump pedal
EN 12 1115-309-001 Rev C.2

AApppplliieedd ppaarrttss -- eelleeccttrriicc lliitttteerr ooppttiioonn
FFiigguurree 44 –– TTyyppee BB aapppplliieedd ppaarrttss -- eelleeccttrriicc lliitttteerr ooppttiioonn
AApppplliieedd ppaarrttss -- PPrriimmee XX ooppttiioonn
FFiigguurree 55 –– TTyyppee BB aapppplliieedd ppaarrttss -- PPrriimmee XX ooppttiioonn
1115-309-001 Rev C.2 13 EN

CCoonnttaacctt iinnffoorrmmaattiioonn
Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
NNoottee -- The user and/or the patient should report any serious product-related incident to both the manufacturer and the
Competent authority of the European Member State where the user and/or patient is established.
To view your operations or maintenance manual online, see https://techweb.stryker.com/.
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.
SSeerriiaall nnuummbbeerr llooccaattiioonn
A
FFiigguurree 66 –– SSeerriiaall nnuummbbeerr llooccaattiioonn
DDaattee ooff mmaannuuffaaccttuurree
The year of manufacture is the first four digits of the serial number.
EN 14 1115-309-001 Rev C.2

SSeettuupp
To unpack your product, see the unpacking instructions that are attached to the product inside of the shipping crate.
WWAARRNNIINNGG
• Always allow the product to reach room temperature before you set up the product or test 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.
Make sure that the product functions before you put the product into service.
1. Apply the brake. Push on the product to make sure that all four casters are locked.
2. Release the brake. Push on the product to make sure that all four casters are unlocked.
3. Raise and lower the litter with the hydraulic lift system.
4. Raise the product to the highest position and put the product in the Trendelenburg position (see
Positioning the product
in Trendelenburg
(page 18)). Make sure that the head end lowers to the full down position.
5. Raise the product to the highest position and put the product in the Reverse Trendelenburg position (see
Positioning the
product in Reverse Trendelenburg
(page 18)). Make sure that the foot end lowers to the full down position.
6. Apply BBiigg WWhheeeell and make sure that it is working.
7. Make sure that the siderails raise, lower, and lock in place.
8. Raise and lower the manual Fowler backrest (head end).
9. Raise and lower the manual Gatch (foot end).
For product with the electric lift or electric litter option:
1. Complete the setup checklist above.
2. Plug the product into a grounded, hospital grade wall outlet. Make sure that the LED lights illuminate on the lockout
keypad.
3. Make sure that each function on the optional siderail patient control panel works.
4. Make sure that each function on the optional foot end operator control panel works.
5. Raise and lower the electric Fowler backrest (head end).
6. Raise and lower the electric Gatch (foot end).
For product with the scale system option-electric litter option (with or without CChhaappeerroonnee option):
1. Complete the setup checklist above.
2. Charge the batteries (
Charging the scale system battery pack option - electric litter option or electric litter option with
Chaperone option - Prime only
(page 31)).
1115-309-001 Rev C.2 15 EN

OOppeerraattiioonn
AAppppllyyiinngg aanndd rreelleeaassiinngg tthhee bbrraakkeess
WWAARRNNIINNGG -- 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.
To apply the brakes, push down on the brake (red) side of the brake/steer pedal. Push on the product to make sure that the
brakes work.
To release the brakes, push down on the steer (green) side of the brake/steer pedal.
PPrriimmee bbaassee ccoonnttrroollss
kg
A
B
C
D
A
B
C
D
A
A
C
A
BD
FFiigguurree 77 –– PPrriimmee bbaassee ccoonnttrroollss aanndd llaabbeell
RRaaiissiinngg tthhee nnoonn--eelleeccttrriicc lliitttteerr
WWAARRNNIINNGG
• 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. 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.
CCAAUUTTIIOONN -- Do not use the hydraulics on the base to raise the product with a patient lift under the product.
EN 16 1115-309-001 Rev C.2