Stryker Xpedition 625700000000 Manual

XXppeeddiittiioonn™™ PPoowweerreedd SSttaaiirr CChhaaiirr
OOppeerraattiioonnss//MMaaiinntteennaannccee MMaannuuaall
625700000000
625705550001
625705550002
650700080301
650700450301
EN
6257-009-001 Rev AF.1 2023-03

SSyymmbboollss
Refer to instruction manual/booklet
Consult instructions for use
General warning
Caution
Warning; crushing of hands
Warning; non-ionizing radiation
No pushing
China RoHS without declarable substances
China RoHS with declarable substances
No stepping
CE mark
UK Conformity Assessment mark
Importer
Unique device identifier
Authorized representative in the European Community
REPCH
Authorized representative in Switzerland
6257-009-001 Rev AF.1 EN

European medical device
Catalogue number
Lot (batch) code

Serial number
 
For US Patents see www.stryker.com/patents
Manufacturer
Date of manufacture
Mass of equipment with safe working load
Safe working load
Type BF 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 ES60601-1:2012 and CAN/
CSA-C22.2 No. 60601-1:14.
Direct current
~
Alternating current
Class II electrical equipment: equipment in which protection against electric shock does not rely
on basic insulation only, but in which additional safety precautions such as double insulation or
reinforced insulation are provided, there being no provision for protective earthing or reliance
upon installation conditions.
Dangerous voltage
IIPP3366 Ingress protection rating
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.
The Rechargeable Battery Recycling Corporation (RBRC) is a non-profit, public service
organization that promotes the recycling of portable rechargeable batteries. Batteries must be
delivered to a battery collection site. Visit the RBRC website (www.rbrc.org) to find a nearby
collection site or call the phone number shown on the recycling symbol.
Two person lift
This way up
EN 6257-009-001 Rev AF.1

Fragile, handle with care
Keep dry
Stacking limit by number
Battery terminal identification (D - data (SMBus data line), C-clock (SMBus clock line), T- T-Pin
or temperature, - negative terminal, + positive terminal)
2800 mAh/71.68 Wh Battery capacity and duration
< 1m > 4m
Chair duty cycle
U.S.A.
English text below this symbol is intended for USA audiences only
Distributed by in the US
MMAADDEE IINN UU..SS..AA.. Product made in the United States of America
Box manufacturer’s certificate
5019398
The AAllvvaarriiuumm charger complies with the requirements of UL 62368-1:2019 Ed. 3 and CSA
C22.2#62368-1:2019 Ed. 3 for audio/video, information and communication technology
equipment, The AAllvvaarriiuumm battery complies with the requirements of UL 62133-2:2020 Ed. 1 and
CSA C22.2#62133-2:2020 Ed. 1 for secondary lithium battery systems.
The AAllvvaarriiuumm battery complies with the requirements of UL 62133-2:2020 Ed. 1 and CSA
C22.2#62133-2:2020 Ed. 1 for secondary lithium battery systems.
Main patient containment system (PCS) restraint straps
6257-009-001 Rev AF.1 EN

TTaabbllee ooff CCoonntteennttss
Warning/Caution/Note Definition ..............................................................................................................................3
Summary of safety precautions ................................................................................................................................3
Introduction ...............................................................................................................................................................6
Product description .................................................................................................................................................6
Indications for use...................................................................................................................................................6
Intended users........................................................................................................................................................6
Clinical benefits ......................................................................................................................................................6
Contraindications....................................................................................................................................................7
Expected service life ...............................................................................................................................................7
Disposal/recycle .....................................................................................................................................................7
Specifications - Xpedition ........................................................................................................................................7
European REACH - Xpedition .............................................................................................................................8
Specifications - Alvarium .........................................................................................................................................9
European REACH - Alvarium ............................................................................................................................10
China RoHS - Alvarium.....................................................................................................................................10
Product illustration - Xpedition................................................................................................................................11
Product illustration - Alvarium.................................................................................................................................12
Contact information...............................................................................................................................................12
Serial number location - Xpedition ..........................................................................................................................13
Serial number location - Alvarium...........................................................................................................................13
Date of manufacture..............................................................................................................................................13
Setup.......................................................................................................................................................................14
Operation ................................................................................................................................................................15
Operating guidelines .............................................................................................................................................15
User controls and LED indicators ...........................................................................................................................16
Checking the battery power level............................................................................................................................17
Unfolding the chair ................................................................................................................................................18
Folding the chair ...................................................................................................................................................18
Inserting the battery ..............................................................................................................................................19
Removing the battery from the product ...................................................................................................................19
Storing the battery.................................................................................................................................................20
Charging the battery..............................................................................................................................................20
Electrical power requirements................................................................................................................................21
Charger setup.......................................................................................................................................................21
Securing the charger mounting plate option ............................................................................................................21
Securing the charger to the charger mounting plate option .......................................................................................22
Powering the charger ............................................................................................................................................23
Disconnecting the charger .....................................................................................................................................24
Transferring the patient to the chair ........................................................................................................................24
Proper lifting techniques ........................................................................................................................................24
Securing the patient with the PCS restraint straps....................................................................................................24
Attaching the chest/waist restraint straps............................................................................................................25
Attaching the ankle restraint strap ..........................................................................................................................28
Attaching the head restraint strap option .................................................................................................................29
Transporting the patient on flat surfaces .................................................................................................................29
Transporting the patient down stairs .......................................................................................................................30
Transporting the patient up stairs ...........................................................................................................................31
Applying or releasing a wheel lock..........................................................................................................................32
Raising or lowering the head end flip-up carry handles option...................................................................................32
Supporting the patient’s feet with the footrest option ................................................................................................33
Positioning operators and helpers for additional assistance ......................................................................................33
Attaching the IV hook option ..................................................................................................................................35
Attaching the oxygen bottle holder option................................................................................................................35
Accessories and parts ............................................................................................................................................37
6257-009-001 Rev AF.1 1 EN

Cleaning the product...............................................................................................................................................39
Cleaning the track frame........................................................................................................................................39
Cleaning the charger.............................................................................................................................................40
Cleaning the battery ..............................................................................................................................................40
Disinfecting the product ..........................................................................................................................................41
Preventive maintenance .........................................................................................................................................42
Regular inspection and adjustments .......................................................................................................................43
EMC information .....................................................................................................................................................44
EN 2 6257-009-001 Rev AF.1

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
• This product can expose you to chemicals including Nickel, which is known to the State of California to cause cancer,
and Bisphenol A (BPA), which is known to the State of California to cause birth defects or other reproductive harm. For
more information go to www.P65Warnings.ca.gov.
• Always use all restraint straps to secure the patient on the product. An unrestrained patient may fall from the product and
be injured.
• Do not apply a wheel lock when you move the product to avoid the risk of tipping.
• Always avoid getting dirt or other obstructions inside the track frame. The track system may not work the same on all
stair surfaces and in all environmental conditions. Based on conditions, you may encounter varying amounts of
resistance.
• Always clean and dry the track belts before stair transport.
• Always clear the path or consider an alternate route to avoid injury. Condensation, water, ice, or debris on the stairs can
affect operator footing and proper operation of the track system and cause unpredictable performance that results in a
sudden change in the weight that the operators must support.
• Do not attempt to transport patient loads greater than what you can safely lift.
• Always clear any obstacles that may interfere and cause injury to the operator or patient before you operate the product.
• Always inspect the product for damage if involved in an ambulance accident. Contact Stryker Customer Service or
Technical Support for more information.
• Always hold onto the grab bar while you extend the tracks. The product is less stable when unoccupied.
• Do not drive the product on winding stairs. Use the carry handles to manually transport the product up and down winding
stairs.
• Do not stand on the footrest option. The footrest option is not intended to support the weight of a standing operator or
patient.
• Always avoid accidental patient contact with the user controls. User control temperature may reach 118.4° F (48° C)
after ten minutes of operation.
• Do not operate if the product is behaving abnormally or erratically.
• Always make sure that the product is locked in the unfolded position before use. An unlocked product may fold during
use. If you accidentally activate the fold-release mechanism, pull back on the product until locked in place.
• Do not remove the battery when the product is active.
• Do not attempt to open the battery pack for any reason to avoid the risk of electric shock. If the battery pack case is
cracked or damaged, do not insert the case into the charger. Return damaged battery packs to a service center for
recycling.
• Always avoid direct contact with a wet battery or battery enclosures. Contact may cause injury to the patient or operator.
• Do not insert a cracked or damaged battery into the charger. Return damaged batteries to a service center for recycling.
6257-009-001 Rev AF.1 3 EN

• Do not connect AC and DC power supplies to the battery at the same time to avoid the risk of fire or electric shock.
• Always have a certified mechanic, familiar with ambulance vehicle construction, secure the charger mounting plate
option and charger.
• Always make sure that the charger mounting plate option is secured to the surface before use.
• Do not use the product to transport patients who have suspected spinal injuries.
• Do not leave a patient unattended. Hold the product while a patient is on the product.
• Always make sure that patient belongings do not interfere with the user interface and track system.
• Do not transfer the patient to or from the product while on uneven surfaces, if possible. Transfer the patient while the
product is on flat surfaces to avoid the risk of tipping.
• Do not push the product with the grab bar in the fully extended position. Pushing the product with the grab bar in the fully
extended position may cause the product to tip when you encounter obstacles.
• Do not press the GO button while transporting on flat surfaces to avoid operator or patient injury.
• Always transport the patient on stairs with a minimum of two trained operators. Additional operators are recommended
for patients who weigh more than 250 pounds.
• Always lock the carry handles in position before you use the carry handles to lift or tip the product back.
• Always lock the track system in position before you transport a patient.
• Do not install or apply a wheel lock on a product with worn wheels.
• Always apply both wheel locks.
• Always clean and disinfect or dispose of contaminated product components to avoid risk of exposure to bloodborne
pathogens and injury to the patient or operator.
• Always secure the oxygen bottle and oxygen bottle accessories so they do not interfere with the operation of the
product.
• Always follow these cleaning and disinfecting guidelines, in addition to your protocols, to maintain hygienic safety.
• Always use any appropriate personal protective equipment while power washing to avoid inhaling contagion. Power
washing equipment may aerate contamination.
• Always wear rubber gloves, in addition to personal protective equipment, when cleaning the battery to reduce the risk of
injury.
• Always disconnect the charger from the wall outlet before cleaning to avoid the risk of electrical hazards.
• Do not spray fluid directly onto the charger.
• Do not power wash the charger.
• Do not use solvents, lubricants, or other chemicals to clean the charger unless otherwise directed.
• Do not immerse the charger in liquid or allow liquid to collect on top of the charger to avoid the risk of electric shock.
• Always use only non-conductive materials to wipe the battery.
• Always avoid excessive water exposure to the battery terminals.
• Do not directly handle or make contact with the battery terminals while cleaning to avoid the risk of injury.
• Do not immerse the battery in liquid or allow liquid to collect on top of the battery to avoid the risk of electric shock.
• Do not use solvents, lubricants, or other chemicals to clean the battery unless otherwise directed.
• Do not power wash the battery.
• Do not use portable RF communications equipment, including peripherals such as antenna cables and external
antennas, closer than 12 inches (30 cm) to any part of XXppeeddiittiioonn, including cables specified by the manufacturer.
• Always avoid stacking or placing other equipment adjacent to XXppeeddiittiioonn to prevent improper operation of the products. If
such use is necessary, carefully observe the chair and the other equipment to verify proper operation.
• Do not use accessories, transducers, and cables, other than those specified or provided by the manufacturer, to avoid
increased electromagnetic emissions or decreased electromagnetic immunity and improper operation.
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.
• Always use caution when you operate the product on stairs with condensation, water, or ice. Smooth tracks may have
reduced traction in these conditions. Grooved tracks are recommended if you regularly operate the product in cold
weather.
EN 4 6257-009-001 Rev AF.1

• Always use caution if you store the product at temperatures < 14° F (-10° C) or > 113° F (45° C). Drive speed may revert
to the low setting at these temperatures.
• Always remove the battery if you do not intend to use the product for more than 24 hours or longer.
• Always place the electrical charger power cord where it will not be stepped on, tripped over, or otherwise subjected to
damage or stress.
• Do not touch the battery receptacle terminals with metal objects.
• Always grasp and pull the plug, not the cord, when you disconnect the charger to avoid the risk of damage to the
electrical plug and cord.
• Always store excess restraint strap material to avoid the risk of tripping.
• Always check for and remove any debris in the casters before transport.
• Always release the red track release bar before you click the track system into the locked position. Try to fold the track
system by pushing down and pulling up on the black cross tube before use. Make sure that both sides of the track
system lock in the extended position.
• Do not load IV hook above the safe working load of 5 lb (2.3 kg).
• Always secure the oxygen bottle in the oxygen bottle holder. Make sure that the regulator valve of the oxygen bottle
does not protrude from the width of the product.
• Always remove the oxygen bottle from the oxygen bottle holder before you attempt to fold or store the product.
• Always use only D-size or JD-size oxygen bottles with the oxygen bottle holder.
• Always remove the battery before you wash the product.
• Do not clean, service, or perform maintenance while the product is in use.
• Do not steam clean or ultrasonically clean the product.
• Do not exceed 180 °F (82 °C) as the maximum water temperature.
• Do not exceed 1500 psi (103.4 bar) as the maximum water pressure. If you are using a hand held wand to wash the
product, keep the pressure nozzle at a minimum of 24 in. (61 cm) from the product.
• Always use authorized parts to avoid the risk of product damage.
• Changes or modifications to the AAllvvaarriiuumm Battery Management System, not expressly approved by Stryker, could void
the user's authority to operate the equipment.
6257-009-001 Rev AF.1 5 EN

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 XXppeeddiittiioonn™ Powered Stair Chair is a seated patient transport device with handles and a powered belt and
track system. The chair is designed to support and transport a maximum weight of 500 lb (227 kg) up and down stairs. The
chair is intended for patients who weigh 50 lb (23 kg) or more and can remain seated in the chair while secured by patient
restraint straps. Handles at the head and foot ends allow operators to control the chair during powered or manual ascent or
descent on stairs. Operators can push and maneuver the chair over various types of terrain that are expected in
commercial and residential environments, as well as lift patients over obstacles. The chair has a removable patient
containment system (PCS) with attachment points for the chest and waist to secure a patient during transport. A fold-out
footrest can be deployed for secure feet placement. A removable, rechargeable battery powers electrical functions
including the motorized drive system for traversing stairs, speed selection, direction selection, ground lighting activation,
battery capacity feedback, drive activation buttons, and LED visual feedback networks. User interfaces at the back of the
chair and the top handle allow for drive system control. The chair has several mechanical activations including wheel locks
to prevent unintended motion on ground, a latch to fold or unfold the chair, a track deployment mechanism to deploy the
stair driving track system, and top and bottom handle length adjustment activations. Options include a footrest, head end
flip-up carry handles, grooved tracks, head restraint, IV clip, and oxygen bottle holder.
AAllvvaarriiuumm™ Battery Management System is comprised of a lithium iron phosphate battery pack and a universal charger.
The rechargeable battery acts as a power source for the XXppeeddiittiioonn chair.
IInnddiiccaattiioonnss ffoorr uussee
XXppeeddiittiioonn transports a patient with a mobility-limiting medical condition or injury, who is physically able to maintain a seated
position while restrained, up or down a set of stairs. XXppeeddiittiioonn is intended for use in residential and commercial
environments including pre-hospital and hospital environments, emergency, and non-emergency applications. All
operators, including healthcare professionals such as emergency medical service personnel and medical first responders,
must be trained by a qualified trainer before product use.
IInntteennddeedd uusseerrss
Operators of this product include trained healthcare professionals such as emergency medical service personnel and
medical first responders.
CClliinniiccaall bbeenneeffiittss
Transport patients up and down stairs
EN 6 6257-009-001 Rev AF.1

CCoonnttrraaiinnddiiccaattiioonnss
The use of XXppeeddiittiioonn is contraindicated for patients who have suspected spinal injuries.
EExxppeecctteedd sseerrvviiccee lliiffee
XXppeeddiittiioonn has a 7 year expected service life under normal use conditions and with appropriate periodic maintenance.
AAllvvaarriiuumm charger has a 7 year expected service life under normal use conditions.
AAllvvaarriiuumm battery has a 2 year expected service life under normal use conditions.
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.
SSppeecciiffiiccaattiioonnss -- XXppeeddiittiioonn
NNoottee -- Safe working load includes weight of the patient,
equipment, and accessories.
500 lb 227 kg
Height 37.5 in. 95.25 cm
Maximum height 56.7 in. 144 cm
Width 20.5 in. 52 cm
Seat pan width 19.6 in. 49.8 cm
Depth 25 in. 63.5 cm
Folded depth 8 in. 20.32 cm
Folded length 37.5 in. 95.25 cm
Folded width 20.5 in. 52 cm
Foot end carry handle stowed length 25 in. 63.5 cm
Minimum stair width 24 in. 60.96 cm
Minimum landing length (for U-shaped stairs) 3.28 ft 1 m
Maximum slope uphill 11.6°
Maximum slope downhill 8.2°
Maximum permissible slope of upper and lower landings 10°
Maximum pitch of stairs 45°
Maximum speed for transporting up and down stairs 71 steps/minute
Maximum direct operating force 208.5 N
Front wheel diameter 5 in. 127 mm
6257-009-001 Rev AF.1 7 EN

Back wheel diameter 8 in. 203 mm
Patient tip back angle on stairs 24°
WWeeiigghhtt
Chair 52.7 lb 23.9 kg
Patient containment system (PCS) 1.25 lb 0.57 kg
Battery 2.15 lb 0.98 kg
CCoommppoonneenntt wweeiigghhtt
Footrest 1.35 lb 0.61 kg
Head end flip-up carry handles 2.65 lb 1.20 kg
SSttaannddaarrddss
ISO 7176 XXppeeddiittiioonn has been successfully tested according to the
standard ISO 7176-28:2012. As classified in Annex A,
XXppeeddiittiioonn is classified as a Type A, assistant-operated,
self-standing stair-climbing chair.
PPoowweerr ssyysstteemm
Battery (650700080301) 25.6 VDC LiFePO4
Charger (650700450301) 100-240 VAC, 50/60 Hz, 1A
12-34 VDC, 5A
Stryker reserves the right to change specifications without notice.
The yellow and black color scheme is a proprietary trademark of Stryker Corporation.
Labels may be unreadable from a viewing distance greater than 12 inches.
EEnnvviirroonnmmeennttaall ccoonnddiittiioonn OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn
Temperature
130 °F
(54.5 °C)
-30 °F
(-34.5 °C)
149 °F
(65 °C)
-40 °F
(-40 °C)
Relative humidity
95%
10%
95%
10%
Atmospheric pressure
1060 hPa
620
1060 hPa
500
EEuurrooppeeaann RREEAACCHH -- XXppeeddiittiioonn
In accordance with the European REACH regulation and other environmental regulatory requirements, the components that
contain declarable substances are listed.
EN 8 6257-009-001 Rev AF.1

DDeessccrriippttiioonn NNuummbbeerr SSuubbssttaannccee ooff vveerryy hhiigghh ccoonncceerrnn
((SSVVHHCC)) cchheemmiiccaall nnaammee
Backdrive PCBA 625700010057 Lead, lead oxide
Battery cable 625700010001 Lead, lead compounds, brominated
flame retardants, antimony flame
retardants, antimony trioxide, chlorinated
flame retardants, PVC, phthalates
Powder coat, black JN156QF Silica, crystalline, carbon black
Powder coat, red EG126QF Titanium dioxide, silica, crystalline
Powder coat, yellow JE032QF Titanium dioxide
Powerbox PCBA 625700010009 Lead, brominated flame retardants,
PVC, PVC copolymers, antimony
trioxide, phthalates
UI module backrest, patient left 625700110200 Lead, carbon black, nickel, antimony
oxide, PVC, PVC copolymers
UI module backrest, patient right 625700110100 Lead, carbon black, nickel, antimony
oxide, PVC, PVC copolymers
UI module, grab bar 625700050020 Lead, carbon black, nickel, antimony
oxide, PVC, PVC copolymers
SSppeecciiffiiccaattiioonnss -- AAllvvaarriiuumm
WWAARRNNIINNGG -- This product can expose you to chemicals including Nickel, which is known to the State of California to cause
cancer, and Bisphenol A (BPA), which is known to the State of California to cause birth defects or other reproductive harm.
For more information go to www.P65Warnings.ca.gov.
CChhaarrggeerr ((665500770000445500330011)) BBaatttteerryy ((665500770000008800330011))
Electrical input 12-34 VDC, 5A Not applicable
Electrical output Not applicable 25.6 VDC LiFePO4
Height 6.09 in. 154.69 mm 3.62 in. 91.95 mm
Width 4.46 in. 113.28 mm 3.18 in. 80.77 mm
Length 7.79 in. 197.87 mm 6.05 in. 153.67 mm
Weight 1.55 lb 0.70 kg 2.15 lb 0.98 kg
Enclosure protection Not applicable IP36
Standards IEC 62368 IEC 62133-2, IEC 60529: IP36, SAE J3043
6257-009-001 Rev AF.1 9 EN

EEnnvviirroonnmmeennttaall ccoonnddiittiioonn OOppeerraattiioonn CChhaarrggiinngg SSttoorraaggee aanndd
ttrraannssppoorrttaattiioonn
Temperature
104 °F
(40 °C)
32 °F
(0 °C)
104 °F
(40 °C)
50°F
(10 °C)
140 °F
(60 °C)
-4 °F
(-20 °C)
Relative humidity
75%
30%
75%
30%
75%
10%
Atmospheric pressure
1060 hPa
700
1060 hPa
700
1060 hPa
500
Specifications are approximate and may vary from product to product or as a result of power supply fluctuations.
EEuurrooppeeaann RREEAACCHH -- AAllvvaarriiuumm
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
Battery charger assembly 650700450301 Lead, lead compounds, diboron trioxide,
bisphenol A (BPA), antimony oxide
(antimony trioxide)
Battery charger PCBA 650700080820 Lead, diboron trioxide
12 VDC cable, automotive 6500-201-247 Lead, fatty acids, C16-18, lead salts,
diarsenic pentaoxide
CChhiinnaa RRooHHSS -- AAllvvaarriiuumm
DDeessccrriipp--
ttiioonn NNuummbbeerr
HHaazzaarrddoouuss ssuubbssttaanncceess
LLeeaadd ((PPbb)) MMeerrccuurryy
((HHgg))
CCaaddmmiiuumm
((CCdd))
HHeexxaavvaalleenntt
cchhrroommiiuumm
((CCrr ((VVll))))
PPoollyybbrroommii--
nnaatteedd
bbiipphheennyyllss
((PPBBBB))
PPoollyybbrroommii--
nnaatteedd
ddiipphheennyyll
eetthheerrss
((PPBBDDEE))
Battery
charger
PCBA
650700080-
820
O X X X X X
This table is prepared in accordance with the provisions of SJ/T 11364.
O: Indicates that said hazardous substance contained in all of the homogenous materials used for this part is below the
limit requirement of GB/T 26572.
X: Indicates that said hazardous substance contained in at least one of the homogenous materials used for this part is
above the limit requirement of GB/T 26572.
Enterprises may further provide in this box technical explanation for marking “X” based on their actual circumstances.
EN 10 6257-009-001 Rev AF.1

PPrroodduucctt iilllluussttrraattiioonn -- XXppeeddiittiioonn
C
DE
F
G
H
I
K
L
M
N
O
J
A
B
FFiigguurree 11 –– XXppeeddiittiioonn
A Grab bar I PCS cam
BHead end flip-up carry handle (option) J Red twist knob
CTrack system K Fold-release handle
DFoot end carry handle L Red track release bar
EFootrest (option) MBattery release latch
F Back wheel N Wheel lock
GUser interface (UI) O Caster
H GO button
6257-009-001 Rev AF.1 11 EN

PPrroodduucctt iilllluussttrraattiioonn -- AAllvvaarriiuumm
C
A
BD
EF
FFiigguurree 22 –– AAllvvaarriiuumm
ABattery
BBattery indicator button
CCharger
DBattery release button
EAC power cord
FDC power cord
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.
EN 12 6257-009-001 Rev AF.1

SSeerriiaall nnuummbbeerr llooccaattiioonn -- XXppeeddiittiioonn
See below for the chair (A) serial number location (Figure 3).
A
FFiigguurree 33 –– SSeerriiaall nnuummbbeerr llooccaattiioonn -- XXppeeddiittiioonn
SSeerriiaall nnuummbbeerr llooccaattiioonn -- AAllvvaarriiuumm
See below for the battery (B) and charger (C) serial number locations (Figure 4 and Figure 5).
B
FFiigguurree 44 –– AAllvvaarriiuumm bbaatttteerryy sseerriiaall nnuummbbeerr llooccaattiioonn
C
FFiigguurree 55 –– AAllvvaarriiuumm cchhaarrggeerr sseerriiaall nnuummbbeerr llooccaattiioonn
DDaattee ooff mmaannuuffaaccttuurree
The year of manufacture is the first 2 digits of the serial number.
6257-009-001 Rev AF.1 13 EN

SSeettuupp
During setup, unpack the cartons and check all items for proper operation. Make sure that the product operates before you
place it into service.
Remove all the shipping and packaging materials from the product before use.
The vehicle patient compartment where the product will be used must be large enough to accommodate the folded
dimensions of the product.
When necessary, modify the vehicle to fit the product. Do not modify the product.
EN 14 6257-009-001 Rev AF.1