Stryker IsoTour Standard 2874 User manual

IIssooTToouurr™™ PPuummpp
OOppeerraattiioonnss MMaannuuaall
SSttaannddaarrdd aanndd pprreemmiiuumm
2874
EN
FR
2874-009-001 Rev B.0 2019/07

SSyymmbboollss
Refer to instruction manual/booklet
Operating instructions/Consult instructions for use
General warning
Caution
Cardiopulmonary resuscitation (CPR), disconnection point
Catalogue number

Serial number
Batch code
Manufacturer
Authorized representative in the European Community
European medical device
2797
CE mark
Mass of product
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.
Indicates that this product does not contain toxic and hazardous substances or elements above
the maximum concentration of all 6 values defined by the China RoHS legislation. This product is
an environmentally friendly product which can be recycled and reused.
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 provisions for protective earthing or reliance
upon installation conditions.
Type B applied part - 2872 IIssooTToouurr support surface
Fuse
2874-009-001 Rev B.0 EN

E347196
MEDICAL
ELECTRICAL
EQUIPMENT
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, IEC
60601-1-8:2012, and CAN/CSA-C22.2 No. 60601-1:16.
IIPP2211 Solids: Protection from touch by fingers and objects greater than 12 mm
Liquids: Protection from the fall of vertical water drops
 
For US Patents see www.stryker.com/patents
Keep dry
6
Do not stack more than 6 high
This side up
Fragile
Do not use sharp objects to open the package
EN 2874-009-001 Rev B.0

TTaabbllee ooff CCoonntteennttss
Symbols .............................................................................................................................................................1
Warning/Caution/Note Definition ....................................................................................................................2
Summary of safety precautions......................................................................................................................3
Introduction ..................................................................................................................................................4
Product description ................................................................................................................................4
Intended use..........................................................................................................................................4
Expected service life...............................................................................................................................4
Disposal/recycle.....................................................................................................................................4
Contraindications ...................................................................................................................................4
Specifications ........................................................................................................................................5
Environmental conditions .................................................................................................................5
Product illustration..................................................................................................................................6
Button and icon descriptions ...................................................................................................................6
Features................................................................................................................................................7
Contact information ................................................................................................................................7
Serial number ........................................................................................................................................8
Date of manufacture...............................................................................................................................8
Setup...........................................................................................................................................................9
Connecting the power cord .....................................................................................................................9
Connecting the hose...............................................................................................................................9
Operation...................................................................................................................................................10
Powering on the pump..........................................................................................................................10
Activating CPR release.........................................................................................................................11
Powering on or off Low Air Loss (LAL) ...................................................................................................11
Selecting TTrruuTTuurrnn................................................................................................................................11
Increasing or decreasing TTrruuTTuurrnn.........................................................................................................12
Pausing or canceling TTrruuTTuurrnn ..............................................................................................................13
Lock or unlock product functions ...........................................................................................................13
Powering off the pump..........................................................................................................................14
Accessories and parts.................................................................................................................................15
Troubleshooting..........................................................................................................................................16
Product alarms ...........................................................................................................................................17
Preventive maintenance..............................................................................................................................18
Cleaning and disinfecting with wipes ............................................................................................................19
Cleaning ....................................................................................................................................................20
Disinfecting ................................................................................................................................................21
EMC information.........................................................................................................................................22
2874-009-001 Rev B.0 1 EN

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.
EN 2 2874-009-001 Rev B.0

SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WWAARRNNIINNGG
• Consult the operations manual for the support surface before you attach the pump.
• Do not use in the presence of flammable anesthetics, nitrous oxide, or oxygen-rich environments. Risk of explosion can
result.
• Do not expose this product to liquids while powered as this could result in a severe electrical hazard.
• Always setup and use in accordance with the instructions to avoid harmful interference to other devices in the vicinity.
This product radiates radio frequency energy.
• Always make sure the hose is routed down and away from the patient. Avoid accidental patient contact at the foot end of
the support surface. Hose temperature may reach 48° C (118.4° F).
• Never transfer or transport a patient while TTrruuTTuurrnn is in use.
• Always raise the bed siderails before you begin TTrruuTTuurrnn, to avoid the risk of patient fall.
• Do not leave the patient unattended until TTrruuTTuurrnn of the patient position is complete.
• Do not modify or change this device. Service should only be completed by qualified personnel. Failure could result in
injury and void your warranty.
• Always unplug the product before you begin cleaning or disinfecting.
• Do not immerse the product in cleaning or disinfectant solutions.
• Do not spray or allow liquids to enter the power cord ports or the hose ports.
• Always make sure that you wipe each product with clean water and dry each product after you clean. Some cleaning
agents are corrosive in nature and may cause damage to the product. Failure to follow the cleaning and disinfecting
instructions may void your warranty.
• 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.
• Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should
be no closer than 12 inches (30 cm) to any part of IIssooTToouurr, 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.
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 allow the product to come to room temperature after exposure to extreme high or low temperatures.
• Always check the power cord for cuts, exposed wires, worn insulation, or other damage that could result in electrical
hazards.
• Do not over expose the product to higher concentration chemical solutions as these may degrade the product.
• Failure to follow manufacturing instructions may also affect useful life of the product.
2874-009-001 Rev B.0 3 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 Model 2874, IIssooTToouurr PPuummpp is an electric pump for use with the Stryker Model 2872, IIssooTToouurr Support Surface.
This pump provides Low Air Loss for the IIssooTToouurr standard or the premium support surface.
The pump, when connected to the premium support surface delivers the air to inflate and deflate the air bladders for the
TTrruuTTuurrnn function.
IInntteennddeedd uussee
The IIssooTToouurr PPuummpp is for use with the IIssooTToouurr support surface assists in the prevention and treatment of pressure injuries
or pressure ulcers (all stages, Unstageable injury, and Deep tissue injury). We recommend you implement this product in
combination with clinical evaluation of risk factors and skin assessments made by a healthcare professional.
This pump is for use with the IIssooTToouurr support surface in an acute care setting. This may include critical care, step down,
progressive care, med/surg, sub-acute care, and post anesthesia care unit (PACU), or other locations as prescribed by a
physician. Operators of this pump include healthcare professionals (such as nurses, nurse aids, or doctors).
This product is not intended to be sterile, does not include a measuring function, and is not for use in a home healthcare
environment.
EExxppeecctteedd sseerrvviiccee lliiffee
The IIssooTToouurr PPuummpp has a 5 year expected service life under normal use, conditions, and with appropriate periodic
maintenance.
The air hose has a 2 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 TTrruuTTuurrnn feature is not intended for use with patients that have unstable spine.
EN 4 2874-009-001 Rev B.0

NNoottee -- TTrruuTTuurrnn requires the IIssooTToouurr pump to be connected for use. The TTrruuTTuurrnn feature is visually identified by the icons
on the IIssooTToouurr pump (Figure 1).
FFiigguurree 11 –– TTrruuTTuurrnn iiccoonn
SSppeecciiffiiccaattiioonnss
Height 17.25 in. 43.8 cm
Width 9.25 in. 23.5 cm
Depth 7.25 in. 18.4 cm
Weight 16.3 lb 7.4 kg
Interface control panel LCD
Input voltage 100-240V 0.7 Amps
Input frequency 50/60 Hz
Noise level <50 dba
Mode of operation Continuous
Power cord Short 3.2 ft 1 m
Long 16.4 ft 5 m
Compliance IEC 60601-1 3.1 Edition; RoHS Directive 2002/95/EC
Reach; IEC 60601-1-8:2012, IEC 60601-1-2:2014
Compatible with bed frame IIssooTToouurr standard and
premium support surface
with an IIssooTToouurr pump
33000022 SS33™™,33000055 SS33™™,IInnTToouucchh™™,SSppiirriitt SSeelleecctt™™
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn
Ambient temperature
Relative humidity (non-condensing)
Atmospheric pressure
2874-009-001 Rev B.0 5 EN

Stryker reserves the right to change specifications without notice.
PPrroodduucctt iilllluussttrraattiioonn
C
L
I
K
A
B
C
E
F
D
G
H
J
AGraphical user interface GBack pump house
B Status indicators H Power inlet
CBumpers I Anti-vibration foot
DTransport handle JHose port
E Hooks K Hose
FHEPA filter LFront pump housing
BBuuttttoonn aanndd iiccoonn ddeessccrriippttiioonnss
The buttons are located on the outside of the graphical user interface.
IIccoonn NNaammee DDeessccrriippttiioonn
Power button See
Powering on the pump (page 10) or Powering off the pump
(page 14)
Cancel icon Cancel current function, returns to the main menu
Pause icon Pause current function
Action button, right User selects a function
Action button, left User selects a function
Lock or unlock icons See Lock or unlock product functions (page 13)
EN 6 2874-009-001 Rev B.0

IIccoonn NNaammee DDeessccrriippttiioonn
Back icon Returns to the previous screen
Low Air Loss (LAL) icon Low Air Loss function active, on by default, see Powering on or off
Low Air Loss (LAL)
(page 11)
Fill default segment 2 icon Select patient turn to the right or to the left
Maximum fill Maximum fill is 3 bars, see Increasing or decreasing TTrruuTTuurrnn
(page 12)
Decrease or increase Decrease or increase patient turn
Check siderails animated icon Reminder to check siderails before TTrruuTTuurrnn is activated
Check air connector alert icon Product detects air connector error
Kinked air hose alert icon Product detects a bend or twist in the air hose
Alarm off Closes and resets pump for kinked hose or check connector
FFeeaattuurreess
TTrruuTTuurrnn Available for the premium support surface. Air bladders inflate to rotate up to 30
degrees. Helps to off-load the sacrum. Turn angle can be customized per patient
tolerance and comfort.
Moisture management The top surface cover is designed to draw excess moisture away from the
patient’s skin and support surface interface.
Low Air Loss (LAL) Provides air flow to help manage microclimate of the skin.
Standard support surface Orange bottom cover, gel and foam core, LAL capable when connected to pump,
handles, and D-rings
Premium support surface Blue bottom cover, gel and foam core, spacer fabric for enhanced air flow,
handles, D-rings, anchor straps, TTrruuTTuurrnn and LAL capable when connected to
pump
CCoonnttaacctt iinnffoorrmmaattiioonn
Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
2874-009-001 Rev B.0 7 EN

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
A
DDaattee ooff mmaannuuffaaccttuurree
The year of manufacture is the first four digits of the serial number.
EN 8 2874-009-001 Rev B.0

SSeettuupp
Unpack the cartons and check all items. Make sure that the product operates before you place into service.
WWAARRNNIINNGG
• Consult the operations manual for the support surface before you attach the pump.
• Do not use in the presence of flammable anesthetics, nitrous oxide, or oxygen-rich environments. Risk of explosion can
result.
• Do not expose this product to liquids while powered as this could result in a severe electrical hazard.
• Always setup and use in accordance with the instructions to avoid harmful interference to other devices in the vicinity.
This product radiates radio frequency energy.
CCAAUUTTIIOONN
• Always allow the product to come to room temperature after exposure to extreme high or low temperatures.
• Always check the power cord for cuts, exposed wires, worn insulation, or other damage that could result in electrical
hazards.
1. Bring the product to room temperature.
2. Place the pump in a secure location. Allow space around the pump to connect and disconnect the hoses and power
cord. Optional placements:
a. Option 1: Hang the pump on a compatible bed. Make sure that the pump is secure.
b. Option 2: Place the pump on the floor. Make sure that the pump is away from foot traffic to avoid the risk of a trip
hazard. Do not place the pump in the path of lifting or lower mechanisms of the bed.
CCoonnnneeccttiinngg tthhee ppoowweerr ccoorrdd
1. Attach the power cord to the pump.
2. Plug the power cord into an accessible hospital grade receptacle.
CCoonnnneeccttiinngg tthhee hhoossee
WWAARRNNIINNGG -- Always make sure the hose is routed down and away from the patient. Avoid accidental patient contact at the
foot end of the support surface. Hose temperature may reach 48° C (118.4° F).
1. Attach the hose to the pump hose ports.
2. Open the hose port (A) on the support surface (Figure 2).
A
B C
FFiigguurree 22 –– HHoossee ccoonnnneeccttiioonn
3. Attach the hose to the support surface hose port. Make sure that rib (B) lines up with the red line on the hose (C).
2874-009-001 Rev B.0 9 EN

OOppeerraattiioonn
PPoowweerriinngg oonn tthhee ppuummpp
1. See Setup (page 9) to prepare the pump for operation.
2. Press the power button once. The startup screen will appear (Figure 3).
IsoTour
FFiigguurree 33 –– SSttaarrtt uupp ssccrreeeenn -- ooppeerraattoorr vviieeww
NNoottee -- The pump will detect either the standard or premium support surface.
3. The pump, on start up, pumps air into the left bladder to determine which compatible mattress is connected.
4. If the pump detects there are no turn bladders, the pump will show the standard software support surface display (Figure
4).
FFiigguurree 44 –– SSttaannddaarrdd ssooffttwwaarree ssuuppppoorrtt ssuurrffaaccee ddiissppllaayy
NNoottee -- TTrruuTTuurrnn is available for the premium support surface only.
5. If the pump detects there are turn bladders, the pump will show the premium software support surface display (Figure
5).
FFiigguurree 55 –– PPrreemmiiuumm ssooffttwwaarree ssuuppppoorrtt ssuurrffaaccee ddiissppllaayy
NNoottee -- TTrruuTTuurrnn is available for the premium support surface only.
EN 10 2874-009-001 Rev B.0

AAccttiivvaattiinngg CCPPRR rreelleeaassee
Remove the hose from the pump to deflate the support surface for CPR. Follow your hospital protocol for CPR.
PPoowweerriinngg oonn oorr ooffff LLooww AAiirr LLoossss ((LLAALL))
LAL is on by default. This function can be turned off or on.
1. Press the action button next to the active (green) LAL icon to turn off this function (Figure 6).
FFiigguurree 66 –– LLAALL oonn
2. Press the action button next to the inactive (white) LAL icon to turn on this function (Figure 7).
FFiigguurree 77 –– LLAALL ooffff
SSeelleeccttiinngg TTrruuTTuurrnn
WWAARRNNIINNGG
• Never transfer or transport a patient while TTrruuTTuurrnn is in use.
• Always raise the bed siderails before you begin TTrruuTTuurrnn, to avoid the risk of patient fall.
• Do not leave the patient unattended until TTrruuTTuurrnn of the patient position is complete.
1. Make sure you read the IIssooTToouurr support surface operations manual before you start TTrruuTTuurrnn.
2. Press the action button next to the patient left or patient right TTrruuTTuurrnn (Figure 8).
2874-009-001 Rev B.0 11 EN

FFiigguurree 88 –– TTrruuTTuurrnn
3. Raise the siderails (Figure 9).
00:30:00
02:00:00
00:00:15
FFiigguurree 99 –– CChheecckk ssiiddeerraaiill
4. Press the action button next to the time to set the turn duration.
• 02:00:00 = 2 hours
• 00:30:00 = 30 minutes
• 00:00:15 = 15 seconds
NNoottee
• Prior to transfer, transport, or other patient handling activity, cancel TTrruuTTuurrnn function. You can either cancel the
TTrruuTTuurrnn function, turn off the pump, or pull the CPR.
• The support surface will turn up to 30 degrees.
• The count down for the time selected will start after the pump has completed the fill.
IInnccrreeaassiinngg oorr ddeeccrreeaassiinngg TTrruuTTuurrnn
After TTrruuTTuurrnn has reached the default angle fill, you can increase or decrease the turn.
To increase the turn, press and hold the action button next to the up arrow.
EN 12 2874-009-001 Rev B.0

29:59
FFiigguurree 1100 –– IInnccrreeaassee oorr ddeeccrreeaassee ttuurrnn
To decrease the turn, press and hold the action button next to the down arrow.
NNoottee -- The increase and decrease arrows turn green when active.
PPaauussiinngg oorr ccaanncceelliinngg TTrruuTTuurrnn
You can only pause TTrruuTTuurrnn when the pump fills the support surface with air. You can cancel TTrruuTTuurrnn at any time.
To pause TTrruuTTuurrnn, press the action button next to the pause icon .
00:30:00
FFiigguurree 1111 –– TTrruuTTuurrnn ffiillll
To cancel TTrruuTTuurrnn, press the action button next to the cancel icon . The turn bladder deflates and returns the surface
to a flat position.
29:59
FFiigguurree 1122 –– AAccttiivvee TTrruuTTuurrnn
LLoocckk oorr uunnlloocckk pprroodduucctt ffuunnccttiioonnss
The lock icon is orange and closed when active.
To turn the lock on or off:
1. Press and hold the unlock icon for 1 second to turn on the lock.
2874-009-001 Rev B.0 13 EN

FFiigguurree 1133 –– UUnnlloocckkeedd
2. Press and hold the lock icon for 2 seconds to turn off the lock.
FFiigguurree 1144 –– LLoocckkeedd
NNoottee -- When the lock is active, the other functions are not available.
PPoowweerriinngg ooffff tthhee ppuummpp
Press the power button and hold for 2 seconds to power off the pump.
NNoottee
• The turn bladder deflates and returns to a flat position.
• Allow the support surface to deflate before you unplug the power cord.
• For optional deflation, remove the CPR plug from the support surface.
EN 14 2874-009-001 Rev B.0

AAcccceessssoorriieess aanndd ppaarrttss
These accessories may be available for use with your product. Confirm availability for your configuration or region.
NNaammee PPaarrtt nnuummbbeerr
IIssooTToouurr air hose 2874-001-200
2874-009-001 Rev B.0 15 EN

TTrroouubblleesshhoooottiinngg
PPrroobblleemm SSccrreeeenn CCaauussee RReeccoommmmeennddeedd aaccttiioonn
Kinked air hoses Air hose is bent or an
obstruction in the hose may
cause air flow to be
compromised
TTrruuTTuurrnn was attempted but
you have a standard Model
(bottom cover is orange).
1. Make sure the hoses are
straight and air flow is not
obstructed.
2. Press the action button
next to the Alarm off icon
to reset the pump.
Contact sales support for
TTrruuTTuurrnn option
Missed connection with air
hoses Air hoses is not connected
to the pump or the support
surface
1. Make sure that the hoses
are seated all the way
onto the hose ports on
the pump or the support
surface.
2. Press the action button
next to the Alarm off icon
to reset the pump.
Power loss, product does
not turn on Power cord not seated, power cord unplugged from
outlet, or possible internal
damage
Make sure the power cord is
plugged into the product and
the outlet.
Power loss, while TTrruuTTuurrnn
is in use Unintentional or intentional
power loss. Turn bladder is
inflated.
Pull the hose from the pump
or the support surface to
activate CPR. The bladder
deflates and returns the
support surface to a flat
position.
Button not responsive
29:59
Lock function active Press and hold the action
button next to the locked icon
for 2 seconds to turn off the
lock.
TTrruuTTuurrnn not shown on
screen Graphical user interface is
for the standard model, not
connected to a premium
IIssooTToouurr bottom cover with
anchor straps
Check for kinked hoses.
Verify that you have premium
bottom cover (black).
Contact sales support for
TTrruuTTuurrnn option
TTrruuTTuurrnn shown on screen Graphical user interface
shows TTrruuTTuurrnn but you
have a standard Model
(bottom cover is orange).
Turn off the pump to reset
the pump features. Make
sure the air hose is
connected before you turn
the pump on.
EN 16 2874-009-001 Rev B.0