Stryker IsoAir 2941 User manual

IIssooAAiirr®® SSyysstteemm
OOppeerraattiioonnss MMaannuuaall
2941
EN
FR
2941-009-001 Rev B.0 2020/05

SSyymmbboollss
Refer to instruction manual/booklet
Consult instructions for use
General warning
Caution
Cardiopulmonary resuscitation (CPR)
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.
Type B applied part, support surface
Catalogue number

Serial number
Batch code
Manufacturer
European medical device
Authorized representative in the European Community
2797
CE mark
Mass of product
Safe working load
Wash by hand
Do not tumble dry
Do not dry clean
2941-009-001 Rev B.0 EN

Do not iron
Allow to air dry
Chlorinated bleach
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.
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.
Fuse
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 and CAN/
CSA-C22.2 No. 60601-1:16. IEC 60601-1-8:2012
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
Stacking limit by number
This side up
Fragile
Do not use sharp objects to open the package
EN 2941-009-001 Rev B.0

TTaabbllee ooff CCoonntteennttss
Warning/Caution/Note Definition ....................................................................................................................2
Summary of safety precautions ...............................................................................................................2
Introduction ..................................................................................................................................................4
Product description ................................................................................................................................4
Intended use..........................................................................................................................................4
Clinical benefits......................................................................................................................................4
Expected service life...............................................................................................................................4
Disposal/recycle.....................................................................................................................................5
Contraindications ...................................................................................................................................5
Specifications ........................................................................................................................................5
IIssooAAiirr 84 in. (213.3 cm) system........................................................................................................5
Environmental conditions .................................................................................................................6
Product illustration - support surface........................................................................................................6
Product illustration - pump................................................................................................................8
Features .........................................................................................................................................8
Button and icon descriptions ...................................................................................................................9
Contact information ..............................................................................................................................11
Serial number location ...................................................................................................................11
Date of manufacture ......................................................................................................................12
Setup.........................................................................................................................................................13
Setup the support surface .....................................................................................................................13
Setup the pump....................................................................................................................................13
Connecting the power cord.............................................................................................................14
Applying linens..............................................................................................................................14
Operation...................................................................................................................................................15
Powering on the pump..........................................................................................................................15
Transferring a patient from one patient support platform to another ..........................................................15
CPR....................................................................................................................................................16
Starting or canceling Max Inflate............................................................................................................16
Starting the static mode without AST .....................................................................................................17
Starting the ALP mode without AST.......................................................................................................19
Starting or stopping the AST mode ........................................................................................................20
Turning the LAL on or off.......................................................................................................................21
Locking or unlocking the screen ............................................................................................................21
Powering off the pump..........................................................................................................................22
Storing the support surface ...................................................................................................................22
Storing the pump..................................................................................................................................23
Troubleshooting..........................................................................................................................................24
Product alarms ...........................................................................................................................................26
Accessories and parts.................................................................................................................................27
Preventive maintenance..............................................................................................................................28
Cleaning and disinfecting with wipes ............................................................................................................29
Cleaning ....................................................................................................................................................30
Disinfecting ................................................................................................................................................31
Top cover replacement................................................................................................................................32
Fire barrier replacement........................................................................................................................32
EMC information.........................................................................................................................................33
2941-009-001 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.
SSuummmmaarryy ooff ssaaffeettyy pprreeccaauuttiioonnss
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WWAARRNNIINNGG
• Always secure the support surface to the bed frame to prevent the shifting of the product while in use.
• Always inspect for foreign objects between the support surface and the bed frame. Foreign objects may cause the
support surface to slide on the support platform.
• Do not use the support surface on a larger or smaller bed frame that does not fit the width, length, or thickness. This is to
avoid the risk of the support surface sliding, patient injury, or interference with moving parts of the bed.
• Do not use the support surface when gaps are present. The risk of entrapment can develop when the support surface is
placed on incompatible bed frames.
• Always plug the power cord into the bed auxiliary outlet or a grounded power respectable. Do not use an extension cord.
• Do not touch patients and the AST socket on the pump at the same time.
• Always secure the pump to the bed frame to prevent the shifting of the product while in use.
• Always check the product before use to make sure there are no broken parts. If the product is damaged call technical
support.
• Always make sure that you do not exceed the safe working load of the bed frame before you mount the pump.
• Always connect the AST cable to the AST socket on the pump to avoid the risk of electrical shock.
• 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.
• This product radiates radio frequency energy. If not setup and used in accordance with the instructions, may cause
harmful interference to other devices in the vicinity.
• Always check patient’s skin regularly. Consult a physician if erythema or skin breakdown occurs. Serious injury could
result if the patient’s skin condition is left untreated.
• Do not use this product with an overlay. Patient stability and siderail coverage may be compromised.
• Always consider the use of siderails. The safe use of the support surface is maximized when used in conjunction with
siderails. There may be an increased risk of falls when siderails are not present. Serious injury or death can result from
the use (potential entrapment) or non-use (potential patient falls) of siderails or other restraints. Consider local policies
regarding the use of siderails. The physician, operator, or responsible parties should determine whether and how to use
siderails based on each patient’s individual needs.
• Always use extra caution with a patient at risk of a fall (such as agitated or confused) to help reduce the likelihood of a
fall.
• Do not use the support surface as a transfer device.
• Do not use the support surface handles to lift or move the support surface with a patient on board.
• Do not stick needles or other sharp objects into a support surface through the support surface cover. Holes may allow
fluids to enter the inside (inner core) of the support surface, product damage, or product malfunction.
EN 2 2941-009-001 Rev B.0

• Do not exceed the safe working load of the hospital bed frame when supporting both the patient and the support surface.
Excess weight could cause unpredictable safety and performance of this product.
• Always make sure that the opposite siderail is raised when you transfer a patient onto the support surface to reduce the
risk of patient fall.
• Always check the CPR connector before use, if visibly soiled, replace. Direct skin contact with soiled material may
increase the risk of infection.
• Always inflate the product and unplug the pump from the mains 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, the hose ports, or the AST socket.
• Always make sure that you wipe each product with clean water and dry each product after cleaning or disinfecting. Some
cleaning and disinfecting agents are corrosive in nature and may cause damage to the product if you use them
improperly. If you do not rinse and dry the product, a corrosive residue may be left on the surface of the product that
could cause premature degradation of critical components. Failure to follow these cleaning or disinfecting instructions
may void your warranty.
• Always disinfect the support surface between patients to avoid the risk of cross-contamination and infection.
• Do not allow fluid to pool on the support surface. Fluids may cause degradation of components and may cause
unpredictable safety and performance of this product.
• 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 the IIssooAAiirr system, that includes 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.
• This equipment/system is intended for use by healthcare professionals only. This equipment/system may cause radio
interference or may disrupt the operation of nearby equipment. It may be necessary to take mitigation measures, such
as reorienting or relocating IIssooAAiirr system or shielding the location.
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.
• Do not tie the support surface to the bed frame with the bottom center D-ring straps to avoid the risk of equipment
damage. The bottom center-D ring straps are for storage only.
• Always be aware of devices or equipment that are placed on the top of the support surface. Damage to the surface may
occur due to the weight of the equipment, heat generated by the equipment, or sharp edges on the equipment.
• Do not put overlays or accessories inside the cover to avoid the risk of reducing pressure redistribution performance.
• Do not place hoses or power cords in walkways to avoid trip hazards.
• 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.
• Always be aware that an X-ray taken on this product may cause visible image artifacts. An image artifact may interfere
with patient diagnoses.
• Always store the product within the specified environmental condition values.
• Always completely dry the support surface covers before storing, adding linens, or placing a patient on the surface.
• Do not overexpose the product to higher concentration chemical solutions as these may degrade the product.
• Always follow the manufacturing instructions, failure may affect the useful life of the product.
2941-009-001 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 2941, IIssooAAiirr® system consists of a support surface and pump. The support surface is an air powered
support surface that consists of air cells and bladders that run across the surface to support the patient and side bolsters.
The surface is outfitted with a pump that provides the pressure source to inflate and deflate the air cells. The pump,
connected to the air cells through flexible hoses, monitors and automatically adjusts the air in the air cells dependent on the
type of therapy selected. This product includes alternating pressure (ALP), low air loss (LAL), max inflate, active sensor
technology (AST), and CPR deflate. Comfort control is provided through five levels of alternating low pressure and static
pressure.
IInntteennddeedd uussee
The IIssooAAiirr system helps in the prevention and treatment of pressure injuries or pressure ulcers (all stages, Unstageable
injury and Deep Tissue injury). Stryker recommends this product to be implemented in combination with clinical evaluation
of risk factors and skin assessments made by a healthcare professional. This product provides pressure redistribution and
is intended to assist in management of the microclimate of the patient skin.
The IIssooAAiirr system is intended for use with a bed frame and a top sheet. The system is intended for use in an acute care
and long-term care units, including general hospital use, critical care, step down care, Med/Surg, PACU, and progressive
care settings.
This product is not intended for use in a home healthcare environments, with pediatric patients, or in behavioral healthcare
units. This product is not sterile.
CClliinniiccaall bbeenneeffiittss
Assists in the prevention and treatment of all pressure ulcers or pressure injuries
EExxppeecctteedd sseerrvviiccee lliiffee
The IIssooAAiirr support surface has a 3 year expected service life under normal use conditions and with appropriate periodic
maintenance.
The IIssooAAiirr pump has a 5 year expected service life under normal use conditions and with appropriate periodic
maintenance.
EN 4 2941-009-001 Rev B.0

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 IIssooAAiirr system is not intended for use with patients that have an unstable spine.
SSppeecciiffiiccaattiioonnss
IIssooAAiirr 8844 iinn.. ((221133..33 ccmm)) ssyysstteemm
NNuummbbeerr PPlluugg ttyyppee PPoowweerr ccoorrdd 11MM PPoowweerr ccoorrdd 55MM
2941-000-001 B 2874-007-001 2874-007-002
500 lb 226 kg
SSuuppppoorrtt ssuurrffaaccee
Model 2941-001-100
Length 84.0 in. 213.3 cm
Width 35.0 in. 88.9 cm
Thickness 8.0 in. 20.3 cm
Weight 25 lb 11.3 kg
Cover material DDaarrtteexx® Endurance cover
Compatible with bed frame 33000022 SS33®, 33000055 SS33®, IInnTToouucchh®, SSppiirriitt PPlluuss®, SSppiirriitt SSeelleecctt®,
GGooBBeedd® II
DDaarrtteexx is a registered trademark of the Dartex Coatings, Ltd.
PPuummpp
Model 2941-001-001
Height 17.25 in. 43.8 cm
Width 9.25 in. 23.5 cm
Depth 7.25 in. 18.4 cm
Weight 15.6 lb 7.07 kg
Interface control panel LCD
Input voltage 100-240 V
Electric current 1.2 A
Input frequency 50/60 Hz
Noise level <50 dBa
2941-009-001 Rev B.0 5 EN

PPuummpp
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 2015/863/EU, Annex II to
directive 2011/65EU; REACH (EC) 1907/2006 EU; IEC 60601-1-
8:2012, IEC 60601-1-2:2014
Stryker reserves the right to change specifications without notice.
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss
EEnnvviirroonnmmeennttaall ccoonnddiittiioonnss OOppeerraattiioonn SSttoorraaggee aanndd ttrraannssppoorrttaattiioonn
Ambient temperature
Relative humidity (non-condensing)
Atmospheric pressure
1060 hPa
500 hPa
PPrroodduucctt iilllluussttrraattiioonn -- ssuuppppoorrtt ssuurrffaaccee
CCAAUUTTIIOONN -- Do not tie the support surface to the bed frame with the bottom center D-ring straps to avoid the risk of
equipment damage. The bottom center-D ring straps are for storage only.
EN 6 2941-009-001 Rev B.0

C
F
G
H
I
A
B
E
D
F
F
F
G
G
G
F
ATop cover E CPR connector
BStrap handle FTie down strap
C Law label location G D-ring (see Applying linens)
D AST cable H D-ring strap, bottom center
I Bottom cover
2941-009-001 Rev B.0 7 EN

PPrroodduucctt iilllluussttrraattiioonn -- ppuummpp
A
B
C
E
F
D
G
C
H
IJ
AGraphical user interface F Power inlet
B Status indicator G Anti-vibration foot
CBumper HHEPA filter
DTransport handle IHose port
E Hook J AST port connector
FFeeaattuurreess
Shear management The product moves with the patient to assist in the
reduction of shear forces at the interface between the
surface and the patient.
Low Air Loss (LAL) The product provides air flow to help manage microclimate
of the skin.
Alternating low pressure (ALP) The support surface is constructed with rows of air cells
connected to two different air lines (C). Odd row air cells
(A) are connected to the A air line and even row cells (B)
are connected to the B air line (Figure 1).
Active sensor technology (AST) When AST is on, sensors in the sacral region (D) of the
support surface help control patient immersion (Figure 1).
Side bolster The left and right side bolsters (E) provide exterior support
to the patient. This helps to secure the patient within the
support surface (Figure 1).
EN 8 2941-009-001 Rev B.0

FFiigguurree 11 –– AAiirr cceellllss
BBuuttttoonn aanndd iiccoonn ddeessccrriippttiioonnss
SSaammppllee ssccrreeeennss
IIccoonn NNaammee DDeessccrriippttiioonn
Power button See Powering on the pump (page 15) or Powering off the pump
(page 22)
Action button, right Allows the operator to select an action on the screen
2941-009-001 Rev B.0 9 EN

IIccoonn NNaammee DDeessccrriippttiioonn
Action button, left Allows the operator to select an action on the screen
Lock or unlock See Locking or unlocking the screen (page 21)
Home Returns to the home screen
Low Air Loss (LAL) on See Turning the LAL on or off (page 21)
Low Air Loss (LAL) off
Static mode on Adjusts comfort settings when used without AST. in this mode, all
cells are set to the same pressure
Static mode off Static mode off when you choose to cancel this therapy
Decrease or increase Adjusts pressure in the air cells
ALP on Provides therapy with pressure differences between alternating air
cells
ALP off ALP mode off when you choose to cancel this therapy
Mode menu Mode menu screen
Max Inflate full Inflates the support surface to a maximum pressure
Max Inflate filling Shows the surface filling to max inflate
Max Inflate mode Max Inflate off, you choose to cancel max inflate or the max inflate
timer has expired
AST on Optimal air pressure recalculates and adjusts as needed every 3
minutes
AST off AST mode off when you choose to cancel this therapy
Disconnected air hose alarm Detects air hose connection error
Kinked air hose alarm Detects a bend or twist in the air hose
AST malfunction alarm Detects the AST malfunction error
EN 10 2941-009-001 Rev B.0

Remove from use alarm Detects error
Alarm off Cancels alarm
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
You will find the serial number and date of manufacture on the law label (B) on the bottom cover of the support surface.
2941-009-001 Rev B.0 11 EN

B
DDaattee ooff mmaannuuffaaccttuurree
The year of manufacture is the first four digits of the serial number.
EN 12 2941-009-001 Rev B.0

SSeettuupp
SSeettuupp tthhee ssuuppppoorrtt ssuurrffaaccee
WWAARRNNIINNGG
• Always secure the support surface to the bed frame to prevent the shifting of the product while in use.
• Always inspect for foreign objects between the support surface and the bed frame. Foreign objects may cause the
support surface to slide on the support platform.
• Do not use the support surface on a larger or smaller bed frame that does not fit the width, length, or thickness. This is to
avoid the risk of the support surface sliding, patient injury, or interference with moving parts of the bed.
• Do not use the support surface when gaps are present. The risk of entrapment can develop when the support surface is
placed on incompatible bed frames.
CCAAUUTTIIOONN
• Always be aware of devices or equipment that are placed on the top of the support surface. Damage to the surface may
occur due to the weight of the equipment, heat generated by the equipment, or sharp edges on the equipment.
• Do not put overlays or accessories inside the cover to avoid the risk of reducing pressure redistribution performance.
To setup the support surface:
1. Remove all shipping and packaging materials from the product before use.
2. Release the tie straps.
3. Unroll and place the support surface with the hose at the foot end of the bed frame.
4. Start with one side of the anchor strap and wrap the strap around the top edge of the litter deck. Push the buckle up
through the slot on the same side.
5. Fasten the buckle and pull the strap to tighten to the bed frame.
6. Place linens on the support surface per hospital protocols.
SSeettuupp tthhee ppuummpp
Unpack the cartons and check all items. Make sure that the product operates before you place into service.
WWAARRNNIINNGG
• Always plug the power cord into the bed auxiliary outlet or a grounded power respectable. Do not use an extension cord.
• Do not touch patients and the AST socket on the pump at the same time.
• Always secure the pump to the bed frame to prevent the shifting of the product while in use.
• Always check the product before use to make sure there are no broken parts. If the product is damaged call technical
support.
• Always make sure that you do not exceed the safe working load of the bed frame before you mount the pump.
• Always connect the AST cable to the AST socket on the pump to avoid the risk of electrical shock.
• 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.
• This product radiates radio frequency energy. If not setup and used in accordance with the instructions, may cause
harmful interference to other devices in the vicinity.
CCAAUUTTIIOONN
• Do not place hoses or power cords in walkways to avoid trip hazards.
• Always allow the product to come to room temperature after exposure to extreme high or low temperatures.
2941-009-001 Rev B.0 13 EN

• Always check the power cord for cuts, exposed wires, worn insulation, or other damage that could result in electrical
hazards.
To setup the pump:
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.
3. Connect the AST cable.
4. Connect the hose.
CCoonnnneeccttiinngg tthhee ppoowweerr ccoorrdd
WWAARRNNIINNGG -- Always plug the power cord into the bed auxiliary outlet or a grounded power respectable. Do not use an
extension cord.
To connect the power cord:
1. Attach the power cord to the pump.
2. Plug in the power cord into an accessible outlet.
3. Place the power cord out of the path of foot traffic to avoid trip hazards.
AAppppllyyiinngg lliinneennss
To apply linens:
1. Part the D-rings (C) (Figure 2).
2. Thread the four linen corners through the D-rings (C) attached to the bottom cover to secure the linens (A) to the support
surface (B).
A
B
C
FFiigguurree 22 –– AAppppllyy lliinneennss
NNoottee -- This product is designed for use with non-fitted sheets. For best results, do not pull the linens too tight to avoid the
hammock effect.
EN 14 2941-009-001 Rev B.0

OOppeerraattiioonn
WWAARRNNIINNGG
• Always check patient’s skin regularly. Consult a physician if erythema or skin breakdown occurs. Serious injury could
result if the patient’s skin condition is left untreated.
• Do not use this product with an overlay. Patient stability and siderail coverage may be compromised.
• Always consider the use of siderails. The safe use of the support surface is maximized when used in conjunction with
siderails. There may be an increased risk of falls when siderails are not present. Serious injury or death can result from
the use (potential entrapment) or non-use (potential patient falls) of siderails or other restraints. Consider local policies
regarding the use of siderails. The physician, operator, or responsible parties should determine whether and how to use
siderails based on each patient’s individual needs.
• Always use extra caution with a patient at risk of a fall (such as agitated or confused) to help reduce the likelihood of a
fall.
CCAAUUTTIIOONN -- Always be aware that an X-ray taken on this product may cause visible image artifacts. An image artifact may
interfere with patient diagnoses.
PPoowweerriinngg oonn tthhee ppuummpp
To power on the pump:
1. Follow
Setup the pump (page 13) to prepare the pump for operation.
2. Press and hold the PPoowweerr button until IIssooAAiirr appears on the screen (Figure 3).
IsoAir
FFiigguurree 33 –– SSttaarrttuupp ssccrreeeenn FFiigguurree 44 –– HHoommee ssccrreeeenn,, ooppeerraattoorr vviieeww
NNoottee -- The ALP, AST, and the LAL modes that are powered on are shown in green on the home screen (Figure 4).
TTrraannssffeerrrriinngg aa ppaattiieenntt ffrroomm oonnee ppaattiieenntt ssuuppppoorrtt ppllaattffoorrmm ttoo aannootthheerr
WWAARRNNIINNGG
• Do not use the support surface as a transfer device.
• Do not use the support surface handles to lift or move the support surface with a patient on board.
• Do not stick needles or other sharp objects into a support surface through the support surface cover. Holes may allow
fluids to enter the inside (inner core) of the support surface, product damage, or product malfunction.
• Do not exceed the safe working load of the hospital bed frame when supporting both the patient and the support surface.
Excess weight could cause unpredictable safety and performance of this product.
• Always make sure that the opposite siderail is raised when you transfer a patient onto the support surface to reduce the
risk of patient fall.
To transfer the patient from one patient support surface to another:
PPrreerreeqquuiissiittee:: Follow hospital protocols required to transfer a patient from one surface to another.
2941-009-001 Rev B.0 15 EN

1. Press and wait for MMaaxx IInnffllaattee to fully inflate. See Starting or canceling Max Inflate (page 16).
2. Position one patient support platform alongside the other patient support platform while minimizing the gap between the
two platforms.
3. Set the brakes to OONN for both patient support platforms.
4. Adjust the patient support platform heights so that they are level with one another.
5. Transfer the patient following all applicable safety rules and institution protocols for patient and operator safety.
CCPPRR
CPR compressions may begin as soon as you remove the CPR connector.
1. Press the tab in on the CPR connector to disconnect.
2. Remove the CPR connector from the pump.
3. Remove the AST cable to prevent damage to the cable (recommended).
SSttaarrttiinngg oorr ccaanncceelliinngg MMaaxx IInnffllaattee
To start or cancel Max Inflate:
1. On the home screen, press the AAccttiioonn button next to the MMooddee icon (Figure 5).
FFiigguurree 55 –– HHoommee ssccrreeeenn
2. To start maximum inflation, press the AAccttiioonn button next to the MMaaxx IInnffllaattee icon (Figure 6).
FFiigguurree 66 –– MMaaxx IInnffllaattee
NNoottee -- The MMaaxx IInnffllaattee icon blinks until the support surface inflates to the maximum pressure setting.
EN 16 2941-009-001 Rev B.0