INSTRUCTIONS FOR USE

Auto Logic

630933EN_09 • 08/2019
WARNING
To avoid injury, always read this Instructions for Use and accompanied documents
before using the product.

Mandatory to read the Instructions for Use

Design Policy and Copyright

® and ™ are trademarks belonging to the Arjo group of companies.
© Arjo 2019.

As our policy is one of continuous improvement, we reserve the right to modify designs
without prior notice. The content of this publication may not be copied either whole or in part
without the consent of Arjo.
 Contents
General Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iii

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
About this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
About Auto Logic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1

Clinical Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6
Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Cautions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Care of the Patient When Sitting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7
Preparing the Systems for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Installing the Mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
To Complete the Mattress Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Installing the Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Installing the Aura Logic Seat Cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

Controls, Alarms and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12

Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Alarms and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
Quick Start . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Comfort Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Autofirm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Power Fail Condition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
To Disconnect the Tubeset . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Transport Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
To Deflate and Store the Auto Logic Mattress. . . . . . . . . . . . . . . . . . . . . . . . . 18
To Deflate the Aura Logic Seat Cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
CPR Control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20

Installing the Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Checking the Status of the Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Charging the Battery Pack. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Battery Storage and Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Decontamination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24

Routine Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25

Auto Logic and Aura Logic Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Auto Logic and Aura Logic Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

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 Auto Logic 110, 175 & 200 Mattresses and Aura Logic Seat Cushion . . . . . . 25
Serial Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

Troubleshooting & Alarm Condition. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26

Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27

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 General Safety
Before you connect the system pump to a mains socket, read carefully all the installation
instructions contained within this manual.
The system has been designed to comply with regulatory safety standards including:
• EN60601-1:2006/A1:2013 and IEC 60601-1:2005/A1:2012.
• EN60601-1-11:2010; IEC 60601-1-11:2010 and IEC60601-1-8:2012.
• ANSI/AAMI ES 60601-1(2005)+AMD(2012)and CAN/CSA-C22.2 No.60601-1(2008)+
(2014).
Safety Warnings
• It is the responsibility of the care giver to ensure that the user can use this product
safely.
• Whilst the patient is unattended, the decision to use safety sides should be based
on clinical assessment and in line with local policy.
• Alignment of the bed frame, safety sides and the mattress should leave no gap
wide enough to entrap a patient's head or body, or to allow egress to occur in a
hazardous manner where entanglement with the mains power cable and tubeset or
air hoses may result. Care should be exercised to prevent occurrence of gaps by
compression or movement of the mattress. Death or serious injury may occur.
• Make sure that the mains power cable and tubeset or air hoses are positioned to
avoid causing a trip or other hazard, and are clear of moving bed mechanisms or
other possible entrapment areas. The mains power cable of this pump is designed
to allow movement of the bed, and should be fitted into the cable management
flaps along the sides of the mattress, as described in this manual.
• When using a seat cushion, the tubeset may be a trip hazard; position the tubeset
so that it does not create a trip hazard, and always supervise babies and small
children when the product is in use.
• Electrical equipment may be hazardous if misused. There are no user-serviceable
parts inside the pump. The pump's case must only be removed by authorised
technical personnel. No modification of this equipment is allowed.
• The mains power socket/plug must be accessible at all times. To disconnect the
pump completely from the electricity supply, remove the plug from the mains
power socket.
• The CPR control and/or the CPR indicator tag must be visible and accessible at all
times.
• Disconnect the pump from the mains power socket before cleaning and inspecting.
• Keep the pump away from sources of liquids and do not immerse in water.
• Do not use the pump in the presence of uncontained flammable liquids or gasses.
• The cover of this product is vapour permeable but not air permeable and may
present a suffocation risk.
• Do not use the mattress without a cover, it provides a protective barrier.
• Bags supplied with this equipment may present a suffocation risk; to avoid the risk
of suffocation keep the bags away from babies and small children.
• There is no Transport facility on the seat cushion.
• Only the pump and mattress combination as indicated by Arjo should be used. The
correct function of the product cannot be guaranteed if incorrect pump and
mattress combinations are used.

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• The battery socket cover on the bottom of the pump must be retained in position at
all times. If there is a need to remove it, then it should be stored in a safe place
away from babies and small children for subsequent reinstalling.
• Due to the inherently lower flame retardancy of the high performance Ventilate IS2
fabric, it is NOT suitable for use in the homecare environment.
• The operator should stay around the pump to prevent from missing the system
alarm.
• If a serious incident occurs in relation to this medical device, affecting the user,
or the patient then the user or patient should report the serious incident to the
medical device manufacturer or the distributor. In the European Union, the user
should also report the serious incident to the Competent Authority in the
member state where they are located.
Side Rails / Patient Restraints
• Whether and how to use side rails or restraints is a decision that should be based on each
patient’s needs and should be made by the patient and the patient’s family, physician and
caregivers, with facility protocols in mind.
• Caregivers should assess risks and benefits if side rail / restraint use (including
entrapment and patient falls from bed) in conjunction with individual patient needs, and
should discuss use of non-use with patient and / or family. Consider not only the clinical
and other needs of the patient but also the risks of fatal or serious injury from falling out of
bed and from patient entrapment in or around the side rails, restraints and other
accessories.
• In the US, for a description of entrapment hazards, vulnerable patient profile and
guidance to further reduce entrapment risks, refer to FDA’s Hospital Bed System
Dimensional and Assessment Guidance To Reduce Entrapment.
• Outside the US, consult the local competent authority or government agency for Medical
Device Safety for specific local guidance. Consult a caregiver and carefully consider the
use of bolsters, positioning aids or floor pads, especially with confused, restless or
agitated patients.
• Make sure a capable patient knows how to get out of bed safely (and, if necessary, how to
release the side rails) in case of fire or other emergency. Monitor patients frequently to
guard against patient entrapment.

When selecting a mattress and overlay combination or MRS, ensure

the distance between the top of side rails (if used) and patient surface
(without compression) is at least 8.66 in (220 mm) to help prevent
inadvertent bed exit or fails. Consider individual patient size, position
(relative to the top of the side rail) and patient condition in assessing fall
risk.

Safety Warnings - Battery Pack (Optional)

THE BATTERY PACK IS NOT SUITABLE FOR USE IN THE HOMECARE ENVIRONMENT.
The following instructions are important for the safe use of the battery pack and to
keep the user (resident/care giver) from harm:
• The battery pack BBP600 for the Auto Logic® pump is rechargeable. For maximum
battery life, charge the battery at least once every five months when the product is
not in use.
• Only use the battery pack designed for use with the pump. If unsure, do not use the
battery pack. Make sure the battery pack belongs to the pump by comparing the

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 battery pack label with the“Technical Description” on page 27. If the battery pack
type cannot be confirmed, contact your local Arjo office.
• Do not expose the battery pack or charger to open flames.
• Do not expose the battery pack connector to water.
• To avoid bodily injury, do not crush, puncture, open, dismantle or otherwise
mechanically interfere with the battery pack.
• Should the battery pack casing crack and cause contents to come in contact with
skin or clothing, rinse immediately with plenty of water.
• If contents come in contact with the eyes, rinse immediately with plenty of water
and seek medical attention.
• Inhalation of the contents can cause respiratory irritation. Provide fresh air and
medical attention.
• Stop using the battery pack if any damage or deformation is noted. Contact your
local Arjo office before further use.
• Refer to the “Battery Storage and Disposal” on page 23 for the correct disposal and
recycling of the battery pack.
Precautions
For your own safety and the safety of the equipment, always take the following
precautions:
• Placing extra layers between the patient and the mattress potentially reduces the benefits
provided by the mattress and should be avoided or kept to a minimum. As part of sensible
pressure area care, it is advisable to avoid wearing clothing which may cause areas of
localised high pressure due to creases, seams, etc. Placing objects in pockets should be
avoided for the same reason.
• Do not expose the system, especially the mattress, to naked flames, such as cigarettes,
etc.
• In the event of a fire, a leak in the seat or mattress could propagate the fire.
• Do not store the system in direct sunlight.
• Do not use phenol-based solutions to clean the system.
• Make sure the system is clean and dry prior to use or storage.
• Never use sharp objects or electrically heated under blankets on or under the system.
• Store the pump and mattress in the protective bags supplied.
• Pets and children must be supervised in the vicinity of the system.
Electromagnetic Compatibility (EMC)
This product complies with the requirements of applicable EMC Standards. Medical electrical
equipment needs special precautions regarding EMC and needs to be installed in accordance
with the following instructions:
• The use of accessories not specified by the manufacturer may result in increased
emissions by, or decreased immunity of, the equipment, affecting its performance.
• Portable and mobile radio frequency (RF) communications equipment (e.g. mobile/cell
phones) can affect medical electrical equipment.
• If this equipment needs to be used adjacent to other electrical equipment, normal
operation must be checked before use.
• For detailed EMC information contact Arjo service personnel.

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Environmental Protection
Incorrect disposal of this equipment and its component parts, particularly batteries or other
electrical components, may produce substances that are hazardous to the environment. To
minimise these hazards, contact Arjo for information on correct disposal.
Expected Service Life
The Auto Logic pump has an expected service life of seven years. To maintain the condition
of the pump, have the pump serviced regularly according to the schedule recommended by
Arjo.
Do NOT use unapproved accessories or attempt to modify, disassemble or otherwise misuse
the Auto Logic system. Failure to observe this caution could result in injury, or in extreme
cases, death.
End of Life Disposal
• Fabric material used on the mattresses or any other textiles, polymers or plastic materials
etc. should be sorted as combustible waste.
• Mattresses at the end of life should be disposed of as waste according to the national or
local requirements which may be landfill or combustion.
• Pump units have electrical and electronic components should be disassembled and
recycled per Waste of Electrical and Electronic Equipment (WEEE) or in accordance with
local or national regulation.

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1. Introduction

About this Manual This manual is your introduction to the Auto Logic Dual
Mode support systems and the Aura Logic® seat
cushion. You must read and fully understand this
manual before using the system.
Use this manual to initially set up the mattress or seat
cushion, keep it as a reference for day-to-day routines
and as a guide to maintenance.
If you have any difficulties in setting-up or using the
Auto Logic and Aura Logic systems, contact your Arjo
sales office, listed at the end of this manual.
Intended Use The intended use of this product is to prevent and/or
manage pressure ulcers for patients up to 200 kg
(440 lb).
The Auto Logic system should be used as part of a
prescribed plan of care (refer to “Indications” on
page 6).
About Auto Logic The Auto Logic systems comprise a mattress
replacement, overlay or seat cushion, all operated by the
same pump. The pump incorporates Self Set
Technology (SST), which adjusts air pressure every
10 minutes for the Active (Alternating) mode and
20 minutes for the Reactive (Constant Lower Pressure)
(CLP) mode to suit the Body Mass Index (BMI) and
position of the patient. Both support systems can be used
on standard hospital beds. The device can be used in the
home care environment.
A full technical description of the Auto Logic system
can be found in the Service Manual, part number
SER0006, available from your Arjo sales office.
Auto Logic Pump The Auto Logic pump comprises a moulded case with
non slip feet on the base and rear and integral hanging
brackets.
The controls are situated on the top of the pump and a
sophisticated alarm system differentiates between
normal operation and genuine system faults. If an alarm
situation is detected an indicator illuminates on the top
and front of the pump and an audible warning sounds.
The Autofirm system, once activated, creates a
temporary firm surface to allow nursing procedures to
be performed.

1
 Control Panel
Power and Alarm
Indicators

Hanging Brackets

Auto Logic 110 The Auto Logic 110 mattress overlay comprises the
Mattress Overlay following components:

Detachable Cover

3 Static Head Cells

(Dark Blue)

Cover Attachment Zips

Cable
Management
CPR Unit

2 Standard Cells (Dark Blue)

10 Side Supporting Cell-in-Cells

(Light Blue)
Fixed 5 Standard Cells (Dark Blue)
Tubeset
Overlay Base Cover (Including Micro Air Loss System)
Serial Label
(Inside Base Cover) Corner Straps

2
 Detachable Cover The standard cover comprises a 2-way stretch PU coated
knitted fabric zipped to a durable polyester base. The
zips are protected by flaps to prevent ingress of
contaminants and allow easy removal of the cover for
cleaning.
Alternative covers with advanced properties, such as
Glide IS2 and Ventilate IS2 are also available (Refer to
“COVER SPECIFICATION” on page 30).
Cells The mattress comprises 20 polyurethane (PU) cells
providing support to the user in either Active
(Alternating) or Reactive (Constant Lower Pressure)
modes. The cells are slightly curved to reduce patient
movement down the mattress.
The side supporting cells incorporate Cell-in-Cell
technology to help the transfer of patients on and off the
bed by keeping the edges of the mattress firm.
Micro Air Loss System A micro air loss system is incorporated into the base
cover which de-humidifies the air surrounding the cells
to reduce heat build up within the mattress and ensure
patient comfort. This system is separate from the cell
inflation to enable both micro air loss and patient
transport modes to be incorporated into the mattress.
CPR Function A CPR (Cardio-Pulmonary Resuscitation) control is
positioned at the head end of the mattress to enable the
air to be evacuated in under 10 seconds.
Tubeset The tubeset has a 3-way pneumatic connection which
incorporates a flexible, compact anti-kink tube that is
resistant to crushing and any subsequent obstruction of
air flow.
NOTE
If the tubeset is disconnected from the pump, the
mattress automatically changes to Transport mode.

Overlay Base Cover The base cover for the mattress overlay is PU coated
polyester on the underside. Four corner retention straps
are incorporated, which slide under the corners of the
base mattress.

3
Auto Logic 175 & 200 Mattress Replacement
The Auto Logic 175 & 200 mattress replacements are of
a similar construction to the overlay with the addition of
a non-slip base. Within the non-slip base, the 175
mattress includes a foam underlay and the 200 mattress
has an air filled zoned sub-mattress both of which
replace the need for a mattress on the bed. The base can
be removed to convert the mattress replacement to an
overlay, refer to Arjo for more information.

Detachable Cover

3 Static Head Cells

(Dark Blue)

Cover Attachment Zips

Cable
Management

CPR Unit

2 Standard Cells (Dark Blue)

10 Side Supporting Cell-in-Cells

(Light Blue)
5 Standard Cells (Dark Blue)
Fixed Tubeset 175 - Non-slip base including foam underlay
Securing Straps 200 - Air Filled Zoned Sub-Mattress (Non-Slip)

Air Sub-Mattress The Sub-Mattress provides an integral constant pressure

(200 Only) support which removes the need for a standard mattress.
The pressure in the central zone of the pad is
automatically adjusted in line with the Active
(Alternating)/Reactive (Constant Lower Pressure)
(CLP) of the mattress. The pressure in the perimeter
zone of the pad is maintained at a higher level to help
transfer of patients on and off the bed.
On the underside of the Sub-Mattress there are eight
straps to attach the mattress replacement to the bed
frame. The straps can be moved to any of the 10 anchor
points to allow attachment of the mattress to different
bed frames.

4
 Aura Logic Seat The Aura Logic seat cushion is an Active (Alternating)
Cushion pressure redistribution system that can be used on
standard hospital chairs.

Detachable Cover

Deflation Valves (on

underside for packing
& storage)
Alternating Cells

Zip

Non-Slip Base Serial Label

(Inside Base Cover)

Fixed Tubeset
Fixing Straps

Caution

The optional battery pack is not suitable for use in the homecare
environment.

Battery Pack The Battery Pack is an optional extra that allows the
(Optional) pump to operate for a minimum of eight hours without a
mains power supply.
The Battery Pack easily slides onto the base of the pump
and will recharge itself when the pump is operating from
the mains power supply.

5
2. Clinical Applications
Indications The Auto Logic systems are indicated for the prevention
and/or management of all categories1 of pressure ulcer,
when combined with an individualised, comprehensive
pressure ulcer protocol: for example, repositioning,
nutritional support, skin care. Selection should be based
upon a holistic assessment of the patient’s individual
care needs.
These systems represent one aspect of a pressure ulcer
management protocol; all other aspects of care should be
considered by the prescribing clinician.
If existing wounds do not improve or the patient's
condition changes the overall therapy regimen should be
reviewed by the prescribing clinician.
The above are guidelines only and should not replace
clinical judgement.
The Auto Logic mattress and cushion are designed for
patients weighing up to 200kg (440 lb).
Contraindications Do not use Auto Logic systems for patients with unstable
spinal fractures.
Cautions If patients have other unstable fractures, or conditions
which may be complicated by a soft or moving surface,
advice should be sought from an appropriate clinician
before use.
While the Auto Logic systems have been designed to
manage patients up to the weight limits indicated above,
those approaching this upper limit are likely to have
additional care and mobility needs and may be better
suited to a specialist bariatric system.
Active (Alternating) therapy cushions may be
unsuitable for patients with poor sitting posture or pelvic
deformity; advice from a seating specialist should be
sought.
Care of the Patient Seated patients are at increased risk of pressure ulcers
When Sitting particularly if they are immobile or have wounds over
the seating area. For optimal outcome, provide a
pressure redistributing seat cushion in a chair which
promotes a good sitting posture and has a level base seat
to support the cushion, in addition to an individualised
repositioning programme.
NOTE
Mattress and cushion combinations may have different upper
weight limits. Cushions should be used in combination with
pressure-redistributing mattresses to provide 24-hour therapy.

1. NPUAP/EPUAP International Pressure Ulcer Guideline, 2009.

6
3. Installation

WARNING

Bags supplied with this equipment may present a suffocation risk;

to avoid the risk of suffocation keep the bags away from babies and
small children.

Preparing the Remove the system from the packaging. You should
Systems for Use have the following items:
• Auto Logic pump including mains power cord and
hanging brackets.
• Auto Logic 110 mattress overlay, Auto Logic 175 or
200 mattress replacement or the Aura Logic seat
cushion, which all have integral tubesets and covers.
NOTE
Do not use the mattress or seat cushion without the cover.

• Battery Pack (optional).

Installing the Mattress

Caution
Do not use the mattress overlay directly on the bed frame.

Auto Logic 110 1. Place the overlay on top of the base mattress, with
Mattress Overlay the tubeset located near the foot end of the bed and
the CPR at the head end. The cells of the mattress
must be uppermost.
2. Secure the overlay to the base mattress by placing
and tightening the four long straps under the
corners of the base mattress.

7
Auto Logic 175 or 200 1. Remove the existing mattress from the bed frame
Mattress Replacement and check that there are no protruding bed springs
or sharp objects on the bed frame surface.
2. Unroll the mattress onto the bed frame and ensure
that the tubeset is located near the foot end of the
bed and the CPR at the head end. The cells of the
mattress must be uppermost.
3. Attach the mattress to the bed frame using the eight
fastener straps.

NOTE
• The eight fastener straps can be moved to any of the
10 anchor points on the base of the mattress
replacement. This allows for attaching the mattress to
different types of bed frame.
• If the bed can be profiled to any position (i.e. raised or
lowered), attach the mattress to the movable parts of
the bed only.
• Care should be taken at all times to check that
tubes/lines are positioned correctly.

To Complete the Complete the installation of the mattress overlay or the

Mattress Installation mattress replacement as follows:
1. If not already fitted, place the protective cover over
the mattress. Ensure that the Arjo logo is uppermost
and at the foot end of the mattress.
k”
“Clic 2. Zip the cover onto the mattress starting from the
head end and taking care not to trap any material in
the zip.
3. Ensure that the CPR unit is clicked into the closed
position.
NOTE
The CPR must be accessible at all times.

WARNING

Make sure that the mains power cable is positioned to avoid

causing a hazard and is clear of moving bed mechanisms or other
possible entrapment areas. Refer to “Cable Management” on
page 9.

8
Installing the Pump 1. Position the pump, feet down, on any convenient
horizontal surface or alternatively suspend from the
bed foot rail by means of the swing out hooks.
2. Ensure that the mattress/seat tubeset is not “kinked”
or twisted and connect it to the pump until it clicks
into place. Ensure that the tubeset is securely
connected to the pump.
3. Insert the mains power plug into a suitable mains
power socket.

”
Click
“

Battery Pack If you have a battery pack, refer to “Installing the

Battery Pack” on page 20.
Cable Management If using the mattress replacement or mattress overlay,
the power cable can be positioned in the cable
management flap running down the side of the mattress
as follows:
1. Locate the flap running along the mattress on the
opposite side to the tubeset and CPR.
2. Run the straight part of the cable along the side of
the mattress securing the flap round the cable using
the press studs.

System Operation The system is now ready for use. Refer to “Controls,
Alarms and Indicators” on page 12 and “Operation” on
page 15 for day-to-day operating instructions.

9
 Installing the The system should be installed as follows:
Aura Logic Seat 1. Check that there are no sharp objects on the chair
Cushion which may puncture the cushion.
2. Place the cushion on top of the chair surface. From
a standing position in front of the chair and facing
it, ensure that:
• The cells are uppermost.
• The tubeset appears from the front right corner of
the cushion.
• The cells in the seat cushion are in a horizontal
position across the chair, with the ‘V’ shape
pointing towards the front.

Cautions

• Do not use the Aura Logic seat cushion without a foam cushion
beneath it.
• Always use the Aura Logic seat cushion with the protective top
cover.
• Always use the Aura Logic seat cushion in the correct
orientation.
• Avoid trailing cables - ensure that cables and tubing are
positioned beneath the chair to avoid causing a hazard.
• Position the tubeset so it does not create a trip hazard and
always supervise babies and small children when the product
is in use.

10
3. Secure the seat cushion to the chair by using the
fixing straps as shown in the following illustrations.
4. If the chair is of the open sided construction, then
fix the cushion as shown below:

5. If the chair is of the closed side type with a

removable seat cushion, fix the seat cushion as
shown below:

6. If the chair is of the closed side type with a non-

removable seat cushion, then security will rely on
the anti-slip base material of the seat cushion.
7. Place the protective cover over the seat cushion and
ensure that the Arjo logo and the orientation icon,
printed on the cover, are uppermost and at the front
of the seat.
8. Zip the cover onto the seat cushion, taking care not
to trap any material in the zip.
9. Connect to the Auto Logic pump, refer to page 9.

11
4. Controls, Alarms and Indicators

Controls

Run/Standby Wait Indicator

Low Pressure Indicator

Autofirm
Alarm Mute
Comfort
Controls

Reactive (CLP) Mode

Battery Low Indicator
Service Indicator Power Fail Indicator

Run/Standby Button Pressing the Run/Standby button will activate the pump.
The green indicators on the control panel and the front
of the pump will illuminate when the pump is on.
To switch the pump to Standby, the button must be
pressed for two seconds. This prevents accidental
operation.
The green indicator will blink twice every 2 seconds to
indicate to the user that the pump is in Standby.
NOTE
Unless Transport mode is required, always put the pump
into Standby before disconnecting mattress or seatpad.

Alarm Mute During an alarm condition (except Power Fail Alarm),

the sound of the alarm can be silenced by pressing this
button. The yellow indicator then remains on but the
alarms will be silenced for 15 minutes or until the alarm
condition has been corrected.
Reactive (CLP) Mode Selects the Reactive (Constant Lower Pressure) (CLP),
non-alternating mode. The yellow indicator illuminates
when the pump is in this mode. When the Active
(Alternating) mode (default) is selected, the yellow
indicator will be switched off.
Press the Reactive (CLP) Mode button for
approximately 4 seconds to activate the reactive mode.
The change in the mode will occur at the end of the next

12
 complete alternating cycle, and so a maximum 10
minute delay may be experienced.
In the Reactive (CLP) mode the patient will not
experience the benefits of Active (Alternating) therapy.
Autofirm Mode Press and hold the Autofirm button for two seconds to
enter Autofirm mode. Once activated, Autofirm creates
a temporary firm surface to allow nursing procedures to
be performed. Autofirm lasts 15 minutes, after which the
pump will default back to the previous setting.
When the pump is in Autofirm mode the Reactive (CLP)
and Comfort Control LEDs are illuminated.
NOTE
This operation does not function whilst a seat cushion is
connected.

Comfort Control Two buttons control the relative firmness/softness of the

mattress/seat cushion for patient comfort.
The pressure setting is indicated by the green indicator
to the left of the buttons.

Alarms and Indicators

Wait Indicator The yellow Wait indicator is illuminated when the
mattress/seat is being inflated. The indicator remains
illuminated until the mattress/seat has been fully
inflated.
Low Pressure The yellow Low Pressure indicator is illuminated
Indicator whenever the pump detects low pressure within the
mattress/seat. An audible alarm sounds unless silenced
by the Alarm Mute button.
The indicator will extinguishes once normal pressure is
reached.
NOTE
See “Troubleshooting & Alarm Condition” on page 26 for
possible causes of Low Pressure.

Battery Low Indicator The yellow Battery Low indicator will illuminate 2
hours before battery failure.
1 hour before battery failure, the pump will default to
Reactive (CLP) mode, an audible alarm will sound and
the yellow indicator will still illuminate.

13
Power Fail Indicator The yellow Power Fail indicator illuminates when a
mains power failure has been detected and no battery
backup is available. An audible alarm sounds until
power is resumed or the pump is switched off using the
Run/Standby button.
If a Power Fail condition arises and no battery is
connected, disconnect the tubeset from the pump. This
will put the mattress into transport mode (Refer to
page 17).
Service Indicator The yellow Service indicator illuminates and remains on
after a set number of running hours. This indicates that
the pump is ready for a service. The pump will continue
to function normally even when the service indicator is
illuminated but you should arrange service as soon as is
convenient.
If the yellow Service indicator illuminates, the pump has
detected an internal fault and a Service Engineer should
be called.

14
5. Operation

These instructions cover day-to-day operation of the system. Other operations, such
as maintenance and repair, should only be carried out by suitably qualified
personnel.

WARNING

Do not place the patient on the mattress until it is fully inflated and
normal operating pressure has been reached.

Quick Start Before using any of the Auto Logic mattress or seat
systems make sure it has been installed correctly in
accordance with “Installation” on page 7 and ensure that
the CPR unit on the mattress is clicked into the closed
position.
1. When the Auto Logic pump is switched on at the
mains supply or a battery pack is connected, an
audible beep sounds and a self-diagnostic check
runs for approximately 10 seconds. When the check
is complete a second audible beep sounds and the
Run/Standby
pump is ready for use.
2. Press the Run/Standby button on the control panel
of the pump. The Run/Standby and Wait indicators
will illuminate together with the comfort indicator
and the green light on the front of the pump.
3. The Wait indicator will extinguish when the pump
and mattress or seat cushion are ready for use.
Approximate timings to inflate fully are:
• 7 minutes for a mattress overlay
• 15 minutes for a mattress replacement
• 3 minutes for a seat cushion
NOTE
The Wait indicator extinguishes when the mattress/seat is
fully inflated.

4. Place a bed sheet over the mattress and tuck in

loosely. Ensure that the CPR unit is clearly visible
at the head end of the bed.
5. You can now put the patient on the mattress.
NOTE
Once the patient is on the mattress, the pump
automatically senses and adjusts the pressure in the cells
using Self Set Technology (SST) to support the patient.

15
 Comfort Control The mattress/seat cell pressure can be manually adjusted
for patient comfort using the buttons on the pump
control panel.

WARNING

Autofirm increases the volume of air in the mattress and therefore

operation of the CPR function will take longer to deflate the
mattress. If there is a risk of adverse patient reactions during
clinical procedures then do not use Autofirm.

Autofirm The Autofirm mode allows the mattress to be pumped to

a steady high pressure to allow nursing procedures that
require a firmer base to be performed.
Autofirm mode lasts for 15 minutes but may be
increased in 5 minute steps up to a maximum of 30
minutes.
Autofirm operation is only possible when a mattress is
connected to the pump.
NOTE
This operation will not function whilst a seat cushion is
connected.

To Activate Autofirm To activate the Autofirm mode hold the Autofirm button
down for 2 seconds.
All comfort LEDs will flash while the pump configures
itself for Autofirm.
The comfort LED's will illuminate in sequence while the
mattress is being inflated to Autofirm pressures.
Once the mattress has reached pressure all comfort
LEDs will remain illuminated, and the pump will beep
three times. The Reactive (CLP) LED will also be
illuminated.

To De-Activate To de-activate the Autofirm mode hold the Autofirm

Autofirm button down for 2 seconds.

16
 To Extend Autofirm During the last minute of Autofirm all comfort LEDs
Duration will flash and the pump will sound a series of tones,
which will increase in both pitch and frequency. During
this alert period the Autofirm mode may be extended by
a further 5 minutes by pressing either comfort key.
The maximum duration of Autofirm mode is 30
minutes.
Following the end of Autofirm the previous pump mode
is restored.
Power Fail Condition If a Power Fail condition arises and no battery is
connected, disconnect the tubeset from the pump. This
will put the mattress into Transport mode and will
support the patient for up to 12 hours. Once power is
resumed, re-connect the tubeset to the pump.
To Disconnect the To disconnect the tubeset at any time, push the button
Tubeset down and pull the tubeset connector away from the
pump.
This puts the mattress into Transport mode but does not
deflate the mattress. To deflate the mattress
Refer to page 18.

Transport Mode To transport a patient using the Auto Logic mattress,

disconnect the tubeset from the pump. This
automatically switches the mattress into Transport
mode.
The patient will remain supported by the mattress for up
to 12 hours.
To resume normal operation, simply reconnect the
tubeset and run the pump.
NOTE
There is no Transport mode on the Aura Logic seat
cushion.

17
 Shut Down Power the pump off by pressing the Run/Standby button
for at least two seconds to select Standby (LED amber).
If you need to completely isolate the pump from the
mains, remove the plug from the mains power socket.
If running from the battery pack, remove it from the
pump.
To Deflate and Store the Auto Logic Mattress
To deflate the 1. Disconnect the tubeset from the pump.
mattress: 2. Activate the CPR control to deflate the mattress.
To store the mattress Following deflation:
1. Bring the tubeset over the mattress to lie parallel to
the foot end of the mattress.
2. Roll the mattress from the foot end toward the CPR
connector at the head end of the mattress.
2

To Deflate the Aura Logic Seat Cushion

To deflate the seat cushion:
1. Disconnect the tubeset from the pump.
2. Push the two valves on the underside of the seat
cushion.

18
 CPR Control

IMPORTANT

IN THE EVENT OF CARDIAC ARREST

In the event of a patient suffering cardiac arrest and CPR

needing to be administered:
To Activate CPR Press the two CPR release buttons simultaneously.

To Reset CPR Push the front of the CPR unit until it clicks into place.

k”
“Clic

19
6. Battery Pack

Caution

The optional battery pack is not suitable for use in the homecare
environment.

Installing the Battery Install the battery pack to the pump as follows:
Pack 1. Remove the battery socket cover from the base of
the pump.
NOTE
Store it in a safe place away from babies and small
children for subsequent reinstalling.

2. From the front of the pump, slide the battery pack

over the guides on the base of the pump and click
into place.
3. To remove the battery pack, depress the reset/status
latch at the rear of the unit and slide the battery
pack out from the base of the pump. Replace the
battery socket cover on the base of the pump.

Battery Socket Cover

Reset/Status Latch

Battery Pack

20
Checking the Status of the Battery Pack
Battery Label
LED 1 LED 2
Jack Socket Polarity

+
80-100% Charge
Battery Pack OK

Battery Pack 30-80% Charge

needs recycling

Battery Pack <30% Charge

Fault

Press Reset / Status Latch

To Check the Battery Pack Status

To check the status of the battery pack:
1. Remove the battery pack from the pump unit.
2. Press the Reset/Status Latch, this activates the two LEDs on the top of the
battery.
If the battery pack is not on charge the LEDs will display one of the following
conditions:

LED 1 LED 2 Battery Status

The Battery Pack is OK. It has > 80% charge.
Green Green

The Battery Pack is OK. It has between 30-80% charge.

Green Green

The Battery Pack is OK. It has < 30% charge.

Green

Red Green The Battery Pack needs recycling (1). It has between 30-80% charge.

Red The Battery Pack needs recycling (1). It has < 30% charge.

The Battery Pack has an error.

Red

The Battery Pack is flat or has an error. Try recharging.

1. Once the battery pack has entered the ‘recycling’ mode it will never show that the battery is fully
charged (Note: this does not indicate a fault condition). It is recommended that the battery pack is
sent back to an Arjo service centre for disposal (refer to “Battery Storage and Disposal” on
page 23).

21
Charging the Battery Pack
The battery pack is automatically recharged whenever it is installed in a pump which
is connected to an AC outlet. Alternatively the battery pack can be recharged away
from the pump by plugging into the battery charger as shown below.
NOTE
It is normal for the battery pack and charger to get warm during use.
Avoid charging the battery near source of heat or in direct sunlight

To ensure the long term performance of the battery pack, periodically run the pump
using the battery pack until the pump switches off. This will fully discharge the
battery pack. Fully recharge the battery pack before further use.
Typical service life of the battery is four years (500 charge/discharge cycles).
For safe handling and to extend the battery lifetime, follow and remember the
instructions:
NOTE
Not following these instructions can cause short battery life and may, in
extreme cases, put the user at risk.

• Only use the battery pack designed and labelled for use with the pump. When not
sure, do not use the battery pack. Make sure the battery pack belongs to the pump
by comparing the battery pack label with the “Technical Description” on page 27.
If the battery pack type cannot be confirmed, contact Arjo.
• Battery pack life depends on many factors. Factors that can influence battery life
are: frequency of use, frequency of charging, temperature of operation, storage
and storage time.

22
• The expected battery pack lifetime depends on care. With correct care, frequent
charging and storage at room temperature, the battery pack life can be prolonged.
It is recommended that the battery pack is replaced every 2 years.
The Ni-MH battery pack should be totally discharged before being recharged in
order to optimize its lifetime.
NOTE
For pump and mattress/seat cushion systems, periodically run the pump
using the battery pack until the pump switches off. Fully recharge the
battery pack before further use.

Make sure there is a replacement battery pack ready when needed. It is

recommended that the facility department keep one in stock.
Battery Storage and Disposal
If the device is not to be used for an extended period, charge (refer to “Charging the
Battery Pack” on page 22), remove and store the battery pack. If the battery packs
are to be put into long term storage they should be recharged at least once every three
to six months.
Faulty battery packs should be sent back to Arjo for recycling or correct disposal.

23
7. Decontamination
The following processes are recommended, but should be adapted to comply with the
local or national guidelines (Decontamination of Medical Devices) which may apply
within the Healthcare Facility or the country of use. If you are uncertain, you should
seek advice from your local Infection Control Specialist.
The Auto Logic system should be routinely decontaminated between patients and at
regular intervals while in use; as is good practice for all reusable medical devices.

WARNING

Remove the electrical supply to the pump before cleaning by

disconnecting the mains power cord from the mains power supply
or removing the battery pack.
Protective clothing should always be worn when carrying out
decontamination procedures.

Caution

Do not use Phenol-based solutions or abrasive compounds or pads

during the decontamination process as these will damage the
surface coating. Do not boil or autoclave the cover.
Avoid immersing electrical parts in water during the cleaning
process. Do not spray cleaning solutions directly onto the pump.

To Clean
Clean all exposed surfaces and remove any organic debris by wiping with a cloth
moistened with a simple (neutral) detergent and water. Dry thoroughly.
Do not allow water or cleaning solutions to collect on the surface of the pump.
Chemical Disinfection
To protect the integrity of the cover we recommend a chlorine-releasing agent, such as
sodium hypochlorite, at a strength of 1,000ppm available chlorine (this may vary from
250ppm to 10,000ppm depending on local policy and contamination status).
Wipe all cleaned surfaces with the solution, then wipe with a cloth moistened in water
and dry thoroughly.
Alcohol based disinfectants (strength 70%) may be used as an alternative.
Ensure the product is dry before storage.
If an alternative disinfectant is selected from the wide variety available we recommend
that suitability for use is confirmed with the chemical supplier prior to use.
Do not wring/mangle, autoclave or use phenolic based solutions.
Thermal Disinfection
For information for the mattress top cover, including laundering guidelines, refer to
‘Cover Specification’ table on page 30.

24
8. Routine Maintenance

Auto Logic and Aura Logic Systems

Maintenance The equipment has been designed to be virtually
maintenance-free between service periods.
Servicing Arjo will make available on request service manuals,
component parts lists and other information necessary
for Arjo trained personnel to repair the system.
Service Period Arjo recommend that the Auto Logic system should be
serviced after 12 months continuous running time, by an
Arjo authorised service agent. This is indicated by the
illumination of the Service symbol.
Auto Logic and Aura Logic Pump
General Care, Check all electrical connections and power cord for
Maintenance and signs of excessive wear or damage.
Inspection If the pump has been subjected to abnormal treatment,
e.g. immersed in water or dropped, the unit must be
returned to an authorised service centre.
Auto Logic 110, 175 & 200 Mattresses and Aura Logic Seat Cushion
General Care Remove the top cover and inspect for signs of wear or
any tears.
Check all zips are secure.
Check integrity of all connectors, including cell to
manifold connections.
Ensure all cell fasteners are correctly connected to the
mattress base sheet and are not loose or damaged.
Serial Labels
Pump The serial number for the pump is on the label on the
back of the pump case.
Mattress The mattress serial label can be found just inside the
base cover above the tubeset, refer to the illustration on
page 2.
Seat Cushion The seat cushion serial label can be found just inside the
front of the base cover, refer to the illustration on page 5.
Quote this serial number when requesting service.

25
9. Troubleshooting & Alarm Condition

The following table provides a troubleshooting guide for the Auto Logic and
Aura Logic systems in the event of malfunction. All the alarm conditions are low
priority, compliance with 60601-1-8.

Indicator Possible Cause Remedy

LOW PRESSURE 1. The pump is inflating the 1. Both indicators will extinguish
mattress/seat. when operating pressure is
reached.
2. CPR not fully closed. 2. Close CPR unit.
and WAIT

LOW PRESSURE 1. The tubeset is not connected 1. Check the tubeset connector
properly. and ensure it is securely
fitted to the pump.
2. CPR not fully closed. 2. Close CPR unit.
3. There is a leak in the system. 3. Call service engineer.

POWER FAILURE Power has been removed from Re-apply power or switch the
the pump. pump off.
If the fully charged battery pack
is fitted the pump will continue to
operate for a minimum of 8
hours.

BATTERY LOW Low battery life. Install a fully charged battery

pack
or
Charge the battery by using
mains power supply to run the
pump.

SERVICE (ON) Pump needs a service. Call service engineer.

To find the serial numbers for the
pump, mattress or seat refer to
“Serial Labels” on page 25.

SERVICE (FLASHING) Pump has detected an internal Switch the pump off and call
fault. service engineer.

AUTOFIRM does not activate 1. Seat pad in use. 1. Autofirm only available for
use with mattresses.
2. Mattress in use. 2. Wait for 2 seconds before
releasing Autofirm button.

NOTE
If the trouble shooting procedures do not return the system to normal
performance, stop using the system immediately and call the service
engineer.

26
10. Technical Description

PUMP
Model: Auto Logic

Part Numbers: 630009KSA KSA

Supply Voltage: 100-230 V 230 V

Supply Frequency: 50-60 Hz 60 Hz

Power Input: 28-68 VA

Size: 375mm x 280mm x 125mm (14.8" x 11" x 5 in.)

Weight: 3.9kg (8.6 lb) (no battery)

4.6kg (10.14 lb) (with battery)

Case Material: ABS Plastic

Plug Fuse Rating: 5A to BS1362 (UK only)

Pump Fuse Rating: 2 x T3.15A H250V

Degree of protection Mains Connected: Class II, Double Insulated without Functional Earth
against electric shock: Type BF

No Mains Connected: Internally Powered (Not Homecare)

Degree of protection IP20 - (Non HomeCare)

against liquid ingress: IP21 - (HomeCare, from serial number: 1500004716) Protection against ingress
of solid objects more than 12.5mm diameter and water droplets falling vertically.

Mode of operation: Continuous

Cycle Time: 10 Mins (Autofirm 15 mins to 30 mins)

27
PUMP
The operator must read this
document (Instructions for Use)
Do not dispose of
before use. Battery Low Indicator
in domestic refuse
Note: This symbol is blue on the
product label.

With respect to electric shock,

fire and mechanical hazards only
in accordance with CAN/CSA- Run/Standby. Note: Unit
CAN/CSA-C22.2
No.60601.1
C22.2 No.60601.1 (2008) + is not isolated from Type BF
(2008) + (2014) (2014) and ANSI/AAMI mains supply.
ANSI/AAMI
ES60601-1 (2005)
ES60601-1 (2005)+AMD(2012).
+ AMD (2012) MEDICAL EQUIPMENT

Refer to this document

i (Instructions for Use) for a

description of the product
classification (3rd Edition).
SN: Serial Number Ref: Model number

Manufacturer: This
Refer to this document
symbol is accompanied
(Instructions for Use) for a
by the name and the
description of the product Double Insulated
address of the
classification (2nd Edition).
manufacturer.

Indicates the product is a Medical CE marking indicating

Device according conformity with
to EU Medical Device Regulation European Community
2017/745 harmonized legislation.
Figures indicate Notified
Body supervision.

ENVIRONMENTAL INFORMATION
Condition Temperature Range Relative Humidity Atmospheric Pressure
Operating +5°C to +40°C 30% to 75% 700hPa to 1060 hPa
(+41°F to +104°F) (non-condensing)
Storage (Long Term) +5°C to +40°C 20% to 95% 700 hPa to 1060 hPa
(+41°F to +104°F) (non-condensing)
Storage (Short Term) -20°C to +65°C 20% to 95% 500 hPa to 1060 hPa
(-4°F to +149°F) (non-condensing)

NOTE
• If the pump is stored in conditions outside the “Operating” ranges, allow time for its
temperature to stabilise to normal before use. Allow a minimum of 8 hours if the pump is
stored at -20°C.
• One of the effects of prolonged exposure to high temperatures is to increase the self-
discharge of the internal battery; this will reduce the duration of power fail alarms. The pump
will fully charge the battery over a 24-hour period when the pump is connected to a mains
power supply.

28
ACCESSORIES
Part: Battery Pack
NOTE: The battery pack is not suitable for use in the homecare environment.
Part Number: BBP600
Weight: 0.8kg
Electrical Rating: 13.8V dc 4Ah (NiMH)
Symbols

Do not dispose of in domestic refuse

Recycle

MATTRESS
Description Cell Material *Foam underlay size Base Pad Material
**Air-filled sub-mattress size
Auto Logic 110 Polyurethane NA NA
Auto Logic 175 Polyurethane *2032 x 838 x 63.5mm (80" x 33" x 2 ½") PU Laminate
Auto Logic 200 Polyurethane **2030 x 860 x 90mm (80" x 34" x 3 ½") PU Laminate

MATTRESS SIZE INFORMATION

Part No. Description Spare Length Width mm Weight Height mm
Cover mm Kg
PXA001DAR Auto Logic 110 (Reliant IS2 ) PXA080 2030 (80") 860 (34") 7.5 115 (4 ½")
PXA201DAR Auto Logic 110 Narrow (Reliant IS2 ) PXA280 2030 (80") 780 (30") 7.5 115 (4 ½")
PXB005DAR Auto Logic 175 (Reliant IS2 ) PXB180 2030 (80") 860 (34") 10.5 175 (7")
PXB001DAR Auto Logic 200 (Reliant IS2 ) PXB080 2030 (80") 860 (34") 10.5 205 (8")
PXB201DAR Auto Logic 200 Narrow (Reliant IS2 ) PXB280 2030 (80") 780 (30") 10.5 205 (8")
PXA001DARW Auto Logic 110 PXA080W 2030 (80") 860 (34") 7.5 115 (4 ½")
(Reliant IS2 welded cover)
PXA201DARW Auto Logic 110 Narrow PXA280W 2030 (80") 780 (30") 7.5 115 (4 ½")
(Reliant IS2 welded cover)
PXB001DARW Auto Logic 200 PXB080W 2030 (80") 860 (34") 10.5 205 (8")
(Reliant IS2 welded cover)
PXB201DARW Auto Logic 200 Narrow PXB280W 2030 (80") 780 (30") 10.5 205 (8")
(Reliant IS2 welded cover)
PXB005DARW Auto Logic 175 PXB180W 2030 (80") 860 (34") 10.5 175 (7")
(Reliant IS2 welded cover)

29
SEAT
Aura Logic Seat Cushion PXS001

Length: 470mm (18 ½")

Width: 455mm (17.9")

Height: 50mm (2")

Cell Material Polyurethane

Sewn Part Number PXS062

Welded Part Number PXS062W

COVER SPECIFICATION
Standard Cover Welded Cover
Feature
(Reliant IS2) (Reliant IS2)

Removable Cover Yes Yes

Moisture Vapour Permeable Low Low

Low Friction No No

Water Resistant / Repellent Yes Yes

Polyurethane coating Yes Yes

includes an antimicrobial
agent to control microbial
deterioration of fabric

Fire Retardant1 BS 7175: 0,1 & 5 BS 7175: 0,1 & 5

2-Way Stretch Yes Yes

Recommended Wash 60°C (140°F) 15 min 60°C (140°F) 15 min.

Temperatures

Maximum Wash Max 95°C (203°F) Max 95°C (203°F)

Temperatures 15 min. 15 min.

Recommended Drying 60°C (140°F) or air dry 60°C (140°F) or air dry
Temperatures

Max Drying Temperatures Max 80°C (176°F) Max 80°C (176°F)

Chlorine at strength of 1000ppm or Chlorine at strength of 1000ppm or

Alcohol at 70% concentration; no Alcohol at 70% concentration; no
Wipedown Chemicals2 phenol; ensure product is dry before phenol; ensure product is dry before
storage storage

1. For additional flammability testing standards, refer to individual product law tags, if applicable
2. Chlorine concentrations may vary from 250ppm to 10,000ppm depending on local policy and
contamination status. If an alternative disinfectant is selected from the wide variety available, Arjo
recommend that suitability for use is confirmed with the chemical supplier prior to use.

30
 MATTRESS CLEANING SYMBOLS
Recommended wash temperature:
Tumble dry at 60°C (140°F)
15 min at 60°C (140°F)
Maximum drying temperature:
Max 95 Maximum wash temperature:
15 Min Max 80 80°C (176°F)
15 min at 95°C (203°F)

Recommended wash temperature:

Tumble dry at 60°C (140°F)
15 min at 60°C (140°F)

Do not iron Do Not Use Phenol-based cleaning Solutions

Wipe surfaces with cleaning solution, then

Use solution diluted to 1000 ppm of Available
wipe with a cloth moistened with water
Chlorine
and dry thoroughly

Electromagnetic Compatibility (EMC)

Product has been tested for compliance with current regulatory standards regarding its
capacity to block EMI (electromagnetic interference) from external sources.
Some procedures can help reduce electromagnetic interferences:
• Use only Arjo cables and spare parts to avoid increased emissions or decreased
immunity which can compromise the correct functioning of the equipment.
• Ensure that other devices in patient-monitoring and/or life-support areas comply to
accepted emissions standards.

WARNING
Wireless communications equipment such as wireless computer network devices, mobile phones, cordless
telephones and their base stations, walkie-talkies, etc. Can affect this equipment and should be kept at least 1.5m
away from the equipment.

Intended Environment: Home Healthcare Environment and Professional Healthcare

facility environment.
Exceptions: HF Surgical Equipment and the RF Shielded room of an ME SYSTEM
for magnetic resonance imaging.

WARNING
Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in
improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify
that they are operating normally.

31
Guidance and manufacturer’s declaration - electromagnetic emissions

Emissions Test Compliance Electromagnetic environment - guidance

RF emissions Group 1
CISPR - 11

RF emissions This equipment uses RF energy only for its internal

Class B
CISPR - 11 function. Therefore, its RF emissions are very low and are
Harmonic emissions not likely to cause any interference in nearby electronic
Class A equipment. This pump is suitable for use in all
IEC 61000-3-2 establishments including domestic and those directly
connected to the public low voltage power supply network
Voltage that supplies buildings used for domestic purposes.
fluctuations/flicker
emissions Complies

IEC 61000-3-3

32
Guidance and manufacturer’s declaration - electromagnetic immunity

Immunity Test IEC 60601-1-2 Compliance Electromagnetic environment - guidance

Test Level Level
Electrostatic ±2kV, ±4kV, ±8kV, ±2kV, ±4kV,
discharge (ESD) ±15kV air ±8kV, ±15kV Floors should be wood, concrete or ceramic tile. If
air floors are covered with synthetic material the relative
EN 61000-4-2 humidity level should be at least 30%.
±8kV contact ±8kV contact

Conducted 3V in 0,15 MHz to 3V in 0,15

disturbances 80MHz MHz to 80MHz
inducted by RF
fields 6V in ISM and
6V in ISM and amateur radio
EN 61000-4-6
amateur radio bands bands Portable and mobile RF communications equipment
between 0,15 MHz between 0,15 should be used no closer to any part of the product,
and 80 MHz MHz and 80 including cables, than 1.0 m, if the transmitter’s
MHz output power rating exceeds 1W (a).
80% AM at 1 kHz Field strengths from fixed RF transmitters, as
80% AM at 1 determined by an electromagnetic site survey a,
kHz should be less than the compliance level in each
frequency range.b
Radiated RF Home Healthcare Home
electromagnetic environment 10 V/m Healthcare
Interference may occur in the vicinity of equipment
field environment
marked with the following symbol:
10 V/m

IEC 61000-4-3 80 MHz to 2.7 GHz 80 MHz to 2.7

GHz

80% AM at 1 kHz 80% AM at 1

kHz

Electrical ±1kV SIP/SOP ports ±1kV SIP/SOP

transient/burst ports
±2kV AC port
±2kV AC port Mains power supply should be that of a typical
EN 61000-4-4 100kHz repetition commercial or hospital environment.
frequency 100kHz
repetition
frequency

Power 30A/m 30A/m Power frequency magnetic fields should be at levels

frequency characteristic of a typical location in a typical
Magnetic field commercial or hospital environment.

EN 61000-4-8

33
Guidance and manufacturer’s declaration - electromagnetic immunity
Surge ±0,5kV ±1kV; ±2 kV, ±0,5kV ±1kV;
AC Mains, Line to ±2 kV,
Ground AC Mains,
Line to
Ground Mains power quality should be that of a typical
±0,5kV ±1kV, AC commercial or hospital environment.
Mains, Line to Line ±0,5kV ±1kV,
IEC 61000-4-5 AC
Mains, Line to
Line

Voltage dips, 0 % UT; 0,5 cycle At 0 % UT; 0,5

short 0°, 45°, 90°, 135°, cycle At 0°,
interruptions 180°, 225°, 270° and 45°, 90°, 135°,
and voltage 315° 180°, 225°,
variations on 270° and 315° Mains power quality should be that of a typical
power supply commercial or hospital environment. If the user of the
input lines 0 % UT; 1 cycle and 0 % UT; 1 product requires continued operation during power
70 % UT; 25/30 cycle and 70 mains interruptions, it is recommended that the
cycles Single phase: % UT; 25/30 product be powered from an uninterrupted power
at 0° cycles Single supply or a battery.
phase: at 0°
IEC 61000-4-11
0 % UT; 250/300 0 % UT;
cycle 250/300 cycle

NOTE: UT is the AC mains voltage prior to application of the test level.

a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land

mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location in which the product is used exceeds the
applicable RF compliance level above, the product should be observed to verify normal operation. If abnormal
operation is observed, additional measures may be necessary, such as reorientating or relocating the product.

b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

34
AUSTRALIA FRANCE POLSKA
Arjo Australia Pty Ltd Arjo SAS Arjo Polska Sp. z o.o.
78, Forsyth Street 2 Avenue Alcide de Gasperi ul. Ks Piotra Wawrzyniaka 2
O’Connor CS 70133 PL-62-052 KOMORNIKI (PoznaĔ)
AU-6163 Western Australia FR-59436 RONCQ CEDEX Tel: +48 61 662 15 50
Tel: +61 89337 4111 Tél: +33 (0) 3 20 28 13 13 Fax: +48 61 662 15 90
Free: +1 800 072 040 Fax: +33 (0) 3 20 28 13 14 E-mail: arjo@arjo.com
Fax: + 61 89337 9077 E-mail: info.france@arjo.com
PORTUGAL
BELGIQUE / BELGIË HONG KONG Arjo em Portugal
Arjo NV/SA Arjo Hong Kong Limited MAQUET Portugal, Lda.
Evenbroekveld 16 Room 411-414, 4/F, Manhattan Centre, (Distribudor Exclusivo)
BE-9420 ERPE-MERE 8 Kwai Cheong Road, Kwai Chung, N.T., Rua Poeta Bocage n.º 2 - 2G
Tél/Tel: +32 (0) 53 60 73 80 HONG KONG PT-1600-233 Lisboa
Fax: +32 (0) 53 60 73 81 Tel: +852 2960 7600 Tel: +351 214 189 815
E-mail: info.belgium@arjo.be Fax: +852 2960 1711 Fax: +351 214 177 413
E-mail: Portugal@arjo.com
BRASIL ITALIA
Arjo Brasil Equipamentos Médicos Ltda Arjo Italia S.p.A. SUISSE / SCHWEIZ
Rua Marina Ciufuli Zanfelice, 329 PB02 Galpão Via Giacomo Peroni 400-402 Arjo AG
- Lapa IT-00131 ROMA Fabrikstrasse 8
São Paulo – SP – Brasil Tel: +39 (0) 6 87426211 Postfach
Fax: +39 (0) 6 87426222 CH-4614 HÄGENDORF
CEP: 05040-000
E-mail: Italy.promo@arjo.com Tél/Tel: +41 (0) 61 337 97 77
Phone: 55-11-3588-5088
Fax: +41 (0) 61 311 97 42
E-mail: vendas.latam@arjo.com MIDDLE EAST
E-mail: servicios.latam@arjo.com Arjo Middle East FZ-LLC SUOMI
Office 908, 9th Floor, Arjo Scandinavia AB
CANADA Riihitontuntie 7 C
HQ Building,North Tower,
Arjo Canada Inc. 02200 Espoo
Dubai Science Park,
90 Matheson Boulevard West Finland
Suite 300 Al Barsha South
Puh: +358 9 6824 1260
CA-MISSISSAUGA, ON, L5R 3R3 P.O Box 11488, Dubai,
E-mail: Asiakaspalvelu.finland@arjo.com
Tel/Tél: +1 905 238 7880 United Arab Emirates
Free: +1 800 665 4831 Institutional Direct +971 487 48053 SVERIGE
Free: +1 800 868 0441 Home Care Fax +971 487 48072 Arjo International HQ
Fax: +1 905 238 7881 Email: Info.ME@arjo.com Hans Michelsensgatan 10
E-mail: info.canada@arjo.com SE-211 20 MALMÖ
NEDERLAND Tel: +46 (0) 10 494 7760
ýESKÁ REPUBLIKA Arjo BV Fax: +46 (0) 10 494 7761
Arjo Czech Republic s.r.o. Biezenwei 21 E-mail: kundservice@arjo.com
Na Strzi 1702/65 4004 MB TIEL
140 00 Praha Postbus 6116 UNITED KINGDOM
Czech Republic 4000 HC TIEL Arjo UK and Ireland
Phone No: +420225092307 Tel: +31 (0) 344 64 08 00 Houghton Hall Park
e-mail: info.cz@arjo.com Fax: +31 (0) 344 64 08 85 Houghton Regis
E-mail: info.nl@arjo.com UK-DUNSTABLE LU5 5XF
DANMARK Tel: +44 (0) 1582 745 700
Arjo A/S NEW ZEALAND Fax: +44 (0) 1582 745 745
Vassingerødvej 52 Arjo Ltd E-mail: sales.admin@arjo.com
DK-3540 LYNGE 34 Vestey Drive
Tel: +45 49 13 84 86 Mount Wellington USA
Fax: +45 49 13 84 87 NZ-AUCKLAND 1060 Arjo Inc.
E-mail: Tel: +64 (0) 9 573 5344 2349 W Lake Street Suite 250
dk_kundeservice@arjo.com Free Call: 0800 000 151 US-Addison, IL 60101
Fax: +64 (0) 9 573 5384 Tel: +1 630 307 2756
DEUTSCHLAND E-mail: nz.info@Arjo.com Free: +1 800 323 1245 Institutional
Arjo GmbH Free: +1 800 868 0441 Home Care
Peter-Sander-Strasse 10 NORGE Fax: +1 630 307 6195
DE-55252 MAINZ-KASTEL Arjo Norway AS E-mail: us.info@arjo.com
Tel: +49 (0) 6134 186 0 Olaf Helsets vei 5
Fax: +49 (0) 6134 186 160 N-0694 OSLO JAPAN
E-mail: info-de@arjo.com Tel: +47 22 08 00 50 Arjo Japan K.K.
Faks: +47 22 08 00 51 ᶡӜ䜭⑟४㱾ɖ䮰йбⴞ  ⮚  ਧǂɱɻɏȫɋ
ESPAÑA E-mail: no.kundeservice@arjo.com ȷㅜ  㱾ɖ䮰ɛɳ  䲾
Arjo Ibérica S.L. 䴫䂡˖  
Parque Empresarial Rivas Futura, C/Marie ÖSTERREICH
Curie 5 Arjo GmbH
Edificio Alfa Planta 6 oficina 6.1-.62 Lemböckgasse 49 / Stiege A / 4.OG
ES-28521 Rivas Vacia, MADRID A-1230 Wien
Tel: +34 93 583 11 20 Tel: +43 1 8 66 56
Fax: +34 93 583 11 22 Fax: +43 1 866 56 7000
E-mail: info.es@arjo.com

Address page - REV 24: 04/2019

www.arjo.com
At Arjo, we are committed to improving the everyday lives of people affected by reduced mobility and age-related health challenges.
With products and solutions that ensure ergonomic patient handling, personal hygiene, disinfection, diagnostics, and the effective
prevention of pressure ulcers and venous thromboembolism, we help professionals across care environments to continually raise
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ArjoHuntleigh AB
Hans Michelsensgatan 10
211 20 Malmö, Sweden
www.arjo.com