Arjo Enterprise 8000X, E8X User guide

INSTRUCTIONS FOR USE

Enterprise 8000X (E8X)

746-585-EN_14 • 12/2020

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 2020.

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

Warnings, Cautions and Notes ........................................................

General Warnings .........................................................................5

1. Introduction ................................................................... 7

Product overview ........................................................................... 9

2. Clinical Applications .................................................. 10

Intended use ...............................................................................10

Indications ...................................................................................10

Contra-indications ....................................................................... 11

3. Installation .................................................................. 12

Electricity supply .........................................................................13

Underbed light ............................................................................. 13

Mattresses ...................................................................................14

4. Operation .................................................................... 16

Brakes and steering .................................................................... 16

Foot Pedal for Adjustment of Bed Height (Optional) ................... 17

How to use the 5th Wheel (Optional) ........................................... 18

Side rails .....................................................................................19

CPR backrest release ................................................................. 21

X-ray cassette tray (Optional) .....................................................22

Operation ....................................................................................22

Bed length adjustment ................................................................24

Bedstripper (linen shelf) (Optional) ............................................. 26

Lifting pole and accessory sockets ............................................. 27

Drainage bag rails ....................................................................... 28

Head and foot boards .................................................................. 29

Adjusting the mattress platform ................................................... 30

Patient controls ...........................................................................31

Caregiver controls .......................................................................31

Patient handset (Optional) .......................................................... 33

Attendant Control Panel (ACP) ................................................... 34

Function lockout ..........................................................................36

Adjusting the calf position ...........................................................37

Backup battery ............................................................................ 38

Duty cycle lockout 39

5. Product Care ............................................................... 40

Mattress platform sections .......................................................... 40

Decontamination ......................................................................... 41

Preventive maintenance .............................................................. 43

Troubleshooting .......................................................................... 46

Fault indications .......................................................................... 47

Product lifetime ...........................................................................47

6. Accessories and Cables ............................................ 48

7. Technical Data ............................................................ 49

8. Warranty and Service ................................................. 53

9. Electromagnetic Compatibility .................................. 54

3

Warnings, Cautions and Notes

Indicates possible hazards in procedures or conditions

WARNING

Caution

NOTE Explains or amplifies a procedure or condition.

which, if not correctly followed, could result in death,
injury or other serious adverse reactions.

Indicates possible hazards in procedures or conditions
which, if not correctly followed, could result in
equipment damage or failure.

4

General Warnings

WARNING

Keep these instructions in a safe place; you may need to refer to them
later on.

Read and understand these instructions before operating the bed.
Caregivers must be trained in the proper use of this product, its
functions and controls, and any accessories.

These instructions are mandatory for the safe and effective use of this
product, including the safety of patients and caregivers.

Unauthorised modifications or repairs to this product may affect its
safety and will invalidate any warranty. Arjo accepts no liability for any
incident, accident or reduction in performance that may occur as a
result of such repairs or modifications.

To avoid the risk of electric shock, this product must only be
connected to an electricity supply with a protective earth.

Do not smoke or use naked flames near this equipment and do not
expose it to extremes of temperature.

Do not use electrically powered beds in the presence of flammable
gases such as anaesthetic agents e.g. in operating theatres.

The bed is intended for indoor use only and should not be used
outside a normal hospital environment.

Do not use accessories that have not been designed or approved for
use with the bed.

The user should carry out a risk assessment before using the bed
with equipment from other suppliers or manufacturers.

Always apply the brakes when the bed is stationary.

To reduce the risk of injury due to falls, lower the bed to minimum
height when the patient is unattended.

Patients should not be left in the Trendelenburg position when
unattended.

To reduce the risk of overbalancing, do not allow the patient to get on
or off the bed when the mattress platform is in a tilted (head down or
foot down) position.

5

WARNING

Where risk assessment indicates that a patient is at high risk of
entrapment owing to their medical condition or other circumstances,
and where there is no medical benefit from their being left in a
contoured position, place the mattress platform in the flat position
when the patient is unattended.

It is recommended to use the Function Lockout facility on the
Attendant Control Panel to prevent unintended movement in
situations where objects may press against the patient’s controls.

When the bed is operated, make sure that obstacles such as feet,
oxygen bottles, bedside furniture or any other objects do not restrict
its movement.

To avoid potential damage or injury, do not leave oxygen bottle or any
other obstacles under the bed frame while operated.

When moving or operating the bed, take care that any accessories
attached to it (e.g. lifting pole) do not strike doors, ceilings, etc.

Hold the head board or foot board when pushing or pulling the bed;
do not hold the side rails or any attached accessories.

Before operating the bed, make sure the patient is positioned
correctly to avoid entrapment or imbalance.

Take care not to squeeze or trap trailing cables from other equipment
between moving parts of the bed.

Take care not to allow clothing or bed linen to become snagged on
moving parts of the bed.

This product complies with the requirements of applicable standards
for electromagnetic compatibility (EMC). However, medical electrical
equipment requires special precautions regarding EMC and should be
installed and used in accordance with the EMC information in the
product service manual.

Medical electrical equipment can be affected by portable and mobile
radio frequency communications equipment, e.g. cellular telephones.

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.

6

1. Introduction

These instructions contain information for the installation, use
and maintenance of the Arjo Enterprise
hospital bed. These beds have multiple functions to provide
the optimum nursing position for both patient and caregiver.

Standard features:

• Folding split side rails with integrated controls

• Electrical adjustment of bed height and leg section

• Electrically operated retracting backrest

•Bio-Contour

• Auto-Chair facility

• Electrical adjustment of head down tilt (Trendelenburg)

• Manual selection of calf section vascular position

• Mattress support surface with removable panels

®

8000X acute care

elevation

®

advanced profiling system

and foot down tilt (reverse Trendelenburg)

• Adjustable length mattress platform

• Drainage bag rails

• Underbed lights

• 125mm single wheel castors

Optional features:

• 150mm (single or dual wheel) castors

• Bedstripper (linen shelf)

• 5th Wheel

• DIN accessory rails

• Lockable foot board

• Full width brake bar

• Radio translucent backrest with X-ray cassette tray

• IndiGo™ Intuitive Drive Assist

• Foot Pedal for Adjustment of Bed Height

• Foot-end mounted Attendant Control Panel (ACP)

Optional features are specified by the customer at the time of
ordering. The chosen options are indicated by the equipment
model number.

7

The model number and serial number can be

ARJO HEALTHCARE LTD
WEDNESBURYWEST MIDLANDS UK

S/No. 012345
Model 5000Bxxxxxxxxx

Made In
Poland

250kg



Duty 10% 2min/20min

Power in 230V 3.0Amp 50Hz

IP54

found on the specification label; this is located on the bed
frame below the head board.

Caution

Specification label

Before using the bed, ensure that the “Power in” rating on the
specification label is compatible with the local electricity supply.

8

Product overview

A

Y

B

C

D

E

F

G

H

I

J

K

L

M

N

O

P

Q

R

S

U

V

G

T

W

X

A. Head board

B. Head end side rail

C. Caregiver controls

D. Backrest section

E. Foot end side rail

F. Patient controls

G. Attendant Control Panel (ACP)

H. Seat section

I. Thigh section

J. Calf section

K. Calf extension sheet

L. Foot board

M. Bedstripper (linen shelf) (Optional)

N. Extension locking handle

NOTE
Flat deck sheets are supplied as standard when the backrest with X-ray cassette tray
is present.

O. Brake pedal / bar (Optional)

P. Accessory socket

Q. Extension catch bar

R. CPR release handle

S. Place for 5th Wheel (Optional, see

page 18)

T. Drainage bag rail

U. Side rail release lever

V. Castor

W. Lifting pole socket

X. Head end brake pedal (Optional)

Y. Roller buffer

9

2. Clinical Applications

WARNING

To ensure the patient can use the bed safely, their age and condition
should be assessed by a clinically qualified person.

The use of head down tilt (Trendelenburg) or foot down tilt (reverse
Trendelenburg) may be contraindicated for certain medical
conditions. The tilt facility should only be used under the guidance of
a clinically qualified person after assessment of the patient’s
condition.

Intended use This product is intended to provide support to patients during a

stay in hospital or other care facility and allows positioning for
CPR and Trendelenburg.

The bed is suitable for use in the following situations:

• Intensive/critical care provided in a hospital where 24­hour medical supervision and constant monitoring is
required, e.g. ITU, ICU and CCU (*Application
Environment 1).

• Acute care provided in a hospital or other medical facility
where medical supervision and monitoring is required,
e.g. general medical and surgical wards (*Application
Environment 2).

• Long term care in a medical area where medical
supervision is required and monitoring is provided if
necessary, e.g. nursing homes and geriatric facilities
(*Application Environment 3).

* Application Environments are defined in
IEC 60601-2-52.

Indications The bed is appropriate for high dependency patients who pose

a movement and handling risk and / or whose clinical condition
requires that they are positioned with minimal physical
handling.

Patients with a moderate amount of independence can, at the
caregiver’s discretion, use the controls to adjust their own
position.

10

The mattress platform can be positioned to assist with such
clinical procedures as may be required in the Application
Environments defined above.

Contra-

185 kg/

250 kg/

407 lb

550 lb

kg

40

146

cm

BMI

17

indications

The bed is not suitable for use in the following situations:

• A domestic area, i.e. home healthcare (*Application
Environment 4).

• Outpatient care (*Application Environment 5).

* Application Environments are defined in
IEC 60601-2-52.

The bed is not suitable for patients under 40kg in weight.

The maximum recommended patient weight is 185kg.

The safe working load (SWL) of the bed is 250kg.

The safe working load is calculated as follows (in accordance
with IEC 60601-2-52):

Maximum patient weight........................................... 185kg

Mattress .................................................................... 20kg

Accessories (including attached loads) ...................... 45kg

TOTAL .................................................................. 250kg

WARNING

If the combined weight of the mattress and accessories exceeds 65kg,
the maximum patient weight must be reduced accordingly.

The recommended patient size is; weight equal or above 40kg,
height between 146cm and 190cm and BMI equal or above 17.

At the discretion of the carer, patients taller than 190cm may be
accommodated by extending the bed -

adjustment" on page 24.

exceed the

“In-bed length” shown on page 50.

Ensure that the patient’s height does not

refer to "Bed length

11

3. Installation

The following chapter describes how to install the bed.

WARNING

If the power supply cord or plug is damaged, the complete assembly
must be replaced by authorised service personnel. Do not remove the
fitted plug, or use a rewireable plug or adapter.

Make sure the power supply cord is not stretched, kinked or crushed.

Do not allow the power supply cord to trail on the floor where it may
cause a trip hazard.

Make sure the power supply cord does not become entangled with
moving parts of the bed or trapped between the bed frame and head
board.

Disconnect the power supply cord from the electricity supply, and
store it as shown, before moving the bed.

Caution

Before the first use, or if the bed has been unused for more than three
months, connect the bed to the electricity supply for at least 24 hours
to allow the backup battery to recharge fully; failure to do this may
reduce the life of the battery. After charging, check that the battery is
fully serviceable by carrying out a battery test as shown on page 45.

12

Electricity
supply

Connect the mains plug to a suitable socket outlet. Make sure
the plug is easily accessible so it can be disconnected quickly
in an emergency.

2

3

1

Power supply cord and potential equalisation terminal

When the bed is connected to the electricity supply, an
indicator will light on the Attendant Control Panel (see
page 34).

The power supply cord (1) is fitted with a plastic hook (2).
When not in use or before moving the bed, clip the hook onto
the head board, coil up the cable and place it over the hook as
shown.

To isolate the bed from the electricity supply, disconnect the
mains plug from the socket outlet.

A potential equalisation terminal (3) is located at the head end
of the bed.

When other electrical equipment is within reach of the patient
or caregiver, potential differences between the equipment can
be minimised by connecting together their potential
equalisation terminals.

Underbed
light

The underbed light illuminates the floor on either side of the
bed.

The underbed light is always on unless the bed is in its low
power state; refer to the section "Low power mode" on
page 39.

13

Mattresses

WARNING

Always use a mattress of the correct size and type. Incompatible
mattresses can create hazards.

Entrapment hazards may exist when using a very soft mattress, even
if it is the correct size.

The maximum recommended mattress thickness for use with side
rails is 18cm.

Read the instructions for use supplied with the mattress.

Where the maximum patient weight specified for the mattress is
different to that specified for the bed, the lower value applies.

A label on the calf extension sheet indicates the correct
mattress size:

Mattress size label

NOTE
The numbers 1, 2 and 3 on the label indicate different mattress platform
refer to Bed length adjustment on page 24.

lengths;

14

Mattresses and
side rails

When choosing bed and mattress combinations, it is important
to consider the use of side rails based on clinical assessment
of each individual patient and in line with local policy.

When assessing the suitability of a mattress for use with side
rails, the following factors should be considered:

• The bed is designed to provide an acceptable side rail
height when used with a foam mattress up to 18cm thick.

• Specialist powered air / foam replacement mattresses
will typically envelop the patient when loaded and can
generally be deeper than a foam mattress without
compromising safety. Other makes of specialist mattress
replacement must be assessed individually prior to use
to verify sufficient clearance is maintained.

• Mattress overlays are not recommended for use with this
bed.

• To ensure compliance with IEC 60601-2-52, an approved
Arjo mattress should be used. Compliance with this
standard when using other mattresses must be validated
by the user.

• For more information on suitable mattresses and
mattress replacements, contact your local Arjo office or
approved distributor. A list of Arjo offices can be found at
the back of this manual.

15

4. Operation

The following chapter describes how to operate the bed.

WARNING

Operate the brake pedals with your feet while wearing suitable shoes.
Do not operate the pedals with your hands.

Brakes and steering

The pedals have three positions as shown below:

• BRAKE: brakes are applied on all four castors.

• FREE: all four castors are free to rotate and swivel.

• STEER: all four castors can rotate, but the steering
castor (see below) is locked so that it cannot swivel. This
helps to keep the bed on a straight line.

BRAKE FREE STEER

Brake pedal
bar

Using the
steering castor

The brake pedals at the foot end of the bed can be linked by a
full width bar.

Position the bed so that all the castors line up in the direction
of travel. Raise the pedals to lock the steering castor and move
the bed by pushing it from the opposite end.

NOTE
The steering castor may be at either end of the bed, as specified by the customer.

NOTE
Brake pedal appearance may alter slightly on actual product, but functionality and
user instructions remains unchanged.

16

Head end brake
pedals

Brake pedals (1) are fitted at the head end of the bed. These
operate in the same way as the foot end pedals.

1

Head end brake pedal

Foot Pedal for Adjustment of Bed Height (Optional)

Bed height can be adjusted from bed control panels and from
the foot pedal located near the foot end of the bed.

Lift cover of pedal with foot and press left side to raise the bed
height. Press right side of pedal to lower the bed height.

17

How to use the 5th Wheel (Optional)

The 5th wheel provides improved mobility and steering.

Activate 5th Wheel:

1. Step down on the head end of the 5th wheel activation pedal (A).

(See Fig. 1)
The 5th wheel (B) will lower until it has contact with the floor.

2. Check that the brakes are unlocked and the brake pedal is in the

“Free” position. (See Fig. 2)

3. The bed is ready for movement.

Deactivate 5th Wheel:

1. Step down on the foot end of the 5th wheel activation pedal (A).

(See Fig. 1)

2. Make sure the 5th wheel (B) is raised from the floor.

Head End

Fig. 1 - 5th wheel activation pedal

Place Brake Pedal in
“Free” position

B

Foot End

A

18

Fig. 2 - Free Position

Side rails

WARNING

The clinically qualified person responsible should consider the age,
size and condition of the patient before allowing the use of side rails.

Side rails are not intended to restrain patients who make a deliberate
attempt to exit the bed.

Ensure that the mattress is suitable for use with side rails - see
Mattresses and side rails on page 15.

To prevent possible entrapment, make sure the patient’s head and
limbs are clear of the side rails when adjusting the mattress platform.

Side rail contact points are identified by this symbol. Keep
hands and fingers away from these areas.

19

To lower the side rail:

Hold either side rail handle (1). Pull the blue release lever (2)
and lower the side rail (3), holding the side rail until it is
completely lowered. The side rail folds down below the
mattress platform.

1

3

2

Side rail operation

NOTE
The head end and foot end side rails operate in the same way.

To raise the side rail:

Hold either side rail handle (1). Pull the side rail up and away
from the bed until it locks in the raised position.

WARNING

Make sure the locking mechanism is securely engaged when the side
rails are raised.

20

CPR backrest release

Manual CPR release handles are located below the calf
section on either side of the bed.

If the patient suffers a cardiac arrest, pull the CPR release
handle (1). This will lower the backrest (2) to enable cardio­pulmonary resuscitation to be carried out.

2

1

CPR backrest release

WARNING

The backrest can fall quickly; keep hands clear to avoid trapping.

Caution

The manual CPR release should only be used in an emergency;
repeated everyday use can cause premature wear.

21

X-ray cassette tray (Optional)

The X-ray cassette tray allows thoracic X-ray photography with
the backrest at any angle and without the patient moving from
the bed.

WARNING

Position the mattress platform at an ergonomic height to allow easy
loading and removal of X-ray cassettes.

Return the X-ray cassette tray to its closed position below the
backrest before raising or lowering the backrest.

Do not sit or place heavy objects on the X-ray cassette tray.

Ensure the X-ray cassette tray is held securely in place by the catch at
all times.

Operation Apply the brakes. Remove the head board from the bed.

Pull the knob (1) to release the catch and slide the tray out (2)
as far as will go.

22

2

1

X-ray cassette tray operation

Release the knob to hold the tray in the fully open position (3).
Position the X-ray cassette (4) on the tray with its bottom edge
against the lip at the foot end of the tray.

3

4

Positioning the X-ray cassette

Pull the knob and slide the tray underneath the backrest.

The red moulding on the top of the X-Ray sitting tool indicates
the top right hand corner of the X-Ray cassette. Use this
feature to assist in accurate positioning.

X-Ray Sitting Tool

Release the knob to hold the tray in one of the latching
positions.

After use, pull the tray out to the fully open position and remove
the X-ray cassette. Return the tray to the closed position below
the backrest and replace the head board.

23

Bed length adjustment

The length of the bed is adjustable to three set positions.
These are typically used as follows:

1 Short, for manoeuvring the bed in confined spaces
2 Standard length, for normal use
3 Extended, to accommodate very tall patients

WARNING

Install a suitable foam mattress extension (squab) at the head end
when the bed is extended.

Always adjust the bed frame and mattress platform to the same length
and make sure both are latched securely in position.

Level the mattress platform before adjusting the bed length.

Take care not to pinch your fingers when lifting the catch bar.

To extend the bed frame:

Pull the blue extension locking handle (1). Pull out the bed
frame (2) to the required position and release the handle.

2

24

1

Extending the bed frame

To extend the mattress platform:

Lift the blue extension catch bar (1). Hold the middle of the end
crossbar (2) and pull out the mattress platform to the required
position. Release the catch bar.

2

1

Extending the mattress platform

WARNING

After extending the mattress platform make sure the calf extension
sheet is clipped over the end of the mattress platform frame.

To shorten the bed:

Reverse the above procedure.

25

Bedstripper (linen shelf) (Optional)

The bedstripper is used for supporting clean linen when the
bed sheets are being changed.

Pull out the bedstripper from its closed position below the foot
board.

After use, push the bedstripper back to its closed position.

Bedstripper (linen shelf)

Caution

The safe working load of the bedstripper is 20kg.

Level the mattress platform before using the bedstripper.

26

Lifting pole and accessory sockets

Lifting pole sockets (1) are located at the head end of the
mattress platform.

Sockets to support compatible accessories are located at the
head end (2) and foot end (3) of the bed.

1

2

Lifting pole and accessory sockets (head end)

3

Accessory sockets (foot end)

27

Drainage bag rails

Rails (1) to support drainage bags, etc. are located below the
thigh and backrest sections on either side of the bed.

(Optional) The bed may also be fitted with DIN accessory rails (2).

1

2

Drainage bag rails and DIN rail

Caution

The maximum weight that can be safely supported by each drainage
bag rail and DIN rail is 5kg.

28

Head and
foot boards

The head and foot boards can be easily lifted off the bed for
access to the patient.

(Optional) The head and foot boards can each be fitted with

locking catches (1) to prevent accidental removal. To unlock
a board: pull out the catches (2) and rotate them a quarter-turn
(3); the board can now be lifted off the bed.

2

3

1

Locking foot board (foot end shown in this example)

After replacing a board on the bed, rotate the catches until they
spring back into the locked position.

29

Adjusting the mattress platform

WARNING

The controls require only a single press to activate. To prevent
unwanted movement of the mattress platform, avoid leaning against
the side rails and keep equipment on and around the bed clear of the
controls.

To avoid potential damage or injury, do not leave oxygen bottle or any
other obstacles under the bed frame while operated.

Controls for use by the patient and caregiver are built into the
head end side rails. These operate the bed’s basic functions.
For patients who find it difficult to use the side rail controls, a
separate handset is available as an optional extra.

An Attendant Control Panel (ACP) for use only by the caregiver
is built into the foot end side rails. This provides full control of
all the bed’s functions.

The functions of the patient and caregiver controls, and the
ACP, are described over the next few pages.

To adjust the mattress platform: press and hold the
appropriate button until the required position is achieved.
Movement will continue until the button is released or the limit
of travel is reached.

NOTE
If a warning tone (beep) sounds when pressing a button, this indicates that the bed is
operating on the backup battery - refer to the section Backup battery on page 38.

NOTE
If a button is held down for more than 90 seconds, the function will be automatically
inhibited until the button is released. The function must then be unlocked as
described in the section Function lockout on page 36.

30

Patient
controls

The patient controls are located on the inside panel of both
head end side rails.

Patient controls (patient’s left hand side)

WARNING

The patient should be shown how to use these controls by the
caregiver.

Caregiver
controls

The caregiver controls are located on the outside panel of both
head end side rails.

Caregiver controls (patient’s right hand side)

31

Thigh section These buttons raise and lower the thigh section.

When the thigh section is first raised from the flat position, the
calf section will be in the Fowler position (angled downwards).

To change the calf section to the vascular (horizontal) position,
refer to the section Adjusting the calf position on page 37.

Backrest angle These buttons raise and lower the backrest.

Bio-Contour The Bio-Contour up button simultaneously raises the backrest

and thigh sections to provide upright patient profiling; the
raised thigh section prevents the patient sliding down the bed.

The Bio-Contour down button returns the mattress platform to
a flat position.

Mattress
platform height

These buttons raise and lower the mattress platform.

When the mattress platform is lowered to 38cm* above the
floor, it will pause then continue to lower until it reaches its
minimum height.

(* 40cm on beds with 150mm castors.)

WARNING

At minimum height, clearance underneath the bed is reduced. Keep
your feet away from the areas below the side rails and take extra care
when using patient hoists or similar equipment.

To avoid potential damage or injury, do not leave oxygen bottle or any
other obstacles under the bed frame while operated.

32

Patient
handset

The controls on this handset operate in the same way as those
on the side rails (see page 32).

(Optional)

WARNING

Store the handset on the side rail using the clip on the back; this will
help to prevent accidental operation of the controls.

The patient should be shown how to use the handset by the caregiver.

Take care not to squeeze or trap the handset cable between moving
parts of the bed.

Patient handset

NOTE
On some models the patient handset does not have mattress platform height,
backrest or thigh section controls.

33

Attendant Control Panel (ACP)

Attendant Control Panels are located on the outside panels of
both foot end side rails. The ACP on the left side and right side
of the bed have different button layouts.

can be mounted at the foot-end of the bed, either clipped onto the
foot board or using an ACP holder (ENT-ACC11) in an accessory
socket. The foot-end mounted ACP has the same button layout as
the right side rail mounted ACP.

Attendant Control Panel (patient’s right hand side)

Additionally, an ACP

Power on indicator - lights when the bed is connected to the
electricity supply.

Battery indicator - refer to the section Backup battery on

.

Mattress
platform height

page 38

These buttons raise and lower the mattress platform.

When the mattress platform is lowered to 38cm* above the
floor, it will pause then continue to lower until it reaches its
minimum height.

(* 40cm on beds with 150mm castors.)

WARNING

At minimum height, clearance underneath the bed is reduced. Keep
your feet away from the areas below the side rails and take extra care
when using patient hoists or similar equipment.

To avoid potential damage or injury, do not leave oxygen bottle or any
other obstacles under the bed frame while operated.

34

Backrest These buttons raise and lower the backrest.

The backrest will pause when it reaches an angle
approximately 30º above the horizontal.

Thigh section These buttons raise and lower the thigh section.

When the thigh section is first raised from the flat position, the
calf section will be in the Fowler position (angled downwards).

To change the calf section to the vascular (horizontal) position,
refer to the section Adjusting the calf position on page 37.

Auto-Chair The Auto-Chair up button simultaneously raises the backrest

and thigh sections, pausing when the backrest reaches 45º.
Continue to hold the up button to lower the foot end of the
mattress platform into a chair position.

If the backrest angle is greater than 45º, it will return to 45º to
prevent the patient from tipping forwards.

The Auto-Chair down button returns the mattress platform to a
flat and level position.

Tilt angle

This button lowers the head end of the mattress platform
(Trendelenburg position).

This button lowers the foot end of the mattress platform
(reverse Trendelenburg position).

NOTE
When returning from a tilted position, the mattress platform will pause at the level
(no tilt) position.

CPR position If the patient suffers a cardiac arrest, press and hold the CPR

button. This will flatten the mattress platform (and lower it if
necessary) to enable cardio-pulmonary resuscitation to be
carried out.

The CPR button overrides the function lockout settings.

35

Function lockout

Function lockout can be used to prevent operation of the
controls, e.g. when inadvertent movement of the mattress
platform could injure the patient.

To lock (prevent) or unlock (allow) functions:

Press the Function Lock button. The indicator above the button
will light.

Press the ACP button(s) corresponding to the function(s) to be
locked or unlocked. The “lock” indicator LED above each
function button shows its current status:

When all functions are locked or unlocked as required, press
the Function Lock button again or wait for five seconds. The
indicator above the Function Lock button will go out and the
lockout settings are stored.

LED on = function locked
LED off = function unlocked.

NOTE
When a function is locked, any associated functions are automatically disabled, e.g.
locking the backrest also disables Bio-Contour and Auto-Chair.

NOTE
Function lockout settings are retained if the bed is disconnected from the electricity
supply.

36

Adjusting the calf position

When the thigh section is raised, the calf section can be
manually changed to the vascular (horizontal) position.

Hold the side of the calf section frame. Lift the calf section
upwards (1) until it latches (2).

1

Changing from Fowler position (left) to vascular

To return the calf section to the Fowler position:

2

Use the caregiver controls or ACP to lower the thigh section to
the flat position; then raise the thigh section again.

WARNING

Take care when lifting the calf section. Observe local manual handling
guidelines.

37

Backup battery

Caution

To ensure the battery is kept fully charged and prevent damage to the
battery, the bed should be connected to the electricity supply at all
times during normal use.

The battery is intended for short term use only. Its life will be reduced
if it is used to power the bed for long periods.

The backup battery allows operation of the bed for short
periods when it is disconnected from the electricity supply or in
emergency situations when the electricity supply is not
available.

The battery’s charge level is indicated as follows:

If an intermittent warning tone (beep-beep-beep) sounds when
operating the bed, the battery is between 75% and 100%
charged.

In this condition all bed functions remain operational.

If a continuous warning tone sounds when operating the bed,
the battery is between 10% and 75% charged.

In this condition, all bed functions remain operational.

If the ACP battery indicator lights red, the battery is less than
10% charged.

In this condition, all functions are locked.

38

Recharging the
backup battery

To recharge the battery, connect the bed to the electricity
supply. Allow at least eight hours to recharge the battery when
it is completely discharged.

While the battery is recharging, the ACP battery indicator lights
yellow. The indicator will go out when the battery is fully
charged.

WARNING

If the battery is left discharged for long periods, its operational life will
be reduced.

The battery must only be recharged using the built-in charger. Do not
use a separate charger or power supply.

The backup battery must be ventilated while recharging. Do not cover
the battery vent hole or obstruct the area around it.

Low power
mode

Duty cycle
lockout

When the bed is disconnected from mains power, it enters a
low power mode to conserve battery power. In this state, the
underbed lights and the indicators on the control panels are
turned off.

Pressing any of the control buttons brings the bed out of low
power mode. The bed will return to low power mode two
minutes after the last control button was pressed.

Continuous operation of the controls may exceed the duty
cycle of the bed’s electrical system, causing the indicators
above the buttons to flash. After 30 seconds, the indicators will
light and all functions are locked.

If this happens, wait for at least 18 minutes then follow the
unlocking procedure described in the section “Function
lockout” on page 36.

39

5. Product Care

WARNING

Disconnect the bed from the electricity supply before starting any
cleaning or maintenance activity. The bed will still operate on battery
power if the function has not been locked on the ACP.

Mattress platform sections

The four mattress platform sections (backrest, seat, thigh and
calf) can be removed by pulling them upwards off the mattress
platform frame.

Lift off the calf extension sheet (1) before removing the calf
section (2).

2 1

Mattress platform sections (top view)

To replace each section, make sure it is correctly positioned on
the mattress platform frame then press down firmly until it
snaps into place.

Replace the calf extension sheet (1) by clipping it over the end
of the mattress platform frame.

40

Decontamination

WARNING

Do not allow the mains plug or power supply cord to get wet.

NOTE
These instructions also apply to accessories but not to mattresses. For lifting straps
and handles, refer to the manufacturer’s instructions supplied with the product.

The bed should be cleaned and disinfected weekly, and before
a new patient uses the bed.

Cleaning Remove the mattress and all accessories from the bed.

The head/foot boards and mattress platform sheets should be
removed from the bed for cleaning.

Wearing suitable protective clothing, clean all surfaces with a
disposable cloth moistened in hand hot water and a neutral
detergent.

Start by cleaning the upper sections of the bed and work along
all horizontal surfaces. Work methodically towards the lower
sections of the bed and clean the wheels last. Take extra care
to clean areas that may trap dust or dirt.

Wipe over with a new disposable cloth moistened with clean
water, and dry with disposable paper towels.

Allow the cleaned parts to dry before replacing the mattress.

Disinfecting After cleaning the bed as described above, wipe all surfaces

with sodium dichloroisocyanurate (NaDCC) at a concentration
of 1,000 parts per million (0.1%) of available chlorine.

In the case of pooling body fluids, e.g. blood, the concentration
of NaDCC should be increased to 10,000 parts per million (1%)
of available chlorine.

Use of other
disinfectants

Arjo recommends sodium dichloroisocyanurate (NaDCC) as a
disinfectant because it is effective, stable and has a fairly
neutral pH. Many other disinfectants are used in healthcare
facilities, and it is not possible for Arjo to test each one to
determine whether it may affect the appearance or
performance of the bed.

If facility protocols require the use of a disinfectant other than
NaDCC (e.g. diluted bleach or hydrogen peroxide), it should be

41

used with care and in accordance with the manufacturer’s
instructions.

Caution

Do not use abrasive compounds or pads, or phenol-based
disinfectants.

Do not use jet stream cleaning or wash tunnels.

Do not remove grease from the actuator pistons.

42

Preventive maintenance

This product is subject to wear and tear during use. To ensure
that it continues to perform within its original specification,
preventive maintenance procedures should be carried out at
the intervals shown.

WARNING

This list indicates the minimum recommended level of preventive
maintenance. More frequent inspections should be carried out when
the product is subjected to heavy use or aggressive environments, or
where required by local regulations.

Failure to carry out these checks, or continuing to use the product if a
fault is found, may compromise the safety of both the patient and
caregiver. Preventive maintenance can help to prevent accidents.

NOTE
Product cannot be maintained and serviced while in use with the patient.

Actions to be done by caregiver Daily Weekly

Check operation of side rails

Visually check castors

Check operation of the manual CPR release
handles on both sides of the bed

Visually check power supply cord and mains plug

Carry out a full test of all electrical bed positioning
functions (backrest, height, tilt, etc.)

Check that the patient controls, caregiver controls
and Attendant Control Panels operate correctly

Check the mattress for damage and fluid ingress

Examine the lifting pole, strap and handle (Optional)

If the result of any of these tests is unsatisfactory, contact Arjo
or an approved service agent.

9

9

9

9

9

9

9

9

43

WARNING

The procedures below must be carried out by suitably trained and
qualified personnel. Failure to do so may result in injury or an unsafe
product.

Actions to be done by qualified personnel Yearly

Check that the bedstripper (linen shelf) (Optional) remains in its
closed position when maximum foot down tilt is applied

Check that the bed operates correctly using the backup battery
as described in the section Battery test on page 45.

Check operation of the castors, paying special attention to
braking and steering functions

Check that the calf section moves to the Fowler position when the
thigh section is raised

Check that the calf section latches securely in the horizontal
(vascular) position when manually raised.

Check that the bed extension locks securely in all three positions

Examine the power supply cord and mains plug; if damaged,
replace the complete assembly; do not use a rewireable plug

Examine all accessible flexible cables for damage and
deterioration

9

9

9

9

9

9

9

9

Check all accessible nuts, bolts and other fasteners are present
and correctly tightened

Check any accessories fitted to the bed, paying particular
attention to fasteners and moving parts

9

9

44

Battery test Check the condition of the backup battery by carrying out the

following test.

1. Disconnect the bed from the electricity supply.

2. Raise the mattress platform to maximum height - ignore
the battery warning tone.

3. Raise the backrest and thigh sections as far as they will
go.

4. Press and hold the CPR button. The mattress platform will
flatten and lower to a mid-height position.

5. Lower the mattress platform to minimum height.

6. Apply maximum head down tilt (Trendelenburg).

7. Return the mattress platform to the level position; then
apply maximum foot down tilt (reverse Trendelenburg).

If this test is not completed successfully, connect the bed to the
electricity supply for at least eight hours to recharge the battery
then perform the test again. If the bed fails a second time,
contact Arjo or an approved service agent.

To maintain best performance, the backup battery should be
replaced every four years by an approved service agent.

45

Troubleshooting

If the equipment fails to operate correctly, the table below
suggests some simple checks and corrective actions. If these
steps fail to resolve the problem, contact Arjo or an approved
service agent.

Symptom Possible Cause Action

Check the power supply
cord is plugged in and

“Beeping” sound when
using the bed

Bed is operating from
the backup battery

the electricity supply is
OK

Check fuse in mains
plug (where fitted)

One or more bed
functions inoperative

Bed is difficult to
manoeuvre

All indicators on ACP lit
or flashing

Mattress platform
cannot be lowered

All functions remain
locked after connecting
mains power after a
near flat battery (ACP
battery indicator was red
before mains power was
connected)

Function(s) locked on
ACP

Brake pedals in “steer”
position

Duty cycle of electrical
system exceeded

Height control software
error

Function(s) locked on all
controls due to a low
power state

Unlock function(s) on
ACP

Place brake pedals in
the “free” position

Refer to the section
Duty cycle lockout on
page 39

Raise the mattress
platform to maximum
height to reset software

To unlock all functions
connect mains power
and then press the
Function Lock button
twice in quick
succession then select
the function(s) to unlock

Bed movement function
buttons do not respond

46

Control software error

Disconnect and then
reconnect the mains
power to clear bed
software errors

Fault indications

The bed’s control software indicates problems in the electrical
system by means of flashing indicators on the Attendant
Control Panel (ACP). If you experience any of the indications
below, contact Arjo or an approved service agent.

Indication Possible cause

ACP mattress platform height and
head down tilt indicators flashing

ACP mattress platform height and
foot down tilt indicators flashing

ACP backrest indicator flashing Backrest actuator fault

ACP thigh section indicator flashing Thigh section actuator

Mattress platform height, head down
tilt, backrest and thigh section
indicators flashing

Height actuator fault
(foot end)

Height actuator fault
(head end)

fault

Control unit fault

Product lifetime

The lifetime of this equipment is typically ten (10) years.
“Lifetime” is defined as the period during which the product will
maintain the specified performance and safety, provided it has
been maintained and operated in conditions of normal use in
accordance with the requirements in these instructions.

47

6. Accessories and Cables

Recommended accessories for the bed are shown in the table
below. Note that some items may not be available in all
countries.

Accessory Product code

Lifting pole with strap and handle ENT-ACC01

IV pole ENT-ACC02

IV pole steel hooks ENT-ACC02 SH

Three-position lifting pole with strap and handle ENT-ACC03

Angled IV pole ENT-ACC04

Fracture frame ENT-ACC05

Syringe pump holder ENT-ACC07

Oxygen bottle holder (for CD, D, E & PD cylinder) ENT-ACC08

Small traction assembly ENT-ACC10

ACP holder ENT-ACC11

Additional hooks for IV pole ENT-ACC14

Power supply cord storage hook (supplied with bed) ENT-ACC15

Oxygen bottle holder (for B5 cylinder) ENT-ACC18

Urine bottle holder ENT-ACC19

Heavy duty IV pole ENT-ACC24

Transducer mounting pole ENT-ACC26

Head end traction assembly ENT-ACC32

ITU head end panel (head board) ENT-ACC34

Oxylog

Bed pan holder ENT-ACC56

Oxygen bottle holder ENT-ACC58

Monitor shelf ENT-ACC64

Lifting pole mounted IV fluid bag holder ENT-ACC65

Foot end infill panels ENT-ACC66

Urine bottle holder ENT-ACC69

IV pole ENT-ACC71

®

equipment bracket ENT-ACC40

Monitor shelf ENT-ACC74

Integrated IV Pole ENT-ACC89

Oxylog is a registered trademark of Dräger Medical.

No. Name Cable Length (m) Whether shielding or not Remark

1 Cable 2.895 No /

48

7. Technical Data

General

Safe working load 250kg

Maximum patient weight 185kg

Product weight (approx.) 150kg

Audible noise 50dB approx.

Operating conditions

Temperature 10°C to 40°C

Relative humidity 20% to 90% at 30°C, non-condensing

Atmospheric pressure 700hPa to 1060hPa

Electrical data

Power input 1.6A max. at 230V a.c. 50/60Hz

1.6A max. at 230V a.c. 60Hz (KSA)

2A max. at 120V a.c. 50/60Hz

Duty cycle 10% (2 min. on, 18 min. off)

Safety standards USA/Canada

Electric shock protection Class I Type B

EMC Complies with IEC 60601-1-2:2014

Potential equalisation terminal

Liquid ingress protection IPX4

Backup battery

EN/IEC 60601-1:2005 AMD1:2012
ANSI/AAMI ES60601-1 (2005) AMD 1
(2012)
CAN/CSA-C22.2 No. 60601-1:14

IEC60601-2-52:2015

Complies with EN 60601-1:2005
AMD1:2012

2 x 12V series connected, sealed,
rechargeable lead/acid gel, 1.3Ah

49

Dimensions (subject to normal manufacturing tolerances)

Overall length Head end board

on mattress
platform

Position 1 (Short) 219cm 224cm

Position 2 (Standard) 230cm 235cm

Position 3 (Extended) 242cm 247cm

In-bed length

Position 1 (Short) 192cm

Position 2 (Standard) 203cm

Position 3 (Extended) 215cm

Overall width 103cm

Height of mattress platform (centre of seat section to floor)

With 125mm castors 32cm to 76cm

With 150mm castors 34cm to 78cm

Head end board
base

Head down tilt angle 12° min.

Foot down tilt angle 12° min.

Mattress size (refer to the section Mattresses on page 14)

Position 2 (Standard) 202cm x 88cm, 12.5 to 18cm thick

Mattress platform angles

End of life disposal

• Equipment that has 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.

• All batteries in the product must be recycled separately. Batteries are to
be disposed in accordance with national or local regulations.

• Components that are primarily made up of different kinds of metal
(containing more than 90% metal by weight) for example bed frame,
should be recycled as metals.

50

Transport and storage

250 kg/
550 lb

185 kg/
407 lb

Handle with care. Do not drop. Avoid shock or violent impact.

This equipment should be stored in a clean, dry and well-ventilated area which
meets the following conditions:

Temperature -10°C to 50°C

Relative humidity 20% to 90% at 30°C, non-condensing

Atmospheric pressure 700hPa to 1060hPa

Caution

If the bed is stored for a long time, it should be connected to the
electricity supply for 24 hours every three months to recharge the
backup battery, otherwise it may become unserviceable.

Symbols

Safe working load

Maximum patient weight

Alternating current (a.c.)

Caution

Refer to instructions for use

Type B applied part

Applied parts are considered to be: Upper frame
section, Bed controls, Safety Sides, Head and Foot
Boards

Manufacturer / date of manufacture

CE marking indicating conformity with European
Community harmonised legislation

Indicates the product is a Medical Device according to
EU Medical Device Regulation 2017/745

51

Symbols (continued)

kg

40

146

cm

BMI

17

=

kg / lb

+

kg / lbkg / lb

Mandatory to read instructions for use

Serial number

Model number

Waste Electrical and Electronic Equipment (WEEE) ­do not dispose of this product in general household or
commercial waste

Potential equalisation terminal

Protective earth (ground)

Recommended mattress size

Recommended patient size

Total weight of the equipment including its safe
working load.

Calf section vascular position

Mattress platform extension

Do not leave Oxygen bottle or any other obstacles under
the bed frame while operated.

52

8. Warranty and Service

Arjo standard terms and conditions apply to all sales; a copy is
available on request. These contain full details of warranty
terms and do not limit the statutory rights of the consumer.

For service, maintenance and any questions regarding this
product, please contact your local Arjo office or approved
distributor. A list of Arjo offices can be found at the back of this
manual.

Have the model number and serial number of the equipment to
hand when contacting Arjo regarding service, spare parts or
accessories.

53

9. Electromagnetic Compatibility

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 life­support 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: 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.

54

Guidance and manufacturer’s declaration – electromagnetic emission

Emission test Compliance Guidance

RF emissions CISPR 11 Group 1

This equipment uses RF energy only for its internal
functions. Therefore its RF emissions are very low

RF emissions CISPR 11 Class A

Harmonic emissions
IEC 61000-3-2

Voltage fluctuations/
flicker emissions IEC
61000-3-3

Class A

Complies

and are not likely to cause any interference in nearby
electronic equipment.
This equipment is suitable for use in all
establishments other than domestic and those directly
connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.

Guidance and manufacturer’s declaration – electromagnetic immunity

Immunity test

Electrostatic
discharge (ESD)

EN 61000-4-2

IEC 60601-1-2
test level

±2kV, ±4kV,
±8kV, ±15kV air

±8kV contact

Compliance level

±2kV, ±4kV, ±8kV, ±15kV air

±8kV contact

Electromagnetic
environment-guidance

Floors should be wood,
concrete or ceramic tile. If
floors are covered with
synthetic material the relative
humidity level should be at
least 30%.

55

Conducted
disturbances
inducted by RF
fields

EN 61000-4-6

Radiated RF
electromagnetic
field
EN 61000-4-3

Proximity fields
from RF wireless
communications
equipment
EN 61000-4-3

3V in 0,15 MHz
to 80 MHz
6V in ISM and
amateur radio
bands between
0,15 MHz and 80
MHz
80% AM at 1
kHz

Professional
Healthcare
environment
3 V/m
80 MHz to 2,7
GHz
80% AM at 1
kHz

385 MHz - 27 V/
m
450 MHz - 28 V/
m
710, 745, 780
MHz - 9V/m
810, 870, 930
MHz - 28 V/m
1720, 1845,
1970, 2450 MHz
– 28 V/m
5240,5500, 5785
MHz - 9V/m

3V in 0,15 MHz to 80 MHz
6V in ISM and amateur radio
bands between 0,15 MHz and
80 MHz
80% AM at 1 kHz

Professional Healthcare
environment

3 V/m

80 MHz to 2,7 GHz

80% AM at 1 kHz

385 MHz - 27 V/m
450 MHz - 28 V/m
710, 745, 780 MHz - 9V/m
810, 870, 930 MHz - 28 V/m
1720, 1845, 1970, 2450 MHz
– 28 V/m

5240,5500, 5785 MHz - 9V/m

Portable and mobile RF
communications equipment
should be used no closer to
any part of the product,
including cables, than 1.0m,
if the transmitter’s output

a

power rating exceeds 1W

.
Field strengths from fixed RF
transmitters, as determined
by an electromagnetic site
survey, should be less than
the compliance level in each

b

frequency range

.
Interference may occur in the
vicinity of equipment marked
with this symbol:

Electrical fast
transient/burst
EN 61000-4-4

Power frequency
Magnetic field
EN 61000-4-8

Surge
IEC 61000-4-5

±1kV SIP/SOP
ports
±2kV AC port
100kHz
repetition
frequency

30A/m
50 Hz or 60 Hz

±0,5kV ±1kV;
±2 kV, AC
Mains, Line to
Ground
±0,5kV ±1kV,
AC Mains, Line
to Line

±1kV SIP/SOP ports
±2kV AC port
100kHz repetition frequency

30A/m
50 Hz

±0,5kV ±1kV; ±2 kV, AC
Mains, Line to Ground
±0,5kV ±1kV, AC Mains,
Line to Line

Mains power supply should
be that of a typical
commercial or hospital
environment.

Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.

56

0% UT; 0,5
cycle

Voltage dips,
short
interruptions and
voltage
variations on
power supply
input lines
IEC 61000-4-11

At 0°, 45°, 90°,
135°, 180°, 225°,
270° and 315°

0% UT; 1 cycle
and
70% UT; 25/30
cycles
Single phase: at
0°

0% UT; 250/300
cycle

0% UT; 0,5 cycle
At 0°, 45°, 90°, 135°, 180°,
225°, 270° and 315°

0% UT; 1 cycle
and
70% UT; 25/30 cycles
Single phase: at 0°

0% UT; 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 performance is observed, additional measures may be necessary.

b

Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 1 V/m.

57

Intentionally left blank

58

AUSTRALIA
Arjo Australia
Building B, Level 3
11 Talavera Road
Macquarie Park, NSW, 2113,
Australia
Phone: [phone]

BELGIQUE / BELGIË
Arjo Belgium
Evenbroekveld 16
9420 Erpe-Mere
Phone: [phone]
Fax: [phone]
E-mail: [e-mail]

BRASIL
Arjo Brasil Equipamentos Médicos Ltda
Rua Marina Ciufuli Zanfelice, 329 PB02
Galpão - Lapa
São Paulo – SP – Brasil
CEP: 05040-000
Phone: [phone]
E-mail: [e-mail]
E-mail: [e-mail]

CANADA
Arjo Canada Inc.
90 Matheson Boulevard West
Suite 300
CA-MISSISSAUGA, ON, L5R 3R3
Tel/Tél: [phone]
Free: [phone] Institutional
Free: [phone] Home Care
Fax: [phone]
E-mail: [e-mail]

ý(6.È5(38%/,.$

Arjo Czech Republic s.r.o.
Na Strzi 1702/65
140 00 Praha
Czech Republic
Phone No: [phone]
e-mail: [e-mail]

'$10$5.

Arjo A/S
Vassingerødvej 52

'./<1*(

Tel: [phone]
Fax: [phone]
E-mail:
[e-mail]

DEUTSCHLAND
Arjo GmbH
Peter-Sander-Strasse 10

'(0$,1=.$67(/

Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

ESPAÑA
ARJO IBERIA S.L.
Poligono Can Salvatella
c/ Cabanyes 1-7
08210 Barberà del Valles
Barcelona - Spain
Telefono 1: [phone]
Telefono 2: [phone]

FRANCE
Arjo SAS
2 Avenue Alcide de Gasperi
CS 70133
FR-59436 RONCQ CEDEX
Tél: [phone]
Fax: [phone]
E-mail: [e-mail]

+21*.21*
$UMR+RQJ.RQJ/LPLWHG

Room 411-414, 4/F, Manhattan Centre,

.ZDL&KHRQJ5RDG.ZDL&KXQJ17
+21*.21*

Tel: [phone]
Fax: [phone]

ITALIA
Arjo Italia S.p.A.
Via Giacomo Peroni 400-402
IT-00131 ROMA
Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

MIDDLE EAST
Arjo Middle East FZ-LLC

2ႈFHWK)ORRU
+4%XLOGLQJ1RUWK7RZHU

Dubai Science Park,
Al Barsha South
P.O Box 11488, Dubai,
United Arab Emirates
Direct [phone]
Fax [phone]
Email: [e-mail]

NEDERLAND
Arjo Nederland BV

%LH]HQZHL

4004 MB TIEL
Postbus 6116
4000 HC TIEL
Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

NEW ZEALAND
Arjo Ltd
34 Vestey Drive
Mount Wellington

1=$8&./$1'

Tel: [phone]
Free Call: 0800 000 151
Fax: [phone]
E-mail: [e-mail]

NORGE

$UMR1RUZD\$6

Olaf Helsets vei 5
N-0694 OSLO
Tel: [phone]
Faks: [phone]
E-mail: [e-mail]

ÖSTERREICH
Arjo GmbH
Lemböckgasse 49 / Stiege A / 4.OG
A-1230 Wien
Tel: [phone]
Fax: [phone]

32/6.$

Arjo Polska Sp. z o.o.

XO.V3LRWUD:DZU]\QLDND
3/.20251,.,3R]QDĔ

Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

PORTUGAL
Arjo em Portugal
MAQUET Portugal, Lda.
(Distribudor Exclusivo)
Rua Poeta Bocage n.º 2 - 2G
PT-1600-233 Lisboa
Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

SUISSE / SCHWEIZ
Arjo AG
Fabrikstrasse 8
Postfach
CH-4614 HÄGENDORF
Tél/Tel: [phone]
Fax: [phone]

SUOMI
Arjo Scandinavia AB
Riihitontuntie 7 C
02200 Espoo
Finland
Puh: [phone]

(PDLO$VLDNDVSDOYHOX¿QODQG#DUMRFRP

SVERIGE
Arjo International HQ
Hans Michelsensgatan 10
SE-211 20 MALMÖ
Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

81,7('.,1*'20
$UMR8.DQG,UHODQG

Houghton Hall Park
Houghton Regis

8.'8167$%/(/8;)

Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

USA
Arjo Inc.
2349 W Lake Street Suite 250
US-Addison, IL 60101
Tel: [phone]
Free: [phone] Institutional
Free: [phone] Home Care
Fax: [phone]
E-mail: [e-mail]

JAPAN

$UMR-DSDQ..

౨ښ౐ߕۢލό໵ࢀ஺໪൬ߺɻ

ϧϱυΡρέ୊ލό໵ϑϩ֌

Tel: [phone]
Fax: [phone]
E-mail: [e-mail]

www.arjo.com

Address page Rev 26 • 11/2020

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

WKHVWDQGDUGRIVDIHDQGGLJQL¿HGFDUH(YHU\WKLQJZHGRZHGRZLWKSHRSOHLQPLQG

ArjoHuntleigh AB
Hans Michelsensgatan 10
211 20 Malmö, Sweden

www.arjo.com