ENTERPRISE 9000X (E9X)

Instruction for Use

746-591-EN_11 • 03/2018 ...with people in mind

Design Policy and Copyright
® and ™ are trademarks belonging to the ArjoHuntleigh group of companies unless otherwise
stated.
© ArjoHuntleigh 2016.
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 wholly or in part without the
consent of ArjoHuntleigh.
Contents
Warnings, Cautions and Notes ...................................................... 4
General Warnings .......................................................................... 5
1. Introduction ...........................................................................7
Product overview ........................................................................... 9
2. Clinical Applications...........................................................10
Intended use ................................................................................ 10
Indications.................................................................................... 10
Contra-indications ........................................................................ 11
3. Installation ...........................................................................12
Weighing system ......................................................................... 13
Electricity supply .......................................................................... 14
Underbed light ............................................................................. 14
Mattresses ................................................................................... 15
4. Operation .............................................................................16
Brakes and steering..................................................................... 16
Foot Pedal for Adjustment of Bed Height (Optional) ................... 17
How to use the 5th Wheel (Optional) ........................................... 18
Split side rails .............................................................................. 19
CPR backrest release ................................................................. 20
X-ray cassette tray (Optional) ..................................................... 21
Operation .................................................................................... 21
Bed length adjustment ................................................................ 23
Bedstripper (linen shelf) (Optional) ............................................. 25
Lifting pole and accessory sockets ............................................. 26
Drainage bag rails........................................................................ 27
Head and foot boards ................................................................. 28
Adjusting the mattress platform .................................................. 29
Patient controls ........................................................................... 30
Caregiver controls ....................................................................... 30
Patient handset (Optional) .......................................................... 32
Attendant Control Panel (ACP) ................................................... 33
Function lockout .......................................................................... 35
Adjusting the calf position ........................................................... 36
Backup battery ............................................................................ 37
Duty cycle lockout ....................................................................... 38
5. Advanced Features ............................................................39
Patient weighing system ............................................................. 39
VariZone™ patient movement detection .................................... 44
Anti-entrapment system (Optional) ............................................. 46
6. Product Care .......................................................................47
Mattress platform sections .......................................................... 47
Decontamination ......................................................................... 48
Preventive maintenance ............................................................. 49
Troubleshooting .......................................................................... 52
Fault indications .......................................................................... 54
Product lifetime ........................................................................... 54
7. Accessories and Cables ....................................................55
8. Technical Data ....................................................................56
9. Warranty and Service ........................................................61
10. Electromagnetic Compatibility .........................................62
3
Warnings, Cautions and Notes
Indicates possible hazards in procedures or conditions which, if not
WARNING correctly followed, could result in death, injury or other serious
adverse reactions.

Indicates possible hazards in procedures or conditions which, if not

CAUTION
correctly followed, could result in equipment damage or failure.

NOTE Explains or amplifies a procedure or condition.

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. ArjoHuntleigh 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 bedside furniture do not
restrict its movement.
The bed can only be moved on firm surfaces. Gradients must not exceed an angle of
10 degrees.
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 when using equipment that needs to be positioned under the base frame to
ensure there is no contact with any part of the bed frame or components.
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.
When operating moving parts of the bed, ensure the bed does not come into contact
with adjacent equipment which could be damaged by the beds operation.
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.

6
1. Introduction

These instructions contain information for the installation, use and

maintenance of the ArjoHuntleigh Enterprise® 9000X acute care 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 elevation
• Electrically operated retracting backrest
• Bio-Contour® advanced profiling system
• Auto-Chair facility
• Electrical adjustment of head down tilt (Trendelenburg) and foot down
tilt (reverse Trendelenburg)
• Manual selection of calf section vascular position
• Mattress support surface with removable panels
• Adjustable length mattress platform
• Drainage bag rails
• Underbed lights
• 125mm single wheel castors
• Full width brake bar
• Patient weighing and patient egress detection

Optional features:
• Anti-Entrapment System
• 150mm (single or dual wheel) castors
• Bedstripper (linen shelf)
• 5th Wheel
• DIN accessory rails
• Lockable foot board and head board
• Radio translucent backrest with X-ray cassette tray
• Flat deck sheets
• IndiGo™ Intuitive Drive Assist

NOTE
Do not combine curved deck sheets with flat deck sheets.

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 found on the
specification label; this is located on the control box tray.

ArjoHuntleigh AB
Hans Michelsensgatan 10
211 20 Malmö, SWEDEN

Specification label

Caution

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

8
Product overview

Fig. 1 - Product overview

A. Head board O. Brake pedal / bar
B. Head end split side rail P. Accessory socket
C. Caregiver controls Q. Extension catch bar
D. Backrest section R. CPR release handle
E. Foot end split side rail S. Weighing / movement detection system
controls
F. Patient controls
T. 5th Wheel (Optional)
G. Attendant Control Panel (ACP)
U. Drainage bag rail
H. Seat section
V. Split side rail release lever
I. Thigh section
W. Anti-entrapment sensor (Optional)
J. Calf section
X. Castor
K. Calf extension sheet
Y. Lifting pole socket
L. Foot board
Z. Head end brake pedal (Optional)
M. Bedstripper (linen shelf) (Optional)
AA.Roller buffer
N. Extension locking handle

NOTE
Flat deck sheets are supplied as standard when the backrest with X-ray cassette tray is
present.
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.
The weighing system is intended to provide reference data only. The weighing system
is not intended to provide readings upon which medication dosage decisions are
made.
Intended use The product is intended to provide support to patients during a stay in
hospital or other care facility. The product allows positioning for CPR and
Trendelenburg and is equipped with a weighing system. The weighing
system is intended to provide reference data only. The weighing system is
not intended to provide readings upon which medication dosage decisions
are made.
The bed is suitable for use in the following situations:
• Intensive/critical care provided in a hospital where 24-hour medical
supervision and constant monitoring is required, e.g. ITU, ICU and
CCU.
• Acute care provided in a hospital or other medical facility where
medical supervision and monitoring is required, e.g. general medical
and surgical wards.
• 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.
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.
The mattress platform can be positioned to assist with such clinical
procedures as may be required in the Application Environments defined
above.

10
Contra- The bed is not suitable for use in the following situations:
indications • A domestic area, i.e. home healthcare.
• Outpatient care.
• By patients under 40kg in weight.
• By children under 12 years old.
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
between146cm and 190cm, and BMI equal or above 17.
At the discretion of the carer, patients taller than190cm may be
40 kg 146 cm BMI 17 accomodated by extending the bed - refer to “Bed length adjustment” in
Chapter 4. Ensure that the patient’s height does not exceed the “In-bed
length” shown in Chapter 7.

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.
Before the first use, or if the bed has been unused for more than three months, read
and understand this IFU and test the functionality of the bed to verify correct
operation. Refer to “Preventive maintenance” on page 49 for a list of functional tests.

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 51.

12
Weighing Position the bed on a flat, level surface and apply the brakes (see page 16).
system
Remove the four transport locking bolts (1) and washers (2); there are two
locking bolts at the head end of the bed and two at the foot end.

2 2

1 1

Fig. 2 - Removing the transport bolts

Retain the bolts and washers in case the bed needs to be transported at a
later date.

CAUTION

To prevent damage to the weighing mechanism, replace the transport locking bolts
and washers before transporting the bed. This is not necessary when moving the bed
short distances over smooth surfaces.
When replacing the transport locking bolts care must be take to avoid trapping or
damaging any cables.

13
Electricity Connect the mains plug to a suitable socket outlet. Make sure the plug is
supply easily accessible so it can be disconnected quickly in an emergency.

2
3

Fig. 3 - 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 33).
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 The underbed light illuminates the floor on either side of the bed.
light The underbed light is always on unless the bed is in its low power state;
refer to the section “Low power mode” on page 38.

14
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 split 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:

1 - 191cm
2 - 202cm
3 - 214cm

12.5 - 18cm

88cm

Mattress size label

NOTE
The numbers 1, 2 and 3 on the label indicate different mattress platform lengths; refer to “Bed
length adjustment” on page 23.
Mattresses and When choosing bed and mattress combinations, it is important to consider
split side rails the use of split 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 split side rails, the
following factors should be considered:
• The bed is designed to provide an acceptable split 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
ArjoHuntleigh 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 ArjoHuntleigh office or approved
distributor. A list of ArjoHuntleigh 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 brake pedals at the foot end of the bed are linked by a full width bar
which makes it easier to operate the pedals, especially when the mattress
platform is at low height.
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

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

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 remain un-changed.

16
Head end brake Brake pedals (1) are at the head end of the bed. These operate in the same
pedals way as the foot end pedals.

Fig. 4 - 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. 5)
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. 6)
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. 5)
2. Make sure the 5th wheel (B) is raised from the floor.

Foot End

A
Head End

Fig. 5 - 5th wheel activation pedal

Place Brake Pedal in

“Free” position
Fig. 6 - Free Position

18
Split side rails

WARNING
The clinically qualified person responsible should consider the age, size and
condition of the patient before allowing the use of split side rails.
Split 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 split side rails - see “Mattresses and
split side rails” on page 15.
To prevent possible entrapment, make sure the patient’s head and limbs are clear of
the split side rails when adjusting the mattress platform.
Split side rail contact points are identified by this symbol. Keep hands and
fingers away from these areas.
To lower the split side rail:
Hold either split side rail handle (1). Pull the blue release lever (2) and lower
the split side rail (3), holding the split side rail until it is completely lowered.
The split side rail folds down below the mattress platform.

2
Fig. 7 - Split side rail operation
NOTE
The head end and foot end split side rails operate in the same way.
To raise the split side rail:
Hold either split side rail handle (1). Pull the split 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 split side rails are
raised.

19
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 cardio-pulmonary resuscitation to be
carried out.

Fig. 8 - 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.

20
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.

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.

21
 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.

22
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.
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.

Fig. 9 - Extending the bed frame

23
 To extend the mattress platform:
Lift the blue extension catch bar (1) and hold the middle of the end crossbar
(2), then pull the mattress platform to the required position. Release the
catch bar.

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

Fig. 10 - 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.

24
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.

Fig. 11 - Bedstripper (linen shelf)

CAUTION

The safe working load of the bedstripper is 20kg.

Level the mattress platform before using the bedstripper.

25
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.

Fig. 12 - Lifting pole and accessory sockets (head end)

3
3

Fig. 13 - Accessory sockets (foot end)

26
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).

Fig. 14 - 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.

CAUTION

Items placed on the drainage bag rails (such as patient drains and urine bags) are
included in the weighing calculation, and can influence measurement of patient weight
- see “Advanced Features” on page 39.

27
Head and The head and foot boards can be easily lifted off the bed for access to the
foot boards patient.
(Optional) The head or foot board may be fitted with two locking catches
(1) to prevent accidental removal. To unlock the head or foot board: pull
out the catches (2) and rotate them a quarter-turn (3); the foot board can
now be lifted off the bed.

2
3

Fig. 15 - Locking foot board (foot end shown in this example)

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

28
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 split side rails and keep equipment on
and around the bed clear of the controls.
Controls for use by the patient and caregiver are built into the head end split
side rails. These operate the bed’s basic functions. For patients who find it
difficult to use the split 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 split 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.

CAUTION

Do not place anything on the electrical box (1) as it may be damaged or obstruct the
movement of the mattress platform.

Fig. 16 - Electrical box

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 37.
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 35.

29
Patient The patient controls are located on the inside panel of both head end split
controls side rails.

Fig. 17 - Patient controls (patient’s left hand side)

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

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

Fig. 18 - Caregiver controls (patient’s right hand side)

30
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 36.

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 These buttons raise and lower the mattress platform.

platform height 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 split side rails and take extra care when using patient hoists
or similar equipment.

31
Patient The controls on this handset operate in the same way as those on the side
handset rails (see page 31).
(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

32
Attendant Control Panel (ACP)
Attendant Control Panels are located on the outside panels of both foot end
split side rails. The ACP on the left side and right side of the bed have
different button layouts.

Fig. 19 - Attendant Control Panel (patient’s right hand side)

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

supply.
Battery indicator - refer to the section “Backup battery” on page 37.

Mattress These buttons raise and lower the mattress platform.

platform height 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
Before lowering the bed, make sure that the space between the mattress frame and
chassis is free of persons, limbs, bedding or other objects.

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

33
 WARNING
If the head end panel has been removed there is an increased risk of entrapment
between the backrest and chassis when the backrest is being lowered. Make sure that
the space between the chassis and backrest is free of persons, limbs, bedding or
other objects.
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 36.

Auto-Chair The Auto-Chair up button simultaneously raises the backrest and thigh
sections, pausing when the backrest reaches 45º. Continue to hold the
button down 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).

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.

34
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:
LED on = function locked
LED off = function unlocked.
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.
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.

35
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).

Fig. 20 - Changing from Fowler position (left) to vascular

To return the calf section to the Fowler position:

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.

36
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.

37
Recharging the To recharge the battery, connect the bed to the electricity supply. Allow at
backup battery 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 When the bed is disconnected from mains power, it enters a low power
mode mode to conserve battery power. In this state, the underbed lights, the
indicators on the control panels and the weighing system display 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.

Duty cycle Continuous operation of the controls may exceed the duty cycle of the bed’s
lockout 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 35.

38
5. Advanced Features

Patient weighing system

The controls for the weighing system are located on the foot end split side
rails.

Fig. 21 - Patient weighing system controls

Display: indicates the patient’s weight in kilograms. It can also be used to

show other information, e.g. bed section angles.

Weigh: this button is used to calculate and display the current patient
weight.

Auto Compensation (tare): this button allows items to be added to or

removed from the bed without affecting the indicated patient weight.

Zero: this button is used to reset the weighing system when the bed is first
set up and before a new patient uses the bed.

Select Weight Display: this button allows the patient weight to be displayed
rounded to the nearest 100g or 500g.

WARNING
The weighing system should only be used by staff trained in the correct use of the
weighing function.
The weighing system should only be used in closely supervised environments, where
factors influencing patient weight (such as additions to the bed) can be controlled as
described in the following instructions for use.

39
Accuracy The weighing system is very sensitive and can be affected by a number of
external factors. For best performance, observe the following precautions:
• Ensure the bed is on a flat, level surface.
• Ensure the transport locking bolts and washers have been removed
before use – refer to page 7.
• Position the bed so that it is clear of obstructions, e.g. walls, furniture,
cables and curtains.
• Ensure the patient is fully on the mattress during weighing.
• While weighing is taking place, the patient should keep as still as
possible and other persons should keep clear of the bed.
• Ensure that the patient, pillows and bed linen do not touch the head
board during weighing.

CAUTION

Any item attached to or placed on any part of the bed other than the head board
(Fig 22, Item 1) and head end lifting pole accessory sockets (Fig 22, Item 2) will
influence the patient weighing system.
Make sure the mains cable is free of the head board and any fixed part of the bed. If
the cable becomes trapped it can affect the accuracy of the weighing system.

2
Areas that do influence patient weighing
Areas that do not influence patient weighing
Fig. 22 - Areas of patient weighing influence
NOTE
Use the AUTO COMPENSATION feature before adding or removing any items (eg: urine
bags, iv poles, mattress pumps, bed-clothes etc.).

40
Initialisation After connecting the bed to the electricity supply, the weighing system must
be initialised as follows:
1. Place the mattress, bed linen and all necessary accessories on
the bed. The patient must not be on the bed at this point.

2. Press the Zero button once.

3. After a few seconds the display will read .

4. The patient can now get onto the bed

5. The bed cannot be re-zeroed once a patient is on the bed. Use

the Auto Compensation feature if adding or removing items from
the bed such as linen or accessories.

WARNING
The weighing system is intended to provide reference data only. The weighing system
is not intended to provide readings upon which medication dosage decisions are
made.

CAUTION

The weighing system MUST be zeroed every time a new patient is to be placed on the
bed.

CAUTION

The weighing system MUST be zeroed every time a mattress is changed.

CAUTION

The weighing system cannot be zeroed if a mattress or accessories weighing more

than 35kg are fitted. To ensure the bed can be zeroed correctly, only use ArjoHuntleigh
approved mattresses.

41
Weighing To calculate and display the patient’s weight:
1. With the patient lying centrally on the bed, press the Weigh
button once.

2. The display will show a moving circular pattern until a stable

weight reading is obtained.

3. The patient’s weight will be displayed for ten seconds then the
display will go blank.

The patient’s weight is usually displayed rounded to the nearest 500g; this
can be temporarily changed to 100g by pressing the Select Weight
Display button. The display will revert to 500g next time the Weigh button
is pressed.
NOTE
The 100g weight display should only be used for comparative readings.

Auto The Auto Compensation facility allows weight (up to a maximum of 100kg)
Compensation to be added to or removed from the bed, without affecting the indicated
patient weight.
1. With the patient lying on the bed, press the Auto Compensation
button once.

2. The display will show a moving circular pattern until a stable

weight reading is obtained.

3. The display will show to indicate that the system is in Auto

Compensation mode.

4. Add or remove accessories, bed linen, pillows, etc. as required.

5. Press the Auto Compensation button again.

6. The display will show a moving circular pattern for a few seconds
then revert to showing the patient’s weight..

CAUTION

The weighing system requires periodic calibration to ensure accuracy. See

“Preventive maintenance” on page 49.

42
Error Codes Error codes are shown on the display. They are used to indicate a problem
with the weighing system; this may be due to an operator error or a possible
fault condition.
The table below shows common error codes with their meanings and
possible causes.

Display Cause Solution

E001 Zero on battery power

Connect bed to mains supply and re-initialise
the weighing system - see page 41

Auto Compensation
E002 weight decrease more
than 100kg
Replace weight removed from bed

Auto Compensation
E003 weight increase more
than 100kg
Remove added weight from bed

A stable weight reading

E102 was not obtained within
10 seconds
Refer to the points listed in the section
“Accuracy” on page 40

NOTE
If the display shows an error code other than those given above, refer to the product service
manual or contact an approved ArjoHuntleigh service agent.

Angle When operating the controls for backrest angle or tilt, the weighing system
indication display shows the approximate angle in degrees of the selected function.
Angles are shown relative to the floor, so the displayed values of backrest
angle and thigh angle change when the mattress platform is tilted.
The tilt angle is shown as a positive value for head down tilt and a negative
value for foot down tilt.

43
VariZone™ patient movement detection
The patient movement detection system can be set to alarm when
undesired movement of the patient occurs. The sensitivity of the patient
movement detection, relative to the centre of the mattress platform, can be
varied incrementally.
The controls for the patient movement detection system are located on the
foot end split side rails.

Fig. 23 - Patient movement detection controls

In Bed: this button activates/deactivates patient movement detection and

increases the sensitivity of the system.

Patient movement detection threshold display: an indicator shows the

current system status and the selected sensitivity of patient movement
detection.

Egress: this button activates/deactivates patient movement detection and

decreases the sensitivity of the system.

WARNING
The patient movement detection function should be checked periodically for correct
operation and before each new patient uses the bed.
Mattresses that are not approved by ArjoHuntleigh should be validated by the user to
ensure correct operation with the VariZone system.

NOTE
Adjusting the mattress platform profile while patient movement detection is active can trigger
an alarm if patient movement detection is set to a high sensitivity.

Operation Before activating patient movement detection, make sure that:

• The patient’s weight has been measured and recorded.
• All additional items (e.g. accessories) have been accounted for using
the Auto Compensation function.
• The weighing system display is blank.

44
 WARNING
Before using patient movement detection, verify that the alarm can be easily heard by
caregivers, e.g. at the nurse’s station.

To activate patient movement detection, press either the In Bed button or

Egress button for two seconds.
The threshold display indicator will flash to show the alarm threshold level.
The further to the left the flashing indicator is, the lower the alarm threshold,
and small movements of the patient in bed will be detected.
The further to the right the flashing indicator is, the higher the alarm
threshold, and only large movements, such as the patient exiting the bed,
will be detected.
Lower Higher
threshold threshold

To increase the patient movement detection threshold:

Press and hold the Egress button; the flashing indicator will move towards
the right. When the required threshold is reached, release the button.
To reduce the patient movement detection threshold:
Press and hold the In Bed button; the flashing indicator will move towards
the left. When the required threshold is reached, release the button.

After a few seconds the indicator will stop flashing and remain lit to show that
patient movement detection is active.
If movement of the patient above the set threshold is detected, an audible
alarm will sound and the threshold indicator will flash.
To cancel the alarm or deactivate patient movement detection:
Press the In Bed button or Egress button once.
The alarm will be silenced and the threshold display indicator will go out to
show that movement detection is deactivated.

45
Anti-entrapment system (Optional)
The anti-entrapment system is designed to detect patient entrapment
between the base and mattress platform when the mattress platform is
lowered, or is placed into tilt or Auto-Chair. The system is permanently
active and cannot be switched off.

2 2
1

Fig. 24 - Anti-entrapment sensors and beam

There are four infra-red sensors (1), one above each castor, which
generate an invisible beam around the base of the bed (3).
If the beam is interrupted (e.g. by a patient’s limb) while the mattress
platform is lowering, the mattress platform stops moving and the weighing
system display shows .Upward movement of the mattress platform is
not affected.

NOTE
The anti-entrapment system may also be triggered if the beam is interrupted by bed linen,
etc.

WARNING
Clean the lenses (2) of the infra-red sensors regularly using a soft dry cloth.

46
6. 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

Fig. 25 - 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.

47
Decontamination

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

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.

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 ArjoHuntleigh recommends sodium dichloroisocyanurate (NaDCC) as a

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

48
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 split side rails 9
Visually check castors 9
Check operation of the manual CPR release handles on both
sides of the bed
9

Visually check power supply cord and mains plug 9

Carry out a full test of all electrical bed positioning functions
(backrest, height, tilt, etc.)
9

Check that the patient controls, caregiver controls and Attendant

Control Panels operate correctly
9

Check that the weighing system controls operate correctly 9

Check operation of the anti-entrapment system and clean the
sensor lenses (see page 46) (Optional)
9

Check the mattress for damage and fluid ingress 9

Examine the lifting pole, strap and handle (Optional) 9

If the result of any of these tests is unsatisfactory, contact ArjoHuntleigh or

an approved service agent.

49
 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
9
Check that the bed operates correctly using the backup battery as described
in the section “Battery test” on page 51.
9
Check operation the of castors, paying special attention to braking and
steering functions
9
Check that the calf section moves to the Fowler position when the thigh
section is raised
9
Check that the calf section latches securely in the horizontal (vascular)
position when manually raised.
9
Check that the bed extension locks securely in all three positions 9
Examine the power supply cord and mains plug; if damaged, replace the
complete assembly; do not use a rewireable plug
9
Examine all accessible flexible cables for damage and deterioration 9
Check all accessible nuts, bolts and other fasteners are present and correctly
tightened
9
Check any accessories fitted to the bed, paying particular attention to
fasteners and moving parts
9
Weighing system
Be sure to follow all local guidelines or regulations regarding weigh scale
verification and calibration.
The weigh system should be re-verified before the date of expiry shown on
the bed. Make sure the bed is re-verified every 12 months. If verification
does not pass, the weigh system should be re-calibrated.
Refer to the product service manual for verification and calibration
procedures or contact an approved ArjoHuntleigh service agent.

Fig. 26 - Weighing Calibration Expiry Label

50
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 ArjoHuntleigh or an approved
service agent.
To maintain best performance, the backup battery should be replaced every
four years by an approved service agent.

51
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 ArjoHuntleigh or an approved service agent.

Symptom Possible Cause Action

Check the power supply cord is
“Beeping” sound when Bed is operating from plugged in and the electricity supply is
using the bed the backup battery OK
Check fuse in mains plug (where fitted)
One or more bed functions Function(s) locked on
Unlock function(s) on ACP
inoperative ACP
Bed is difficult to Brake pedals in Place brake pedals in the “free”
manoeuvre “steer” position position
Duty cycle of
All indicators on ACP lit or Refer to the section “Duty cycle
electrical system
flashing lockout” on page 38
exceeded
Mattress platform cannot Height control Raise the mattress platform to
be lowered software error maximum height to reset software
Remove pressure from control
Control button
Error code E300 is buttons. If error code does not clear
pressed for more than
displayed call an ArjoHuntleigh approved service
90 seconds
engineer
Remove obstruction(s) from below the
Mattress platform cannot
Anti-Entrapment mattress platform. If bed still cannot be
be lowered and error code
system activated lowered, call an ArjoHuntleigh
AES is displayed
approved service engineer
Call an ArjoHuntleigh approved
Error code E410 Service Error
service engineer
Alarm sounds when Movement detection
Increase VariZone threshold setting
patient moves on the bed threshold set too low
Check the mattress platform is not
touching furniture, curtains, cables,
Errors in indicated patient Mattress platform etc.
weight obstructed Check that weight has not been added
to the bed without using the auto-
compensation function.
Backrest does not lower Insufficient patient
Push the backrest down to initiate
using the manual CPR weight applied to the
lowering
release handle backrest
Connect bed to mains supply and re-
Error code E001 Zero on battery power initialise the weighing system - see
page 41

52
Symptom Possible Cause Action
Auto Compensation
Error code E002 weight decrease more Replace weight removed from bed
than 100kg
Auto Compensation
Error code E003 weight increase more Remove added weight from bed
than 100kg
A stable weight
reading was not Refer to the points listed in the section
Error code E102
obtained within 10 “Accuracy” on page 40
seconds

53
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 ArjoHuntleigh or an
approved service agent.

Indication Possible cause

ACP mattress platform height and head Height actuator fault (foot end)
down tilt indicators flashing

ACP mattress platform height and foot Height actuator fault (head
down tilt indicators flashing end)

ACP backrest indicator flashing Backrest actuator fault

ACP thigh section indicator flashing Thigh section actuator fault

Mattress platform height, head down tilt, Control unit fault

backrest and thigh section indicators
flashing

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.

54
7. 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® equipment bracket ENT-ACC40
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
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 /

55
8. Technical Data

General
Safe working load 250kg
Maximum patient weight 185kg
Product weight (approx.) 180kg
Audible noise 50dB approx.
Operating conditions
Temperature 10°C to 40°C (50°F to 104°F)
Relative humidity 20% to 90% at 30°C, non-condensing
Atmospheric pressure 700hPa to 1060hPa

Electrical data
3A max. at 230V a.c. 50/60Hz
3A max. at 230V a.c. 60Hz (KSA)
Power input
5.8A max. at 120V a.c. 60Hz
6.8 max. at 100V a.c. 50/60Hz
Duty cycle 10% (2 min. on, 18 min. off)
Safety standards USA/Canada 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

Electric shock protection Class I Type B

EMC Complies with EN 60601-1-2:2002 and

2007
Complies with EN/IEC 60601-1:2005
Potential equalisation terminal AMD1:2012
Liquid ingress protection IPX4
2 x 12V series connected, sealed,
Backup battery
rechargeable lead/acid gel, 1.2Ah
Patient weighing system
Minimum verification interval (scale division) e 500g
Minimum capacity 10kg
Maximum capacity 250kg

56
 EC type approval no. UK3074. Complies
Approvals
with 2014/31/EU Class III.
Dimensions (subject to normal manufacturing tolerances)
Overall length
Position 1 (Short) 224cm
Position 2 (Standard) 235cm
Position 3 (Extended) 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)
32cm to 76cm Curved Deck Sheets
With 125mm castors
34cm to 78cm Flat Deck Sheets
34cm to 78cm Curved Deck Sheets
With 150mm castors
36cm to 80cm Flat Deck Sheets
Head down tilt angle 12° min.
Foot down tilt angle 12° min.
Mattress size (refer to the section “Mattresses” on page 15)
Position 2 (Standard) 202cm x 88cm, 12.5 to 18cm thick

Mattress platform angles

57
Environmental protection
Incorrect disposal of this equipment and its component parts, particularly gas springs,
actuators, batteries and other electrical devices, may produce substances that are
hazardous to the environment. To minimise these hazards, contact ArjoHuntleigh for
information on correct disposal.

Transport and storage

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 (14°F to 122°F)
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, Split side rails, Head and Foot Boards

Manufacturer / date of manufacture

Complies with the European Medical Device Directive 93/42/

EEC

58
Symbols (continued)
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

40 kg 146 cm BMI 17

+ = kg / lb Total weight of the equipment including its safe working load

kg / lb kg / lb

Calf section vascular position

Mattress platform extension

Calibration expiry Label

INSTRUMENT
RECONNU CONFORME

1 LIMITE DE 7
2
3
VALIDITE
20XX
8
9
Calibration expiry Label (France)
4 10
5 11
6 12

59
Symbols (continued)

Refer to manual

Brake operation Label LH

Brake operation Label RH

Refer to manual

Indicates min / max temp for use of weigh scales

Metrology Notified Body number, complies with NAWI

directive 2014/31/EU
M15 1234 Fictitious example above included “15” representing 2015 for
year of affixing and “1234” representing metrology Notified
Body.

60
9. Warranty and Service

ArjoHuntleigh 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 ArjoHuntleigh office or approved distributor. A list of
ArjoHuntleigh offices can be found at the back of this manual.

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

61
10. Electromagnetic Compatibility

The bed is intended for use in the electromagnetic environment specified in the tables below. The
customer or the user of the bed should ensure that it is used in such an environment. Failing to
ensure that these tables are properly followed may result in the product not working properly.

Portable and mobile frequency communication equipment may affect the normal use of E9000X,
please use E9000X under the recommended electromagnetic environment.

CAUTION

The use of non-approved accessories may result in increased emissions or reduced

immunity of the equipment. A list of approved accessories is included in the product
instructions for use. See chapter 7- Accessories and cables.
When this equipment is used adjacent to other electronic devices, the user should
observe the equipment to verify normal operation.

Guidance and manufacturer’s declaration – electromagnetic emissions

The bed is intended for use in the electromagnetic environment specified below. The customer or the user of
the bed should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment - guidance

The bed uses RF energy only for its internal function. Therefore
RF emissions
Group 1 its RF emissions are very low and are not likely to cause any
CISPR 11
interference in nearby electronic equipment.

RF emissions
Class B
CISPR 11
The bed is suitable for use in all establishments, including
Harmonic emissions
Class A domestic establishments and those directly connected to the
IEC 61000-3-2
public low-voltage power supply network that supplies buildings
Voltage fluctuations/ used for domestic purposes.
flicker emissions Complies
IEC 61000-3-3

62
 Guidance and manufacturer’s declaration – electromagnetic immunity
The bed is intended for use in the electromagnetic environment specified below. The customer or the user of the
bed should assure that it is used in such an environment.
IEC 60601 Compliance
Immunity test Electromagnetic environment - guidance
test level level

Electrostatic Floors should be wood, concrete or ceramic tile. If

± 6kV contact ± 6kV contact
discharge (ESD) floors are covered with synthetic material, the
± 8kV air ± 8kV air
IEC 610000-4-2 relative humidity should be at least 30%

± 2kV for power

Electrical fast ± 2kV
supply lines Mains power quality should be that of a typical
transient/burst
± 1kV for input/ commercial or hospital environment.
IEC 61000-4-4 Not applicable
output lines
± 1kV line to
± 1kV
Surge line Mains power quality should be that of a typical
IEC 61000-4-5 ± 2kV line to commercial or hospital environment.
± 2kV
earth

70% UT
70% of input
(30% dip in UT)
voltage for 500ms
for 25 cycles
Voltage dips, 40% UT Mains power quality should be that of a typical
40% of input
short interruptions (60% dip in U ) commercial or hospital environment.
T voltage for 100ms
and voltage
for 5 cycles
variations on <5% UT If the user of the bed requires continued operation
<5% of input
power supply during power mains interruptions, it is
(>95% dip in voltage for 10ms
input lines recommended that the bed be powered from an
IEC 61000-4-11 U T) for 0.5 cycle uninterruptible power supply or battery.
<5% UT <5% of input
voltage for
(>95% dip in
5000ms
UT) for 5 sec.

Power frequency
Power frequency magnetic fields should be at
(50/60Hz)
3A/m 3A/m levels characteristic of a typical location in a
magnetic field
typical commercial or hospital environment.
IEC 61000-4-8

NOTE UT is the a.c. mains voltage prior to the application of the test level

63
 Guidance and manufacturer’s declaration – electromagnetic immunity
The bed is intended for use in the electromagnetic environment specified below. The customer or the user of
the bed should assure that it is used in such an environment.
IEC 60601 test Compliance
Immunity test Electromagnetic environment - guidance
level level

Portable and mobile RF communication s

equipment should be used no closer to any part of
the bed, including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance

Conducted RF 3V rms
3V d 1.2 P
IEC 61000-4-6 150kHz to 80MHz
Radiated RF 3V/m
3V/m d 1.2 P 80 MHz to 800MHz
IEC 61000-4-3 80MHz to 2.5GHz

d 2.3 P 800MHz to 2.5GHz

Where P is the maximum output power rating of

the transmitter in watts (W) according to the
transmitter manufacturer and d is the
recommended separation in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,a
should be less than the compliance level in each
frequency range.b
Interference may occur in the vicinity
of equipment marked with the
following symbol:

NOTE 1 At 80MHz and 800MHz, the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
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
bed is used exceeds the applicable RF compliance level above, the bed should be observed to verify normal
operation. If abnormal performance is observed additional measures may be necessary, such as reorienting
or relocating the bed.
b Over the frequency range 150kHz to 80MHz, field strengths should be less than 3V/m.

64
 Recommended separation distances between portable and mobile RF
communications equipment and the bed

The bed is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the bed can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the bed as
recommended below, according to the maximum output power of the communications equipment.

Separation distance according to frequency of transmitter

m

Rated maximum output 150kHz to 80MHz 80MHz to 800MHz 800MHz to 2.5GHz

power of transmitter
W
d 1.2 P d 1.2 P d 2.3 P
0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
metres (m) can be estimated using the equation applicable to the power of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80MHz and 800MHz, the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by
NOTE 2
absorption and reflection from structures, objects and people.

65
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66
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
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90 Matheson Boulevard West Biotechnology & Research Park, Riihitontuntie 7 C
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Tel/Tél: +1 905 238 7880 Tel: +971 (0)4 447 0942 Puh: +358 9 6824 1260
Free: +1 800 665 4831 Institutional E-mail: [email protected] E-mail: Asiakaspalvelu.[email protected]
Free: +1 800 868 0441 Home Care
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E-mail: [email protected] Arjo BV Arjo International HQ
Biezenwei 21 Hans Michelsensgatan 10
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ESPAÑA $UMR-DSDQ..
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Parque Empresarial Rivas Futura, C/Marie Arjo GmbH 㝵
Curie 5 Lemböckgasse 49 / Stiege A / 4.OG 㟁ヰ㸸
Edicio Alfa Planta 6 ocina 6.1-.62 A-1230 Wien
ES-28521 Rivas Vacia, MADRID Tel: +43 1 8 66 56
Tel: +34 93 583 11 20 Fax: +43 1 866 56 7000
Fax: +34 93 583 11 22 Address page - REV 21: 02/2018
E-mail: [email protected]

www.arjo.com
ArjoHuntleigh AB
Hans Michelsensgatan 10
211 20 Malmö, Sweden
www.arjohuntleigh.com

ArjoHuntleigh is a world-leading provider of integrated products and

solutions that improve the lives of patients and residents with reduced
mobility. We help healthcare facilities deliver wellness
and effective everyday care, early mobilisation, safe patient handling,
venous thromboembolism prevention, pressure injury prevention,
hygiene routines, bariatric care and diagnostics. With extensive know-
ledge and experience, we strive to improve efficiency and ensure
a safer and dignified environment for caregivers and their patients.