Arjo Alpha Trancell Deluxe User manual

Alpha Trancell Deluxe
500934US-P_06 • 04/2019
INSTRUCTIONS FOR USE

Design Policy and Copyright
® and ™ are trademarks belonging to the Arjo group of companies.
© Arjo 2019.
As our policy is one of continuous improvement, we reserve the right to modify designs without
prior notice. The content of this publication may not be copied either whole or in part without the
consent of Arjo.
WARNING
To avoid injury, always read this Instructions for Use and accompanied documents
before using the product.
Mandatory to read the Instructions for Use

(i)
Contents
General Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . iii
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
About this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1
About Alpha Trancell Deluxe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Clinical Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Indications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Care of the patient when sitting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Preparing the System for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Installing the Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Installing a Mattress Overlay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
Installing the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Inflating the Mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Rapid Deflate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Stopping Therapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Decontamination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Routine Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Alpha Trancell Deluxe Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Alpha Trancell Deluxe Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Mattresses and Seats . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Serial Number Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Troubleshooting Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

(ii)
Technical Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Environmental Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Pump Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
Mattress Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
Product . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
Cover Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
Cleaning Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20
Seat Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21

(iii)
GENERAL SAFETY
Before you connect the system pump to a mains socket, read carefully all the installation instructions
contained within this manual.
The system has been designed to comply with regulatory safety standards including:
EN60601-1:2006/A1:2013 and IEC 60601-1:2005/A1:2012
EN60601-1-11:2010; IEC 60601-1-11:2010 and IEC60601-1-8:2012
ANSI/AAMI ES 60601-1(2005)+AMD(2012) and CAN/CSA C22.2 No.60601-1(2008)+(2014).
Safety Warnings
• It is the responsibility of the care giver to ensure that the user can use this product
safely.
• Whilst the patient is unattended, the decision to use safety sides should be based on
clinical assessment and in line with local policy.
• Alignment of the bed frame, safety sides and the mattress should leave no gap wide
enough to entrap a patient's head or body, or to allow egress to occur in a hazardous
manner where entanglement with the mains power cable and tubeset or air hoses may
result. Care should be exercised to prevent occurrence of gaps by compression or
movement of the mattress. Death or serious injury may occur.
• Make sure that the mains power cable and tubeset or air hoses are positioned to avoid
causing a trip or other hazard, and are clear of moving bed mechanisms or other possible
entrapment areas. Where cable management flaps are provided along the sides of the
mattress, these should be used to cover the mains power cable.
• Electrical equipment may be hazardous if misused. There are no user-serviceable parts
inside the pump. The pump's case must only be removed by authorised technical
personnel. No modification of this equipment is allowed.
• The power switch must be accessible at all times. Use the power switch to disconnect the
pump completely from the power supply.
• The Rapid Deflate indicator tag must be visible and accessible at all times.
• Disconnect the pump from the mains power socket before cleaning and inspecting.
• Keep the pump away from sources of liquids and do not immerse in water.
• Do not use the pump in the presence of uncontained flammable liquids or gasses.
• The cover of this product is vapour permeable but not air permeable and may present a
suffocation risk.
• Bags supplied with this equipment may present a suffocation risk; to avoid the risk of
suffocation keep the bags away from babies and small children.
• There is no Transport facility on the Alpha Trancell®Deluxe seat cushion.
• Only the pump and mattress combination as indicated by Arjo should be used. The
correct function of the product cannot be guaranteed if incorrect pump and mattress
combinations are used.
• 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.

(iv)
Precautions
For your own safety and the safety of the equipment, always take the following precautions:
• Placing extra layers between the patient and the mattress potentially reduces the benefits
provided by the mattress and should be avoided or kept to a minimum. As part of sensible
pressure area care, it is advisable to avoid wearing clothing which may cause areas of localised
high pressure due to creases, seams, etc. Placing objects in pockets should be avoided for the
same reason.
• Do not expose the system, especially the mattress, to naked flames, such as cigarettes, etc.
• In the event of a fire, a leak in the seat or mattress could propagate the fire.
• Do not store the system in direct sunlight.
• Do not use phenol-based solutions to clean the system.
• Make sure the system is clean and dry prior to use or storage.
• Never use sharp objects or electrically heated under blankets on or under the system.
• Store the pump and mattress in the protective bags supplied.
• Pets and children must be supervised in the vicinity of the system.
• When the pump is in use the operator should remain in area in case the system alarms.
Electromagnetic Compatibility (EMC)
This product complies with the requirements of applicable EMC Standards. Medical electrical
equipment needs special precautions regarding EMC and needs to be installed in accordance with
the following instructions:
• The use of accessories not specified by the manufacturer may result in increased emissions by,
or decreased immunity of, the equipment, affecting its performance.
• Portable and mobile radio frequency (RF) communications equipment (e.g. mobile/cell phones)
can affect medical electrical equipment.
• If this equipment needs to be used adjacent to other electrical equipment, normal operation must
be checked before use.
• For detailed EMC information contact Arjo service personnel.
Environmental Protection
Incorrect disposal of this equipment and its component parts, particularly batteries or other electrical
components, may produce substances that are hazardous to the environment. To minimise these
hazards, contact Arjo for information on correct disposal.
Expected Service Life
The Alpha Trancell Deluxe pump has an expected service life of seven years. To maintain the
condition of the pump, observe the service information.
Do NOT use unapproved accessories or attempt to modify, disassemble or otherwise misuse the
Alpha Trancell Deluxe system. Failure to observe this caution could result in injury, or in extreme
cases, death.
End of Life Disposal
• Fabric material used on the mattresses or any other textiles, polymers or plastic materials etc.
should be sorted as combustible waste.
• Mattresses at the end of life should be disposed of as waste according to the national or local
requirements which may be landfill or combustion.
• Pump units have electrical and electronic components should be disassembled and recycled per
Waste of Electrical and Electronic Equipment (WEEE) or in accordance with local or national
regulation.

1
1. Introduction
About this Manual This manual is your introduction to the Alpha Trancell®Deluxe
systems. You must read and fully understand this manual before
using the system.
Use this manual to initially set up the system, and keep it as a
reference for day-to-day routines and as a guide to maintenance.
If you have any difficulties in setting-up or using the Alpha Trancell
Deluxe system, contact your local Arjo sales office, listed at the end
of this manual.
Intended Use The intended use of this product is to prevent and/or manage
pressure ulcers for patients up to 120 kg (264 lb).
The Alpha Trancell Deluxe system should be used as part of a
prescribed plan of care (refer to “Indications” on page 5).
About Alpha Trancell
Deluxe
The Alpha Trancell Deluxe is a pressure relief system which
consists of a pump and a choice of mattresses or a seat cushion:
•Alpha Trancell Deluxe mattress overlay
•Alpha Trancell Deluxe mattress replacement
•Alpha Trancell Deluxe seat cushion
•Alpha PREVENT™mattress overlay
•Trancell®II mattress overlay
Depending on the choice of mattress, the system is indicated for
patients who are at risk of developing pressure ulcers.
The Alpha Trancell Deluxe system can be used in acute care, long-
term care and home care environments, including private homes.
A full technical description of the Alpha Trancell Deluxe system can
be found in the Service Manual, part numbers SER0004 (pump)
and SER0005 (mattresses), available from Arjo.

2
Product Description
Pump Unit
Alpha PREVENT
Overlay
Pressure Control Knob
Low Pressure Indicator
Tubeset Connections
Fuse Holder
Power:Connect / Power:Disconnect Switch
Suspension Hooks
on Rear Case
Setting Up Instructions on Rear Case
Power Indicator
Power Fail Indicator
Wait Indicator
Tube Protector
Air Feed Tubes
Corner Straps
Clip
Pump Connectors

3
Trancell II Overlay
Alpha Trancell Deluxe Overlay
Cover
Air Feed Tubes
Securing Apron
Cells
Fixing Strap
Rapid deflate tag
Top Cover
Corner Straps
Cells
Zips
Transport Facility
Rapid Deflate
Pump Connectors

4
Alpha Trancell Deluxe Mattress Replacement
Alpha Trancell Deluxe Seat Cushion
Top Cover
Foam Base Pad
Cells
Top Cover Zips
Bottom Cover Zips
Transport Facility
Rapid Deflate
Base Cover
Straps
Pump Connectors
Cover
Straps
Cells Pump Connectors

5
2. Clinical Applications
Indications The Alpha Trancell Deluxe systems are indicated for the prevention
and/or management of pressure ulcers, when combined with an
individualised, comprehensive pressure ulcer protocol: for
example, repositioning, nutritional support, skin care. Selection
should be based upon a holistic assessment of the patient’s
individual care needs.
These systems represent one aspect of a pressure ulcer
management protocol; all other aspects of care should be
considered by the prescribing clinician.
If existing wounds do not improve or the patient's condition changes
the overall therapy regimen should be reviewed by the prescribing
clinician.
The above are guidelines only and should not replace clinical
judgement.
Alpha PREVENT Indicated for prevention and/or management of pressure ulcers up
to category 21. Maximum patient weight 90 kg.
Alpha Trancell Deluxe/
Trancell II
Indicated for prevention and/or management of all categories of
pressure ulcer. Maximum patient weight 120 kg.
Alpha Trancell Deluxe
Seat Cushion
Indicated for prevention and/or management of all categories of
pressure ulcer for patients weighing between 40 to 90 kg.
Contraindications Do not use these systems for patients with unstable spinal
fractures.
Cautions If patients have other unstable fractures, or conditions which may
be complicated by a soft or moving surface, advice should be
sought from an appropriate clinician before use.
While these systems have been designed to manage patients up to
the weight limits indicated above, those approaching this upper limit
are likely to have additional care and mobility needs and may be
better suited to a specialist bariatric system.
Active therapy (alternating) cushions may be unsuitable for patients
with poor sitting posture or pelvic deformity; advice from a seating
specialist should be sought.
Care of the patient
when sitting
Seated patients are at increased risk of pressure ulcers particularly
if they are immobile or have wounds over the seating area. For
optimal outcome, provide a pressure redistributing seat cushion in
a chair which promotes a good sitting posture and has a level base
seat to support the cushion, in addition to an individualised
repositioning programme.
1. NPUAP/EPUAP International Pressure Ulcer Guideline, 2014.
NOTE
Mattress and cushion combinations may have different upper weight limits. Cushions should be
used in combination with pressure-redistributing mattresses to provide 24-hour therapy.

6
3. Installation
Preparing the System for Use
The system is simple to set up using the following guidelines.
Remove the contents from the packaging. You should have the
following items:
•Alpha Trancell Deluxe pump with integral mains power cord and
hanging bracket.
• Mattress overlay, mattress replacement or a seat cushion.
Installing the
Pump
1. The pump should be placed feet down on any convenient
surface or alternatively suspended from the bed foot rail by
means of the swing out hooks.
2. Plug the pump power cable into wall socket. Leave the
Power:connect / Power:disconnect switch in the
Power:disconnect position.
Installing a Mattress
Overlay
If you have an Alpha Trancell Deluxe, Trancell II or Alpha
PREVENT, mattress overlay, it should be installed as follows:
1. Place overlay on top of the normal mattress surface with the
air feed tubes located near the pump at the foot end of the
bed.
2. Secure the mattress overlay by tucking the securing aprons
under each end of the mattress and/or securing the corner
straps under each corner of the bed mattress.
3. When using the Trancell II or Alpha Trancell Deluxe
mattresses, ensure that the Rapid Deflate stopper at the head
end of the bed is securely fitted.
4. When using the Trancell II mattress overlays, place protective
cover over the mattress overlay and adjust fixing strap around
overlay or bed mattress. Make sure the cover is fitted loosely
around mattress to prevent hammocking.
WARNING
Bags supplied with this equipment may present a suffocation risk; to avoid the
risk of suffocation keep the bags away from babies and small children.
WARNING
Do not use the mattress overlay directly on the bed frame.
NOTE
Trancell II overlays are supplied with separate connector adaptors
to suit the Alpha Trancell Deluxe pump. Ensure these are fitted to
the overlay pump connectors before use.

7
Alpha Trancell Deluxe
Mattress Replacement
If you have the Alpha Trancell Deluxe mattress replacement system,
it should be installed as follows:
1. Remove the existing mattress from the bed frame and check
that there are no protruding bed springs or sharp objects on the
bed frame surface.
2. Place the mattress onto the bed frame and ensure that the
tubeset is located at the foot end of the bed. The cells of the
mattress must be uppermost.
3. Ensure the mattress has been secured to the bed frame using
the straps provided.
4. Ensure that the Rapid Deflate stopper at the head end of the
bed is securely fitted.
Alpha Trancell Deluxe
Seat Cushion
The seat cushion should be installed as follows:
1. Check that there are no sharp objects on the chair which may
puncture the cushion.
2. Place the cushion on top of the chair surface. From a standing
position in front of the chair and facing it, ensure that:
• The cells are uppermost.
• The tube-set appears from the front right corner of the
cushion.
3. Secure the seat cushion to the chair by using the fixing straps
as shown in the following illustrations.
4. If the chair is of the open sided construction, then fix the
cushion as shown below:
NOTE
The cells are in a horizontal position across the chair, not from front
to back.
Cautions
• Do not use the Alpha Trancell Deluxe seat cushion without a foam cushion
beneath it.
• Always use the Alpha Trancell Deluxe seat cushion with the protective top
cover.
• Always use the Alpha Trancell Deluxe seat cushion in the correct orientation.
• Avoid trailing cables - ensure that cables and tubing are positioned beneath
the chair to avoid causing a hazard.

8
5. If the chair is of the closed side type with a removable seat
cushion, fix the seat cushion as shown below:
6. If the chair is of the closed side type with a non-removable
seat cushion, then security will rely on the anti-slip base
material of the seat cushion.
7. Position the protective cover over the seat cushion and
ensure that the Alpha Trancell Deluxe logo is uppermost and
at the front of the seat.
To complete the
system installation
Complete the installation of the system as follows:
1. If not already fitted, place the protective cover over the
mattress. Ensure that the Alpha Trancell Deluxe logo is
uppermost and at the foot end of the mattress.
2. Connect tubeset to pump ensuring that the tubes are not
kinked or twisted.
3. The system is now ready for use. Refer to “Controls and
Indicators” on page 9 and “Operation” on page 10 for day-to-
day operating instructions.

9
4. Controls and Indicators
Controls
Pressure Control This is situated on the front panel and is adjusted by the carer to suit
the weight of the patient.
Power:Connect/
Power:Disconnect
Switch
This is situated on the side panel of the pump and is used to
activate the unit and reset alarms. Mains isolation should be
performed with the pump disconnected from power.
To isolate the pump from the mains power, switch the pump to
Power: disconnect ( ) and then remove the plug from the mains
power socket.
Indicators
Power On A light on the front panel indicates that the pump is running.
Wait When the overlay is being inflated the amber Wait indicator remains
illuminated until the overlay is correctly inflated.
Low Pressure In the event of low pressure in the overlay, the yellow Low Pressure
alarm indicator starts flashing and an audible alarm sounds.
Power Fail In the event of mains power failure, the yellow alarm indicator starts
flashing and an audible alarm sounds. If the power supply is
returned the audible alarm stops, but the alarm light remains
illuminated until the system is reset (UK only).
Alarm
Alarm Priority All the alarm conditions are low priority, compliance with 60601-1-8.
Alarm Reset When the cause of the alarm has been resolved, the pump needs
to be reset. This can be achieved by switching the pump to
Power:disconnect and back to Power:connect using the
Power:connect / Power:disconnect switch on the side panel.
Self Test Every time the pump is switched on all indicator lights illuminate for
approximately two seconds. During this period, the system self
tests its circuits.
(Power:Connect)
(Power:Disconnect)

10
5. Operation
These instructions cover day-to-day operation of the system. Other operations, such as maintenance
and repair, should only be carried out by suitably qualified personnel.
Installing the System Before using the Alpha Trancell Deluxe system make sure that it
has been installed correctly in accordance with
Section 3, Page 6 “Installation”.
Where fitted, make sure:
• The rapid deflate stopper on the mattress is securely fitted.
• The Transport control on the mattress is set to Normal.
Inflating the Mattress 1. Connect the pump to the mains power supply using the
supplied cable.
2. Set the Power:connect / Power:disconnect switch to
Power:connect ( ). The pump performs a diagnostic self test,
illuminating all four indicators and sounding the audible alarm.
3. At the end of this start-up sequence, the pump starts to inflate
the mattress or seat cushion.
• The green Power indicator and amber Wait indicator are
illuminated while the mattress or seat cushion is inflating.
• The pump may take up to 10-15 minutes to fully inflate a
mattress or 2-3 minutes for the seat cushion. The amber
Wait indicator extinguishes when the system is fully
inflated.
NOTE
Refer to Section 4, Page 9 “Controls and Indicators” for a comprehensive description of the
controls and indicators on the pump.
NOTE
If the operation of the pump changes during use, refer to “Troubleshooting Guide” on page 16 of
this manual before calling a service engineer or contacting your local Arjo sales office.
WARNING
Make sure that the mains power cable and mattress tubeset are positioned to
avoid causing a trip or strangulation hazard, and are clear of moving bed
mechanisms or other possible entrapment areas.
Do not place the patient on the mattress or seat cushion until it is fully inflated,
when the Wait indicator is extinguished.

11
To Adjust the Pressure
Control Knob Position
The pressure control knob (2) is locked in position to prevent
accidental rotation.
To adjust the position of the pressure control knob:
1. Lift the lock pin (A) to release the control knob.
2. Rotate the control knob (B) whilst the lock pin is raised.
3. Release the lock pin when the pressure control knob is in the
desired position to lock the control knob.
Initial Pressure Setting 4. If you are using the Alpha Trancell Deluxe seat cushion, set
the pressure control to the maximum position (8).
5. If you are using a mattress, adjust the pressure for the
appropriate patient weight. Refer to the patient weight guide
on the back of the pump for the correct setting. In the case of
a patient sitting in bed, increase the pressure control knob by
two settings.
Lock
Pin
A
B
NOTE
Rotate the pressure control knob clockwise to increase and
counterclockwise to decrease pressure.
WARNING
The weight guide is only an indication and should not replace clinical judgement.
kg lbs Alpha PREVENT Trancell II Alpha Trancell
Deluxe
If Patient
Sitting in Bed
40 88 2 1 1
60 132 2-4 1-2 2-3
80 176 4-5 2-3 4
100 220 Trancell II 3+ 5-6
+2

12
Rapid Deflate Located at the head end of the mattress (on the same side as the
tubeset) is a tag with a Rapid Deflate picture. In the event of cardiac
arrest, pull this tag for rapid mattress deflation.
To reinflate the mattress, simply replace the stopper securely into
the manifold and ensure secure connection of the mattress to the
pump.
IMPORTANT
• The Rapid Deflate facility is fitted to the Trancell II and Alpha Trancell
Deluxe mattresses only.
• In the event of a cardiac arrest, pull the Rapid Deflate tag firmly at the head
end of the mattress and disconnect the tubeset connectors at the pump.
NOTE
When the Rapid Deflate stopper is removed, the low pressure
alarm will activate on the pump. To cancel the alarm, switch the
pump OFF then ON again.
Ensure that the pump is connected to the power supply and
switched on.

13
Transport Mode The transport facility is located on the tubeset near the pump. The
patient may be transported on the Alpha Trancell Deluxe systems
as follows:
1. Turn the control knob 90 degrees as shown below.
2. Remove the tubeset from the pump.
3. Switch the pump to Power:disconnect.
The pressure in the two sets of cells will equalise and the patient
continues to be supported (with the mattress static) for 1 - 2 hours
with the patient in the supine (lying) position.
Normal Mode To return to normal alternating mode, push the tubeset onto the
pump, make sure the pump is switched on and then turn the
control knob 90 degrees counter-clockwise so that the arrows
align with the tubeset.
Stopping Therapy To stop the therapy, switch the pump to the Power:disconnect ( )
position.
• To completely isolate the pump from the mains, remove the
plug from the mains power socket.
IMPORTANT
• The Transport facility is fitted to the Alpha Trancell Deluxe mattress
replacement and the mattress overlay only.
• There is no Transport facility on the Alpha Trancell Deluxe seat cushion.
NOTE
To obtain the maximum use of the transport facility ensure that the patient remains in the supine
position and the mattress is put in transport mode when all cells are inflated.

14
6. Decontamination
The following processes are recommended, but should be adapted to comply with the local or
national guidelines (Decontamination of Medical Devices) which may apply within the Healthcare
Facility or the country of use. If you are uncertain, you should seek advice from your local Infection
Control Specialist.
The Alpha Trancell Deluxe system should be routinely decontaminated between patients and at
regular intervals while in use; as is good practice for all reusable medical devices.
To Clean Clean all exposed surfaces and remove any organic debris by wiping
with a cloth moistened with a simple (neutral) detergent and water.
Dry thoroughly.
Do not allow water or cleaning solutions to collect on the surface of
the pump.
Chemical Disinfection To protect the integrity of the cover we recommend a chlorine-
releasing agent, such as sodium hypochlorite, at a strength of
1,000ppm available chlorine (this may vary from 250ppm to
10,000ppm depending on local policy and contamination status).
Wipe all cleaned surfaces with the solution, then wipe with a cloth
moistened in water and dry thoroughly.
Alcohol based disinfectants (strength 70%) may be used as an
alternative.
Ensure the product is dry before storage.
If an alternative disinfectant is selected from the wide variety
available we recommend that suitability for use is confirmed with the
chemical supplier prior to use.
DO NOT WRING/MANGLE, AUTOCLAVE OR USE PHENOLIC
BASED SOLUTIONS.
Thermal Disinfection For mattress top cover information including laundering guidelines,
refer to “Cover Specification” on page 19.
Re-use with multiple
patients
Professional hygiene maintenance is required before re-use of the
system with a different patient.
WARNING
Remove the electrical supply to the pump by disconnecting the mains power cord
from the mains power supply before cleaning.
Protective clothing should always be worn when carrying out decontamination
procedures.
Caution
Do not use Phenol-based solutions or abrasive compounds or pads during the
decontamination process as these will damage the surface coating. Do not boil or
autoclave the cover.
Avoid immersing electrical parts in water during the cleaning process. Do not
spray cleaning solutions directly onto the pump.