Direct Healthcare Group Dyna-Form Mercury Advance User manual

DIRECTHEALTHCAREGROUP.COM
User Manual
Trolley
Mercur
y Advance

2
DYNA-FORM MERCURY ADVANCE TROLLEY
DIRECTHEALTHCAREGROUP.COM

USER MANUAL
3
DIRECTHEALTHCAREGROUP.COM
The Dyna-Form Mercury Advance Trolley Mattress has been designed especially for users considered to be that of Very High
Risk of pressure ulcer development in potentially lengthy A&E waiting environments. This product can be made to measure in
order to fit most trolley designs and is ideal for use in busy A&E departments that have an extensive patient turnover. Offering high
levels of patient comfort, this system has the facility to “step up” to that of a dynamic mattress when clinically required. Similarly,
the mattress function can be downgraded as the patient’s condition improves. These features make it particularly beneficial for use
in an acute environment and help reduce moving and handling, logistical and decontamination impact costs. A higher maximum
weight capacity, up to 40 stone / 254kg, allows the product to meet the modern challenges of those heavier clients. All component
parts are interchangeable and replaceable, maximising product life and reducing environmental impact. The outer cover
comprising a high frequency welded, multi stretch and vapour permeable fabric satisfies the strictest infection control policies.
1. Introduction .....................................................................................................................................................................4
2. Quick Reference Guide & Frequently Used Functions............................................................................................................4
3. Troubleshooting ...............................................................................................................................................................6
4. Installation .......................................................................................................................................................................7
5. Operation .........................................................................................................................................................................7
6. Transportation ..................................................................................................................................................................8
7. Warnings .........................................................................................................................................................................8
8. Maintenance Procedures...................................................................................................................................................9
9. Technical Specification ...................................................................................................................................................10
10. Technical Data..............................................................................................................................................................14
11. Optimum Conditions for Use ...........................................................................................................................................14
12. Symbols Guide & Contraindications for Use .....................................................................................................................14
13. Detachable / Removable Parts .......................................................................................................................................15
14. Disposal ......................................................................................................................................................................15
Contents
Trolley
Mercur
y Advance

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DYNA-FORM MERCURY ADVANCE TROLLEY
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1. Introduction
The Mattress consists of a foam head cell and series of 14 transverse air cells, each containing a unique
foam profiled insert, which are in turn held within a foam U Core, all protected by a vapour permeable
waterproof cover. The single head end cell and the formers consist of foam only. The transverse cells are
arranged into alternate pairs of A and B cells which are filled and emptied in sequence.
In Static Mode, the mattress attains the pressure reducing properties of the Dyna-Form Mercury
static foam mattress (details available on request), whilst in Alternating Mode the mattress is able to
offer similar properties to a pressure relieving dynamic system.
The digitally controlled Power Unit controls a pump that allows air to flow into, or out of the air cells
as required according to the operating mode selected. It also maintains the air pressure within the
mattress at the required level and controls the action of the audible/visual Audible Warning System in
the event of mains supply failure or over or under inflation pressure. A CPR Valve located at the pump
end of the umbilical hose permits the rapid deflation of the Mattress in an emergency.
Power Switch Audible Warning Reset
The power switch simply switches the mains power to the pump on and off.
When the pump detects an Audible Warning condition, this can be silenced (see page 5)
and re-set by switching the pump off and then back on again.
CPR Valve
Please ensure that the CPR connector is always placed fully home, prior to inflating the mattress.
NB: The mattress will NOT inflate properly should this not be the case.
The CPR connector is only to be used in the event of a clinical emergency for priority use.
However, disconnecting this function will cleverly deflate air rapidly from the mattress in
readiness for transport / static mode.
2. Quick Reference Guide (Frequently used functions)
This is a quick reference guide for the Dyna-Form Mercury Advance Trolley System
Product Code MAT/ADV/TROL/SIZE

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This symbol when illuminated (The green indicator light) is not used to indicate that the
equipment is on or ready for use.
When a patient requires a true dynamic function or indeed more pressure in the cells, as they
may be uncomfortable or feel as though the support surface is too soft or unstable, then please
select a “High” setting (pressure 26mmHg). This must only be used by a trained clinician as often
too high pressures can further agitate certain patient conditions.
When a patient requires less pressure in the cells, as they may be uncomfortable or indeed hyper
sensitive to cell movement or indeed if the patient is still reddening further, then please select a
“Low” setting (pressure 18mmHg). This must only be used by a trained clinician.
This function is used to silence the Audible Warning. The LED will remain lit if the Audible
Warning has been silenced previously, however a fault is still detected. Refer to the power switch
in order to re-set fully. If the Audible Warning continues to sound repeatedly, along with an
illuminated light, then an engineer must be called.
This symbol indicates an “Audible Warning Failure”.
Please see troubleshooting guide below for how to re-set.
This symbol when illuminated indicates a Service is required.
DHG recommends a service every 8760 hours of operation (one continuous year running).
LED Mode Settings
Note: Please ensure (when available) that all securing straps on the base of the mattress are secured onto
the MOVING PARTS of the bed frame.
For shut down procedure, see 4.2 Power Unit (Pump) section.
Power On / Off
True Dynamic /Firmer Setting
Silence Audible Warning
Audible Warning Failure
Service Indicator
Low / Comfort Pressure Setting

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Warning / Fault Cause
Control Unit does
not operate;
no display lights
illuminate
The Control
Unit may not be
attached to a
power source or
a fuse may need
replacing.
1. Check the Control Unit is connected to mains power outlet with the correct voltage.
2. Check the Control Unit is switched on. Switch off and unplug the unit before restarting.
3. Check the mains plug fuse (5 AMP) then check both Control Unit fuses (1 AMP) –
fuses can be released using a screwdriver to push and turn.
Do not try to open the Control Unit. Opening the unit could cause personal injury
or equipment damage.
Ensure the replacement of fuses is carried out accordance with local legislation.
Warning LED C
+ audible warning
Mains failure /
Other
See above,
plus:
1. Reset the audible warning – turn off power and press the audible warning mute button.
2. Check the handle is intact, ensuring all four sealing connectors are firmly fitted to the control unit
and the air hoses. Check the CPR tag is attached and all sealing connectors are firmly secure.
3. Check all air hoses along the inside of the mattress – each should be firmly connected.
Check each air cell is securely attached to its connecting air pipe.
4. Check all cells, pipes and hoses for any air leakage.
5. Switch on power.
Warning LED B
+ audible warning
Pressure too low 1. Reset the warning – turn off power and press the audible warning mute button.
2. Check the handle is intact, ensuring all four sealing connectors are firmly fitted to the control unit
and the air hoses. Check the CPR tag is attached and all sealing connectors are firmly secure.
3. Check all air hoses along the inside of the mattress – each should be firmly connected.
Check each air cell is securely attached to its connecting air pipe.
4. Check all cells, pipes and hoses for any air leakage.
5. Check that the air filter cover is correctly secured and the air filter is clean.
6. Switch on power.
Warning LED B+C
+ audible warning
Pressure too low /
Air pipe kinked
1. Check all air hoses along the inside of the mattress – each should be firmly connected.
Check each air cell is securely attached to its connecting air pipe.
Warning LED A
+ audible warning
Pressure
too high
1. Reset the warning – turn off power and press the audible warning button.
2. Disconnect the air hoses to reduce pressure, reconnect when pressure
has decreased.
3. Check for twists in the air hoses between Mattress and Control Unit.
4. Switch on power.
Warning LED A+B
+ audible warning
Alternating
Mode Failure (no
alternation)
1. Reset the warning – turn off Power and press the audible warning mute button.
2. Disconnect the air hoses to reduce pressure – reconnect when pressure has decreased.
Warning LED A,B+C
+ audible warning
Initialising Failure 1. Press the audible warning mute button to silence the audible warning.
2. Check the power cable is firmly plugged into the mains outlet and the Control Unit;
and check the mains power is switched on.
3. Check the Control Unit fuse (1 AMP) – fuses can be released using a screwdriver
to push and turn.
Solution
3. Troubleshooting

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4. Installation
4.1 Mattress (This is the applied part type BF)
Place the Dyna-Form® Mercury Advance Trolley Mattress directly on to the bed platform ensuring
that the Blue multi-stretch waterproof cover is on top and that the umbilical hose is located at
the left hand corner at the foot end of the bed. Note: The umbilical hose can be located inside the
cover under the “Open Here for Air Inlet” printed in the bottom left hand corner of the mattress.
Cover the Mattress with a loose fitting sheet.
Static Mattress Use
The Dyna-Form® Mercury Advance Trolley Mattress can be used as a pressure reducing mattress
for patients at High Risk of pressure ulcer damage without the need to attach the pump.
Alternating Mattress Use
If / When required, the Dyna-Form® Mercury Advance Trolley Mattress can be used as an
alternating mattress system by attaching the Dyna-Form® Mercury Advance Trolley Power Unit
(Pump) system.
No other system should be attached to the mattress as the design settings and internal
air pressure properties of the Dyna-Form® Mercury Advance Trolley Power Unit (Pump) are
specific to this mattress only.
The Dyna-Form® Mercury Advance Trolley is a replacement mattress system and should NOT be
placed on top of any existing mattress.
The startup time from static to dynamic mode is immediate.
4.2 Power Unit (Pump)
Hang the Power Unit (Pump) onto the footboard. The mounting hooks swivel to suit the thickness
of the footboard or rail. Connecting the Umbilical Hose to the Power Unit (Pump), place the 3-pin
electrical plug into the wall outlet and switch on:
(a) Open the zip located at the bottom left hand side of the mattress and pull out the Blue Umbilical hose.
(b) Attach the Blue Umbilical Hose to the Power Unit (Pump) by connecting the air connector
at the end of the Umbilical Hose to the air inlet connector at the bottom left hand side of the
pump. Ensure that the Red CPR Release button is located on top of the Air Inlet connector after
connection is complete.
(c) Re-close the zip as far as possible without clamping the Blue Umbilical Hose to ensure the
mattress and air cells are sealed within the cover.
(d) Shut down is the reverse of items a, b & c above.
5. Operation
Attach the mains cable to the pump by inserting the “kettle” type connector into the recess
located on the left hand side of the pump. The mains cable has been designed specifically as a
removable part to aid in easy replacement should it become damaged in use.
The mains plug should be turned off and removed from wall socket as a means of isolation.
Plug the mains cable into a suitable 230v mains socket and switch on the Power Unit using the
on/off switch.
After the pump has been turned on both the “High “and the “Low” lights will flash together
intermittently until the pump has attained its initial operating pressure. Once the pump has
attained its initial operating pressure the “Low” light will stay on constantly and the mattress is
ready for use.

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DYNA-FORM MERCURY ADVANCE TROLLEY
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5.1 Low / High Settings
The Dyna-Form® Mercury Advance Trolley Mattress, in Alternating Mode, has two pressure settings.
The initial setting that the pump will revert to upon set up is “Low”. The “Low” comfort setting is
ideal for the lighter patient or those who feel discomfort when on a normal alternating air type
mattresses system. However, for patients with existing pressure damage or those at Very High
Risk, it is recommended that dependant on the clinical judgement of the clinician,
the “High” setting is activated by pressing the +/- button once, which is located on top of the
pump.
In “High” Mode the pump attains more of the characteristics of an alternating air mattress system
whilst still utilising the advantages of the static foam inserts. Repeatedly pressing the ‘mode’
button enables the Low & High modes to be selected in turn.
5.2 CPR Deflation
The CPR system consists of a manually operated button located on the Air Inlet connector
attached to the pump. By pressing the Red Button, which will release the connector locking
system, the user can remove the connector unit which will deflate the mattress air system back
to that of a static foam mattress.
Note: After a short period as the Mattress deflates the ‘Low Pressure’ Audible Warning is
activated and can be cancelled by switching the Power Unit off.
5.3 Troubleshooting
For assistance (if needed) in setting up, using or maintaining the Mercury Advance System, or to
report unexpected operation or events, please contact Direct Healthcare Group on the contact
details on the reverse of this manual.
6. Transportation
To change the location of the mattress, remove the Umbilical Cord and allow the mattress to
return to its Static Mattress form. Switch off the Power Unit (Pump) using the on/off switch and
disconnect the electrical supply cable from the mains socket. The mattress can now be moved to
a new location where it must immediately be reconnected to the mains electrical supply and the
Power Unit (Pump) switched back on. Once the Mattress has been refilled, the ‘Alternating’ mode
will automatically revert back to the Low setting and should be reselected to High should this be
desired by the clinician.
Warning: The Mattress will not ‘alternate’ when disconnected from the Power Unit (Pump)
and /or the mains electrical. Also refer to environmental conditions section at rear of this manual.
7. Warnings
Warning conditions are indicated by a flashing red display accompanied by an audible warning.
In each case the user should respond by turning the Power Unit’s switch off and investigating the cause.
7.1 High Pressure Warning
This condition could be caused, for example by a kinked Umbilical Hose or visitors,
and others, sitting suddenly on the Mattress.
7.2 Low Pressure Warning
This condition could be caused, for example, by incorrect fitting of the air inlet connector,
opening of the CPR Valve or a leak in the Mattress due to a cut or puncture.
7.3 Mains Failure Warning
This condition may be caused, for example if Mains power is lost.

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8. Maintenance Procedures
8.1 Safety Warning
Only qualified technicians trained or formally approved by Direct
Healthcare Group Ltd. in the operation and maintenance of
Direct Healthcare Group products may carry out maintenance,
modification or repair work on the equipment. Unqualified
personnel attempting to work on Direct Healthcare Group Power
Units risk serious injury to themselves and others and possibly
death by electrocution. Inlet fuse NOT to be replaced by operator
or patient, to be replaced by service personnel only.
Warning – Do not modify this equipment without
authorisation of Direct Healthcare Group.
8.1.1 Servicing
A service light will illuminate when a service is due.
Direct Healthcare Group (DHG) recommend that the Power
Unit (Pump) should be serviced every 8760 hours of operation (one
continuous year running). The unit contains no user serviceable
parts and should only be carried out by persons as described in
section 8.1. DHG will make available on request service manuals,
component parts lists and other information necessary for any
suitably qualified person (As in 8.1) to carry out repair or service
the system. For Service, maintenance and any questions regarding
this please contact DHG.
8.2 Cleaning Procedures
Warning: Before cleaning the System make sure that the Power
Unit (Pump) is disconnected from the mains electricity supply.
Do not immerse the Power Unit (Pump) in water or other fluids.
Do not autoclave, nor use phenol for cleaning.
Do wash hands before commencing the cleaning process.
Wear appropriate protective clothing such as gloves, apron
and a mask.
Ensure all work surfaces are cleaned before and after contact
with the Mattress.
8.3 Warning – Cleaning the Mattress
1. Cleaning should take place after use or between patients.
2. With cover left on the Mattress disconnect the Mattress from
the Power Unit (Pump).
3. Clean the surface of the wash down table with Hypochlorite
solution or equivalent disinfectant.
4. Wash Mattress top using hot water (60 degrees C) containing
detergent – dry with a paper towel.
5. Use a Hypochlorite solution 1,000 parts per million available
chlorine. For heavy contamination use a Hypochlorite solution
10,000 parts per million available chlorine.
Please ensure
thorough rinsing after cleaning.
6. Using suitable brush, hot water, detergent or Hypochlorite
solution, clean Umbilical Hose and CPR Valve. Dry with
paper towel.
7. If required, the Mattress Cover may be removed and
machine-washed at a temperature of 80 degrees C, for not
less than 10 minutes. The individual Air Cells can be wiped
down with established disinfectants.
8. To avoid shrinkage of the cover line dry in an indoor clean
environment or tumble dry on a low heat setting not
exceeding 40 degrees C and not for longer than 10 minutes.
Covers must be thoroughly dried before re-fitting to the
mattress.
8.4 Warning – Cleaning the Power Unit (Pump)
The Power Unit can be cleaned by wiping with a cloth dampened
with a detergent solution or Hypochlorite solution.
Also refer to symbol chart.
8.4.1 Warning
Ensure the Mercury Advance System is not exposed to:
1. Excessive heat sources e.g. fires, radiators etc.
2. Water, particularly immersion of the pump.
7.4 Alternating Mode Failure (no alternation)
This will be indicated by a warning LED on A and B and an audible warning.
1. R eset the warning – turn off Power and press the audible warning mute button.
2. Disconnect the air hoses to reduce pressure – reconnect when pressure has decreased.
7.5 Initialising Failure
This will be indicated by a warning LED on A, B and C and an audible warning.
1. Press the audible warning mute button to silence the audible warning.
2. Check the power cable is firmly plugged into the mains outlet and the Control Unit;
and check the mains power is switched on.
3. Check the Control Unit fuse (1 AMP) – fuses can be released using a screwdriver
to push and turn.

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9. Technical Specification
Guidance and manufacturer’s declaration – electromagnetic emission
The MAT1260001 is intended for use in the electromagnetic environment specified below.
The customer or the user of the system should ensure that it is used in such an environment.
Emission test Compliance Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1 The system uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely
to cause any interference in nearby electronic equipment.
RF emission
CISPR 11
Class B The system is suitable for use in all establishments, including
domestic establishments and those directly connected to
the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/flicker
emissions
IEC 61000-3-3
Complies
Declaration – electromagnetic emissions - for all ME EQUIPMENT and ME SYSTEMS

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9. Technical Specification
Declaration – electromagnetic immunity
Guidance and manufacturer’s declaration – electromagnetic immunity
The MAT1260001 is intended for use in the electromagnetic environment specified below.
The customer or the user of the system should ensure that it is used in such an environment.
Immunity test IEC 60601
test level
Compliance level Electromagnetic
environment – guidance
Electrostatic discharge (ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood,
concrete or ceramic tile.
If floor are covered with
synthetic material, the relative
humidity should be at least
30%.
Electrical fast transient/burst
IEC 61000-4-4
±2 kV for power
supply lines
±1 kV for input/output line(s)
±2 kV for power
supply lines
±1 kV for input/output line(s)
Mains power quality
should be that of a typical
commercial or hospital
environment.
Surge Immunity Test
IEC 61000-4-5
± 1 kV line(s) to line(s) ±1 kV differential mode Mains power quality
should be that of a typical
commercial or hospital
environment.
Voltage dips, short
interruptions and voltage
variations on power supply
input lines
IEC 61000-4-11
Voltage Dips
%U T
Period
(Cycles)
Voltage Dips
%U T
Period
(Cycles)
Mains power quality
should be that of a typical
commercial or hospital
environment. If the user of
the Span system requires
continued operation during
power mains interruptions,
it is recommended that the
system be powered from an
uninterruptible power supply
or a battery.
30 25 30 25
60 5 60 5
>95 0.5 >95 0.5
Voltage
Interruption
% U T
Seconds Voltage
Interruption
% U T
Seconds
>95 5 >95 5
Power frequency (50Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
NOTE U T is the a.c. mains voltage prior to application of the test level.

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Guidance and manufacturer’s declaration – electromagnetic immunity
The MAT1260001 is intended for use in the electromagnetic environment specified below.
The customer or the user of the system should ensure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment – guidance
Conducted RF
IEC 61000- 4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m (Professional
Healthcare Environment)
10 V/m (Home
Healthcare Environment)
80 MHz at 2.7 GHz
3 Vrms
10 V/m
Portable and mobile RF communications equipment
should be used no closer to any part of the CT515,
including cables, than the recommended separation
distance calculated from the equation applicable to the
frequency of the transmitter
Recommended separation distance
d = 1.167√P
d = 1.167√P 80 MHz to 800 MHz
d = 2.333√P 800 MHz to 2.5 GHz
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
distance in meters (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 80 MHz and 800 MHz, 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 Span system is used exceeds the applicable RF compliance level above, the system should
be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as
reorienting or relocating the system.
b. Over the frequency range 150kHz to 80MHz, field strengths should be less than 3V/m.
9. Technical Specification
Declaration – electromagnetic immunity – for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING

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9. Technical Specification
Recommended separation distances between portable and mobile RF communications equipment and the MAT1260001
Alternating Control Unit
The MAT1260001 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the system can help prevent electromagnetic interference by maintaining a minimum distance between
portable and mobile RF communications equipment (transmitters) and the system as recommended below, according to the maximum
output power of the communications equipment.
Rated maximum output
power of transmitter (W)
Separation distance according to frequency of transmitter (m)
150 KHz to 80 MHz
d = 1.167√P
80 MHz to 800 MHz
d = 1.167√P
800 MHz to 2.5 GHz
d = 2.333
√ P
0.01 0.117 0.117 0.233
0 .1 0.369 0.369 0.738
11.16 7 1.16 7 2.333
10 3.689 3.689 7.379
100 11.667 11.667 23.333
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be
estimated using the equation applicable to the frequency 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 80 MHz and 800 MHz, the separation distance for 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.
Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT
or SYSTEM – for ME EQUIPMENT or ME SYSTEM that are not LIFE – SUPPORTING

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10. Technical Data
9.1 Power Unit (Pump)
Serial Number ............................As per label on rear of pump
Electrical Supply. ................................220 – 240 volt, 50 Hz
Power Consumption ...............................................10 watts
Fuses ................................................................TA1H 250V
Protection against shock ...........................................Class 2
Noise Level ...............................................Approx. 30 dB (A)
Dimensions ...........................................245 x 160 x 95 mm
Weight...................................................................... 1.7 kg
Service Interval ............................... 12 months / 8760 hours
Expected life ............................................................5 years
Shelf life of parts ......................................................5 years
9.2 Mattress
Serial Number .....................Label on inside of mattress cover
Number of Air Cells ................ 14 Air Cells / 1 Static Foam Cell
Dimensions ..............................................Made to Measure
Weight........................................................................10kg
Expected life of Mattress ...........................................5 years
Shelf life of Mattress parts .........................................5 years
11. Optimum Conditions
(Applies to Mattress and Pump)
10.1 Environment Conditions for Use
Transport .................................................... -25˚C – +70˚C
Storage ...................................................... -25˚C – +70˚C
Usage ......................................................... +5˚C – +40˚C
Humidity .......................................................... 10% – 93%
Atmospheric Pressure ........................... 700hPa – 1060hPa
Operational Altitude .............................................. ≤ 2000m
10.2 Exposure
Exposure to direct sunlight, dust, lint and general debris is not
considered to be an issue with the Mercury Advance System.
REFER TO
USER MANUAL
SERVICE
REQUIRED
TUMBLE DRY ON LOW
0843
DO NOT IRON
DO NOT USE
SHARP INSTRUMENTS
WASH AT 80˚
REFER TO
USER MANUAL
DO NOT BLEACH
MAXIMUM USER
WEIGHT LIMIT
254 KG / 40 ST
ONES
DOUBLE INSULATED
CLASS II
NO SMOKING
DO NOT USE
PHENOL
DO NOT DRY CLEAN
TYPE BF
APPLIED PART
DO NOT DISPOSE OF
WITH HOUSEHOLD WASTE.
PLEASE REFER TO DHS WEBSITE
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF SERIOUS INJURY
OR OTHERWISE ADVERSE
REACTIONS WITH THE USE
OR MISUSE OF THE DEVICE
WARNING
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF A PROBLEM
WITH THE SYSTEM ASSOCIATED
WITH ITS USE OR MISUSE
CAUTION
CAUTION
HUMIDITY
LIMITATION
ATMOSPHERIC PRESSURE
LIMITATION
PROTECT FROM HEAT
AND RADIOACTIVE SOURCES
TEMPERATURE
LIMITATION
0843
IP: INGRESS PROTECTION
2: PROTECTION AGAINST FINGERS OR
OTHER OBJECT NOT GREATER THAN
80MM IN LENGTH AND 12MM IN DIAMETER
1: PROTECTION FROM VERTICALLY
DRIPPING WATER
Mattress Symbols
12. Symbols Guide
General Symbols
REFER TO
USER MANUAL
SERVICE
REQUIRED
TUMBLE DRY ON LOW
0843
DO NOT IRON
DO NOT USE
SHARP INSTRUMENTS
WASH AT 80˚
REFER TO
USER MANUAL
DO NOT BLEACH
MAXIMUM USER
WEIGHT LIMIT
254 KG / 40 STONES
DOUBLE INSULATED
CLASS II
NO SMOKING
DO NOT USE
PHENOL
DO NOT DRY CLEAN
TYPE BF
APPLIED PART
DO NOT DISPOSE OF
WITH HOUSEHOLD WASTE.
PLEASE REFER TO DHS WEBSITE
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF SERIOUS INJURY
OR OTHERWISE ADVERSE
REACTIONS WITH THE USE
OR MISUSE OF THE DEVICE
WARNING
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF A PROBLEM
WITH THE SYSTEM ASSOCIATED
WITH ITS USE OR MISUSE
CAUTION
CAUTION
HUMIDITY
LIMITATION
ATMOSPHERIC PRESSURE
LIMITATION
PROTECT FROM HEAT
AND RADIOACTIVE SOURCES
TEMPERATURE
LIMITATION
0843
IP: INGRESS PROTECTION
2: PROTECTION AGAINST FINGERS OR
OTHER OBJECT NOT GREATER THAN
80MM IN LENGTH AND 12MM IN DIAMETER
1: PROTECTION FROM VERTICALLY
DRIPPING WATER
Pump (Unit) Symbols
REFER TO
USER MANUAL
SERVICE
REQUIRED
TUMBLE DRY ON LOW
0843
DO NOT IRON
DO NOT USE
SHARP INSTRUMENTS
WASH AT 80˚
REFER TO
USER MANUAL
DO NOT BLEACH
MAXIMUM USER
WEIGHT LIMIT
254 KG / 40 STONES
DOUBLE INSULATED
CLASS II
NO SMOKING
DO NOT USE
PHENOL
DO NOT DRY CLEAN
TYPE BF
APPLIED PART
DO NOT DISPOSE OF
WITH HOUSEHOLD WASTE.
PLEASE REFER TO
DHS WEBSITE
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF SERIOUS INJURY
OR OTHERWISE ADVERSE
REACTIONS WITH THE USE
OR MISUSE OF THE DEVICE
WARNING
THIS IS A STAT EMENT THAT
ALERTS THE USER TO THE
POSSIBILITY OF A PROBLEM
WITH THE SYSTEM ASSOCIATED
WITH ITS USE OR MISUSE
CAUTION
CAUTION
HUMIDITY
LIMITATION
ATMOSPHERIC PRESSURE
LIMITATION
PROTECT FROM HEAT
AND RADIOACTIVE SOURCES
TEMPERATURE
LIMITATION
0843
IP: INGRESS PROTECTION
2: PROTECTION AGAINST FINGERS OR
OTHER OBJECT NOT GREATER THAN
80MM IN LENGTH AND 12MM IN DIAMETER
1: PROTECTION FROM VERTICALLY
DRIPPING WATER

USER MANUAL
15
DIRECTHEALTHCAREGROUP.COM
Contraindications For Use (Warning)
The Mercury Advance System should not be used for patients with
unstable fractures, gross oedema, burns, or intolerance
to motion.
General Information (Caution) (Warning)
• There are no special skills required to operate the system.
• The Medical Professional is responsible for applying his/her
best medical judgment when using the system.
• The electricity supply is of the type indicated on the Power
Unit (pump).
• Check the mains lead is free from damage and is positioned
so as not to cause an obstruction, or injury. E.g. Strangulation
of a child or trip hazard.
• Ensure the mains lead cannot become trapped or crushed,
e.g. by raising or lowering of the bed or bed rails or any other
moving object.
• The power unit (pump) must only be used with a suitably
approved power cord and plug set as supplied by DHG.
• The system is not to be used in the presence of flammable
anaesthetics.
• Suitable for continuous use.
• Not suitable for sterilisation.
• Do not position the power unit to make it difficult to disconnect
the power supply or plug.
• Do not place the System on or close to a source of heat.
• Do not use with hot water bottles or electric blankets.
• DHG strongly advise against smoking whilst the Power Unit
(pump) is in use. This is to prevent accidental secondary ignition
of items which may be flammable e.g. bed linen. The materials
used in the manufacture of the Mercury Advance System
comply with the required fire safety regulations.
• Do not use sharp objects on or near the mattress system
as this will cause damage.
• Do not store in damp conditions.
• Do not use in an oxygen enriched environment.
• Not suitable for use in an Outdoor Environment.
• Intended for both Home Healthcare and Professional Healthcare
environments.
• Do not connect to any other medical device or equipment.
• Correct fuse rating MUST be used. Failure to do so could result
in the risk of a fire.
• The System should be cleaned after use or between patients.
Refer to Cleaning section.
• All internal and external hoses must be free of twists, kinks.
The external hose should also be properly connected and
positioned so that the risk of obstruction or injury is eliminated.
• Do not use bleach, phenols. Chlorine based products which
exceed 1000ppm. Solvents or alcohol based cleaners.
• All the above warnings and cautions together with safety
considerations should be observed at ALL times during its use.
• Select correct setting ‘Hi’ or ‘Low’ as required. Care should be
taken not to accidentally change settings once set. This may
affect the desired requirement of the therapy. This could also be
caused by pets, pests or children.
• This device does not emit radiation.
13. Detachable/Removable Parts
1. Mattress (Detached from the pump by removing the CPR
connector). Part No. MAT/ADV/TROL/SIZE (or variants
of for the size)
2. Electric power cable. (Removed from the pump by pulling the
cable away from the mains inlet on the side of the pump).
Part No. DHG/ADV/MLEAD
N.B. The battery is an integral part of the PCB and is not
removable or changeable.
Caution
Use of detachable parts not listed is not recommended by
Direct Healthcare Group.
14. Disposal
Please refer to DHG website for recommendations and
responsibilities for disposal within the UK WEEE guidelines.

Direct Healthcare Group
Withey Court, Western Industrial Estate
Caerphilly, United Kingdom
CF83 1BF
T: [phone]
F: [phone]
E: [email protected]
C22773
DIRECTHEALTHCAREGROUP.COM
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LIT-00008 Issue 4
Date: February 2018
Asia Pacific
Direct Healthcare Group PTY Ltd.
PO Box 562, Wembley
Western Australia 6913
T: [phone]
E: [email protected]
Intelligent Pressure Care
Specialist Seating
Rental & Service Solutions