LPG Cellu M6 Integral Series User manual

GU 0902 - EN
Edition D dated10/2020
OPERATOR’S MANUAL
Please read the complete manual carefully
before using your equipment
© LPG Systems 2020. LPG®, Cellu M6®, Integral, Keymodule and endermowear™ are registered trademarks of
LPG SYSTEMS and/or trademarks on which it holds exclusive rights.
Reproduction, even in part, is strictly prohibited.

1
In order to respond better to customer requirements and expectations, LPG Systems is continuously
researching ways of improving the design and quality of its products. This will explain the few minor
differences between your equipment and the item described in this guide.
↗ATTENTION
Congratulations on the purchase of your Cellu M6®Integral i device. This model
represents many years of research in the design and production of cutaneous
tissue treatment systems. You will be able to fully appreciate the technical
perfection and reliability that have made LPG Systems the leader in this field.
This operator’s manual contains the operating description, basic maintenance
instructions to be performed periodically and the safety instructions. Your device
is intended for use in the treatment of connective tissue. It should be used only
by a professional who has attended the manufacturer’s training provided by LPG
Systems or an approved provider if you live outside of France. If you have any
doubts whatsoever concerning the operation or maintenance of your equipment,
please do not hesitate to contact LPG Systems via your distributor.

2
Unpacking instructions to be retained.
↗ATTENTION
→PACKAGE CONTENTS
Depending on the version you have (see serial number on the nameplate; “B”, “2i” or
“i”), some protocols are not activated and their accessories are not provided.
>One Cellu M6®Integral unit
>One main Ergodrive head
>One KeymoduleTM (KM80)
>One TR50 head
>One set of auxiliary heads (TR15 et TR30)
>One set of micro-nozzles/micro-heads
>One Ergolift head
>Two Ergolift chambers (Lift 20 and Lift 10)
>One set of Lift heads
>One operator’s manual
>One electrical power cord
>One POS marketing set

33
>One Cellu M6®Integral unit
>One main Ergodrive head
>One KeymoduleTM (KM80)
>One TR50 head
>One set of auxiliary heads (TR15 et TR30)
>One set of micro-nozzles/micro-heads
>One Ergolift head
>Two Ergolift chambers (Lift 20 and Lift 10)
>One set of Lift heads
>One operator’s manual
>One electrical power cord
>One POS marketing set
Version 2 i Version i Version i B
Ergodrive √ √ √
KM80 √ √ √
TR50 √ √ √
TR30, TR15 √ √ √
Micro-nozzles
Micro-heads √ √ √
Ergolift
Lift 20
Lift 10
√
Lift heads
TML30
TML20
TML10
√
GU √ √ √
Power cord √ √ √
POS √ √ √

4
The manufacturer reserves the right to amend the product technical specifications without prior
notice. Any reproduction – even in part – is prohibited. All the illustrations in this operator’s manual
are non-binding.
↗ATTENTION
→TABLE OF CONTENTS
1. DEVICE DESCRIPTION .......................5
2. CONTROLS DESCRIPTION .....................7
3. IMPORTANT SAFETY INFORMATION ..............10
4. MAINTENANCE ..........................14
5. TROUBLESHOOTING .......................23
6. TECHNICAL SPECIFICATIONS
..................24
7. TREATMENT HEADS .......................26
8. ENDERMOWEAR™ ........................46
9. WARRANTY ............................47
GENERAL WARRANTY CONDITIONS ......................47
LIMITATION AND EXONERATION OF LIABILITY .............49
WARRANTY ACTIVATION .................................50
10. APPENDIX: ELECTROMAGNETIC COMPATIBILITY .......51

5
→THE CELLU M6®INTEGRAL
DEVICE DESCRIPTION
1
INTENDED USE
The Cellu M6®Integral i device is intended for body and face treatment of connective
tissues transformations for beauty and therapeutic purposes. It can be used to:
1) Reduce secondary lymphedema of the arm after a mastectomy
2) Improve secondary lymphedema
3) Improve lymphatic circulation in the treated area
4) Relieve minor muscle aches and pains
5) Relieve muscle spasms
6) Temporarily improve local blood circulation
7) Temporarily relieve minor muscular pain associated with DOMS (Delayed Onset
Muscle Soreness)
8) Improve local circulation during burn rehabilitation
9) Reduce the appearance of cellulite and the circumference of treated areas
10) Temporarily improve lymphatic circulation and local blood circulation to improve
skin trophicity in the treated areas
11) Improve skin quality, scars, fibrosis
12) Improve skin aging (wrinkles, fine lines, skin sagging, fat infiltration, firmness,
elasticity, complexion and eye bags
13) Stimulate fibroblasts (collagen, elastin and hyaluronic acid synthesis)
It utilizes mecano-stimulation treatment heads for bodycontouring and anti-aging
applications. The device can be used in hospitals, therapy centers and institutions
by specialists and physiotherapists It is an independent device not to be combined
with other devices. It is to be used by professionals who are specially trained by LPG
Systems in the use of the device and is not suitable for home use.
It should be used on adult patients only.
OPERATING PRINCIPLES:
The operating principles of the Cellu M6®Integral i medical device consist of a suction
force coupled with movements of rolls/valves performed with treatment heads.
These heads are placed on the healthy skin of the patient and then moved across the
area to be treated by the professional who has been trained by LPG Systems.

6
The device can only operate if it is connected to the power supply by its power cord and provided the
ON switch has been actuated and the green voltage light is on.
After switching on the unit, please wait a few seconds for the screen to display information.
↗ATTENTION
DEVICE DESCRIPTION
1→THE CELLU M6®INTEGRAL (CONT’D)
LIGHT STRIP
CASTER LOCKING MECHANISM
LEFT HOSE
RIGHT HOSE
FORWARDFACING TOUCH
SCREEN
HEAD HOLDER
HEAD STORAGE DRAWER
HEAD STORAGE TRAY
ADAPTER HOLDER
CASTERS
FILTER ACCESS
POWER CORD
HOLDER
IDENTIFICATION
PLATE
FILTER ACCESS DOOR
POWER SWITCH, SOCKET
AND POWER INDICATOR
Before use, ensure that the power cord is completely unwound.

7
For detailed instructions on using the touch interface, refer to the touch interface operating manual
received during training and available from customer service.
↗ATTENTION
→HEAD STORAGE DRAWER AND FILTER ACCESS
DEVICE DESCRIPTION
2
→CONTROL SCREEN
POWER INDICATOR
TREATMENT INFORMATION
TOUCHSCREEN
ETHERNET PORT
AUDIO OUTPUT
USB PORT
TOOLBAR
TREATMENT
CONTROL SETTINGS
LEFT HOSE FILTER
RIGHT HOSE FILTER
HEAD STORAGE DRAWER FILTER ACCESS
The filters are accessible via
the back of the unit

8
→ERGODRIVE HEAD
CONTROLS DESCRIPTION
2
→TR50 HEAD
QUICK CONNECT
QUICK CONNECT
SETTING CONTROL
BUTTONS
CONTROL SCREEN
TRIGGER BUTTONS
(TO REVERSE DIRECTION
OF ROLLERS)
SETTING CONTROL
BUTTONS
KEYMODULE
CONTROL SCREEN
SELECTION BUTTONS
ROLLERS
SEALING VALVE
HOLDER
LOCK RING
ROLLER LOCK SLIDER

9
In cases where the unit has not been moved for a long time, it is possible that marks may form on
the ground where the casters are. This phenomenon is the result of a chemical reaction between the
components of some floorings and those of the wheels of the Cellu M6®Integral idevice.
↗ATTENTION
→ADAPTER
→CASTERS
CONTROLS DESCRIPTION
2
UNLOCKED TO LOCK LOCKED
The Cellu M6®Integral idevice is equipped with locking casters.
Please follow the procedure indicated below to lock or unlock the casters.
SELECTION BUTTONS
QUICK CONNECT

10
Any serious incident that occurring with your device should be reported to your local LPG®distributor and
competent authority.
ATTENTION: KEEP THESE INSTRUCTIONS
→IMPORTANT SAFETY INFORMATION
IMPORTANT SAFETY INFORMATION
3
Your device should be used on clean and healthy skin. It is important to read and respect the
following precautions and contraindications before using your device.
• Never touch the patient and the device’s
unprotected cables or connectors
simultaneously.
• Never use the auxiliary adapter as a
treatment head or allow it to come into
direct contact with the skin.
• Do not use the main head to carry out
treatment on the scalp.
• Only use treatment heads supplied with your
unit or recommended by LPG Systems.
• Only use LPG Systems treatment garments.
• LPG Systems will not be liable for any
inappropriate use of the equipment.
• With respect to treated tissue, some
settings may cause pain or tissue lesions.
• The operator must ensure that the settings
(intensity, sequentiality, differential, etc.)
are always adapted to the cutaneous tissue
being treated.
• Do not lean, rest or sit on the unit.
• When crossing a threshold or step, we
recommend moving the unit carefully to
avoid tipping.
• Do not use the USB and ethernet
connections during treatment.
• Do not operate the unit in unsuitable
environmental conditions (see technical
specifications).
• Do not use the treatment heads directly on
the skin. Wear the treatment suit provided
by LPG Systems, ENDERMOWEARTM.
• Do not use this device on unhealthy/
damaged skin. Avoid affected areas and any
area of the body that have undergone plastic
surgery until eccymosis, oedema and pain
disappear.

11
1 Europe: VII-H05VVF3G1,50-C19 ; Italy: I/3/16-H05VVF3G1,50-C19 ;
Switzerland: 23G-H05VVF3G1.50-C19; UK BS13/13-H05VVF3G1,50-C19 ;
Japan 498GJ-VCTF3X2.00-C19 ;
USA, Canada, Mexico: N5/15-SJT3X14AWG-C19 (connect to Hospital grade receptacle in hospital environment)
IMPORTANT SAFETY INFORMATION
3
→WARNING
→IMPORTANT SAFETY INFORMATION
All safety precautions must be observed while
using electrical equipment. Please read all
safety notices and precautions prior to use of
the equipment.
DANGER - TO MINIMISE THE RISK OF
ELECTRICAL SHOCK:
• Always disconnect the device from the
electrical supply outlet after use and before
cleaning and maintenance.
• Check that the supply voltage of the device
indicated on the data plate complies with the
power supply voltage.
• The unit must be connected by the power
cord1supplied to a grounded outlet in
accordance with current electrical standards.
Electrical adapters must not be used with this
equipment.
TO MINIMISE THE RISK OF BURNS, FIRE,
ELECTRICAL SHOCK OR INJURY
• The device must not be left unattended while
connected to the electrical supply.
• Disconnect the unit from the electrical
supply if it is not going to be used for a long
period.
• Special attention is required while using
the equipment with, or in the proximity of,
children or disabled persons.
• Never use the unit for purposes other than
those recommended by LPG Systems. Only
use the treatment heads supplied with your
unit or those recommended by LPG Systems.
• Never use the device if:
- the electrical power cord or outlet
is damaged.
- the device does not function correctly.
- the device is damaged or has fallen
or been dropped.
- the device has been exposed
to excessive humidity.
In such cases, return the equipment to an
approved LPG Systems service centre.
• Do not move the unit by pulling the electrical
power cord.
• Fully unwind the electrical power cord and
keep it away from warm surfaces.
• Never use the equipment if the ventilation
ports are obstructed. Ensure that the
ventilation ports are kept clear of dust or
other contaminants.
• Do not allow solid debris, liquid or other
foreign bodies to fall or be sucked into the
unit, as these could cause damage.
• Never use the equipment on a dusty, uneven
floor or in a moist atmosphere.
• Never use the equipment in the presence of
aerosols or oxygen.
• Before disconnecting the unit from the
electrical supply, set all controls to the ‘off’
position and unplug the unit.
• It is prohibited to modify this equipment
without prior authorisation from LPG
Systems.
• It is prohibited to use components or spare
parts non recommended by LPG Systems.
↗ATTENTION

12
This device contains programs to help the operator obtain the best anticipated results for each case
undergoing treatment. Under no circumstances may these programs be construed as a guarantee of
successful treatment, which varies depending on the morphology, physiology and eating behaviour of
each patient.
↗ATTENTION
→CONTRAINDICATIONS
IMPORTANT SAFETY INFORMATION
3
• Do not treat open wounds, eyes, intracavity
areas, mucous membranes, genitals or
nipples.
• This device is not recommended for pregnant
women. In the event of pregnancy, do not
treat the lumbar-abdominal region. Consult
with a doctor regarding this treatment.
• Do not treat a patient with an infectious
disease, a growing tumour, a phlebitis, a
wound or an infected area.
• Do not treat a patient with skin cancer, a
visible tumour or other cancerous lesions.
Consult with a doctor in cases where the
patient has a case history of tumours or is in
remission.
• Do not treat inflamed or swollen areas or
scars from a recent surgery without medical
advice and LPG®device training for the
affected areas.
• Do not treat patients with circulatory
problems without first consulting their
doctor.
• Do not treat any swollen or inflamed areas
without seeking medical advice and without
having had LPG®technical training in this
particular area.
• Do not treat a patient after an invasive
medical treatment without medical advice or
the surgeon who carried out the treatment
and without training in LPG®device for the
affected areas. Stop treatment immediately
if the patient experiences pain and consult
a doctor.
• This device should not be used on skin
rashes, herpes, inflammatory or infectious
acne or vitiligo.
• To avoid bruising, exercise caution when
determining a patient’s level of sensitivity
and avoid use on patients taking anti-
coagulant drugs.
• As this list is not exhaustive, always seek out
medical advice in the event of doubt.
• Because of the risk of interference, it is
important that the professional ensures
the patient is not equipped with a personal
medical device such as a pacemaker.
If this is the case, the professional should
obtain details about the device in question to
ensure that any interference will not affect
the correct use of the equipment.
• As this list is not exhaustive, always seek out
medical advice in the event of doubt.
• For a more detailed list of the indications and
contraindications of endermologie®, please
refer to the training manuals.
• Service precaution: risk of explosion if the
Microbattery Button Cell located on the HMI
board (type 3V 190 mAH, VARTA 6 032 101
501) is replaced by an incorrect type. Dispose
used Cell according to country regulation.

13
→INDEX
MAINTENANCE
4
IDENTIFICATION RATING PLATE ................................................14
CLEANING THE UNIT..........................................................15
REPLACING THE FILTER CARTRIDGES AND FOAM ................................16
CONNECTING/DISCONNECTING THE MOTORISED TREATMENT HEADS ..............18
DISCONNECTING THE HOSES ..................................................19
CONNECTING/DISCONNECTING THE ADAPTER ...................................20
REPLACING THE POWER CORD.................................................21
MAINTENANCE LOG SHEET ....................................................21

14
The identification rating plate is located on the underside at the back of the unit.
Identification rating plates may vary. The approved one is one on your machine.
↗ATTENTION
MAINTENANCE
4→IDENTIFICATION RATING PLATE
This symbol indicates that the unit was
sold after August 13, 2006. In conformity
with the 2002/96/CE directive, it cannot
be thrown away with standard household
waste but must be disposed of by means
of recycling. When your device reaches
the end of its useful life, it must be
brought to an appropriate recycling
center or returned to your dealer. By
doing so, you help the environment
by contributing to the conservation of
natural resources and the protection of
human health.
This symbol indicates that some specific
warnings or precautions associated with
this device are not on the label.
This symbol means always consult the
accompanying documents before using
your device.
This symbol indicates the name
and address of the manufacturer.
This symbol means that your device has
type BF applied parts which come into
contact with the patient. These parts
are electrically isolated from all of the
device’s other parts. These applied
parts are the treatment heads.
This symbol means store the device
somewhere protected from inclement
weather.
This symbol indicates temperature
limits.
This symbol indicates relative
humidity limits.
This symbol means
“Do not push.“
This symbol means
“Danger: High Voltage.“
This symbol means
“Use under prescription.“ (US only)
Your unit is identified by a serial number shown
on the rating plate.
The rating plate also shows the permitted
supply voltage for the unit.
If you need to contact LPG Systems because of
a technical problem, please indicate the serial
number of your Cellu M6®Integral i device.
This serial number provides information on the
year and month of manufacture of your unit.
The letter indicates the year the device was
manufactured.
Z=2009, A=2010, B=2011, etc.
The two digits indicate the production month:
01=January; 02=February; 03=March; etc.
serial number
voltage, frequency
and power

15
Do not use corrosive products such as acetone, trichloroethylene or rubbing alcohol.
↗ATTENTION
MAINTENANCE
4
→CLEANING THE UNIT
It is recommended that you clean your unit as often as possible, not only for hygienic and
aesthetic reasons, but also because cleaning the unit will help keep it in a good state of
repair and extend its useful life.
Using a vacuum cleaner with a fine nozzle, clean the following sections:
• Interior of the head storage drawer.
• Interior of the head storage tray.
• Interior of the filter access door.
Using a moist sponge, clean the following sections:
• All the external hoods.
• Hoses.
• The electrical power cord.
Using a cloth soaked with a small amount of alcohol-free domestic cleaning product,
clean the following sections:
• Control screen and control panel.
• Interior of the head storage drawer.
• Interior of the head storage tray.
• Interior of the filter access door.

16
The device must never be used without a filter. If no filter is fitted, the device must be switched off.
MAINTENANCE
4→REPLACING THE FILTER CARTRIDGES AND FOAM
Your device contains two filter cartridges and one filter foam.
These components guarantee the efficiency of your unit and prolong its useful life.
The ‘filter change’ screen indicates
which filter requires changing (Fig. 5).
Ensure that they are changed as
soon as the command screen
displays one of these messages
(Fig. 1-2).
Icon indicating a filter change is
required (Fig. 2).
Access the ‘filter change’ menu as
follows:
Select the ‘maintenance’ menu by
pressing the icon indicated (Fig. 3).
Select the ‘filter’ menu by pressing
the icon indicated (Fig. 4).
FILTER TO CHANGE
FIG. 5
PRESS THIS ICON
FIG. 4
FIG. 1
PRESS THIS ICON
FIG. 3
CHANGE THE FILTERS
FIG. 2
↗ATTENTION

17
→REPLACING THE FILTER CARTRIDGES AND FOAM
(CONT’D)
MAINTENANCE
4
FILTER METER
FIG. 5
Replace the filter cartridges as follows:
1. Open the filter access door.
2. Unscrew and remove the filter
cartridges and replace them with
new ones.
3. Remove the filter foam and
replace it with a new one.
4.
Remember to purchase new filter
cartridges from the LPG Systems
Customer Service Department so
you always have a spare
.
FIG. 1 FIG. 2
FIG. 3 FIG. 4
5.Once the filter cartridge is
replaced, the filter meter should
be reset by pressing the icon
indicated (Fig. 5).
1
2

18
→CONNECTING/DISCONNECTING
THE MOTORISED TREATMENT HEADS
MAINTENANCE
4
FIG. 3
LOCKED
POSITION
LOCKING RING
ORNAMENTAL
RING
WHITE
RING
HOSE KEY
KEY SLOT
To connect the heads to the hose, follow the
procedure below:
Position the locking ring in the locked position
(Fig. 1).
Position the end of the hose so that the hose key
is lined-up with the key slot of the treatment
head connection (Fig. 2).
Push the hose into the treatment head connection
until it clicks into place.
To disconnect the heads, position the locking ring
in the unlocked position (Fig. 3).
Pull the locking ring towards the hose (Fig. 4).
Carefully remove the hose by pulling it by the
white ring (Fig. 5).
FIG. 5
FIG. 1
UNLOCKED
POSITION
FIG. 4
UNLOCKED LOCKED
FIG. 2

19
MAINTENANCE
4
→DISCONNECTING THE HOSES
FIG. 3
FIG. 2
FIG. 4
• Unscrew the screws on the movable arms (Fig. 1).
• Unclip the covers from the movable arms (Fig. 2 - 3).
• Disconnect the electrical connection, as described in the previous section (Fig. 4).
FIG. 1