LPG CELLU M6 Alliance Lab Medical User manual

GU 1603 - EN
Indice B1 - 09/2020
OPERATOR’S MANUAL
Please read the complete manual carefully before using your equipment
© LPG Systems 2020. LPG®, ENDERMOWEARTM and ENDERMOLOGIE®are registered trademarks of
LPG SYSTEMS.
Reproduction, even in part, is strictly prohibited.
CELLU M6
Alliance®Lab - Medical
Registered design

1
In order to better respond 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 Alliance®Lab Medical 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. With the aim to continuously provide satisfaction, your device is equipped
with a specific software ensuring connection with the LPG dedicated server. The
data collected through this software will allow LPG to give you better services in
terms of support and maintenance.
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 official distributor 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 via the Customer Service
Department of your distributor.
[phone]
CELLU M6
Alliance®Lab - Medical

2
→PACKAGE CONTENTS
Unpacking instructions to be retained.
↗ATTENTION
>One CELLU M6 Alliance® Lab Medical device
> One Alliance 80 treatment head
> One Alliance 50 treatment head
> One TR30 treatment head
> One set of micro-nozzles and micro-heads
> One Ergolift treatment head
> Two Ergolift chambers (Lift20 and Lift10)
> One electrical power cord
> One unpacking instructions and quick installation guide
> One marketing set

33
Depending on the version you have, (see serial number on the nameplate), some protocols are
not activated and their accessories are not provided.
Accordingly, the paragraphs describing them do not concern this version (see table below).
In case you have any doubt about the operation of your device or to evolve into a complete
model, please contact LPG Systems’ After Sales Service.
List of accessories provided with your device:
Cellu M6 Alliance®
Lab Medical
Cellu M6 Alliance®
Lab Medical Plus
Cellu M6 Alliance®
Lab Medical
Premium
Alliance 80 √ √ √
Alliance 50 √ √
TR30 √ √
Micro-nozzles
and micro-heads √ √
Ergolift
Unpacking
instructions and
quick installation
guide
√ √ √
Cord √ √ √
Marketing set √ √ √

4
→TABLE OF CONTENTS
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
1. DEVICE DESCRIPTION .......................5
2. CONTROLS DESCRIPTION .....................8
3. IMPORTANT SAFETY INFORMATION ..............12
4. MAINTENANCE ..........................18
5. TROUBLESHOOTING .......................28
6. TECHNICAL SPECIFICATIONS
..................29
7. TREATMENT HEADS .......................30
8. ENDERMOWEARTM ........................45
9. GENERAL WARRANTY CONDITIONS...............46
10. APPENDIX: ELECTROMAGNETIC COMPATIBILITY .......50

5
DEVICE DESCRIPTION
1
→DEVICE DESCRIPTION
INTENTED USE
The CELLU M6 Alliance®Lab Medical device is intended for therapeutic use.
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 boost lymphatic circulation and local blood circulation to improve skin
trophicity in the treated areas
11. Improve skin quality, scars and fibrosis
12. Improve skin ageing (wrinkles, fine lines, sagging skin, fat infiltration, firmness,
elasticity, complexion and dark circles and puffiness)
13. Stimulate fibroblasts (collagen, elastin and hyaluronic acid synthesis)
The device can be used in hospitals, therapy centers and institutions by specialists and
physiotherapists. It can be used on adult patients only, of any sex, with a maximum
weight of 135 kg. It is an independent device that cannot be combined with other
machines. 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.
OPERATING PRINCIPLES:
The operating principles of the CELLU M6 Alliance®Lab Medical device consist of
a suction coupled with movements of rolls/flaps, 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 unit can only operate if it is connected to the power supply by its power cord and provided the
ON button is switched on and the green voltage light is on. After switching on the unit, please wait
a few seconds for the screen to display information.
↗ATTENTION
HOSE HOLDER
HEAD
HOLDER
FILTER
ACCESS DOOR
HEAD
STORAGE TRAY
FRONT SIDE TOUCHSCREEN
IHM ARMS
HEAD HOLDER
DRAWER
MAINS PLUS,
SWITCH AND POWER
ADJUSTABLE TREATMENT
TABLE
BOX
HOSE
→THE CELLU M6 ALLIANCE®LAB MEDICAL DEVICE
DEVICE DESCRIPTION
1

7
→FILTER ACCESS 1
DEVICE DESCRIPTION
FILTER
THE FILTER IS ACCESSIBLE ON THE SIDE OF THE BOX

8
USB PORT ACCESS
TOUCHSCREEN
POWER INDICATOR
For detailed instructions on using the touch interface, refer to the touch interface operating manual received
during training and available from customer service.
↗ATTENTION
→CONTROL SCREEN
→ALLIANCE 80 TREATMENT HEAD
CONTROLS DESCRIPTION
2
PARAMETER SETTING
BUTTONS
EMBELLISHER FLAP
BRIGHT LEDS
ADJUSTMENT SLIDER
POSITION FOR ROLL AND FLAP
MOTORISED ROLL AND FLAP

9
→ALLIANCE 50 TREATMENT HEAD AND TR30 HEAD
→ADAPTER ERGOLIFT HEAD
CONTROLS DESCRIPTION
2
PARAMETER SETTING
BUTTONS
EMBELLISHER FLAP
MOTORISED ROLLS
AND FLAP
ADJUSTMENT SLIDER
POSITION ROLL
AND FLAP
ALLIANCE 50 TR30
SEALING FLAP
MOTORISED ROLLS
ADJUSTEMENT
SLIDER
POSITION ROLL
SELECTION BUTTON FOR TREATMENT TYPE
POWER INCREASE BUTTON
POWER DECREASE BUTTON
ON/OFF BUTTON
HOSE CONNECTION
ERGOLIFT CHAMBER CONNECTION
They can be connected and disconnected
by a simple push-pull action.

10
2→HEIGHT ADJUSTMENT
→FRONT SIDE ADJUSTMENT
CONTROLS DESCRIPTION
The front side can be adjusted using the
articulated dial.
To adjust the front side, simply move it to
the desired position.
ARTICULATED DIAL
BACK DOWN
BUTTON
TABLE DOWN
BUTTON
BACK UP
BUTTON
TABLE UP
BUTTON
The table and back height are adjustable using the controls on the table (see photo).
Simply press the appropriate buttons.

11
2
→TAB
CONTROLS DESCRIPTION
TREATMENT HEAD HOLDER
LINE
TREATMENT
HEAD HOLDER
The CELLU M6 Aliance®Lab Medical device is equipped with two shelves to hold the different
treatment heads.
These shelves can be moved along the length of the table by sliding it along the provided rail.

12
→IMPORTANT SAFETY INFORMATION
3
All safety precautions must be observed while using electrical equipment. Please read all
safety notices and precautions prior to use of the equipment.
• Always disconnect the equipment from the electrical supply outlet after use and before
cleaning and maintenance.
• Check that the supply voltage of the unit indicated on the data plate complies with the power
supply voltage.
• The unit must be connected by the power cord supplied to a grounded outlet in accordance with
current electrical standards. Electrical adapters must not be used with this equipment.
• Ensure that the unit is connected to a system with a differential protection against DC and AC.
DANGER - TO MINIMISE THE RISK OF ELECTRICAL SHOCK:
IMPORTANT SAFETY INFORMATION
↗ATTENTION
Any serious incident occurring with your device should be reported to your local LPG distributor and competent
authority

13
→WARNING
• 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 device 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 recommended by LPG.
• Never use the equipment if:
• The electrical power cord or outlet is damaged.
• The equipment does not function correctly.
• The equipment is damaged or has fallen or been dropped.
• The equipment has been exposed to excessive humidity.
• 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. The disconnection of the unit is disconnecting the power outlet.
• It is prohibited to modify this equipment without prior authorisation from the manufacturer.
• It is prohibited to use components or spare parts not recommended by LPG Systems.
Return the device to LPG Systems Service Center for examination and repair.
IMPORTANT SAFETY INFORMATION
3
↗ATTENTION
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 environnement)

14
→IMPORTANT SAFETY INFORMATION
• Never touch the patient and the device’s
unprotected cables or connectors
simultaneously.
• Never use the adapter as a treatment head
or allow it to come into direct contact with the
skin.
• Only use treatment heads supplied with your
unit or recommended by LPG®.
• Do not use the treatment heads directly on the
skin. Use the treatment suits provided by LPG
Systems only, ENDERMOWEARTM.
• LPG Systems will not be liable for any
inappropriate use of the equipment.
• Improper use of the device can cause tissue
damage or pain.
• The operator must be particularly attentive to
the sensations felt by the patient undergoing
treatment.
• The operator must ensure that the settings
(intensity, sequentiality, differential, etc.) are
always adapted to the tissue being treated..
• Do not put more than 135 kg on the seat.
• Do not put more than 10 kg on the head
storage tray.
• When the table is being used without
supervision, it should be put in the lowest
position to avoid the risk of falling.
• After use, put the table in the lowest position
to avoid the risk of falling.
• Do not lean, rest or sit on the head storage
tray.
• Do not use the USB connection during
treatment.
• Do not operate the unit in unsuitable
environmental conditions (see technical
specifications).
• It is recommended to use a treatment sheet on
the seat.
• The power plug is used as a disconnect device.
The disconnection of the unit is possible by
disconnecting the power plug.
• Please position your device so that the power
supply unit is always accessible.
• Do not touch the patient and the hose
connectors simultaneously.
• Do not use vegetable oil on the treatment
heads.
ATTENTION : KEEP THESE INSTRUCTIONS.
Your device should be used on healthy skin. It is important to read and respect the following
precautions and contraindications before using your device.
3
IMPORTANT SAFETY INFORMATION

15
→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 inflammatory areas or scars without medical advice and LPG®technical
training for the affected areas.
• Do not treat patients with circulatory problems without first consulting their doctor and
without training in LPG®technology for the affected areas.
• Do not treat a patient with an unexplained and persistent pain without medical advice and
without training in LPG technology for the affected areas.

16
This unit 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
3
IMPORTANT SAFETY INFORMATION
• 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.
• To avoid bruising, exercise caution when determining a patient’s level of sensitivity and avoid
use on patients taking anticoagulant drugs.
• Stop treatment immediately if the patient experiences pain and consult a doctor.
• This device should not be used on all dermatoses, skin rashes, herpes, inflammatory or
infectious acne or vitiligo.
• 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 indications and contraindications, refer to training manuals.

17
→ELECTROMAGNETIC COMPATIBILITY 3
• Your CELLU M6 Alliance®Lab Medical device requires special care concerning the EMC; it must
be installed and serviced according to the information provided in this user guide.
• Portable and mobile RF communication devices must not be used within 30 cm of your device;
they can cause undesired operation.
• The use of treatment heads other than those provided by LPG Systems may result in increased
emissions or decreased immunity of the device.
• Your CELLU M6 Alliance®Lab Medical device should not be used adjacent to or stacked with
other medical devices.
• The Cellu M6 Alliance®Lab Medical device does not manage essential performances.
• Interference may occur near equipment marked with the following symbol:
For more information about electromagnetic compatibility, refer to the “Electromagnetic
Compatibility” appendix
IMPORTANT SAFETY INFORMATION

18
→IDENTIFICATION RATING PLATE
MAINTENANCE
4
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 Alliance®Lab
Medical 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,
frenquency
and power

19
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
This icon 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
centre 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 icon indicates that some specific warnings
or precautions associated with
this device are not on the label.
This symbol means you must 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 that the
maximum permissible weight on
this device is 135 kg.
This symbol indicates relative humidity limits
This symbol means
“Danger: High Voltage.”
This symbol means
“Use under prescription.” (US only)
This symbol indicates the year of the
manufacturing.
This symbol means “Fragile, handle with
care.”
This symbol indicates to keep the device up
right.
This symbol indicates to not reverse the
device.
This symbol indicates atmospheric pressure
limits.
This symbol indicates “Do not sit.”
→IDENTIFICATION RATING PLATE
MAINTENANCE
4
voltage,
frenquency
and power