Winncare Automorpho User manual

User manual
*PA0010122*
MAJ 27/03/2014 UK

ASKLÉSANTÉ
TABLE OF CONTENTS
INTRODUCTION..............................................................................................................................................................................- 1 -
Necessary information for the patient and those around them ........................................- 1 -
Advice for use ..................................................................................................................................- 1 -
Indications.........................................................................................................................................- 2 -
Counterindications .........................................................................................................................- 2 -
Precautions .......................................................................................................................................- 2 -
Warning..............................................................................................................................................- 2 -
Definition of symbols.......................................................................................................................- 4 -
USE .......................................................................................................................................................................................................- 4 -
Contents of packaging.................................................................................................................- 4 -
Operating principle ........................................................................................................................- 4 -
Installation .........................................................................................................................................- 5 -
Use.......................................................................................................................................................- 7 -
Emergency cardiopulmonary resuscitation: CPR ..................................................................- 8 -
Heel Grounding Valves: ................................................................................................................- 8 -
De-installation ..................................................................................................................................- 9 -
Storage and transport....................................................................................................................- 9 -
AXENSOR® CONNECT: ............................................................................................................................................................- 10 -
MAINTENANCE - DISINFECTION............................................................................................................................................- 10 -
Compressor and AXENSOR® system:.......................................................................................- 10 -
Macro-particle filter:.....................................................................................................................- 10 -
Mattresses and Covers: ...............................................................................................................- 11 -
Diagram of advised maintenance and disinfection...........................................................- 12 -
ALARMS and TROUBLESHOOTING ......................................................................................................................................- 13 -
MAINTENANCE - CHECK..........................................................................................................................................................- 14 -
Frequency of checks: ..................................................................................................................- 14 -
Use of the "info" button ................................................................................................................- 14 -
DISPOSAL OF THE MEDICAL DEVICE ..................................................................................................................................- 15 -
Protection of the environment ..................................................................................................- 15 -
WARRANTY.....................................................................................................................................................................................- 15 -
TECHNICAL FEATURES ...............................................................................................................................................................- 16 -
ELECTROMAGNETIC COMPATIBILITY..................................................................................................................................- 17 -

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INTRODUCTION
NECESSARY INFORMATION FOR THE PATIENT AND THOSE AROUND THEM
This product is a support to help prevent and treat bedsores.
Why have you been prescribed this support?
Your state of health impairs your mobility and puts you at risk of bedsores.
What is a bedsore?
A bedsore is a more or less skin deep lesion caused by putting excessive and
prolonged pressure on tissues between the body and a load bearing surface. This
excessive pressure can obstruct blood flow and lead to bedsores.
A bedsore can take several forms: a simple redness lasting more than one day,
hardening of the skin, or a wound of varying depth, which, in serious cases, can reach
the muscles or the underlying bone.
The appearance of a bedsore may be linked to lack of mobility and/or a chronic
illness.
How does this support work?
This support reduces the pressure supported and allows for better blood flow in the
skin, in order to help prevent bedsores.
ADVICE FOR USE
A support alone cannot prevent bedsores; other preventative measures are also
essential:
– changing position frequently (at least every 2 to 3 hours);
– maintaining skin hygiene and avoiding maceration;
– in cases of incontinence, regularly changing protection;
– monitoring or having the skin condition monitored on a daily basis;
– ensuring sufficient and suitable nutrition;
– regularly drinking a sufficient quantity of liquid.
If one of these measures cannot be taken, it is essential to inform your doctor or nurse
as soon as possible.
Informing your doctor or nurse as soon as possible of any abnormal event such as, for
example, fever, pain or even redness or whitening of support points (head, shoulder,
back, hip, shoulder blade, pelvis, heel, etc.).
It is important to limit the number of layers between the body and the support as much
as possible, with the exception of sheets for a bed support, clothing and any complete
change. Favour loose cotton clothing without seams in the supporting area, if possible.
Do not use folded towels or sheets, an additional pillow, etc.
Ensure the absence of any foreign bodies such as tubing, crumbs, grease, etc.
For hygiene purposes, each support to help prevent bedsores must be used by one
person only.

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INDICATIONS
According to the CNEDiMTS (the French National Committee for Evaluation of Medical
Devices and Health Technologies) report of 22 December 2009 and in accordance
with expert medical opinions:
Prevention and aid in the treatment of bedsore(s) in stages 1 to 4 (according to
medical opinion) for patients up during the day, in bed for more than 15 hours and
presenting an "average" (AT12) to "high" (AT15) risk of bedsore(s), according to a
validated scale and medical opinion.
COUNTERINDICATIONS
Patients whose weight is over 165kg for the VAXT6/AUTO and 180kg for the
VAXT6/MAX. Use in a hyperbaric chamber. Use on a stretcher.
PRECAUTIONS
Unstabilised bone and/or muscle injury in contact with the support;
In the first few days following bedsore surgery (skin graft or flaps) [use static low
pressure mode] ;
Patient monitored at home with no possibility of medical intervention;
WARNING
In accordance with Annex 1 of Directive 93/42/EEC on essential requirements
applicable to medical devices, only compatibility between the systems assembled
by the manufacturer ASKLESANTE guarantees safe usage of the AXTAIR
AUTOMORPHO AXENSOR® motorised air mattress.
The features and performance of the motorised air support shall only be maintained
by using the pump (ref. VAXT6/PUMP/AUTO) associated with the mattress (ref.
VAXT6/MA/AUTO and VAXT6/MA/MAX), without any modification and, optionally,
the inflation/deflation kit (ref. VKIT/AXT).
The national authority responsible for healthcare safety and health products may, at
any time, take steps to monitor the conditions in which products are put on the
market and take the necessary measures in the event of danger or violation of
regulation. In the event of failing to comply with the instructions for use given above,
the user is likely to be held liable in case of an accident.
Products in the Axtair motorised air range area therapeutic mattresses, as defined
by standard CEI 60601-2-52 on evaluation of protection against the mechanical
dangers of Electro-Mechanical equipment (EM) and EM systems; in this respect, they
are excluded from the scope of application of testing according to figures 201.107,
201.108 and table 201.101 on measuring the Dimension "D".

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In order to comply with risk assessment under ISO standard 14971, an assessment was
carried out on all "hospital bed - therapeutic mattresses (Axtair) - accessories". The
risk assessment shows that there may be a risk of bodily trapping if the bedridden
person presents mental confusion and/or agitation. Use of the device has been
approved in order to improve the service rendered in terms of therapeutic aid
and/or prevention of bedsores.
We have approved this product in order to improve the service offered in the
prevention and aid in treatment of bedsores versus the risk of trapping of the
bedridden person.
Keep packaging, the transporting bag as well as the mattress out of reach of
children in order to avoid any risk of suffocation.
In order to avoid any risk, any modification of this product or unspecified use of its
accessories is prohibited.

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DEFINITION OF SYMBOLS
Warning - see user manual and (or) instructions for use
Class II device (Double insulation)
In accordance with the essential requirements of European
Directive 93/42/EEC, applicable to medical devices (modified
2007/47/EEC)
Warning - electrical and electronic equipment subject to
separate collection of waste
Manufacturer
Series number
BF electrical device (applied to blankets)
Patient weight range
USE
CONTENTS OF PACKAGING
1 mattress, rolled up in a transporting bag
1 dirty/clean label
1 identification label
1 AXENSOR® device, located in the blanket cover
1 compressor integrated into a rolled-up mattress
1 electrical power cable with 2 hooks systems for connecting to the sides of a
hospital bed
1 user manual
OPERATING PRINCIPLE
Alternating pressure helps to avoid prolonged vascular compression which is likely to
lead to tissue hypoxia.
The static low pressure mode allows for the care of people requiring immobilisation
(fractures, neurological injury, etc.), reducing secondary pain to a minimum,
promoting the patient's rest and carrying out a weaning process before putting in
place a static mattress, etc..
The "care" mode (fixed) allows for the maintenance of certain acts of care and
transfers.
Adjustment of the level of inflation is automatic based on the patient's shape and
size and the angle of the backrest, thanks to AXENSOR® technology. No external
intervention is necessary.

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NOTES:
Contact the store or service provider from which the product was purchased for
any assistance relating to the set-up, use or repair of the product.
INSTALLATION
1. Unroll the mattress.
2. Position it on the base of the bed, using the "head" and "feet" symbols on the
cover.
3. Hang the compressor on the end of the bed (feet end) using the hooks.
4. Run the electric cable for the compressor along the bed to the nearest power
socket, attach it to the side of the bed using the 2 hooks on the cable and switch
on the power: The lights will turn on for 1 second and a beep will sound.
5. If you have a rapid inflation pump, follow these steps. If not, proceed to step 9.
6. Open the CPR valve, positioning it to OPEN, .
7. Connect the rapid inflation pump to the CPR.
Keep the CPR and the pump on the same line to avoid jamming the CPR with the
weight of the pump. Improper use may lead to reduced airtightness of the CPR.
8. Press down on the rapid inflation button on the pump until the mattress is inflated
(around 1 minute) - Note: The level of inflation is not important as this will be
adjusted automatically by the compressor.
9. Close the CPR valve, positioning it to CLOSED, .
10. Connect the mattress to the compressor.
11. After the timer light has gone off, the patient can be placed on the mattress.

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NOTES:
The necessary information for use of the compressor is noted on the side of the latter:
simplified instructions
After 30 minutes without selection, the intensity of lights will dim so as not to bother
the patient during the night. Pressing a button re-activates the maximum intensity for
30 minutes.
The pneumatic connector is self-blocking and rebalances the pressure in the
mattress when it is disconnected from the compressor.
• The passage in static mode requires the finalization of pressure calculation. If the
static mode is activated when the calculation is completed, the compressor inform
you and alternate until the end of the calculation.
The end of this calculation requires the presence of a patient on the support. In case
of the absence of patient, the alternate pressure will continue even in static mode.
At the end of the calculation pressure, the compressor will switch into the selected
mode.
WARNING:
The electrical cable must be installed so as to avoid any crossover with the
articulated parts or wheels of the bed and prevent staff from tripping. Risk of bodily
injury and material damage. Use the detachable hook systems provided.
The power cable makes up the isolation system for the device.
The compressor keypad, the power cable, the pneumatic connector and the CPR
valve must be visible and accessible at all times.
The AXENSOR® box must always be placed in the elastic pouch located on the inner
side of the ad-hoc mattress.

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USE
Indicates the compressor is on
Flickers to indicate inflation of the mattress
After it has gone off, the patient can be placed on it
When this light is lit, it indicates that the keypad is locked: it is not
possible to change mode.
To unlock the keypad, you must press down continuously for 4
seconds.
Locking is automatic after 5 minutes or can be ordered by pressing
down continuously for 4 seconds.
Low pressure dynamic mode: triggers alternation of one in two cells
(except the 3 head cells). Alternation takes place every 7 minutes.
Care mode (static): makes the surface of the mattress firm in order to
facilitate handling of the patient during care or getting them up (eg.
transfer to a flat bed chair).
Duration of this mode is limited to 30 minutes.
Securing care mode: flickering of the care mode light indicates that
the mode is almost finished. It is triggered 5 minutes before the end. A
sound signal is emitted when triggered.
At the end of the 30 minutes, the compressor automatically switches
into the mode previously used.
Low pressure static mode: inflates all cells in the mattress at a constant
pressure depending on the shape and size of the patient and
promotes their immersion in the support in order to increase the
supporting surface and thus reduce the average interface pressure.
Fixed LED: Low severity alarm. (see alarm chapter)
Flickering LED: Medium severity alarm. (see alarm chapter)
Pressing on the button: stops sound alarm
Allows you to get technical information on operation (see
maintenance-revision chapter)
The following terms of use must be respected:
Temperature: between +15°C and + 40°C
Humidity levels: between 30% and 93%
Altitude: less than 2000m

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EMERGENCY CARDIOPULMONARY RESUSCITATION:CPR
In case of heart stoppage:
1. Turn the end of the CPR valve to the "OPEN" position.
2. The mattress deflates and the back of the thorax will be flat on the base of the
bed in less than 15 seconds in order to allow External Cardiac Massage to be
carried out.
HEEL GROUNDING VALVES:
The range of mattresses is equipped with 4 independent heel grounders at the levels
of the cells at the foot of the mattress.
In position A
The cell, with the air vented,
deflates.
In position B
The cell is re-inflated.
WARNING:
Do not simultaneously deflate more than 2 out of 4 cells in order to guarantee
the comfort and safety of the patient.
Do not leave a heel grounder in a position between A and B.
A notch on the A and B position ensures proper positioning.

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DE-INSTALLATION
1. Unplug the compressor from the mains
2. Open the CPR valve to deflate the mattress. Total removal of air from the mattress
can be facilitated by use of the inflation/deflation pump connected to the CPR.
3. Position the compressor in the centre of the mattress.
4. Roll the mattress up, starting at the feet
5. Strap up the mattress.
6. Insert the mattress into the transporting bag provided upon delivery of the
product.
7. Position the dirty/clean label so as to make the yellow face visible.
Blue label: the mattress is clean
Yellow label: the mattress is dirty
(risk of contamination)
STORAGE AND TRANSPORT
A model identification label allows you to identify which product from the Axtair range
is in the bag. This label must be visible during storage.
The following storage and transport conditions must be respected:
Temperature: between -25°C and + 70°C
Humidity levels: between 30% and 93%
Atmospheric pressure: between 50kPa and 106 kPa
WARNING:
Keep the device away from sources of humidity, direct sunlight and constant heat
sources.
Prevent the risk of shocks or damage by sharp objects.
NOTE:
The MANUFACTURER shall make available, on request, the circuit diagrams, lists of
components, descriptions, calibration procedures and any other useful information
to UPKEEP and MAINTENANCE STAFF to carry out authorised repairs in accordance
with the contract which ties the requesting party to the manufacturer, ASKLE.

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AXENSOR® CONNECT:
Details on the operation of the compressor can be transmitted on a PC via a
Bluetooth connection.
Visit the site www.winncare.fr , AXENSOR® CONNECT menu to download the software
and find out how it works.
When you stop using the software, check that the compressor starts up again in one of
the three operating modes (DYNAMIC, STATIC or CARE). Otherwise, contact your
maintenance service.
MAINTENANCE -DISINFECTION
The method used depends on the degree of disinfection required. Techniques and
products will be applied according to validated good practice recommendations.
See the diagram at the end of the paragraph
- Daily upkeep of the compressor is carried out on the connection between the
mattress and connector.
- It is essential to unplug the electric cable linked to the compressor from the mains.
The light indicating the presence of mains power must be off.
- Do not use high pressure jets to clean an Axtair AUTOMORPHO AXENSOR®
compressor.
- Do not put the compressor on the floor. Hang it at a distance of ≥ 60 cm from a
water source.
Do not use corrosive cleaning products such as industrial cleaning agents,
acetone solvents, ether or colouring products (alcohol iodine, potassium
permaganate, silver nitrate, etc.). Do not use abrasive materials such as steel wool or
Scotchbrite pads.
COMPRESSOR AND AXENSOR® SYSTEM:
Use a dishcloth lightly doused in a CE certified surface detergent or detergent/disinfection solution at
the concentration recommended for use by the manufacturer. Adhere to the recommended
time periods.
Attention: do not project liquid in order to avoid any damage to the compressor due to
seepage of liquid into the interior of the box.
MACRO-PARTICLE FILTER:
The macro-particle filter provided by ASKLE SANTE must be changed at least every 6
months or more frequently, depending on the environmental conditions (dust, smoke,
etc.). This filter is located on the back of the compressor in a transparent cover.

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MATTRESSES AND COVERS:
Two zips located inside the cover at the foot and head of the mattress allow the
elements to be quickly separated.
The cells and the AXENSOR® system remain attached and must be manually disinfected:
use a dishcloth doused in a CE certified surface detergent or detergent/disinfection
solution at the concentration recommended for use by the manufacturer. Adhere to
the recommended time periods.
* CE certification obligatory under Directive 94/42/EEC for products to be used on the
surfaces of Medical Devices.
For the covers and the base, the following maintenance recommendations must be respected:
Washed at a maximum water temperature of 90°C, reduced
mechanical action, rinsing at decreasing temperature, reduced
spin dry.
Whitening possible, chlorination at 5000ppm allowed.
Do not iron.
Do not dry clean, do not use solvent-based stain remover.
Tumble drying allowed moderate temperature.

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DIAGRAM OF ADVISED MAINTENANCE AND DISINFECTION
* Broad-spectrum alcohol-based disinfectant cleaner, standardised: bactericide
EN1040, EN13727, Fungicide EN1275, EN13624, NF T72-190, Sporicide EN13697, EN14561,
Polyvirus EN14476, HBV, HCV.
Limit spraying on cells
**Detergent-Disinfectant for maintenance of floors and surface (Positive List of
Disinfectants)
*** Neutral detergent (domestic detergent)
NO
YES
NO
YES
YES
Receipt
of Full Device
Pre-Treatment of surface (Decontamination)
Spread over surface by µfibres
Alcohol-based solution [Recommended: hygiene
mask, gloves, apron]
Physical
cleanliness
Unacceptable
Bio-cleaning surface maintenance
Method: 3 operations
Product: Detergent-Disinfectant**
[Recommended: gloves, apron]
Machine wash cover at 90°C
(Detergent ***)
Replacement cover identical
to the original protection
Conformance of
Mattress and
Compressor
Assemble
Register
Spray surface
Detergent-Disinfectant**
[Recommended: hygiene mask]
Release of product
Condition
NO
Product
expertise
Cover changed?
Removal by the waste
industry
Surface maintenance
1 Operation
Detergent-Disinfectant

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ALARMS AND TROUBLESHOOTING
The following table shows all the device alarms, what triggers them, their severity as
well as possible troubleshooting.
Signal
Severity
Trigger
Possible troubleshooting
Condition
Time
perio
d
Flickering light
alarm
and presence of
mains electricity
light off
+
+ sound signal
Medium
Electrical fault:
the compressor is
not being
supplied by the
mains
0 min
1- Plug the compressor back in
2 - Check that state of the
electrical grid
3- Change the fuse
4 -Unplug the mattress from the
compressor
5 - Contact your maintenance
service
Flickering light
alarm
and presence of
mains electricity
light on
+ sound signal
Medium
Problem with
compressor
system
0 to 1
min
1 - Check that the mattress is
properly connected to the
compressor
2 - Check that the CPR is
properly closed
3 - Remove the patient from
the support
4 - Contact your maintenance
service
The compressor
is measuring zero
pressure when it
pumps
1 min
The compressor
is measuring too
much pressure
1 min
Inflation
impossible
10
min
Fixed light alarm
+ sound signal
Low
First inflation
impossible
40
min
1 - Check that the mattress is
properly connected to the
compressor
2 - Check that state of the
AXENSOR® box
3 - Check that the CPR is
properly closed
4 - Contact your maintenance
service
Problem with
mattress system
0 min
NOTES:
When the compressor is unplugged, even voluntarily, there is automatically an
electrical fault alarm to prevent accidental handling.
When there is an alarm related to loss of communication, it is not necessary to
remove the patient as the compressor runs a default safe operation mode.
The triggers in the above table are ranked based on their severity.
Sound and visual alarms are designed to be visible and audible from 2 metres
away from the compressor.

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WARNING:
After accidental deflation of the mattress due to prolonged power cut, check during
re-inflation that the patient does not have any part of their body trapped between
the mattress and the bars of the bed.
MAINTENANCE -CHECK
FREQUENCY OF CHECKS:
It is recommended to check compressors and AUTOMORPHO AXENSOR® mattresses
after every 2 years of use.
In order to facilitate management and planning of these checks, operation timers let
you know how long the compressor and mattress have been in use.
To see this information, you require specific equipment; contact your distributor for
more information.
WARNING:
Checks can only be carried out by designated people, contact your distributor.
USE OF THE "INFO"BUTTON
Continuously pressing this button allows you to get information on the last
recorded alarm and the need for a check.
Alarm key: Signal
Meaning
Fixed lock light
Problem with mattress
system
Flickering lock light
Problem with compressor
system
Flickering dynamic light
No pressure
Fixed care light
First inflation impossible
Flickering care light
Inflation impossible
Flickering static light
Too much pressure

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Key to need for
check: Signal
Meaning
Timer flickering
quickly
Recommended date of revision past
(operating time higher than 17,500 hours since
last revision)
Timer flickering
slowly
Revision scheduled within 2 months
Timer fixed
Revision scheduled in over 2 months
DISPOSAL OF THE MEDICAL DEVICE
PROTECTION OF THE ENVIRONMENT
This piece of equipment contains several recyclable materials.
This symbol tells you that this equipment is recyclable and that used
equipment must not be mixed with other waste.
Recycling equipment will be carried out as safely as possible to limit the
effects on the environment and human health, in the case of dangerous substances
being present, in accordance with European directive 2002/96/EC on electrical and
electronic waste equipment at the end of its life cycle.
You can take the compressor to your closest waste sorting centre at the
end of its life cycle. The device must be placed in the mixed small
appliances receptacle.
You can contact the shop or service provider from which the product was
bought to find out where your nearest collection points for used equipment are.
Before any disposal, the device must be cleaned, following the instructions in the
MAINTENANCE - DISINFECTION chapter to avoid any risk of contamination.
We thank you for doing your bit to protect the environment.
WARRANTY
The compressor and mattress are guaranteed for 2 years from the date of purchase
against any manufacturing fault, in the recommended conditions of use specified in
the instructions. This warranty does not substitute any legal guarantees.
In order to make use of it, it is essential to retain your product receipt.
In the case of a manufacturing flaw and if the product is still under warranty, you may
contact your service provider and present the product in question to them. The latter
will take the necessary steps with our company to proceed to repair the product.

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WARNING:
A guarantee seal is located under the simplified instructions on the side of the
compressor. The presence of this seal ensures that the compressor has successfully
passed all control tests, as well as its inviolability.
In case of removal of this label by the user or an unauthorised third party, the integrity
of the compressor can no longer be proven; ASKLE SANTE may refuse to carry out the
repair under guarantee, and is authorised to cancel the latter.
TECHNICAL FEATURES
SUPPORT FEATURES
VAXT6/MA/AUTO
VAXT6/MA/MAX
Validated user weight
30 – 165 kg
30 – 180 kg
Weight of support
8 Kg
10 kg
Size of support
195 x 87 x 17 cm
195 x 87 x 20.5 cm
Therapeutic air cells
Number: 18
Height: 12 cm
Material: Ether
polyurethane
Number: 18
Height: 15.5 cm
Material: Ether
polyurethane
Head cells
3 static cells
Rapid inflation (CPR valve)
less than 15 secs.
Foam mattress
Polyether foam (detachable) - Height 5cm
Upper cover
- Detachable
- Waterproof and permeable to water vapour.
Polyurethane/polycarbonate mesh with ionic silver.
Assembled by welding
- Location for comfort pillow
Lower cover
- Detachable
- Material: non-slip PU/PVC
Independent life of
disconnected mattress
> 8 hours
Fire regulations
EN 597-1&2 and GPEM D1-90 & D1-89bis
Warranty
2 years against any manufacturing flaw
Life cycle
6 years
Rapid inflation pump
Compatible (ref. VKIT/AXT)

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COMPRESSOR FEATURES
Operating modes
- Alternating: 1 cell out of 2
- Static low pressure
- Care: renewable, lasting 30 minutes
Weight of compressor
2.7 Kg
Size of compressor
22 x 25 x 11.5 cm
Pressure adjustment
Automatic
Cycle times
Between 17 and 20 mins
Maximum output
8 litres/min
Mattress inflation time:
- around 20 minutes
- less than 1 minute with a rapid inflation pump
Acoustic level
< 35 dBA
Alarms
visual and sound
Power supply
220-240 volts – 50 Hertz
Length of supply cable
4.5 m
Fuse
T 0,63A H 250 V
Max. apparent power used
13 VA
Average consumption noted
5 Wh
Protection against electric
shocks
class II,
BF insulation applied to mattress and AXENSOR®
B insulation applied to compressor
Box materials
Fire resistant plastic material
Warranty
2 years against any manufacturing flaw
Life cycle
6 years
Regulations
IEC 60601-1 Ed.3 ; IEC 60601-1-2
ELECTROMAGNETIC COMPATIBILITY
The Axtair AUTOMORPHO AXENSOR® is in accordance with the relevant
electromagnetic compatibility regulations (EMC).
The Axtair AUTOMORPHO AXENSOR® requires special precautions in terms of
electromagnetic compatibility and must be installed and commissioned in
accordance with the EMC information provided on demand by ASKLE SANTE, and
which are available on its website.
Portable and mobile radio frequency communications equipment can affect the
Axtair AUTOMORPHO AXENSOR®.
The use of accessories and cables other than those provided and specified by ASKLE
SANTE may result in increased emissions by the Axtair AUTOMORPHO AXENSOR® or
decreased immunity, affecting its operation as well as its performance.

ASKLÉSANTÉ Groupe Winncare – 200, rue Charles Tellier – Actiparc de Grézan – 30 034 Nîmes Cedex 1 (France)
Tel: [phone] – Fax. : [phone] – Email: [e-mail]
www.winncare.fr
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