Winncare MEDICALYS 2 User manual

1
4 Le Pas du Château
85670 SAINT PAUL MONT PENIT
TEL : [phone]
FAX : [phone]
Email : [e-mail]
Site Internet : http://www.winncare.fr
USER MANUAL
MEDICALYS 2ième GENERATION (MS4…)
Creation 2020_02_11
Update 2020_05_01
580244 Anglais

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1. TRANSPORT AND STORAGE 4
2. BED ENVIRONMENT CONDITIONS 4
3. GENERAL USE 4
3.1. PREREQUISITES BEFORE USE AND INSTRUCTIONS FOR USE 4
3.1.1. TRAINING AND QUALIFICATIONS OF THE PERSON USING THE DEVICE 4
3.1.2. INDICATIONS 5
3.1.3. CONTRAINDICATIONS 5
3.2. CLINICAL BENEFIT,DEVICE PERFORMANCE,ACTION MECHANISM DEPENDING ON THE FUNCTIONS,OPTIONS OR ACCESSORIES USED 5
3.2.1. DEVICE PERFORMANCE CHARACTERISTICS 5
3.2.2. EXPECTED CLINICAL BENEFITS 5
3.2.3. INFORMATION FOR HEALTHCARE PROFESSIONALS 5
3.3. PRECAUTIONS FOR USE 5
3.4. ELECTRICAL CHARACTERISTICS 7
3.4.1. ELECTRICAL DATA 7
3.4.2. ELECTROMAGNETIC COMPATIBILITY 8
3.4.3. EQUIPOTENTIALITY 9
4. BED BOARDS 90CM/100CM WIDTH COMPATIBLE 10
4.1. BED BOARD REFERENCES FOR APPLICATION ENVIRONMENTS 1AND 2 10
5. COMPATIBLE ACCESSORIES 11
6. USE 12
6.1. PURPOSE OF DEVICE 12
6.2. SPECIFIC PRECAUTIONS FOR USE 12
6.2.1. RESIDUAL RISKS ANS ADVERSE SIDE EFFECTS 12
6.3. GENERAL DESCRIPTION 12
6.4. TECHNICAL CHARACTERISTICS 13
6.4.1. DIMENSIONS 13
6.4.2. WEIGHT 14
6.4.3. NOISE 14
6.4.4. ELECTRICAL COMPONENTS 14
6.4.5. PROTECTION LEVEL AGAINST DUST AND LIQUID PENETRATION 14
6.5. ELECTRICAL CONNECTION DIAGRAM 15
6.6. REMOTE CONTROL 16
6.6.1. MOBILE CARER CONTROL ACO (OPTION) 17
6.7. CENTRALIZED BRAKING 18
6.8. EMERGENCY DECLINATION 18
6.8.1. POSITIONING OF THE EMERGENCY DECLINATION 18
6.8.2. RESETTING THE BOX SPRING 18
7. OPERATION OF THE SLEEPING SURFACE 19
7.1. BACK REST 19
7.1.1. STANDARD BACK REST 19
7.1.2. BACK REST WITH TRANSLATION 19
7.1.3. EMERGENCY RELEASE OF THE BACK REST (CARDIO PULMONARY RESUSCITATION) 20
7.2. LEG REST 20
7.2.1. LEG REST WITH MANUAL CRANK (C/) 20

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7.2.2. LEG REST WITH ELECTRIC FOLDING (P/) 20
8. INSTALLATION OF ACCESSORIES 20
8.1. BOARDS 20
8.2. METAL SIDE RAILS 21
8.3. WOODEN BARRIERS 22
8.4. ALUMINUM HALF SIDE RAILS 23
8.5. ANGLED LIFTING POLE AND IV STAND 24
9. SPECIFIC FUNCTIONALITIES 25
9.1. 3POSITIONS WALL STOP 25
9.2. MECHANICAL BACK TILT /FORWARD TILT AND/OR RELEASE OF THE TRENDELEBURG (OPTION) 25
9.3. BATTERY 26
10. MAINTENANCE 27
10.1. IDENTIFICATION 27
10.2. INSTRUCTIONS FOR DISMANTLING THE MOTORS 27
10.3. MAINTENANCE 28
10.4. QUALITY INSPECTION OF MEDICAL BEDS 29
10.5. CLEANING AND DISINFECTION 30
10.6. LIFETIME 31
10.7. GARANTIES 31
10.8. TROUBLESHOOTING GUIDE 32
11. SCRAPPING 33

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It is strictly forbidden to stack packages weighing over 60kg/m², whatever
position they are in.
Before transporting or dismantling the bed, make sure the back and leg rests
are fixed to the frame of the bed base.
Dear Sir/Madam,
You have acquired a WINNCARE medical bed equipped with its accessories, and we thank you for your
custom.
Our class I medical devices are designed and manufactured in accordance with Annex VIII of Regulation
(EU) 2017/745.
They are tested in conformity with standard IEC 60601-2-52 (2010) in their commercial configurations,
including the boards and accessories that we manufacture, so as to ensure you maximum safety and
performance.
As a result, maintenance of the contracted good’s warranty depends on compliance with the conditions for
use recommended by WINNCARE and the use of original accessories, which also guarantees you safe use
of the medical bed and its accessories.
1. TRANSPORT AND STORAGE
For transport, the bed should be in its low position, and strapped and protected. The wired control and supply
lead should be attached to the bed base.
The head and footboards are protected and strapped to the sleeping surface.
The bed should be transported upright when in its original packaging in compliance with the instructions printed
on the packaging.
2. BED ENVIRONMENT CONDITIONS
The bed, along with the boards and accessories, must be transported and stored
at a room temperature of between -10°C and +50°C,
The bed, along with the boards and accessories, must used at a room
temperature of between +10°C and +38°C,
Relative humidity of between 30% and 75%.
Atmospheric pressure between 700hPa and 1060hPa
3. GENERAL USE
Before use, it is essential to read these instructions carefully. They contain advice on using and looking after
the bed to guarantee optimum safety.
The latest updated version of this manual is available on our website www.winncare.fr.
The photos, images and diagrams included in this manual may not correspond to your product depending on
the versions or options you have.
3.1. Prerequisites before use and instructions for use
3.1.1. Training and qualifications of the person using the device
Users must be trained by people who have been trained and approved by the relevant business entities, in
particular when it comes to safety and reporting non-conformities.
Observe the specified
environmental conditions

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3.1.2. Indications
Suitable for patients with temporary or permanent decreased independence due to their illness or disability.
3.1.3. Contraindications
To be determined by the prescribing doctor based on the patient’s condition, the medical treatment and the
type of relevant accessories. Patient weight higher than the safe operating load defined.
3.2. Clinical benefit, device performance, action mechanism depending on the functions,
options or accessories used
3.2.1. Device performance characteristics
Variable height (ergonomics of care, transfer aid), low bed (reduces the severity of falls from the bed),
Trendelenburg, reverse Trendelenburg, chest rest, leg rest, flat, chair position (preserves or improves the
patient’s physical and/or psychological state, helps with administering care), 30° chest rest and/or with Fowler
or semi-Fowler positions (helpsprevent pressure sores), 5° Trendelenburg (helps lift the patient), rails(protects
the patientand/or caregivers), lateral stop (stabilizes the mattress), removable bed panels (prevents the patient
from falling out of bed, acts as a fixed walking aid, helps with head and foot care).
3.2.2. Expected clinical benefits
To preserve the patient’s state of health, mobility, activity and transfers. To reduce the repercussions of the
immobilization syndrome. To protect the health and safety of users or others.
3.2.3. Information for healthcare professionals
Identify possible combinations of risks and benefits for each intended use. Assess the patient’s ability to use
and understand the overhead remote control and the caregivers’ knowledge of how the medical bed and its
accessories work.
Any serious incident occurring in connection with the device must be reported to the manufacturer and to the
competent authority of the Member State in which the user and/or patient is established. Inform the competent
authority if you think or have a reason to believe that the device presents a serious risk or is faulty.
3.3. Precautions for use
Although the bed is conforming with Electromagnetic Compatibility, some devices may alter how it functions,
in which case they must be used at a distance or not used at all.
The bed is a medical device and must not be modified under any circumstances. You must ensure its
traceability, including that of the boards and its accessories.
If you are assembling medical devices not provided by the bed manufacturer, you must check the conformity
of the assembly and make the EU declaration of conformity of the new medical device.
The electric parts (jack, supply box, wired control, etc.) shall only be repaired by the manufacturer Linak.
The bed is not suitable for use with an inflammable anaesthetic mixture with air or oxygen or nitrous oxide.
The loads permitted (see bed characteristics) must be distributed evenly over the bed base.
Do not activate all the motors at the same time when the patient is in the bed (only one motor is authorised at
one time, except elevation by 2 motors or simultaneous function).
The user and staff must be trained and aware of the risks associated with
using the bed. He must not allow it by children and be vigilant when used by
confused or disoriented people.

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After each use and while care is being administered to the patient, the brakes must be activated.
We recommend putting the bed in its low position after every use and while the patient is resting, to reduce the
height of falls by a confused or agitated person. Remember to lock the function(s) (if the option is available).
On change of height or angle of the parts of the bed, make sure that there are no objects and no parts of the
patient’s or carer’s body caught between the bed, the boards, the accessories and the ground or between the
boards and base or between the cross braces.
Do not sit down on the side of the back rest or leg rest if this is not flat.
In the case of a prolonged more than 50 ° tilt bust semi-sitting position, it is recommended to vary the position
of the person in bed every 2 hours.
When the bed is being moved, keep the power lead well away from the ground and wheels.
When use of an adaptor, extension lead or connection plug proves necessary, you must check that its
characteristics are suitable for the bed.
Connection to the supply box must be done using a mains complying with the standards in force and
corresponding to a voltage of use indicated on the device.
The mains plug must be disconnected before the bed is moved.
Do not pull on the mains leads to disconnect the mains plug.
During any handling, try not to catch the leads of the motors and remote control and do not get them knotted.
The wired control must be hooked to the headboard when not in use.
In the case of the use of infrared remote control(s), WINNCARE allows the establishment of a single bed in the
same room (or in a close environment) or a second bed only if the infrared options of 2 beds concerned are
different (I and I1).
The condition of the leads must be checked frequently. If the slightest modification is observed, the person in
charge for maintaining the bed must be contacted to carry out the necessary repairs.
If repairs are required, the person in charge of maintenance must be contacted.
For greater safety, some side rails can be adapted (see accessories).
Side rails should not be used to manipulate or move the medical bed.
To assist patient mobility, it is possible to fit a Mobility Aid System (S.A.M.).
For assistance, if necessary, in mounting, operation or maintenance or to report unexpected operation or
events, call your supplier or Winncare.
The cleaning instructions recommended must be complied with.
Only use original parts and accessories supplied by WINNCARE to guarantee safety and maintain product
conformity. The bed must not be modified.
Abnormal use of the bed may damage it or cause accidents to users, in which case the warranty shall be
annulled. Abnormal use means failure to comply with the precautions for use, maintenance instructions and
other uses not related to the bed’s normal purpose, such as: use of the bed by several people at the same time
(except DUO DIVISYS bed), use outdoors, moving the bed on a slope that is steeper than 10°, etc.
Put the bed in the designated room, foreseeing an appropriate perimeter of use for the different functions
(variable height, TR, etc.), especially if the bed has a lifting pole or side rails. Check that there is sufficient
ceiling height if a lifting pole is fitted.
Brake the wheels.
The mains socket should remain accessible to enable the bed to be disconnected quickly.

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- Check that the bed operates properly after installing it in accordance with the check-list
appended in this document. (Test all of its functions)
- The patient is a planned operator of the bed. Users must be trained in how to use the
equipment.
- Inform the patient and his visitors of the safety instructions to be observed.
Plug in the power lead, checking that the mains comply with the standards in force and that it is suitable for the
supply box voltage.
Also ensure that the power lead, the remote control lead as well as the cables of possible other devices are
positioned correctly to prevent any risks of getting caught between the moving parts of the bed.
3.4. Electrical characteristics
3.4.1. Electrical data
Classe II (double
insulation)
Frequency
Protection level against
dust and liquid penetration
Operating time
In accordance with DEEE
Internal reference
Voltage
Current type
XXX-XXX-XXX
IP XX
xxxV ~ xxH
Z
FACTEUR DE SERVICE :
xx% max. x min/xx min
PUISSANCE ABSORBEE :
Xxx VA
ET-xxxxx
Protection level against
electric shocks (type BF)
Absorbed power
Internal reference

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The bed is an electromedical device requiring special precautions with regard to electromagnetic
compatibility. The device must be installed and put into service according to the EMC information
provided in this manual.
The use of accessories, transducers, and cables other than those specified or supplied by the
manufacturer may cause increased electromagnetic emissions or a decrease in the immunity of
the device and may cause improper operation.
3.4.2. Electromagnetic compatibility
The bed will not move automatically when subject to electromagnetic disturbances within the limit of the values
indicated below.
Manufacturer’s declaration and guide – electromagnetic emissions
The medical bed (see references in contents) has been designed for use in the electromagnetic environment specified below. The user should ensure that it is used in such
an environment.
Emissions test
Compliance
ELECTROMAGNETIC ENVIRONMENT - GUIDE
RF emissions
CISPR 11
Group 1
The medical bed (see references in contents) uses RF energy only for its internal functions.
Therefore, its RF emissions are very low and are not likely to cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class B
The medical bed (see references in contents) can be used in all domestic environments,
including those directly connected to the public low-voltage power supply network that supplies
buildings for domestic purpose.
[ ]
Harmonic emissions
EN 61000-3-2
Class A
Voltage fluctuations / Flicker
EN 61000-3-3
Compliant
RF emissions
CISPR 14-1
Not Applicable
The medical bed (see references in contents) has not been designed for connection to other
equipment.
Manufacturer’s declaration and guide - electromagnetic immunity
The medical bed (see references in contents) has been designed for use in the electromagnetic environment specified below. The user should ensure that it is used in such
an environment.
IMMUNITY TEST
IEC 60601
Severity level
COMPLIANCE LEVEL
Electrostatic discharge
EN 61000-4-2
8 kV contact
15 kV air
8 kV contact
15 kV air
Radiated RF
EN 61000-4-3
3 V/m
80Mhz –2,7Ghz
80% AM at 1kHz
3 V/m
80Mhz –2,7Ghz
80% AM at 1kHz
Proximity fields from RF
wireless communication
equipment
EN 610004-3
See table below
See table below
Electrical fast transients
EN 61000-4-4
2 kV for feeders
1 kV for input/output lines
Repetition frequency at 100 kHz
2 kV for feeders
1 kV for input/output lines
Repetition frequency at 100 kHz
Surges
EN 61000-4-5
Differential mode 1 kV
Common mode 2 kV
Differential mode 1 kV
Common mode 2 kV
Conducted RF
EN 61000-4-6
3V
0,15 –80 MHz
6V in ISM band between 0.15 and 80 MHz
3V
0,15 –80 MHz
6V in ISM band between 0.15 and 80 MHz
Magnetic fields
IEC 61000-4-8
30A/m
50 Hz or 60 Hz
30A/m
50 Hz or 60 Hz
Voltage dips
EN 61000-4-11
0% UT; 0,5 cycle at 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°
0% UT; 1 cycle
70% UT; 25/30 cycles at 0°
0% UT; 0,5 cycle at 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°
0% UT; 1 cycle
70% UT; 25/30 cycles at 0°
Voltage interruptions
EN 61000-4-11
0% UT ; 250/300 cycles
0% UT; 250/300 cycles
NB: UTis the nominal value of power voltage applied during the test.

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Test specification for immunity to RF wireless communications devices
Test frequency (MHz)
Modulation
Immunity test level (V/m)
385
Pulse Modulation : 18 Hz
27
750
FM + 5 Hz deviation : 1 kHz sine
28
710 –745 –780
Pulse Modulation : 217 Hz
9
810 –870 –930
Pulse Modulation : 18 Hz
28
1720 –1845 –1970
Pulse Modulation : 217 Hz
28
2450
Pulse Modulation : 217 Hz
28
5240 –5500 - 5785
Pulse Modulation : 217 Hz
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3.4.3. Equipotentiality
Under the head-half of the bed base you will find an equipotentiality socket, identified by the label, enabling
you to connect any electromedical devices. The leads of these devices must pass through the head end and
not on the side.
Equipotentiality

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4. BED BOARDS 90cm/100cm WIDTH COMPATIBLE
(1) Bed board incompatible with the XPRESS transport kit
(2) Long pan option incompatible with the XPRESS transport kit
(3) Emergency removable option incompatible with the XPRESS transport kit
(4) Board incompatible with the centralised brake option of the ALDRYS bed
(5) The blanket hoop option is incompatible with the XPRESS transport kit, XPRIM III and
AERYS bed
(6) Bed board incompatible with the XPRESS transport kit.
4.1. Bed board references for application environments 1 and 2
➢Mattress
Observe the mattress dimensions prescribed. See user guide
Width of base in
cm
Characteristics of compatible mattresses
90
Width 86 cm minimum with a high resilience foam of 34Kg/m³ minimum
100
Width 96 cm minimum with a high resilience foam of 34Kg/m³ minimum
Item
L=90cm
L=100cm
MEDIDOM II (2)(4)
P318-00
19
P323-00
21
MEDIDOM II HOTELIER (4)(6)
P326-00
34
COTE DE LUMIERE (5)
P360-00
21
DAGONE (5)
P388-00
20
ELEGANTTI
P414-00
17
LOUIS PHILIPPE (1)(2)
P415-00
15
COTE DE LUMIERE with wooden barriers (2)(5)
P549-00
21
VAL DE VIE with wooden barriers (2)(4)
P552-00
19
P553-00
21
WINNEA® (3)(5)
P609-00
19
AUZENCE II (5)
P611-00
18
WINNEA® CIC (1)(5)
P615-00
15
ABELIA II
P616-00
15
P636-00
17
CARMEN II with wooden barriers (2)
P620-00
30
P630-00
33
MADELIA II
P624-00
13
P634-00
14
CARMEN II
P625-00
27
P635-00
30
CARMEN II HOTELIER (6)
P629-00
42
ABELIA II Aluminum side rails (6)
P631-00
20
P637-00
21
STYLVIA Aluminum side rails (6)
P632-00
32
P638-00
34
NOVIDA Aluminum side rails (6)
P633-00
32
P639-00
34
VAL DE VIE (4)(5)
P704-00
17
Item
L=90cm
WINNEA HAND RAILS
P609-00
WINNEA CIC BOARDS
P615-00
Incompatible mattresses can pose RISKS
There must be at least 220 mm between the top of the side rail and uncompressed and no
therapeutic mattress surface. It will be advisable to tend towards this specification in the case
of the use of a therapeutic mattress.

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5. COMPATIBLE ACCESSORIES
Only accessories and boards supplied by WINNCARE guarantee you a
compatibility with our products.
Incompatible accessories and boards can pose RISKS

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6. USE
6.1. Purpose of device
➢The device is intended to compensate for a handicap and as a preventive measure.
➢Depending on their configuration, Medicalys beds are intended for environments 1, 2, 3 and 5 defined
by the standard. EN 60601-2-52.
➢Medicalys are intended for persons whose size is greater than or equal to 146 cm, with a weight
greater than or equal to 40 kg and a body mass index (BMI) greater than or equal to 17.
6.2. Specific precautions for use
The bed can be used as a stretcher except with wheels Ø100.
6.2.1. Residual risks ans adverse side effects
6.3. General description
Manual crank or electric folding leg rest depending on version.
DANGER
RESULT
REQUIREMENTS FOR THE USER
Trapping
Hands pinched
Handle legsrest or backrest up by handles or at specified
locations
Trapping
Crushing body or object
Before lowering the bed, check that the area between
the bed and the floor is free
Trapping
Crushing body or object
Check before operating the central brake pedal that the
area between the pedal and the floor is free
ADVERSE SIDE EFFECTS
Fall of the person. Immobilization syndrome. Aggravation of fractures that have not been stabilized
and/or procedural pain when the articulated parts of the bed frame are moved.
Slatted back rest
Mattress side stop
Bed base
Headboard
Angled lifting
pole slots
IV stand slots
Footboard
Wall stop
3 positions
Back rest handle
Base and
cross braces
Forward slant /
back slant pedal
Centralised
brake pedal
Slat leg rest
Leg rest handle
Calculation of BMI :
BMI = m / h²
m : weight in kg
h : size in m
Warning refer to
user’s manual

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4°
P/
-16°
6.4. Technical characteristics
6.4.1. Dimensions
.
Ø wheels
Height
lower position
Height
top position
Height under base
(for lifter or dinner table)
12,5cm
37cm
86,5cm
14,5cm
15cm
39,5cm
89cm
17cm
Forward slant
17°
Back slant
12.5°
223,5cm
105,5cm
672 mm
947 mm
Version C/ R/
847 mm
739 mm
394 mm
553 mm
Version P/
26° (P)
C/
12°

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Maximum operating time: Read the recommendations on the electrical label
on the bed.
6.4.2. Weight
Normal load in use: 230 kg (Patient 165 kg, Mattress 20kg. Accessories 45kg)
TOTAL
Médicalys bed (C/)
Version manual crank leg rest (without boards)
103 kg
Médicalys bed (P/)(R/)
Version electric folding leg rest (without boards)
106 kg
Médicalys bed (P/)(R/)
Version electric folding leg rest and back/forward slant (without boards)
120 kg
6.4.3. Noise
The measurement of the maximum audible sound power in accordance with ISO 3746 is 53 dB(A).
6.4.4. Electrical components
6.4.5. Protection level against dust and liquid penetration
Index
1st number (decade)
Protection against solids
2nd number (unit)
Protection against water intrusion
0
No protection.
No protection.
1
Protected against solid bodies greater than 50
mm.
Protected against vertical drops of water drops.
2
Protected against solid bodies greater than 12,5
mm.
Protected against falling drops of water up to 15° from
the vertical.
3
Protected against solid bodies greater than 2,5
mm.
Protected against rain water up to 60 ° from vertical.
4
Protected against solid bodies greater than 1
mm.
Protected against splashing water from all directions.
5
Protected against dust and other microscopic
residues.
Protected against jets of water from all directions at the
lance (6.3 mm nozzle, distance 2.5 m to 3 m, flow 12.5 l /
min ± 5%).
6
Totally protected against dust.
Protected against strong jets of water from all directions
to the lance (12.5 mm nozzle, distance 2.5 m to 3 m, flow
100 l / min ± 5%).

15
6.5. Electrical connection diagram
1
2
3
Variable height jack
Back rest jack
4
Plug
1
Control box CA 40
Remote control
2
HB
Legs or plug falls
Back rest jack
Variable height jack
Plug
Legs or plug falls
Battery or plug falls
Remote contrôle or
infrared recever
1
2
Control box CO 41
40

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6.6. Remote control
Carry out a test cycle when the bed is empty to familiarise yourself with the bed functions
Lifting and lowering of back rest
Lifting and lowering of variable
height
Lifting and lowering of electric
folding
Simultaneous lifting and lowering
of back rest and folding
KEY IN VERTICAL
POSITION : THE FUNCTION
IS UNLOCKED
TURN THE KEY SLIGHTLY TO
THE RIGHT TO LOCK THE
FUNCTION
KEY TO LOCK A FUNCTION

17
6.6.1. Mobile carer control ACO (option)
Clipsable on the handrail of the foot board.
To activate the functions, press the « arrow » key (up or down) at the same time as the desired function.
To lock functions (raise back, variable height, leg rest, back tilt, forward tilt), press the « key » key and the key
for the function to be locked. Make the same thing to unlocked a function.
Back rest
Chair position
fauteuil
Leg rest
Locking indicator light
Back slant /
forward slant
Flatten
« Key » key to lock functions : press simultaneously with
the function to be locked
Variable height
The mobile carer control (ACO) connects to the connection
box

18
12°
6.7. Centralized Braking
6.8. Emergency declination
6.8.1. Positioning of the emergency declination
6.8.2. Resetting the box spring

19
7. OPERATION OF THE SLEEPING SURFACE
7.1. Back rest
7.1.1. Standard back rest
In the event of a power cut or failure, flatten the back rest as follows :
a) Disconnect the power supply.
b) Dismantle the headboard .
c) Stand at the head of the bed and take hold of the back rest handle with one hand. Push or lift to
compensate the pressure exerted by the patient and unhook the clip by the connecting rod with the
other hand. The back rest jack will then pivot downwards.
d) Put the headboard back.
Version with handle on the back rest Version without handle on the back rest
7.1.2. Back rest with translation
Same operation for flattening as the standard back rest.
The back rest with translation avoids to slip forward..
1
1
1
1
2
2
3
3
10 cm

20
1) Grasp the back rest with one hand.
2) With the other hand, activate one of the two handles on the back rest while
lowering.
If the handle is released, the back rest will stop moving.
.
To reactivate the cardiopulmonary resuscitation system of high-load beds
(270Kg), actuate the backrest electric actuator to its minimum position by pressing the
down button on the remote control.
7.1.3. Emergency release of the back rest (Cardio Pulmonary Resuscitation)
7.2. Leg rest
7.2.1. Leg rest with manual crank (C/)
To lift, lift the leg rest using the handle at the end.
To lower, relieve the leg rest slightly or to its maximum with the hand to release the catch, then lower the leg
rest.
7.2.2. Leg rest with electric folding (P/)
Memory folding: This function keeps a position of the tibia section horizontal when the jack is activated
upwards. To use this function, the 1st crank catch must be engaged when the leg rest is flat.
Folding without memory : the end of the tibia section stays in contact with the bed base.
8. INSTALLATION OF ACCESSORIES
8.1. Boards
➢Installing a bed board :
Release handles
O
K