Medicatlantic XXL User manual

2015_10_15 580040 Anglais
4 Le Pas du Château
85670 SAINT PAUL MONT PENIT
TEL : [phone]
FAX : [phone]
Email : [e-mail]
Site Internet : http://www.winncare.fr
IXX3L08/11-120/140
IXL4L08/11-120/140
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XX XL L D DI IV VI IS SY YS S
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1. TRANSPORT AND STORAGE.............................................................................................................. 3
2. BED ENVIRONMENT CONDITIONS .................................................................................................... 3
3. GENERAL USE......................................................................................................................................... 3
3.1. Precautions for use ................................................................................................................................ 3
3.2. First use..................................................................................................................................................... 5
3.3. Use .............................................................................................................................................................. 6
3.3.1. Easy Move boards............................................................................................................................... 6
3.3.2. Metal side rails..................................................................................................................................... 7
3.3.3. Wooden barriers.................................................................................................................................. 8
3.3.4. Angled lifting pole and IV stand...................................................................................................... 8
3.3.5. Separate braking................................................................................................................................. 9
3.3.6. Remote control .................................................................................................................................... 9
3.3.7. Leg rest................................................................................................................................................ 10
3.4. Technical characteristics.................................................................................................................... 10
3.4.1. Electrical data..................................................................................................................................... 10
3.4.2. Equipotentiality.................................................................................................................................. 12
3.5. Putting the back rest flat..................................................................................................................... 13
If the bed is fitted with an emergency release for the back rest (Cardio Pulmonary
Resuscitation).................................................................................................................................................. 13
4. MAINTENANCE...................................................................................................................................... 14
4.1. Instructions for dismantling the motors......................................................................................... 14
4.2. Maintenance ........................................................................................................................................... 14
4.3. Cleaning and disinfection................................................................................................................... 17
4.4. Warranties............................................................................................................................................... 19
4.5. Identification........................................................................................................................................... 19
5. CONDITIONS FOR SCRAPPING........................................................................................................ 19
6. ASSEMBLING AND DISMANTLING .................................................................................................. 20
6.1. Assembling the bed XXL XPress...................................................................................................... 20
6.2. Assembling the bed XXL XPress...................................................................................................... 24
6.3. Dismantling the bed XXL and XXL XPress..................................................................................... 25
6.4. Fold the base of the XXL XPress ...................................................................................................... 26
7. BED BOARDS – 120/140/160cm WIDTH - COMPATIBLE............................................................ 27
8. COMPATIBLE ACCESSORIES........................................................................................................... 28
9. SPECIFIC USE........................................................................................................................................ 30
9.1. Purpose of bed....................................................................................................................................... 30
9.2. General description.............................................................................................................................. 30
9.3. Specific precautions for use.............................................................................................................. 30
9.4. Electrical connection diagram........................................................................................................... 30
9.5. Specific technical data......................................................................................................................... 31
9.5.1. Noise..................................................................................................................................................... 31
9.5.2. Weight .................................................................................................................................................. 31
9.5.3. Dimensional........................................................................................................................................ 31

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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 MEDICATLANTIC medical bed equipped with its accessories, and we thank you for
your custom.
Our beds and their accessories are designed and manufactured in compliance with the essential requirements
of the European Directive 93/42/EEC and 2007/47/EEC.
They are tested in conformity with standard EN 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 MEDICATLANTIC 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, on a pallet, 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,
stored and used at a room temperature of between -10°C and +50°C,
and relative humidity of between 30% and 75%.
Atmospheric pressure between 700hPa and 1060hPa
3. GENERAL USE
3.1. Precautions for 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.
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 user and staff must be trained and aware of the risks associated with using
the bed, and children, confused or disorientated persons must not be allowed
on it.
Observe the specified
environmental conditions

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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 assemble different types of medical devices, you must conduct a risk analysis and make the CE
declaration.
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).
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 of 230 V.
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. MEDICATLANTIC prohibits the
establishment of two beds in a room or in a too close environment as infrared remote command the two beds
together.
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.
Moreover, the telephone number of the company to be contacted for any repairs is given in this document.
When using side rails, the distance between the top of the rail and the uncompressed top surface of the
mattress should be at least 22 cm.
For greater safety, the side rails can be adapted (see accessories).
To assist patient mobility, it is possible to fit a Mobility Aid System (S.A.M.).

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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)
- Users must be trained in how to use the equipment.
Inform the patient and his visitors of the safety instructions to be observed.
The cleaning instructions recommended must be complied with.
Only use original parts and accessories supplied by MEDICATLANTIC 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, use outdoors, moving the bed on a slope that is steeper than 10°, etc.
3.2. First use
Remove the packaging protective devices, adhesive tape, packing straps and holding clamps (see
unpacking instructions on the pallet).
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.
 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 and the remote control lead are positioned correctly to prevent any
risks of getting caught between the moving parts of the bed.

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Assemble the highest board on the head side.
3.3. Use
3.3.1. Easy Move boards
 Installing an Easy Move bed board :
 Removing an Easy Move bed board :
1 to 2 cm
1
1 to 2 cm
2
3

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If the side rail is poorly positioned, safety of the patient may be endangered or a
malfunctioning may occur. The side rails must not be used when the patient is a child (under
12) or if s/he is too small (≤146 cm).
Check that the side rail is locked by trying to fold it without using the release pin.
There must be at least 220 mm between the top of the side rail and uncompressed mattress
surface.
3.3.2. Metal side rails
To positionning the side rail.
1
2
1Insert amount of the side rail in the grip jaw on the head side of the bed.
2Tighten the Rondo screws of the grip jaws on the bed base.
To remove the side rail, in reverse operation 2and operation 1by pulling the release pin on the grip jaw of
the head side.
To lower the side rail.
To raise the side rail.
Head side
Feet side
Feet side
Head side

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Check that the high guide engage in the
right direction in the low guide.
3.3.3. Wooden barriers
See the attached instructions for fitting the wooden side rail.
To raise the side rail.
 Raise the top side rail with both hands until it locks.
 Check that it is properly slot in.
To lower the side rail.
 Raise the top side rail with one hand.
 Press on the unlocking button with the other hand.
 Support the rail as it lowers.
 Repeat steps to for the other side.
3.3.4. Angled lifting pole and IV stand
The lifting pole is intended to help the patient lift him/herself up and change position in the bed. It is not
meant to help with transferring.

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KEY IN VERTICAL
POSITION: THE FUNCTION
IS UNLOCKED
TURN THE KEY SLIGHTLY TO THE
RIGHT TO LOCK THE FUNCTION
Key to lock a function
3.3.5. Separate braking
Check that the wheels are locked by trying to move the bed. If this is not done, the patient or another person
who leans on the bed may fall.
3.3.6. 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

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Maximum operating time:
Read
the
recommendations
on
the
electrical
label on
the
bed.
3.3.7. Leg rest
Manual crank version (11):
To lift, lift the leg rest using the wire 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.
Version with electric folding (08):
Memory folding: This function keeps a position of the tibia section horizontal when the jack is activated
upwards. To use this function, the 1
st
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.
3.4. Technical characteristics
3.4.1. Electrical data
TYPE PROTECTION
INDEX VOLTAGE FREQUENCY
LINAK jack
LA27 / LA24 / LA34 IP 66 24V DC -
Supply box
CB6 / CB16 IP 66 230 V AC 50 HZ
Connection box
MJB IP 66 24V DC -
Operator’s side control console
ACC IP 66 24V DC -
Operator’s mobile control
console
ACO IP 66 24V DC -
Wired control
HB72 / HB74 IP 66 24V DC -
Lockable wired control
HL72 / HL74 IP 54 24V DC -
Flexible arm control
FPP IP 66 24V DC -
Battery
BA1812- IP 66 24V DC -
Infrared control
HB21 IP 21 3V DC -
Essential performances
The bed will not move automatically when subject to electromagnetic disturbances within the limit of the
values indicated below.
Class II (double insulation) Bed code
Voltage
Current type
Frequency
Operating time
Absorbed power
Protection level against
liquid penetration
Protection level against electric
shocks (type B)

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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
Harmonic emissions
EN 61000-3-2 Class A
Voltage fluctuations / Flicker
EN 61000-3-3 Applicable
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.
[ ]
RF emissions
CISPR 14-1 Compliant 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 Electromagnetic environment - Guide L
Electrostatic discharge
EN 61000-4-2 ±6 kV contact
±8 kV air
±6 kV contact
±8 kV air Floors should be wood, concrete, or ceramic tile. If floors are covered with
synthetic material, the relative humidity should be at least 30%.
Electrical fast transients
EN 61000-4-4 ±2 kV for feeders
±1 kV for input/output lines
±2 kV for feeders
±1 kV for input/output lines
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
Surges
EN 61000-4-5 Differential mode ±1 kV
Common mode ±2 kV
Differential mode ±1 kV
/
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations
EN 61000-4-11
•<5% UT- for 10 ms
•40% UT- for 100 ms
•70% UT- for 500 ms
•<5% UT- for 5 s
•<5% UT– for 10 ms
•40% UT - for 100 ms
•70% UT- for 500 ms
•<5% UT- for 5 s
The quality of the main power supply must be the same as for a typical
commercial or hospital environment.
If the user of the medical bed (see references in contents) wants to be
able to continue to use the bed during interruptions in the main power
supply, it is recommended that the bed be powered by a converter or
battery.
Power frequency
magnetic field
(50/60 Hz)
3 A/m 3 A/m Power frequency magnetic fields should be at levels characteristic of a
location in a typical commercial or hospital environment.
NB: UTis the nominal value of power voltage applied during the test.
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 Electromagnetic environment - Guide
Portable and mobile RF communications equipment should be used no closer to the medical
bed (see references in contents), including leads, than the recommended separation
distance, calculated using equations applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6 3 Vrms 150 kHz to 80 MHz 3 V
Pd 17,1=
Radiated RF
EN 61000-4-3 3 V/m 80 MHz to 2.5 GHz 3 V/m
80 to 800 MHz
Pd 17,1=
80 MHz to 800 MHz
Pd 33,2=
800 MHz to 2.5 GHz
2 to 2.5 GHz
10 V/m where
P
is the maximum output power rating of the transmitter in watts (W) according to

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800 MHz to
2 GHz the transmitter manufacturer and dthe recommended separation distance in meters (m).
The field strengths transmitted by fixed RF transmitters, determined by an electromagnetic
measurement of the site a, must be less than the conformity level in each range of
frequencies.
Disturbances can occur near devices marked with this symbol:
Note 1 At 80 MHz and 800 MHz, the upper frequency range applies.
Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
A Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast
and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site
survey should be considered. If the measured field strength in the location in which the medical bed (see references in contents) is used exceeds the applicable RF
compliance level above, the normal operation of the bed must be checked. If abnormal performance is observed, additional measures may be necessary, such as re-
orienting or relocating the medical bed.
B Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distances between portable and mobile RF communications equipment and the medical bed (see references in contents)
The medical bed (see references in contents) is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The user of the bed can help
prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the bed as recommended below,
according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Rated maximum power of transmitter
W
Pd 17,1= Pd 17,1=
Pd 33,2=
0.01 0.12 / 0.116 0.12 / 0.116 0.23 / 0.233
0.1 0.37 / 0.316 0.37 / 0.366 0.74 / 0.736
1 1.17 / 1.16 1.17 / 1.16 2.33 / 2.33
10 3.70 / 3.66 3.70 / 3.66 7.37 / 7.36
100 11.70 / 11.6 11.70 / 11.6 23.30 / 23.3
For transmitters rated at a maximum output power not listed above, the recommended separation distance din meters (m) can be estimated using the equation applicable to the frequency of
the transmitter, where Pis the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
3.4.2. 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 the sides.
Label 
Equipotentiality 

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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.
3.5. Putting the back rest flat
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
If the bed is fitted with an emergency release for the back rest (Cardio Pulmonary Resuscitation)
Release handles
2 1
3
1
2
3

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Disconnect the 230 volts connection before dismantling.
4. MAINTENANCE
4.1. Instructions for dismantling the motors
•Dismantle when the bed is empty or in the side position.
•If dismantling in any other position, keep a firm hold of the moving parts to avoid any shearing.
•Unblock the safety clips 

, unplug the motor leads, and remove them from the securing seals.
•Put the motors back in place and put in the same direction as at the beginning.
4.2. Maintenance
Quality control of medical beds will be made by technical staff or trained biomedical and taking into account
the normal conditions of use specified in the user guide, on a bed with its specific security barriers.
The bed must be available to perform all quality control at least once a year, but also on special request and
corrective maintenance on the performance that could be affected by the intervention. However, to save time
this may be associated with preventive maintenance. In this case, it is not useful to make a further
examination of already controlled performance.
R ECOMMENDATIONS FOR PREVENTIVE MAINTENANCE :
Preventive maintenance should be carried out in accordance with our specifications and at least once a year
by the organisation or person who installed the bed.
Between two maintenance sessions and at least once a year, the following should be carried out:
- Verification that the electrical leads are connected all along the metal jambs to prevent shearing of these
leads when the variable height is being activated.
- Verification that all of the electrical leads and plugs are in good condition. Replacement if there is the
slightest alteration (wear, shearing, damage, etc.).
- Verification of the external appearance (traces of damp and good overall condition of protective covers in
particular) and that the motors and jacks function properly.
- Verification that the bed is in good working order (test all functions).
- Verification that the frame, bed base and mechanical joints are all in good condition.
When maintenance is carried out at the patient’s home as part of a long-term contract, the installer must also:
- Check that the bed is properly installed (check to see that there hasn’t been any modification contrary to the
safety instructions made by the user since the bed’s installation).
- Remind the users of the safety instructions.
- All installation and preventive maintenance operations must be recorded. See table model below. This
record must be kept in a designated area throughout the bed’s lifetime.
Safety clip

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QUALITY INSPECTION OF MEDICAL BEDS
IDENTIFICATION OF MEDICAL BED ESTABLISHMENT
CATEGORY
TYPE MODEL TRADEMARK
SERIAL NO. SERVICE SITE
INVENTORY NO.
DATE OF MANUFACTURE
TEST DEVICES CHECKED AND CONFORMING WITH STANDARDS
Description Type/model Identification/serial no.
Mass continuity tester
Dielectrimeter
Fault current to patient
Qualitative aspects NA
(1) YES NO
VISUAL CHECKS
General condition
User’s manual available
Headboard and footboard present
Good overall condition (head and footboards, bed corners, protective
stops)
General cleanliness
Acceptable state of corrosion given the requirements of the user
department
Identification/label/serigraphy in good condition
Mechanical condition
Lifting pole in good condition (positioning and strap)
Mechanical leads in good condition
Sleeping surface in good condition (bed base)
Boards lock and tighten well (head and footboards)
Chest rest functions properly
Leg rest functions properly
Half-seated position functions properly
Manual leg rest functions properly
TR/RTR positions function properly
Bed base extension functions properly
Castors function properly (pivoting, rolling, etc.) including the steering
castor where applicable.
Bed immobilises properly (castor brakes, etc.)
Verification of tightenings, diverse nuts and bolts, pins, pivot, IV stand

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Qualitative aspects NA
(1) YES NO
Verification that welds are in good condition
Absence of sound disturbances (squeaking, lubrications)
Electrics, hydraulics and pneumatics
Electrical leads, plugs and connectors are in good condition (not
sheared, not caught, etc.)
Electrical parts in good condition (leads, motors, boxes, etc.)
Hydraulic and pneumatic parts in good condition (pumps, compressors,
jacks, dampers, etc.)
Remote controls, displays and lights in good condition
Bed-specific side rails NA
(1) YES NO
The rails in place and specific to the bed and/or comply with the
manufacturer’s specifications
Properly positioned and secured
Side rail locking functions properly in raised position
Check that the height measured from the top of the barrier to the
uncompressed mattress surface, excluding therapeutic mattresses, is
more than or equal to 220 mm (complies with the standard in force) 2
Safety check NA
(1) YES NO
Locking of operational functions
Inactivation of variable height control pedals
Check that the headboard extracts or
retracts properly in an emergencyCardio Pulmonary Resuscitation (CPR)
emergency flattening of the
back rest Check that the chest rest emergency
flattening function works properly
Withstands jack load well
Visual and sound alarms in good working order
Quantitative aspects NA
(1) YES NO
Bed functions properly using the battery
Check the scale of movements
Maximum angle when propped = Maximum angle of specifications
claimed by the manufacturer (±2°)
Maximum height = Maximum height of specifications claimed by the
manufacturer (±20 mm)
Minimum height = Minimum height of specifications claimed by the
manufacturer (±20 mm)
Electrical safety
Electrical safety inspection (Values comply with EN 60601-1)

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Comments
Conclusion YES NO
Operational (is the safety of the patient, carers and technical staff at risk?)
Plan of action (see comments) 3
Recommended date of next quality inspection
OPERATOR
NAME Establishment
DATE Signature
1 Not Applicable
2 If the height measured does not comply with the standard, the health manager responsible for correct
application must be informed. Failure to comply is not a criterion for a non-operational status.
3 The manager decides on the actions to take and which people to contact depending on the results of the
quality inspection and the comments made.
4.3. Cleaning and disinfection
High-pressure cleaning is forbidden.
Unplug the mains lead.
Check that all the electrical parts are connected together. All the sockets of the supply box must be used,
otherwise its watertightness is not guaranteed.
Clean the electric covers of the jacks and wired control straightaway if any bodily fluids, particularly urine,
have sprayed on to them.
The medical bed is a non-critical appliance requiring “Low Level” disinfection.
We draw your attention to the fact that the recommendations below are drawn up according to the rules of
good practice but are not a protocol. Contact the hospital hygiene department.
AIM
To recondition the bed and prevent the transmission of germs from one patient to another.
To eliminate all organic soiling by:
- physical action (cleaning)
- chemical action (disinfection)
INDICATION
Physical and bacteriological cleanliness of the bed and its accessories

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EQUIPMENT
Microfiber wipes
Detergent or Detergent-Disinfectant (Surface DD with CE mark) and surface Disinfectant (Chlorine
substances, alcohol base < 30%)
Attention: DD products and Javel water must not be used undiluted. A remanence time must be applied
according to the disinfectant manufacturer’s instructions (the drying time without human presence is often the
same as the remanence time)
SANIVAP steam appliance with accessories
TECHNICAL
-Daily maintenance with a surface DD product in one operation.
-Maintenance when the patient leaves, or periodically, by the process known as Bio cleaning
observing the 3 operations:
oCleaning is done by means of a cloth soaked in a surface detergent or Detergent-Disinfectant
(DD) solution
oRinsing is done with cloth rinsed in clean water
oDisinfection is done by means of a cloth soaked in a surface disinfectant solution.
-Specific maintenance by specialist contractors after removal of the bed from the establishment:
oDispose of the packaging after decontamination of the inside by spraying with a Detergent-
Disinfectant solution
oBio cleaning operation, or,
oSteam cleaning (accessory with microfiber band) of the flat surfaces and the base slats.
Change the washing mops regularly to prevent water accumulating. Clean the parts that are
difficult to access with a steam nozzle (wheels, hinges after opening, corners, etc.). For tubes,
use the steam nozzle with a microfiber cloth. Never direct the nozzles onto electrical boxes or
actuators.
oDry hinges with compressed air
oAttention: Disinfect jacks, electrical boxes and remote controls with a microfiber cloth soaked
in disinfectant.
Do not rinse or wipe.
Check the operation of all the bed functions
Repair if necessary
Pack in thermoplastic film
Attention:
-In the event of additional precautions (Contact precautions, Droplets or Air), apply the measures
recommended by the hospital hygiene department
-The use of a Javel water solution of more than 5000ppm (0.5% of active chlorine) should be justified
by a microbiological risk and only applied for the required time (Risk of ageing of some materials,
especially their colour).
-The concentration of alcohol-based surface disinfectant solutions should be less than 30%.
Note: The use of the terminal disinfection process is compatible with the medical bed and its accessories.
Product for external use. Do not swallow, keep away from heat sources and
avoid contact with eyes.

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Refer to user’s manual
Refer to user’s manual
4.4. Warranties
All of our products carry a warranty against any manufacturing defect, provided the normal conditions
for use and maintenance are complied with.
Labour costs due to changes in structures or parts under warranty are not taken into account.
Please refer to the standard terms of sale for the specific terms of warranty for each product.
Every time you contact us for possible maintenance, you must quote us the information on the bed
identification label and on the electric parts if these are concerned.
Original parts shall be supplied for replacement, within the term of warranty, by our customer sales
network determining the beginning of the term of warranty.
Defective parts must be returned to ensure proper application of this warranty and also to avoid any
invoicing.
4.5. Identification
5. CONDITIONS FOR SCRAPPING
The product must be scrapped if the main requirements are no longer met, particularly when the product no
longer has its original characteristics and has not been subject to corrective action during the manufacturing
process.
Measures should therefore be taken to ensure that the bed is no longer used for the purpose it was originally
intended.
Manufacturer
CE marking
Manufacturer's address
Product identification
Serial number
and date of
manufacture
Safe operational load
Maximum patient
weight
xxx kg
yyy kg