Medisa Majestic II Parts list manual

REV.09/2018
USER’S MANUAL AND TECHNICAL DESCRIPTION
MAJESTIC II BED

Page 2
Dear Customer:
With our beds, you have chosen a product of our company made with the highest
demands in terms of quality in its components, ensuring the fulfilment of all
requirements throughout its useful life. Thanks to the careful selection of materials, the
most modern production technology and precise work of our employees, our products
and services are focused on ensuring the requirements of our customers and achieve
their full satisfaction by providing safe, reliable and consistent functionality.
We are aware that requirements in market are increasing, so Medical Iberica brings a
broad knowledge in socio-sanitary equipment and furniture offering a wide range of
products, which together with the values of environmental and ethical and professional
awareness, give optimum results

User manual
MAJESTIC II bed
Page 3
Index
1) Introduction. .............................................................................................................................................................................................6
a. Delivery. ............................................................................................................................................................................7
2) Safety instructions................................................................................................................................................................................7
3) Environment conditions. .....................................................................................................................................................................8
4) Technical parameters...........................................................................................................................................................................9
a. Power supply ...............................................................................................................................................................11
b. Important information about EMC......................................................................................................................12
5) Specifications of the variant..........................................................................................................................................................17
6) Bed description.....................................................................................................................................................................................18
7) Installation..............................................................................................................................................................................................19
a. Connection to power supply. ................................................................................................................................20
b. Potentials connection..............................................................................................................................................20
c. Battery charge.............................................................................................................................................................20
8) Bed adjustment....................................................................................................................................................................................21
a. Standard movements...............................................................................................................................................22
i. Backrest section adjustment...........................................................................................................22
ii. Upper leg rest section adjustment................................................................................................22
iii. Lower leg rest section adjustment...............................................................................................23
iv. Synchronized adjustment for backrest and leg rest (auto-contour)..............................23
v. Height adjustment ...............................................................................................................................23
vi. Programmed positions configuration...........................................................................................24
b. Nurse panel...................................................................................................................................................................26
i. Nurse panel description .....................................................................................................................26
ii. Locking of movements .......................................................................................................................27
c. Patient handset..........................................................................................................................................................28
d. Embedded controls on side rails..........................................................................................................................28
9) CPR backrest release.....................................................................................................................................................................28
10) Automatic auto-regression backrest system......................................................................................................................29
11) Leg rest................................................................................................................................................................................................29
12) Headboard and footboard. ..........................................................................................................................................................29
13) Side rails..............................................................................................................................................................................................30
a. Split side rails adjustment......................................................................................................................................31
14) Central brake.....................................................................................................................................................................................32
15) Bed extension...................................................................................................................................................................................33
16) Accessories. .......................................................................................................................................................................................34
a. IV pole and lifting pole.............................................................................................................................................34
b. Small accessories holder.........................................................................................................................................35
c. Other accessories.......................................................................................................................................................36
17) Sections cover extraction............................................................................................................................................................36
18) Cleaning and disinfection............................................................................................................................................................36
a. Basic instructions before cleaning procedures.............................................................................................36
b. Cleaning procedures. ................................................................................................................................................37
c. Cleaning recommendations...................................................................................................................................38
19) Maintenance......................................................................................................................................................................................38
a. Safety notes.................................................................................................................................................................38
b. Maintenance schedule.............................................................................................................................................39
c. Technical checking ....................................................................................................................................................40
i. Visual inspection...................................................................................................................................40
ii. Functional checking of side rails....................................................................................................41
iii. Functional checking of brakes ........................................................................................................42
iv. Functional checking of motors........................................................................................................42
v. Power supply cable ..............................................................................................................................42
vi. Cables.........................................................................................................................................................42
vii. Mechanical checking............................................................................................................................42
viii. Measures according to DIN en62353 ..........................................................................................43
20) Problems and solutions................................................................................................................................................................43
21) Storage. ...............................................................................................................................................................................................44
22) Use life and environmental protection..................................................................................................................................45
23) Warranty and service.....................................................................................................................................................................46
24) Symbols ...............................................................................................................................................................................................47
25) Finished product certificate. ......................................................................................................................................................48
26) Labels with lot numbers...............................................................................................................................................................49
27) Contact.................................................................................................................................................................................................49
28) Declaration of Conformity...........................................................................................................................................................50

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List of figures
Figure N. 1-
Electric connections ....................................................................................................................................11
Figure N. 2-
MAJESTIC II bed..............................................................................................................................................18
Figure N. 3-
Equipotential connector ............................................................................................................................20
Figure N. 4-
Trendelemburg and reverse Trendelemburg positions................................................................25
Figure N. 5-
Nurse panel.....................................................................................................................................................26
Figure N. 6-
Patient handset. ..........................................................................................................................................27
Figure N. 7
- Controls embedded on side rails. ...........................................................................................................28
Figure N. 8 –
CPR backrest release.................................................................................................................................28
Figure N. 9
- Feet section adjustment ...........................................................................................................................29
Figure N. 10
- Unblocking lever for headboard and footboard............................................................................30
Figure N. 11
- Insert spikes into structures.................................................................................................................30
Figure N. 12
- Headboard / footboard fixing...............................................................................................................30
Figure N. 13-
Split folding side rails. .............................................................................................................................31
Figure N. 14-
Central brake...............................................................................................................................................32
Figure N. 15-
Bed extension system ............................................................................................................................33
Figure N. 17-
Bed extension.............................................................................................................................................33
Figure N. 18 and 18b –
IV and lifting poles sockets...............................................................................................35
Figure N. 19 -
Small accessories socket.......................................................................................................................35
Figures N. 20 –
Bottle holder support...........................................................................................................................36
Figure N. 21-
Functional checking of side rails.........................................................................................................41
Figure N. 22-
Equipotential connection diagram. ....................................................................................................43

User manual
MAJESTIC II bed
Page 5
Tables list
Table N. 1
- Technical parameters for Majestic II..............................................................................................................................................9
Table N. 2
- Bed dimensions ....................................................................................................................................................................................10
Table N. 3
- Cables and electric components list ...........................................................................................................................................10
Table N. 4
- Guide and manufacturer declaration – electromagnetic emissions. ............................................................................13
Table N. 5
- Guide and manufacturer declaration – electromagnetic immunity 1 ..........................................................................14
Table N. 6
- Guide and manufacturer declaration – electromagnetic immunity - 2 ...................15
Table N. 7
- Recommended separation distances between portable and mobile RF communications equipment..........16
Table N. 8-
Battery signal.......................................................................................................................................................................................21
Table N. 9-
Accessories list ....................................................................................................................................................................................34
Table N. 10-
Recommended mattresses ..........................................................................................................................................................34
Table N. 11
- Spanish MOH recommended disinfectants...........................................................................................................................37
Table N. 12
- Cleaning recommendations.........................................................................................................................................................38
Table N. 13
- Maintenance schedule...................................................................................................................................................................40
Table N. 14
- Dimensions for functional checking of side rails...............................................................................................................41
Table N. 15
- Problems and solutions .................................................................................................................................................................44

Page 6
1)Introduction.
Bed model MAJESTIC II has been designed for adult patients (above 12 years or above
146 cm height) for standard hospital wards and long stay units wards (application
environment 2 and 3). Nevertheless, it can be used in ICU wards, but that decision is
under Hospital responsibility (application environment 1)
The articulated bed model MAJESTIC II is not designed for patients with
mind illness diseases or to be used in operating theatres.
Any other use of the Medisa bed that is not the planned one, excludes the Company for
any liability.
MAJESTIC II bed is classified as Class I medical device according to RD
1591/2009 (7.9.2.2)
This product respects UE Directive
2007/47/CEE
, related to medical devices,
and also UE Directive
2004/108/CEE,
regarding electromagnetic
compatibility.
Our Managing systems are according to
ISO 9001:2008, EN ISO
13485:2012
e
ISO 14001:2004
According the requirements of rule EN 60601-2-38, an electric hospital bed
must allow achieving Trendelemburg position, even without power supply.
Due to this, MAJESTIC II bed is equipped with a battery. Otherwise, it does
not achieve the requirements of such rule and a Declaration of Conformity is
issued for the same
The standard configuration of MAJESTIC II allows Trendelemburg position,
so a Declaration of Conformity is issued according to EN 60601-2-38 rule.
Before using this bed, it is important to be familiarized with this
manual. All operations must be carried out as defined in this manual.
The manufactu
rer shall not be liable for any damage or jury caused by
the user´s failure to follow the instructions defined in this manual, as
regards the improper use of this bed, or by the use of it for other
purposes different from those it was designed.
Thus, it is very important that the user's manual is accessible to patient or user
along the whole life of the bed.

User manual
MAJESTIC II bed
Page 7
WARNING:
Medisa is not responsible of any harm, damage, injury or accident that may
occur due to misuse, carelessness or negligence.
Safety and product use instructions must be strictly followed
Medisa reserves the right to modify this manual due to product upgrades or
technical changes. The information provided in this manual may be slightly
different with respect to the basic design of the product.
a. Delivery
The bed is delivered fully assembled, except for its optional accessories, and headboard
and footboard. In this case, these components should be assembled before use
according to chapter
Headboard and footboard. On delivery note it must be stated that
the bed has been complete delivered.
Any failure or damage must be reported to the
carrier and Medisa (see Contact) before accepting the order.
When the bed is moved during loading and unloading, the brakes shall be unblocked
(see chapter
Central braking system) . Wheels have been designed for use in an indoor
space and for movement in smooth, clean and stable soils (tiled floors, linoleum,
gypsum, etc.) Wheels could be damaged if the bed is moved on steep, uneven or dirty
surfaces.
2) Safety instructions.
Before using this bed the staff must be familiarized with this user manual and the
operations described therein all operations must be carried out as defined in it.
RF communication equipment can affect electro medical devices.
Avoid the use of non-original or not approved by the manufacturer accessories,
since they can affect the electromagnetic performance.
During maintenance or cleaning in the space between base and mattress,
adjustment controls must be blocked in nurse panel to avoid accidents due to
an accidental activation of the pedals and the following unexpected movements.
In the event of any defect which may jeopardize the patient or user safety or which may
damage the bed or the building contents, remove the bed and do not use it until the
defect is corrected.
Before using the bed, connect the battery (check that it is connected to the power
supply at the delivery); battery duration will depend on workload and functioning cycles.
In order to ensure the correct operation of the bed, it must be operated only by those
who have been properly trained or those having enough experience.
The person responsible must inform the patient lying on the bed of its positioning
features, including the correct use of handset.
Before using the bed, test every function and check that it is in perfect conditions of
use. Check chapter Use conditions
This bed must only be used on clean, hard, flat surfaces.
Never exceed the maximum load capacity of the bed, even in brief periods.
When a patient is lying on the bed, the braking system must be locked (except for
transporting the bed); this will eliminate the risk of roll over and other possible
accidents when getting on and off the bed. If exceeding the maximum load capacity of
the bed is absolutely necessary, its sections must be adjusted to their lowest position.
The angle of the sections must be appropriate for the state of the patient.

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To avoid damage due to patient fall, it is recommended (except under medical
prescriptions) that the bed should be adjusted in its lowest positions and with brakes
actuated (except for transport) After activating brakes, check that the bed is properly
fixed and the wheels correctly braked
Select height according to patient needs. No other one is allowed to sit on the bed next
to the patient.
When adjusting the sections of bed, check that there is no risk for the patient, other
people or the accessories to be trapped.
In case that there are accessories fixed to the bed, check that they have enough room
to move together with the bed.
During Trendelemburg position, staff must pay attention to the distance between the
lifting pole (if it is used) or IV pole and the wall, and the objects placed in the bed or any
other environment, since there is a risk of collision or damages.
Unplug the power cable of the bed before carrying out cleaning or maintenance
activities.
Do not use the bed an environment where there is a risk of explosion or in the
presence of anaesthetics or other inflammable products
During maintenance, use only proper and original components. Medisa will not be
responsible of damages or injuries that may arise.
Use only mattresses and accessories from Medisa; in the contrary, a malfunction may
occur on the side rails adjustment, jeopardizing patient safety.
During transport, power supply cable must be hold in a plastic hook placed in one of
the bed ends or in other safe place to avoid cable entrapments that could damage it.
Do not push the bed over more than 2 cm height obstacles. Maximum angle of the floor
must not exceed 10º.
Power supply cable must be guided in a way that it won’t be rolled up in any
component. An electric shock may occur.
An inadequate handling of the power supply cable may injure any person that handles
it
The patient or user might be injured if:
-The bed rolls on an inappropriate floor.
- The maintenance activities for this bed are not carried out
according to the indicated instructions.
Damages and wear of mobile components should be checked unless once a month
In case of power failure, or electric tension were not enough, sections can be adjusted
through battery and with CPR backrest manual manoeuvre (check RCP backrest
release chapter).
Undercarriage must not be used as storage area. In case of placing an object in the
area under mattress structure, bed or objects could be damaged when height is
adjusted.
As the bed is not delivered sterilized, cleaning and disinfecting it is recommended
before using it for the first time, as well as before and after each usage.
Any major repair work must be carried out by qualified staff.
Use only the cleaning and disinfectant agents recommended in this manual.
3) Environment conditions
We recommend you to install the bed in a dry place, essentially, indoors.
The temperature varies between 10⁰Cand 40⁰C.
The relative humidity varies between 30% and 75%.
The atmospheric pressure varies between 70 kPa and 106 kPa.

User manual
MAJESTIC II bed
Page 9
If you find other conditions, contact us.
Bed has been designed for medical wards. So, electric installations of the
room must satisfy the requirements of the standard related to electric
conditions in special conditions (for example, a storm)
4) Technical parameters
Maximum safe working load of the bed is 250 kg. To calculate the maximum weight of the
patient, the maximum safe load will be subtracted 20 kg for the mattress and 45 kg for the
accessories when the bed is used in application environments 1 and 2. When used in an
application environment 3, the values are 20 kg for the mattress and 15 kg for accessories as
well as the weight carried by the accessories
Table N.1 - Technical Parameters of MAJESTIC II bed
Weight Specifications Variation
Net weight 136 Kg UNPACKED ±2 kg
Gross weight 164 Kg PACKED ±2 kg
Maximum safe working
load
250 Kg Patient weight ± 185 (
in
application environments
1
y 2)
Mattress weight ± 20kg
Accessories weight ±45kg
Patient weight ± 215 (
in
application environments
3)
Mattress weight ± 20kg
Accessories ±15kg
and
whatever is placed in the
accessories
±5 kg
NOTE: MAJESTIC II weight (standard) can
vary depending on accessories or installed
variation

Page 10
Bed dimensions
Table N. 2 -
Approximate measures of standard beds
Component/
element
Measures (cm) Specifications
Length Width
Mattress 208-214 94
±1 cm
Without packaging
Length without bed extension. Optional bed
extension : +15 cm length

Without bumpers or side rails
Patient mattress 200 85
±1 cm
Length can vary depending on bed extension
Width does not change
Maximum measures of
the bed 215-230 94
Without packaging
Maximum overall measures
Width with side rails
Length without and with optional bed extension.
Height with the mattress in his lowest and highest
Maximum measures
when packaged
220 108
Packaged
Height 73 cm

Without accessories
Volume: 2,40 m3
NOTE: Packaging measures can vary depending on accessories and variants
Steel side rail 147 30 3
Not folded
Without packaging
Height from floor
Table N. 3
-
List of cables and electric components
Nurse panel Timotion TNP6-223-0A6-31
Patient handset Timotion TH12-B422-20AA6-101
Backrest motor Timotion
TA7-2J-090312-21122-
21211-MT
Legrest motor Timotion
TA7-2J-090312-21122-
21211-MT
Height motor (column) Timotion TL8-5A-300300-20123-0
Power supply Timotion TC1-4A42-A240-61
Battery Timotion TBB2-211-2
Power cable Timotion
TYC-2-11120-0200-02101-
0000-02101-0000-2

User manual
MAJESTIC II bed
Page 11
Figure N. 1 –
Electric connections
a) Power supply.
The power supply is covered by a highly resistant plastic housing. Its main function is to
convert the signals it receives from the patient's command and from the supervisor.
Everything is controlled analogically. Each actuator is controlled separately by the
corresponding handset, which can be blocked by the nurse panel. The power supply is
designed to connect to networks of 100V / 120 / 220-240V and alternating current of
50-60 Hz, so it allows its use in different countries without any problem (specify when
ordering).
The design of the power supply includes the following security systems:
•
EOP safety system
(electrical protection against overloads): protects the actuator
against overloads by disconnecting the current in case of overload during operation.
•
EAS safety system
(electrical protection against short circuits or power cut): the
power supply is designed so that the terminals short circuit the actuator when the
actuator is not in operation. This property gives the actuator a greater self-locking
capacity. It also has a safety system that cuts off the current and stops the actuators
when the consumption reaches the limit value.
•
Class 1
protective earth cable to avoid the derivation of both the patient and the
users who are in contact with the bed.
It allows to connect different optional accessories, such as a 24V (1.2 Ah) external
battery for the operation of the bed without connection to the network

Page 12
NOTE:
Upon request, the beds can be delivered with electric options depending on the country
standards (different voltage, type of plugs, etc. )
Power supply should be changed periodically to ensure a perfect state for
use of the Equipment.
Due to electric supply, the most sensitive components could be affected
by electromagnetic fields. To avoid the risk of unwanted effects, the bed
has been manufactured under normative EN 60601-1-1. It must be used
according to this manual to avoid those problems.
b) Important information about electromagnetic compatibility (EMC)
Important information about Electromagnetic Compatibility
(EMC)
Due to the growing number of existing electronic devices, such as computers and mobile
phones, it is possible that medical electrical equipment is susceptible to electromagnetic
interference received from other devices. Electromagnetic interference may cause the
medical equipment to malfunction and create a potentially unsafe situation.
Medical devices should also not interfere with other devices.
In order to regulate the requirements for EMC (Electromagnetic Compatibility) and to avoid
unsafe product situations, the IEC60601-1-
2 standard has been implemented. This
standard defines the levels of immunity to electromagnetic interfe
rence, as well as the
maximum levels of electromagnetic emissions for electro medical equipment.
Medical electrical equipment manufactured by Medical Ibérica complies
with this
IEC60601-1-2 standard for both immunity and emissions.
However, it is necessary to take special precautions:
The use of accessories and cables not specified by Medical Ibérica, with the exception of
cables sold by Medical
Ibérica as spare parts for internal components, could cause an
increase in emissions or a reduction in the immunity of the device.
• A medical device must not be used together or on top of other equipment. In the event
that it is necessary to use it under these circumstances, the medical electromedical
equipment must be controlled to verify its normal operation in the configuration in which it
will be used.
• The MAJESTIC II
electromedical equipment needs special precautions regarding
electromagnetic compatibility (EMC) and needs to be installed and used according to the
information contained in this documentation.
The MAJESTIC II
electromedical equipment may receive interference from other
equipment, even if this other equipment complies with the emission requirements

User manual
MAJESTIC II bed
Page 13
Table N. 4 – Guide and manufacturer declaration – electromagnetic emissions
Electromanetic emissions
The MAJESTIC II device it is intended for use in an electromagnetic environment specified below. The client
or the user of the MAJESTIC II bed should ensure that it is used in said environment
Emissions Test
Conformity
Electromagnetic environment – Guide
RF Emissions
CISPR 11 Group 1
The MAJESTIC II uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not likely to
cause any interference in nearby electronic
equipment.
RF Emissions
CISPR 11 Class A Th
e MAJESTIC II is suitable for use in all
establishments other than domestic
establishments, and can be used in
domestic establishments and those directly
connected to the public low-voltage power
supply network that feeds buildings used
for domestic purpos
es, provided that The
following warning is considered:
Harmonics emissions
IEC 6100-3-2 Class A
Tension fluctuations/
Flickers emissions
IEC 61000-3-3
Complies

Page 14
Table N.5 – Guide and manufacturer declaration – electromagnetic immunity
Electromagnetic immunity
The MAJESTIC II device it is intended for use in an electromagnetic environment specified below. The client
or the user of the MAJESTIC II bed should ensure that it is used in said environment
Immunity Test
Test according
Rule IEC 60601
Conformity Level
Electromagnetic immunity -
guide
Electrostatic
discharge (DES)
IEC 61000-4-2
±6 kV by contact
±8 kV by air
±6 kV by contact
±8 kV by air
The floor should be made of wood,
concrete or ceramic tile. If the floors
are covered with synthetic material,
the relative humidity should be at
least 30%
Transients / Rapid
bursts
IEC 61000-4-4
± 2 kV for power
supply lines
± 1 kV for input /
output lines
± 2 kV for power
supply lines
±1 kV
for input /
output lines
The quality of the power network
should be that of a typical commercial
environment or that of a hospital.
Shock waves
IEC 61000-4-5
±1 kV line to line
±2 kV line to line
±1 kV línea a línea
±2 kV línea a tierra
The quality of the power network
should be that of a typical commercial
environment or that of a hospital.
Voltage drops,
interruptions and
voltage variations in
the input lines of
the power supply.
IEC 61000-4-11
<5% Ut
( >95% dip in Ut)
for 0,5 cycles
40% Ut
(60% dip en Ut)
for 5 cycles
70% Ut
(30% dip en Ut)
for 25 cycles
>5% Ut
(>95% dip en Ut)
for 5 seconds
<5% Ut
( >95% dip in Ut)
for 0,5 cycles
40% Ut
(60% dip en Ut)
For 5 cycles
70% Ut
(30% dip en Ut)
For 25 cycles
>5% Ut
(>95% dip en Ut)
For 5 seconds
The quality of the power network
should be that of a typical commercial
environment or that of a hospital. If
the user of the MAJESTIC II requires
continuous operation during power
interruptions, it is recommended that
the MAJESTIC II be powered by an
uninterruptible power supply or a
battery
Magnetic field at
network frequency
(50/60 Hz)
IEC 61000-4-8
3 A/m 3 A/m
The quality of the power network
should be that of a typical commercial
environment or that of a hospital
Note: Utis the alternating current supply voltage before the application of the test level

User manual
MAJESTIC II bed
Page 15
Table N. 6 – Guide and manufacturer declaration – electromagnetic immunity
Guide and manufacturer declaration – electromagnetic immunity
The MAJESTIC II device it is intended for use in an electromagnetic environment specified below. The client
or the user of the MAJESTIC II bed should ensure that it is used in said environment
Immunity Test
Test according
Rule IEC 60601
Conformity Level
Electromagnetic immunity - guide
RF conducted
IEC 61000-4-6
RF radiated
IEC 61000-4-3
3 Vrms
150 kHz a 80 MHz
3 v/m
80 MHz a 2,5 GHz
3 Vrms
3 V/m
80 MHz a 2,5 GHz
(due to laboratory
limitation)
Mobile and portable RF communications
equipment should not be used closer to
any part of the MAJESTIC II, including
cables, than the recommended separation
distance at the transmitter frequency.
Recommended separation distance
d = 1,17 √ P 150 kHz to 80 MHz
d =1,17√ P 80 MHz to 800 MHz
d=2,33√ P 800 MHz to 2,5 GHz
Where P is the maximum assigned output
power of the transmitter and d is the
re
commended separation distance in
meters (m).
The field strengths from the fixed RF
transmitter, as determined by an
electromagnetic study of the site, should
be less than the compliance level in each
frequency range.
Interference can occur in the vicinity of the
equipment marked with the following
symbol:
NOTE 1: A 80 MHz y 800 MHz, highest frequency level is applied
NOTE 2: These guidelines cannot be applied in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
aThe field strengths of fixed transmitters, such as base stations for radio telephones (cellular / cordless) and land mobile
radios, amateur broadcasters, AM and FM radio broadcasts and TV emitters cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, a study of the electromagnetic site
should be considered. If the measurement of the field strength at the location where the MAJESTIC II is used exceeds
the applicable prior RF compliance level, the MAJESTIC II should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as reorientation or relocation of the MAJESTIC II.
bOver the frequency range of 150 kHz to 80 MHz, the field strength should be less than 3 V.

Page 16
Table N. 7 – Recommended separation distances between portable and mobile RF
communications equipment
Recommended separation distances between portable and mobile RF
communications equipment and MAJESTIC II bed
The MAJESTIC II bed is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or user of the MAJESTIC II can help prevent electromagnetic
interference by maintaining a minimum distance between the portable and mobile RF communications
equipment (transmitters) and the MAJESTIC II as recommended below, in accordance with the maximum
power output of the communications equipment.
Maximum assigned
output power of the
transmitter
W
Separation distance according to the frequency of the transmitter
m
150 kHz to 80 MHz
d = 1,17 √P
80 MHz to 800 MHz
d =1,17√P
800 MHz to 1 GHz
d=2,33√P
0,01 0,12 0,12 0,23
0,1 0,38 0,38 0,74
1 1,2 1,2 2,3
10 3,8 3,8 7,3
100 12 12 23
For assigned transmitters with a maximum output power not listed above, the recommended separation distance d in
meters (m) can be determined using the equation applicable to the transmitter frequency, where P is the maximum rated
output power in watts (W) according to the manufacturer of the transmitter.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the highest frequency range applies.
NOTE 2 These guidelines cannot be applied in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
c) Electric actuators or motors.
The MAJESTIC II models have two column actuators to perform the movements of:
• Bed elevation,
• Trendelemburg and antitrendelemburg
And two linear actuators to perform the movements of backrest adjustment and leg
section
Linear actuators are very compact, have long life and great performance. The shaft and
plunger are made of highly resistant and non-corrosive stainless steel. They have a
great resistance thanks to the protection of the housing of the plastic actuator.

User manual
MAJESTIC II bed
Page 17
An incorrect assembly can be dangerous for the user. If you notice that this
component is not correctly installed, do not handle it, leave the bed out of service
and contact the technical service for proper assembly
5) Specifications of the variant
The next features are the standard equipment, as well as the possibilities for
personalizing bed MAJESTIC II.
Standard equipment
oTotally electric bed with columns height adjustment.
oMaximum safe working load up to 250 kg.
oElectric Trendelemburg y reverse Trendelemburg positions
oABS side rails
oPatient handset (except with ABS side rails with embedded controls)
oNurse panel
oSafety “GO” button
oAuto contour ( 11cm backrest/7 cm pelvis )
oRechargeable long life battery
o150mm wheels
oBumpers on each corner
oAbs base cover
oIV and accessories sockets
oCentral brake system
oAngle indicator for Tren and reverse trendelemburg
oDetachable headboard and footboard
Optional equipment
oABS side rails with embedded controls
oSteel side rails
oXR backrest with cassette holder
o5th wheel
oLateral fixing for pump of air mattress
oAccessories fixing system
oNight light
oPendent handset
oHeadboard with table
oBi-lateral pedal for height with blocking system
Accessories
oUrine bag holder
oLifting pole
oIV pole

Page 18
6) Bed description
Figure N.2
– Majestic II bed
COMPONENTS:
1. Round bumpers on each corner.
2. Four ABS sections cover, easily detachable C
3. Base.
4. Four 150 mm wheels. Central brake and steer.
5. Accessories sockets (for IV pole, lifting pole, Balkan beam, etc.).
6. Easily detachable ABS footboard
7. Set of split side rails (4 units) with optional embedded controls or epoxy coated
steel side rails.
8. Easily detachable ABS headboard.
9. Nurse panel
2
7
8
4
1
5
3
6
9

User manual
MAJESTIC II bed
Page 19
7) Installation
1. Remove the packaging completely and dispose of it respecting the environment.
2. If beds are delivered in double package (two beds in the same pallet, one above
the other) take out carefully the top bed and leave it on the floor. This process
must be done by two person at least
3. Check that no components are missing according to the delivery note and if any
damage due to transport mishandling has occurred. Note any damage and report it
to your supplier immediately.
4. Read carefully this user manual.
5. Install the bed ends. The easily-detachable head end and foot end must be placed
in the corresponding sockets at the corners of the upper frame. As for the sliding
head end, place the support bars in the corresponding sockets of the upper frame.
6. If the temperature during transport or storage of the bed differs from the
operating temperature, do not connect the bed to the power supply until at least
24 hours have elapsed to adapt it to indoor temperature conditions.
7. Attach the accessories.
6. To install both the lifting pole and the I.V. pole:
Place the accessory in one of the sockets at the corners of the upper frame.
8. Connect the bed to power supply, including connection for potential (consult
chapter) and charge battery
9. Fix the ABS covers on backrest and leg rest sections
10. Check the following:
- Visual inspection
i. It must be ensured that the bed does not show visible signs of damage.
ii. It must be ensured that the electrical insulation of the wiring is intact.
- Functional inspection
i. The adjustment of the bed parts in their maximum position, as well as the
inclination and elevation of the bed.
ii. The operation of the control of the wheels, the guard rails, the extension
of the bed and the supports of the bed (if they have been ordered with it).
iii. The functions of the patient's command, the control and medical
supervision panel and the controls integrated in the handrails (if requested).
Before being used by a new patient, check the previous points

Page 20
a. Connection to power supply.
The Equipment has a cable with plug to connect and disconnect it from power supply. It
is important to place the bed in a place where it is easy to operate in this plug in case of
disconnection needs.
Insert the plug into power supply. The cable has a plastic hook for handling during
transport.
Check that the cable is not damaged. If it is, do not use the bed and retire it
until replacement by a correct one.
To avoid the risk of electric shock, this equipment should only be
connected to a power supply network with protective earth
The bed must be connected to a proper tension supply. Otherwise, the
functions would be disabled.
b. Equipotential connection.
Since it is possible to place the instruments
connected to the patient intravascularly or intra
cardiac, the bed has a conne
ction called
"equipotential" that allows the adjustment of the
potentials between the bed and these
instruments.
The mass connection designed for this is located
under the C / P of the bed.
Figure N. 3- Equipotential connector
Note:The following label marks the connection position
c. Battery charge
As standard Equipment, MAJESTIC II bed includes battery. Before using the product,
check that the battery is connected to the control box. Battery should be charged
connecting the bed to the power supply. Charging process can be observed in the nurse
panel.
To achieve a longer life, use battery in a proper and correct way.