LINET ELEGANZA 5 Parts list manual

User Manual and Technical
Description
ELEGANZA 5
Positionable Bed for Intensive Care
D9U001GE0-0101
Version: 02
Publication Date: 2017-04-21

D9U001GE0-0101_022
Manufacturer:
Linet spol. s r.o.
Želevčice 5
274 01 Slaný
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
http://www.linet.com
Eleganza 5
Positionable bed for intensive care
Author: LINET, s.r.o.
Related links: www.linet.com
D9U001GE0-0101
Version: 02
Publication Date: 2017-04-21
Copyright © LINET, s.r.o., 2017
Translation © LINET, 2017
All rights reserved.
All trademarks and brands are the property of the appropriate owners. The manufacturer reserves the right to changes in the
contents of this manual that relate to the product´s technical regulations. It is for this reason that the contents of this manual may
indicate differences from the current manufacture of the product.

D9U001GE0-0101_02 3
Table of Contents
1 Symbols and Denitions.............................................4
1.1 Warning Notices .........................................................4
1.1.1 Types of Warning Notices........................................ 4
1.1.2 Structure of Warning Notices...................................4
1.2 Instructions .................................................................4
1.3 Lists ............................................................................4
1.4 Symbols and Labels on the Bed.................................5
1.5 Serial Labels with UDI ................................................6
1.6 Denitions...................................................................7
1.7 Abbreviations..............................................................7
2 Safety Instructions ......................................................8
3 Intended Use................................................................9
4 Product Description ....................................................10
5 Technical Specication...............................................11
5.1 Identication of Applied Parts (Type B).......................11
5.2 Scales.........................................................................11
5.3 Mechanical Specications (Eleganza 5)..................... 11
5.4 Electrical Specications (Eleganza 5) ........................12
5.5 Electromagnetic Compatibility ....................................12
5.6 Manufacturer’s Manual and Declaration - Electromagnetic
Radiation ..........................................................................12
5.7 Manufacturer’s Manual and Declaration - Electromagnetic
Resistance........................................................................13
6 Use and Storage Conditions ......................................15
7 Scope of Delivery and Bed Variants .......................... 16
7.1 Delivery.......................................................................16
7.2 Scope of Delivery .......................................................16
7.3 Eleganza 5 Variants.................................................... 16
8 Initial Instructions........................................................17
8.1 Battery Activation........................................................17
8.2 Installation ..................................................................18
8.3 Before Use..................................................................19
8.4 Transport ....................................................................19
9 Mains Power Cable......................................................20
10 Battery ........................................................................20
10.1 Replacing the battery................................................21
10.2 Removing the Bed from Use ....................................22
10.3 Deactivating the Battery ...........................................22
11 Manipulation...............................................................23
11.1 Control Elements ......................................................23
11.1.1 iBoard ....................................................................24
11.1.2 Additional Supervisor Panel...................................36
11.1.3 Handset (optional) .................................................37
11.1.4 Integrated Control Panels for Patient..................... 38
11.1.5 Foot Control Bed Height (optional) ........................ 39
11.1.6 Foot Control Lateral Tilt (standard)........................ 39
11.2 Bed Positioning.........................................................40
Backrest............................................................................40
Thighrest ..........................................................................41
Calfrest ............................................................................42
Bed Height........................................................................42
Autocontour ......................................................................44
Examination Position........................................................44
Emergency Trendelenburg Position .................................45
Anti-Trendelenburg and ...................................................45
Trendelenburg Tilt.............................................................45
Bed Extension ..................................................................46
CPR Position ....................................................................46
Cardiac Chair Position......................................................47
Mobilisation Position.........................................................47
Ergoframe.........................................................................48
Lateral Tilt.........................................................................48
11.3 Siderails ....................................................................49
11.4 CPR Backrest Release.............................................50
11.5 Safe Stop (optional)..................................................50
11.6 Bed Illumination ........................................................50
11.7 Castor Control...........................................................51
i-Brake® (optional) ...........................................................51
11.8 i-Drive Power (optional) ............................................52
11.9 Mobi-Lift® (optional)...................................................57
11.10 X-Ray Lung Examination (optional)........................58
12 Mattress......................................................................59
12.1 Installation of Passive Mattress................................59
12.2 Installation of Integrated Mattress ............................59
Installation of SCU (System Control Unit) ........................60
12.3 Mattress Display and Keyboard Description.............60
13 Accessories ...............................................................61
13.1 Accessories at Bed Ends..........................................61
Lifting Pole........................................................................61
Infusion Stand...................................................................61
Ventilation Circuit Holder .................................................. 62
Oxygen Bottle Holder .......................................................62
Writing Shelf .....................................................................63
Monitor Shelf ....................................................................63
13.2 Accessories on Siderails...........................................64
Nurse Call.........................................................................64
Protector...........................................................................65
13.3 USB Connector.........................................................66
13.4 Urine Bag Holder......................................................66
14 Cleaning/Disinfection................................................67
14.1 Cleaning (Eleganza 5)..............................................67
14.1.1 Daily Cleaning .......................................................68
14.1.2 Cleaning before Changing Patients.......................68
14.1.3 Complete Cleaning and Disinfection .....................68
15 Troubleshooting ........................................................69
16 Maintenance...............................................................70
16.1 Monthly maintenance ...............................................70
16.2 Maintenance every 3 months ...................................70
16.3 Maintenance every 12 months .................................70
16.3.1 Spare Parts............................................................70
16.3.2 Completeness........................................................70
16.3.3 Wear......................................................................70
16.3.4 Functioning............................................................70
16.3.5 Electric Control ......................................................71
16.3.6 Castors ..................................................................71
16.3.7 Accessories ...........................................................71
16.4 Safety Checks ..........................................................71
16.5 Maintenance Active Mattress....................................72
16.6 Linet ® Service Department ......................................72
17 Disposal......................................................................73
17.1 Environment Protection ............................................73
17.2 Disposal....................................................................73
17.2.1 Eleganza 5.............................................................73
18 Warranty .....................................................................74
19 Standards and Regulations......................................75

D9U001GE0-0101_024
1 Symbols and Denitions
1.1 Warning Notices
1.1.1 Types of Warning Notices
Warning notices are differentiated by the type of danger using the following key words:
► CAUTION warns about the risk of material damage.
► WARNING warns about the risk of physical injury.
► DANGER warns about the risk of fatal injury.
1.1.2 Structure of Warning Notices
SIGNAL WORDS!
Type and source of danger!
► Measures to avoid the danger.
1.2 Instructions
Structure of instructions:
► Perform this step.
Results, if necessary.
1.3 Lists
Structure of bulleted lists:
■ List level 1
□ List level 2
Structure of numbered lists:
a. List level 1
b. List level 1
1. List level 2
2. List level 2

D9U001GE0-0101_02 5
1.4 Symbols and Labels on the Bed
READ INSTRUCTIONS FOR USE
SAFE WORKING LOAD
DESIGNATION OF HOSPITAL BED FOR ADULTS
USE MATTRESS RECOMMENDED BY MANUFACTURER
DO NOT PUT ANY OBJECTS ON UNDERCARRIAGE
CALFREST LOAD
WARNING AGAINST CRUSHING OR TRAPPING
JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION
CPR LEVER
POSSIBLE RISK
POSSIBLE RISK (on Serial Label)
APPLIED PARTS TYPE B

D9U001GE0-0101_026
THERMAL PROTECTION FOR TRANSFORMER
SAFETY ISOLATING TRANSFORMER, GENERAL
ONLY SUITABLE FOR INDOOR USE
MAXIMUM WEIGHT OF PATIENT
WEIGHT OF BED
CE MARK
1.5 Serial Labels with UDI
Fig. 1 Serial Label with UDI (Eleganza 5)

D9U001GE0-0101_02 7
1.6 Denitions
Basic Bed Conguration the pricelist model conguration, not including a mattress
Bed Weight The value depends on the product conguration, accessories or
customer adjustments.
Clearance of Undercarriage the height from the oor to the lowest point of the undercarriage
between the castors, for the manipulation of accessories under a
braked bed in the standard position
Duty Cycle cycle of operation of the motor: time of activity/time of rest
Ergoframe Ergoframe is the kinematic system of Mattress Platform Adjus-
tment whose effect is the elimination of pressure on the patient´s
abdomen and pelvic area and frictional forces on the patient‘s
back and legs.
Safe Working Load the highest allowable load on the bed (patient and accessories)
Siderail Height the height of the upper crossbar or the edges of the siderails (not
the highest point of the siderail controls) from the patient surface
Standard Bed Position - The height of the patient surface with regard to the oor is 400
mm
- The mattress platform, including the individual parts, has to be in
a horizontal (level - 0°) position.
- The siderails are always locked in the upper position.
- The basic position of the integrated extension.
1.7 Abbreviations
AC Alternating Current
CE European Conformity
CPR Cardiopulmonary Resuscitation
dB Sound Intensity Unit
DC Direct Current
EMC Electromagnetic Compatibility
FET Field-effect transistor
HF High Frequency
ICU Intensive Care Unit
IV Intravenous
LED Light Emitting Diodes
ME Medical Electrical (Equipment)
SCU System Control Unit
SWL Safe Working Load
UDI Unique Device Identication (for medical devices)
USB Universal Serial Bus

D9U001GE0-0101_028
2 Safety Instructions
► Follow the instructions carefully.
► Use the bed exclusively if it is in perfect working order.
► If necessary, check the bed functions daily or at each shift change.
► Ensure any user has read and understood this manual completely before operating the product.
► Use the bed exclusively with the correct mains supply.
► Ensure that the bed is operated exclusively by qualied personnel.
► Ensure that the patient (health permitting) has been informed about the operation of the bed and all applicable safety
instructions.
► Move the bed exclusively on even, hard-surfaced oors.
► Replace any damaged parts immediately with original spare parts.
► Ensure that maintenance and installation are performed exclusively by qualied personnel who have been trained by the
manufacturer.
► During peak loads or unavoidable excess loads (CPR), place Mattress Platform in the lowest position.
► Ensure that only one adult patient uses the bed at any time.
► Take care to avoid injuries or squeezing when operating moving parts.
► When using lifting poles or infusion stands, ensure that nothing will be damaged when you move or adjust the bed.
► Brake the castors when the bed is occupied.
► Keep the mattress platform in the lowest position at any time when the healthcare personnel are not treating the patient
in order to prevent the patient from falling or injuries.
► Ensure that siderails are operated exclusively by healthcare personnel.
► Never use the bed in areas where there is a hazard of explosion.
► Enable or disable functions on patient controls using the iBoard supervisor panel as appropriate for the patient’s
physical and mental state. Verify that the function is actually disabled.
► Never handle the mains plug with wet hands.
► Disconnect the product from the mains exclusively by pulling the mains plug.
► When pulling the mains plug, always hold the plug, not the cable.
► Position the mains cable so that there are no loops or kinks in the cable; protect the cable from mechanical wear and tear.
► Improper handling of mains cable can cause an electric shock hazard, other serious injuries or damage to the mattress
replacement system.
► Ensure that the stipulated duty cycle of motor is not exceeded.
► To change fuses or cables contact servise organisation authorized by manufacturer.
► Ensure that the moving parts of the bed are not blocked.
► To prevent failures, use exclusively the manufacturer’s original accessories and mattresses.
► Ensure that the stipulated safe working load is not exceeded.
► If the patient‘s condition could lead to an entrapment, leave the mattress support platform in the at position whilst
unattended.
► Adjust bed height when transporting the bed in order to facilitate overcoming possible obstacles.
► Do not exceed maximum load of 80 kg (176.37 lbs) for mattress platform extension.
► Do not modify bed and its components without the manufacturer´s approval.
► Use the mattress system exclusively as specied in this manual and in perfect working order.
► Use the mattress system exclusively with the correct mains supply (see Electrical Specications).
► Use the mattress system exclusively in its original state and do not modify it in any way.
► Have the mattress system used exclusively by or under supervision of trained and qualied nursing personnel.
► Have the mattress system serviced and installed exclusively by qualied personnel trained and authorised by the
manufacturer.
► Do not exceed the maximum patient weight limit (see Mechanical Specications).
► Do not use the SCU near ammable gases. (This does not apply to oxygen cylinders.)
► Do not hang anything on any cable.
► Never use the mattress replacement system near radiators or other heat sources.
► Never cover the SCU while in use.
► Select a suitable location for the placement of bed accessories and other objects to prevent involuntary activation of
buttons or controls which may result in the adjustment of bed positioning.
► Do not use the bed in the event parts have been removed (e.g. parts of mattress platform) unless these parts are de
signed to be removed (e.g. head and/ or foot end of the bed).
► Never place any accessories or handset on the siderails where keyboards are located.
► After each emergency situation always check if any of the controllers (in side rails, hand set or ACP) is not involuntarily
pressed by the bed accessories or by the mattress.
► The weighing system must be calibrated at regular intervals and in accordance with the metrological regulations of the
relevant country. All testing and certication must be carried out by qualied personnel. The healthcare provider is
responsible for ensuring the required testing frequency and testing procedure of the weighing system is carried out.
► To avoid injury or crushing, take extra caution when operating any moving parts of the bed.
► To avoid unintended activation of moving parts during any use of the bed always check that none of the control elements
of the bed is not involuntary pressed by persons, mattress or other objects.

D9U001GE0-0101_02 9
3 Intended Use
Eleganza 5 is a positionable bed for intensive care. Its purpose is to support patient and to facilitate treatment and
manipulation with patient for nursing personnel. Eleganza 5 is equipped with weighing system designed for weighing pati-
ents. Eleganza 5 is compatible with an integrated mattress replacement system approved by the manufacturer.
Eleganza 5 must be used exclusively by or under supervision of trained and qualied nursing personnel.
Eleganza 5 is suitable for:
■Patients
□ Standard bed:
● With weight ≥ 40 kg
● With height ≥ 146 cm
● With BMI ≥ 17
□ Bed equipped with Junior Kit:
● Older than 4 years with minimal height of 90 cm
□ Whose weight (including mattress and accessories) does not exceed the SWL
in long-term treatment (depending on bed type)
■Personnel
□ qualied medical staff
□ patient (condition permitting)
■Use
□ intensive/critical care units
□hospital rooms
□patient transport
■Transport
□in original bag
■Medical purpose
□ support for patients in Eleganza 5 beds
□ pressure ulcer prevention
■Location
□ The bed is determined for application environment 1 and 2 according to EN 60601-2-52:2010.
NOTE For information concerning uses other than those, please contact Linet ®.

D9U001GE0-0101_0210
4 Product Description
1. Removable Foot Board
2. Split Siderail – Middle Section with Integrated Control Panels for Patient
3. Split Siderail – Head Section
4. Removable Head Board
5. iBoard
6. CPR Lever – Backrest Release
7. Poles Adaptor
8. Foot Switch
9. Siderail Release Lever
10. Four-part Mattress Platform with Ergoframe® System (under the mattress)
11. Castor Control Lever
12. Mobilift® Handle
13. Castor Diameter 150 mm (5.9 in.)
14. Safety Lock
15. Bumper
Fig. 2 Bed Overview (Eleganza 5)
5
6
7
12 910 8
11
15
14
13
1 2 43

D9U001GE0-0101_02 11
5 Technical Specication
5.1 Identication of Applied Parts (Type B)
All part of the bed (and accessories) the patient can reach are type B Applied Parts.
■ Mattress Platform Frame, Covers and all Movable Parts
■Head and Foot End
■Siderails
■ Mobilift Handles
■Handset
5.2 Scales
Accuracy of displayed weight values:
■ 0,5 kg (1,1 lbs)
■ Scales Class III
5.3 Mechanical Specications (Eleganza 5)
Parameter Value
External Dimensions in Standard Bed Position (length x width) 219 cm x 100 cm
Siderail Height above Mattress Platform 45 cm
Bed Extension 0 cm - 22 cm
Dimensions of Mattress (length x width) 208 cm x 90 cm
Maximum Mattress Height 23 cm
Clearance in Standard Position 14,2 cm
castors 15 cm
Minimum-Maximum Mattress Platform Height above oor
(without Mattress)
43,5 cm - 81,5 cm
Ergoframe (Backrest/Thighrest) 7,4 cm / 4 cm
Maximum Backrest Angle 65°
Maximum Thighrest Angle 30°
Maximum Calfrest Angle 33°
Lateral Tilt Adjustment +15°/-15°
Trendelenburg/Anti-Trendelenburg Position (Angle) +14°/-14°
Bed Weight in Basic Conguration 210 Kg
SWL (Bed Safe Working Load) 250 Kg
SWL (Lifting Pole Safe Working Load) 75 Kg
SWL (Patient Safe Working Load) 185 Kg
Application Environment in accordance with EN 60601-2-52 1, 2
Environment Conditions
Ambient Temperature 10°C-40°C
Relative Humidity 30% - 75 %
Atmospheric Pressure 795 - 1060 hPa
Storage and Transport Conditions
Ambient Temperature -20°C- 50°C
Relative Humidity 20% - 90 %
Atmospheric Pressure 795 - 1060 hPa

D9U001GE0-0101_0212
5.4 Electrical Specications (Eleganza 5)
Input Voltage 230 V, 50/60 Hz
Maximum Power Input Max. 1,6 A, 370 VAC
Ingress Protection (EN 60529) IPX4
Protection Class Class I
Electrical Motor Duty Cycle 2 minutes ON /18 minutes OFF
Battery Pb AKU 2 x 12 V / 1,2 Ah / Fuse 15A
Fuse 2 x T3.15A L 250V for 230 V
NOTE Upon request, Linet ® can deliver hospital beds with electrical specications that comply with regional standards (custom
voltage, different mains plugs).
5.5 Electromagnetic Compatibility
WARNING!
Increased electromagnetic radiation or reduced electromagnetic resistance due to unsuitable accessories,
converters or cables!
► Consult Linet® or local dealer before using other parts than those provided by Linet®.
WARNING!
Medical electrical equipment or medical electrical system should not be used in extremely short distances
within the bed! In the case it is necessary to use medical electrical equipment in this extremely short distances
within the bed observe this conguration regularly to verify the normal functions of the bed in this congurati-
on.
► Consult Linet® or local dealer before using medical electrical equipment where inuence on the bed can be
strong.
NOTE IEC 60601-1-2 certied medical electrical equipment used in ICU is not restricted.
Eleganza 5 requires special preliminary measures pertaining to EMC that necessitate installation and commissioning in conformity
with the EMC information given in this Manual.
Portable and mobile HF communication equipment can inuence bed functions.
NOTE It does not concern xed installations of hospital communication systems and nets (DECT, pager, WiFi) and other mobile
devices which are certied according to local telecommunication legislation.
5.6 Manufacturer’s Manual and Declaration - Electromagnetic Radiation
Eleganza 5 is intended for the application in electromagnetic environment as specied below. The customer or user of the bed is
responsible for the fact that these requirements are met.
Radiation Test Conformity Electromagnetic Environment
High-frequency radiation CISPR 11 Group 1 Eleganza 5 utilises high-frequency
energy for its internal function only. The
high-frequency radiations are very low
and unlikely to cause any interference to
nearby electronic devices.
High-frequency radiation CISPR 11 Class B Eleganza 5 is suitable for all institu- tions,
including households and objects directly
connected to the public low-voltage
mains supplying residential buildings.
Harmonic radiations IEC 61000-3-2 Class A
Fluctuating voltage/Flashing radia- tion
CE 61000-3-3
Satisfactory

D9U001GE0-0101_02 13
5.7 Manufacturer’s Manual and Declaration - Electromagnetic
Resistance
Eleganza 5 is intended for the application in electromagnetic environment as specied below. The customer or user of the bed is
responsible for the fact that these requirements are met.
Resistance Test Test Level as per IEC 60601 Level of Compliance Electromagnetic Environment
Electrostatic
discharge (ESD)
IEC 61000-4-2
± 6 kV for contact
± 8 kV for air
± 6 kV for contact
± 8 kV for air
► Ensure that the following
requirements are met: Floors:
wood, concrete or ceramic tiles
Relative humidity: >30%.
Electrical fast transient
response/
group of impulses
IEC 61000-4-4
± 2 kV in feeder line
± 1 kV in input/output
line
± 2 kV in feeder line
± 1 kV in input/output line
► Ensure the mains quality is
suitable for a commercial or
hospital environment.
Shock pulse
IEC 61000-4-5
± 1 kV between lines
± 2 kV between line (lines)
and earth
± 1 kV in differential mode
± 2 kV in co-phasal
mode
► Ensure the mains quality is
suitable for commercial or hospi-
tal environment.
Short-time voltage
drop, short-duration
interruptions
and slow voltage
changes on the feeder
input line
IEC 61000-4-11
<5 % UT
(>95 % short-duration
drop of UT)
within 0.5 cycles
40 % UT
(60 % short-duration
drop of UT)
within 5 cycles
70 % UT
(30 % short-duration
drop of UT)
within 25 cycles
<5 % UT
(>95 % short-duration
drop of UT)
within 5 s
<5 % UT
(>95 % short-duration
drop of UT)
within 0.5 cycles
40 % UT
(60 % short-duration
drop of UT)
within 5 cycles
70 % UT
(30 % short-duration
drop of UT)
within 25 cycles
<5 % UT
(>95 % short-duration
drop of UT)
within 5 s
► Ensure that mains quality
is suitable for a commercial or
hospital environments.
► For permanent operation
during a power failure, connect
the bed to a power generator as
the back-up battery’s capacity is
limited.
Magnetic eld of
network frequency
(50/60 Hz)
IEC 61000-4-8
3 A/m 3 A/m ► Ensure the magnetic elds of
the network frequency conform
to the normal levels of commer-
cial or hospital environments.
NOTE UT refers to the AC mains voltage before the test level is applied.

D9U001GE0-0101_0214
Resistance Test Test Level as per IEC 60601 Level of Compli-
ance
Electromagnetic Environment
Conducted high frequency
phenomena
IEC 61000-4-6
3 Vrms
150 kHz to 80 MHz
3 Vrms ► It is recommended to use portable
and mobile HF communication equi-
pment around the bed in distances
defined below.
Recommended distances:
d = 1.2 √P
d = 1.2 √P 80 MHz to 800 MHz
d = 2.3 √P 800 MHz to 2.5 GHz
Pis the rated maximum output power of
the transmitter in Watts (W) dened by
the transmitter‘s
manufacturer.
d is the recommended separating di-
stance in metres (m).
► Ensure the eld intensities of perma-
nent HF transmitters determined by the
summary of electromagnetic characteri-
stics for the given place do not exceed
the satisfactory level b in each frequen-
cy range.
Interferences are possible in the vicinity
of the instrument marked with the fo-
llowing symbol:
Radiated high-frequency
phenomena
IEC 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
1) It is not possible to accurately indicate eld intensities from permanent transmitters (e.g. radio base stations of
the radio, phones and ground mobile and amateur radio stations, AM and FM radio and television broadcasting).
To assess the electromagnetic environment for permanent HF transmitters, take into account the on-site electromagnetic
characteristics.
If the measured eld intensity is higher than the pertinent satisfactory HF level stated above, observe whether
the bed is functioning normally.
If any abnormal properties are observed, move or relocate the bed.
2) The eld intensity in the entire frequency range from 150 kHz to 80 MHz should be lower than 3 V/m.
NOTE With 80 MHz and 800 MHz, the higher frequency range is applicable.
NOTE The absorption and reection of buildings, objects and people will inuence electromagnetic propagation.

D9U001GE0-0101_02 15
Recommended separation distances between portable and mobile RF communications equipment and the Eleganza 5
Medical Bed
The Eleganza 5 Medical Bed is intended for use in an electromagnetic environment in which radiated RF disturbances are cont-
rolled. The customer or the user of the Eleganza 5 Medical Bed can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Eleganza 5 Medical Bed
as recommended below, according to the maximum output power of the communications equipment.
Rated maximum output of
transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
0,01 0,12 0,40 0,40
0,1 0,37 1,26 1,26
1 1,17 4,00 4,00
10 3,69 12,65 12,65
100 11,67 40,00 40,00
For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres (m) can be
estimated using the equation applicable to the frequency of the transmitter, where P is 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 reection
from structures, objects and people.
6 Use and Storage Conditions
DANGER!
Danger to life due to electric shock!
To ensure the bed’s class I protection against electric shocks:
► Ground the mains.
► Use exclusively Hospital Grade or Hospital Only receptacles for grounding.
Eleganza 5 is designed for use in rooms for medical purposes. Electrical installations must therefore meet local norms laying down
the necessary conditions for electrical installations.
► Disconnect the bed from the mains in exceptional cases (i.e. lightnings, earthquake).
Eleganza 5 is not suitable for indoor environments containing ammable gases (except oxygen cylinders).

D9U001GE0-0101_0216
7 Scope of Delivery and Bed Variants
7.1 Delivery
► Upon receipt, check that the shipment is complete as specied on the delivery note.
► Notify the carrier and supplier of any deciencies or damages immediately as well as in writing or make a note on the
delivery note.
7.2 Scope of Delivery
■ Eleganza 5 hospital bed
■ User Manual
7.3 Eleganza 5 Variants
s = standart
o = optional
Optional bed features:
■ Undercarriage
□ Standard undercarriage with IV pole and lifting pole bushing
■ Integrated Mattress
□ with integrated mattress
□ without integrated mattres
■ Scales
□ with scales (with bed exit alarm)
■Castors
□ Tente Integral 150 mm (5.9 in.) single castors (s)
□ Tente Integral 150 mm (5.9 in.) double castors (o)
□ Tente Integral 150 mm (5.9 in.) single castors + retractable 5th castor (o)
□ Tente Integral 150 mm (5.9 in.) double castors + retractable 5th castor (o)
□ Tente Integral 150 mm (5.9 in.) single castors + i-Drive Power (o)
□ Tente Integral 150 mm (5.9 in.) double castors + i.Drive Power (o)
■Control Elements
□ iBoard in both head sections of the siderails (s)
□ Additional Supervisor Panel (s)
□ Handset with illuminated buttons and adapter for simple connection Plug and Play (o)
□ Foot Control for Lateral Tilt (s)
□ Foot Control for Height Adjustment (o)
□ Patient Control Elements integrated in both middle sections of the siderails (s)
□ Patient Control Elements integrated in head sections of the siderails (0)
■ 1 pair of Mobi-Lift® handles (o)
■ i-Brake® (o)
■ x-ray cassette holder (0)
■ EMR ready bed (o)
■ Nurse call (o)
■ i-Drive Power® (o)
■ Safe Stop (o)
■ USB (o)

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8 Initial Instructions
Set up the bed as follows:
► Unpack the bed.
► Check the delivery (see Scope of Delivery and Bed Variants).
► Remove isolating foil from the mains control box (see Battery Activation).
► Install equipment and accessories (see Installation).
► In case of delivery with dismantled bed ends, mount the head and foot ends (see Bed Ends).
► Set up the bed exclusively on a suitable oor surface (see Transport).
► Ensure that the mains cable does not collide or get stretched when adjusting the bed.
► Check that the plug is inserted correctly.
► Do not leave any extension cords or power strips loose on the oor.
► Ensure that all of the required mechanical and electrical prevention mechanisms are available on site.
► There is no mains switch on the bed, i.e. the mains cable is the only means to isolate the bed from the mains. Ensure that
the mains cable is always accessible.
► Have the separable plug of the mains cable changed and maintained exclusively by qualied and trained service techni
cians authorised by the manufacturer.
CAUTION!
Material damage due to temperature difference!
► If there is a considerable temperature difference between the bed and the place of operation
(after transport/storage), leave bed unconnected for 24 for the difference to balance itself.
8.1 Battery Activation
Control Section Placement
Removing the Isolating Foil
Fig. 3 Control Section Placement
Fig. 3a Isolating Foil Placement
Fig. 3b Detail of Isolating Foil
To remove isolating foil:
► Remove isolating foil from mains control box 1 by
pulling strap 2.
► Check if isolating foil is complete and
undamaged as shown in Fig. 3b.
► If isolating foil is damaged, contact the
manufacturer’s service department immediately.
NOTE It is recommended to wear gloves when removing
the isolating foil.

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8.2 Installation
WARNING!
Risk of injury when working on the bed!
► Ensure that the bed is disconnected from the mains connection prior to assembly, disassembly and
maintenance.
► Ensure that the castors are locked prior to assembly, disassembly and maintenance.
CAUTION!
Material damage due to incorrect assembly!
► Ensure that assembly is performed exclusively by customer service or trained hospital personnel.
NOTE For safe, easy handling, Linet ® recommends having two technicians assemble the bed.
Bed Ends
Dismount the bed ends as follows:
► Unlock sleeve tting.
► Pull bed ends from sleeve tting.
► Lock sleeve tting.
Install the bed ends as follows:
► Unlock sleeve tting.
► Slide bed ends into sleeve tting.
► Lock sleeve tting.
Mattress Platform
Eleganza 5 without x-ray cassette holder has four removable parts of Mattress Platform (1,2,3 and 4).
Fig. 4 Locking of the bed ends
Fig. 5 Parts of Mattress Platform
2
1
34
LEFT SIDE
RIGHT SIDE
HEAD END
FOOT END

D9U001GE0-0101_02 19
Potential Equalisation
The bed is equipped with a standard protective connector. This connector is used for potential equalisation between the bed and
any intravascular or intracardiac device connected to the patient to protect the patient from static electric hocks.
Use equalisation connector if:
■ the patient is connected to any intravascular or intracardiac device.
Before connecting the patient to an intravascular/intracardiac device:
► Connect the ground wire of the device to the potential equalisation connector 2 on the bed on which the patient in question
is lying.
► Use a standard hospital connector 1.
► Make sure that the connectors match.
► Make sure that there is no possibility for inadvertent disconnection.
Before moving the bed:
► Disconnect the patient from the intravascular or intracardiac device.
► Disconnect the potential equalisation connector.
8.3 Before Use
Prepare the bed for use as follows:
► Connect the bed to the mains.
► Charge the battery.
► Raise and tilt the mattress platform to the highest position.
► Lower and tilt the mattress platform to the lowest position.
► Check that the castors as well as main brake work correctly.
► Check that the bed extension works correctly.
► Check that it is possible to remove the head and foot boards.
► Check all of the functions on the control elements.
► Check that the siderails function properly.
► Dispose of all packaging (see Disposal).
8.4 Transport
For a safe transport, observe the following:
► Ensure that no cables are run over when moving a bed.
► Ensure that the mains cable is attached with a hook (at the head end of the bed).
► Ensure that the castors are unlocked before moving the bed during the loading/unloading process (see Castor Control).
► Adjust bed height to at least 20 cm below maximum height.
► Push bed by handles on head or foot end.
► Move the bed exclusively on suitable oor surfaces.
Suitable surfaces:
■Tile
■Hard linoleum
■ Poured ooring
Fig. 6a Potential equalisation
connector - female
Fig. 6b Potential equalisation - male

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Unsuitable surfaces:
■ Too soft, unsealed or defective ooring
■ Soft wooden ooring
■ Soft and porous stone oors
■ Carpeted oors with underlay
■Soft linoleum
► For longer distances, ensure that the castor steering function (main control) is activated.
► Ensure that the brakes are released while moving the bed.
9 Mains Power Cable
Attachment plug is means of connecting and disconnecting bed from the mains.
Mains power cable must be attached with a hook at the head end of the bed during transport.
CAUTION!
Disconnecting bed from the mains does not stop motions of the bed!
► Stop the bed before disconnection bed from the mains.
Where the integrity of the external protective conductor in the installation or its arrangement is in doubt
► operate the bed from internal battery only.
10 Battery
Purpose
The battery serves as a backup during power failures or for emergency bed positioning.
► Use only batteries approved by the manufacturer.
► Check the batteries’ functionality at least once a month in accordance with the user and service manuals and have the
batteries changed if necessary.
► Use exclusively batteries approved by the manufacturer.
NOTE The service life of the batteries depends on the frequency and method of use.
The manufacturer will assume no responsibility for any damage to the bed or the battery caused by:
■ non-observance of the manufacturer’s instructions in the user manual
■ using batteries not approved by the manufacturer
Warranty
The manufacturer provides a 6-month warranty for the full function of the batteries.
Charging
The battery supplied with the bed is delivered uncharged.
For declared lifetime period of leaded accumulators is recommended during storage:
► To prevent accumulators from deep discharging (state-of-charge under 70%) and to keep accumulators at least partly
charged by regular recharging
► To store accumulators on dry and cold places (from 10°C to 0°C)
► To prevent accumulators from being in the sunshine
To charge the battery:
► Connect the bed to the mains.
NOTE Some bed adjustment options are not available without a battery, for example, Height Adjustment under a load of above
200 kg.