LINET ELEGANZA 4 Parts list manual

User Manual and Technical
Description
ELEGANZA 4
Positionable Bed for Intensive Care
D9U001GE4-0101
Version: 05
Publication Date: 2019-05
version with scales and without scales

D9U001GE4-0101_052
Manufacturer:
LINET spol. s r.o.
Želevčice 5
274 01 Slaný
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
http://www.LINET.com
Eleganza 4
Positionable bed for intensive care
Author: LINET, s.r.o.
Related links: www.LINET.com
D9U001GE4-0101
Version: 05
Publication Date: 2019-05
Copyright © LINET, s.r.o., 2019
Translation © LINET, 2019
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. Reproduction, also excerpts, only with prior permission of the
publisher. Subject to changes due to technical developments. All technical data are rated data and are subject to construction and
manufacturing tolerances.

D9U001GE4-0101_05 3
1 Symbols and Denitions .............................................4
1.1 Warning Notices..........................................................4
1.1.1Types of Warning Notices ........................................4
1.1.2 Structure of Warning Notices ...................................4
1.2 Instructions..................................................................4
1.3 Lists.............................................................................4
1.4 Symbols on the Package ............................................5
1.5 Symbols and Labels on the Bed .................................5
1.6 Serial Label with UDI ..................................................9
1.7Acoustic signalisation.................................................. 10
1.8 Illumination.................................................................. 10
1.9 Denitions ...................................................................11
1.10 Abbreviations ............................................................12
2 Safety Instructions.......................................................13
3 Intended Use ................................................................15
3.1 Contraindications ........................................................15
4 Product Description.....................................................16
5 Technical Specication ...............................................17
5.1 Identication of Applied Parts (Type B) .......................17
5.2 Scales .........................................................................17
5.3 Mechanical Specications (Eleganza 4) .....................17
5.4 Environment Conditions.............................................. 18
5.5 Electrical Specications (Eleganza 4)......................... 18
5.6 Electromagnetic Compatibility.....................................18
5.6.1 Manufacturer instructions - electromagnetic emissions
..........................................................................................19
5.6.2 Manufacturer instructions - electromagnetic susceptibility
..........................................................................................19
6 Use and Storage Conditions ....................................... 20
7 Scope of Delivery and Bed Variants...........................21
7.1 Delivery .......................................................................21
7.2 Scope of Delivery........................................................ 21
7.3 Eleganza 4 Variants ....................................................21
8 Putting into Service .....................................................22
8.1 Accumulator Activation................................................22
8.2 Head Board and Foot Board ....................................... 23
8.3 Mattress support platform ...........................................23
8.4 Potential Equalisation .................................................24
8.5 Before Use .................................................................. 25
8.6Transport.....................................................................25
9 Power Cable .................................................................26
10Accumulator ...............................................................26
10.1 Replacing the accumulator .......................................27
10.2 Removing the Bed from Use..................................... 28
10.3 Deactivating the Accumulator ...................................28
11 Manipulation ............................................................... 29
11.1 Siderails.....................................................................29
11.2 Castor Control ........................................................... 32
11.3 CPR Backrest Release.............................................. 32
11.4 Control Elements.......................................................33
11.4.1 Nurse Control Panel (optional)...............................34
11.4.2 iBoard Basic (standard)..........................................37
11.4.3Attendant Control Panel ......................................... 39
11.4.4 Handset (optional)..................................................41
11.4.5 Foot Switch - Bed Height (optional)........................42
11.4.6 Patient Control Panels............................................ 42
11.5 Bed Positioning .........................................................43
11.5.1 Backrest .................................................................43
11.5.2Thighrest ................................................................44
11.5.3 Mechanical Calfrest Adjustment .............................46
11.5.4 Bed Height..............................................................47
11.5.5Autocontour ............................................................49
11.5.6 Examination Position..............................................50
11.5.7 Emergency Trendelenburg Position .......................52
11.5.8Anti-Trendelenburg Tilt and Trendelenburg Tilt ......53
11.5.9 CPR Position ..........................................................55
11.5.10 Mechanical Bed Extension ...................................56
11.5.11 Cardiac Chair Position..........................................59
11.5.12 Mobilisation Position.............................................60
11.5.13 Ergoframe.............................................................60
12 Scales Control (only version with scales) ...............61
12.1 Preparation ...............................................................61
12.2Taring ........................................................................61
12.3 Displaying .................................................................61
12.4 Hold Mode.................................................................62
12.5 Bed Overload ............................................................62
12.6 Bed Underload .......................................................... 62
12.7 Weighing in tilt........................................................... 62
12.8 Zeroing Scales .......................................................... 62
13 Bed Exit Monitoring (only version with scales) ......63
13.1 Preparation ...............................................................63
13.2 Activation of Bed Exit Monitoring ..............................63
13.3 Monitored Zone......................................................... 63
13.4 BED EXIT ALARM.....................................................64
13.4.1Alarm Volume.........................................................64
13.5 PAUSE ......................................................................64
13.6 Deactivation of Bed Exit Monitoring ..........................64
14 Equipment ..................................................................65
14.1 Accessory Rail with plastic hooks (optional) .............65
14.2 Linen Shelf (standard)...............................................65
14.3 Mobi-Lift® (optional) ...................................................66
14.4 Brake Signal (optional)..............................................66
14.5 i-Brake® (optional) .....................................................66
14.6 Retractable Fifth Castor (optional) ............................66
14.7 X-Ray Examination (optional) ...................................67
14.8 Undercarriage Cover.................................................68
15 Mattress ......................................................................69
15.1 Installation of Passive Mattress ................................69
15.1.1 Straps with side release buckles............................ 69
15.2 Installation of Active Mattress ...................................70
15.2.1 Straps with side release buckles............................ 70
16Accessories ................................................................71
16.1 Lifting Pole ................................................................72
16.2 Infusion Stand ........................................................... 73
16.3 Oxygen Bottle Holder ................................................ 74
16.4 Ventilation Circuit Holder...........................................75
16.5 Writing Shelf..............................................................76
16.6 Monitor Shelf............................................................. 76
16.7 USB Connector (optional) .........................................77
16.8 Urine Sack Holder ..................................................... 77
16.9 SafetyMonitor............................................................ 78
17 Cleaning/Disinfection ................................................80
17.1 Cleaning (Eleganza 4) ..............................................80
17.1.1 Daily Cleaning........................................................ 81
17.1.2 Cleaning before Changing Patients .......................81
17.1.3 Complete Cleaning and Disinfection ...................... 81
18 Troubleshooting .........................................................82
19 Maintenance ...............................................................83
19.1 Monthly maintenance performed by the user............ 83
19.2 Maintenance every 3 months performed by the user 83
19.3 Maintenance every 12 months performed by the service
department of the manufacturer .......................................83
19.3.1 Spare Parts ............................................................ 83
19.3.2 Completeness ........................................................ 83
19.3.3 Wear.......................................................................83
19.3.4 Functioning ............................................................83
19.3.5 Electric Control.......................................................84
19.3.6 Castors...................................................................84
19.3.7Accessories............................................................ 84
19.4 Safety Technical Checks ...........................................84
19.5 Maintenance Active Mattress .................................... 85
19.6 LINET ® Service Department.....................................85
20 Disposal ...................................................................... 86
20.1 Environment Protection.............................................86
20.2 Disposal ....................................................................86
20.2.1 Eleganza 4 ............................................................. 86
Table of Contents

D9U001GE4-0101_054
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
● List level 3
21 Warranty......................................................................87
22 Standards and Regulations ......................................87
22.1 EU Declaration of Conformity (Eleganza 4 with scales)
..........................................................................................88
22.2 EU Declaration of Conformity (Eleganza 4 without scales)
..........................................................................................89

D9U001GE4-0101_05 5
1.4 Symbols on the Package
FRAGILE, HANDLE WITH CARE
THIS WAY UP
KEEP DRY (PROTECT FROM HUMIDITY)
PAPER RECYCLING SYMBOL
OVERSEAS PACKAGE: STACKING LIMIT BY NUMBER (4 PACKAGES FOR STORAGE)
OVERSEAS PACKAGE: STACKING LIMIT BY NUMBER (2 PACKAGES FOR TRANS-
PORT)
DO NOT USE HAND TRUCK HERE
DO NOT STACK DURING STORAGE
1.5 Symbols and Labels on the Bed
READ INSTRUCTIONS FOR USE
GO BUTTON (PRESS TO ACTIVATE CONTROL ELEMENT)
STOP BUTTON (PRESS TO INTERRUPT BED POSITIONING)

D9U001GE4-0101_056
SAFE WORKING LOAD
DESIGNATION OF HOSPITAL BED FOR ADULTS
USE MATTRESS RECOMMENDED BY MANUFACTURER
DO NOT PUT ANY OBJECTS ON UNDERCARRIAGE
BED EXTENSION
WARNING AGAINST CRUSHING OR TRAPPING
JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION
CPR LEVER
WARNING
WARNING
BED BOARD REMOVAL INSTRUCTION
MAXIMUM CALFREST LOAD

D9U001GE4-0101_05 7
APPLIED PARTS TYPE B
THERMAL PROTECTION FOR TRANSFORMER
SAFETY ISOLATING TRANSFORMER, GENERAL
ONLY SUITABLE FOR INDOOR USE
MAXIMUM WEIGHT OF PATIENT
WEIGHT OF BED
CE MARK (ELEGANZA 4 WITHOUT SCALES)
CE MARK (ELEGANZA 4 WITH SCALES)
WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,
DO NOT PUT INTO THE HOUSEHOLD WASTE)
MANUFACTURER
MANUFACTURING DATE

D9U001GE4-0101_058
REFERENCE NUMBER (PRODUCT TYPE DEPENDING ON CONFIGURATION)
SERIAL NUMBER
DO NOT POLLUTE THE ENVIRONMENT
RECYCLING SYMBOL
DO NOT OPEN
Fig. Scales label (WS17)
Scales Abbreviations
Max maximum capacity of the weighing instrument
Min minimum capacity of the weighing instrument
everi cation scale interval
Ttare value

D9U001GE4-0101_05 9
1.6 Serial Label with UDI
Pictures of serial labels below serve just for explanation of the signs and elds on the serial labels.
Fig. Serial Label with UDI (Eleganza 4 with scales)
1
1
5
5
6
6
7
7
8
8
9
9
10
10
4
4
2
2
3
3
1 Address of Distributor
2Manufacturing Date (Year-Month-Day)
3DI (Device Identier) / GTIN (Global Trade Item Number)
41D Bar code GS1-128 (Serial Number)
5 Symbols
6Conguration number
7Electrical Specication
8 Serial Number
9PI (Product Identier)
10 2D Bar Code (GS1 DataMatrix) DI+PI=UDI
Fig. Serial Label with UDI (Eleganza 4 without scales)

D9U001GE4-0101_0510
1.7 Acoustic signalisation
SOUND MEANING
CONTINUOUS SOUND overheating, scales overload, actuator overload, accumulator
overcurrent
REPEATED DISCONTINUOUS SOUND
(0,6s sound / 2,6s silence) STOP error (all STOP buttons are disabled)
(melody: 3 beeps, pause, 2 beeps, longer pause, 3 beeps,
pause, 2 beeps)
Bed Exit Alarm
DISCONTINUOUS SOUND
(duration 0,3s) conrmation
signalisation of stopping or signalisation of locked function
transition from tilt (Trendelenburg, Antitrendelenburg) to hori-
zontal position
Bed Exit Monitoring: transition from OFF to ON, transition from
PAUSE to ON
(duration 0,5s) start of service mode or end of service mode
keyboard error (positioning blocked)
(duration 3s) system error
(duration 3 min: 1,1s sound / 1,1s silence) Brake Signal
1.8 Illumination
NIGHT LIGHT
Bed illumination helps the nursing staff as well as the patient to orientate. The lowered intensity of lightning is set up after turning
the bed on. The night light is turned off during accumulator operation.
The bed is equipped with three-phase illumination:
1. Lowered intensity of illumination
2. Full intensity of illumination
3. Illumination is turned off
After pressing any button:
► The bed illumination will light up at full intensity for 10 minutes.
After 10 minutes the bed illumination will be lowered.
After disconnection of the bed from the mains illumination lights up for few seconds.
Turning off bed illumination:
► Disconnect bed from the mains.
After disconnection of the bed from the mains illumination lights up for few seconds.

D9U001GE4-0101_05 11
1.9 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 support platform
Adjustment 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.
Maximum Patient Weight Maximum Patient Weight depends on the application environ-
ment according to IEC 60601-2-52. For application environment
1 (intensive/critical care) and 2 (acute care) reduce Safe working
Load by 65 kg. For application environment 3 (long-term care) and
5 (ambulatory care) reduce Safe working Load by 35 kg.
Safe Working Load the highest allowable load on the bed (patient, mattress, accesso-
ries and the load supported by those 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 support 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.

D9U001GE4-0101_0512
AC ( ~ ) Alternating Current
ACP Attendant Control Panel
CE European Conformity
CPR Cardiopulmonary Resuscitation
dBA Sound Intensity Unit
DC ( ) Direct Current
CUC Conguration number
EMC Electromagnetic Compatibility
FET Field-effect transistor
HF High Frequency
HPL High Pressure Laminate
HW Hardware
ICU Intensive Care Unit
INT. Duty Cycle
IP Ingress Protection
IV Intravenous
LED Light Emitting Diodes
ME Medical Electrical (Equipment)
ON Activation
OFF Deactivation
ppm parts per million, millionth (1000 ppm = 0,1%)
REF Reference Number (product type depending on conguration)
SCU System Control Unit (active mattress)
SN Serial Number
SW Software
SWL Safe Working Load
UDI Unique Device Identication (for medical devices)
USB Universal Serial Bus
WEEE Waste Electrical and Electronic Equipment
1.10 Abbreviations

D9U001GE4-0101_05 13
2 Safety Instructions
WARNING!
Eleganza 4 bed should be left in its lowest position when the patient is unattended in order to reduce risk of
injury due to falls!
WARNING!
Siderails of Eleganza 4 should be located in the „up“ position to reduce the risk of the patient accidentally
slipping or rolling off the mattress!
WARNING!
Incompatible siderails and mattresses can cause an entrapment hazard!
WARNING!
Inappropriate handling of the power supply cord, e. g. by kinking, shearing or other mechanical damages is
hazardous!
WARNING!
When routing cables from other equipment in the Eleganza 4 bed avoid squeezing those between parts of the
Eleganza 4 bed!
WARNING!
Eleganza 4 bed should not be used with bed hoists and bed lifts!
WARNING!
The bed is intended for adults.
►Follow the chapter Intended use.
WARNING!
Incompatible mattresses can create hazards.
WARNING!
To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective
earth.
WARNING!
No modication of this equipment is allowed.
WARNING!
Do not modify this equipment without authorization of the manufacturer.
WARNING!
If this equipment is modied, appropriate inspection and testing must be conducted to ensure continued safe
use of the equipment.
WARNING!
An additional multiple socket-outlet or extension cord shall not be connected to the medical electrical system.

D9U001GE4-0101_0514
WARNING!
During specic investigations or treatments the signicant risks of reciprocal interference posed by ME equip-
ment may occur.
► 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 support 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 support 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.
► Enable or disable functions on Patient Control Panels using the iBoard Standard Attendant Control Panel as appropriate
for the patient’s physical and mental state. Verify that the function is actually disabled.
► Ensure that siderails are operated exclusively by healthcare personnel.
► Never use the bed in areas where there is a hazard of explosion.
► 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 for bed 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 support platform) unless these parts are
designed 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, handset 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.

D9U001GE4-0101_05 15
► Before setting the Extra Low position, ensure there is no risk of any parts of the bed colliding with servers,
accessories or body parts.
► Close Linen Shelf before using the Anti-Trendelenburg Tilt or Cardiac Chair Position.
3 Intended Use
Eleganza 4 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 4 (only version with scales) is equipped with weighing system
designed for weighing patients. Eleganza 4 is compatible with mattresses approved by the manufacturer.
Eleganza 4 must be used exclusively by or under supervision of trained and qualied nursing personnel.
Eleganza 4 is suitable for:
■Patients
□ Standard bed:
● With weight ≥ 40 kg
● With height ≥ 146 cm
● With BMI ≥ 17
□ 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 4 beds
■Location
□ The bed is determined for application environment 1 and 2 according to IEC 60601-2-52.
Other uses of Eleganza 4 bed are not allowed!
3.1 Contraindications
Staff expert assessment is needed to consider all individual cases of contraindications!
Certain bed positions are not suitable for specic diagnosis/medical conditions. Fowler position is not suita-
ble for spinal cord injuries! Trendelenburg position is not suitable for patients with higher intracranial pressu-
re!
Length adjustment of the bed must be proportional to the height of patient!
Risk of trapping or squeezing because of patient´s body constitution disproportionate to the size of mattress
support platform!

D9U001GE4-0101_0516
4 Product Description
1. Removable Head Board
2. Head Siderail
3. Mobi-Lift Handle - Bed Height
4. Patient Control Panel
5. Foot Siderail
6. Removable Foot Board
7. Corner Bumper
8. Foot Board Lock
9. Linen Holder
10. Castor Control Lever
11. Foot Switch - Bed Height
12. Four-part Mattress support platform with Ergoframe® System
13. Siderail Release Mechanism
14. Accessory Rail
15. CPR Lever – Backrest Release
16. Castor
17. Accessory Adaptor
18. Nurse Control Panel
19. iBoard Basic
Fig. Bed Overview (Eleganza 4)
111213 10 9141516
7
8
17
18
19
64 531 2

D9U001GE4-0101_05 17
5 Technical Specication
All technical data are rated data and are subject to construction and manufacturing tolerances.
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 support platform Frame, Covers and all Movable Parts
■Head and Foot End
■Siderails
■Mobi-Lift® Handles
■Handset
■Patient Control Panels
5.2 Scales
Accuracy of displayed weight values:
■0,5 kg
■Scales Class III
5.3 Mechanical Specications (Eleganza 4)
Parameter Value
External Dimensions in Standard Bed Position (length x width) 217,5 cm x 100 cm
Maximum Siderail Height above Mattress support platform 45 cm
Bed Extension 11 cm, 22 cm
Maximum Dimensions of Mattress (length x width) 208 cm x 90 cm
Maximum Mattress Height 23 cm
Clearance of Undercarriage 15 cm
Castor diameter 15 cm
Minimum-Maximum Mattress support platform Height (above oor,
without Mattress)
41 cm - 79 cm
Ergoframe (Backrest/Thighrest) 7,4 cm / 4 cm
Maximum Backrest Angle 65°
Maximum Thighrest Angle 25°
Maximum Calfrest Angle 20°
Angle between Calfrest and Thighrest 225°
Trendelenburg Angle 14°
Anti-Trendelenburg Angle 14°
Bed Weight (depending on conguration) 156 - 190 Kg
SWL (Bed Safe Working Load) 250 Kg
SWL (Lifting Pole Safe Working Load) 75 Kg
Maximum Patient Weight 185 Kg
Sound Pressure Level 57 dBA
Minimum Sound Pressure Level of Bed Exit Alarm 60 dBA

D9U001GE4-0101_0518
5.4 Environment Conditions
Use Conditions
Ambient Temperature 10°C - 40°C
Relative Humidity 30% - 75 %
Atmospheric Pressure 795 hPa - 1060 hPa
Storage and Transport Conditions
Ambient Temperature -20°C - 50°C
Relative Humidity 20% - 90 %
Atmospheric Pressure 795 hPa - 1060 hPa
5.5 Electrical Specications (Eleganza 4)
Input Voltage
Version 1
Version 2
230 V AC, 50/60 Hz
120 V AC, 50/60 Hz
Maximum Power Input 370 VAC
Ingress Protection (EN 60529) IP X4
Protection Class Class I
Electrical Motor Duty Cycle 2 minutes ON /18 minutes OFF
Accumulator Pb AKU 2 x 12 V / 1,2 Ah / Fuse 15 A
Fuse
Version 1
Version 2
2 x T1.6A L 250V for 230 V
2 x T3.15A L 250V for 120 V
NOTE Upon request, LINET ® can deliver hospital beds with electrical specications that comply with regional standards (custom
voltage, different mains plugs).
5.6 Electromagnetic Compatibility
Bed is intended for hospitals except for near active HF surgical equipment and the RF shielded room of a medical system
for magnetic resonance imaging, where the intensity of EM disturbances is high.
Bed has dened no essential performance.
WARNING!
It is recommended to avoid the use of this device next to or in block with other device, because it could lead to
improper operation. If such use is needed, this device and the other equipment should be under surveillance
to verify proper operation.
List of used cables:
► Mains cable, maximum length 6 m
► Attendant Control Panel, maximum length 3m
► Handset, maximum length 3m
WARNING!
Use of the accessories, converters and other cables, than specied and provided by manufacturer of this bed
could lead to increase of electromagnetic emission or lower the electromagnetic immunity of this bed and lead
to improper operation.
WARNING!
Mobile RF communication device (including end use devices like antenna cables and external antenna) should
not be used closer than 30 cm (12 inches) from any part of this bed Eleganza 4, including cables specied by
manufacturer. Otherwise this could lead to deterioration of functionality of this bed.
WARNING!
Do not overload the bed (SWL), respect the duty cycle (INT.) and consider chapter 19 Maintenance in order to
maintain the basic safety with regard to electromagnetic disturbances for the expected service life.

D9U001GE4-0101_05 19
5.6.1 Manufacturer instructions - electromagnetic emissions
Emission Test Compliance
RF emissions
CISPR 11
Group 1
RF emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Class A
Voltage uctuations / icker emissions
IEC 61000-3-3
Complies
5.6.2 Manufacturer instructions - electromagnetic susceptibility
Immunity Tests Compliance level
Electrostatic discharge (ESD)
IEC 61000-4-2
± 8 kV for contact discharge
± 15 kV for contact discharge
Radiated RF
IEC 61000-4-3
Proximity elds from RF wireless communications equipment
IEC 61000-4-3
3 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz
See Table 1
Fast electrical transients / burst
IEC 61000-4-4
±2 kV for power line
repetition frequency 100 kHz
Surge
IEC 61000-4-5
± 1 kV Line-to-line
± 2 kV Line-to-ground
Conducted RF
IEC 61000-4-6
3 V (0,15 MHz – 80 MHz)
6 V in ISM bands between 0,15 MHz and 80 MHz
80 % AM at 1 kHz
Power frequency (50/60 Hz) magnetic eld
IEC 61000-4-8
30 A/m
Voltage dips, short interruptions on power supply input lines
IEC 61000-4-11
0 % UT; 0,5 cycle
At 0°, 45°, 90°, 135°, 180°, 225°, 270° a 315°
0 % UT; 1 cycle and 70 % UT; 25/30 cycle
Single phase: at 0°
0 % UT; 250/300 cycle

D9U001GE4-0101_0520
Table 1 - IMMUNITY to RF wireless communications equipment
Test frequency (MHz) Band (MHz) Service Modulation Immunity Test Level
V/m
385 380 - 390 TETRA 400 Pulse modulation 18 Hz 27
450 430 - 470 GMRS 460, FRS 460 FM ± 5 kHz deviation 1
kHz sine
28
710
745
780
704 - 787 LTE band 13, 17 Pulse modulation 217
Hz
9
810
870
930
800 - 960 GSM 800/900, TETRA
800, iDEN 820, CDMA
850,
LTE band 5
Pulse modulation 18 Hz 28
1 720
1 845
1 970
1 700 - 1 990 GSM 1800; CDMA
1900; GSM 1900;
DECT; LTE band 1, 3,
4, 25; UMTS
Pulse modulation 217
Hz
28
2 450 2 400 - 2 570 Bluetooth, WLAN,
802.11 b/g/n, RFID
2450,
LTE band 7
Pulse modulation 217
Hz
28
5 240
5 500
5 785
5 100 - 5 800 WLAN 802.11 a/n Pulse modulation 217
Hz
9
NOTE There are applied no deviations to requirements of IEC 60601-1-2 ed. 4
NOTE There are no known other measures for keeping the basic safety based on EMC phenomena.
NOTE Beds equipped with communication module meet standard for IEEE 802.11 b/g/n (2400,0 MHz – 2483,5 MHz, modulation
DSSS (IEEE 802.11 b ), OFDM (IEEE 802.11 g/n) 20MHz bandwidth, EIRP = 0,34 W).
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 4 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 4 is not suitable for indoor environments containing ammable gases (except oxygen cylinders).