LINET ELEGANZA 5 Parts list manual

User Manual and Technical
Description
ELEGANZA 5
Positionable Bed for Intensive Care
D9U001GE5-0110
Version: 06
Publication Date: 2018-10
and OptiCare integrated mattress replacement system

D9U001GE5-0110_062
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
D9U001GE5-0110
Version: 06
Publication Date: 2018-10
Copyright © LINET, s.r.o., 2018
Translation © LINET, 2018
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.

D9U001GE5-0110_06 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 and Labels on the Bed .................................4
1.5 Symbols and Labels on the Mattress .......................... 7
1.6 Serial Labels with UDI................................................. 9
1.7Acoustic signalisation.................................................. 11
1.8 Illumination.................................................................. 11
1.9 Denitions ................................................................... 12
1.10 Abbreviations ............................................................12
2 Safety Instructions.......................................................13
3 Intended Use ................................................................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 5) ..................... 17
5.4 Environment conditions (Eleganza 5) ......................... 18
5.5 Electrical Specications (Eleganza 5)......................... 18
5.6 Mechanical Specications (OptiCare)......................... 18
5.7 Environment conditions (OptiCare)............................. 18
5.8 Electrical Specications (OptiCare) ............................19
5.9 Electromagnetic Compatibility.....................................19
5.9.1 Manufacturer instructions - electromagnetic emissions
...........................................................................................19
5.9.2 Manufacturer instructions - electromagnetic susceptibility
..........................................................................................20
6 Use and Storage Conditions ....................................... 21
7 Scope of Delivery and Bed Variants...........................21
7.1 Delivery ....................................................................... 21
7.2 Scope of Delivery........................................................ 21
7.3 Eleganza 5 Variants ....................................................21
8 Initial Instructions ........................................................ 22
8.1 Battery Activation ........................................................22
8.2 Putting into Service ..................................................... 23
8.2.1 Potential Equalisation ..............................................24
8.3 Before Use .................................................................. 24
8.4Transport..................................................................... 24
9 Power Supply Cord (Mains Power Cable).................. 25
10 Battery.........................................................................25
10.1 Replacing the battery ................................................26
10.2 Removing the Bed from Service ............................... 27
10.3 Deactivating the Battery............................................ 27
11 Manipulation ...............................................................27
11.1 Control Elements.......................................................27
11.1.1 iBoard Standard .....................................................28
11.1.2 Additional Supervisor Panel ...................................35
11.1.3 Handset (optional)..................................................36
11.1.4 Integrated Control Panels for Patient .....................37
11.1.5 Foot Control Bed Height (optional).........................38
11.1.6 Foot Control Lateral Tilt (standard).........................38
11.2 Bed Positioning .........................................................39
11.2.1 Backrest .................................................................39
11.2.2 Thighrest ...............................................................40
11.2.3 Calfrest ..................................................................41
11.2.4 Bed Height.............................................................. 41
11.2.5Autocontour ............................................................ 43
11.2.6 Emergency Trendelenburg Position .......................44
11.2.7Anti-Trendelenburg and Trendelenburg Tilt ............44
11.2.8 Examination Position..............................................45
11.2.9 Bed Extension ........................................................46
11.2.10 CPR Position ........................................................46
11.2.11 Cardiac Chair Position..........................................47
11.2.12 Mobilisation Position............................................. 47
11.2.13 Lateral Tilt.............................................................48
11.3 Scales Control ...........................................................49
11.4 Bed Exit Monitoring ...................................................51
11.5 CPR Backrest Release.............................................. 54
11.6 Castor Control ...........................................................54
11.7 Siderails..................................................................... 55
12 Equipment ..................................................................56
12.1 i-Brake® (optional) .....................................................56
12.2 Retractable Fifth Castor (optional) ............................ 56
12.3 i-Drive Power (optional) ............................................56
12.3.1 i-Drive Power Activation/Deactivation ....................58
12.3.2 Powered Drive .......................................................59
12.3.3 Braking................................................................... 59
12.3.4 Free Drive .............................................................. 60
12.4 Mobi-Lift® (optional) ...................................................61
12.5 Safestop (optional).................................................... 61
12.6 X-Ray Lung Examination (optional) .......................... 62
12.7 Nurse Call ................................................................. 63
13 Mattress ...................................................................... 64
13.1 Passive Mattress.......................................................64
13.2 Active Mattress (not integrated) ................................ 64
13.3 OptiCare (integrated mattress) .................................65
13.3.1 Intended Use..........................................................65
13.3.2 Contraindications ................................................... 65
13.3.3 Installation of OptiCare ..........................................67
13.3.4 Installation of SCU (System Control Unit).............. 68
13.3.5 Replacing the mattress ..........................................68
13.3.6 Preparing OptiCare for patient ............................... 69
14Accessories ................................................................75
14.1 Lifting Pole ................................................................75
14.2 Hercules.................................................................... 76
14.3 Infusion Stand ........................................................... 77
14.4 Oxygen Bottle Holder................................................ 78
14.5 Ventilation Circuit Holder...........................................79
14.6 Writing Shelf..............................................................80
14.7 Monitor Shelf............................................................. 80
14.8 Protector ...................................................................81
14.9 USB Connector ......................................................... 82
14.10 Urine Bag Holder ....................................................82
15 Cleaning/Disinfection ................................................ 83
15.1 Cleaning (Eleganza 5) ..............................................83
15.1.1 Daily Cleaning........................................................ 84
15.1.2 Cleaning before Changing Patients .......................84
15.1.3 Complete Cleaning and Disinfection ...................... 84
15.2 Cleaning (OptiCare) .................................................. 85
15.2.1 Routine Cleaning and Disinfection ......................... 85
15.2.2 Full Cleaning and Disinfection ...............................86
15.2.3 Removing the Mattress Cover: ..............................86
15.2.4 Machine Washing Symbioso Hi-MVP Slippy Mattress
Cover................................................................................87
16 Troubleshooting .........................................................88
17 Maintenance ............................................................... 89
17.1 Monthly maintenance................................................ 89
17.2 Maintenance every 12 months.................................. 89
17.2.1 Spare Parts ............................................................ 89
17.2.2 Completeness ........................................................ 89
17.2.3 Wear.......................................................................89
17.2.4 Functioning ............................................................89
17.2.5 Electric Control.......................................................90
17.2.6 Castors...................................................................90
17.2.7Accessories............................................................ 90
17.3 Safety Checks........................................................... 90
17.4 Maintenance OptiCare .............................................. 91
17.5 Linet ® Service Department.......................................91
18 Disposal ...................................................................... 91
18.1 Environment Protection.............................................91
18.2 Disposal .................................................................... 91
18.2.1 Eleganza 5 ............................................................. 92
18.2.2 OptiCare.................................................................92
Table of Contents

D9U001GE5-0110_064
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
1.4 Symbols and Labels on the Bed
READ INSTRUCTIONS FOR USE
GO BUTTON (PRESS TO ACTIVATE CONTROL ELEMENT)
STOP BUTTON (PRESS TO INTERRUPT BED POSITIONING)
19 Warranty......................................................................92
20 Standards and Regulations ......................................93
20.1 Eleganza 5 ................................................................ 93
20.2 OptiCare....................................................................93
20.3 Manufacturer............................................................. 93

D9U001GE5-0110_06 5
SAFE WORKING LOAD
PHYSICAL DESCRIPTION OF AN ADULT
(DESIGNATION OF MEDICAL BED FOR ADULTS)
USE MATTRESS RECOMMENDED BY MANUFACTURER
DO NOT PUT ANY OBJECTS ON UNDERCARRIAGE
CALFREST LOAD LIMIT
WARNING AGAINST CRUSHING OR TRAPPING OF HANDS
JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION
CPR LEVER
GENERAL WARNING SIGN
CAUTION
TYPE B APPLIED PARTS
THERMAL PROTECTION FOR TRANSFORMER

D9U001GE5-0110_066
SAFETY ISOLATING TRANSFORMER (GENERAL)
FOR INDOOR USE ONLY
MAXIMUM PATIENT WEIGHT
WEIGHT OF BED
MET MARK FOR Eleganza 5
CE MARK FOR OptiCare
WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,
DO NOT PUT INTO THE HOUSEHOLD WASTE)
RECYCLING SYMBOL
RECYCLING SYMBOL
RECYCLING SYMBOL
DO NOT OPEN

D9U001GE5-0110_06 7
MANUFACTURER
MANUFACTURING DATE
REFERENCE NUMBER (PRODUCT TYPE DEPENDING ON CONFIGURATION)
SERIAL NUMBER
1.5 Symbols and Labels on the Mattress
DO NOT IRON!
DO NOT USE PHENOL!
DO NOT WRING!
REGULARLY INSPECT THE INSIDE OF THE COVER FOR CONTAMINATION
MACHINE WASH AT MAX. 71°C FOR 3 MINUTES

D9U001GE5-0110_068
TUMBLE DRY ON LOW HEAT SETTING (MAX. 60°C)
HANDWASH WITH DETERGENT
(INITIAL TEMPERATURE OF HOT WATER SHOULD NOT EXCEED 50°C)
DISINFECT USING SOLUTION CONTAINING LESS THAN 1000 ppm OF CHLORINE
(REFER TO INSTRUCTIONS FOR USE)
WIPE WITH WATER
DRY
COVER MATERIALS ARE FIRE RESISTANT TO BS7175, SOURCE 0, 1 AND 5
MATTRESS FOOT PART (OptiCare)

D9U001GE5-0110_06 9
Fig. Serial Label with UDI (Eleganza 5 with scales)
1
5 6 789 10 4
2 3
1.6 Serial Labels with UDI
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

D9U001GE5-0110_0610
1
Fig. Serial Label with UDI (OptiCare - SCU)
8
9
4
2
3
10
Fig. Scales label (WS17)
8
9
4
2
3
10
Fig. Serial Label with UDI (OptiCare - mattress)
1
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)
8 Serial Number
9PI (Product Identier)
10 2D Bar Code (GS1 DataMatrix) DI+PI=UDI

D9U001GE5-0110_06 11
1.7 Acoustic signalisation
SOUND MEANING
CONTINUOUS SOUND overheating, scales overload, actuator overload, battery over-
current
BEEP + CONTINUOUS SOUND lateral tilt + head siderail or foot siderail in down position
REPEATED DISCONTINUOUS SOUND
(0,6s sound / 2,6s silence) STOP error (all STOP buttons are disabled)
(0,6s sound / 0,6s silence) Bed Exit Alarm
DISCONTINUOUS SOUND
(duration 0,3s) conrmation
signalisation of stopping or signalisation of locked function
lateral tilt 15° achieved
transition from tilt (lateral tilt, Trendelenburg, Antitrendelenburg)
to horizontal 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 Alarm
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 battery 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 17 minutes.
After 17 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.

D9U001GE5-0110_0612
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 custo-
mer 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 Adjus-
tment whose effect is the elimination of pressure on the patient´s abdo-
men and pelvic area and frictional forces on the patient‘s back and legs.
Maximum Patient Weight Maximum Patient Weight depends on the application environment accor-
ding 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 envi-
ronment 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, accessories 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.
1.10 Abbreviations
AC Alternating Current
CE European Conformity
CPR Cardiopulmonary Resuscitation
dB Sound Intensity Unit
DC Direct Current
CUC Conguration number
EMC Electromagnetic Compatibility
FET Field-effect transistor
HF High Frequency
HPL High Pressure Laminate
ICU Intensive Care Unit
INT. Duty Cycle
IP Ingress Protection
IV Intravenous
LED Light Emitting Diodes
ME Medical Electrical (Equipment)
MET MET Laboratories testing and certifying for the U.S. market
ppm parts per million, millionth (1000 ppm = 0,1%)
REF Reference Number (product type depending on conguration)
SCU System Control Unit
SN Serial Number
SWL Safe Working Load
UDI Unique Device Identication (for medical devices)
USB Universal Serial Bus
WEEE Waste Electrical and Electronic Equipment

D9U001GE5-0110_06 13
2 Safety Instructions
WARNING!
Eleganza 5 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 5 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 5 bed avoid squeezing those between parts of the
Eleganza 5 bed!
WARNING!
Eleganza 5 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.

D9U001GE5-0110_0614
WARNING!
During specic investigations or treatments the signicant risks of reciprocal interference posed by ME equi-
pment 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 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 Standard 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.
► Use the mattress system exclusively with the correct mains supply.

D9U001GE5-0110_06 15
► 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 for OptiCare).
► Do not use the SCU (System Control Unit) near ammable gases (This does not apply to oxygen cylinders.).
► Never use the mattress replacement system near radiators or other heat sources.
► Never cover the SCU while in use.
► Never cover the lter of SCU while in use.
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 pa-
tients. Eleganza 5 is compatible with OptiCare integrated mattress replacement system. The OptiCare mattress system is
intended to aid in the prevention and treatment of pressure injuries of patients. The OptiCare mattress can only be used
when installed on a Linet Eleganza 5 bed frame.
Eleganza 5 must be used exclusively by or under supervision of trained and qualied nursing personnel.
Eleganza 5 with OptiCare integrated mattress system 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)
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!
■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 IEC 60601-2-52.
NOTE For information concerning uses other than those, please contact Linet ®.

D9U001GE5-0110_0616
4 Product Description
1. Removable Foot Board
2. Split Siderail – Middle Siderail with Integrated Control Panels for Patient
3. Split Siderail – Head Siderail with Integrated Control Panels for Patient
4. Removable Head Board
5. iBoard Standard
6. CPR Lever – Backrest Release
7. Poles Adaptor
8. Foot Switch (Lateral Tilt)
9. Siderail Release Lever
10. Foot Switch (Bed Height)
11. Four-part Mattress Platform with Ergoframe® System (under the mattress)
12. Castor Control Lever
13. Mobi-Lift® Handle
14. Castor
15. Foot Board Safety Lock
16. Bumper
Fig. Bed Overview (Eleganza 5)
5
6
7
13 911 10 8
12
16
15
14
1 2 43

D9U001GE5-0110_06 17
5 Technical Specication
All technical data are rated data and are subject to construction and manufacturing tolerances.
WARNING!
If Eleganza 5 bed is used with OptiCare integrated mattress system respect values of mechanical and
electrical specications which can harm none of them!
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
■Mobi-Lift 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 14,2 cm (minimum), 45 cm (maximum)
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 (with fth castor 11,3 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 30°
Angle between Thighrest and Calfrest 120°
Lateral Tilt Adjustment +15°/-15°
Trendelenburg/Anti-Trendelenburg Position (Angle) +14°/-14°
Bed Weight in Basic Conguration (depending on conguration,
without mattress)
210 Kg (462 lbs) - 248 Kg (545,6 lbs)
SWL (Bed Safe Working Load) 250 Kg (550 lbs)
SWL (Lifting Pole Safe Working Load) 75 Kg
Maximum Patient Weight 185 Kg (407 lbs)
Application Environment in accordance with IEC 60601-2-52 1, 2

D9U001GE5-0110_0618
5.4 Environment conditions (Eleganza 5)
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 5)
Input Voltage, Frequency 230 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
Battery Pb AKU 2 x 12 V / 1,2 Ah / Fuse 15A
Fuse 2 x T2.0A 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).
5.6 Mechanical Specications (OptiCare)
Parameter Value
External Dimensions
Inated Mattress 214 cm x 86 cm x22 cm
SCU 36 cm x 22 cm x10 cm
Weight
Inated Mattress 10 kg (22 lbs)
SCU 6 kg (13.1 lbs)
Ination time after storage max. 15 min (typical < 10 min)
CPR deation time (depending on patient weight, chosen mode -
optimization or maximum internal pressure - and on type of CPR
- electric or manual)
max. 30 s
Max. Mattress Load 250 kg / 550 lbs / 39 stones
Min. Mattress Load 40 kg
5.7 Environment conditions (OptiCare)
Use Conditions
Ambient Temperature 10°C - 40°C
Relative Humidity 30% - 75 %
Atmospheric Pressure 700 - 1060 hPa
Remain Inated in Transport Mode 12 hours (whem starting from Maximum Inate Mode)
Noise Level max. 45 dBa (normal operation without alarm)
Storage and Transport Conditions
Ambient Temperature -40°C - 70°C
Relative Humidity 10% - 100 % (non-condensing)
Atmospheric Pressure 500 - 1060 hPa

D9U001GE5-0110_06 19
5.8 Electrical Specications (OptiCare)
Input Voltage, Frequency 100/127 VAC, 50/60 Hz (Model 110V)
Maximum Power Input max. 40 VA (when operating from mains supply)
Ingress Protection (EN 60529) IPX4
Protection Class Class I with Applied Parts Type B
Electrical Safety in conformity with EN 60601-1
Fuse 2 x T1A Anti-surge Fuse
5.9 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 surveillan-
ce to verify proper operation.
List of used cables:
► Mains cable, maximum length 6 m
► Additional Supervisor 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 5, 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 17 Maintenance in order to
maintain the basic safety with regard to electromagnetic disturbances for the expected service life.
5.9.1 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

D9U001GE5-0110_0620
5.9.2 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
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).