Instructions for Use

and Technical Description

ELEGANZA 2
A smart acute bed

D9U001GRA-0101

Version: 12

Publication Date: 2021-09

Manufacturer:

L I N E T spol. s r.o.
Želevčice 5
274 01 Slaný

Tel.: +420 312 576 111

Fax: +420 312 522 668

E-mail: [email protected]
http://www.linet.com
Service department: [email protected]

Eleganza 2
A smart acute bed

Author: L I N E T, s.r.o.
Related links: www.linet.cz

D9U001GRA-0101
Version: 12
Publication Date: 2021-09

Copyright © L I N E T, s.r.o., 2021

Translation © L I N E T, 2021

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 the instructions for use that relate to the product´s technical regulations. It is for this reason that the con-
tents of the instructions for use 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.

2 D9U001GRA-0101_12
Table of Contents 13.1 Siderails.....................................................................34
13.1.1 Collapsible siderail (3/4 siderail)............................. 35
13.1.2 Split plastic siderails...............................................36
1 Symbols and Definitions..............................................4 13.1.3 Split plastic siderails with Junior Kit....................... 38
1.1 Warning Notices...........................................................4 13.2 Castor Control and Bed Transport............................ 39
1.1.1 Types of Warning Notices.........................................4 13.3 CPR backrest release................................................40
1.1.2 Structure of Warning Notices....................................4 13.4 Mattress Platform.......................................................41
1.2 Instructions...................................................................4 13.4.1 Auto-Regression.....................................................41
1.3 Lists..............................................................................4 13.4.2 Mechanical Calfrest Adjustment.............................. 41
1.4 Symbols on the Package.............................................5 13.4.3 Mattress Platform Extension................................... 41
1.5 Symbols and Labels on the Bed..................................6 13.4.4 Shortened Bed........................................................44
1.6 Serial Label with UDI...................................................8 13.5 Control Elements.......................................................45
1.7 Acoustic signalisation (Eleganza 2 with PB43 control unit) 13.5.1 ACP – Attendant Control Panel............................... 46
..........................................................................................8 13.5.2 Attendant Control Panel with SafeSense® 3 Control
1.8 Acoustic signalisation (Eleganza 2 with PB11 control unit) ..........................................................................................49
..........................................................................................8 13.5.3 Handset...................................................................55
1.9 Visual signalisation......................................................9 13.5.4 Satellite Control Panel (optional)............................ 56
1.9.1 Mains Power LED (Attendant Control Panel)............ 9 13.5.5 Foot Control............................................................57
1.9.2 Accumulator Indicator (Attendant Control Panel)...... 9 13.5.6 Control Element Integrated in Siderail (optional).... 58
1.9.3 Lock LED (Attendant Control Panel)......................... 9 14 Equipment...................................................................59
1.9.4 Illumination................................................................10 14.1 Accessory Rails..........................................................59
1.10 Definitions..................................................................11 14.2 Urinary bottle holder...................................................59
1.11 Abbreviations..............................................................12 14.3 Redon bottle holder....................................................60
2 Safety Instructions........................................................13 14.4 Mobi-Lift®...................................................................60
3 Intended use (Eleganza 2)............................................16 14.5 Angle indicators..........................................................61
3.1 User population............................................................16 14.6 X-Ray Backrest (optional)..........................................62
3.2 Contraindications.........................................................16 14.7 SafeSense® 3 ready bed...........................................63
3.3 Operator.......................................................................16 15 Mattress.......................................................................64
4 Intended use (Eleganza 2 with Junior Kit).................. 16 16 Accessories.................................................................64
4.1 User population............................................................16 16.1 Lifting Pole.................................................................65
4.2 Contraindications.........................................................16 16.2 Infusion Stands..........................................................66
4.3 Operator.......................................................................17 16.3 External holder for infusion stand/pump.................... 66
5 Incorrect Use.................................................................17 16.4 Oxygen Bottle Holder.................................................67
6 Product Description......................................................18 16.5 Handy box – storage pocket for siderails................... 67
6.1 Eleganza 2 (1GR) – Split Plastic Siderails................... 18 16.6 Head Board and Foot Board Holder.......................... 68
6.2 Eleganza 2 (1GR) – Single Collapsible Siderails......... 19 16.7 Name holder..............................................................68
7 Technical Specification................................................20 16.8 Chart Holder...............................................................68
7.1 Applied parts type B....................................................20 16.9 Handset Holder..........................................................69
7.2 Mechanical Specification (standard version).............. 20 16.10 Monitor Shelf............................................................69
7.3 Mechanical Specification (shortened version)............ 21 16.11 Compressor Holder..................................................70
7.4 Environment Conditions...............................................21 16.12 Towel holder.............................................................70
7.5 Electrical Specifications (Eleganza 2).......................... 22 16.13 Extension Holder......................................................70
7.6 Electromagnetic compatibility......................................22 16.14 Soft Guards for Siderails.........................................71
7.6.1 Manufacturer instructions - electromagnetic emissions 16.15 Protector®...............................................................71
..........................................................................................23 16.16 Siderail extension – „Extender®“ (SR55)................. 73
7.6.2 Manufacturer instructions - electromagnetic susceptibility 16.17 SafeSense..............................................................74
..........................................................................................23 16.18 SafeSense® 3..........................................................75
8 Use and Storage Conditions........................................24 17 Cleaning/Disinfection.................................................76
9 Scope of Delivery and Bed Variants............................ 25 17.1 Safety Instructions for Cleaning and Disinfection of the Bed
9.1 Scope of Delivery.........................................................25 ..........................................................................................77
9.2 Bed Variants.................................................................25 17.2 General Instructions for Cleaning and Disinfection.... 77
10 Putting into Service....................................................26 17.2.1 Daily Cleaning.........................................................77
10.1 Accumulator Activation...............................................27 17.2.2 Cleaning before Changing Patients........................ 77
10.1.1 Placement of Control Section................................. 27 17.2.3 Complete Cleaning / Cleaning before First Use...... 77
10.1.2 Removing Isolating Foil...........................................27 17.2.4 Cleaning of Spilled Fluids....................................... 77
10.1.3 Isolating Foil............................................................27 17.2.5 Damaged Foam Mattress....................................... 77
10.2 Head Board and Foot Board......................................28 17.3 Mode of Cleaning and Disinfection............................ 78
10.3 Mattress Platform.......................................................29 17.4 Steam Cleaning........................................................79
10.4 Potential Equalisation................................................30 18 Troubleshooting..........................................................80
10.5 Before Use.................................................................30 19 Maintenance................................................................81
10.6 Transport....................................................................31 19.1 Regular maintenance.................................................81
10.7 Firmware....................................................................31 19.2 Spare Parts................................................................81
11 Power Supply Cord (Mains Power Cable)................. 31 19.3 Safety Technical Checks............................................81
12 Accumulator................................................................32 20 Disposal.......................................................................82
12.1 Status Faulty Accumulator.........................................33 20.1 Environment Protection..............................................82
12.2 Status Discharged Accumulator................................. 33 20.2 Disposal.....................................................................82
12.3 Removing the Bed from Service............................... 34 20.2.1 Within Europe.........................................................82
12.4 Deactivating the Accumulator................................... 34 20.2.2 Outside Europe.......................................................82
13 Manipulation................................................................34 21 Warranty.......................................................................83

D9U001GRA-0101_12 3
22 Standards and Regulations.......................................83
22.1 AFSSAPS Declaration...............................................84

1 Symbols and Definitions

1.1 Warning Notices
1.1.1 Types of Warning Notices
Warning notices are differentiated by the type of danger using the following signal words:

► CAUTION - risk of material damage.

► WARNING- risk of physical injury.
► DANGER - 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

4 D9U001GRA-0101_12
1.4 Symbols on the Package

FRAGILE, HANDLE WITH CARE

THIS WAY UP

KEEP DRY (PROTECT FROM HUMIDITY)

PAPER RECYCLING SYMBOL

DO NOT USE HAND TRUCK HERE

DO NOT STACK DURING STORAGE

D9U001GRA-0101_12 5
1.5 Symbols and Labels on the Bed

READ INSTRUCTIONS FOR USE

ATTENTION

THERMAL PROTECTION OF TRANSFORMER

ONLY SUITABLE FOR INDOOR USE

PROTECTION AGAINST ACCIDENTS DUE TO ELECTRICAL CURRENT – TYPE B

APPLIED PARTS

SAFETY ISOLATING TRANSFORMER, GENERAL

CE MARK OF CONFORMITY WITH EU REGULATION

JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION

SAFE WORKING LOAD

WARNING AGAINST CRUSHING OR TRAPPING

MAXIMUM WEIGHT OF PATIENT

USE MATTRESS RECOMMENDED BY MANUFACTURER

6 D9U001GRA-0101_12
 WEIGHT OF BED

DO NOT PUT ANY OBJECTS HERE

DESIGNATION OF HOSPITAL BED FOR ADULTS

EAC MARKING

WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,

DO NOT PUT INTO THE HOUSEHOLD WASTE)

MEDICAL DEVICE (COMPATIBLE WITH MEDICAL DEVICE REGULATION)

RECYCLING SYMBOL

DO NOT POLLUTE THE ENVIRONMENT

D9U001GRA-0101_12 7
1.6 Serial Label with UDI
Serial label of the Eleganza 2 is placed on the right foot end side of the mattress support platform frame. The serial label contains
information about Address of Manufacturer, Manufacturing Date (Year-Month-Day), Product Reference Number, Product Serial
Number, Global Trade Item Number (GTIN), Unique Device Identification (UDI), symbols, weight specifications and electrical speci-
fications.

1.7 Acoustic signalisation (Eleganza 2 with PB43 control unit)

SOUND MEANING
CONTINUOUS SOUND overheating
accumulator overcurrent
actuator overload
REPEATED BEEP: 0,6s sound / 2,6s silence STOP error (all STOP buttons are disabled)
REPEATED BEEP: 0,1s sound / 3s silence switching of the transformer winding error (Brazil)
BEEP lasting 0,3s confirmation
stopping or locked function
optionally: transition from tilt (Trendelenburg, Antitrendelen-
burg) to horizontal position
BEEP lasting 0,5s start of service mode or end of service mode
keyboard error (positioning blocked)
BEEP lasting 3s system error
REPEATED BEEP during 3 minutes: 1,1s sound / 1,1s silen- Brake Signal (only version with Brake Signal)
ce

1.8 Acoustic signalisation (Eleganza 2 with PB11 control unit)

There are no acoustic signals in the case of Eleganza 2 bed with PB11 control unit.

8 D9U001GRA-0101_12
1.9 Visual signalisation
1.9.1 Mains Power LED (Attendant Control Panel)
MAINS POWER LED MEANING

lit connected to the mains

flashing: 0,6s lit / 0,6s not lit keyboard error (flashing inverted to Lock LED)
error (first fault)
flashing: 0,1s lit / 0,1s not lit service mode
not lit disconnected from the mains power
transformer switching error

1.9.2 Accumulator Indicator (Attendant Control Panel)

ACCUMULATOR INDICATOR MEANING

lit accumulator disconnected or faulty

flashing: 1,6s lit / 0,2s not lit accumulator deeply discharged
flashing: 0,1s lit / 0,1s not lit accumulator discharged
flashing: 0,2s lit / 1,6s not lit accumulator is charging
not lit accumulator charged

1.9.3 Lock LED (Attendant Control Panel)

VISUAL
SIGNALISATION flashing:
lit 0,6s lit / 0,6s not lit not lit

LOCK LED

Thighrest Lock LED locked lock keyboard motion unlocked

error error blocked
Backrest Lock LED locked lock keyboard motion unlocked
error error blocked
Bed Height, Trendelenburg and An- locked lock keyboard motion unlocked
titrendelenburg Tilt Lock LED error error blocked
Foot Control Lock LED locked lock keyboard motion unlocked
error error blocked

D9U001GRA-0101_12 9
1.9.4 Illumination
The bed is equipped with three-phase illumination:

1. Full intensity of illumination

2. Lowered intensity of illumination
3. Illumination is turned off

The lowered intensity of illumination is set up after the bed is turned on.

After pressing the GO button:

► The controllers in siderails, handset, angle indicator and bed illumination will light up at full intensity.

After elapsing the GO period:

► The illumination intensity of handset, siderail controller and angle indicator will be lowered.

7 minutes after GO period has elapsed:

► The intensity of bed illumination will be lowered.

In the event any button is pressed (supervisor, handset or siderail) outside of GO period:
► The bed illumination will light up at full intensity for 10 minutes and after that, the illumination will be lowered.
► Simultaneously, the handset, siderail controller and angle indicator will light up at full intensity for 7 seconds. After that the
illumination will be lowered.

After activating the bed via the foot controller (mini GO function):
► The full intensity of bed illumination will be activated for 9 minutes and 40 seconds.

In case of pressing the foot controller once outside the active “mini GO” period:
► All the controllers (handset, siderail controllers and angle indicator) will light up at full intensity for 7 seconds and after the
illumination will be lowered.
► The full intensity of bed illumination will be activated for 10 minutes and after the illumination will be lowered.

Turning off all illumination:

► Press button (20) and all illumination on the bed (handset, siderail controllers, angle indicator and bed illumination) will be
turned off. This function is not blocked by the activation GO button.

Illuminated angle indicator:

► The bed in the lowest (safe) position is indicated by green illumination of the angle indicator.
► The bed in all other positions, except lowest position, is indicated by white illumination of the angle indicator.

10 D9U001GRA-0101_12
1.10 Definitions
Basic Bed Configuration the pricelist model configuration, not including a mattress
Bed Weight The value depends on the product configuration, accessories or customer
adjustments.
Clearance of Undercarriage the height from the floor 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 pel-
vic area and frictional forces on the patient‘s back and legs.
Maximum Patient Weight Maximum Patient Weight depends on the application environment 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 environ-
ment 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 lowest height of the patient surface with regard to the floor
► 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.
Adult Patient having a physical size equal to or more than 146 cm, a mass equal
to or more than 40 kg and a body mass index (BMI) equal to or more than 17
(according to IEC 60601-2-52).

D9U001GRA-0101_12 11
1.11 Abbreviations
AC ( ~ ) Alternating Current
ACP Attendant Control Panel
CE European Conformity
CPR Cardiopulmonary Resuscitation
dBA Sound Intensity Unit
DC ( ) Direct Current
CUC Configuration 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 configuration)
SCU System Control Unit (active mattress)
SN Serial Number
SW Software
SWL Safe Working Load
UDI Unique Device Identification (for medical devices)
USB Universal Serial Bus
WEEE Waste Electrical and Electronic Equipment

12 D9U001GRA-0101_12
2 Safety Instructions
WARNING!
Eleganza 2 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 2 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 2 bed avoid squeezing those between parts of the
Eleganza 2 bed!

WARNING!
Eleganza 2 bed should not be used with bed hoists and bed lifts!

WARNING!
The Eleganza 2 bed is intended for adults.
► Follow chapter Correct 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 modification of this equipment is allowed!

WARNING!
Do not modify this equipment without authorization of the manufacturer.

WARNING!
If this equipment is modified, appropriate inspection and testing must be conducted to ensure continued safe
use of the equipment.

D9U001GRA-0101_12 13
 WARNING!
An additional multiple socket-outlet or extension cord shall not be connected to the medical electrical system.

WARNING!
During specific investigations or treatments the significant risks of reciprocal interference posed by medical
electrical equipment may occur.

WARNING!
Length adjustment of the bed must be proportional to the height of patient!

WARNING!
Risk of trapping or squeezing because of patient´s body constitution disproportionate to the size of mattress
support platform!

WARNING!
Risk of injury or death due using of incorrect equipment!
► Always conduct the risk assessments required for the selection of suitable equipment.

WARNING!
Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the
competent authority of the Member State in which the user and/or patient is established!

WARNING!
Only authorised and trained person using the tool is allowed to change fuses and power supplies!

WARNING!
This medical device is not intended for oxygen enriched environment!

WARNING!
This medical device is not intended for use with flammable substances!

WARNING!
This medical device is not portable medical electrical equipment!

WARNING!
Make sure the duty cycle (2 min ON/18 min OFF) is not exceeded during bed positioning!

WARNING!
Patient is allowed to use selected control elements only if hospital personnel had assessed that the patient´s
physical and psychological state is in accordance with use of them and only if the hospital personnel had
trained the patient in accordance with the instructions for use!

14 D9U001GRA-0101_12
► It is necessary to read the instructions for use before operating the bed.
► Follow the instructions carefully.
► Use the bed exclusively in its original condition.
► If necessary, check the bed functions daily or at each staff rotation.
► Use the bed exclusively with the correct mains supply.
► Ensure that the bed is operated by qualified personnel only who have been trained according to the instructions for use.
► Ensure that the patient (health permitting) has been informed about the operation of the bed and all applicable safety
instructions.
► Ensure the bed is only moved or positioned upon even, hard floor surfaces.
► Replace any damaged parts immediately with original spare parts.
► Ensure maintenance and installations are performed only by qualified personnel who have been trained by the
manufacturer.
► Do not apply excess weight or load to the bed according to SWL (safe working load).
► Only one adult patient can use the bed at any time.
► Take care to avoid injuries or squeezing when operating moving parts.
► When using lifting poles or infusion stands, ensure nothing will be damaged when you move or adjust the bed.
► Ensure castors are braked when the bed is not being moved, regardless of whether the bed is occupied or empty.
► Keep the mattress platform in the lowest position at any time when the healthcare personnel are not trea- ting the patient
in order to prevent the patient from falling or sustaining injuries.
► Ensure that siderails are operated by healthcare personnel only.
► Never use the bed in areas where there is a hazard or risk of explosion.
► Enable or disable functions on the handset using the Attendant Control Panel as appropriate for the patient’s phy- sical
and mental state. Verify that the function is actually disabled.
► Never handle the mains plug with wet hands.
► Unplug the mains cable by pulling on the plug only.
► Position the mains cable so there are no loops or bends in the cable; protect the cable from mechani- cal wear and tear.
► Incorrect handling of the mains cable can cause an electric shock hazard, other serious injuries or damage to the bed.
► Ensure the specified duty cycle (on-time) is not exceeded (see INT. on product label).
► Ensure moving parts of the bed are not blocked.
► To prevent failures, use exclusively the manufacturer’s original accessories and mattresses.
► Ensure the safe working load is not exceeded.
► Adjust bed height to approx. 20 cm below maximum height when transporting the bed in order to facilitate overcoming
possible obstacles.
► Do not exceed the 75 kg safe working load of the mattress platform extension.
► Ensure the bed and its components are exclusively modified with the manufacturer´s approval.
► Any non-observance of this manual may lead to injuries or material damage.
► Ensure there is no risk of crushing or otherwise injuring the patient’s limbs (e.g. between siderails and mattress platform,
between movable parts etc.) before positioning the bed or folding down the siderails.
► Close linen shelf before using the Reverse Trendelenburg or Cardiac chair position.
► Do not put any objects (e.g. accessories, infusions, cables) between or on siderails and movable parts. Or between
mattress platform and undercarriage of the bed.
► Ensure that nobody can get injured while folding the siderails.
► Ensure no injuries will occur when folding the siderails.
► Use exclusively split plastic or split telescopic siderails for confused or disoriented patients or add Protector to the single
collapsible siderails.
► Ensure there is no risk of damaging the cables of the Attendant Control Panel or handset when they are stored on
siderails or head board and foot board.
► To prevent collisions, do not put oxygen bottle holders directly under the mattress platform.
► If the patient is left without supervision of hospital personnel during sleep, adjust the mattress platform to its lowest positi
on with straight sleeping surface in order to prevent the patient from falling or sustaining injuries.
► If the patient is left without supervision of hospital personnel during day, adjust the mattress platform to recommended
daily position (Fowler’s position) with mattress platform in lowest position and backrest adjusted to the angle of 30° in
order to prevent the patient from falling or sustaining injuries.
► The hospital personnel must consider locking all positioning functions of the bed in case the patient is left without
supervision depending on health and mental status of the patient.
► Manual positioning of parts of the bed which are designed for electronic positioning (e.g. backrest) is forbidden.
Otherwise there is a risk of damaging and dysfunction of the backrest actuator or unprompted fall of the backrest.

D9U001GRA-0101_12 15
3 Intended use (Eleganza 2)
The intended use is the hospitalization of the patient in the acute and long-term care units, which includes above all the
following aspects:
► Adjustment of the specific positions needed for the preventive reasons, routine nursing, treatments, mobilization, physio-
therapy, examinations, sleeping, and relaxation. These positions are further specified and described in the clinical evaluation of this
device, together with their potential clinical outcomes and benefits.
► Providing the safe environment for the patient during all relevant procedures. The particular requirements on patient safety
are the subject of the clinical evaluation, including evaluation of the risk/benefit ratio. The relevant safety issues are the part of the
risk management file.
► Patient in-bed indoor transport out of the patient room.
► Providing the suitable working conditions for the caregivers to perform the routine and specific tasks during the patient
hospitalization.

3.1 User population

► Adult patients (weight >= 40 kg, height >= 146 cm, BMI >= 17) in the acute and long-term care units (Application Environ-
ment 2 and 3, as in IEC 60601-2-52)
► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

3.2 Contraindications
► The medical device is not intended for the pediatric patients use.
► Certain positions are not suitable for specific diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position,
higher ICP patients vs. Trendelenburg). Staff expert assessment / nursing consideration is needed in all individual case of contrain-
dication.

3.3 Operator
► Caregiver
► Patient (based on individual patient status assessment by caregiver the patient can utilize dedicated device functions)

4 Intended use (Eleganza 2 with Junior Kit)

The intended use is the hospitalization of the patient in the acute and long-term care units, which includes above all the
following aspects:
► Adjustment of the specific positions needed for the preventive reasons, routine nursing, treatments, mobilization, physio-
therapy, examinations, sleeping, and relaxation. These positions are further specified and described in the clinical evaluation of this
device, together with their potential clinical outcomes and benefits.
► Providing the safe environment for the patient during all relevant procedures. The particular requirements on patient safety
are the subject of the clinical evaluation, including evaluation of the risk/benefit ratio. The relevant safety issues are the part of the
risk management file.
► Patient in-bed indoor transport out of the patient room.
► Providing the suitable working conditions for the caregivers to perform the routine and specific tasks during the patient
hospitalization.

4.1 User population

► Patients with length more than 125 cm in the standard care units (based on individual patient status assessment by care-
giver the patient can utilize dedicated device functions)
► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

4.2 Contraindications
► The medical device is not intended for the pediatric patients shorter than 125 cm.
► Limited patient handling leads to development of pressure injury.
► Certain positions are not suitable for specific diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position,
higher ICP patients vs. Trendelenburg). Staff expert assessment / nursing consideration is needed in all individual case of contrain-
dication.

16 D9U001GRA-0101_12
4.3 Operator
► Caregiver
► Patient (based on individual patient status assessment by caregiver the patient can utilize dedicated device functions)

5 Incorrect Use
Eleganza 2 is not suitable for:

■ Patients
□ Not fulfilling conditions stated in chapter “Intended use”
■ Use
□ Home care
□ Other than described in the instructions for use

NOTE For information concerning uses other than those outlined in the “Intended use” section above, please contact LINET®.

LINET®’s efforts in research, design and manufacture ensure LINET® products are of the highest quality and fit for their intended
purpose. However, LINET® can take no responsibility for any damage to the products or any harm to patients, staff or other indivi-
duals resulting from:
■ Not following the instructions in the manual, including warning notices.
■ Using the product for a purpose other than the intended purpose stated in the relevant documentation provided by
LINET® (see Intended use).

D9U001GRA-0101_12 17
6 Product Description
6.1 Eleganza 2 (1GR) – Split Plastic Siderails

Fig. Overview Eleganza 2 – Split Plastic Siderails

1. Foot Board
2. Siderail release mechanism with SoftDrop function
3. Mattress platform with removable plastic sections
4. Integrated MobiLift controller in siderails
5. Integrated control panel in siderails
6. Split plastic siderails
7. Head Board
8. CPR control lever – backrest release
9. Castor control lever
10. Castor 150 mm (Tente Motion with plastic cover)
11. Angle indicator
12. Fifth castor
13. Foot control
14. Linen/Attendant Control Panel holder
15. Foot board unlocking mechanism
16. Protective bumber

18 D9U001GRA-0101_12
6.2 Eleganza 2 (1GR) – Single Collapsible Siderails

Fig. Overview Eleganza 2 – Single Collapsible Siderails

1. Foot Board
2. Siderail release mechanism
3. Single collapsible siderails
4. Mattress platform with mattress
5. Head Board
6. CPR control lever – backrest release
7. Castor 150 mm (Tente Motion with plastic cover)
8. Accessory rail
9. Fifth castor
10. Foot control
11. Castor control lever
12. Protector®
13. Linen/Attendant Control Panel holder
14. Foot board unlocking mechanism
15. Protective bumper

D9U001GRA-0101_12 19
7 Technical Specification
7.1 Applied parts type B
All the accesories the patient can reach are type B applied parts.

List of type B applied parts:

■ ACP Attendant Control Panel

■ Handset
■ Satellite controller
■ Siderails
■ Integrated siderail controllers
■ Head board and Foot board
■ Mattress platform

All technical data are rated data and are subject to construction and manufacturing tolerances.

7.2 Mechanical Specification (standard version)

Parameter Value
External dimensions
With split plastic siderails and standard bumpers (10 cm) 223,3 cm x 99,5 cm
Mattress dimensions 200 cm x 90 cm
Maximum Height of Mattress 18 cm (depending on configuration)
Siderail length
Split plastic head siderail 104,2 cm
Split plastic foot siderail 95,5 cm
Maximal clearance underneath the bed 15 cm
Siderail Height above Mattress Platform (without Mattress) 9 cm (minimum), 40 cm (maximum)
Bed Extension 0 cm / 15 cm / 32 cm
Mattress Platform Height Adjustment 39,5 cm – 77,5 cm
Castor (diameter) 15 cm
Maximum Backrest Angle 64°
Maximum Calfrest Angle 15°
Maximum Thighrest Angle 32°
Auto-regression 11 cm
Trendelenburg Position 16°
Reverse Trendelenburg Position 16°
Weight (Depending on Equipment) 156 kg
Safe Working Load (including Mattress and Accessories) 250 kg
Maximum Patient Weight
Application environment 1, 2 185 kg
Application environment 3, 5 215 kg
Maximum Lifting Pole Load 75 kg

20 D9U001GRA-0101_12
7.3 Mechanical Specification (shortened version)
Parameter Value
External dimensions
With split plastic siderails and small bumpers (8,5 cm) 222 cm (212 cm) x 99,5 cm
Mattress dimensions 190 cm x 90 cm
Maximum Height of Mattress 18 cm (depending on configuration)
Siderail length
Split plastic head siderail 104,2 cm
Split plastic foot siderail 95,5 cm
Maximal clearance underneath the bed 15 cm
Siderail Height above Mattress Platform (without Mattress) 9 cm (minimum), 40 cm (maximum)
Bed Shortening 0 cm / -10 cm
Mattress Platform Height Adjustment 39,5 cm – 77,5 cm
Castor (diameter) 15 cm
Maximum Backrest Angle 64°
Maximum Calfrest Angle 15°
Maximum Thighrest Angle 32°
Auto-regression 11 cm
Trendelenburg Position 16°
Reverse Trendelenburg Position 16°
Weight (Depending on Equipment) 156 kg
Safe Working Load (including Mattress and Accessories) 250 kg
Maximum Patient Weight
Application environment 1, 2 185 kg
Application environment 3, 5 215 kg
Maximum Lifting Pole Load 75 kg

7.4 Environment Conditions

Use conditions
■ Temperature 10 °C — 40 °C
■ Humidity 30% — 75%
■ Atmospheric Pressure 795 hPa — 1060 hPa
Storage and Transport Conditions
■ Temperature -20°C — 50°C
■ Humidity 20% — 90% (non-condensing)
■ Atmospheric Pressure 795 hPa —1060 hPa

D9U001GRA-0101_12 21
7.5 Electrical Specifications (Eleganza 2)
DANGER!
Danger to life due to electric shock!
► Ensure that maintenance and service of electrical parts are performed only by qualified personnel if the bed is
connected.

Parameter Value
Input Voltage
Version 1 230 V~, 50/60 Hz
Version 2 100 V~, 50/60 Hz
Version 3 110 V~, 50/60 Hz
Version 4 120 V~, 50/60 Hz
Version 5 127 V~, 50/60 Hz
Version 6 110 - 127 V~, 50/60 Hz or 220 V~, 50/60 Hz
Maximum Power Input 370 VA
Ingress Protection IPX4
Safety Class Class I (with type B applied parts)
Electrical Motor Duty Cycle max. 2 min ON / 18 min OFF
Accumulator Pb ACCU 2 x 12 V / 1,2 Ah / Fuse 15 A

Fuse
Version 1 2x T1.6A L 250 V for 230 V, 110-127 V or 220 V version
Version 2 2x T3.15A L 250 V for 100 V, 110 V, 120 V, 127 V, 110-127 V
or 220 V version

NOTE Upon request, LINET® can deliver hospital beds with electrical specifications that comply with regional standards (custom
voltage, different mains plugs).

Electrical system of Eleganza 2 is characterized by overcurrent protection against overload of each actuator.

7.6 Electromagnetic compatibility

Bed is intended for hospitals except for near active HF surgical equipment and the RF shielded room of a medical system for mag-
netic resonance imaging, where the intensity of EM disturbances is high.

Bed has defined 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:

1. Mains cable, maximum length 6 m
2. ACP Attendant Control Panel, maximum length 3m
3. Handset, maximum length 3m

WARNING!
Use of the accessories, converters and other cables, than specified 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 2, including cables specified 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 14 Maintenance in order to
maintain the basic safety with regard to electromagnetic disturbances for the expected service life.

22 D9U001GRA-0101_12
7.6.1 Manufacturer instructions - electromagnetic emissions
Emission Test Compliance
RF emissions Group 1
CISPR 11
RF emissions Class B
CISPR 11
Harmonic emissions Class A
IEC 61000-3-2
Voltage fluctuations / flicker emissions Complies
IEC 61000-3-3

7.6.2 Manufacturer instructions - electromagnetic susceptibility

Immunity Tests Compliance level
Electrostatic discharge (ESD) ± 8 kV for contact discharge
IEC 61000-4-2 ± 15 kV for contact discharge
Radiated RF 3 V/m
IEC 61000-4-3 80 MHz – 2,7 GHz
80 % AM at 1 kHz
Proximity fields from RF wireless communications equipment
IEC 61000-4-3 See Table 1
Fast electrical transients / burst ±2 kV for power line
IEC 61000-4-4 repetition frequency 100 kHz
Surge ± 1 kV Line-to-line
IEC 61000-4-5 ± 2 kV Line-to-ground
Conducted RF 3 V (0,15 MHz – 80 MHz)
IEC 61000-4-6 6 V in ISM bands between 0,15 MHz and 80 MHz
80 % AM at 1 kHz
Power frequency (50/60 Hz) magnetic field 30 A/m
IEC 61000-4-8
Voltage dips, short interruptions on power supply input lines 0 % UT; 0,5 cycle
IEC 61000-4-11 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

D9U001GRA-0101_12 23
 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 28
kHz sine
710 704 - 787 LTE band 13, 17 Pulse modulation 217 9
745 Hz
780
810 800 - 960 GSM 800/900, TETRA Pulse modulation 18 Hz 28
870 800, iDEN 820, CDMA
930 850,
LTE band 5
1 720 1 700 - 1 990 GSM 1800; CDMA Pulse modulation 217 28
1 845 1900; GSM 1900; Hz
1 970 DECT; LTE band 1, 3,
4, 25; UMTS
2 450 2 400 - 2 570 Bluetooth, WLAN, Pulse modulation 217 28
802.11 b/g/n, RFID Hz
2450,
LTE band 7
5 240 5 100 - 5 800 WLAN 802.11 a/n Pulse modulation 217 9
5 500 Hz
5 785

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).

8 Use and Storage Conditions

The bed may not be used and stored in indoor environments:
■ Where there is a risk of explosion.
■ Containing inflammable anaesthetics.

The bed is designed for use in rooms for medical purposes. Electrical installations must therefore meet local stan-dards laying
down the necessary conditions for electrical installations.
► Disconnect the bed from the mains in exceptional cases (i.e. earthquake, lightning).

24 D9U001GRA-0101_12
9 Scope of Delivery and Bed Variants
9.1 Scope of Delivery
Delivery:
■ Upon receipt, check that the shipment is complete as specified on the delivery note.
■ Notify the carrier and supplier of any deficiencies or damages immediately as well as in writing or make a note on the
delivery note.
■ The bed is delivered with deactivated accumulator. To activate accumulator see chapter “Accumulator activation”.

9.2 Bed Variants

Features - Eleganza 2 Model 1GR (for model number see serial label):

s = standard
o = optional

■ Mattress Platform
□ mattress platform consisting of removable plastic segments (s)
□ mattress platform with bed shortening (-10 cm) and with HPL on calfrest (o)
■ Siderails
□ Without siderails (s)
□ Split plastic siderails, with integrated controllers (o)
□ Split plastic siderails, without integrated illuminated controllers (o)
□ Single collapsible siderails, powder coated (o)
□ Split plastic siderails with Junior Kit (o)
■ Head board and foot board
□ Design Eleganza 2 – plastic panels with coloured inserts (s)
■ Castors
□ 150 mm Tente Motion, with central braking sytem (o)
□ 150 mm Tente Motion + fifth castor (o)
□ 150 mm Tente Motion, with plastic cover (o)
□ 150 mm Tente Motion, with plastic cover + fifth wheel (o)
□ 150 mm Tente Integral, double castors (o)
□ 150 mm Tente Integral, double castors + fifth wheel (o)
■ Control Elements
□ ACP Attendant Control Panel (s)
□ Handset with illuminated keyboard (s)
□ Handset without illuminated keyboard (o)
□ Foot control (o)
□ Satellite control panel (o)
□ Integrated in siderails (o)
□ Mobi-Lift in head siderail (o)
■ Other
□ Mattress platform extension (s)
□ Linen shelf (o)
□ One pair of universal accessory holders (o)
□ Urinary bag holder integrated in siderails (s)
□ Universal box (o)
□ Segufix holders (o)
□ Universal handset holder (o)
■ Powder Coating Colors
□ RAL 9002 (grey) (s)
□ Powder-coated metal parts, RAL 9006 (light grey) + RAL 7043 (dark grey) (o)
■ SafeSense® 3 ready bed

D9U001GRA-0101_12 25
10 Putting into Service
WARNING!
Risk of injury when working on the bed!
► Ensure that the bed is disconnected from the mains connection prior to putting into service, putting out of service
and maintenance.
► Ensure that the castors are locked prior to putting into service, putting out of service and maintenance.

CAUTION!
Material damage due to incorrect putting into service!
► Ensure that putting into service is performed exclusively by manufacturer´s customer service or trained hospital
personnel.

Set up the bed as follows:

► Unpack the bed.
► Check the delivery (see Scope of Delivery and Bed Variants).
► Remove isolating foil from mains control box (see Removing Isolating Foil).
► Install equipment and accessories.
► In case of delivery with dismounted head board and foot board, mount the head board and foot board (see Head Board
and Foot Board).
► Set-up the bed only on a suitable floor surface (see Transport).
► Ensure the mains cable does not collide or get stretched when adjusting the bed. Check the plug is inserted correctly.
► Do not leave any extension cords or power strips loose on the floor.
► Ensure all 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 the mains cable is always accessible.
► The plug on the mains cable should only be changed and maintained by qualified and trained service technicians authoris-
ed by the manufacturer.

26 D9U001GRA-0101_12
10.1 Accumulator Activation
10.1.1 Placement of Control Section

10.1.2 Removing Isolating Foil

PULL

10.1.3 Isolating Foil

Check if isolating foil is complete and undamaged as shown:

If isolating foil is damaged, contact the manufacturer’s service department immediately.

NOTE: It is recommended to wear gloves when removing the isolating foil.

D9U001GRA-0101_12 27
10.2 Head Board and Foot Board
WARNING!
Risk of injury when inserting the head board and foot board!
► To insert head board and foot board into corner posts, hold them by the corner handles on top with both hands.
► Install head board and foot board before the first use.

WARNING!
Risk of injury due to incorrectly installed head board and foot board!
► Ensure head board and foot board are correctly inserted, especially when moving the bed.
► Ensure head board and foot board locks are locked, especially when moving the bed.

WARNING!
Risk of injury when removing the head board and foot board!
► Before removing head board and foot board, ensure siderails are folded down and there are no accessories atta-
ched to the head board and foot board.
► If a patient is lying in a bed with the head and/or foot board removed, supervise the bed at all times.

WARNING!
Material damage due to excess load!
► Ensure nobody sits on the head board and foot board.

NOTE: The head board and foot board may be delivered in several decor colour variants.

1. Locked
2. Unlocked

1 2
To remove head board or foot board:
► Press head board lock or foot board lock. The lock will stay unlocked (2).
► Release the lock button and take finger out of locking mechanism.
► Remove the head board or foot board.

To install head board or foot board:

► Insert head board or foot board to the bushings.
► Press lock button to lock head board or foot board. The lock will stay locked (1)

NOTE: It is possible to install head board and foot board to the bushings with locked lock.

28 D9U001GRA-0101_12
10.3 Mattress Platform
The mattress platform consists of removable plastic sections.

Fig. Correct placement of mattress platform sections

A. Back section / Calf section

B. Loins section / Thigh section
C. Seat section

NOTE Sections A and B are replaceable. It is possible to change back section A for calf section A. Same applies for B sections.
Section C is not replaceable.

To remove/install sections of the mattress platform:

► Pull out mattress platform sections.
► Install mattress platform section.
► The correct fitting of section is signalized by hearable “click”.
► Ensure that mattress platform sections are fitted correctly by trying pull the section up with little manpower.

D9U001GRA-0101_12 29
10.4 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 shocks.

Fig. Potential equalisation connector -

female
Fig. Potential equalisation connector – male

Use equalisation connector if:

■ The patient is connected to any intravascular or intracardiac device.

Before connecting the patient to an intravascular/intra-cardiac device:

► Connect the ground wire of the device to the potential equalisation connector on the bed on which
the patient in question is lying.
► Use a standard hospital connector.
► Make sure the connectors match.
► Make sure there is no possibility of accidental disconnection.

Before moving the bed:

► Disconnect the patient from the intravascular or intracardiac device.
► Disconnect the potential equalisation connector.

10.5 Before Use

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 hours to allow the temperature to equalise.

Prepare the bed for service as follows:

► Dispose of all packaging (see Disposal).
► Connect the bed to the mains.
► Charge the accumulator.
► Raise the mattress platform to the highest position.
► Remove the isolating foil from control section.
► Lower and tilt the mattress platform to the lowest position.
► Check the castors and main brake work correctly.
► Check the bed extension works correctly.
► Check it is possible to remove the head and foot boards.
► Check all of the functions on the control elements (Attendant Control Panel etc.).
► Check the siderails function properly.

30 D9U001GRA-0101_12
10.6 Transport
For safe transport, observe the following:
► Ensure no cables are run over when moving a bed.
► Ensure the mains cable is attached with a hook (at the head end of the bed).
► Ensure the castors are unlocked before moving the bed during the loading/unloading process
(see Castor Control and Bed Transport).
► Ensure the siderails are lifted and locked during transport of the bed.
► Move the bed only on suitable floor surfaces.

Suitable surfaces:
■ Tile
■ Hard linoleum
■ Hard flooring

Unsuitable surfaces:
■ Soft, unsealed or defective flooring
■ Soft wooden flooring
■ Soft and porous stone floors
■ Carpeted floors with underlay
■ Soft linoleum
□ For longer distances, ensure the castor steering function is activated.
□ Ensure the brakes are released while moving the bed.

10.7 Firmware
The bed includes firmware that can be updated only by an authorised service technician.
This firmware is protected against unauthorised access by mechanical housing (tool is needed to access), by seal (com-
ponents with processor are sealed), by exclusive compatibility with an authorised software tool and by check of compati-
bility of the new firmware with the bed.

11 Power Supply Cord (Mains Power Cable)

CAUTION!
Disconnecting bed from the mains does not stop motions of the bed!
► Stop the bed before disconnection bed from the mains.

Attachment plug is means of connecting and disconnecting bed from the mains.
Power supply cable (mains power cable) must be attached with a hook at the head end of the bed during transport.

Where the integrity of the external protective conductor in the installation or its arrangement is in doubt
► operate the bed from internal accumulator only.

D9U001GRA-0101_12 31
12 Accumulator
CAUTION!
Risk of reducing accumulator durability due to incorrect use!
► Use bed on accumulator only in crisis situations (e.g.: power blackout, patient complications during transport,
etc.).
► After reconnecting bed to the mains charge accumulator to full capacity (see chart Accumulator charge status).

CAUTION!
Risk of damage or destruction of accumulator!
► If the accumulator is faulty, degassing may occur. In rare cases this might cause deformations of the accumulator
case, control panel housing or cable.
► If this occurs stop using the bed immediately (see Removing the Bed from Service).
► Inform the manufacturer’s service department immediately.
► Charging and accumulator capacity is indicated by the yellow LED placed on the ACP control panel.

The accumulator supplied with the bed is delivered uncharged. The accumulator serves as a backup during power failures or
while transporting the patient.

► Use only accumulators approved by the manufacturer.

► The manufacturer provides a 6-month warranty for the full function of accumulators.
► Check the accumulator functionality at least once a month in accordance with the user and service manuals
and have the accumulator changed if necessary.
► The manufacturer will assume no responsibility for any damage to the bed or the accumulator caused by:
■ Non-observance of the manufacturer’s instructions in the instructions for use.
■ Using accumulators not approved by the manufacturer.
■ Accumulator replacement non-qualified service organisation.

To charge the accumulator:

► Connect the bed to the mains and check the yellow LED on the Attendant Control Panel according to the following table.

NOTE: Some bed adjustment options are not available without a accumulator, for example, height adjustment under a load of
above 200 kg.

Accumulator lifetime could be up to 5 years if operated under optimum conditions.

Accumulator capacity can be significantly reduced if:

► too high ambient temperature
► many accumulator charge/discharge cycles
► recurrence of deep discharge
► bed is often powered only by the accumulator

32 D9U001GRA-0101_12
The LED indicates the accumulator charge status (Attendant Control Panel):

Yellow LED Accumulator charge status

Not lit Accumulator capacity is sufficient (charging completed)

Short flashing (short, intermittent illumination) Accumulator is charging - continue charging until the LED is
(circa 1.8 sec.) extinguished. In emergency cases, the accumulator can be
used as a backup power source for a short period. If LED is still
flashing after 12 hours of charging or stops flashing, but you
cannot position with bed, accumulator is defective or broken.
Contact manufacturer.
Long flashing (long illumination) (circa 0.2 sec.) Low accumulator voltage - accumulator cannot be used as a
backup power supply even for a short period; accumulator is
completely discharged or defective (if this type of signalisation
persists, it is necessary to replace the accumulator - service
action)
Long, intermittent illumination for several hours (circa 10 Accumulator absence or failure condition (accumulator is
hours), when bed is connected to the mains. connected incorrectly, line between the power supply and
accumulator is broken or accumulator fuses are faulty); contact
service department of the manufacturer in case of such signa-
lisation.

To maintain maximum functionality of the accumulator:

► Unplug the bed from the mains as least as possible.

In case the accumulator cover or control section is deformated by heat

► Unplug the bed from the mains.
► Do not use the bed (see. Removing the Bed from Service).
► Contact service of the manufacturer.

12.1 Status Faulty Accumulator

The accumulator is regarded as faulty if at least one of the following conditions applies:
► Accumulator charging constantly
► Low voltage on accumulator
► Low charging current of accumulator

Status “faulty accumulator” is indicated:

► By the accumulator status indicator being constantly lit.
► A fault accumulator status can be cancelled by pressing the STOP button.
► Accumulator status data is saved to the Linis system and written to the “Blackbox”.

12.2 Status Discharged Accumulator

The accumulator is regarded as discharged if the following condition is met:
► Defined decrease of voltage depending on discharging current

Status “discharged accumulator” is:

► Status is indicated by the accumulator status indicator flashing quickly.
► The electric CPR position is the only possible position.
► This status will be cancelled automatically when the bed switches to sleep mode.

D9U001GRA-0101_12 33
12.3 Removing the Bed from Service
How to remove the bed from service:
► Disconnect the bed from the mains.
► Disconnect the ground wire.
► Deactivate the accumulator (see Deactivating the Accumulator).
► Remove accessories.
To prevent damage during storage:
► Pack or cover the bed and accessories.
► Ensure storage conditions are the same as the operating conditions.

12.4 Deactivating the Accumulator

To avoid damaging the bed and the environment during storage:
► Deactivate the accumulator on the Attendant Control Panel.
To deactivate the accumulator on the Attendant Control Panel:
► Disconnect the bed from the mains.
► Disconnect the ground wire.
► Activate the keypad by pressing the GO button on the Attendant Control Panel.
► Press the Thighrest Up + Thighrest Down + Trendelenburg Position buttons at the same time and hold
them for three seconds.
► The accumulator is deactivated.

NOTE: Try some functions to ensure the accumulator is deactivated.

To activate the accumulator again:

► Connect Power Cable to the mains.

13 Manipulation
WARNING!
Risk of injury when adjusting the bed!
► Ensure there are no body parts between the mattress platform elements and the mattress platform frame
when adjusting the bed.
► Ensure there are no body parts below the mattress platform frame before adjusting the bed.
► Secure or remove any items on the bed.

13.1 Siderails
WARNING!
Risk of injury due to crushing!
► Ensure that there are no objects or body parts between siderail and mattress platform when folding the
siderail up or down.
► Ensure that no body part or object are under the siderail when folding the siderail down.
► It is necessary to take extra care and attention when locking the siderails in the top position. Hospital
staff must ensure the siderail is locked in its highest position by pushing the siderail to head end and foot end
of the bed. The risk of spontaneous folding of the siderail may occur when the siderail is not properly locked
and it can injure the patient, staff or the third parties.

Model variants:
■ Without siderails
■ With single collapsible siderails
■ With split plastic siderails

34 D9U001GRA-0101_12
13.1.1 Collapsible siderail (3/4 siderail)
WARNING!
The hospital personnel is responsible for locking the siderails in the highest position when the patient is on
the bed or when the bed is transported.

WARNING!
Ensure that there are no objects or body parts between the bars of siderail when folding the siderail up or
down.

Collapsible siderails are situated on both sides of the bed. Both collapsible siderails are integral parts of the bed in contact with pati-
ent and cannot be removed.

2 2 2 1

3
Fig. Collapsible Siderail (3/4 Siderail) 1. Release Mechanism
2. Siderail Bars
3. Siderail Stop

Fig. Releasing mechanism of the Single Collapsible Siderails

To fold siderails down:

■ Take hold of release mechanism and push siderail towards head end to unlock locking system 1.
■ Press button 2 to unlock.
■ Fold siderail down as required 3.
■ To fold the siderail up push the siderail up. Siderail will click into place and lock automatically.

D9U001GRA-0101_12 35
13.1.2 Split plastic siderails
WARNING!
Risk of injury due to crushing!
► Ensure that there are no objects or body parts between siderail and mattress platform when folding the
siderail up or down.
► Ensure that no body part or object are under the siderail when folding the siderail down.

WARNING!
Risk of injury due to patient falling out of bed!
► Ensure that folded-up siderails are securely anchored.
► Press against siderails from inside in order to check stability.
► Hospital personnel are responsible for ensuring siderails are folded-up when the bed is occupied.

The split plastic siderails are components of the bed, the siderails cannot be removed. The SoftDrop function enables smooth and
quiet folding of the siderails.

Fig. Eleganza 2 with split plastic siderails.

36 D9U001GRA-0101_12
Fig. Folding down the split plastic siderail.

To fold siderails down:

► Push the siderail towards the mattress support platform (1).
► Unlock siderails by pulling the release handle (2).
► The siderail will fold down smoothly due to Soft Drop function (3).

NOTE: If pressure is placed on the siderail from inside the bed (by either the mattress or patient) and it is not possible to fold
down the siderail, grip the siderail by the upper section and push the siderail towards the middle of the bed and then repeat steps 2
and 3.

To fold siderails up:

► Grip the siderail by the upper part.
► Pull siderail up until it latches.
► The locking of each siderail is indicated by an audible ‘click‘ when locked in place.
► Ensure that the siderail is locked properly.

D9U001GRA-0101_12 37
13.1.3 Split plastic siderails with Junior Kit
CAUTION!
Risk of damaging the bed due to incorrect use!
► Do not hang anything on the prop in siderail if the bed is equipped with Junior Kit.

Eleganza 2 with Junior Kit is intended for patients with length more than 125 cm.
Split plastic siderail with Junior Kit can be recognized according to a prop in the opening of the head siderail.

Fig. Eleganza 2 with Junior Kit

38 D9U001GRA-0101_12
13.2 Castor Control and Bed Transport
CAUTION!
Material damage due to incorrect transport or involuntary movement!
► Prior to assembly, disassembly and maintenance, ensure the castors are locked.
► Ensure the castors are locked while the bed is occupied and/or not being transported.
► Prior to transport, ensure that bed is disconnected from mains.
► Put mains cable on hook provided for transport.
► Have the bed transported only by nursing or trained personnel.

CAUTION!
Objects on undercarriage can damage the bed!
► Do not place any objects on the undercarriage or in the space under the mattress platform.

Castor Control Levers:

1
2
3
Fig. Central braking system lever

The central braking system facilitates movement of the bed by a single person. The bed has a main lock control lever for the four
castors. The brakes are at the foot end of the undercarriage.

Castor control:
1. Forward Movement: The front left castor is locked. The bed moves straight ahead. If the bed is equipped with a fifth
castor, this castor determines the direction of movement.
2. Unrestricted Movement: All of the castors are unlocked.
3. Braked: All of the castors are locked.

To move the bed:

► Adjust the bed height to at least 20 cm below maximum height.
► Push the bed using handles on head board or foot board.

D9U001GRA-0101_12 39
13.3 CPR backrest release
WARNING!
Risk of injury due to lowering the backrest too quickly!
► Ensure single collapsible siderails are in their lowest position.
► Ensure split plastic siderails are in their highest position.
► Ensure there are no body parts between siderails and backrest.
► Press the backrest down only by the mattress guard handle or the siderail.

The bed permits quick mechanical lowering of the backrest for emergency resuscitation (CPR) procedures.

Fig. CPR backrest release

1. Mattress guard handle

2. CPR mechanical handle

Set the position as follows:

■ Grab and hold backrest using:
► Mattress guard handle (1).
► Upper part of the siderails (in case the split siderails are in upper position)
■ Pull and hold release handle 2.
■ Press the backrest down using:
► Mattress guard handle (1)
► Upper part of the siderails (in case the split siderails are in upper position)

40 D9U001GRA-0101_12
13.4 Mattress Platform
13.4.1 Auto-Regression
Ergoframe® enlarges the space for pelvic area during Auto-contour. Because of increasement of the space the force applied results
in decrease of the pressure that can cause pressure injuries in the pelvic area.

Benefits of auto-regression:
■ Prevents decubitus.
■ Increases the sitting area by 11 cm in the maximum upright position.

13.4.2 Mechanical Calfrest Adjustment

You can adjust the calfrest mechanically. A special locking mechanism allows the position to be adjusted.

To raise the calfrest:

► Pull on calfrest handle until the desired position is reached.

To lower the calfrest:

► Hold handle and pull the calfrest to the upper most position.

13.4.3 Mattress Platform Extension

WARNING!
Risk of crushing the patient due to incorrect extension/shortening!
► If the bed is equipped with split siderails, lower the foot siderail before extending the mattress platform by 15 cm.
► The patient should not be left unattended by healtcare personnel when the 15 cm bed extension is used.

WARNING!
Damage to property due to excess load!
► Ensure nobody sits on the extended bed end.

Fig. Bed extension by 15 cm. Fig. Bed extension by 32 cm.

D9U001GRA-0101_12 41
Fig. Mattress Platform Extension Safety Lock

1. Locked
2. Unlocked (it is possible to set up bed extension)

Fig. Mattress retainer positions during bed extensions.

1. 0 cm
2. +15 cm
3. + 32 cm

To lengthen/shorten the bed:

► Pull out the safety catches 1 at the foot end of both sides of the frame.
► Turn the safety catches 1 by 90° (2).

The safety lock is released.

► Pull the foot board out as far as it will go.
► Adjust wire mattress retainer located under the mattress to bed extension position.
► Turn the safety lock by 90° and push them in.
► Ensure that both of the safety locks are locked properly.

NOTE: In the event of incorrect closure of the safety lock, move the foot end of the bed until the locking point is reached.

42 D9U001GRA-0101_12
Positions of the mattress retainer:

Fig. Mattress retainer in the position without bed extension (default postion)

Fig. Mattress retainer in the position with bed extension by 15 cm

Fig. Mattress retainer in the position with bed extension by 32 cm

D9U001GRA-0101_12 43
13.4.4 Shortened Bed

WARNING!
Use the bed shortening carefully when a patient is on the bed to avoid risk of crushing, trapping or squeezing.

Eleganza 2 medical bed can be delivered in the version with bed shortening. Purpose of this shortened
version is to facilitate bed transport. It is recommended to use mattress (with length of 190 cm) with foam extension (with
length of 10 cm).

Fig. Shortened bed with length of 212 cm

Fig. Standard mattress platform of the Shortened version of Eleganza 2

44 D9U001GRA-0101_12
13.5 Control Elements
The bed is operated by different control elements.

Control elements:
► ACP Attendant Control Panel
► Attendant Control Panel with SafeSense® 3 Control
► Handset
► Foot control
► Satellite control panel
► Controls integrated in siderails
► Mobi-Lift®

Disabling individual functions on the Attendant Control Panel affects all of the control elements.

If the bed does not react to individual position settings:

► Check whether the function is disabled on the Attendant Control Panel.

NOTE: If the bed is equipped with “Automatic Stop of Backrest at 30°” then this function works on every control element which
allows backrest adjustment.

NOTE: To detect if the bed is equipped with function “Automatic Stop of Backrest at 30°” see Attendant Control Panel where the
“30° STOP” symbol on the backrest adjustment button is located. In case the bed is not equipped with this function, the buttons do
not contain those symbols.

D9U001GRA-0101_12 45
13.5.1 ACP – Attendant Control Panel
ACP Attendant Control Panel is main control panel of the bed. Nurse controller can be placed in the shelf. We recommend placing
this control panel on the head board or foot board or hold it in the hands while controlling the bed.

Fig. ACP - Attendant Control Panel

1. Central „STOP“ Button

2. Central „GO“ Button
3. Thighrest Positioning Buttons
4. Lock Indicators
5. Lock Buttons for Respective Functions
6. Backrest Positioning Buttons (symbol „30° STOP“ indetifies equipment of the bed with this function)
7. Height Adjustment Buttons
8. Auto-Contour Buttons (simultaneous setting of backrest and thighrest)
9. Foot Control Lock Button
10. Button Anti Trendelenburg (mattress platform tilt only)
11. Button Trendelenburg (mattress platform tilt only)
12. Button Examination Position
13. Button CPR (Resuscitation) Position
14. Emergency Trendelenburg Button
15. Button Cardiac Chair Position
16. LED Accumulator charge status
17. LED Mains power
18. Bed Lights Control Button (ON/OFF)

To set positions:
► Activate the keypad by pressing the GO button.
► Press and hold corresponding button until required position is reached.

Central STOP Button

The central STOP button 1 immediately interrupts all bed movements.
Pressing central STOP button 1 for at least 0.3 seconds immediately stops all electronic bed movements.

NOTE: The bed can be stopped by pressing two different buttons even on two different controllers. If the press of the buttons is
longer than 0,5 second the bed will stop all the movements immediately.

46 D9U001GRA-0101_12
Activating GO Button
The GO button 2 activates the keypads on all control elements except the foot control.
A GO button is included on a number of different control elements. The function of the GO button is identical on all control ele-
ments.

After pressing GO button 2, the keypad will remain active for 3 minutes. It is possible to control every function on the bed except the
locked functions.

Pressing a function button will keep the keypad active for another 3 minutes.

It is necessary to activate the keypad again if the 3 minute period without pressing any function is passed.

Function Buttons
Function buttons 3, 6, 7 and 8 allow the setting of different positions, for example the height and tilt of the mattress platform, adjust
individual mattress platform elements, etc.

To set a position:
► Activate the keypad by pressing the GO button.
► Press and hold the respective button until required position is reached.
► If the bed is equipped with “Automatic Stop of Backrest at 30°” function the backrest will stop
automatically. To continue with positioning simply press and hold button until the desired position is reached.

NOTE: If the bed is equipped with “Automatic Stop of Backrest at 30°” then this function works on every control element which
allows backrest adjustment.

Lock Buttons
Lock button 5 allows disabling individual functions on the Attendant Control Panel.

To disable functions:
► Activate the keypad by pressing the GO button 2.
► Press respective lock button 5.
The respective LED flashes 4 to indicate the lock.

NOTE: The individual functions are locked in the central control panel, the satellite control, the handset, and the siderail control.
The foot controllers are locked separately.

To enable disabled functions:

► Activate the keypad by pressing the GO button 2.
► Press the respective lock button 5.
The respective LED goes out (4). The function is enabled.

D9U001GRA-0101_12 47
Position Buttons
WARNING!
Risk of injury due to moving parts!
► Ensure that no body parts are trapped between moving parts of bed and mattress platform.
► Ensure that no persons or body parts are close to bed or accessories (e.g. infusion stand, lifting pole) when
mattress platform is moving

CAUTION!
Damage to property due to moving parts!
► Ensure that no objects (e.g. cables) are trapped between moving parts of bed and mattress platform.
► Ensure that no objects are close to bed or accessories (e.g. infusion stand, lifting pole) when mattress platform is
moving.

The therapeutic and safety-related positions are pre-programmed. When a position is set, several parts of the bed and mattress
platform will move simultaneously.

Programmed positions:
► Cardiac chair position 15
► Trendelenburg position 14
► CPR (resuscitation) position 13
► Examination Position 12

To set the programmed positions:

► Activate the keypad by pressing the GO button.
► Press and hold corresponding function button until the desired position is reached.

Cardiac chair position (15)

The cardiac chair position is suitable for patients with cardiac arrhythmia and breathing difficulties.

Settings after pressing and holding the Cardiac chair button (15):
► Calfrest tilts into lowest position, thighrest moves into the upright position (34°).
► 6 second after positioning calfrest and thighrest the backrest will move into an upright position (62°).

Trendelenburg position (14)

The Trendelenburg position serves as an anti-shock position. All parts of the mattress platform are flattened. Mattress platform tilts
head down.

CPR (Resuscitation) Position (13)

The CPR position is for resuscitating the patient in an emergency.

Settings after pressing and holding the CPR button (13):

► Mattress platform moves into a horizontal position.

NOTE: For quick mechanical positioning, see CPR Backrest Release.

Examination Position (12)

Examination position is designed for personnel and allows comfortable patient examination.

Settings after pressing and holding the Examination Position button (12):
► The mattress platform will move into the most appropriate position for patient examination and the mattress platform will
flatten.

48 D9U001GRA-0101_12
13.5.2 Attendant Control Panel with SafeSense® 3 Control

The Attendant Control Panel with SafeSense® 3 Control is a control element for Eleganza 2 medical bed. The Attendant Control
Panel with SafeSense® 3 Control indicates Bed Exit Monitoring, Motion Monitoring, Decubitus/Movement Notification and Wetness
Monitoring. This Attendant Control Panel can be hung on the foot board or on the siderails if required or it can be stored in the
Linen Shelf. It is possible to hold this Attendant Control Panel in the hand while operating.

► Ensure that exclusively trained nursing staff operates the Attendant Control Panel with SafeSense® 3 Control.

17 18 19 20 21

2
16
3
4
5

15 14 13 12 11 10 9 8 7 6
Fig. Attendant Control Panel with SafeSense® 3 Control for Eleganza 2 medical bed

1. Activating GO Button
2. Central STOP Button
3. CPR (Resuscitation) Position Button
4. Mains Power LED
5. Emergency Trendelenburg Position Button
6. Accumulator Charge Status LED
7. PLAY and STOP Button (SafeSense® 3 Monitoring System)
8. SELECT and TIME Button (SafeSense® 3 Monitoring System)
9. Examination Position Button
10. Autocontour Buttons (simultaneous adjustment of Backrest and Thighrest)
11. Mobilisation Position Button
12. Backrest Adjustment Buttons
13. Cardiac Chair Position Button
14. Thighrest Adjustment Buttons
15. Antitrendelenburg Tilt Button
16. Height Adjustment Buttons (UP or DOWN or EXTRA LOW)
17. Lock Button for Bed Height Adjustment with respective LED indicator
18. Lock Button for Thighrest Adjustment with respective LED indicator
19. Lock Button for Backrest Adjustment with respective LED indicator
20. Bed Lights Control Button (ON/OFF)
21. SafeSense® 3 Display (SafeSense® 3 Monitoring System)

D9U001GRA-0101_12 49
To set positions:
► Activate the keypad by pressing the GO button (1).
► Press and hold corresponding button until required position is reached.

Central STOP Button

The central STOP button 2 immediately interrupts all bed movements.
Pressing central STOP button 2 for at least 0.3 seconds immediately stops all electronic bed movements.

Activating GO Button
The GO button 1 activates the keypads on all control elements except the foot control. A GO button is included on a number of
different control elements. The function of the GO button is identical on all control elements. After pressing GO button 1, the keypad
will remain active for 3 minutes. It is possible to control every function on the bed except the locked functions. Pressing a function
button will keep the keypad active for another 3 minutes. It is necessary to activate the keypad again if the 3 minute period without
pressing any function is passed.

Function Buttons
Function buttons 5, 9, 10, 11, 12, 13, 14, 15 and 16 allow the setting of different positions, for example the height and tilt of the
mattress platform, adjust individual mattress support platform elements, etc.

NOTE: The bed can be stopped by pressing two different buttons even on two different controllers. If the press of the buttons is
longer than 0,5 second the bed will stop all the movements immediately.

To set a position:
► Activate the keypad by pressing the GO button.
► Press and hold the respective button until required position is reached.

Backrest Adjustment (12)

During continuous positioning Backrest stops automatically in 30 degrees. To continue in positioning release the button, then press
and hold button until the desired position is reached.

Antitrendelenburg Tilt (15)

During positioning from Trendelenburg Position to Antitrendelenburg Tilt (or vice versa) the bed stops in the horizontal position (0°).
To continue tilting, press the Antitrendelenburg Tilt Button once more.

Lock Buttons (17, 18 and 19)

Lock buttons allow disabling individual functions on the Attendant Control Panel.

To disable functions:
► Activate the keypad by pressing the GO button 1.
► Press respective lock button.
The respective LED flashes to indicate the lock.

NOTE: The individual functions are locked in the central control panel, the satellite control and the handset.

To enable disabled functions:

► Activate the keypad by pressing the GO button.
► Press the respective lock button.
The respective LED goes out. The function is enabled.

50 D9U001GRA-0101_12
Mains Power LED Signalisation (4)

MAINS POWER LED MEANING

lit connected to the mains

flashing: 0,6s lit / 0,6s not lit keyboard error (flashing inverted to Lock LED)
error (first fault)
flashing: 0,1s lit / 0,1s not lit service mode
not lit disconnected from the mains power
transformer switching error

Accumulator Charge Status LED Signalisation (6)

ACCUMULATOR INDICATOR MEANING

lit accumulator disconnected or faulty

flashing: 1,6s lit / 0,2s not lit accumulator deeply discharged
flashing: 0,1s lit / 0,1s not lit accumulator discharged
flashing: 0,2s lit / 1,6s not lit accumulator is charging
not lit accumulator charged

Position Buttons
WARNING!
Risk of injury due to moving parts!
► Ensure that no body parts are trapped between moving parts of bed and mattress platform.
► Ensure that no persons or body parts are close to bed or accessories (e.g. infusion stand, lifting pole) when
mattress platform is moving

CAUTION!
Material damage due to moving parts!
► Ensure that no objects (e.g. cables) are trapped between moving parts of bed and mattress support platform.
► Ensure that no objects are close to bed or accessories (e.g. infusion stand, lifting pole) when mattress support
platform is moving.

The therapeutic and safety-related positions are pre-programmed. When a position is set, several parts of the bed and mattress
support platform will move simultaneously.

Programmed positions:
► Cardiac Chair Position
► Emergency Trendelenburg Position
► CPR (resuscitation) Position
► Examination Position
► Mobilisation Position
► Extra Low Position

To set the programmed positions:

► Activate the keypad by pressing the GO button.
► Press and hold corresponding function button until the desired position is reached.

D9U001GRA-0101_12 51
Cardiac chair position (13)
The cardiac chair position is suitable for patients with cardiac arrhythmia and breathing difficulties.

Settings after pressing and holding the Cardiac chair button (13):
► Calfrest tilts into lowest position, thighrest moves into the upright position (34°).
► 6 second after positioning calfrest and thighrest the backrest will move into an upright position (62°).

Emergency Trendelenburg Position (5)

The Emergency Trendelenburg Position serves as an anti-shock position. All parts of the mattress support platform are flattened.
Mattress support platform tilts head down.

CPR (Resuscitation) Position (3)

The CPR Position is for resuscitating the patient in an emergency.

Settings after pressing and holding the CPR button (3):

Mattress support platform moves into a horizontal position.

NOTE: For quick mechanical positioning, see CPR Backrest Release.

Examination Position (9)

Examination Position is designed for personnel and allows comfortable patient examination.

Settings after pressing and holding the Examination Position button:

The mattress support platform will move into the most appropriate position for patient examination and the mattress support plat-
form will flatten.

Mobilisation Position (11)

The Mobilisation Position makes it easier for the patient to get out of the bed. Mattress support platform is in the lowest position and
backrest is upright.

Extra Low Position (16)

The bed height adjustment stops above Extra Low Position during lowering, mattress support platform is adjusted to flat position
and beep is performed. After this adjustment the lowering continues to Extra Low Position.

52 D9U001GRA-0101_12
SafeSense® 3 Display (21)

8 1 2 1. Activation Symbol (selected type (or types) of

monitoring is (are) activated)
2. Indicator of communication between Hub and
Attendant Control Panel (black arrows - communication
works, orange cross over black arrows - communication
does not work)
3. Indicator of discharged Hub battery
4. Indicator of activated Motion Monitoring
3 5. Period during which the absence of patient
movement on the bed is tolerated. Countdown to the
selected time (e.g. 4 hours) starts again from the begi-
nning after patient movement on the mattress.
7 4 6. Period during which the Bed Exit alerts are
not triggered unless patient is on the bed (e.g. no alert
during 30 minutes)
7. Indicator of activated Bed Exit Monitoring (pati-
ent presence on the mattress is monitored)
8. Indicator of Wetness Monitoring (Wetness Mo-
6 5 nitoring is activated)

Fig. SafeSense® 3 Display - monitoring ON

7 1 2 1. Deactivation Symbol
2. Indicator of communication between Hub and
Attendant Control Panel (black arrows - communication
works, orange cross over black arrows - communication
does not work)
3. Indicator of activated Decubitus/Movement
Notification
4. Period after which nursing staff is notified to
check position of the patient
5. Period during which the Bed Exit alerts are
not triggered unless patient is on the bed (e.g. no alert
during 30 minutes)
6 3 6. Indicator of activated Bed Exit Monitoring (pati-
ent presence on the mattress is monitored)
7. Indicator of Wetness Monitoring (Wetness Mo-
nitoring is activated - The more black symbol of drop,
the higher degree of the wetness is monitored.)
5 4

Fig. SafeSense® 3 Display - monitoring OFF

Orange square symbol is displayed instead of the green activation symbol when no monitoring is activated.
Indicator of Wetness Monitoring is not displayed when Wetness Monitoring is not activated.
Indicator of Wetness Monitoring changes according to the degree of monitored wetness. The more black symbol of drop, the higher
degree of the wetness is monitored.

D9U001GRA-0101_12 53
 Fig. Bed Exit Alert (monitored patient is not present
on the mattress)

Fig. Motion Monitoring Alert (expired period during

which the absence of patient movement on the
mattress was tolerated)

Fig. Decubitus/Movement Notification Alert (nursing

staff is notified to check position of the patient)

54 D9U001GRA-0101_12
13.5.3 Handset
The handset is included as a standard feature. The handset is available with and without button illumination. The button illumination
of the illuminated handset is active when the bed is connected to the mains. The functions of both handsets are identical. Where
the handset is to be stored on the bed depends on the patient’s condition.

1. Thighrest Adjustment Button

2. Thighrest/Backrest Lock LED
3. Backrest Adjustment Button
4. Activating GO Button
5. Auto-Contour Button
6. Height Adjustment Button
7. Height Lock LED
8. Flashlight Button
9. Flashlight

Fig. Handset

To switch on the flashlight:

► Press and hold flashlight button 8 and flashlight 9 on the top of the handset will light up.

Set the positions as follows:

► Activate the keypad by pressing the GO button.
► Press and hold the function button until the desired position is reached.

NOTE: Depending on the patient’s condition, the nursing staff decides whether the patient is allowed to adjust the bed’s position.

If required, prevent the patient from adjusting the bed as follows:

► Disable functions.
► Unplug handset (if the bed is equipped with Plug and Play).

NOTE: The handset can be plugged into another LINET® hospital bed with the Plug and Play slot.

NOTE: If the bed is equipped with “Automatic Stop of Backrest at 30°” then this function works on every control element which
allows backrest adjustment.

D9U001GRA-0101_12 55
13.5.4 Satellite Control Panel (optional)
The satellite control panel is an optional control element. The satellite control panel is attached to the backrest with a flexible arm.

1. Activating GO Button
2. Thighrest Adjustment Buttons
3. Backrest Adjustment Buttons
4. Height Adjustment Buttons

Fig. Satellite control panel

To set positions:
► Activate the keypad by pressing the GO button.
► Press and hold corresponding button until required position is reached.

NOTE: Depending on the patient’s condition, the nursing staff decides whether the patient is allowed to adjust the bed’s position.

If required, prevent the patient from adjusting the bed as follows:

► Move the satellite panel out of the patient’s reach.
-or-
► Disable functions.

NOTE: The satellite control panel can be fixed on the right or left side of the bed.

NOTE: If the bed is equipped with “Automatic Stop of Backrest at 30°” then this function works on every control element which
allows backrest adjustment

56 D9U001GRA-0101_12
13.5.5 Foot Control
WARNING!
Risk of injury due to moving parts!
► Ensure no body parts are trapped between moving parts of bed and mattress platform.
► Ensure no persons or body parts are close to bed or accessories (e.g. infusion stand, lifting pole) when the
mattress platform is moving.

It is possible to equip the bed with a foot control. The foot controllers enable the adjustment of the bed height or pre-programmed
examination positions.

1. Foot Switch Lower Mattress Platform

2. Foot Switch Examination Position
3. Protection Frame against Unwanted Activation
4. Foot Switch Raise Mattress Platform

Fig. Foot control

Set the position as follows:

► Press foot switch for activation (mini GO function).
► Press and hold foot switch until desired position is reached.

D9U001GRA-0101_12 57
13.5.6 Control Element Integrated in Siderail (optional)

It is possible to equip the Eleganza 2 bed with integrated illuminated controllers in the siderails.The optional control element is atta-
ched to the siderail. The controllers are positioned on both sides of the bed.

1. Thighrest Adjustment Buttons

2. Backrest Adjustment Buttons
3. Activating GO Button
4. Auto-Contour Buttons
5. Height Adjustment Buttons

Fig. Control Element Integrated in the Siderail

To set positions:
► Activate the keypad by pressing the GO button.
► Press and hold corresponding button until required position is reached.

NOTE: Depending on the patient’s condition, the nursing staff decide whether the patient is allowed to adjust the bed’s position.

NOTE: If the bed is equipped with “Automatic Stop of Backrest at 30°” then this function works on every control element which
allows backrest adjustment.

If required, prevent the patient from adjusting the bed as follows:

► Disable functions in siderails by locking the functions with ACP Attendant Control panel.

58 D9U001GRA-0101_12
14 Equipment
14.1 Accessory Rails
WARNING!
Risk of injuring the personnel, patients or risk of damaging the bed due to incorrect placement of the
accessories!
► Always ensure the accessory placed on the accessory rail is not in collision with bed or with patient.
► Never place holders directly above the foot controllers.

Load capacity:
► Maximum load per hook is 5 kg.
► Maximum load per rail is 10 kg.

Accessories suitable for hanging on the accessory rail:

► Urine bag holder
► Urine bottle holder
► Cannula holder
► Redon bottle holder
► DIN rail for accessories

Fig. Accessory rail

14.2 Urinary bottle holder

Urinary bottle holder is designed for placing urinary bottle into

wire basket.

Placement:
► On the accessory rail

Load capacity:
► Maximum load of holder is 10 kg.

Fig. Urinary bottle holder

D9U001GRA-0101_12 59
14.3 Redon bottle holder
WARNING!
Risk of damaging the bed or injuring the personnel or patient due to incorrect use!
Ensure the length of the tube is long enough to prevent tearing the drain when manipulating the patient.

Fig. Redon bottle holder

14.4 Mobi-Lift®
It is possible to equip the Eleganza 2 with integrated Mob-iLift® controllers. Controllers are integrated in both head siderails. Mobi-
-Lift® helps the patient with standing up from the bed.

Fig. Mobi-Lift® in head siderail

When standing up from the bed:

► Press GO button on any bed controller for activation.
► Grip the head siderail where Mobi-Lift® controller is placed.
► Press and hold the up button 1 to adjust the height of the bed when standing up from the bed.

60 D9U001GRA-0101_12
14.5 Angle indicators
It is possible to equip the Eleganza 2 with integrated angle indicators. The angle indicators are integrated in all siderails. The angle
indicator in foot siderails is not illuminated and is used for angle measurement when the bed is positioned in the Trendelenburg and
Reverse Trendelenburg positions.
The angle indicator in the head siderails are illuminated and are equipped with lowest (safe) position indication. A green light indica-
tes the lowest (safe) position of the bed. A white light indicates all other positions.
The angle of tilt is indicated on the outer circuit of the angle indicator.

Fig. Angle indicator in foot siderail Fig. Angle indicator in head siderail

D9U001GRA-0101_12 61
14.6 X-Ray Backrest (optional)
WARNING!
Respect maximum dimensions of x-ray cassettes!
► Maximum dimensions of any x-ray cassette for X-Ray Cassette Holder are 67 cm x 46 cm x 1,7 cm!

Fig. Backrest X-ray option

Upon request it is possible to equip Eleganza 2 with x-ray translucent backrest which consists of HPL. The bed is equipped with x-
-ray cassette holder located under the backrest. This design allows taking x-ray images of the patient’s lungs and upper body parts
without moving the patient.

Necessary steps before the examination:

► Ensure the patient is in the centre of the bed.
► Adjust backrest up using one of the bed positioning functions.
► Insert x-ray cassette by wider side 1.
► Position cassette to desired position using slider 2.
► Lock slider 2.
► Lock safety pin 3.

NOTE: The bed with backrest x-ray cannot be equipped with Junior Kit.

Fig. Cassette holder

1. Cassette holder
2. Cassette slider
3. Locked safety pin

62 D9U001GRA-0101_12
14.7 SafeSense® 3 ready bed
WARNING!
Before use of the SafeSense® 3 Monitoring System with Eleganza 2 medical bed read the instructions for use
for SafeSense® 3 Monitoring System!

CAUTION!
Risk of material damage due to steam cleaning of the SafeSense 3 Monitoring System!
► Always remove the components of the SafeSense® 3 Monitoring System (Hub Box, Air Pad, Wetness Pad and
cables) from the Eleganza 2 medical bed on which the system has been installed!

Specific configuration of the Eleganza 2 medical bed is compatible with SafeSense® 3 Monitoring system.
SafeSense® 3 ready Eleganza 2 medical bed includes Attendant Control Panel with SafeSense® 3 Control, accessory rail with
Power Supply/Data cable in safety position, holder of the interconnecting elements for Nurse Call cable and LAN cable behind the
accessory rail on the right side of the Eleganza 2 bed and holder of the interconnecting elements for Nurse Call cable and LAN
cable at head end of the Eleganza 2 bed.

Fig. SafeSense 3 ready Eleganza 2 bed

D9U001GRA-0101_12 63
15 Mattress
The manufacturer recommends the use of the following mattress systems on the Eleganza 2 bed:
► EffectaCare 10, EffectaCare 20, PrimaCare 10, PrimaCare 20, CliniCare 10, CliniCare 20, CliniCare 30

16 Accessories
WARNING!
Risk of injury due to incompatible accessories!
► Only the manufacturer’s original accessories can be used.

WARNING!
Risk of injury due to damaged accessories!
► Use exclusively accessories in perfect condition.

NOTE: The manufacturer assumes no responsibility for the use of accessories not approved by the manufacturer.

NOTE: All accessories conform to IEC 60601-2-52.

The following accessories are suitable for the Eleganza 2:

■ Lifting pole
■ Triangular holder for lifting pole
■ Pole for devices and accessories
■ IV holder
■ External IV holder
■ Urinary bag holder
■ Urinary bottle holder
■ Redon bottle holder
■ Head Board and Foot Board Holder
■ Oxygen bottle holder
■ Compressor holder
■ Cannula holder
■ Name holder
■ Chart holder
■ Extension holder
■ Towel holder
■ Monitor shelf
■ Writing shelf
■ Handset holder
■ Handy box – storage pocket on the siderails
■ Protector
■ Extender
■ Soft guards for siderails
■ SafeSense®
■ SafeSense® 3

NOTE: Detailed information on SafeSense® is available in the instructions for use for this product. Detailed information on Safe-
Sense® 3 is available in the instructions for use for this product.

64 D9U001GRA-0101_12
16.1 Lifting Pole
WARNING!
Risk of patient‘s injury or damage to the bed due to incorrect use!
► Never exceed the maximum load of lifting pole – 75 kg.
► Never use the lifting pole for rehabilitation exercises.
► To prevent the bed from tipping over, ensure the lifting pole does not project out from the bed.
► Replace plastic handle every 4 years.
► The lifting pole is not designed for hanging any kind of accessories, controllers etc. except triangular holder.

Fig. Bushing for lifting pole or infusion stand Fig. Lifting pole

Placement:
■ In the bushings for lifting pole and infusion stands in the corners of the head end.

Load capacity:
■ Maximum load of lifting pole is 75 kg.

Lifting pole variants:

■ Lifting pole for beds with fixed head board and foot board – powder coated
■ Lifting pole for beds with fixed head board and foot board – chrome plated

Lifting pole positions:

■ Over the backrest (working position).
■ Parallel to the head board (when not in use).

To install the lifting pole:

► Insert lifting pole into corresponding bushings at the head end of the bed (corners).
► Ensure the safety pin locks are in place.
► Hang the grab handle on the lifting pole.

NOTE: The lifting pole is not a part of the delivery and needs to be ordered separately.
NOTE: The date of manufacture is marked on the grab handle. LINET® recommends replacing the plastic grab handle every
four years.

D9U001GRA-0101_12 65
16.2 Infusion Stands
WARNING!
Risk of injury or collision due using of unsuitable accessories!
► Use infusion stands exclusively for accessories listed in the instructions for use.
► Only mount an infusion pump to the lower (wider) telescopic section of an infusion stand above the head board /
foot board.
► Never mount an infusion pump to the upper (thiner) telescopic section of an infusion stand.
► Ensure the infusion pump will not collide with any movable parts of the bed (especially Backrest part) or with the
patient. This must be verified DURING installation.
► In case of failure to comply those instructions there is a risk of collision of accessories with movable parts of the
bed or injury of the patient.
► Do not use the infusion stand as driving/pushing device during the bed transport.

It is possible to insert infusion stands into the bushings at the head and foot ends of the bed.
► Use exclusively infusion stands with 4 hooks for hanging IV bags or baskets for intravenous solutions.
► Ensure that the weight-bearing capacity of the 4 hooks is not exceeded.
Capacity per hook: 5 kg
► Ensure that the infusion stand’s weight-bearing capacity is not exceeded.

Placement:
■ In the bushings for lifting pole and infusion stands in the corners of the head
end.

Use:
■ Use exclusively infusion stands with 4 hooks for hanging IV bags or baskets for
intravenous solutions.

Load capacity:
■ Maximum load per hook is 2 kg.
■ Ensure the capacity of infusion stand and per hook is not exceeded.

Fig. Infusion stand

16.3 External holder for infusion stand/pump

WARNING!
Risk of patient’s injury or damaging the holder due to incorrect use!
► Never place lifting pole into external holder for infusion stands/pumps.

External holder is designed for placing infusion stands or pumps on the bar under the head board.

Placement:
■ On the head bar under the head board.

Load capacity:
■ Maximum load of holder is 25 kg.

Fig. External infusion stand/pump holder

66 D9U001GRA-0101_12
16.4 Oxygen Bottle Holder
WARNING!
Risk of injury by the oxygen bottle holder or due to incorrect use or due to careless transport!
► Ensure the oxygen bottle holder is correctly fitted in the correct position.
► Be aware of persons or objects in close proximity when moving or manipulating the bed equipped with oxygen
bottle holder.
► Ensure the oxygen bottle valve is not damaged by careless or incorrect manipulation or by placement.

Oxygen bottle holder is designed for placement and transport of oxygen bottles. It is possible to use oxygen bottles with weight of
15 kg and a volume of 5 litres.

Variants and correct placement of oxygen bottle holders:

■ Horizontal oxygen bottle holder
■ Vertical oxygen bottle holder

Placement:
■ On the head bar under the head board.

Load capacity:
■ Maximum load of holder is 15 kg.

Fig. Horizontal holder Fig. Vertical holder

16.5 Handy box – storage pocket for siderails

Storage pocket “Handy box” is designed for storing small personal items of
the patient (e.g. glasses, cell phone, keys etc.)

Placement:
■ On the upper edge of the siderail

Load capacity:
■ Maximum load capacity of the box is 2 kg.

Fig. Handy box

D9U001GRA-0101_12 67
16.6 Head Board and Foot Board Holder
Head Board and Foot Board Holder is designed for hanging deferred head
board or foot board to the holder.

Placement:
■ On the upper edge of the head board or foot board

Fig. Head Board and Foot Board Holder

16.7 Name holder

Name holder is designed for placing patient’s name in the holder.

Placement:
■ In the middle of upper edge of the head board or foot board

Fig. Name holder

16.8 Chart Holder

Chart holder is designed for placing charts, which are registering the development of health condition of the
patient.

Placement:
■ In the middle of upper edge of the head board or foot board

Fig. Chart holder

68 D9U001GRA-0101_12
16.9 Handset Holder
WARNING!
Risk of injuring the patient or damaging the bed due to incorrect placement!
► Never place handset holder on the skewed edge of head board and foot board.
► Never place handset holder to the handles near the Mobilift controller.
► Handset holder must be placed on the siderails.
► Ensure there is no collision between handset holder and movable parts of the bed or with the patient.

Holder is designed for placing handset to the holder on the siderails.

Placement:
■ On the upper edge of the siderail

Install holder on the bed as follows:

► Put the handset on the siderail handle.
► Place handset in the holder.

Fig. Correct placement of the handset holder

16.10 Monitor Shelf

WARNING!
Risk of injury by shelf due to incorrect use!
► Never place infusion pumps on the shelf.
► Placement of the shelf on the bed with removed head board and foot board is forbidden.
► Shelf must only be placed to the foot board.

Monitor shelf is designed for placement to the foot board. The shelf must head into the bed after placement.
Controlling the shelf:
Working position:
► Place the shelf to the bushings on the foot end. Longer
part of the shelf is heading into the bed.
► Unlock the shelf by pulling the locking lever.
► Flip the shelf into the bed.

Storage position:
► Unlock the shelf by pulling the locking lever.
► Flip the shelf so it vertically copies the head board or foot board.

Fig. Monitor shelf in working position

Position:
► To the bushings on the foot end corners
Load capacity:
► Maximum load of shelf is 35 kg.

D9U001GRA-0101_12 69
16.11 Compressor Holder
Compressor holder is designed for handing compressor on the foot
board.

Placement:
■ On the foot board, between foot board handles

Load capacity:
■ Maximum load of the holder is 10 kg.

Fig. Compressor holder

16.12 Towel holder

Towel holder is designed for hanging the towel on the holder.

Placement:
■ On the head board or foot board to the head board or foot board
handles

Load capacity:
■ Maximum load of the holder is 2 kg.

Fig. Towel holder

16.13 Extension Holder

WARNING!
Risk of injuring the patient due to incorrect use!
► Placement of the extension holder on the bed with removed head board and foot board is forbidden.

Holder is designed for placing extension on the holder.

Placement:
■ To the bushings on the foot/head end corners

Load capacity:
■ Maximum load of the holder is 75 kg.

Install extension holder as follows:

► Insert holder to the bushings on the foot/head end corners.
o Horizontal tube is heading outside the bed.
► Ensure the safety pin is securely locked in the bushings.

Fig. Extension holder

70 D9U001GRA-0101_12
16.14 Soft Guards for Siderails
WARNING!
Risk of damaging the guards due to incorrect use!
► Always take down the guards before transporting the bed.
► Always remove the foam insert from the guards before washing.
► Ensure the transparent nets are bears on the control elements of the bed. There is a risk of damaging the guards
in case of their replacement.

Soft guards for siderails are designed for raising the patient safety while he is staying on the bed. Guards are protecting patient
against bruising from siderails.

Install the guards as follows:

► Unzip the zip on the bottom of the guard.
► Put the guard on the siderail so the transparent net is placed on the control or information element of the bed
(angle indicators, Mobilift)
■ Head siderail – 2 nets: one for Mobilift + angle indicator, second for siderail controller
■ Foot siderail – 1 net: for angle indicator
► Zip the zip on the siderail guard.

Uninstall the guards as follows:

► Unzip the zip on the bottom of the guard.
► Carefully pull down the guard from the siderail so it will not get damaged.
► Zip the zip on the siderail guard.
► Store the guards on the suitable, dry place for storage of the medical devices.

Fig. Bed with installed siderail guards

16.15 Protector®
WARNING!
Risk of injury due to patient falling out of bed!
► Ensure that Protector® is securely anchored to the bushing.
► To check stability, pull the protector up without touching the release button.
► Always check that the siderail is properly locked.

WARNING!
Risk of damage to the bed or patient injury!
► Do not mount head board or foot board to accessory bushing (3).
► Do not mount lifting pole to accessory bushing (3) on the foot end.
► Do not use protector with bed extension.

Protector® is not a component of the bed. Protector® is optionally available

D9U001GRA-0101_12 71
 Fig. Closed Protector® Fig. Opened Protector®

1. Releasing button
2. Tube of Protector®
3. Bushing of Protector®

Fig. Safety pin anchored in bushing

Mount Protector® to closed position as follows:

► Insert the tube of protector (2) into bushing near foot end of the bed (3) so the protector is facing the siderail.
► Safety pin must be locked in place.

Mount Protector® to open position as follows:

► Insert the tube of protector (2) into bushing near foot end of the bed (3), so the protector is facing out from bed.

Dismount Protector® as follows:

► Press and hold the releasing button (1).
► Pull the protector up.

72 D9U001GRA-0101_12
16.16 Siderail extension – „Extender®“ (SR55)
WARNING!
Risk of injury or collision due to incorrect use!
► The Extender® can be used with single collapsible siderails only. The manufacturer will not be held responsible
for any consequences if the Extender® is used with other types of siderails.
► Movement of the bed must be considered if the Extender® is installed.
► Use of the Extender® in a manner other than stated in the instructions for use is on the responsibility of
personnel.
The manufacturer shall not be held liable for incorrect use!

It is recommended to use Extender® (model number SR55) if a mattress higher than the recommended height was placed on the
bed. The Extender® is used to raise the height of the siderails and helps to secure patients safety. The Extender® is designed for
single collapsible siderails only.

It is recommended to use Extender® with the following mattresses:

■ Passive mattress: with maximum height 22 cm
■ Active mattress: with maximum height 22 cm
□ Virtuoso

Fig. Installation of Extender®

Fig. Securing Extender®

Install the Extender® as follows:

► Place the Extender® (without securing screws) on the upper edge of the siderail. Siderails must be in upper position.
Square hole is pointed into the mattress platform.
► Insert screws from the inside of the bed thru the securing holes in Extender®.
► Secure the screws with the plastic rosette nuts and tighten. The rosette nu ts are pointed outside from the bed.
► Check if the Extender® is secured correctly by pushing it sideways.

D9U001GRA-0101_12 73
16.17 SafeSense
Purpose:
SafeSense system is intended for informing nursing staff as soon as the resident/patient leaves the bed or does not return to the
bed when expected.

Description:
SafeSense system consists of Sensor mat, Bed-Exit Box, Plug and Play adapter and connecting cables.

Placement:
Bed-Exit Box and Plug and Play adapter are located on accessory rail on the right side of the bed.
Nurse Call connector is fixed on the crossbar of head end.
Sensor mat should be fixed on the seat section of mattress platform. Follow instructions for use for SafeSense.

Fig. SafeSense (Sensor mat)

74 D9U001GRA-0101_12
16.18 SafeSense® 3
CAUTION!
Eleganza 2 bed is compatible with Stand-alone version of the SafeSense® 3 Monitoring System and with Sa-
feSense® 3 Monitoring System in Version for Eleganza 2. Eleganza 2 bed must be SafeSense® 3 ready for use
with SafeSense® 3 in Version for Eleganza 2 so the compatilility depends on configuration of the bed.

Purpose:

The SafeSense® 3 Monitoring System is intended to use for the automated, contactless and unobtrusive continuous mobility detec-
tion of patients in bed, bed exit and continuous wetness detection in the context of healthcare and nursing facilities.

Description of the SafeSense® 3 Monitoring System in Version for Eleganza 2:

■ SafeSense® 3 Hub
■ Comb-like part securing connectors connected to the Hub
■ Hub Holder
■ SafeSense® 3 Air Pad
■ Air Hose
■ Cables (Nurse Call cable, LAN cable)
■ Wetness Pad with Wetness Pad Cable (optionally)

Placement:

Hub Box must be safely placed on the accessory rail on the right side of the Eleganza 2 bed. Air Pad must be fixed on the Backrest
of the Eleganza 2 bed and under the compatible mattress. Wetness Pad must be placed on the seat section of the compatible
mattress and Air Hose and each cable must be safely installed according to the Instructions for use for SafeSense® 3 Monitoring
System.

Eleganza 2 Control Unit

Inputs
3 15
Wetness Pad

ACP with Air Pad

SafeSense 3 Connectivity Hub Air
Control Box Hose
Hirschmann
7 pin
connector

Nurse Call System

LAN/WiFi

Fig. Diagram of the SafeSense® 3 Monitoring System with Eleganza 2 bed

D9U001GRA-0101_12 75
17 Cleaning/Disinfection
WARNING!
Risk of injury when working on the bed!
► Prior to assembly, disassembly, cleaning and maintenance, ensure that all adjustment functions are locked.
► Ensure the bed is disconnected from the mains during cleaning process.
► Pay extra attention when cleaning any movable or controlling mechanisms of the bed to prevent involuntary
activation, entrapping or crushing.
► Cleaning should be entrusted to the person who has been trained to control the bed.

WARNING!
Risk of damaging the bed due to use of incorrect cleaning detergents or cleaning processes!
► The bed is not designed for machine washing.
► The selection of cleaning detergents/disinfections and their correct concentration is responsibility of responsible
person in charge of cleaning/disinfection in accordance with the informations provided in this manual.
► Never use germicidal or other radiants for disinfection of the bed, if those radiants act directly on the bed.
► Follow these instructions and follow the prescribed dosage by the manufacturer of cleaning detergents.
► Not following recommended processes may result in damaging or deterioration of the bed condition.
► Check if used cleaning agents and disinfectants are compatible with materials that the product consists
of! For information see the following table.

BED COMPONENTS THAT ARE MATERIALS (SURFACES OF THE MENTIONED BED COMPONENTS)
INTENDED TO BE CLEANED

Do not clean what is not mentioned Competent user is responsible for check if used cleaning agents and disinfectants
in this column! are compatible with mentioned materials!
Head board and foot board Polypropylene (PP) + Lacquered steel
Head siderails and foot siderails Polypropylene (PP) + Acrylonitrile butadiene styrene (ABS) + Polyamide (PA6) + La-
cquered steel
Mattress support platform covers blown plastic mattress support plat- version with x-ray plastic mattress supp-
(Backrest) form covers: Polypropylene (PP) cassette holder: High ort platform covers:
Pressure Laminate Acrylonitrile butadiene
(HPL) styrene (ABS)
Mattress support platform covers blown plastic mattress support plat- plastic mattress support platform covers: Acrylo-
(Thighrest, Calfrest) form covers: Polypropylene (PP) nitrile butadiene styrene (ABS)
Seat section Polypropylene (PP)
Castors Polyurethane (PUR) + Polypropylene (PP)
Castor control levers standard: Polyamide (PA6) + Thermoplastic elastomer (TPE)
Frame of the mattress support plat- Polyamide (PA6) + Lacquered steel
form
Columns Aluminium (Al) + Acrylonitrile butadiene styrene (ABS) + Polyoxymethylene (POM)
Undercarriage cover two-part undercarriage cover: Acry- one-part undercarriage cover: Acrylonitrile butadi-
lonitrile butadiene styrene (ABS) + ene styrene (ABS)
Lacquered steel
Corner covers Acrylonitrile butadiene styrene (ABS)
Corner bumpers Polypropylene (PP)
Keyboards (Attendant Control Panel, Polyethylene terephthalate (PET)
Handset, control elements integrated
in the siderails)
CPR levers Polypropylene (PP)
Labels Polyethylene terephthalate (PET)
Accessory rail Polyoxymethylene (POM) + Lacquered steel
Actuators Polyamide (PA6) + Aluminium (Al)

76 D9U001GRA-0101_12
17.1 Safety Instructions for Cleaning and Disinfection of the Bed
Preparation for cleaning:
► Drive the bed on a place where the cleaning process will be performed and then brake the bed.
► Position the mattress platform to its highest positions and also position the backrest and thighrest parts so the back side
of those parts are accessible for cleaning.
► Lock all adjustment functions of the bed to prevent involuntary adjustment of the bed or injuries during cleaning.
► Disconnect the bed from the mains.
► Check if all connectors are properly fixed (controllers, actuators and control unit).

Recommendations for cleaning:

► Only use detergents designed for cleaning the medical technologies.
► Dilute the detergents in accordance with instructions from manufacturer of detergents.
► Never use any strong acids or bases. Optimal pH range is 6-8.
► Never use abrasive powders, steel wool or other materials and detergents that may damage the surface of the bed.
► Never use detergents with solvents that may affect the structure and consistency of the plastic parts (benzene, toluene,
acetone etc.).

Cleaning process:
► Clean by wiping the bed with damp, well-wrung textile material.
► The detergent can be applied by spraying on bed or on the textile material.
► Perform cleaning and disinfection of the bed in the appropriate range. The range of cleaning and disinfection should be
distinguished according to the degree of contamination of the bed and the cleaning mode (daily, before changing patient or
complete).
► Electronic parts that may be contaminated clean carefully and only their outer side. Never open those connectors due to
cleaning or disinfection. Those components should not be exposed to prolonged or continuous exposure to moisture.
► Let the bed dry completely after cleaning or disinfection process.
► After drying the bed place the mattress back on the mattress platform.
► After drying the bed check functions of the bed.

17.2 General Instructions for Cleaning and Disinfection

17.2.1 Daily Cleaning
It is recommended to clean all parts of the bed which are touched by patient or personnel (e.g. siderails, head board and foot
board, handset, lifting pole etc.) and all handles, all control elements and accessory rails.

17.2.2 Cleaning before Changing Patients

It is recommended to completely clean and disinfects all parts of the bed which are touched by patient or personnel (see Daily Cle-
aning), mattress platform, columns, undercarriage covers and mattress.

17.2.3 Complete Cleaning / Cleaning before First Use

It is recommended to clean the bed completely before the first use and then at least once in 4-8 weeks.

17.2.4 Cleaning of Spilled Fluids

Spilled fluids should be cleaned as soon as possible. Always disconnect the bed from mains before cleaning the spilled fluids.
Some fluids used in health care may cause permanent stains.

17.2.5 Damaged Foam Mattress

Mattress should be periodically checked for cracks, holes or cracks that may affect the integrity, water resistance or resistance to
infections of the cover. Contact the service department of the manufacturer according to scope of damage to cover.

D9U001GRA-0101_12 77
17.3 Mode of Cleaning and Disinfection

Part of bed – Eleganza 2 Daily C&D Changing patient C&D Complete C&D
Stickers (Split plastic siderails)   
Stickers (Single collapsible 
siderails)  
Siderails mechanism   
Head board and foot board 
(stickers)  
Controllers (cables)   
Mattress platform covers   
Undercarriage cover   
Telescopic columns   
Corner bumpers   
Mains cable   
Undercarriage frame   
Castors   
Actuators   

78 D9U001GRA-0101_12
17.4 Steam Cleaning
WARNING!
Observe the instructions from instructions for use of the bed before, during and after each steam cleaning!
► The bed could be damaged and LINET withdraws from warranty of the bed if these instructions are not followed.

► Disconnect bed from the mains before each steam cleaning.

► Use just steam cleaners intended for medical devices for steam cleaning of the bed.
► Medical staff is allowed to perform the steam cleaning of the bed only in accordance with instructions for use of the bed
and with instructions for use of the steam cleaner.
► Before each steam cleaning the bed must be tempered to ambient temperature of a room where the steam cleaning will
be performed in order to prevent condensate from being produced redundantly on the bed surface.
► Do not use any chemicals with the steam cleaner.
► Speed of the steam cleaning (processing speed) must not be less than 10 cm per second. Temperature compensation
of the cleaned surface and of the ambient environment must happen before hot steam will be applied to the same place
again.
► Set and check the temperature parameter on control panel of the steam cleaner. The temperature of the hot steam must
never exceed value 90 °C. Set pressure must not exceed value 5 bars.
► Clean the labels on the bed by steam with lower pressure and avoid mechanical contact with material of the labels during
each steam cleaning. Do not use any brushes to clean the labels.
► Do not use any accessories like high-pressure hose with nozzle to clean non-metal parts of the bed and
electrocomponents.
► Use the steam cleaner only with soft non-metal brushes and with soft cloth in order to reduce pressure of the steam
cleaner.
► Do not leave open the connectors of electrocomponents during each steam cleaning in order to prevent steam and water
from penetrating the connectors.
► During each steam cleaning of the bed be careful not to overheat and damage sensitive parts of the bed, e.g. keyboards
of control elements, displays, control units, actuators, connectors, decors and labels.
► After each steam cleaning let the bed surface become dry during at least 60 minutes and do not use the bed unless
ambient tempreture and bed temperature are compensated. Never connect plug of the power supply cord to the mains
unless the plug is completely dry after the previous steam cleaning.
► After each steam cleaning it is necessary to check whether each control element of the bed works in accordance with user
manual of the bed.

D9U001GRA-0101_12 79
18 Troubleshooting
DANGER!
Danger to life due to electric shock!
► If a fault occurs ensure the electric motor, power box and other electrical parts checked by qualified personnel
only.
► Do not open protective covers of the electric motor or power box.

Error/Fault Cause Solution

Adjusting with position buttons not possible GO button was not pressed Press the GO button.
Function disabled on Attendant Control Panel Enable disabled function.
Check the mains connection.
Drive motors have no power Defective drive
Notify the service department of
motors Defective accumulator
the manufacturer.
Plug inserted incorrectly Insert the mains plug correctly.
Notify the service department of
Faulty power box
the manufacturer.
Notify the service department of
Faulty control element
the manufacturer.
Faulty mattress platform height/tilt adjus- There is an object on the
Remove the object.
tment undercarriage cover
Function disabled on Attendant Control Panel Enable disabled function.
Drive motors have no power Check the mains connection.
Defective drive motors Notify the service department of
Defective accumulator the manufacturer.
Plug inserted incorrectly Insert the mains plug correctly.
Notify the service department of
Faulty power box
the manufacturer.
Notify the service department of
Faulty control element
the manufacturer.
Lowering backrest from the upright position Object under the backrest or in the drive me-
Remove the object.
not possible chanism
Notify the service department of
Locking handle is defective
the manufacturer.
Adjusting siderails not possible The siderail lock is dirty Clean the locking mechanism.
Notify the service department of
Locking handle is defective
the manufacturer.
Faulty brakes The brakes are blocked by dirt Clean the brake system.
Notify the service department of
The brake mechanism is defective
the manufacturer.

80 D9U001GRA-0101_12
19 Maintenance
WARNING!
Risk of injury when working on the bed!
► Ensure that the bed is disconnected from the mains power prior to installation, putting into service, maintenance
and deinstallation.
► Ensure that the castors are locked prior to installation, putting into service, maintenance and deinstallation.

WARNING!
Risk of injury due to defective bed!
► Have a defective bed repaired immediately.
► If the defect cannot be repaired, do not use the bed.

CAUTION!
Material damage due to incorrect maintenance!
► Ensure that maintenance is performed exclusively by manufacturer´s customer service or by authorised service
personnel certified by the manufacturer.
► If the defect cannot be repaired, do not use the bed.

LINET ® recommends attaching the maintenance plaque to the bed.

19.1 Regular maintenance

► Check regularly movable parts for wear.
► Perform regularly visual check of the product (with delivery note if necessary).
► Ask service department of the manufacturer for addition of the original spare parts if some product parts are missing.
► Ask service department of the manufacturer for replacement of any damaged product parts by the original spare parts.
► Check that the accumulator is working properly. Disconnect the bed from the mains power to check signalisation of
accumulator indicator according to the instructions for use.
► Have the accumulator replaced if it is not working properly.
► Check regularly that all accessories are working properly.
► Replace damaged accessories immediately.

19.2 Spare Parts

The serial label is located on the frame of the mattress support platform. The serial label contains information for claims and orde-
ring replacement parts.

Information about spare parts is available from:

■ Manufacturer´s customer service
■ Sales department

19.3 Safety Technical Checks

WARNING!
Risk of injury due to incorrect safety technical checks!
► Ensure that safety technical checks are performed exclusively by manufacturer´s customer service or by authori-
sed service personnel certified by the manufacturer.
► Ensure that the safety technical checks are recorded in the service and maintenance log.

Safety technical check of the medical bed must be performed at least once every 12 months.

The procedure for performing the safety technical check is stipulated in EN 62353:2014.

NOTE On request, the manufacturer will provide service documentation (e.g. circuit diagrams, component part lists, descriptions,
calibration instructions etc.) for service personnel for the repair of ME equipment designated by the manufacturer as repairable by
service personnel.

D9U001GRA-0101_12 81
20 Disposal
20.1 Environment Protection
The company LINET® is aware of the importance of environmental protection for future generations. Within this company the
environmental management system is applied in accordance with the internationally agreed standard ISO 14001. The compliance
with this standard is annually tested by the external audit executed by an authorised company. Based on the Directive No. 2002/96/
EC (Directive WEEE - Waste, Electric and Electronic Equipments) the company LINET, s. r. o. is registered in the List of Electric
and Electronic Equipment Producers (Seznam výrobců elektrozařízení) on the Ministry of the Environment of the Czech Republic
(Ministerstvo životního prostředí).

Materials used in this product are not environmentally hazardous. LINET® products meet valid requirements of national and Euro-
pean legislation in the areas of RoHS and REACH, so they do not contain any prohibited substances in excess quantities.
None of the wooden parts is made of tropical wood (such as mahogany, rosewood, ebony, teak etc.) or made of timber from the
Amazon region or from similar rainforests. Product noise (sound pressure level) meets requirements of the regulations for the pro-
tection of public health against undesirable effects of noise and vibration in protected interior spaces of buildings (according to stan-
dard IEC 60601-2-52). Used packaging materials are in accordance with requirements of the Packaging Act (Zákon o obalech).
For disposal of packaging materials after installation of products contact your sales representative or manufacturer´s customer
service about the possibility of a free take-back of packaging through an authorized company (more details on www.linet.cz).

20.2 Disposal
The main objective of the obligations arising from the European Directive No. 2012/19/EU on Waste, Electric and Electronic Equip-
ments (nationally regulated in Act No. 185/2001 Coll. as amended. On Waste and in Decree of the Ministry of the Environment No.
352/2005 Coll. as amended), is to increase the re-use, material recovery and recovery of electric and electronic equipment at the
required level, thereby avoiding the production of waste and thereby avoiding the possible harmful effects of hazardous substances
contained in electric and electronic equipment on human health and the environment. LINET® electric and electronic equipments
that have a built-in accumulator or accumulator are designed so that the used accumulators or batteries can be safely removed by
LINET® qualified service technicians. There is an information about its type on the built-in accumulator or accumulator.

20.2.1 Within Europe

To dispose of the electric and electronic equipment:

► The electric and electronic equipment must not be disposed of as household waste.
► Dispose of this equipment at designated collection points or take-back points.

To dispose of the other equipment:

► The equipment must not be disposed of as household waste.

► Dispose of this equipment at designated collection points or take-back points.

LINET® participates in a collective system with take-back company REMA System (see www.remasystem.cz/sberna-mista/).
By bringing electric and electronic equipment to a take-back point, you participate in recycling and you save primary raw material
resources while protecting your environment from effects of unprofessional disposal.

20.2.2 Outside Europe

► Dispose of the product or its components in accordance with local laws and regulations!
► Hire an approved waste disposal company for disposal!

82 D9U001GRA-0101_12
21 Warranty
LINET ® will only be held responsible for the safety and reliability of products that are regularly serviced, maintained and used in
accordance with the safety guidelines.

Should a serious defect arise that cannot be repaired during maintenance:

► Do not continue to use the bed.

This product is covered by a 24-month warranty from the date of purchase. The warranty covers all material and manufacturing-re-
lated failures and errors. Failures and errors caused by incorrect use and external effects are not covered. Justified complaints will
be fixed free of charge during the warranty period. Proof of purchase, with the date of purchase, is required for all warranty service.
Our standard terms and conditions apply.

22 Standards and Regulations

Apllied norms are stated on Declaration of Conformity.

The bed equipped with Junior Kit complies with all requirements of AFSSAPS (Agence française de sécurité sanitaire des
produits de santé). We declare that our product Eleganza 2 with universal twin plastic siderails equipped with Junior Kit is
safe under condition of common use in compliance with instructions and that measures have been taken to ensure the
conformity of recommendation by AFSSAPS described in letter dated 18.6.2014.

The manufacturer adheres to a certified quality management system in compliance with the following standards:
■ ISO 9001
■ ISO 14001
■ ISO 13485
■ MDSAP (Medical Device Single Audit Program)

D9U001GRA-0101_12 83
22.1 AFSSAPS Declaration

84 D9U001GRA-0101_12