User Manual and Technical

Description

Image 3

Hospital bed for acute care

D9U001AM0-0101

Version: 04

Publication Date: 2018-05

Manufacturer:

LINET spol. s r. o.
Želevčice 5
274 01 Slaný
Czech Republic

Tel.: +420 312 576 111

Fax: +420 312 522 668
E-mail: info@linet.cz
http://www.linet.com

Image 3
Hospital bed for acute care

Author: LINET, s.r.o.

Related links: www.linet.cz

D9U001AM0-0101
Version: 04
Publication Date: 2018-05

Copyright © LINET, s.r.o., 2018

Translation © LINET, 2018

All rights reserved. All trademarks and brands are the property of the appropriate owners. The manufacturer
reserves the right to changes in the contents of this manual that relate to the product´s technical regulations. It is
for this reason that the contents of this manual may indicate differences from the current manufacture of the
product.

D9U001AM0-0101_04 2
Table of Content

1 Symbols ........................................................................................................................... 5
1.1 Warning Notices ..................................................................................................................................5
1.2 Instructions ..........................................................................................................................................5
1.3 Lists 5
1.4 Symbols and Labels on the Product ...................................................................................................6
1.5 Serial Label with UDI ...........................................................................................................................7
1.6 Definitions ...........................................................................................................................................8
1.7 Abbreviations ......................................................................................................................................9

2 Safety and Dangers ....................................................................................................... 10

2.1 Safety instructions .............................................................................................................................11
2.2 Conditions of Use ..............................................................................................................................13
2.3 Specifications of Use.........................................................................................................................13

3 Standards and Regulations .......................................................................................... 13

4 Functioning .................................................................................................................... 14
4.1 Correct use ........................................................................................................................................14
4.2 Incorrect Use .....................................................................................................................................14

5 Scope of Delivery and Bed Variants............................................................................. 15

5.1 Scope of Delivery ..............................................................................................................................15
5.2 Bed Variants ......................................................................................................................................15
5.3 Applied parts type B ..........................................................................................................................16

6 Setup .............................................................................................................................. 17
6.1 Transport ...........................................................................................................................................17
6.2 Setup 17

7 Battery Activation .......................................................................................................... 18

7.1 Placement of Control Section ..........................................................................................................18
7.2 Removing the Isolating Foil ..............................................................................................................18
7.3 Isolating Foil ......................................................................................................................................18

8 Assembly ....................................................................................................................... 19
8.1 Potential Equalisation........................................................................................................................19
8.2 Mattress support platform .................................................................................................................20
8.3 Standard version: Image 3 (1AM) – Split Telescopic Siderails .........................................................21
8.4 Washable version: Image 3 (1AMW) – Split Telescopic Siderails .....................................................22
8.5 Head Board and Foot Board .............................................................................................................23

9 Operation ....................................................................................................................... 24
9.1 Initial Operation .................................................................................................................................24
9.2 Battery ...............................................................................................................................................25
9.3 Battery charging ................................................................................................................................25
9.4 Status Faulty Battery .........................................................................................................................26
9.5 Status Discharged Battery ................................................................................................................26
9.6 Removing the Bed from Service .......................................................................................................27
9.7 Deactivating the Battery ....................................................................................................................27

10 Manipulation .................................................................................................................. 27

D9U001AM0-0101_04 3
10.1 Supervisor control panel (nurse controller) .................................................................................28
10.2 Handset .......................................................................................................................................32
10.3 Night Bed Lightning .....................................................................................................................35
10.4 Bed Illumination ...........................................................................................................................35
10.5 CPR backrest release ..................................................................................................................36
10.6 Siderails .......................................................................................................................................37
10.7 Castor Control and Bed Transport ...............................................................................................39

11 Accessories ................................................................................................................... 41

12 Cleaning and Disinfection ............................................................................................. 49

12.1 Safety Instructions for Cleaning and Disinfection of the Bed ......................................................49
12.2 General Instructions for Cleaning and Disinfection .....................................................................50
12.3 Choosing of Detergents or Disinfections .....................................................................................51
12.4 Machine washing .........................................................................................................................52

13 Troubleshooting ............................................................................................................ 54
13.1 Sound signals of the bed .............................................................................................................54

14 Maintenance................................................................................................................... 55
14.1 Maintenance Work .......................................................................................................................55
14.2 Functioning ..................................................................................................................................56
14.3 Beds designed for machine washing ...........................................................................................58

15 Disposal ......................................................................................................................... 59
15.1 Environmental Protection ............................................................................................................59
15.2 Disposal .......................................................................................................................................59

16 Warranty ......................................................................................................................... 60

17 EC Declaration of Conformity ....................................................................................... 61

18 Technical Specifications ................................................................................................ 62

18.1 Mechanical Specifications (Standard Version) ............................................................................62
18.2 Mechanical Specifications (Washable Version) ...........................................................................63
18.3 Environment Conditions (Standard and Washable Version) .......................................................63
18.4 Electrical Specification (Standard and Washable Version) .........................................................64
18.5 Electromagnetic Compatibility .....................................................................................................65

D9U001AM0-0101_04 4
1 Symbols

1.1 Warning Notices

1.1.1 Types of Warning Notices

Warning notices are differentiated by the type of danger using the following key words:

 Caution - 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.
Result, if necessary.

1.3 Lists

Structure of bulleted lists:

 List level 1
 List level 2

D9U001AM0-0101_04 5
1.4 Symbols and Labels on the Product

Read user manual.

Attention

Thermal protection of transformer

Only suitable for indoor use

Protection against accidents due to electrical current

– Type B applied parts

Safety isolation 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

Weight of bed

Do not put any objects here

D9U001AM0-0101_04 6
 Bed is designed for cleaning in decontamination
devices, which meets criteria stated in standard
AK:BWA 2009.

Designation of hospital bed for adults

EAC marking (Eurasian Conformity)

Do not open!

Recycle symbols

WEEE symbol (recycle as electronic waste)

1.5 Serial Label with UDI

Address of Distributor 1D Bar code GS1-128 Manufacturing Date DI (Device Identifier) / 2D Bar Code
(Serial Number) (Year-Month-Day) GTIN (Global Trade (GS1 Data
Item Number) Matrix)
DI+PI=UDI

Symbols Electrical Specification Serial Number PI (Product Identifier)

Fig. Serial Label with UDI (Image 3 standard)

D9U001AM0-0101_04 7
 Address of Distributor 1D Bar code GS1-128 Manufacturing Date DI (Device Identifier) / 2D Bar Code
(Serial Number) (Year-Month-Day) GTIN (Global Trade (GS1 Data
Item Number) Matrix)
DI+PI=UDI

Symbols Electrical Specification Serial Number PI (Product Identifier)

Fig. Serial Label with UDI (Image 3 washable)

1.6 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
pelvic 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 environment 3 (long-term care) and 5 (ambulatory care)
reduce Safe working Load by 35 kg.
Safe Working Load the highest allowable load on the bed (patient, mattress and accessories)

Siderail Height the height of the upper crossbar or the edges of the siderails (not the
highest point of the siderail controls) from the patient surface
Standard Bed Position  The height of the patient surface with regard to the floor is 400 mm
 The mattress support platform, including the individual parts, has to be in
a horizontal (level - 0°) position.
 The siderails are always locked in the upper position.
 The basic position of the integrated extension.

D9U001AM0-0101_04 8
1.7 Abbreviations
AC Alternating Current
CE European Conformity
CPR Cardiopulmonary Resuscitation
dB Sound Intensity Unit
DC Direct Current
EAC Eurasian Conformity
EMC Electromagnetic Compatibility
FET Field-effect transistor
HF High Frequency
ICU Intensive Care Unit
INT. Duty Cycle
IV Intravenous
LED Light Emitting Diodes
ME Medical Electrical (Equipment)
OFF Deactivated
ON Activated
REF Reference number (product type depending on configuration)
SCU System Control Unit
SN Serial number
SWL Safe Working Load
UDI Unique Device Identification (for medical devices)
USB Universal Serial Bus

D9U001AM0-0101_04 9
2 Safety and Dangers

WARNING!
Image 3 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 Image 3 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 Image 3 bed avoid squeezing those between parts of
the Image 3 bed!

WARNING!
Image 3 bed should not be used with bed hoists and bed lifts!

WARNING!
The Image 3 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!

D9U001AM0-0101_04 10
 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.

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.

2.1 Safety instructions

 It is necessary to read the user manual 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 the bed is operated by training and/or qualified personnel.
 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 support 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 supervisor 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.

D9U001AM0-0101_04 11
  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 support 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 support 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 support 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.
 Before setting the extra-low position, ensure there is no risk of any parts of the bed colliding with servers,
accessories or body parts.
 Ensure there is no risk of damaging the cables of the supervisor control panel or handset when they are
stored on siderails or on head board and foot board.
 To prevent collisions, do not put oxygen bottle holders directly under the mattress support platform.
 Always set mattress support platform to its lowest position and single parts of mattress support platform to
horizontal position in case the patient is left on the bed without supervision of personnel and if his health
and mental status may indicate increase risk of falling out of the bed or entrapment.
 Personnel must consider overall adjustment of the bed and locking all of the positioning functions in
accordance to health and mental status of patient, especially if the patient is left without supervision (even
for short period of time) of the personnel.
 Manual positioning of parts of the bed which are designed for electronic positioning (e.g. back rest) is
forbidden. Otherwise there is a risk of damaging and dysfunction of the back rest actuator or unprompted
fall of the back rest.

D9U001AM0-0101_04 12
2.2 Conditions of Use

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. a storm).

2.3 Specifications of Use

Medical purpose:
 Hospital bed for acute care, support for patient in various positions (Horizonal position, Trendelenburg,
Cardiac chair, etc.)
Patient:
 See chapter “Correct use”. Weight of patient + mattress + accesories can not be higher than safe working
load (SWL). Condition of patient is not important.
Personnel:
 Qualified medical staff (nurse, doctor) with medical school or university (EU). Any person familiar with the
manual. Patient if the condition permits.
Location:
 The bed is determined for application environments 1, 2, 3 and 5 according to IEC 60601-2-52: 2009. The
stable undercarriage with 4 castors makes it possible for the bed to be handled by one person. However,
the manufacturer recommends that at least two persons handle the bed.

3 Standards and Regulations

The bed complies with the following standards and directives:

 EN 60601-1:2006/A1:2013
 EN 60601-1-2:2007
 EN 60601-1-6:2010
 EN 60601-2-52:2010
 EN ISO 15223-1:2012
 EN ISO 10993-5:2009
 EN ISO 10993-10:2010
 93/42/EEC
 2011/65/EU
 AK-BWA:2009 (only Image 3 washable version)

The manufacturer adheres to a certified quality management system in compliance with the following
standards:
 EN ISO 9001
 EN ISO 14001
 EN ISO 13485

D9U001AM0-0101_04 13
4 Functioning

4.1 Correct use

DANGER!
Risk of injury or death due to use of incorrect equipment!
 Always conduct the risk assessments required for the selection of suitable equipment.

Image 3 is an acute care hospital bed. It is designed for supporting the patient in several positions such as
horizontal, Trendelenburg, Cardiac Chair etc.

Image 3 is suitable for:

 Patients
 With weight ≥ 40 kg
 With height ≥ 146 cm
 With BMI ≥ 17
 With a maximum weight (Follow chapter Technical Specifications)
 Whose weight (including mattress and accessories) does not exceed the SWL

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

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

 Personnel
 Qualified medical staff
 Any person familiar with the manual
 Patient (condition permitting)
 Use
 Acute care
 Standard care
 Location
 Application environments 1, 2, 3 and 5 according to IEC 60601-2-52.

4.2 Incorrect Use

Image 3 is not suitable for:

 Patients
 Not fulfilling conditions stated in chapter “Correct use”
 Use
 Other than described in the user manual
NOTE For information concerning uses other than those outlined in the “Correct 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 individuals 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 Correct Use).

D9U001AM0-0101_04 14
5 Scope of Delivery and Bed Variants

5.1 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 battery. To activate battery see chapter “Battery activation”.

5.2 Bed Variants

CAUTION!
Damage to the bed due to incorrect use!
 Use 125 mm castors exclusively on flat, even surfaces without any gaps.

5.2.1 Standard version: Image 3 – 1AM

Features – Image 3 Model 1AM (model no. see product label):
 Mattress Support Platform
 Mattress support platform consisting of removable plastic segments
 Siderails
 Without siderails
 Split telescopic siderails
 Single collapsible siderails, powder coated
 Head board and foot board
 Aluminium head/foot board with fixed coloured HPL panels
 Plastic head board and foot board, design Eleganza 1 and Eleganza 3
 Head board and foot board light design - powder coated tube with HPL
 Removable head board and foot board design A+ hotel look with HPL panels
 Castors
 125 mm Tente Linea with central braking system
 150 mm Tente Linea, with central braking system
 150 mm Tente Linea with 5th castor
 150 mm Tente Integral
 150 mm Tente Integral with 5th castor
 Control Elements
 ACP Nurse control panel (supervisor control panel)
 Handset with illuminated keyboard
 Handset without illuminated keyboard
 Other
 Linen shelf
 Vertical safety bumpers
 One pair of universal accessory holders
 One pair of urine bag holder
 CPR emergency backrest release
 Segufix holders
 Colour concept
 Powder coated metal parts RAL 9006 (light grey) + RAL 7043 (dark grey)
 Powder coated metal parts RAL 9002 (white)

D9U001AM0-0101_04 15
  Powder coated metal parts RAL 9006 (light grey)

5.2.2 Washable version: Image 3 – 1AMW

Features – Image 3 Model 1AMW (model no. see product label):
 Mattress Support Platform
 Mattress support platform consisting of removable plastic segments
 Siderails
 Split telescopic siderails
 Single collapsible siderails, powder coated
 Head Board and Foot Board
 Aluminium head/foot board with fixed coloured HPL panels, stainless bar on the head/foot board.
 Plastic head board and foot board, design Eleganza 1
 Castors
 125 mm Tente Linea with central braking system
 150 mm Tente Linea, with central braking system
 150 mm Tente Linea with 5th Castor
 150 mm Tente Integral
 150 mm Tente Integral with 5th castor
 Control Elements
 ACP Nurse control panel (supervisor control panel)
 Handset with illuminated keyboard
 Handset without illuminated keyboard
 Other
 Linen shelf
 Vertical safety bumpers
 One pair of universal accessory holders
 One pair of urine bag holder
 CPR emergency backrest release
 Segufix holders
 Colour concept
 Cataphoresis-coated metal parts RAL 9006 (light grey) + RAL 7043 (dark grey)
 Cataphoresis-coated metal parts RAL 9002 (white)

5.3 Applied parts type B

All the accesories the patient can reach are type B applied parts.

List of type B applied parts:

 ACP Nurse control panel (supervisor control panel)
 Handset
 Siderails
 Head Board and Foot Board
 Mattress support platform

D9U001AM0-0101_04 16
6 Setup

6.1 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 while the patient is on the bed during the transport.
 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 (main control) is activated.
 Ensure the brakes are released while moving the bed.

6.2 Setup

Set up the bed as follows:

 Unpack the bed.
 Check the delivery (see Scope of Delivery).
 Remove isolating foil from mains control box (see Removing Isolating Foil).
 Install equipment and accessories (see Assembly).
 In case of delivery with dismounted head board and foot board, mount the head and foot boards (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 authorised by the manufacturer.

D9U001AM0-0101_04 17
7 Battery Activation

7.1 Placement of Control Section

7.2 Removing the Isolating Foil

Pull

7.3 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: Isolating Foil is sharp-edged. Remove it carefully not to cut yourself.

D9U001AM0-0101_04 18
8 Assembly

WARNING!
Risk of injury when working on the bed!
 Ensure the bed is disconnected from the mains connection prior to assembly, disassembly and
maintenance.
 Ensure the castors are locked prior to assembly, disassembly and maintenance.

CAUTION!
Material damage due to incorrect assembly!
 Ensure the assembly is performed only by seller´s customer service or trained hospital personnel.

8.1 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. 1 Potential equalisation connector – male Fig. 2 Potential equalisation connector – female

Use equalisation connector if:

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

Before connecting the patient to an intravascular/intracardiac device:

 Connect the ground wire of the device to the potential equalisation connector (Fig. 1) on the bed on which
the patient in question is lying.
 Use a standard hospital connector (Fig. 2).
 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.

D9U001AM0-0101_04 19
8.2 Mattress support platform

The mattress support platform consists of removable plastic sections.

To remove/install sections of the mattress support platform:

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

Fig. 3 Bed sides (H=head, F=foot, R=right, L=left)

D9U001AM0-0101_04 20
8.3 Standard version: Image 3 (1AM) – Split Telescopic Siderails

Fig. 4a Standard Image 3 with split telescopic siderails

1. Foot board
2. Supervisor panel
3. Split telescopic siderails
4. Removable plastic segments
5. Head board
6. Handset
7. Central castor control system lever
8. Castor
9. CPR emergency lever – backrest release
10. Siderail release mechanism
11. Linen shelf

NOTE: For safe, easy handling, LINET® recommends that two technicians assemble the bed.

D9U001AM0-0101_04 21
8.4 Washable version: Image 3 (1AMW) – Split Telescopic Siderails

Fig. 4b Washable Image 3 with split telescopic siderails

1. Foot board
2. Split telescopic siderails
3. Siderail release mechanism
4. Head board
5. Bumper
6. Castor Tente Linea 150mm
7. CPR emergency lever – backrest release
8. Central castor control system lever
9. Linen shelf
10. Symbol indicating the bed is suitable for machine washing

NOTE: For safe, easy handling, LINET® recommends that two technicians assemble the bed.

D9U001AM0-0101_04 22
8.5 Head Board and Foot Board

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

WARNING!
Risk of injury when inserting the bed ends!
 To insert head board or foot board into corner posts, hold them by the corner handles on top with both
hands.
 Install head board or foot board before the first use.

WARNING!
Risk of injury due to incorrectly installed bed ends!
 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 bed ends!
 Before removing head board and foot board, ensure siderails are folded down and there are no
accessories attached to the head board and foot board.
 If a patient is lying in a bed with the head board 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 or foot board.

Fig. 5 Locking the head board or foot board

1. Locked
2. Unlocked

Install the head board or foot board as follows:

 Unlock safety levers on corner posts (red arrow marks direction).
 Slide head board or foot board into slots on corner posts with coloured panel on the outside.
 Lock safety levers on corner posts.

Remove the head board or foot board as follows:

 Unlock safety levers on corner posts.
 Pull head board or foot board upward.

D9U001AM0-0101_04 23
Fig. 6 Installing the head board or foot board
1. Right
2. Wrong

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

9 Operation

9.1 Initial Operation

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 battery.
 Raise the mattress support platform to the highest position.
 Remove the isolating foil from control section.
 Lower and tilt the mattress support 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 (supervisor control panel etc.).
 Check the siderails function properly.

D9U001AM0-0101_04 24
9.2 Battery

For declared lifetime period of leaded accumulators is recommended during storage:

1) To prevent accumulators from deep discharging (state-of-charge under 10%) and to keep accumulators
at least partly charged by regular recharging
2) To store accumulators on dry and cold places (from 10°C to 0°C)
3) To prevent accumulators from being in the sunshine

CAUTION!
Risk of reducing battery durability due to incorrect use!
 Use bed on battery only in crisis situations (e.g. power blackout, patient complications during transport,
etc.).
 After reconnecting bed to the mains charge battery to full capacity (see chart Battery charge status).

CAUTION!
Risk of damage or destruction of battery!
 If the battery is faulty, degassing may occur. In rare cases this might cause deformations of the battery
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.

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

 Use only batteries approved by the manufacturer.

 The manufacturer provides a 6-month warranty for the full function of batteries.
 Check the battery functionality at least once a month in accordance with the user and service manuals
and have the batteriy changed if necessary.
 The manufacturer recommends to replace the battery by qualified service organization after 2 (two) years
of use. After this period the supposed service life of battery ends and the manufacturer cannot guarantee
the battery service life after this period.
 The battery must be replaced with the new battery approved by manufacturer after maximum 5 (five)
years of use at the latest.
 The manufacturer will assume no responsibility for any damage to the bed or the battery caused by:
o Non-observance of the manufacturer’s instructions in the user manual.
o Using batteries not approved by the manufacturer.
o Battery replacement non-qualified service organisation.

9.3 Battery charging

To charge the battery:

 Connect the bed to the mains and check the yellow LED on the Supervisor control panel according to the
table 1.

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

D9U001AM0-0101_04 25
  Charging and battery capacity is indicated by the yellow LED placed on the ACP control panel.

The LED indicates the battery’s charge status:

Yellow LED
Not lit
Short flashing (short, intermittent illumination)
(circa 1.8 sec.)
Long flashing (long illumination) (circa 0.2 sec.)
Long, intermittent illumination for several hours (circa
10 hours), when bed is connected to the mains.
Table 1 ACP control panel – battery signalization
Battery charge status
Battery capacity is sufficient (charging completed)
Battery is charging - continue charging until the LED
is extinguished. In emer-gency cases, the battery 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 can not position with bed,
battery is defective or broken. Contact manufacturer.
Low battery voltage - battery can not be used as a
backup power supply even for a short period; battery
is completely discharged or defective (if this type of
signalisation persists, it is necessary to replace the
battery - service action)
Battery absence or failure condition (battery is
connected incorrectly, line between the power supply
and battery is broken or battery fuses are faulty);
contact service department of the manufacturer in
case of such signalisation.

To maintain maximum functionality of the battery:

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

In case the battery 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.

9.4 Status Faulty Battery

The battery is regarded as faulty if at least one of the following conditions applies:
 Battery charging constantly
 Low voltage on battery
 Low charging current of battery
Status “faulty battery” is indicated:
 By the battery status indicator being constantly lit.
 A fault battery status can be cancelled by pressing the STOP button.
 Battery status data is saved to the Linis system and written to the “Blackbox”.

9.5 Status Discharged Battery

The battery is regarded as discharged if the following condition is met:
 Defined decrease of voltage depending on discharging current
Status “discharged battery” is:
 Status is indicated by the battery 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.

D9U001AM0-0101_04 26
9.6 Removing the Bed from Service
How to remove the bed from service:
 Disconnect the bed from the mains.
 Disconnect the ground wire.
 Deactivate the battery (see Deactivating the Battery).
 Remove accessories.
To prevent damage during storage:
 Pack or cover the bed and accessories.
 Ensure storage conditions are the same as the operating conditions.

9.7 Deactivating the Battery

To avoid damaging the bed and the environment during storage:
 Deactivate the battery on the supervisor control panel.
To deactivate the battery on the supervisor control panel:
 Disconnect the bed from the mains.
 Disconnect the ground wire.
 Activate the keypad by pressing the GO button on the supervisor control panel.
 Press the Thigh Rest Up + Thigh Rest Down + Trendelenburg Position buttons at the same time and hold
them for three seconds.
 The battery is deactivated.

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

10 Manipulation

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

The bed is operated by different control elements.

Control elements:
 ACP Nurse control panel (supervisor control panel)
 Handset

Disabling individual functions on the supervisor 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 supervisor control panel.

D9U001AM0-0101_04 27
10.1 Supervisor control panel (nurse controller)

Supervisor panel is main control panel of the bed. Nurse controller can be placed in the shelf. We recommend
placing ACP panel on the head board or foot board or hold it in the hands while controlling the bed.

Fig. 7 Supervisor control panel

1. Lock indicators
2. Lock Buttons for respective functions
3. Thighrest Positioning Buttons
4. Backrest Positioning Buttons
5. Height Adjustment Buttons
6. Auto-Contour Buttons (simultaneous setting of back- and thighrest)
7. Central STOP button
8. Button Trendelenburg (mattress support platform tilt only)
9. Button Reverse Trendelenburg (mattress support platform tilt only)
10. Button Examination Position
11. Button Extra-low Position
12. Button CPR (Resuscitation) Position
13. Emergency Trendelenburg Button
14. Button Cardiac Chair Position
15. Button Mobilisation Position
16. LED Battery charge status (only for beds with backup battery)
17. LED Mains power
18. Activating GO Button
19. Bed Lights Control Button (ON/OFF)

NOTE: In case that the bed is not equipped with bed light control , button 19 is not on the controller.

D9U001AM0-0101_04 28
To set positions:
 Activate the keypad by pressing the GO button.
 Press and hold corresponding button until required position is reached.

10.1.1 Central STOP Button

The central STOP button 7 immediately interrupts all bed movements.
Pressing central STOP button 7 for at least 0.3 seconds immediately stops all electronic bed movements.

10.1.2 Activating GO Button

The GO button 18 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 18, 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.

10.1.3 Function Buttons

Function buttons 3, 4, 5 and 6 allow the setting of different positions, for example the height and tilt of the
mattress plat-form, 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.

10.1.4 Lock Buttons

Lock button 2 allows disabling individual functions on the supervisor control panel.

To disable functions:
 Activate the keypad by pressing the GO button 18.
 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.

10.1.5 Mains power LED

Status Meaning
lit LED connected to the mains
unlit LED disconnected from the mains
flashing LED system error

D9U001AM0-0101_04 29
10.1.6 Position Buttons

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

CAUTION!
Material damage due to moving parts!
 Ensure no objects (e.g. cables) are trapped between moving parts of the bed and mattress support
platform.
 Ensure no objects are close to the bed or accessories (e.g. infusion stand, lifting pole) when the 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
 Trendelenburg Position
 CPR (resuscitation) Position
 Examination Position
 Mobilisation 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.

Trendelenburg Position (8)

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

Cardiac Chair Position (button 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 (70°).

CPR (Resuscitation) Position

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

Settings after pressing and holding the CPR button (12):

 Mattress support platform moves into a horizontal position.
NOTE: For quick mechanical positioning, see CPR Backrest Release.

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

Settings after pressing and holding the Examination Position button:

D9U001AM0-0101_04 30
  The mattress support platform will move into the most appropriate position for patient examination and the
mattress support platform will flatten.

Mobilisation Position (15)

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.

D9U001AM0-0101_04 31
10.2 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.

Fig. 8 Handset

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

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 from Plug and Play slot if the bed is equipped with it.

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

D9U001AM0-0101_04 32
10.2.1 Standard version

Standard version is not equipped with Plug and Play connector.

10.2.1.1 Handset with Plug and Play connector (optional)

The Plug and Play connector allows the use of the handset on the right or left side of the bed according to staff or
patient needs.

The Plug and Play connector is located on both sides of the bed.

To connect the handset on the opposite side of the bed:

 If the handset cable is plugged into the Plug and Play connector, unplug it.

 Cover the free Plug and Play connector on this side of the bed with a plastic cap.

 Plug the handset cable into the Plug and Play connector on the opposite side of the bed.

10.2.2 Washable version

The Plug and Play connector is located at the end of a cable that can be attached to both sides of the bed.

Fig. 9a Handset and Plug and Play connector Fig. 9b Handset and Plug and Play connector

1. Handset 1. Handset
2. Cable holder 2. Cable clamps
3. Plug and Play connector 3. Plug and Play connector

To connect the handset on the opposite side of the bed:

 If the Plug and Play connector is slotted into the side holder on the side of the bed, turn it to the right and

remove (Fig. 9a).

 Pull the cable with the handset between the mattress support platform sections towards the cable clamp

(Fig. 9b).

D9U001AM0-0101_04 33
  Remove the cable from the cable clamp and secure it in the cable clamp on the opposite side of the bed

(Fig. 9b).

 Pull the cable with the handset between the mattress support platform sections towards the side holder

on the opposite side of the bed. (Fig. 10)

Fig. 10 Pulling the cable with the handset between the mattress support platform sections

 Insert the Plug and Play connector into the metal holder and secure it by turning left (Image 11a)

Fig. 11a Securing the Plug and Play connector

into the side holder

Fig. 11b Releasing the Plug and Play connector

from the side holder

D9U001AM0-0101_04 34
10.3 Night Bed Lightning

It is possible to equip Image 3 with undercarriage lightning. The lightning helps the patient or hospital personnel to
better orientate in room with lowered or turned off light. The lowered intensity of lightning is set up after turning the
bed on. For additional informations about bed lightning see chapter “Bed Illumination”.

10.4 Bed 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 handset and bed illumination will light up at full intensity.

After elapsing the GO period:

 The illumination intensity of handset 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 will light up at full intensity for 7 seconds. After that the illumination will
be lowered.

Turning off all illumination:

 Press button (19) and all illumination on the bed (handset and bed illumination) will be turned off.
This function is not blocked by the activation GO button.

D9U001AM0-0101_04 35
10.5 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. 12 Backrest release CPR

Set the position as follows:

 Pull and hold CPR backrest release lever and simultaneously press backrest down by the mattress
guard handle.

NOTE: In some cases (e.g. with bed in Trendelenburg position without power supply) it is possible to use the
CPR lever to raise the backrest.

D9U001AM0-0101_04 36
10.6 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 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.

10.6.1 Telescopic Siderails

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!
Hospital staff is responsible for assessing if the physical and psychological state of the patient is
in accordance with use of the telescopic siderails in middle positions!

Split telescopic siderails are components of the bed. The siderails cannot be dismounted. Telescopic siderails can
be adjusted to the lowest position, the highest position and to the two middle positions. The middle positions are
intended for making work of the hospital personnel easier and for facilitating mobilization of the patient in good
mental condition.

To fold the siderail up or down:

 Hold release mechanism and push both locking buttons
simultaneously.
 Fold siderail up or down to the required position.
The siderail will click into place and lock automatically. Arrows on the
figure 14 show positions of yellow catches.

Fig. 13 Control of Telescopic siderails

D9U001AM0-0101_04 37
Fig. 14 Positions of telescopic siderails

10.6.2 Collapsible Siderails (3/4 Siderails)

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.

The collapsible siderails are components of the bed. The siderails cannot be dismounted.

Fig. 15 Control of Collapsible siderail

To fold siderails down:

 Take hold of release mechanism and push siderail towards head end (1) to unlock locking system.
 Press button 2 to unlock.
 Fold siderail down (3) as required.

D9U001AM0-0101_04 38
To fold siderails up:
 Push the siderail up. Siderail will click into place and lock automatically.

Fig. 16 Collapsible Siderail (3/4 Siderail)

10.7 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.

10.7.1 Bed with Castor Control Levers

The castor control levers are located on both sides of the foot end.

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

Fig. 17 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.

Centrally operated castors:

Standard: 2 levers, foot bed side operated, push from the foot side
Options:
4 levers, foot bed side operated, push from the foot side
4 levers, head bed side operated, push from the head side
2 levers, foot bed side operated, push from the head side
4 levers, foot bed side operated, push from the head side

D9U001AM0-0101_04 39
 2 levers 2 levers 4 levers 4 levers 4 levers
foot side foot side operated foot side operated head side operated foot side operated
operated push from the head push from the head push from the head push from the foot
push from the side side side side
foot side

To move the bed:

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

10.7.2 The Fifth Castor

th
The bed can be equipped with a 5 castor to make it easier to manoeuvre and control the bed. The standard
th
locking castor will automatically be excluded from the bed specification if the 5 castor is requested as this will
th
replace the need for this function. The control lever for the 5 castor is identical to the control lever for the
th
braking system. To activate the 5 castor, press the foot operated lever shown in Figure 14, position 1.

WARNING!
Damage to the fifth castor may occur during movement across ridges
(incline greater than 15%)!
 Make sure you avoid movement with the bed over ridges.

10.7.3 Brake Alarm – Signalization of Unbraked Bed

It is possible to equip Image 3 with signalization of unbraked bed. The signalization of unbraked bed signalizes,
that bed is connected to the mains but is not braked. This status is signalized by acoustic signal. To shut down
acoustic signal brake the bed or unplug bed from the mains.

D9U001AM0-0101_04 40
11 Accessories

WARNING!
Risk of injury due to incompatible accessories!
 Only the manufacturers original accessories can be used.

NOTE: The manufacturer assumes no responsibility for the use of accessories not approved by the
manufacturer.
NOTE: All accessories conform to EN 60601-2-52:2010.

The following accessories are suitable for the Image 3:

 Lifting pole
 powder-coated
 chrome-plated
 Triangular holder, grey plastic
 for lifting pole
 for lifting pole, adjustable by retractor
 IV holder
 for lifting pole, 3 hooks, powder-coated
 for lifting pole, 3 hooks, stainless steel
 for lifting pole, 4 hooks, chrome-plated
 Telescopic IV pole
 4 plastic hooks, chrome-plated
 4 plastic hooks, chrome-plated, S-shaped top part, with lock against unwanted rotation
 4 metal hooks, chrome-plated, lock against unwanted rotation
 4 metal hooks, stainless steel, S-shaped top part, lock against unwanted rotation
 Infusion bottle basket
 for IV pole, stainless steel
 IV pump holder
 cross-shaped, chrome-plated
 Pole for devices and accessories
 chrome-plated
 Urine bag holder
 self-adjusting level, powder-coated
 Writing shelf
 white, for plastic or metal head/foot board
 Name holder
 plastic, for plastic head/foot board
 Chart holder
 plastic, for plastic head/foot board
 SafeSense

NOTE: Detailed information on SafeSense is available in the attached user manual for this product.

D9U001AM0-0101_04 41
11.1.1 Lifting Pole

It is possible to equip the bed with lifting pole. The lifting pole must be placed only to the bushing on the head end.

Fig. 18 Bushing for lifting pole and infusion stand

Lifting pole variants:

 Lifting pole for beds with fixed bed end

To ensure safe use of the lifting pole:

 Never exceed the maximum load of 75 kg of lifting pole.
 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.

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.
A plastic grab handle with an adjustable strap is attached to the lifting pole.

NOTE: The date of manufacture is marked on the grab handle. LINET® recommends replacing the plastic grab
handle every four years.

D9U001AM0-0101_04 42
11.1.2 Infusion stand

WARNING!
Risk of injury due to use of incorrect accessories or due toincorrect use!
Infusion Stands must only be used for their intended purpose. Always read the instructions for use!
 Only mount an infusion pump on the lower (wider) telescopic section of the infusion stand above the
head/foot end of the bed.
 Never mount an infusion pump on the upper (thinner) telescopic section of the infusion stand.
 Ensure the infusion pump does not collide with any movable parts of the bed (especially the back rest) or
with the patient. This must be verified after installation.
 Do not over tighten the infusion pump clamps when mounting. Over tightening may damage the infusion
stand.

It is possible to insert infusion stands in the sockets at the head and foot ends of the bed.
 Only use infusion stands with 4 hooks for hanging IV bags or baskets for intravenous solutions.
 Ensure the 2kg maximum Safe Working Load of individual hooks on the infusion stand is not exceeded.
o Capacity per hook: 2 kg (4.41 lbs.).
 Ensure the 20kg maximum Safe Working Load of the infusion stand is not exceeded.
o The total maximum load of the IV/Infusion pole must not exceed 20 Kg (44.1 lbs.).

Fig. 19a Infusion stand Fig. 19b Infusion pump – correctly mounted

D9U001AM0-0101_04 43
11.1.3 Additional hooks for accessories

WARNING!
Risk of damaging the bed or injuring staff or patients due to incorrect use!
 Always install additional hooks on the lowest partition of the telescopic siderail!
 Never install additional hooks between movable partitions of the telescopic siderail!
 The manufacturer recommends placing a maximum of 2 hooks on one siderail!
 Ensure any accessories placed on the hooks do not collide with the bed or the patient.

Additional hooks are designed to be placed on the telescopic siderails or on the bed ends. It is possible to place
additional bed accessories on these hooks. The hook must be placed on the lowest partition of the telescopic
siderail.
Capacity:
 Maximum load capacity per hook is 5 kg.

Install additional hooks on the telescopic siderail as follows:

 Place the hook on the lowest partition of the siderail.
 Ensure the hook is installed correctly.

11.1.4 Oxygen bottle holder

WARNING!
Risk of injury by the oxygen bottle holder due to incorrect use or due to careless transport!
 Ensure the oxygen bottle holder is correctly fitted in the correct position.
 The oxygen bottle holder (with or without O2 bottle) must be fitted before transport to secure the transport
position.
 Be aware of people or objects in close proximity when moving or manipulating a bed equipped with an
oxygen bottle holder.
 Secure the oxygen bottle from falling or involuntary movement using the rubber strap.
 Place the oxygen bottle holder on the bed according to the instructions in the following text.
 Ensure the oxygen bottle valve is not damaged by careless or incorrect manipulation or placement.

Oxygen bottle holders are suitable for transporting oxygen bottles with a weight of up to 15 kg and a volume of 5
liters.

Fit horizontal oxygen bottle holder as follows:

 Place the oxygen bottle holder on the diagonal profile at the head of the bed.
 Secure the oxygen bottle holder with rubber straps.
 Ensure the holder and bottle are fitted correctly.


Fig. 20 Horizontal oxygen bottle holder

D9U001AM0-0101_04 44
11.1.5 Cannula holder
The cannula holder is designed to place cannulas on the holder.

The cannula holder can be placed on:

 the accessory rail
 the lowest partition of the telescopic siderail

11.1.6 Urine bottle holder

The urine bottle holder is designed for placing a urine bottle in the wire basket. The urine bottle holder must be
placed on the lowest partition of the siderail.

Place urine bottle holder as follows:

For telescopic siderails
 Place urine bottle holder on a hook on the lowest partition of the siderail.

Fig. 21 Urine bottle holder with a bottle on a hook on the siderail

11.1.7 Radon bottle holder

WARNING!
Risk of damaging the bed or injuring staff or patients due to incorrect use!
 Always install additional hooks on the lowest partition of the telescopic siderail!
 Never install additional hooks between movable partitions of the telescopic siderail!
 Ensure any accessories placed on the hooks do not collide with the bed or the patient.
 Ensure the length of the tube is long enough to prevent tearing the drain when manipulating the patient.

The radon bottle holder is designed to hold two radon bottles.

Capacity:
 Maximum load capacity of holder is 10 kg
The radon bottle holder can be placed on:
 The lowest partition of the telescopic siderail

D9U001AM0-0101_04 45
11.1.8 Siderails Extension – Extender®

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 then stated in this user manual is on the responsibility of
personnel. The manufacturer shall not be held liable for incorrect use!
It is recommended the siderail extension – Extender® be used 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 that the Extender® be used with the following mattresses:

 Passive mattress: higher than 14 cm

 Active mattress: with maximum height 25 cm

Fig. 22a Installing the Extender® on the siderail Fig. 22b Inserting the screw

Fig. 22c Securing the Extender® Fig. 22d Image 3 with installed Extender®

Install the Extender® as follows:

 Place the Extender® on the upper edge of the siderail (Fig. 22a). Siderails must be in the upper position.
 Insert the screw from the inside of the bed thru the securing hole in the Extender® (Fig. 22b). The square
hole is pointed into the mattress support platform.
 Secure the screw with the plastic rosette nut and tighten (Fig. 22c). The rosette nut is pointed out from the
bed.
 Check that the Extender® is secured correctly.

D9U001AM0-0101_04 46
11.1.9 Image 3 Protector®

WARNING!
Risk of injury due to patient falling out of bed!
 Ensure the Protector® is securely anchored to the housing.
 To check stability, push 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 attach the head board or foot board to accessory housing (3).
 Do not use the Protector with bed extension.
 The Protector® can be used with powder coated head/foot board only.

The Protector® is not a component of the bed. The Protector® is an optional accessory.

® ®
Fig. 23a Closed Protector Fig. 23b Open Protector

Mount the Protector in the closed position as follows:

 Put the tube of the Protector (2) into the housing near the foot of the bed (3), so that the Protector is facing
the siderail.
 The safety pin must be locked in place.

Mount the Protector in the open position as follows:

 Put the tube of the Protector (2) into the housing near the foot of the bed (3), so that the Protector is facing
out from bed.
 The safety pin must be locked in place.

Dismount the Protector as follows:

 Press and hold the release button (1).
 Push the Protector up.

D9U001AM0-0101_04 47
11.1.10Accessory Rails

Fig. 24 Accessory Rail

Load capacity:
 Maximum load of 5 kg without leverage.
 Maximum load of hook pair 10 kg.

Accessories for hanging on the accessory rail:

 Cannula holder
 Urine bag holder
 Urine bottle basket
 DIN steel bar

11.1.11DIN rail (optional)

Siderail can be equipped with DIN rail intended for accessories approved by the manufacturer.

11.1.12Mattress

The manufacturer recommends the use of the following mattress systems on the Image 3 bed:
 EffectaCare 10, EffectaCare 20, PrimaCare 10, PrimaCare 20, CliniCare 10, CliniCare 20, CliniCare 30
 Air2Care, CliniCare 100 HF, ProphyCair

D9U001AM0-0101_04 48
12 Cleaning and 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 bed is not designed for cleaning by spraying, showering nor for pressure or steam cleaners.
 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.

12.1 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 support platform to its highest positions and also position the back rest and thigh
rest 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 support platform.
 After drying the bed check functions of the bed.

D9U001AM0-0101_04 49
12.2 General Instructions for Cleaning and Disinfection

12.2.1 Daily Cleaning

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

12.2.2 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 Cleaning), mattress support platform, columns, undercarriage covers and mattress.

12.2.3 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.

12.2.4 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.

12.2.5 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.

D9U001AM0-0101_04 50
12.3 Choosing of Detergents or Disinfections

CAUTION!
Risk of damaging the bed due to use of incorrect detergent!
 Always consult choosing of the detergent and its dilution with manufacturer of the detergents according to
the material table below.

Changing
Part of bed – Image 3 Material (*) Daily C&D Complete C&D
patient C&D
Siderails (stickers)
 Split telescopic ALU, POM (ABS)   
 Single collapsible S, ABS (ABS)   
Head board and Foot board PP, S, (ABS)   
(stickers)
Controllers (cables) ABS, (PU)   
Mattress support platform PP   
covers
Undercarriage cover ABS   
Corner bumpers EP, ABS   
Mains cable PU   
Undercarriage frame S   
Castors ABS, S, PU   
Actuators ABS, ALU   

Material (*) Shortcut

Akrylonitrilbutadienstyren ABS
Aluminium ALU
Ethylene propylene EP
High-pressure laminate HPL
Polyester P
Polyamide PA
Polycarbonate PC
Polyethersulfone PES
Polyoxymethylene POM
Polypropylene PP
Polyurethane PU
Polyvinyl chloride PVC
Iron (powder coated) S
Anti-corrosive iron – chrome plated S-CR

D9U001AM0-0101_04 51
12.4 Machine washing

WARNING!
Material damage to the bed or its parts due to not following the instructions for machine washing!
 Always follow the instructions from manufacturer for machine washing due to securing maximal service
life and functionality of the bed designed for machine washing. Otherwise serious damage to the bed may
occur.
 Not following those instructions may lead to the void of warranty.
 Do not use any strong acids or bases. Optimum pH range 6 – 8.
 Never use detergents with solvents that might affect the structure and consistency of the plastics.
 Never exceed the dosage prescribed by the manufacturer.
 Never use high pressure wap cleaner for cleaning the bed.
 The cooling of the bed with cold water is not allowed.

WARNING!
Material damage to the accessories due to incorrect use in the washing machine!
 In the washing machine use accessories intended for machine washing only.

CAUTION!
Risk of damaging the accessories due to machine washing!
 Never place any accessories to the washing machine.
 The only allowed accessories for washing machine is lifting pole and infusion stand.
 Always check if the allowed accessory is not colliding with washing machine or if it is not preventing from
its trouble-free service.

If the bed is designed for the machine washing, then it this symbol is located on the frame
under the foot end. Also it is labeled as 1AMW on the serial label (serial label is located on
the frame of the bed).

12.4.1Preparing for cleaning

 Disconnect the bed from the mains.
 Ensure all connectors are correctly plugged on its place.
 Ensure the plug&play connector is closed correctly.
 Allowed detergents:
Washing cycle Detergent Manufacturer
Cleaning and disinfection Sekumatic FDR Ecolab
Neodisher Dekonta AF Dr. Weigert
Rinsing Sekumatic FKN Ecolab
Neodisher TN Dr. Weigert
 Recommended position of the bed before machine washing:
 Height of the mattress support platform: approx. 42 cm above the ground
 Siderails: in the highest position
 Linen shelf: pulled out, as much as the washing machine allows
 Bed extension: pulled in
 Mattress support platform: flat
 ACP controller: placed on the head board or foot board
 Handset: placed on the siderail
 Mains cable: hanged on the head frame
 Accesories: lifting pole, infusion stand (suitable for machine washing)
other accessories is not designed for machine washing

D9U001AM0-0101_04 52
  Place the bed in the washing machine.

Fig. 25 Recommended position of bed for machine washing

12.4.2 Machine washing

The following conditions for machine washing must be met:

 Maximal lenght of machine washing: 7 minutes
 Maximal pressure of washing machine jet: 5-6 bar
 Maximal water temperature: 85 °C
 Maximal temperature of bed: 70 °C
 Relative humidity: 100%
 Maximal water hardness: 5 dH

12.4.3 After machine washing

 After finishing of the machine washing and before next use of the bed, check that:
 Ensure the connector of network cable is dry. Dry if needed.
 None of the electronic parts is visibly damaged.
 Wait 5-6 minutes until the bed cools down to its working temperature.
 Try some of the adjustment functions of the bed.

NOTE: It is recommended to visually check bed for any signs of damage after each machine washing
(especially damage on the painted parts). In case of that damage, repair it using paint. This
will extend service life of the bed.
NOTE: After machine washing it is recommended to use Trendelenburg position (headend is folded down) in
order to get rid of water from all parts of the bed.

D9U001AM0-0101_04 53
13 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
Adjusting with position buttons not
possible
Faulty mattress support platform
height/tilt adjustment
Lowering backrest from the
upright position not possible
Adjusting siderails not possible
Faulty brakes
Inserting head and foot boards not
possible
13.1 Sound signals of the bed
D9U001AM0-0101_04
Cause
GO button was not pressed
Function disabled on supervisor
control panel
Drive motors have no power
Defective drive motors Defective
battery
Plug inserted incorrectly
Faulty power box
Faulty control element
There is an object on the
undercarriage cover
Function disabled on supervisor
panel
Drive motors have no power
Defective drive motors Defective
battery
Plug inserted incorrectly
Faulty power box
Faulty control element
Object under the backrest or in
the drive mechanism
Locking handle is defective
The siderail lock is dirty
Locking handle is defective
The brakes are blocked by dirt
The brake mechanism is defective
The head or foot board is in the
wrong position
Defective mechanism
Function locked on Supervisor control panel (signal 0,2s)
Unbraked bed (signal 2,5s, pause 0,5s)
Engine overload
Solution
Press the GO button.
Enable disabled function.
Check the mains connection. Notify
the service department.
Insert the mains plug correctly.
Notify the service department.
Notify the service department.
Remove the object.
Enable disabled function.
Check the mains connection. Notify
the service department.
Insert the mains plug correctly.
Notify the service department.
Notify the service department.
Remove the object.
Notify the service department.
Clean the locking mechanism.
Notify the service department.
Clean the brake system.
Notify the service department.
Check the locking mechanism.
Position the head or foot board
correctly.
Notify the service department.
54
14 Maintenance

WARNING!
Risk of injury when working on the bed!
 Ensure that the bed is disconnected from the mains connection prior to assembly, disassembly and
maintenance.
 Ensure that the castors are locked prior to assembly, disassembly and maintenance.
 Ensure that the adjustment function on the nurse control panel is locked prior to assembly, disassembly,
cleaning and maintenance

WARNING!
A defective bed can cause injuries!
 A defective bed should be inspected and repaired immediately.
 If the defect cannot be repaired, do not use the bed.

CAUTION!
Incorrect maintenance can damage the bed!
 Ensure maintenance is performed by a LINET® service engineer service or trained hospital technicians
only.

14.1 Maintenance Work

 The connector replacement should only be carried out by service personnel trained by LINET ®. For
service related instructions, please refer to the service documentation.
 Ensure the following maintenance work is performed every 12 months by the manufacturer or by a
qualified service organisation trained and certified by the manufacturer. Service documentation and
electrical schemes are available for qualified service organisation trained by Linet.
 The manufacturer will provide the service organisation with service training certification to confirm the
organisation is qualified to carry out maintenance on LINET® products.
 Do not use the bed If any malfunction or defect occurs. In this case contact the manufacturer or service
organisation immediately.

14.1.1 Spare Parts

The product label is located on the longitudinal rail of the mattress support platform frame. The product label
contains information required for product queries and ordering replacement parts.

Information about spare parts is available from:

 Seller´s customer service
 Sales
 Our technical support department

14.1.2 Completeness
 Perform a visual check (with delivery note if necessary).
 Have any missing parts replaced.

D9U001AM0-0101_04 55
14.1.3 Wear
 Check all bolts and tighten if necessary.
 Check all locking mechanisms.
 Check the bed for wear, scratches or rub marks.
 Eliminate the cause if necessary.
 Have any defective parts replaced.

14.2 Functioning

 Check that all bed adjustments reach the maximum position.

 If necessary, clean, lubricate or replace any worn areas and parts.

14.2.1 Electric Control

Plug Connections
 Replace O-rings on connectors.
 Check the plug connections for dirt and defects.
 Clean or replace if necessary.
 Check the plug connectors are properly seated.
Motors
 Check motor movement (adjust bed positions). Check for incorrect and interrupted movements.
 Have defective motors replaced if necessary.
 Check cables for signs of wear and entanglement.
 Install new cable or replace the motor if necessary.
Battery
 Check the battery is working properly (disconnect the bed from the mains).
 Replace the battery if necessary.

14.2.2 Castors
 Clean the castors completely.
 Grease the castors if necessary. Use Caro EP 2 by DEA or an equivalent grease
 Check the castors work properly.
o Forward Movement
o Unrestricted Movement
o Braked
 Have the brakes adjusted if necessary.
 Have any defective castors replaced.

14.2.3 Accessories
 Check all accessories (for example, lifting pole, siderails, infusion stand, etc.) are working properly.
 Replace if necessary.

D9U001AM0-0101_04 56
14.2.4 Safety checks

WARNING!
Incorrect safety checks can cause injuries!
 Ensure that safety checks are performed by qualified or authorised personnel certified by the
manufacturer.
 Ensure that the safety checks are recorded in the service and maintenance log.

WARNING!
A defective bed can cause injuries!
 A defective bed must be inspected and repaired immediately.
 If the defect cannot be immediately repaired, do not continue to use the bed.

Technical Safety Check of the hospital bed must be performed at least once every 12 months.

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

NOTE: The manufacturer will give a certificate to service organisations in which the manufacturer declares that
the service organisation is qualified to perform maintenance on LINET® products. On request, the LINET® will
provide service documentation and circuit diagrams for qualified service technicians trained by LINET®.

D9U001AM0-0101_04 57
14.3 Beds designed for machine washing

The manufacturer recommends performing technical check after 25 cycles of machine washing.

The technical check must grease the following:

Place on the bed No. Recommended grease Manufacturer
Siderail mechanism 1 BIO FLUID WEICON GmbH & Co. KG
Gliders of the linen holder 2 BIO FLUID WEICON GmbH & Co. KG
Bed extension 3 MOL Liton LT 2/3 MOL-LUB
Mechanism of the mattress support 4 MOL Liton LT 2/3 MOL-LUB
platform lift

Fig. 26 Recommended places for greasing

The technical check must check the following:

 Functionality of the adjustable functions of the bed
 Rust on the bed components
 Status of the battery

D9U001AM0-0101_04 58
15 Disposal

15.1 Environmental Protection

Linet ® is aware of the importance of environmental protection for future generations. Within the whole LINET
company is applied the environmental management system, which is in accordance with the internationally
agreed standards ISO 14001. The international system recognition and certification ISO are based on the external
audits executed by specialists from reputable international TŰV company. Materials used in our product have the
minimal ballast on the environment. Noise emissions and vibrations are in accordance with applicable regulations
for the place of use. The product is made of recyclable materials. Waste is eliminated through an authorized
company for waste management under the applicable legislation. None of the wooden parts is made of tropical
wood (such as mahogany, rosewood, ebony, teak etc.) or from timber from the Amazon region or similar
rainforests. Our products do not contain hazardous substances based on heavy metals, asbestos, PCBs and
CFCs. For disposal of packaging materials after installing beds contact your sales representative or service Linet
about the possibility of a free take-back of packaging through an authorized company www.linet.cz

15.2 Disposal

15.2.1 Within Europe

To dispose of the appliance:

 When you dispose of your appliance do not put it into household waste.
 Appliances should be taken to an authorised electrical appliance recycling location.

Materials of the appliance may be reused. When recycling or reusing old appliances you are making an important
contribution in the protection of the environment.

Ask the responsible environmental protection authorities for the appropriate disposal point.

15.2.2 Outside Europe

 Dispose of the bed or its components in accordance with local laws and regulations:
 After using the bed
 Following maintenance and installation work
 Hire an approved waste disposal company for disposal.

D9U001AM0-0101_04 59
16 Warranty

LINET® will only be held responsible for the safety and reliability of products that are regularly serviced 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-related 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.

D9U001AM0-0101_04 60
17 EC Declaration of Conformity

D9U001AM0-0101_04 61
18 Technical Specifications

18.1 Mechanical Specifications (Standard Version)

Dimensions
221 cm* x 104 cm*
Siderail Height above Mattress support platform
with split telescopic siderails (version 1) 6,5 cm (MIN), 40 cm (MAX)
with split telescopic siderails (version 2) 8,5 cm (MIN), 42 cm (MAX)
with collapsible siderails 4,7 cm (MIN), 39 cm (MAX)
Siderail length
split telescopic siderails 98,5 cm
collapsible siderails 146,5 cm
Maximum mattress height
with split telescopic siderails (version 1) 18 cm
with split telescopic siderails (version 2) 20 cm
with collapsible siderails 17 cm
Mattress dimensions 200 cm x 86 cm (90 cm*)
Bed extension 0 cm / 10 cm / 22 cm / 30,5 cm
Mattress support platform height adjustment 28 cm – 80 cm (85 cm*)
Maximum Backrest Angle 70°
Maximum Thighrest Angle 34°
Ergoframe® 10 cm / 6 cm
Trendelenburg/Reverse Trendelenburg position 14° / 14°
Weight of bed 160 kg*
Max. Lifting Pole Load 75 kg
Safe Working Load (including Mattress and Accessories) 265 kg
Maximum patient weight
Application environment 1, 2 200 kg
Application environment 3, 5 230 kg
* Depending on configuration

D9U001AM0-0101_04 62
18.2 Mechanical Specifications (Washable Version)

Dimensions
221 cm* x 104 cm*
Siderail Height above Mattress support platform
with split telescopic siderails (version 1) 6,5 cm (MIN), 40 cm (MAX)
with split telescopic siderails (version 2) 8,5 cm (MIN), 42 cm (MAX)
with split telescopic siderails 4,7 cm (MIN), 39 cm (MAX)
Siderail length
split telescopic siderails 98,5 cm
collapsible siderails 146,5 cm
Maximum mattress height
with split telescopic siderails (version 1) 18 cm
with split telescopic siderails (version 2) 20 cm
with collapsible siderails 17 cm
Mattress dimensions 200 cm x 86 cm (90 cm*)
Bed extension 0 cm / 10 cm / 22 cm / 30,5 cm
Mattress support platform height adjustment 28 cm – 80 cm (85 cm*)
Maximum Backrest Angle 70°
Maximum thighrest adjustment (electric) 34°
Ergoframe® 10 cm / 6 cm
Trendelenburg/Reverse Trendelenburg position 14° / 14°
Weight of bed 160 kg*
Max. Lifting Pole Load 75 kg
Safe Working Load (including Mattress and Accessories) 265 kg
Maximum patient weight
Application environment 1, 2 200 kg
Application environment 3, 5 230 kg
* Depending on configuration

18.3 Environment Conditions (Standard and Washable Version)

Environmental Conditions - Operation

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

D9U001AM0-0101_04 63
18.4 Electrical Specification (Standard and Washable Version)

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.

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 230 V, 50/60 Hz
Maximum Power Input max. 370 VA
EN 60529 Ingress Protection for 1AM (standard) IP X4
EN 60529 Ingress Protection for 1AMW (washable) IP X6
Safety Class Class I (with type B applied parts)
Electrical Motor Operating Time max. 2 minutes ON / 18 minutes OFF
Battery Pb AKU 2 x 12 V / 1,2 Ah / Fuse 15A
Fuse 2x T1.6A L 250 V for 230 V version
2x T3.15A L 250 V for 100-127 V version

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

D9U001AM0-0101_04 64
18.5 Electromagnetic Compatibility

WARNING!
Increased electromagnetic radiation or reduced electromagnetic resistance due to unsuitable
accessories, converters or cables!
 Consult Linet® or local dealer before using other parts than those provided by Linet®.

WARNING!
Medical electrical equipment or medical electrical system should not be used in extremely short
distances within the bed! In the case it is necessary to use medical electrical equipment in this
extremely short distances within the bed observe this configuration regularly to verify the normal
functions of the bed in this configuration.
 Consult Linet® or local dealer before using medical electrical equipment where influence on the bed can be
strong.

NOTE IEC 60601-1-2 certified medical electrical equipment used in ICU is not restricted.

Image 3 requires special preliminary measures pertaining to EMC that necessitate installation and

commissioning in conformity with the EMC information given in this Manual.

Portable and mobile HF communication equipment can influence bed functions.

NOTE It does not concern fixed installations of hospital communication systems and nets (DECT, pager, WiFi)
and other mobile devices which are certified according to local telecommunication legislation.

18.5.1 Manufacturer’s Manual and Declaration - Electromagnetic Radiation

Image 3 is intended for the application in electromagnetic environment as specified below. The customer or user
of the bed is responsible for the fact that these requirements are met.

Radiation Test Conformity Electromagnetic Environment

High-frequency radiation CISPR 11
High-frequency radiation CISPR 11
Harmonic radiations IEC 61000-3-2
Fluctuating voltage/Flashing radia- tion
CE 61000-3-3
Group 1 Image 3 utilises high-frequency
energy for its internal function only.
The high-frequency radiations are
very low and unlikely to cause any
interference to nearby electronic
devices
Class B Image 3 is suitable for all institu-
Class A tions, including households and
Satisfactory objects directly connected to the
public low-voltage mains supplying
residential buildings

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18.5.2 Manufacturer’s Manual and Declaration - Electromagnetic Resistance

Image 3 is intended for the application in electromagnetic environment as specified below. The customer or user of
the bed is responsible for the fact that these requirements are met.

Resistance Test Test Level as per Level of Compliance Electromagnetic

IEC 60601 Environment
Electrostatic ± 6 kV for contact ± 6 kV for contact  Ensure that the
discharge (ESD) ± 8 kV for air ± 8 kV for air following requirements
IEC 61000-4-2 are met: Floors: wood,
concrete or ceramic
tiles Relative
humidity: >30%
Electrical fast transient ± 2 kV in feeder line ± 2 kV in feeder line  Ensure the mains
response/ ± 1 kV in input/output ± 1 kV in input/output quality is suitable for a
group of impulses line line commercial or hospital
IEC 61000-4-4 environment.
Shock pulse ± 1 kV between ± 1 kV in differential  Ensure the mains
IEC 61000-4-5 lines mode quality is suitable for
± 2 kV between line ± 2 kV in co-phasal commercial or hospital
(lines) and earth mode environment.
Short-time voltage <5 % UT <5 % UT  Ensure that mains
drop, short-duration (>95 % short-duration (>95 % short-duration quality is suitable for a
interruptions drop of UT) drop of UT) commercial or hospital
and slow voltage within 0.5 cycles within 0.5 cycles environments.
changes on the feeder  For permanent
input line 40 % UT 40 % UT operation during a
IEC 61000-4-11 (60 % short-duration (60 % short-duration power failure, connect
drop of UT) drop of UT) the bed to a power
within 5 cycles within 5 cycles generator as the back-
up battery’s capacity is
70 % UT 70 % UT limited.
(30 % short-duration (30 % short-duration
drop of UT) drop of UT)
within 25 cycles within 25 cycles

<5 % UT <5 % UT
(>95 % short-duration (>95 % short-duration
drop of UT) drop of UT)
within 5 s within 5 s
Magnetic field of 3 A/m 3 A/m  Ensure the magnetic
network frequency fields of the network
(50/60 Hz) frequency conform to
IEC 61000-4-8 the normal levels of
commercial or hospital
environments.

NOTE UT refers to the AC mains voltage before the test level is applied.

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 Resistance Test Test Level as per Level of Electromagnetic Environment
IEC 60601 Compliance
Conducted high 3 Vrms 3 Vrms  Portable and mobile HF
frequency 150 kHz to 80 MHz communication equipment should
phenomena not be used nearer than in the
IEC 61000-4-6 recommended distance calculated
Radiated high-frequency 3 V/m 3 V/m from suitable equation for frequency
phenomena 80 MHz to 2.5 GHz of transmiter in relation to any part
IEC 61000-4-3 of the medical electrical bed
(including cables).

Recommended distances:
d = 1.2 √P
d = 1.2 √P 80 MHz to 800 MHz
d = 2.3 √P 800 MHz to 2.5 GHz
P is the rated maximum output power of the
transmitter in Watts (W) defined by the
transmitter's manufacturer.
d is the recommended separating distance
in metres (m).
 Ensure the field intensities of
permanent HF transmitters
determined by the summary of
electromagnetic characteristics for
the given place do not exceed the
satisfactory level b in each
frequency range.
Interferences are possible in the vicinity of
the instrument marked with the following
symbol:

a It is not possible to accurately indicate field intensities from permanent transmitters (e.g. radio base stations of
the radio, phones and ground mobile and amateur radio stations, AM and FM radio and television broadcasting).
To assess the electromagnetic environment for permanent HF transmitters, take into account the on-site
electromagnetic characteristics.
If the measured field intensity is higher than the pertinent satisfactory HF level stated above, observe whether
the bed is functioning normally.
If any abnormal properties are observed, move or relocate the bed.
b The field intensity in the entire frequency range from 150 kHz to 80 MHz should be lower than 3 V/m.

NOTE With 80 MHz and 800 MHz, the higher frequency range is applicable.

NOTE The absorption and reflection of buildings, objects and people will influence electromagnetic propagation

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 Recommended separation distances between
portable and mobile RF communications equipment and the Image 3 Medical Bed
The Image 3 Medical Bed is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the Image 3 Medical Bed can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the Image 3 Medical Bed as recommended below, according to
the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
Rated maximum
output of 3,5 3,5 7
transmitter d [ ] P d [ ] P d [ ] P
V1 E1 E1
W
0,01 0,12 0,12 0,40

0,1 0,37 0,37 1,2

1 1,1 1,1 4

10 3,6 3,6 12

100 11 11 40
For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres (m)
can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power
rating of the transmitter in watts (W) according to the transmitter manufacturer.

NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.

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