LINET Image 3 XXL Operating instructions

Image 3 B

Bariatric hospital bed for acute care

D9U001AM2-0101

Version: 07

Publication Date: 2023-03

Instructions for Use

and Technical Description

D9U001AM2-0101_072

Manufacturer:

L I N E T spol. s r. o.

Želevčice 5

274 01 Slaný

Czech Republic

Tel.: +420 312 576 111

Fax: +420 312 522 668

E-mail: [email protected]

http://www.linet.cz

Service department: [email protected]

Authorized Representative in Great Britain:

LINET UK Ltd

11 Brunel Way

Segensworth East

Fareham

Hampshire

PO15 5TX

United Kingdom

Authorized Representative in Switzerland:

Bigla Care AG

Bernstrasse 3

CH-3421 Lyssach

Switzerland

Authorized Representative in Malaysia:

Emergo Malaysia Sdn. Bhd.

Level 16, 1 Sentral, Jalan Stesen Sentral 5

KL Sentral

50470 Kuala Lumpur

Malaysia

Authorized Representative in Peru:

Drogería Emergo Peru S.R.L.

Calle Las Orquídeas Nro. 585, Int. 1301

San Isidro, Lima

Director Técnico Renato Delgado Rivera

RUC: 205 52 75 65 35

Peru

Authorized Representative in Philippines:

Biomedica Healthcare Inc.

Unit 2103 City land 10, Tower 1

Ayala Corner, Dela Costa Street

Makati City, Metro Manila

Philippines

D9U001AM2-0101_07

3

Image 3 B

Bariatric hospital bed for acute care

Author: L I N E T, s.r.o.

Related links: www.linet.cz

D9U001AM2-0101

Version: 07

Publication date: 2023-03

Translation © L I N E T, 2023

changes in the contents of the instructions for use that relate to the product´s technical regulations.

It is for this reason that the contents of the instructions for use may indicate dierences from the current manufacture of the pro-

duct. Reproduction, also excerpts, only with prior permission of the publisher. Subject to changes due to technical developments.

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

D9U001AM2-0101_074

1 Symbols and Denitions .............................................5

1.1 Warning Notices .......................................................... 5

1.1.1 Types of Warning Notices ........................................5

1.1.2 Structure of Warning Notices ...................................5

1.2 Instructions ..................................................................5

1.3 Lists .............................................................................5

1.4 Symbols on the Package ............................................6

1.5 Symbols and Labels on the Bed .................................7

1.6 Acoustic signalisation ................................................. 10

1.7 Visual signalisation......................................................10

1.7.1 Mains Power LED (Attendant Control Panel) ...........10

1.7.2 Accumulator Indicator (Attendant Control Panel) ..... 10

1.7.3 Lock LED (Attendant Control Panel) ........................ 11

1.8 Night Bed Illumination .................................................11

1.9 Denitions ...................................................................12

1.10 Abbreviations ............................................................13

2 Safety Instructions .......................................................14

3 Intended use ................................................................. 17

3.1 User population ........................................................... 17

3.2 Contraindications ........................................................17

3.3 Operator ...................................................................... 17

4 Incorrect Use ................................................................17

5 Product Description ..................................................... 18

5.1 Image 3 B (1AM2) - Single Collapsible Siderails and Powder

Coated Head Board and Foot Board ................................ 18

6 Technical Specication ...............................................19

6.1 Applied parts type B ...................................................19

6.2 Mechanical Specication ...........................................19

6.3 Environment Conditions .............................................. 19

6.4 Electrical Specications ..............................................20

6.5 Electromagnetic compatibility .....................................20

6.5.1 Manufacturer instructions - electromagnetic emissions

..........................................................................................21

6.5.2 Manufacturer instructions - electromagnetic susceptibility

..........................................................................................21

7 Use and Storage Conditions ....................................... 22

8 Scope of Delivery and Bed Variants ........................... 23

8.1 Scope of Delivery ........................................................ 23

8.2 Bed Variants ................................................................23

8.2.1 Standard version: Image 3 B Model 1AM2 .............23

9 Putting into Service .....................................................24

9.1 Accumulator Activation ................................................ 25

9.1.1 Placement of Control Section ..................................25

9.1.2 Removing the Isolating Foil ......................................25

9.1.3 Isolating Foil ............................................................. 25

9.2 Head Board and Foot Board .......................................26

9.2.1 Aluminium head board and foot board .....................26

9.2.2 Powder coated head board and foot board ..............27

9.2.3 Correct Orientation of Head Board and Foot Board .27

9.3 Mattress support platform ...........................................28

9.4 Potential Equalisation .................................................29

9.5 Before Use ..................................................................30

9.6 Transport ..................................................................... 30

9.7 Firmware .....................................................................30

10 Power Supply Cord (Mains Power Cable) ................31

11 Accumulator ...............................................................31

11.1 Status Faulty Accumulator .........................................32

11.2 Status Discharged Accumulator ................................ 32

11.3 Removing the Bed from Service...............................32

11.4 Deactivating the Accumulator ................................... 33

12 Manipulation ............................................................... 33

12.1 ACP – Attendant Control Panel (nurse controller) .....34

12.1.1 Central STOP Button .............................................35

12.1.2 Activating GO Button ..............................................35

12.1.3 Function Buttons ....................................................35

12.1.4 Lock Buttons ..........................................................35

12.1.5 Position Buttons .....................................................35

12.2 Handset .....................................................................37

12.3 CPR backrest release ...............................................38

12.4 Siderails ....................................................................39

12.5 Castor Control and Bed Transport ............................ 39

12.5.1 Bed with Castor Control Levers .............................39

13 Equipment ..................................................................40

13.1 Accessory Rails .........................................................40

13.2 The Fifth Castor ........................................................40

13.3 Brake Signal – Signalization of Unbraked Bed ........40

14 Mattress ......................................................................40

15 Accessories ................................................................41

15.1 Lifting Pole ................................................................42

15.2 Infusion Stands .........................................................42

15.3 Siderails Extension – Extender® ..............................43

15.4 Image 3 B Protector® ...............................................44

16 Cleaning/Disinfection ................................................45

16.1 Safety Instructions for Cleaning and Disinfection of the Bed

..........................................................................................46

16.2 General Instructions for Cleaning and Disinfection ... 46

16.2.1 Daily Cleaning ........................................................ 46

16.2.2 Cleaning before Changing Patients .......................46

16.2.3 Complete Cleaning / Cleaning before First Use .....46

16.2.4 Cleaning of Spilled Fluids ......................................46

16.2.5 Damaged Foam Mattress ......................................46

16.3 Modes of Cleaning and Disinfection .........................47

17 Troubleshooting ......................................................... 48

18 Maintenance ...............................................................49

18.1 Regular maintenance ................................................ 49

18.2 Spare Parts ...............................................................49

18.3 Safety Technical Checks ........................................... 49

19 Disposal ......................................................................50

19.1 Environment Protection .............................................50

19.2 Disposal ....................................................................50

19.2.1 Within Europe ........................................................50

19.2.2 Outside Europe ......................................................50

20 Warranty ......................................................................51

21 Standards and Regulations ......................................51

Table of Contents

D9U001AM2-0101_07

5

1 Symbols and Denitions

1.1 Warning Notices

1.1.1 Types of Warning Notices

Warning notices are dierentiated by the type of danger using the following signal words:

► CAUTION warns about the risk of material damage.

► WARNING warns about the risk of physical injury.

► DANGER warns about the risk of fatal injury.

1.1.2 Structure of Warning Notices

SIGNAL WORDS!

Type and source of danger!

► Measures to avoid the danger.

1.2 Instructions

Structure of instructions:

► Perform this step.

Results, if necessary.

1.3 Lists

Structure of bulleted lists:

■ List level 1

□ List level 2

● List level 3

D9U001AM2-0101_076

1.4 Symbols on the Package

FRAGILE, HANDLE WITH CARE

THIS WAY UP

KEEP DRY (PROTECT FROM HUMIDITY)

PAPER RECYCLING SYMBOL

DO NOT USE HAND TRUCK HERE

DO NOT STACK DURING STORAGE

D9U001AM2-0101_07

7

1.5 Symbols and Labels on the Bed

READ INSTRUCTIONS FOR USE

WARNING

THERMAL PROTECTION OF TRANSFORMER

ONLY SUITABLE FOR INDOOR USE

PROTECTION AGAINST ACCIDENTS DUE TO ELECTRICAL CURRENT – TYPE B

APPLIED PARTS

SAFETY ISOLATING TRANSFORMER, GENERAL

CE MARK OF CONFORMITY WITH EU REGULATION

JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION

SAFE WORKING LOAD

WARNING AGAINST CRUSHING OR TRAPPING

MAXIMUM WEIGHT OF PATIENT

D9U001AM2-0101_078

USE MATTRESS RECOMMENDED BY MANUFACTURER

WEIGHT OF BED

DO NOT PUT ANY OBJECTS HERE

WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,

DO NOT PUT INTO THE HOUSEHOLD WASTE)

MEDICAL DEVICE (COMPATIBLE WITH MEDICAL DEVICE REGULATION)

RECYCLING SYMBOL

DO NOT POLLUTE THE ENVIRONMENT

MANUFACTURER

MANUFACTURING DATE

REFERENCE NUMBER (PRODUCT TYPE DEPENDING ON CONFIGURATION)

SERIAL NUMBER

D9U001AM2-0101_07

9

GO BUTTON (PRESS TO ACTIVATE CONTROL ELEMENT)

STOP BUTTON (PRESS TO INTERRUPT BED POSITIONING)

HEAD BOARD UNLOCKED OR FOOT BOARD UNLOCKED (POWDER COATED HEAD

BOARD AND FOOT BOARD)

HEAD BOARD LOCKED OR FOOT BOARD LOCKED (POWDER COATED HEAD

BOARD AND FOOT BOARD)

MASS OF MOBILE HOSPITAL BED (MASS OF EMPTY BED + SAFE WORKING LOAD)

UK CONFORMITY ASSESSED (UKCA) MARKING (PRODUCT NORMATIVELY

HARMONIZED FOR GREAT BRITAIN ECONOMIC AREA)

AUTHORIZED REPRESENTATIVE IN GREAT BRITAIN

AUTHORIZED REPRESENTATIVE IN SWITZERLAND

REPCH

D9U001AM2-0101_0710

1.6 Acoustic signalisation

SOUND MEANING

CONTINUOUS SOUND overheating

accumulator overcurrent

actuator overload

REPEATED BEEP: 0,6s sound / 2,6s silence STOP error (all STOP buttons are disabled)

REPEATED BEEP: 0,1s sound / 3s silence switching of the transformer winding error (Brazil)

BEEP lasting 0,3s conrmation

stopping or locked function

optionally: transition from tilt (Trendelenburg, Antitrendelenburg)

to horizontal position

BEEP lasting 0,5s lowering to the lowest position

start of service mode or end of service mode

keyboard error (positioning blocked)

BEEP lasting 3s system error

REPEATED BEEP during 3 minutes: 1,1s sound / 1,1s silen-

ce

Brake Signal (only version with Brake Signal)

ACCUMULATOR INDICATOR MEANING

lit accumulator disconnected or faulty

ashing: 1,6s lit / 0,2s not lit accumulator deeply discharged

ashing: 0,1s lit / 0,1s not lit accumulator discharged

ashing: 0,2s lit / 1,6s not lit accumulator is charging

not lit accumulator charged

MAINS POWER LED MEANING

lit connected to the mains

ashing: 0,6s lit / 0,6s not lit keyboard error (ashing inverted to Lock LED)

error (rst fault)

ashing: 0,1s lit / 0,1s not lit service mode

not lit disconnected from the mains power

transformer switching error

1.7 Visual signalisation

1.7.1 Mains Power LED (Attendant Control Panel)

1.7.2 Accumulator Indicator (Attendant Control Panel)

D9U001AM2-0101_07

11

VISUAL

SIGNALISATION

LOCK LED

lit

ashing:

0,6s lit / 0,6s not lit not lit

Thighrest Lock LED locked lock error keyboard error motion blocked unlocked

Backrest Lock LED locked lock error keyboard error motion blocked unlocked

Bed Height, Trendelenburg and An-

titrendelenburg Tilt Lock LED

locked lock error keyboard error motion blocked unlocked

1.7.3 Lock LED (Attendant Control Panel)

1.8 Night Bed Illumination

It is possible to equip Image 3 B with undercarriage illumination. The lightning helps the patient or hospital personnel to better ori-

entate in room with lowered or turned o light. The lowered intensity of lightning is set up after turning the bed on.

The bed is equipped with three-phase illumination:

1. Full intensity of illumination

2. Lowered intensity of illumination

3. Illumination is turned o

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 (Attendant Control Panel, Handset) 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 o all illumination:

► Press Bed Lights control Button on the Attendant Control Panel and all illumination on the bed (handset and bed illuminati-

on) will be turned o. This function is not blocked by the activation GO button.

D9U001AM2-0101_0712

1.9 Denitions

Basic Bed Conguration the pricelist model conguration, not including a mattress

Bed Weight The value depends on the product conguration, accessories or customer

adjustments.

Clearance of Undercarriage the height from the oor to the lowest point of the undercarriage between

the castors, for the manipulation of accessories under a braked bed in the

standard position

Duty Cycle cycle of operation of the motor: time of activity/time of rest

Ergoframe Ergoframe is the kinematic system of Mattress support platform Adjustment

whose eect is the elimination of pressure on the patient´s abdomen and pel-

vic area and frictional forces on the patient‘s back and legs.

Maximum Patient Weight Maximum Patient Weight depends on the application environment according

to IEC 60601-2-52. For application environment 1 (intensive/critical care) and

2 (acute care) reduce Safe working Load by 65 kg. For application environ-

ment 3 (long-term care) and 5 (ambulatory care) reduce Safe working Load

by 35 kg.

Safe Working Load the highest allowable load on the bed (patient, mattress, accessories and the

load supported by those accessories)

Siderail Height the height of the upper crossbar or the edges of the siderails (not the highest

point of the siderail controls) from the patient surface

Standard Bed Position ■ The height of the patient surface with regard to the oor is 400 mm

■ The mattress support platform, including the individual parts, has to be in a

horizontal (level - 0°) position.

■ The siderails are always locked in the upper position.

■ The basic position of the integrated extension.

Adult Patient having a physical size equal to or more than 146 cm, a mass equal

to or more than 40 kg and a body mass index (BMI) equal to or more than 17

(according to IEC 60601-2-52).

Mass of mobile hospital bed Sum of empty bed mass and Safe Working Load.

D9U001AM2-0101_07

13

AC ( ~ ) Alternating Current

ACP Attendant Control Panel

CE European Conformity

CPR Cardiopulmonary Resuscitation

dBA Sound Intensity Unit

DC ( ) Direct Current

CUC Conguration number

EMC Electromagnetic Compatibility

FET Field-eect transistor

HF High Frequency

HPL High Pressure Laminate

HW Hardware

ICU Intensive Care Unit

INT. Duty Cycle

IP Ingress Protection

IV Intravenous

LED Light Emitting Diodes

ME Medical Electrical (Equipment)

ON Activation

OFF Deactivation

ppm parts per million, millionth (1000 ppm = 0,1%)

REF Reference Number (product type depending on conguration)

SCU System Control Unit (active mattress)

SN Serial Number

SW Software

SWL Safe Working Load

UDI Unique Device Identication (for medical devices)

USB Universal Serial Bus

WEEE Waste Electrical and Electronic Equipment

1.10 Abbreviations

D9U001AM2-0101_0714

2 Safety Instructions

WARNING!

Image 3 B 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 B should be located in the „up“ position to reduce the risk of the patient accidentally

slipping or rolling o 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 B bed avoid squeezing those between parts of the

Image 3 B bed!

WARNING!

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

WARNING!

The bed is intended for adults.

Follow chapter Intended use.

WARNING!

Incompatible mattresses can create hazards.

WARNING!

To avoid the risk of electric shock, this equipment must only be connected

to a supply mains with protective earth.

WARNING!

No modication of this equipment is allowed.

WARNING!

Do not modify this equipment without authorization of the manufacturer.

WARNING!

If this equipment is modied, appropriate inspection and testing must be conducted to ensure continued safe

use of the equipment.

D9U001AM2-0101_07

15

WARNING!

An additional MULTIPLE SOCKET-OUTLET or extension cord shall not be connected to the MEDICAL ELECTRI-

CAL SYSTEM.

WARNING!

During specic investigations or treatments the signicant risks of reciprocal interference posed by ME equip-

ment may occur.

DANGER!

Risk of injury or death due to use of incorrect equipment!

► Always conduct the risk assessments required for the selection of suitable equipment.

WARNING!

Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the

competent authority of the Member State in which the user and/or patient is established!

WARNING!

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

WARNING!

This medical device is not intended for oxygen enriched environment!

WARNING!

This medical device is not intended for use with ammable substances!

WARNING!

This medical device is not portable medical electrical equipment!

WARNING!

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

WARNING!

Patient is allowed to use selected control elements only if hospital personnel had assessed that the patient´s

physical and psychological state is in accordance with use of them and only if the hospital personnel had

trained the patient in accordance with the instructions for use!

D9U001AM2-0101_0716

► Follow the instructions for use carefully.

► Any non-observance of this manual may lead to injuries or material damage.

► Exclusively use the bed if it is in perfect working order.

► If necessary, check the bed functions daily or at each shift change.

► Use the bed exclusively in its original condition.

► Use the bed exclusively with the correct mains supply.

► Ensure that the bed is operated exclusively by qualied personnel who have been trained according to the instructions for

use.

► Ensure that the patient (health permitting) has been informed about the operation of the bed and all applicable safety

instructions.

► Move the bed exclusively on even, hard-surfaced oors.

► Replace any damaged parts immediately with original spare parts.

► Ensure that maintenance and installation are performed exclusively by qualied personnel who have been trained by the

manufacturer.

► Do not apply excess weight or loads to the bed according to SWL (safe working load).

► During peak loads or unavoidable excess loads (CPR), place mattress platform in the lowest position.

► Ensure that only one adult patient uses the bed at any time.

► Take care to avoid injuries or squeezing when operating moving parts.

► When using lifting poles or infusion stands, ensure that nothing will be damaged when you move or adjust the bed.

► Ensure that castors are braked when the bed not being moved, regardless of whether the bed is occupied or empty

► Keep the mattress platform in the lowest position at any time when the healthcare personnel are not treating the patient in

order to prevent the patient from falling or injuries.

► Ensure that siderails are operated exclusively by healthcare personnel.

► Never use the bed in areas where there is a hazard of explosion.

► Enable or disable functions on the handset using the Attendant Control Panel as appropriate for the patient’s physical and

mental state. Verify that the function is actually disabled.

► Never handle the mains plug with wet hands.

► Unplug the mains cable exclusively by pulling on the plug.

► Position the mains cable so that there are no loops or bends in the cable; protect the cable from mechanical wear and tear.

► Improper handling of mains cable can cause an electric shock hazard, other serious injuries or damage to the bed.

► Ensure that the stipulated duty cycle (on-time) is not exceeded (see INT. on product label).

► Ensure that the moving parts of the bed are not blocked.

► To prevent failures, use exclusively the manufacturer’s original accessories and mattresses.

► Ensure that the stipulated safe working load is not exceeded.

► If the patient‘s condition could lead to an entrapment, leave the mattress support platform in the at position while the

patient is unattended.

► Adjust bed height to approx. 20 cm below maximum height when transporting the bed in order to facilitate overcoming

possible obstacles.

► Do not exceed maximum load of 75 kg for mattress platform extension.

► Ensure that the bed and its components are exclusively modied with the manufacturer´s approval.

► Ensure there is no risk of crushing or otherwise injuring the patient’s limbs (e.g. between siderails and mattress platform,

between movable parts etc.) before positioning the bed or folding down the siderails.

► Close linen shelf before using the Antitrendelenburg position.

► Do not put any objects (e.g. accessories, infusions, cables) between or on siderails and movable parts.

► Use exclusively split plastic or split telescopic siderails for confused or disoriented patients.

► 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 Attendant Control Panel or handset when they are stored on siderails or

head board/foot board.

► To prevent collisions, do not put oxygen bottle holders directly under mattress platform.

► Always set mattress platform to its lowest position and single parts of mattress 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. backrest) is forbidden. Otherwise

there is a risk of damaging and dysfunction of the backrest actuator or unprompted fall of the backrest.

D9U001AM2-0101_07

17

3 Intended use

The intended use is the hospitalization of the patient in the acute and long-term care units, which includes above all the

following aspects:

► Adjustment of the specic positions needed for the preventive reasons, routine nursing, treatments, mobilization, physio-

therapy, examinations, sleeping, and relaxation. These positions are further specied and described in the clinical evaluation of this

device, together with their potential clinical outcomes and benets.

► Providing the safe environment for the patient during all relevant procedures. The particular requirements on patient safety

are the subject of the clinical evaluation, including evaluation of the risk/benet ratio. The relevant safety issues are the part of the

risk management le.

► Patient in-bed indoor transport out of the patient room.

► Providing the suitable working conditions for the caregivers to perform the routine and specic tasks during the patient

hospitalization.

3.1 User population

► Adult overweight patients in the standard care units (based on individual patient status assessment by caregiver the pati-

ent can utilize dedicated device functions)

► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

3.2 Contraindications

► The medical device is not intended for the pediatric patients use.

Certain positions are not suitable for specic diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position, higher ICP

patients vs. Trendelenburg). Sta expert assessment / nursing consideration is needed in all individual case of contraindication.

3.3 Operator

► Caregiver

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

4 Incorrect Use

Image 3 B is not suitable for:

■ Use

□ Other than described in the instructions for use

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

LINET®’s eorts in research, design and manufacture ensure LINET® products are of the highest quality and t for their intended

purpose. However, LINET® can take no responsibility for any damage to the products or any harm to patients, sta or other indivi-

duals resulting from:

► Not following the instructions in the manual, including warning notices.

► Using the product for a purpose other than the intended purpose stated in the relevant documentation provided by LINET®

(see Intended use).

D9U001AM2-0101_0718

5 Product Description

5.1 Image 3 B (1AM2) - Single Collapsible Siderails and Powder Coated

Head Board and Foot Board

Fig. Overview Image 3 B – Single Collapsible Siderails

1. Foot board

2. Virtuoso II compressor

3. Siderail release mechanism

4. Siderail extension – Extender®

5. Virtuoso II active mattress for bariatrics

6. Head board

7. Single collapsible siderails

8. Handset

9. Castor control lever

10. Castor

11. CPR control lever – backrest release

12. Accessories rail

13. Fifth castor

14. Calfrest handle / Mattress holder

15. Housing for the Protector®

16. Foot board unlocking mechanism

17. Attendant Control Panel

18. Protective bumper

NOTE For safe, easy handling, LINET® recommends that two technicians put the bed into service.

D9U001AM2-0101_07

19

6 Technical Specication

6.1 Applied parts type B

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

List of type B applied parts:

► ACP Attendant Control Panel

► Handset

► Satellite controller

► Siderails

► Head board and foot board

► Mattress support platform

6.2 Mechanical Specication

Parameter Value

Dimensions 220 cm x 110 cm

Siderail Height Above Mattress Support Platform 48 cm

Siderails Length 146 cm

Maximum Mattress Height 26 cm

Mattress Support Platform Dimensions (Mattress) 200 cm x 100 cm

Mattress Support Platform Extension 0 cm / 10 cm / 22 cm / 30,5 cm

Mattress Support Platform Height Adjustment 28 cm – 80 cm (85 cm - depending on congu-

ration)

Undercarriage Clearance 13 cm (15,5 cm - depending on conguration)

Castor Diameter 12,5 cm

Maximum Backrest Angle 70°

Maximum Thighrest Angle 34°

Ergoframe® 10 cm / 6 cm

Trendelenburg 14°

Antitrendelenburg position 14°

Bed Weight 160 kg

Maximum Lifting Pole Load 100 kg

Safe Working Load (including Mattress and Accessories) 320 kg

Mass Of Mobile Hospital Bed (Mass Of Empty Bed + Safe Working

Load)

492 kg

Maximum patient weight

Application environment 1, 2

Application environment 3, 5

255 kg

285 kg

6.3 Environment Conditions

Environmental Conditions - Operation

■ Ambient Temperature

■ Relative Humidity

■ Atmospheric Pressure

10 °C — 40 °C

30 % — 75 %

795 hPa — 1060 hPa

Environmental Conditions - Storage and Transport

■ Ambient Temperature

■ Relative Humidity

■ Atmospheric Pressure

-20°C — +50°C

20% — 90% (non-condensing)

795 hPa — 1060 hPa

D9U001AM2-0101_0720

6.5 Electromagnetic compatibility

Bed is intended for hospitals except for near active HF surgical equipment and the RF shielded room of a medical system for mag-

netic resonance imaging, where the intensity of EM disturbances is high.

Bed has dened no essential performance.

WARNING!

It is recommended to avoid the use of this device next to or in block with other device, because it could lead to

improper operation. If such use is needed, this device and the other equipment should be under surveillance

to verify proper operation.

List of used cables:

1. Mains cable, maximum length 6 m

2. ACP Attendant Control Panel, maximum length 3m

3. Handset, maximum length 3m

6.4 Electrical Specications

DANGER!

Danger to life due to electric shock!

► Ensure that maintenance and service of electrical parts are performed only by qualied personnel if the bed is

connected.

Parameter Value

Input Voltage 230 V AC, 50/60 Hz

100 V AC, 50/60 Hz

110 V AC, 50/60 Hz

120 V AC, 50/60 Hz

127 V AC, 50/60 Hz

110-127 V AC, 50/60 Hz or 230 V AC, 50/60 Hz

Maximum Power Input 370 VA

Ingress Protection IP X4

Safety Class Class I (with type B Applied Parts)

Electrical Motor Duty Cycle max. 2 minutes ON / 18 minutes OFF

Accumulator

Fuse

Version 1

Version 2

Version 3

Pb ACCU 2 x 12 V / 1,2 Ah / Fuse 15A

2x T1.6A L 250 V for 230 V version

2x T3.15A L 250 V for 100-127 V version

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 specications that comply with regional standards (custom

voltage, dierent mains plugs).

WARNING!

Use of the accessories, converters and other cables, than specied and provided by manufacturer of this bed

could lead to increase of electromagnetic emission or lower the electromagnetic immunity of this bed and lead

to improper operation.

WARNING!

Mobile RF communication device (including end use devices like antenna cables and external antenna) should

not be used closer than 30 cm (12 inches) from any part of this Image 3 B bed, including cables specied by

manufacturer. Otherwise this could lead to deterioration of functionality of this bed.

WARNING!

Do not overload the bed (SWL), respect the duty cycle (INT.) and consider chapter 18 Maintenance in order to

maintain the basic safety with regard to electromagnetic disturbances for the expected service life.

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LINET Image 3 XXL Operating instructions

LINET Image 3 XXL Operating instructions

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