LINET Multicare Parts list manual

Multicare
Positionable bed for intensive care with
scales and without scales
D9U001MC0-0101
Version: 16
Publication Date: 2020-02
Instructions for Use
and Technical Description

D9U001MC0-0101_162
Manufacturer:
LINET spol. s r.o.
Želevčice 5
274 01 Slaný
Tel.: [phone]
Fax: [phone]
E-mail: [e-mail]
http://www.linet.com
Multicare
Positionable bed for intensive care with scales and without scales
Author: LINET, s.r.o.
Related links: www.linet.com
D9U001MC0-0101
Version: 16
Publication date: 2020-02
Copyright © LINET, s.r.o., 2020
Translation © LINET, 2020
All rights reserved.
All trademarks and brands are the property of the appropriate owners. The manufacturer reserves the right to changes in the con-
tents of the instructions for use that relate to the product´s technical regulations. It is for this reason that the contents of the instruc-
tions for use may indicate differences from the current manufacture of the product.

D9U001MC0-0101_16 3
1 Symbols and Denitions .............................................4
1.1Warning Notices..........................................................4
1.1.1Types of Warning Notices ........................................4
1.1.2Structure of Warning Notices ...................................4
1.2Instructions..................................................................4
1.3Lists.............................................................................4
1.4Symbols on the Package ............................................5
1.5 Symbols and Labels on the Bed .................................6
1.6Serial Label with UDI ..................................................9
1.7Acoustic signalisation .................................................10
1.8 Visual signalisation......................................................11
1.8.1 Mains Power LED (Multiboard, Attendant Control Panel)
..........................................................................................11
1.8.2 Accumulator Indicator (Multiboard, Attendant Control Pa-
nel)....................................................................................11
1.8.3 Lock LED (Attendant Control Panel)........................11
1.9 Denitions ...................................................................12
1.10 Abbreviations ............................................................13
2 Safety Instructions.......................................................14
3 Intended use.................................................................18
3.1User population...........................................................18
3.2Contraindications ........................................................18
3.3Operator......................................................................18
4 Product Description.....................................................19
5 Technical Specication ...............................................20
5.1 Identication of Applied Parts (Type B) .......................20
5.2 Scales (only version with scales) ................................20
5.3 Mechanical Specications (Multicare).........................20
5.4 Environment Conditions..............................................21
5.5 Electrical Specications (Multicare) ............................21
5.6 Electromagnetic compatibility .....................................22
5.6.1 Manufacturer instructions – electromagnetic emissions
..........................................................................................22
5.6.2 Manufacturer instructions – electromagnetic susceptibility
..........................................................................................23
6 Use and Storage Conditions ....................................... 24
7 Scope of Delivery and Bed Variants...........................25
7.1 Delivery ......................................................................25
7.2 Scope of Delivery........................................................25
7.3Multicare Variants........................................................25
8 Putting into Service .....................................................26
8.1 Accumulator Activation................................................27
8.1.1 Placement of Control Section ..................................27
8.1.2 Removing the Isolating Foil......................................27
8.2 Head Board and Foot Board .......................................28
8.3 Potential Equalisation .................................................29
8.4 Before Use .................................................................30
8.5 Transport.....................................................................30
8.6 Firmware .....................................................................30
9 Power Supply Cord (Mains Power Cable)..................31
10Accumulator ............................................................... 31
10.1Accumulator Operation .............................................31
10.2Replacing the accumulator .......................................32
10.3 Removing the Bed from Use.....................................33
10.4 Deactivating the Accumulator ...................................33
11 Manipulation ...............................................................34
11.1Siderails.....................................................................34
11.2 Castor Control and Bed Transport.............................35
11.2.1Central Castor Control............................................35
11.2.2 Bed transport..........................................................35
11.3 CPR Backrest Release..............................................36
11.4Control Elements.......................................................37
11.4.1 Multiboard with LCD Touchscreen in Both Head Siderails
..........................................................................................37
11.4.2Attendant Control Panel .........................................39
11.4.3 Handset..................................................................40
11.4.4Patient Control Panels............................................40
11.4.5 Bed Height Foot Control.........................................41
11.4.6Lateral Tilt Foot Control..........................................41
11.4.7Quick-Action Panels ...............................................41
11.5 LCD Touchscreen......................................................42
11.5.1 Menu Bar Icons ......................................................42
11.5.2 Positioning Screen .................................................43
11.5.3 Lock Screen ...........................................................44
11.5.4 Settings Screen......................................................44
11.5.5 Help Screen............................................................45
11.5.6 Pop-Ups .................................................................45
12ALT (Automatic Lateral Therapy)..............................47
12.1 Resetting Bed to Initial Position ................................47
12.2Test ALT cycle ...........................................................48
12.3ALT Cycle ..................................................................48
13 Scales Control............................................................49
13.1 Scales Screen (WS17) .............................................49
13.1.1Preparation ...........................................................49
13.1.2Taring .....................................................................49
13.1.3Displaying ..............................................................50
13.1.4 Hold Mode..............................................................50
13.1.5 Saving Weight of Patient........................................50
13.1.6 History Subscreen..................................................50
13.1.7 Bed Overload .........................................................51
13.1.8 Bed Underload .......................................................51
13.1.9Weighing in tilt........................................................51
13.1.10 Zeroing Scales .....................................................51
14 Bed Exit Monitoring ...................................................52
14.1Preparation ...............................................................52
14.2 Activation...................................................................52
14.3 Control of Bed Exit Monitoring .................................53
14.4Monitored Zone.........................................................53
14.5 PAUSE ......................................................................53
14.6ALARM......................................................................54
14.7 Deactivation ..............................................................54
14.8 Fault Status (disconnected from the mains) .............54
15 Patient Transfer ..........................................................55
16 Equipment ..................................................................55
16.1Accessory rails ..........................................................55
16.2 i-Brake® (optional)....................................................55
16.3 Retractable 5th wheel i-Drive® (optional) .................55
16.4 Mobi-Lift®..................................................................56
16.4.1 Using the Support Handles ....................................56
16.5 Safety Night Light......................................................56
16.6 i-Drive Power (optional) ............................................57
16.6.1 i-Drive Power System - Basic Description .............57
16.6.2 Safety instruction for i-Drive Power........................57
16.6.3 Specications of Use .............................................57
16.6.4Manipulation...........................................................58
16.6.5 Powered Drive .......................................................59
16.6.6 Braking...................................................................59
16.6.7 i-Drive Power Activation/Deactivation ....................60
16.6.8 Free Drive ..............................................................60
16.6.9Accumulator ...........................................................60
16.6.10Fault Signalization................................................61
16.6.11Light Indicators .....................................................61
16.6.12 Technical Specications.......................................61
16.6.13 Electrical specication..........................................61
16.6.14 I-Drive Power Maintenance..................................62
16.7X-Ray Lung Examination ..........................................62
16.7.1Necessary Steps before the Examination..............62
16.7.2Examination with C-arm.........................................62
17 Mattress ......................................................................63
17.1 Passive Mattress.......................................................63
17.1.1Straps with side release buckles............................63
17.2 Active Mattress (not integrated) ................................64
17.3 OptiCare and Symbioso (integrated mattress)..........64
18Accessories ................................................................65
18.1 Lifting Pole ................................................................65
18.2 Infusion Stands .........................................................66
Table of Contents

D9U001MC0-0101_164
1 Symbols and Denitions
1.1 Warning Notices
1.1.1 Types of Warning Notices
Warning notices are differentiated by the type of danger using the following key words:
► CAUTION warns about the risk of material damage.
► WARNING warns about the risk of physical injury.
► DANGER warns about the risk of fatal injury.
1.1.2 Structure of Warning Notices
SIGNAL WORDS!
Type and source of danger!
► Measures to avoid the danger.
1.2 Instructions
Structure of instructions:
► Perform this step.
Results, if necessary.
1.3 Lists
Structure of bulleted lists:
■ List level 1
□ List level 2
● List level 3
18.3 Stabilising ALT Pads .................................................66
18.4 Ventilation Circuit Holder...........................................67
18.5 Monitor Tray .............................................................67
18.6 Oxygen Bottle Holders ..............................................68
18.7 Protector ...................................................................69
19 Cleaning/Disinfection ................................................70
19.1 Cleaning (Multicare)..................................................71
19.1.1Daily Cleaning........................................................71
19.1.2Cleaning before Changing Patients .......................72
19.1.3Complete Cleaning and Disinfection......................72
20 Troubleshooting .........................................................73
21 Maintenance ...............................................................74
21.1Regular maintenance................................................74
21.2 Spare Parts ...............................................................74
21.3Safety Technical Checks ...........................................74
22 Disposal ...................................................................... 75
22.1 Environment Protection.............................................75
22.2Disposal ....................................................................75
22.2.1Within Europe ........................................................75
22.2.2 Outside Europe ......................................................75
23 Warranty......................................................................76
24 Standards and Regulations ......................................76

D9U001MC0-0101_16 5
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

D9U001MC0-0101_166
1.5 Symbols and Labels on the Bed
READ INSTRUCTIONS FOR USE
THERMAL PROTECTION FOR TRANSFORMER
WARNING
ONLY SUITABLE FOR INDOOR USE
APPLIED PARTS TYPE B
SAFETY ISOLATING TRANSFORMER, GENERAL
CE MARK (MULTICARE WITH SCALES)
CE MARK (MULTICARE WITHOUT SCALES)
JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL EQUALISATION
SAFE WORKING LOAD
WARNING AGAINST CRUSHING OR TRAPPING
USE MATTRESS RECOMMENDED BY MANUFACTURER

D9U001MC0-0101_16 7
DO NOT PUT ANY OBJECTS ON UNDERCARRIAGE
MAXIMUM WEIGHT OF PATIENT
WEIGHT OF BED
DESIGNATION OF HOSPITAL BED FOR ADULTS
ANTIBACTERIAL SURFACE FINISH
WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,
DO NOT PUT INTO THE HOUSEHOLD WASTE)
EAC MARKING (EURASIAN CONFORMITY)
DO NOT POLLUTE THE ENVIRONMENT
TÜV MARK
GO BUTTON (PRESS TO ACTIVATE CONTROL ELEMENT)
STOP BUTTON (PRESS TO INTERRUPT BED POSITIONING)

D9U001MC0-0101_168
RECYCLING SYMBOL
MEDICAL DEVICE (COMPATIBLE WITH MEDICAL DEVICE REGULATION)

D9U001MC0-0101_16 9
1.6 Serial Label with UDI
Pictures of serial labels below serve just for explanation of the signs and  elds on the serial labels.
Fig. Serial Label with UDI (Multicare with scales)
1
1
5
5
6
6
7
7
8
8
9
9
10
10
4
4
2
2
3
3
1 Address of Manufacturer
2Manufacturing Date (Year-Month-Day)
3DI (Device Identi er) / GTIN (Global Trade Item Number)
41D Bar code GS1-128 (Serial Number)
5Symbols
6Con guration number
7Electrical Speci cation
8Serial Number
9PI (Product Identi er)
10 2D Bar Code (GS1 DataMatrix) DI+PI=UDI
Fig. Serial Label with UDI (Multicare without scales)

D9U001MC0-0101_1610
Fig. Serial Label (WS17)
Scales Abbreviations
Max maximum capacity of the weighing
instrument
Min minimum capacity of the weighing
instrument
everication scale interval
Ttare value
1.7 Acoustic signalisation
SOUND MEANING
CONTINUOUS SOUND overheating
accumulator overcurrent
scales overload (only version with scales)
actuator overload
BEEP + CONTINUOUS SOUND Siderail Signal (lateral tilt + head siderail or foot siderail down)
REPEATED BEEP: 0,6s sound / 2,6s silence STOP error (all STOP buttons are disabled)
MELODY: 3 beeps, pause, 2 beeps, longer pause, 3 beeps,
pause, 2 beeps
Bed Exit Alarm (only version with scales)
BEEP lasting 0,3s conrmation
stopping or locked function
lateral tilt 15° achieved
transition from tilt (lateral tilt, Trendelenburg, Antitrendelenburg)
to horizontal position
4 TIMES REPEATED BEEP lasting 0,3s disconnected from the mains
positioning powered by the accumulator
BEEP lasting 0,5s start of service mode or end of service mode
keyboard error (positioning blocked)
BEEP lasting 3s system error
BEEP lasting 5s SCU disconnected (only if integrated mattress is used)
scale module disconnected (only version with scales)
REPEATED BEEP during 3 minutes: 1,1s sound / 1,1s silen-
ce
Brake Signal (only version with Brake Signal)

D9U001MC0-0101_16 11
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
1.8 Visual signalisation
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
1.8.1 Mains Power LED (Multiboard, Attendant Control Panel)
1.8.2 Accumulator Indicator (Multiboard, Attendant Control Panel)
VISUAL
SIGNALISATION
LOCK LED
lit
ashing:
0,6s lit / 0,6s not lit not lit
Thighrest, Calfrest
and Bed Extension Lock LED
locked lock
error
keyboard
error
motion
blocked
unlocked
Backrest Lock LED locked lock
error
keyboard
error
motion
blocked
unlocked
Bed Height, Lateral Tilt,
Trendelenburg and Antitrendelen-
burg Tilt Lock LED
locked lock
error
keyboard
error
motion
blocked
unlocked
Foot Switch Lock
LED
locked lock
error
keyboard
error
motion
blocked
unlocked
1.8.3 Lock LED (Attendant Control Panel)

D9U001MC0-0101_1612
1.9 Denitions
Basic Bed Conguration the pricelist model conguration, not including a mattress
Bed Weight The value depends on the product conguration, accessories or customer
adjustments.
Clearance of Undercarriage the height from the oor to the lowest point of the undercarriage between
the castors, for the manipulation of accessories under a braked bed in the
standard position
Duty Cycle cycle of operation of the motor: time of activity/time of rest
Ergoframe Ergoframe is the kinematic system of Mattress support platform Adjustment
whose effect is the elimination of pressure on the patient´s abdomen and 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).

D9U001MC0-0101_16 13
AC ( ~ ) Alternating Current
ALT Automatic Lateral Therapy
CE European Conformity
CPR Cardiopulmonary Resuscitation
dB Sound Intensity Unit
CUC Control Unit Conguration Number
DC ( ) Direct Current
EAC Euroasian Conformity
EMC Electromagnetic Compatibility
FET Field-effect transistor
HF High Frequency
HPL High Pressure Laminate
ICU Intensive Care Unit
INT. Duty Cycle
IP Ingress Protection
IV Intravenous
LED Light Emitting Diodes
ME Medical Electrical (Equipment)
OFF Deactivated
ON Activated
ppm parts per million, millionth (1000 ppm = 0,1%)
REF Reference Number (product type depending on conguration)
SCU System Control Unit
SN Serial Number
SWL Safe Working Load
UDI Unique Device Identication (for medical devices)
USB Universal Serial Bus
WEEE Waste Electrical and Electronic Equipment
1.10 Abbreviations

D9U001MC0-0101_1614
2 Safety Instructions
WARNING!
Multicare 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 Multicare should be located in the „up“ position to reduce the risk of the patient accidentally sli-
pping 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 Multicare bed avoid squeezing those between parts of the
Multicare bed!
WARNING!
Multicare bed should not be used with bed hoists and bed lifts!
WARNING!
To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
WARNING!
During specic investigations or treatments the signicant risks of reciprocal interference posed by medical
electrical equipment may occur.
WARNING!
No modication of this equipment is allowed.
WARNING!
The bed is intended for adults.
► Follow chapter Specications of 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.

D9U001MC0-0101_16 15
WARNING!
No modication of this equipment is allowed.
WARNING!
Do not modify this equipment without authorization of the manufacturer.
WARNING!
If this equipment is modied, appropriate inspection and testing must be conducted to ensure continued safe
use of the equipment.
WARNING!
An additional multiple socket-outlet or extension cord shall not be connected to the medical electrical system.
WARNING!
During specic investigations or treatments the signicant risks of reciprocal interference posed by ME equip-
ment may occur.
WARNING!
Staff expert assessment is needed to consider all individual cases of contraindications!
WARNING!
Certain bed positions are not suitable for specic diagnosis/medical conditions. Fowler position is not suitable
for spinal cord injuries! Trendelenburg position is not suitable for patients with higher intracranial pressure!
WARNING!
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!
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!

D9U001MC0-0101_1616
► Follow the instructions in the instructions for use carefully.
► Use the bed exclusively if it is in perfect working order.
► If necessary, check the bed functions daily or at each shift change.
► Ensure any user has read and understood this manual completely before operating the product.
► Use the bed exclusively with the correct mains supply.
► Ensure that the bed is operated exclusively by qualied personnel 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.
► During peak loads or unavoidable excess loads (CPR), place mattress platform in the lowest position.
► Ensure that only one adult patient uses the bed at any time.
► Take care to avoid injuries or squeezing when operating moving parts.
► When using lifting poles or infusion stands, ensure that nothing will be damaged when you move or adjust the bed.
► Brake the castors when the bed is occupied.
► Keep the mattress platform in the lowest position at any time when the healthcare personnel are not trea- ting the patient
in order to prevent the patient from falling or injuries.
► Ensure that siderails are operated exclusively by healthcare personnel.
► Never use the bed in areas where there is a hazard of explosion.
► Enable or disable functions on patient controls using the Multiboard panel as appropriate for the patient’s physical and
mental state. Verify that the function is actually disabled.
► Never handle the mains plug with wet hands.
► Disconnect the product from the mains exclusively by pulling the mains plug.
► When pulling the mains plug, always hold the plug, not the cable.
► Position the mains cable so that there are no loops or kinks in the cable; protect the cable from mechani- cal wear and
tear.
► Improper handling of mains cable can cause an electric shock hazard, other serious injuries or damage to the mattress
replacement system.
► Ensure that the stipulated duty cycle (on-time) is not exceeded.
► Ensure that the moving parts of the bed are not blocked.
► To prevent failures, use exclusively the manufacturer’s original accessories and mattresses.
► Ensure that the stipulated safe working load is not exceeded.
► If the patient‘s condition could lead to an entrapment, leave the mattress support platform in the at position whilst
unattended.
► When adjusting the ALT (automatic lateral therapy), ensure that the process does not pose any risk of the patient falling or
getting injured, or of any lines or tracheal tubes getting pulled out.
► 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 80 kg for mattress platform extension.
► Ensure that the bed and its components are exclusively modied with the manufacturer´s approval.
► Use the mattress system exclusively as specied in this manual and in perfect working order.
► Use the mattress system exclusively with the correct mains supply.
► Use the mattress system exclusively in its original state and do not modify it in any way.
► Have the mattress system used exclusively by or under supervision of trained and qualied nursing per- sonnel.
► Have the mattress system serviced and installed exclusively by qualied personnel trained and authorised by the
manufacturer.
► Do not use the SCU near ammable gases.
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!
WARNING!
Hospital personnel is allowed to use the weighing system (scales) for weighing patients only if they had been
trained according to the instructions for use!

D9U001MC0-0101_16 17
► Use the mattress system exclusively in its original state and do not modify it in any way.
► Have the mattress system used exclusively by or under supervision of trained and qualied nursing per- sonnel.
► Have the mattress system serviced and installed exclusively by qualied personnel trained and authorised by the
manufacturer.
► Do not exceed the maximum patient weight limit (see Mechanical Specications (OptiCare or Symbioso)).
► Do not use the SCU (System Control Unit) near ammable gases (This does not apply to oxygen cylinders.).
► Never use the mattress replacement system near radiators or other heat sources.
► Never cover the SCU while in use.
► This does not apply to oxygen cylinders.
► Never use the mattress replacement system near radiators or other heat sources.
► Select a suitable location for the placement of bed accessories and other objects to prevent involuntary activation of
buttons or controls which may result in the adjustment of bed positioning.
► Do not use the bed in the event parts have been removed (e.g. parts of mattress platform) unless these parts are de
signed to be removed (e.g. head and/ or foot board).
► Never place any accessories or handset on the siderails in the area where the integrated siderail controller is located.
► After each emergency situation always check if any of the controllers (in siderails, handset or ACP) is not involuntarily
pressed by the bed accessories or by the mattress.
► The weighing system must be tested at regular intervals and in accordance with the metrological regulations of the
relevant country. All testing and certication must be carried out by qualied personnel. The healthcare provider is
responsible for ensuring the required testing frequency and testing procedure of the weighing system is carried out.
► To avoid injury or crushing, take extra caution when operating any moving parts of the bed.
► To avoid unintended activation of moving parts during any use of the bed always check that none of the control elements
of the bed is not involuntary pressed by persons, mattress or other objects.

D9U001MC0-0101_1618
3 Intended use
The intended use is the hospitalization of the patient in the intensive and acute care units, which includes above all the
following aspects:
► Adjustment of the specic positions needed for the preventive reasons, routine nursing, treatments, mobilization,
physiotherapy, 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.
► Indicative measurement of the patient weight, used as supportive feature without direct diagnostic effect. It helps staff to
assess the general patient status and apply the nutrition and medicaments (valid for the version of the beds with in-bed
scales).
3.1 User population
► Adult patients (weight >= 40 kg, height >= 146 cm, BMI >= 17) in the intensive and acute care units (Application
Environment 1 and 2 as in IEC 60601-2-52)
► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)
3.2 Contraindications
► The medical device is not intended for the pediatric patients use.
► Certain positions are not suitable for specic diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position,
higher ICP patients vs. Trendelenburg). Staff expert assessment / nursing consideration is needed in all individual case of
contraindication.
3.3 Operator
► Caregiver
► Patient (based on individual patient status assessment by caregiver the patient can utilize dedicated device functions)

D9U001MC0-0101_16 19
1. Removable Foot Board with Safety Lock
2. Foot Siderail with Integrated Control Panels for Patient
3. Split Siderail – Head Siderail
4. Four-part Mattress Platform with Ergoframe® System (under the mattress)
5. Multiboard with LCD Touchscreen
6. Quick-Action Panel
7. Removable Head Board
8. CPR Control Lever – Backrest Release
9. X-Ray Cassette Holder
10. Accessory Holder
11. Siderail Release Lever
12. Bi-lateral Accessory Rail
13. Castor Control Lever
14. Castor Diameter 150 mm (5.9 in.) with Main Control Lever
15. Mobilift® Handles
16. Bumpers
NOTE For safe, easy handling, LINET® recommends having two technicians assemble the bed.
Fig. Overview of Multicare
4 Product Description

D9U001MC0-0101_1620
5 Technical Specication
All technical data are rated data and are subject to construction and manufacturing tolerances.
WARNING!
If Multicare bed is used with OptiCare integrated mattress replacement system or with Symbioso integrated
mattress replacement system, respect values of mechanical and electrical specications which can harm
none of them!
5.1 Identication of Applied Parts (Type B)
All part of the bed (and accessories) the patient can reach are type B Applied Parts.
■ Mattress support platform frame, Covers and all Movable Parts
■ Head Board and Foot Board
■Siderails
■ Mobi-Lift Handles
■ Handset
5.2 Scales (only version with scales)
Accuracy of displayed weight values:
■ 0,5 kg (1,1 lbs)
■Scales Class III
5.3 Mechanical Specications (Multicare)
Parameter Value
Dimensions (With Folded-up Siderail) 215 cm x 105 cm
Bed Extension 0 cm - 22 cm
Recommended Mattress Dimensions 208 cm x 86 cm
Maximum Mattress Height 23 cm
Bed Height 44 cm - 82 cm
Siderail length
Head section
Central section
54 cm
100 cm
Castor (Diameter) 15 cm
Maximum Backrest Angle 70°
Maximum Thighrest Angle 30°
Maximum Calfrest Angle 38°
Maximum Lateral Tilt Angle 30°
Trendelenburg 13°
Anti-Trendelenburg Position 16°
Siderail Height (above Mattress Platform) 45 cm
Bed Weight (Basic Equipment) 224 kg
Safe Working Load 250 kg
Maximum Lifting Pole Load 75 kg
Maximum Patient Weight
Application environment 1, 2
Application environment 3, 5
185 kg
215 kg