Hillrom Primo P02033 User manual

PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
PT
ES
IT
DA
SVNL
DE
FR
EN
*170924*
User Manual - Manuel d’utilisation
Gebrauchsanweisung - Gebruikershandleiding
Användarhandbok - Brugermanual
Manuale d’uso - Manual de Usuario
Manual do Utilizador
Primo
P02033 /P02034 /P02044 /P02047
170924
Rev.002

170924(2) - Primo
PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012

PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
EN
*170924*
User Manual
Primo
P02033 /P02034 /P02044 /P02047
170924
Rev.002

170924(2) - EN - Primo™User Manual
PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Hill-Rom Industries S.A.
188, Rue du Caducée
Parc Euromédecine
34195 MONTPELLIER Cedex 5 - FRANCE
Tel: [phone]
Fax: [phone]
www.hill-rom.com
First edition, first printing: june 2012
170924, Rev.002 / October 2012
The information contained in this manual is confidential and may not be
reproduced or divulged in any form or by any means without the prior
written permission of Hill-Rom.
Hill-Rom® is a registered trademark of Hill-Rom Services, Inc.
I-mmersion
™
is a trademark of Hill-Rom Services, Inc.
Primo
™
is a trademark of Hill-Rom Services, Inc.
Velcro® is a registered trademark of Velcro Industries BV.
Hill-Rom reserves the right to make changes to the design, characteristics
and models without prior notice. The only warranty Hill-Rom makes is the
express written warranty extended on the sale or rental of its products.
To order copies of this manual, refer to the last page, identify your national
Hill-Rom representative and order the article with the part number 170924.
© 2012 Hill-Rom Services, Inc. ALL RIGHTS RESERVED.

Introduction,
specifications
Installing the patient Mobilizing and securing
the patient
Moving thedevice Disinfection, servicing Accessories and spare
parts
Appendix
170924(2) - EN - Primo™User Manual Page i
PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Table of Contents
Introduction, specifications
Structure of the manual. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Symbol definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Applications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Indication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Contraindication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Safety and Usage Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Putting into service. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Risk prevention. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Technical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Essential performances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Therapeutic Mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Control unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Conditions for transport, storage and use . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Special conditions of use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Product overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
General symbols on the device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
General symbols on the upper cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
General symbols on the control unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Buttons and light indicators on the control unit. . . . . . . . . . . . . . . . . . . . . . . . 11
General symbols on the labels. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Product identification labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Control unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Packaging. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Upper and bottom covers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Installing the patient
Before placing the patient on the Primo™. . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
List of compatible bed frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Mobilizing and securing the patient
Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Therapeutic mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Maximum inflation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
CPR. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Alarm silence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Mains power fault . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Malfunction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Moving the device
Transport mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

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Page ii 170924(2) - EN - Primo™User Manual
Transferring the mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Storing the mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Disinfection, servicing
Cleaning and Disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Safety Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Infection control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
General recommendations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Frequency of cleaning and disinfection of different parts of the mattress . . . 27
Clean and disinfect after the departure of a patient
or when changing the linen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Cleaning and disinfection at regular intervals or in the event of high risk of
contamination. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Final steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Safety recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Preventive maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
De-commissioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Accessories and spare parts
Seat cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Deflating and packing the seat cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Cleaning and Disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Upper covers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Quick inflate/deflate kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Transport bag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Appendix
Warranty and after sales service conditions . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Regulatory requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Manufacturer’s declaration - Electromagnetic Compatibility . . . . . . . . . . . . . . 39
Electromagnetic emissions compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Electromagnetic immunity compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Recommended separation distances. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40

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170924(2) - EN - Primo™User manual Page 1
Introduction
Specifications
Introduction, specifications
Structure of the manual
For every type of use, Hill-Rom mattresses provide patients with optimal comfort
and greater independence for a feeling of well-being that is conducive to a swift
recovery. They are also easy to use for caregivers.
PATIENT
CAREGIVER
EASE OF USE
INDEPENDENCE
WELL BEING
COMFORT
SAFETY
INSTALLATION
MOBILIZATION
HELP WITH
CARE
MOVEMENT

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Page 2 170924(2) - EN - Primo™User manual
Symbol definitions
This manual contains different typefaces and icons designed to improve readability
and increase understanding of its content. Note the following examples:
• Standard text: used for regular information.
•Bold text: emphasizes a word or phrase.
•highlights special information or explains very important instructions.
The symbols below represent different risks or hazards:
Symbol Description
WARNING
• This symbol indicates that the failure to follow the
associated recommendation can put the patient or
the user in danger, or damage the equipment.
CAUTION
• This symbol indicates that the failure to follow the
associated recommendation can result in damage
to the equipment.
Tip
Risk of falling
Caught hazard warning
Risk of crushing an upper limb
Chemical Hazard Warning
Electric Shock Hazard
Biological danger

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PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Introduction
Specifications
Applications
Description
The Primo
™
is a therapeutic mattress equipped with a pressure control system
designed to operate in continuous (or static) low-pressure mode. The Primo
™
is a
therapeutic solution by I-mmersion
™
that distributes pressure and reduces the
shearing effects on the surface of the patient's skin.
The Primo™ comprises a mattress and an external control unit.
It offers the following functionality:
• a CPR valve to facilitate external cardiac massages;
• a maximum inflation mode for greater patient mobility.
Indication
The Primo
™
therapeutic mattress helps to prevent and treat pressure ulcers in low
to moderate risk adult patients, within the recommended patient weight limits of 30
to 150 kg, in order to achieve clinical performance assessed in all the usual
positions of the adjustable head section.
It can be used as a mattress in the following environments, as defined in the
standard IEC 60601-2-52:
• application environment 2 (short-term care in hospitals or other medical
establishments);
• application environment 3 (long-term care in medical establishments);
• application environment 4 (care administered at home);
• application environment 5 (outpatients or ambulatory care).
The Primo
™
is intended to be used with a sheet between the patient skin and the
surface of the mattress.
In accordance with the NPUAP/EPUAP directives1, we recommend that the
condition of each patient be regularly checked. For patients with special needs,
we recommend the use of the more suitable I-mmersion™Therapy system.
Caregivers are responsible for taking this decision, in accordance with modern
care practices.
Contraindication
The Primo™must not be used with patients:
• suffering from an unstable fracture of the spine.
For any other unstable fractures, a medical examination is necessary to
decide whether the use of the device is appropriate;
• with atypical anatomies;
• suffering from cervical or trans-bone traction.
1. NPUAP / EPUAP - Pressure Ulcer Prevention - Quick Reference Guide, January 2010
NPUAP / EPUAP - Pressure Ulcer Treatment - Quick Reference Guide, December 2009

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Page 4 170924(2) - EN - Primo™User manual
Safety and Usage Tips
Putting into service
Before using the mattress, it is essential to have a thorough
understanding of this manual. This manual contains instructions for
general use and maintenance and guarantees improved safety.
Caregivers must have access to this manual.
Caregivers must be informed of the risks that may be encountered in the use of
electric devices. Product training can be provided on demand.
When using the mattress with medical devices (accessories), the user must ensure
that safety and conformity requirements are met.
Before using the mattress for the first time or when removing from storage:
• check the condition and conformity of the electrical system with the
applicable safety standards;
• connect the control unit of the Primo™device to the mains (See “Electrical
safety” page 5).
• make sure that all the functions of the device (See “Installation” page 16) are
in good conditions of operation;
• make sure that the device and the care environment are in a good state of
hygiene (See “Disinfection” page 28).
Risk prevention
Improper use of the device Primo™can result in risks for the patient or the user. The
following recommendations must be read and followed.
In view of the multitude of models of frames and siderails, and for
safety reasons, Hill-Rom advises that all necessary precautions must
be taken, especially with regard to the height of the siderails and the
dimensions of the sleep surface. If this device is used on a bed with
siderails that are less than 22cm above the mattress, patients must not
be left unattended.
For safety reasons, it is advisable to use the lock-out functions of the bed in the
following situations:
• during all interventions on the patient or the device (e.g.: examinations,
transfers, maintenance);
• if the patient suffers from particular behavioral difficulties (e.g. : agitation,
confusion, disorientation, obsessional behavior and aged and frail patients).
Properly trained medical staff should determine how the device should be used
and the required level of monitoring or constraint.

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PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Introduction
Specifications
It is imperative to observe the practices relating to the safety of caregivers. Special
attention must be taken when redistributing the load application points, since there
is a danger that the bed will tip when the frame is moved.
Surface impermeability and therapy capabilities could be affected by needle sticks
or other mattress bladder punctures. Caregivers should be instructed to prevent
mattress bladder punctures caused by needle sticks.
Avoid mechanical impacts.
Electrical safety
The mains power supply must comply with following standards:
• NF C15-100 and NF C15-211 (France);
• International Electrotechnical Commission (IEC) 60364 for other countries.
Check that the power requirements of the device Primo
™
on the identification label
correspond to the power supply voltage of the hospital (See “Product identification
labels” page 13).
The Primo
™
should be connected to a power system equipped with
a maximum 30 mA earth leakage circuit breaker, in compliance
with IEC 60364-5-53.
Connect the device to the nearest wall plug in order to leave
the shortest possible length of cable on the floor.
In compliance with standards relating to electromagnetic
interference for medical devices, this product does not interfere with other medical
devices or is not susceptible to interference when combined with other medical
devices that also comply with the electromagnetic standards in force.
Some devices, particularly older ones that do not comply with the electromagnetic
compatibility standards, may however undergo interference or may themselves
interfere with the working of this product.
The users of such devices are responsible for ensuring that any malfunctions will
not endanger the patient or any other person.
When intravascular or intracardiac connections are in use, the electric potentials of
all the unprotected metal parts of the appliance and the bed need to be equalized.
This label indicates that oxygen tents must never be used and that only
the use of nasal tubes and oxygen masks is authorized. For reasons of
safety, masks and tubes should always be kept at a higher level than the
mattress support platform.

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Technical specifications
Hill-Rom has a continuous improvement policy for its products. Therefore
specifications are liable to be altered without notice.
Essential performances
* Data source : IFTH 2006 National Body Measurement Campain in France (target
population: men and women aged between 18 and 70).
Values in mbar +/- 8%.
Therapeutic Mattress
Percentile P5-P30* Woman P75-P95* Man
Angle of the adjustable
head section 0° 45° 0° 45°
I-mmersion
™
setting 22 mbar 26 mbar 35 mbar 40 mbar
Characteristics Description
Model P02033 P02047 P02034 P02044
Length (inflated) 200 cm / 79’’ 200 cm / 79’’
Width (inflated) 85 cm / 33.5’’ 77 cm / 30.5’’
Height (inflated) 16 cm / 6’’ 16 cm / 6’’
Weight 8.4 kg / 18.5 lb
Autonomy in transport mode 2 hours
Upper cover
Polyurethane coating on polyester material
Low-friction, stretchable in both directions, breathing,
bacteriostatic, fungistatic and antimicrobial. Can be wiped and
washed.
Bladders Polyurethane
Safe working load,
including the total weight of the patient, accessories (if they are
supported by the support system of the medical bed) and the
load supported by these accessories (excluding the weight of
the patient).
Maximum pressure of relief
valve 1psi / 69 mbar
Degree of protection against
electric shock
Type BF applied parts protected against defibrillation shocks
(labeled 1 and 6 on page 9).
Degree of protection
provided by the cover
(IEC 60529)
IP24: protected against access to hazardous parts with a finger
and against splashing water.
250250

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Introduction
Specifications
Control unit
Front view of the control unit of the Primo™
Characteristics Description
Model P02033 P02047 P02034 P02044
Dimensions 15x29x12 cm / 6x11.5x5’’
Weight 3.5 kg / 8 lb
Power supply 220-240V
50/60 HZ
220-240V
50/60HZ 120V 60HZ 220-240V 50/60HZ
Apparent power 20 VA 20 VA 32 VA 20 VA
Maximum energy consumed 16.4 Wh 16.4 Wh 16.4 Wh 16.4 Wh
Operation of the device Continuous
Sleeve material ABS PC V0
Device : sound pressure level /
sound power (ISO 3744) 41 dB(A) / 52 dB(A)
Alarm : sound pressure level /
sound power (IEC60601-1-8) 56 dB(A) / 67 dB(A)
Fuses T160 mA T160 mA T 200mA T160 mA
Compression 0 - 180 mbar 0 - 180 mbar 0 - 215 mbar 0 - 180 mbar
Compressor flow rate 10 l/min 10 l/min 12 l/min 10 l/min
Device classification according
to IEC 60601-1 Class II
Degree of protection provided
by the cover (IEC 60529)
IP21 : protected against access to hazardous parts with a
finger and against vertically falling water drops.
Protection against inflammable
anesthetic mixtures
Not for use with flammable anesthetics.
Battery life 1 hour
Control
panel

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Page 8 170924(2) - EN - Primo™User manual
Conditions for transport, storage and use
The device must be stored in its original packaging:
• protected against light and damp,
• at least 10 cm above floor level to prevent fluid ingress;
• protected against dust;
• outside passageways.
Never stack more than 5 mattresses.
Special conditions of use
A number of special precautions must be taken when using the device in a
domestic environment.
Strangulation warning:
Never leave children aged under 3 or animals alone in the vicinity of the device. They may
become caught up in the power cord and be strangled.
Suffocation warning:
Never leave the electric connection accessories supplied with the device within the reach of
children or animals.
Do not use the device in dusty environments and avoid the presence of soft toys and ash
(cigarettes, etc.).
Do not expose the device to excessive light, including sunlight.
Do not install the device close to a source of intense heat (fireplace, heaters, etc.) or of
excessive humidity (sprayers, kettles, etc.).
Do not install the device close to pets, insects or pests.
Protect the device against misuse by children.
Symbol Features Use Transport, storagea
a. Applicable only if the device is stored in its original packaging.
The device is designed for indoor use only.
Temperature +5°C - +40°C -25°C - +70°C
Humidity 15% - 93% 0% - 93 %
Atmospheric
pressure 700 mbar - 1,060 mbar 700 mbar - 1,060 mbar

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Introduction
Specifications
Product overview
Item Name Item Name
1 Upper cover 5 Foam sub-mattress
2 Air mattress 6 Bottom cover
3 Control unit 7 CPR valve
4 Sensor 8 Straps
9 Sensor box
2
1
9
5
3
6
7
8
4
8

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General symbols on the device
General symbols on the upper cover
General symbols on the control unit
CPR symbol
Do not walk on or run over the power cord
Adjust the head and foot end straps
Foot end
Zone for notes
Always install the mattress so that the I-mmersion™Therapy
text is visible
A Connection for inflation of the seat cushion
B
Fuse 220-240 VAC
Fuse 120 VAC
A
B

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PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Introduction
Specifications
Buttons and light indicators on the control unit
The control unit is very easy to use and, thanks to the automatic pressure
regulation, no manual adjustments are necessary
Buttons
1 - Alarm silence button :
Inhibits the audible alarms (see “Alarm silence” page 21).
2 - On/Off Button .
NOTE:
To switch off the control unit:
Press to silence the battery, in this case no mains power fault alarm will be
reported ;
Unplug the control unit from the mains.
3 - Maximum inflation button :
Increases the pressure inside the mattress to the maximum value for 5
minutes. See “Maximum inflation” page 19.
Is also used to inflate the seat cushion (see “Seat cushion” page 33).
Indicator lights / alarms
A - Malfunction alarm :
In case of malfunction, the audible alarm sounds and the visual alarm
yellow comes on (see “Malfunction” page 21).
B - Mains power fault alarm :
In case of power failure,
the audible alarm sounds and the visual alarm
yellow comes on (see “Mains power fault” page 21).
C - On/Off Indicator:
The green indicator light at the bottom comes on when the control unit is on.
D - Inflation Indicator :
The green indicator light flashes for 5 minutes while the inflation.
C
ABD
12
3

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Page 12 170924(2) - EN - Primo™User manual
General symbols on the labels
a.The product part number contains the following information:
- P+5 figures = model,
- B = product version letter.
 See “Product identification labels” page 13 .
Manufacturer IP21
Control unit protected
against access to hazardous
parts with a finger and
against vertically falling
water drops.
Product referenceaIP24
Cover protected against
access to hazardous parts
with a finger and against
splashing water.
Serial number
Type BF applied part
protected against
defibrillation shocks
(mattress).
Alternating Current Class II Device
CAUTION,
read the safety instructions
carefully
Compliant with Directive
93/42/EEC
Refer to the user manual. Temperature range
DO NOT DISCARD.
Obey local recycling rules. Atmospheric pressure range
Interior use Humidity range
Warning :
high voltage !
(label on the power supply
card in the control unit)
Width of the mattress (model
P02044 only)

170924(2) - EN - Primo™User manual Page 13
PROPRIETARY AND CONFIDENTIAL DRAFT: octobre 11, 2012
Introduction
Specifications
Product identification labels
Control unit
To identify your device model and serial number, refer to the identification label on
the rear of the control unit.
The label showing the
conditions of use and
specifications of the device is
also located on the rear of the
control unit
(right-hand side).
See “General symbols on the
labels” page 12.
Packaging
To check the model of the device on the packaging label, refer to the example
below:
See symbols in paragraph “Conditions for transport, storage and use” page 8.

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Upper and bottom covers
Open the zip fastener on the mattress to access the upper and bottom covers.
See details of the symbols for cleaning and disinfection in section:
“Disinfection, servicing” page 25.
Upper Cover
P02033/P02034 P02044 P02047
Bottom Cover
P02033/P02034 P02044 P02047