Hillrom P290 User manual

*213960EN* EN
213960EN Rev.01
P290 Mattress
Instructions for Use
P290A1
P290A2
P290A3

213960EN(1) - P290 Mattress Instructions for Use
Hill-Rom S.A.S.
Z.I. du Talhouet
56330 PLUVIGNER - FRANCE
Tel: + 33 (0)2 97 50 92 12
Fax: + 33 (0)2 97 50 92 03
hillrom.com
Edition 1 - September 2020
First Printing: September 2020
The information contained in this manual is confidential and may not be reproduced
or transmitted in any form or by any means without the prior written permission of
Hill-Rom.
Hillrom™ is a trademark of Hill-Rom Services, Inc.
Velcro®
is a registered trademark of Velcro Industries BV.
Terralin®
is a registered trademark of Schülke & Mayr GmbH.
Dismozon®
is a registered trademark of Bode Chemie GmbH.
Sanivap®
is a registered trademark of Sanivap S.A.
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, contact your national Hill-Rom representative or go to
hillrom.com and order the part number 213960EN.
© 2020 Hill-Rom Services, Inc. ALL RIGHTS RESERVED.

Destination
Specifications
Installing the Patientt Mobilizing the Patient Moving the Device Disinfection
Servicing
Accesssories Standards
213960EN(1) - P290 Mattress Instructions for Use Page i
Table of Contents
Section 1: Destination and Specifications
Structure of the Manual and Symbols Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Safety and Usage Tips. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Indications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Intended Users. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Identifying the Models of the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
First Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Preventing Risks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Complying with Electrical Safety Standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Complying with Conditions for Transport, Storage and Use. . . . . . . . . . . . . . . . . . . . . 7
Technical Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Essential performances of the device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Mattress Topper and Mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Viewing the Whole Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Understanding the Symbols on the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Symbols on the Upper Cover . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Symbols on the Control Unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Symbols on the Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Locating the Labels on the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Labels on the Control Unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Upper and Bottom Covers Identification Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Serial number of the mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Section 2: Installing the Patient
Before Placing the Patient on the Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Checking the Compatibility of Bed Frame and Mattresses . . . . . . . . . . . . . . . . . . . . . . . . . 21
Installing the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Section 3: Mobilizing and Securing the Patient
Selecting the Operating Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Activating the CPR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Locking the User Interface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Understanding the Audible Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Audible Indicator Silence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Mains Power Fault Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Low Pressure Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Malfunction Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
X-ray cassette pouch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Page ii 213960EN(1) - P290 Mattress Instructions for Use
Evacuation Handles* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Section 4: Moving the Device
Moving the Patient on the Bed in Transport Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Transferring the Device from One Bed to Another. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Storing the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Section 5: Disinfecting and Servicing
Cleaning and Disinfecting the Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Complying with Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Controlling Infection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Complying with Hill-Rom Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Frequency of Cleaning and Disinfection of Different Parts of the Mattress . . . . . . 37
Cleaning and Disinfecting after the Departure of a Patient or when Changing the
Sheets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Cleaning and Disinfecting at Regular Intervals or in the Event of High Risk of
Contamination. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Performing the Final Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Servicing of the Device. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Complying with Safety Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Performing Preventive Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Complying with Warranty Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
De-commissioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Section 6: Accessories and additional parts
Recommended accessories**. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Recommended additional parts** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
ReFlex™ Seat Cushion (M04177)** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Symbols on the upper cover. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Locate the seat cushion labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Installing the Seat Cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Deflating and Packing the Seat Cushion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Cleaning and Disinfecting the Seat Cushion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Transport Bag. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Section 7: Compliance
Electromagnetic Compatibility
Compliance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
CE conformity mark . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Standards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Electromagnetic Emissions Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Electromagnetic Immunity Compliance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

213960EN(1) - P290 Mattress Instructions for Use Page 1
Destination
Specifications
Destination and Specifications
Structure of the Manual and Symbols Definition
For every type of use, Hillrom™ 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

Page 2 213960EN(1) - P290 Mattress Instructions for Use
Understanding the Symbols
Symbol Description
Highlights special information or explains important
instructions.
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
Entrapment Hazard Warning
Risk of Crushing an Upper Limb
Chemical Hazard Warning
Electric Shock Hazard
Biological Danger

213960EN(1) - P290 Mattress Instructions for Use Page 3
Destination
Specifications
Safety and Usage Tips
Intended Use
This device benefits are phase I to phase IV pressure ulcers prevention and treatment
help.
Indications
This device helps to prevent and treat pressure ulcers in low to high risk adult patients,
within the recommended patient weight limits of 30 to 140 kg,
in order to achieve
validated clinical performance in all the typical head of bed positions.
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 5 (outpatient or ambulatory care).
This device is not designed to come into direct contact with damaged skin
and must to
be used with a sheet between the patient’s skin and the surface of the mattress.
In accordance with the NPUAP/EPUAP directives1, Hill-Rom recommends that the
condition of each patient be regularly checked. For patients with special needs, Hill-
Rom recommends the use of the more suitable I-mmersion™Therapy system.
Caregivers are responsible for taking this decision, in accordance with modern care
practices.
Contraindications
This device 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.
Intended Users
The P290 mattresses are designed to be used by Qualified Staff for patient care and from
several care application environments.
Features
This device offers :
• Two therapeutic modes with manual adjustment of the parameters of comfort:
Continuous Low Pressure (CLP) and Alternating Low Pressure (ALP).
• Two functions: Mattress Firming and Maximum Inflation (Pmax).
1. NPUAP / EPUAP - Prevention and treatment of Pressure Ulcers - Quick Reference Guide, 2014

Page 4 213960EN(1) - P290 Mattress Instructions for Use
Identifying the Models of the Device
 See “Locating the Labels on the Device”on page 16 .
Certain features or accessories may be available or not, depending on the destination
country. These features are identified with an asterisk (*) and the accessories or the
additional parts are identified by two asterisks (**).
To identify your mattress model, its serial number SN (HRPMXXXXXXXX), its UDI, its
date of manufacture and its reference (REF), refer to the identification label (see
“Locating the Labels on the Device” on page 16).
REF: P290Axyz00000:
• P290 = Device Name
• A =Revision
•x=Type
•y=Voltage
•z=X-Ray
• 00000 = a unique five-figure numerical code encoding various
characteristics, such as the power cable, evacuation handles, the language,
etc.
SN: HRPMXXXXXXXX: HRPM = Hill-Rom Pluvigner Mattress; XXXXXXXX = incremental
code.
UDI: Unique Device Identification.
First Use
Before using the device, it is essential to have a thorough understanding of
this manual. This manual contains instructions for general use and
maintenance and guarantees improved safety. Access to this manual
should be made available to caregivers.
Caregivers must be informed of the risks that may be encountered in the use of
electric devices.
Product training is available upon request.
Model Type
P290A1 Overlay Air Mattress (in combination with a foam
mattress below)
P290A2 Foam base + top air Mattress
P290A3 Air Mattress

213960EN(1) - P290 Mattress Instructions for Use Page 5
Destination
Specifications
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 device to the mains power supply (See “Complying
with Electrical Safety Standards” on page 6);
• Allow access to the wall outlet to disconnect the mattress when needed;
• Make sure that all the functions of the device are in good conditions of operation
(See “Installing the Device” on page 21);
• Make sure that the device and the care environment are in a good state of hygiene
(See “Disinfecting and Servicing” on page 35).
• Check the safe positioning of the device in its working environment
(See “Before Placing the Patient on the Device”page 21).
Preventing Risks
Improper use of the device 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 mattress support platform. 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);
• In the case of patients suffering from particular behavioral difficulties (e.g.
agitation, mental confusion, loss of sense of direction, obsessive behavior, old
patients, weakness, etc.).
Properly trained medical staff should determine how the device should be used and the
required level of monitoring or constraint.
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.

Page 6 213960EN(1) - P290 Mattress Instructions for Use
Avoid mechanical impacts.
Notice to Users and/or Patients:
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.
Complying with Electrical Safety Standards
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 supply voltage of the device shown on the identification label matches
the voltage of the establishment’s mains power system (See “Locating the Labels on
the Device” on page 16).
The device 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 device does not interfere
with other medical devices nor is it susceptible to interference when combined with
other medical devices that also comply with the electromagnetic standards in place.
However, some devices, particularly older ones that do not comply with the
electromagnetic compatibility standards, may undergo interference or may themselves
interfere with the functionality 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
.

213960EN(1) - P290 Mattress Instructions for Use Page 7
Destination
Specifications
Complying with 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.
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 +10°C to +40°C -30°C to +50°C
Hygrometry 30% - 85% 20% - 85%
Atmospheric
Pressure
700 hPa - 1,060 hPa 700 hPa - 1,060 hPa

Page 8 213960EN(1) - P290 Mattress Instructions for Use
Technical Specifications
Specifications are subject to change.
Essential performances of the device
The P290 is a therapeutic mattress. It has two operating modes: continuous low
pressure (CLP) and alternating low pressure (ALP). The mattress firmness is adjustable
from the control unit.
Mattress Topper and Mattress
Characteristics Values
Mattress Topper and Mattress
Mattres model P290A1 P290A2 P290A3
Length (inflated) 200 cm / ~ 80’’
Width (inflated) 90 cm / ~ 36’’
Height (inflated) 10 cm / 4" 17 cm / 7"
Weight 6,1 kg / 13,4 lb 12 kg / 26,5 lb 7,5 kg / 16,5 Ib
Range in transport mode 2 hours
Upper cover (applied part of
the device)
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 is the
greatest permissible load
that can be applied after
which a damage may occur
on the mattress.
Safe working load,
including the total weight
of the patient, accessories
and the load supported by
these accessories .
Pressure relief valve
threshold
1.5 psi / 10,3 kPa
Degree of protection
against electric shock
Type BF applied part
Cushions pressure.
Adjustable range
from 8"H2O to 30"H2O
Control Unit
Control Unit model
212290 212291
Dimensions 29 x 20 x 12 cm / 11.4" x 8" x 4.6"
Weight 2.2 kg / 5 lb
Power supply 220-240 V~, 50/60 Hz 120 V~, 50/60 Hz
2
250

213960EN(1) - P290 Mattress Instructions for Use Page 9
Destination
Specifications
Front and Back Views of the P290 Control Unit
The control unit may generate noise and vibration that can cause discomfort to the
patient.
Rated power 0.07 A @ 220-240 Vac 0.17 A @ 120 Vac
Maximum energy
consumed
5.2 Wh
Operation of the device Continuous
Sleeve material ABS PC
Device: sound pressure level
/ sound power (ISO 3744)
45 dB(A) / 61 dB(A)
Fuses T1AL, 250V
Compression 0-10,5 kPa
Compressor flow rate 10 l/min
IEC 60601-1 Classification Classe II
Degree of protection
provided by the cover
(IEC 60529)
IP41: Protected against access to hazardous parts with a
wire and against vertically falling water drops
Protection against
inflammable anesthetic
mixtures
Not for use with flammable anesthetics.
Characteristics Values
Control Panel
Hose Connector
Fuses
Filter
Main Switch
Power Socket
Handle Attachment

Page 10 213960EN(1) - P290 Mattress Instructions for Use
Viewing the Whole Device
Item P290A1
A Control Unit
B Detachable Upper Cover
CPneumaticMattress
DHeelZoneFoam
E Bottom Cover
FPowerCord
GHose
B
F
A
G
D
E
C

213960EN(1) - P290 Mattress Instructions for Use Page 11
Destination
Specifications
Item P290A2
A Control Unit
B Detachable Upper Cover
CPneumaticMattress
DHeelZoneFoam
E Bottom Cover
FPowerCord
GHose
HFoamBase
I Mattress Bottom Cover
JX-raybag
K Evacuation handles*
B
F
A
G
D
E
C
H
I
K
J

Page 12 213960EN(1) - P290 Mattress Instructions for Use
Item P290A3
A Control Unit
B Detachable Upper Cover
C Pneumatic Upper Mattress
D Pneumatic Lower Mattress
E Bottom Cover
FPowerCord
GX-raybag
H Evacuation handles*

213960EN(1) - P290 Mattress Instructions for Use Page 13
Destination
Specifications
Understanding the Symbols on the Device
Symbols on the Upper Cover
A Do not walk on or run over the power cord
B Foot End
C Adjust the head and foot end straps
DSafeWorkingLoad
EAttach the mattress using the straps at the head
and foot ends
FX-Raybag
F
EDCA
B
2

Page 14 213960EN(1) - P290 Mattress Instructions for Use
Symbols on the Control Unit
Buttons and Indicator Lights
Buttons Indicator Lights
Symbol Description Symbol Description
A Alternating Pressure
Cycles (every
5 minutes)
1 Maximum Inflation
(P-max)
BComfortSetting:
Reduce the Pressure
2Alternating
Low Pressure Mode
CComfortSetting:
Increase
the Pressure
3Continuous
Low Pressure Mode
D Selection
of the Operating
Mode
4 Mattress Firming
E Security Lock 5 Mains Power Fault
Indicator
F On/Off 6 Low Pressure
Indicator
GAudibleIndicator
Silence
7 Malfunction Indicator
A
B
D
EF
C
G
1234
5
6
7

213960EN(1) - P290 Mattress Instructions for Use Page 15
Destination
Specifications
Symbols on the Labels
a.The device part number contains the following information:
- P+6 Figures = Model,
- A = Device Revision Letter.
 See “Locating the Labels on the Device”on page 16 .
Manufacturer IP41 Control unit protected
against access to hazardous
parts with a wire and against
vertically falling water drops.
Device ReferenceaIP24 Cover protected against
access to hazardous parts
with a finger and against
splashing water.
Serial Number Type BF Applied Part
Fuse Class II Device
CAUTION
read the Safety
Instructions Carefully
Medical Device conformity
mark
Refer to the User Manual Alternating Current
DO NOT DISCARD
Obey Local Recycling Rules
Temperature Limits
Interior Use Atmospheric Pressure Limits
WARNING
High Voltage
(Label on the Power
Supply Card in the Control
Unit)
Hygrometry Limits
Unique Device Identification Medical Device
Date of manufacture

Page 16 213960EN(1) - P290 Mattress Instructions for Use
Locating the Labels on the Device
Labels on the Control Unit
The labels showing the serial number, the conditions of use and the specifications of
the device (A), (B) are located on the rear of the control unit.
(A) Conditions of Use and Specifications of the Device
(B) Serial Number
P290A160XXXXX
P290A260xxxxx
P290A261xxxxx
P290A360XXXXX
P290A361xxxxx
P290A130XXXXX
P290A230XXXXX
P290A231XXXXX
P290A330XXXXX
P290A331XXXXX
P290A160XXXXX / P290A260XXXXX
P290A261XXXXX / P290A360XXXXX
P290A361XXXXX
P290A130XXXXX / P290A230XXXXX
P290A231XXXXX / P290A330XXXXX
P290A331XXXXX
A
BC