Hillrom Centuris Pro User manual

*194568* EN
Centuris™ Pro Bed
Instructions for Use
LI900B1
194568 Rev. 6

194568 (6) - Instructions for Use Electric Bed Centuris™ Pro
Hill-Rom S.A.S.
Z.I. du Talhouët
56330 PLUVIGNER - FRANCE
Tel: + 33 (0)2 97 50 92 12
Fax: + 33 (0)2 97 50 92 03
hillrom.com
Edition 6: October 2020
First printing 2015
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.
ClinActiv® is a registered trademarks of Hill-Rom Services, Inc.
Hillrom™, Centuris™ Pro and AutoContour™ are trademarks of Hill-Rom
Services, Inc.
MCM™ is a trademark of Hill-Rom SARL.
Sabina™, Viking™, Golvo™ et LowBase™ are trademarks of Liko R&D AB.
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 article with the part number 194568.
© 2020 by Hill-Rom Services, Inc. ALL RIGHTS RESERVED.

Introduction
Specifications
Installing the patient Mobilizing the patient Securing the patient Help with care Moving the bed Decontamination,
Maintenance
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Table of Contents
Introduction, specifications
The structure of the Instructions for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Symbol definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Bed model and country of use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Safety and Usage Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Intented Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Features. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Intended Users. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
First use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Risk prevention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
General precautions for the place of use . . . . . . . . . . . . . . . . . . . . . . . . . 10
Precautions for transport and storage . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Technical specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
General Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Function Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Electrical controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Installing the patient
Before placing the patient on the bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Accessories and peripheral equipments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Mattress** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Recommended accessories** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Recommended additional parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Recommended patient lifts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Recommended bed dining tables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Endboards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Installing the endboards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Bed frame extension*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Wall stop AD277A* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Mobilizing the patient
Electrical Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Control pendant* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Caregiver half-siderails* controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Patient half-siderails* controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Raising/lowering the sleep surface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Raising/lowering the head and thigh sections . . . . . . . . . . . . . . . . . . . . . 31
Trendelenburg/Reverse Trendelenburg. . . . . . . . . . . . . . . . . . . . . . . . . . 32
Mechanical adjustable foot section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Patient helpers** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33

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Egress handles*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Securing the patient
Siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
AD271B** siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Removing the long siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Installing the the long siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Siderail safety net (AD312A)**. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Half-siderails*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Foot gap panels (AD288A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Fittings for the restraining strap handles . . . . . . . . . . . . . . . . . . . . . . . . . 42
Electrical function management. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Bed not in lowered position indicator* . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
CPR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Equipotential terminal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Equipotential cable (AC968A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Help with care
Fixed IV pole (AD294A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Telescopic IV pole (AD298A-AD299A) . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Linen holder* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
Drainage bag holder pins. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Oxygen Cylinder Holder (AC959A-AD101A-AD102A). . . . . . . . . . . . . . . 49
Pivoting 3L Bottle Holder (AC962A)** . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Monitor stand (AD244B) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Syringe-driver holder (AC963A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
IV line manager & support (AD286A)** . . . . . . . . . . . . . . . . . . . . . . . . . . 52
X-ray-transparent adjustable head section (AD242A)**. . . . . . . . . . . . . . 53
Chrome-plated IV hook (AC953A)** . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Label holder (AC325A)** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Movement/Transfer
Braking/steering . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Securing the power cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Removable frame (AD270B) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Decontamination, Maintenance
Decontamination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Safety recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Recommendations for cleaning and disinfection . . . . . . . . . . . . . . . . . . . 61
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Safety recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Preventive maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
De-commissioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Appendix
Warranty and after sales service conditions . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67

Introduction
Specifications
Installing the patient Mobilizing the patient Securing the patient Help with care Moving the bed Decontamination,
Maintenance
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Electromagnetic conformance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Complies with electromagnetic emission standards . . . . . . . . . . . . . . . . 68
Electromagnetic conformance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
Complies with electromagnetic emission standards . . . . . . . . . . . . . . . . 69
Compliance with electromagnetic immunity. . . . . . . . . . . . . . . . . . . . . . . 70
Recommended separation distances. . . . . . . . . . . . . . . . . . . . . . . . . . . . 72

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194568 (6) - Instructions for Use Electric Bed Centuris™ Pro Page 1
Introduction
Specifications
Introduction, specifications
The structure of the Instructions for Use
For every type of use, Hillrom™ beds 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 194568 (6) - Instructions for Use Electric Bed Centuris™ Pro
Symbol definitions
This Instructions for Use contains different typefaces and icons designed to
improve readability and increase understanding of its content. Note the following
examples:
• standard text - normal character style used for “basic” information.
•Boldface 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

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Introduction
Specifications
Bed model and country of use
Certain bed 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 bed model, its serial number SN (HRPXXXXXXXXX), its UDI and
its date of manufacture, refer to the identification label (see “Electrical
characteristics” page 13). Your bed model, LI900B1, is composed of a
chassis/sleep surface whose reference REF starts with CS900B1 and two
endboards (a headboard and a footboard).
• REF: CS900B1XXXXXX: CS900 = Centuris™ Pro ; B = Version; 1XXXXXX =
unique 7-figure numerical code according to different criteria, such as the
voltage, the electrical functions, the language, etc.
• SN: HRP
XXXXXXXXX : HRP = Hill-Rom Pluvigner; XXXXXXXXX =
incremental code.
• UDI; Unique Device Identification.

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Safety and Usage Tips
Intented Use
The Centuris™ Pro beds LI900B1 with electric comfort Trendelenburg / Reverse
Trendelenburg are variable-height beds designed for acute, general and
ambulatory care or care during long hospital stays for
adult patients ( EN 60601-2-
52, application environments 2, 3 and 5). They are designed with the needs of the
whole medical team in mind and the benefits are to facilitate the use of monitoring
equipment and the transfer of patients to examination wards, etc.
Contraindications
• children (aged less than 12 or under 1.46 m tall),
• persons measuring more than 1.85m in height,
• persons with BMI below 17,
• persons weighing less than 40 kg,
Features
The Centuris™ Pro beds:
• are fitted with batteries providing protection against power outages. The
electric Trendelenburg is not an emergency function.
• fitted with Ø 150mm casters can be used to transfer patients.
Intended Users
The Centuris™ Pro beds are designed to be used by Qualified Staff. Patients and
Visitors can also use the Centuris™ Pro medical beds depending on authorization
given by Qualified Staff.
First use
Before using the bed, 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.
Training can be provided on demand.
Caregivers must be informed of the risks that may be encountered in the use of
electric beds.
The many sources and types of accessories, hardware, or medical devices that
may be used together with this bed do not enable Hill-Rom to guarantee both the
safety and conformity of all the combinations thus created. The operator who
creates these device combinations must therefore ensure that security and
conformity requirements are met.

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Introduction
Specifications
Use of accessories, transducers and cables other than those specified or provided by
Hill-Rom could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation.
Waste packaging (plastic, cardboard, metal, wood, etc.) must follow suitable
recovery circuits with a view to being recycled.
Before installing the bed for the first time or after bringing the bed and its
accessories out of storage:
• ensure that the bed and its various parts are at room temperature,
• only connect the bed to a mains electric power supply with earth protection
(see “Electrical safety” page 8),
• the power plug must be accessible to disconnect the bed,
• wait 12 hours until the battery is fully charged before using the bed without
the mains power supply,
• make sure that all the moving parts are in good working order,
• make sure that the bed has been cleaned and disinfected (see
“Decontamination” page 61).
Risk prevention
General recommendations
In general:
• check that nothing (e.g. objects, accessories or power cable) or any persons
(e.g. children, limbs) will interfere with the movement of the mobile parts of the
bed before actuating them. An intermittent beep sounds when one of the bed’s
movements is hindered.
• during a movement or combination of movements of a mobile part of the bed
(eg, backrest, sleep surface, siderail), be vigilant (for oneself, the patient or
any other person) on the risks of pinching or crushing between moving parts
or with a fixed part.
• always check (e.g. to and fro movements) that the various locking mechanisms
are in good working order (e.g. siderails, extensions, grip handles, brakes).
• sufficiently qualified nursing staff determine the usage condition suitable for
the various functions and the degree of supervision to ensure that the patient
uses the bed safely.

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When the patient is left unattended:
• apply the brakes to prevent any risks of falling, especially if the patient leans on
the bed when getting in or out,
• leave the sleep surface in the lowest position to avoid serious consequences in
the event of falling,
• use the siderails to secure the patient and reduce the risk of falling accidentally,
• lock any function that, if misused, could worsen existing injuries or pathologies,
or even result in bodily injury,
• never leave the bed in the Trendelenburg position.
Never modify the bed without Hill-Rom's prior written consent. Alterations could
result in injury to the patient or damage to the bed.
Only use manufacturer's parts and accessories.
Never place objects or equipment on the chassis or use it to support a person.
Do not use of the bed with loads in excess of the safe working load.
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.
Recommendations for the siderails
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 ascertain how the
siderails should be used (irrespective of the model or type), whether the patient
should be monitored closely or immobilized and whether the patient helpers should
be left in position, in order to ensure that patients use the bed in complete safety.
Certain national health authorities have issued guidelines risks to patients and the
reduction of these hazards, as indicated below.
It is recommended that patients at risk be identified in each establishment or ward
so that the safety measures most appropriate to their particular needs can be
implemented.
One measure which has already proved effective is to draw up a protocol
specifying:
1. situations and conditions for siderail use and authorized mattress type or
model,
2. for all patient monitoring procedures, both for restrained and unrestrained
patients, including during intervals,
3. circumstances under which patients must be restrained according to the
instructions and recommendations of the manufacturer of the said
restraining devices.
The siderails are designed to help reduce the risk of patients falling out of bed
accidentally. They are not designed to restrain or immobilize the patient. Restraining
straps or other devices must not be fastened to the half-length siderails (e.g., straps).

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Introduction
Specifications
Recommendations for the mattresses
Hill-Rom shall not be held liable for any problems occurring if the mattress used is
not included in the list of equipment recommended by Hill-Rom (see “References
of recommended mattresses” page 24).
Despite the protective height above the mattress and the top of the siderail,
patients can still potentially fall or become trapped in the spaces around the
mattress.
Use of a mattress thicker than the thickness recommended in “References of
recommended mattresses” page 24 may reduce the effectiveness of the siderails.
Thicker mattresses can increase the risk of falling and narrower mattresses can
increase the risk of patients becoming trapped. In such cases, the patient must be
monitored closely.
As assessed by the “Hospital Bed Safety Workgroup” guide and the standard EN
60601-2-52, the mattress label on page 22 lists the mattresses recommended for
use on the Centuris™ Pro to offer the safest conditions. The therapeutic benefits of
the other therapeutic mattresses listed in page 22 outweigh the residual risk of
entrapment or fall incurred by their use.
Other mattresses may be used, but the manufacturer must always be consulted to
make sure that the bed/mattress/siderail combination does not affect the bed's
performance, its suitability for use or its safety characteristics.
If the bed is fitted with an electrically powered air mattress, the power cord must be
routed so as to prevent it from being cut by the moving parts of the bed (refer to the
instructions of the mattress).
Users must check the compatibility of the patient's weight and the accessories placed
on the bed and the mattress system in view of the specifications of the medical bed and
the mattress system.
If the mattress power cord is unplugged, it is advisable to store it on the support
provided by the mattress supplier.

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Recommendations for the function lockouts
The electrical function management control prevents any unintended bed
movements that might cause injury to the patient.
For safety reasons, it is advisable to use the lock-out functions when treating the
patient or working on the bed (e.g., examinations, transfers, maintenance), when
the patient is left unattended and when caregivers believe that the patient is not in
a fit state of health to operate the controls in safety.
It is thus the responsibility of the nursing staff to authorize the patient to use certain
bed functions, including the HiLow.
The Trendelenburg / Reverse Trendelenburg functions must only be accessible
to caregivers.
Electrical safety
When direct intravascular or intracardiac connections are in use, the electric
potentials of all the unprotected metal parts need to be equalized. The bed must be
connected to a mains electric power supply with earth protection.
In an environment where the electrostatic discharges are prevalent, we recommend
using an antistatic caster.
The mains power supply for the bed must comply with relevant standards:
• NF C 15-100 and NF C 15-211 (France),
• International Electrotechnical Commission (IEC) 364 for other locations.
Check that the bed’s power requirements on the identification label (see “Electrical
characteristics” page 13) correspond to the power supply voltage of the hospital.
The power supply should be equipped with a maximum 30 mA earth
leakage circuit breaker, in compliance with IEC 364-5-53.
All the parts of the bed that are within the patient's reach, even if they are under
the frame, are applied parts.
If the integrity of the protective conductor is in doubt, the beds fitted with batteries
must be used in battery mode.
In compliance with standards relating to electromagnetic interference for medical
equipment, 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.

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Introduction
Specifications
The users of such devices are responsible for ensuring that any malfunctions will
not endanger the patient or any other person.
Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment
and the other equipment should be observed to verify that they are operating
normally.
Ensure that the power cord is unplugged and hooked to the bed before moving the
bed (see “Securing the power cable” page 59).
Only duly qualified and authorized staff should carry out electrical maintenance.
Never clean or service the bed without unplugging it from the mains power supply
and disconnecting the battery.
The battery backup must never be left in direct contact with fire, placed in liquid, or
discarded in a refuse bin. In the event of the battery being damaged, see “De-
commissioning” page 66.
This label indicates that the bed
must never be used with an
oxygen tent or in explosive atmospheres
(presence of
inflammable gases or vapors)
. Use only nasal tubes and oxygen
masks. For reasons of safety, masks and tubes should always be
kept at a higher level than the sleep surface.
Always lock out the HiLow function before any cleaning or
maintenance operations.
If the bed is equipped with a battery, and the bed is stored for long periods of time, the
battery must be charged every 3 months. Failure to do so could result in damage to the
battery.
A continuous beep when activating a movement sounds to indicate that the
battery needs recharging.

PROPRIETARY AND CONFIDENTIAL DRAFT: novembre 02, 2020
Page 10 194568 (6) - Instructions for Use Electric Bed Centuris™ Pro
General precautions for the place of use
It is advisable not to use the bed under the following conditions:
• in hospital wards other than the intended ward (see “Bed model and country of
use” page 3),
• climatic conditions outside the corresponding ranges recommended by Hill-
Rom,
• in hyperbaric chambers,
• in explosive atmospheres,
• in the presence of flammable gases or vapors,
• with oxygen tent type respiration devices or devices that extend below the sleep
surface,
• outdoors or to transport a patient in a vehicle,
• moving the bed over soft ground or inappropriate surfaces,
• moving the bed along slopes of over 10° (with or without a patient).
Climatic restrictions
Service temperature 10° and +40°
Service humidity 30% - 85%
Working atmospheric pressure 700 hPa to 1,060 hPa

194568 (6) - Instructions for Use Electric Bed Centuris™ Pro Page 11
PROPRIETARY AND CONFIDENTIAL DRAFT: novembre 02, 2020
Introduction
Specifications
Precautions for transport and storage
The following conditions must be met to ensure that the bed and its accessories
are shipped and stored in complete safety.
During shipment or storage, beds should not be stacked one on top the other.
During shipmenta, the bed must be:
a. Transport does not include the transfer of the bed between wards with or without patients.
Climatic restrictions on transport and storage
When stored, the bed must be:
- in the lowered position
- all functions locked out
- covered, brakes applied and all
moving parts secured
- protected from fluid ingress
- in the lowered position
- all functions locked out
- covered, brakes applied
- protected from fluid ingress
Transport/storage temperature -30° and +50°
Transport/storage hygrometry 20% - 85%
Transport/storage atmospheric pressure 700 hPa to 1,060 hPa

PROPRIETARY AND CONFIDENTIAL DRAFT: novembre 02, 2020
Page 12 194568 (6) - Instructions for Use Electric Bed Centuris™ Pro
Technical specifications
Hill-Rom has an ongoing continuous improvement policy. Therefore
specifications are liable to be altered without notice.
Features Value
Maximum width (W) 995 mma
Maximum length (without extension) (L) 2162 mma
Maximum length (with extension closed) (L) 2162 mma
Maximum length (with extension open) (L+) 2362 mma
Length of long siderail protection (B) 1421 mmb
Height of long siderail protection (without mattress) (S) 385 mmab
Length of the head half-siderail protection (B1) 499 mma
Length of the foot half-siderail protection (B2) 631 mma
Height of long siderail protection (without mattress) (S1) 393 mma
Low position (150ddiameter casterscd) (h) 397 mma
High position (150ddiameter casterscd) (H) 768 mma
Chassis clearance (150ddiameter casterscd) (C) 203 mma
Head sectioneincline + 65°a
Thigh sectione incline + 28°a
Foot sectione incline - 3° to -22°a
Trendelenburg/Reverse Trendelenburg + 17°/- 17°a
L
L+
B
W
65°
28°
S
H
hC
B1 B2
S1

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PROPRIETARY AND CONFIDENTIAL DRAFT: novembre 02, 2020
Introduction
Specifications
Electrical characteristics
Maximum patient weight 220 kg SWL version 155-185 kgf
Maximum tare of long siderailsg125 kg
Maximum tare of half-siderails without an extensiong133 kg
Maximum tare of half-siderails with an extensiong137 kg
Maximum temperature of applied parts at 40° C 56,5° C
Unweighted peak acoustic pressure levels <120 dB
Maximum measured level of weighted acoustic pressure 42 dBA
a. These are average values, which may vary according to manufacturing tolerances.
b. Bed fitted with AD271B siderails
c. Dimensions in mm.
d. An antistatic version is also available.
e. Maximum inclination in relation to sleep surface
f. SWL 220 kg / the maximum patient weight varies according to the mattress and accessories
- 155 kg as per EN60601-2-52 (acute care)
- 185 kg as per EN60601-2-52 (other environments).
g. Without mattress or accessories.
Characteristic 120V* 230V*
Voltage 120V AC 230V AC
Frequency 50/60 Hz 50/60 Hz
Power supply unit maximum power load 300 VA 300 VA
Power supply unit fuse rating 2 x 2.0 A T 2 x 1.25 A T
Electric shock protection Class I
Class according to IEC 60601-1 Type B
Protection against harmful ingress of water
(according to IEC 60529) IPX4 / IPX6a
a. Option
Duty cycle 10% (2min/18min)b
b. Do not operate electrical functions continuously for more than 2 minutes in any 18 minute
period when the bed is loaded at the safe working load value as this may damage electrical
components. The power supply of the actuator is temporarily cut off if the load factor is
exceeded when using the HiLow.
Features Value

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Page 14 194568 (6) - Instructions for Use Electric Bed Centuris™ Pro
Overview
Bed with half-siderails
Item Name Item Name
AHalf siderailsa
a. Equipment varies depending on bed model
HExtension + linen holdera
B Headboard I Bumper (4)
C 2 sockets for I.V. pole and patient
helper
J Central brake and steer bar
control
DControl pendantaK 150 mm diameter single band
casters
EHead section “CPR” controlaL HRP and identification labels
F General lock-out unit of the
electrical functions
MCaregiver half-siderails controlsa
G Footboard N Patient half-siderails controlsa
D
A
G
H
I
J
E
B
C
FK
L
N
M