Hillrom 900 Series User manual

PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
*171051*
Hill-Rom® 900
User Manual
LI900B0, LI900B2 and LI900B3
171051 Rev.009
EN

171051(9) - Hill-Rom® 900 Electric Bed User Manual
PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
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
www.hill-rom.com
Edition 9: May 2018
First printing 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®, Hill-Rom® 900, Navicare®, Duo® and ClinActiv® are
registered trademarks of Hill-Rom Services, Inc.
Accella™ is a registered trademark of Hill-Rom Services, Inc.
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 171051.
© 2018 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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PROPRIETARY AND CONFIDENTIAL DRAFT: 18 May 2018
Table of Contents
Introduction, specifications
The structure of the manual. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Symbol definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Applications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Bed model and country of use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Safety and Usage Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
First use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Risk prevention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
General precautions for the place of use . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Precautions for transport and storage . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Technical specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
General Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Function Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Installing the patient
Before placing the patient on the bed . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Mattress** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Endboards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Installing the endboards. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Endboard fastening system* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Bed frame extension*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Wall stop AD277A* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Mobilizing the patient
Electrical Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Control pendants* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Caregiver half-siderail* controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Patient half-siderail* controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Bilateral HiLow pedal with caregiver mode*. . . . . . . . . . . . . . . . . . . . . . . 36
Foot control pendant*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Control unit on a flexible arm* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Raising/lowering the sleep surface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Raising/lowering the head and thigh sections . . . . . . . . . . . . . . . . . . . . . 38
Trendelenburg/Reverse Trendelenburg* . . . . . . . . . . . . . . . . . . . . . . . . . 39
Chair position* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Place sleep surface flat . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Bed exit aid*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Mechanical adjustable foot section*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Patient helpers** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Egress handles*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46

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Patient position monitor half-siderail control* . . . . . . . . . . . . . . . . . . . . . . 47
NaviCare® system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Securing the patient
Siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
AD271B* siderails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
AD272B* siderails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Removing the long siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Installing the the long siderails. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Half-siderails*. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Space Filler panel (AD288A)** . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Fittings for the restraining strap handles . . . . . . . . . . . . . . . . . . . . . . . . . 58
Electrical function management. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
Bed not in lowered position indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Night light* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
CPR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Equipotential terminal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Equipotential cable (AD968A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Nurse call* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62
Help with care
Fixed IV pole (AD294A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Telescopic IV pole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Linen holder* . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Drainage bag holder pins. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
Oxygen Cylinder Holder (AC959A-AD101A-AD102A). . . . . . . . . . . . . . . 66
Monitor stand (AD244B) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67
Syringe-driver holder (AC963A) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
Line manager & support (AD286A)** . . . . . . . . . . . . . . . . . . . . . . . . . . . . 68
X-ray-transparent adjustable head section (AD242A)**. . . . . . . . . . . . . . 69
Movement/Transfer
Brake and steer system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73
Securing the power cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Removable frame (AD270B) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Decontamination, Maintenance
Decontamination of the bed. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Safety recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Recommendations for cleaning and disinfection . . . . . . . . . . . . . . . . . . . 77
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
Safety recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
Preventive maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
De-commissioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
Appendix
Warranty and after sales service conditions . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83

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 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
Complies with electromagnetic emission standards . . . . . . . . . . . . . . . . 84
Compliance with electromagnetic immunity. . . . . . . . . . . . . . . . . . . . . . . 86
Recommended separation distances. . . . . . . . . . . . . . . . . . . . . . . . . . . . 88

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PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
171051(9) - Hill-Rom® 900 Electric Bed User Manual Page 1
Introduction
Specifications
Introduction, specifications
The structure of the manual
For every type of use, Hill-Rom 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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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 - 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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PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
Introduction
Specifications
Applications
The Hill-Rom® 900 medical beds with emergency Trendelenburg / Reverse
Trendelenburg are beds for intensive care for adult patients (the emergency
Trendelenburg function remains operational in the event of a power cut: SHOCK)
(EN60601-2-52 application environment 1). They are designed for use in intensive
care wards and also in general care and surgery care wards and allow the use of
advanced techniques used in specialist units.They are designed with the needs of
the whole medical team in mind and facilitate the use of monitoring equipment and
the transfer of patients to examination wards.
The Hill-Rom® 900 beds with electric comfort Trendelenburg / Reverse
Trendelenburg or without Trendelenburg / Reverse Trendelenburg are variable-
height beds designed for intensive, 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
facilitate the use of monitoring equipment and the transfer of patients to
examination wards, etc.
The Hill-Rom® 900 LI900B0 and LI900B2 beds:
• can be fitted with batteries providing protection against power outages as an
option.
• fitted with Ø 150mm casters can be used to transfer patients.
The Hill-Rom® 900 LI900B3 beds:
• are equipped with batteries providing protection against power outages.
• fitted with Ø 125 mm double-band casters or Ø 150 mm casters can be used
to transfer patients.
• are equipped with a patient position detection system.
• can be equipped with a nurse call function*.

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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 are identified by two asterisks (**).
To identify your bed model, its serial number SN (HRPXXXXXXXXX) and its date
of manufacture, refer to the identification label (see “Overview” page 14). Your
LI900BX bed is made up of a chassis/sleep surface, with a REF reference starting
with CS900B0 or CS900B2 or CS900B3 and two endboards (a headboard and a
footboard).
• REF: CS900B0XXXXXX or CS900B2XXXXXX or CS900B3XXXXXX: CS900
=
Hill-Rom® 900 ; B = Version; 0XXXXXX or 2XXXXXX or 3XXXXXX = unique
7-figure numerical code according to different criteria, such as the voltage,
the electrical functions, the language, etc.
• SN: HRPXXXXXXXXX: HRP = Hill-Rom Pluvigner; XXXXXXXXX =
incremental code.
Safety and Usage Tips
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.
Waste packaging (plastic, cardboard, metal, wood, etc.) must follow suitable
recovery circuits with a view to being recycled.

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Introduction
Specifications
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 of the bed” page 77).
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.
• 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.
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.

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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.
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).
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 29).
Use of a mattress thicker than the thickness recommended in “References of
recommended mattresses” page 29 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.
The mattress label page 27
recommends the mattresses to be used for the best
conditions of safety for the use of the Hill-Rom® 900, as assessed by the “Hospital
Bed Safety Workgroup” guide and the standard EN 60601-2-52.

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Introduction
Specifications
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.
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 "Shock"*, Trendelenburg, Reverse Trendelenburg, chair* and return to flat*
functions must only be accessible to caregivers.

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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.
The users of such devices are responsible for ensuring that any malfunctions will
not endanger the patient or any other person.
Ensure that the power cord is unplugged and hooked to the bed before moving the
bed (see “Securing the power cable” page 76).
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 82.

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PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
Introduction
Specifications
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.
If a continuous alarm sounds when activating a movement, the battery needs to
be recharged.
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 “Applications” 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

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Page 10 171051(9) - Hill-Rom® 900 Electric Bed User Manual
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

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PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
Introduction
Specifications
Technical specifications
Hill-Rom has an ongoing continuous improvement policy. Therefore
specifications are liable to be altered without notice.
LI900B2 with long siderails
Features Value
Maximum width (W) 995 mma/1010 mmc
Maximum length (without extension) (L) 2158 mma
Maximum length (with extension closed) (L) 2158 mma
Maximum length (with extension open) (L+) 2358 mma
Length of long siderail protection (B) 1421 mmb/1397 mmc
Long siderail protection height (without mattress) (S) 385 mmab/380 mmc
Length of the head half-siderail protection (B1) 499 mma
Length of the foot half-siderail protection (B2) 631 mma
Long siderail protection height (without mattress) (S1) 393 mma
Low position (double-band 125ddiameter casterse) (h) 386 mmaf
Low position (125 diameter castersdg) (h) 377 mmah/419 mmaf
Low position (double band 150ddiameter casterse) (h) 389 mmah/431 mmaf
L
L+
B
W
65° 28°
S
H
hC
B1 B2
S1
LI900B0/LI900B2/LI900B3/LI900B2 with half-siderails

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Page 12 171051(9) - Hill-Rom® 900 Electric Bed User Manual
Low position (150 diameter castersde) (h) 397 mmah/439 mmaf
High position (double-band 125 diameter castersde) (h) 755 mmaf
High position (125 diameter castersdg) (H) 748 mmah/788 mmaf
High position (double band 150 diameter castersde) (H) 760 mmah/800 mmaf
High position (150 diameter castersde) (H) 768 mmah/808 mmaf
Chassis clearance (double-band 125 diameter castersde) (C) 150 mma
Chassis clearance (125 diameter castersdg) (C) 183 mma
Chassis clearance (double band 150 diameter castersde) (C) 195 mma
Chassis clearance (150 diameter castersde) (C) 203 mma
Head sectioniincline + 65°
Thigh sectioniincline* + 28 °
Foot sectioniincline* - 3° to -22°
Trendelenburg/Reverse Trendelenburg + 17°/- 17°
Emergency Trendelenburg (“Shock”)hi - 12 °/30 sec
Maximum patient weight for the SWL version: 220 kg 155-185 kgj
Maximum patient weight for the SWL version: 250 kg* 185-215 kgk
Bed weight LI900B0/LI900B2l (no mattress or accessories) 144 kg
Bed weight LI900B2 (no mattress or accessories) 120 kg
Bed weight LI900B3 (no mattress or accessories) 170 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. Bed fitted with AD272B siderails
d. Dimensions in mm.
e. An antistatic version is also available.
f. LI900B3 model
g. Incompatible with the CFS 250 kg version, LI900B0 or LI900B2 with half-siderail.
h. LI900B0 and LI900B2 models
i. Maximum incline in relation to the sleep surface
j. SWL 220 kg / the maximum patient weight varies according to the mattress and accessories
used
- 155 kg as per EN60601-2-52 (acute care or intensive care)
- 185 kg as per EN60601-2-52 (other environments).
k. SWL 250 kg / the maximum patient weight varies according to the mattress and accessories
used
- 185 kg as per EN60601-2-52 (acute care)
- 215 kg as per EN60601-2-52 (other environments).
l. LI900B2 models with half-siderails
Features Value

171051(9) - Hill-Rom® 900 Electric Bed User Manual Page 13
PROPRIETARY AND CONFIDENTIAL DRAFT: May 18, 2018
Introduction
Specifications
Electrical characteristics
Characteristic 100V* 120V* 230V*
Voltage 100V AC 120V AC 230V AC
Frequency 50/60 Hz 50/60 Hz 50/60 Hz
Power supply unit maximum power load 300 VA 300 VA 300 VA
Power supply unit fuse rating 2 x 2.5 A T 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
Intermittent operation 10% (2min/18min)a
a. 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.
Conditions required to connect the nurse call system
For more information about the connections required to use the nurse call
function, please refer to the SideCom® Communication System Design and
Application Manual (DS059).

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Page 14 171051(9) - Hill-Rom® 900 Electric Bed User Manual
Overview
LI900B0
Item Name Item Name
AHalf siderailsa
a. Equipment varies depending on bed model
JCaregiver unita
B Headboard K Footboard
C 2 sockets for I.V. pole and patient
helper
L Electric emergency
Trendelenburg (Shock)ab
b. Incompatible with the 250 kg SWL version
DControl pendantaMExtension + linen holdera
EFoot control pendantaN Bumper (4)
FControl unit on a flexible armaO Central brake and steer bar
control
G Head section “CPR” control P 150 mm diameter single band
castersa
H Head section angle indicator Q Bilateral HiLow pedal with
caregiver modea
INight lightaR HRP and identification label
D
A
F
F
K
M
N
O
P
G
Q
JILH
B
C
R