Secure® II

MedSurg Bed
Model 3002

Operations Manual

For parts or technical assistance call:

USA: 1-800-327-0770
2011/12 B.2 3002-509-001 REV B www.stryker.com
 Table of Contents

Symbols and Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6

Warning/Caution/Note Definition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Intended Use – Styker 3002 Secure® II . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Intended Use – iBed® Wireless with iBed Awareness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Mattress Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Bed Illustration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Safety Tips and Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Safety Tips and Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Zoom® Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
iBed Awareness Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
iBed® Wireless Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Setup Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Zoom® Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
iBed® Wireless Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Base Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Brake Pedal Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Steer Pedal Operation (Beds without the Zoom Drive Wheel Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Litter Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
CPR Emergency Release . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Foot Prop Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Fracture Frame Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Foley Bag Hooks Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Patient Restraint Strap Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Positioning Siderails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Siderail Control Panel Lights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Operating I.V. Poles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Night Light Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Nurse Call Backup Battery (Optional Equipment) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Using the 110 Volt Outlet (Optional Equipment) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
CPR Board Usage (Optional Equipment) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Footboard Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Footboard Control Panel Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
LED Display Panel Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Function Lockout System Usage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Chaperone® Bed Exit (Optional Equipment) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Chaperone® Bed Exit With Zone Control (Optional Equipment) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Chaperone® Zone Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Scale System Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Scale System Control Panel Guide (Optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Preparing The Bed For Patient Stay / Zeroing The Scale System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Activating The Scale System And Displaying Patient Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

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 Table of Contents

Scale System Operation Guide (Continued)

Adding Or Removing Items During A Patient’s Stay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Converting The Patient’s Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Displaying The Weight Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Viewing Patient Weight In Gain / Loss Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Changing The Numerical Value Of Displayed Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Optional Pendant Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Zoom™ Option Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Drive Wheel Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Head End Control Panel Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Battery Charging And Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Optional iBed Awareness Operation Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Footboard Control Panel Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Footboard Control Panel Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
LED Indicators: Footboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
LED Indicators: Dashboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Display Screens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Main Menu Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
iBed Awareness Functionality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
iBed Awareness Light Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
iBed Awareness Side LEDs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
iBed Awareness Button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
iBed Awareness Monitoring and Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Low Height . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Brakes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Siderails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Bed Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Additional Alarm Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
iBed Awareness Locks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Fowler 30+ Lock button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Bed Motion Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Patient Control Locks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52
Optional Infrared (IR) Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
Optional iBed Locator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Inside Siderail Function Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Outside Siderail Function Guide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Product Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60

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 Table of Contents

Recycling Passport . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
EMC Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Limited Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
To Obtain Parts and Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Service Contract Coverage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Service Contract Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Return Authorization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
Damaged Merchandise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77
International Warranty Clause . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 77

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 Symbols and Definitions

Warning, consult accompanying documentation

Safe Working Load Symbol

Dangerous Voltage Symbol

~ Alternating Current

Direct Current

Protective Earth Terminal

Potential Equalization Symbol

Type B Equipment: equipment providing a particular degree of protection against electric shock,
particularly regarding allowable leakage current and reliability of the protective earth connection.

Class 1 Equipment: equipment in which protection against electric shock does not rely on BASIC
INSULATION only, but which includes an additional safety precaution in that means are provided
for the connection of the EQUIPMENT to the protective earth conductor in the fixed wiring of the
installation in such a way that ACCESSIBLE METAL PARTS cannot become live in the event of a
failure of the BASIC INSULATION.

Mode of Operation: Continuous

IPX4 Protection from liquid splash

Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock, Fire,
Mechanical and Other Specified Hazards Only in Accordance with UL 60601−1, First Edition (2003)
and CAN/CSA C22.2 No. 601.1−M90 with updates 1 and 2 and IEC 60601-1 (1998) with Amendment
1 (1991) and Amendment 2 (1995).
In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment,
this symbol indicates that the product must not be disposed of as unsorted municipal waste, but
should be collected separately. Refer to your local distributor for return and/or collection systems
available in your country.

Non-ionizing radiation; i.e. RF transmitter (WiFi)

This icon means the iBed Locator is connected.

X This icon means the iBed Locator is not connected.

This icon means the Network is connected.

X This icon means the Network is not connected.

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 Symbols and Definitions

WARNING/CAUTION/NOTE DEFINITION

The words Warning, Caution and Note carry special meanings and should be carefully reviewed.

WARNING
Alerts the reader about a situation, which if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.

CAUTION
Alerts the reader of a potentially hazardous situation, which if not avoided, may result in minor or moderate injury to the
user or patient or damage to the equipment or other property. This includes special care necessary for the safe and
effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or
misuse.

Note
This provides special information to make maintenance easier or important instructions clearer.

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 Introduction
This manual is designed to assist you with the operation of the Model 3002 Secure® II MedSurg Bed. Read it thoroughly
before using the equipment.

INTENDED USE – STYKER 3002 SECURE® II

This device is an AC-powered adjustable hospital bed intended for medical purposes that consists of a bed with a
built-in motor and remote controls that can be operated by the patient to adjust the height and surface contour of the
bed. The device includes movable and latchable siderails.

INTENDED USE – iBED® WIRELESS WITH iBED AWARENESS

The intended use for the iBed® Wireless (with iBed Awareness) is to assist clinical staff to monitor bed parameters
on specific Stryker beds. The desired bed parameters will be set by clinicians at the bedside. The iBed® Wireless
software is intended to be used only with specifically enabled Stryker beds that have been verified and validated with
the iBed® Wireless software, and is not intended to provide bed status information for non-Stryker beds. The iBed®
Wireless software is not intended to communicate any patient status information, nor to permanently store any type
of data. The iBed® Wireless with iBed Awareness System is not intended to provide automated treatment decisions
or as a substitute for professional healthcare judgment. The iBed® Wireless with iBed Awareness System is not a
replacement or substitute for vital signs monitoring or alert equipment. All patient medical diagnosis and treatment are
to be performed under direct supervision and oversight of an appropriate health care professional.

SPECIFICATIONS
Safe Working Load
Note: Safe Working Load indicates the sum of the 500 lbs 227 kg
patient, mattress, and accessory weight.
Scale System Capacity (optional equipment). Loads weighing up to 500 lbs 227 kg
Scale System Accuracy (optional equipment) ± 2 pounds at 0° - ± 10° Trendelenburg for
patients weighing 100 pounds or less
± 2% of the total patient weight at 0° - ± 10°
Trendelenburg for patients weighing greater
than 100 pounds
Overall Length/ Standard Bed (Inside Siderails Up 93” x 42.5” 236 cm x 108 cm
Width US and Canada) Siderails Down 93” x 40” 236 cm x 101.6 cm
Standard Bed (Outside Siderails Up 93” x 42.5” 236 cm x 108 cm
US and Canada) Siderails Down 93” x 36” 236 cm x 92 cm
Short Bed (Inside Siderails Up 85” x 42.5” 216 cm x 108 cm
US and Canada) Siderails Down 85” x 36” 216 cm x 92 cm
Zoom® Bed (Inside Siderails Up 95” x 42.5” 241 cm x 108 cm
US and Canada) Siderails Down 95” x 40” 241 cm x 101.6 cm
Zoom® Short Bed (Inside Siderails Up 87” x 42.5” 221 cm x 108 cm
US and Canada) Siderails Down 87” x 36” 221 cm x 92 cm
Patient Sleep Surface - Standard Bed 84” x 35” 213 cm x 89 cm
Patient Sleep Surface - Short Beds 76” x 35” 193 cm x 89 cm
Bed Height to Top of Seat Standard 16” to 30” ±0.5 41 cm to 76 cm
Litter - 6” Casters Beds with Zoom® Option 19.75” x 30” 50 cm x 76 cm
Short Beds w/Zoom® Option 20.5” x 30” 52 cm x 76 cm

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 Introduction
SPECIFICATIONS (CONTINUED)
Litter Platform Full Up Head End Siderail 15.75” 40 cm
to Top of Full Up Foot End Siderail 15.25” 38.7 cm
Siderail Outside US/Canada Head End Siderail 15” 38.1 cm
Outside US/Canada Foot End Siderail 14” 35.5 cm
Space Between Siderails (Full Up) 9.75” 24.7 cm
Outside the US and Canada 9.125” (8”) 23.1 cm
Knee Gatch Angle 0° to 40°
Fowler Angle 0° to 60°
Trendelenburg/Reverse Trendelenburg Non-Zoom Trend 12° ± 1°
Rev. Trend -10° ± 1°
Zoom® Trend 10° ± 1°
Rev. Trend -10° ± 1°
Electrical Requirements - all electrical requirements meet UL 2601 115 VAC, 60 Hz, 8.0 A
specifications. Optional: 230 VAC, 50/60 Hz, 4.0 A
Wireless Radio (iBed® Wireless Option) 802.11 b/g, 2.4 GHz
• Minimum Operational Signal Strength:
-65 dB
• Supported Securities:
WEP
WPA-PSK (TKIP)
WPA2-PSK (CCMP/AES)
• Supports IPv4 and DHCPv4
Outlet Option 110 VAC, 60 Hz, 10.0 A
(not available with Zoom® Option)
iBed® Wireless iBed Locator • Uses infrared based Stryker proprietary
(Optional Wireless Connection) (Wall Module) communication scheme.
IR Module • Uses infrared based Stryker proprietary
(Bed) communication scheme.
• Communication is line of sight based.
WiFi Module • Communication scheme used is IEEE 802.11 b/g (2.4
(Bed) GHz Band)

MATTRESS SPECIFICATIONS
Thickness 6” 15.2 cm
Width >= 35” >= 88.9 cm
Length >= 84” >= 213.4 cm
ILD 80 lbs 36.3 kg

The above stated mattress specifications assist in ensuring the product conforms to HBSW and IEC specifications.
Stryker reserves the right to change specifications without notice.
Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.

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 Bed Illustration

HEAD END
PATIENT’S
RIGHT
CPR Release
Handle

PATIENT’S
LEFT

I.V. and
Fracture Frame
Footboard Mount
Control Steer
Panel Pedal

Siderail Release
Handle

Brake Pedal

Foley Bag Hooks

FOOT END (Standard)
I.V. and
Fracture Frame
Mount (Behind Foot Board)

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 Safety Tips and Guidelines

SAFETY TIPS AND GUIDELINES

Before operating the Secure Bed, it is important to read and understand all information in this manual. Carefully read
and strictly follow the safety guidelines listed on this page. It is important that all users have been trained and educated
on the inherent hazards associated with the usage of electric beds.

WARNING
• Danger: Explosion hazard. Do not use in the presence of flammable anesthetics.
• Always apply the caster brakes when a patient is getting on or off the bed.
• Always keep the caster brakes applied when a patient is on the bed (except during transport). After the brake
pedal is applied, push on the bed to ensure the brakes are locked. Serious injury could result if the bed moves
while a patient is getting in or out of bed.
• Ensure the brakes are completely released prior to attempting to move the unit. Attempting to move the unit with
the brakes actuated could result in injury to the user and/or patient.
• Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal
is activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when
the steer pedal is activated may cause injury to the user.
• The Secure II Bed is not intended for use with patients less than two years of age. Serious injury can result if
caution is not used when operating the unit. Operate the unit only when all persons are clear of the electrical and
mechanical systems.
• To help reduce the number and severity of falls by patients, always leave the bed in the lowest position when the
patient is unattended.
• When attaching equipment to the frame, ensure it will not impede normal frame operation. For example: hooks
on hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, etc. Use
only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly which
may result in patient or user injury.
• The Secure II is equipped with a hospital grade plug for protection against shock hazard. It must be plugged
directly into a properly grounded three prong receptacle. Grounding reliability can be achieved only when a
hospital grade receptacle is used.
• When using the manual override shaft to manually actuate bed functions, always unplug the bed power cord from
the wall socket to avoid injury in the event of a sudden return of power to the bed.
• When raising the siderails, listen for the ”click” that indicates the siderail has locked in the up position. Pull firmly
on the siderail to ensure it is locked into position. Siderails are not intended to be a patient restraint device. It is
the responsibility of attending medical personnel to determine the degree of restraint and the siderail positioning
to ensure a patient will remain safely in bed.
• The Bed Exit System is intended only to aid in the detection of a patient exiting the unit. It is NOT intended
to replace patient monitoring protocol. The bed exit system signals when a patient is about to exit. Adding or
subtracting objects from the frame after zeroing the weigh system may cause a reduction in the sensitivity of the
bed exit system.
• Always unplug the bed power cord from the wall socket and push the battery power on/off switch to the“OFF”
position before servicing or cleaning the bed. When working under the bed with the bed in the high position,
always place blocks under the litter frame and apply the brakes to prevent injury in case the Bed Down switch is
accidently pressed.
• The CPR emergency release on the Short Bed frame may require assistance to lower the back when the back is
in the highest position. Attempting to lower the back in this position without assistance may result in injury to the
operator.
• Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by equipment
used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not exceed 300uA.
Grounding continuity should be checked periodically.

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 Safety Tips and Guidelines

WARNING (CONTINUED)
• To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or
receptacle.
• Do not use the optional 110V outlet for life sustaining equipment.
• To avoid pinching your fingers, place the I.V. pole in the upright position before using the drive handle.
• When using any mattress and/or mattress overlay that increases the overall height greater than 6” extra caution
and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.

To avoid possible injury and to assure proper operation when using a powered mattress replacement system such as
XPRT:
• Confirm proper scale system operation following mattress installation. For best results, secure the therapy mattress
power cord to prevent damage to the cord or interference with the bed frame and the scale system.
• Do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn Assist active. Patient motion
and position resulting from the dynamic therapy mattress may adversely affect scale system performance.
• Do no initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and
position resulting from the dynamic therapy mattress may adversely affect bed exit system performance.
• When using an XPRT Therapy Mattress extra caution and/or operator supervision is required to help reduce the
likelihood of a patient fall occurring.

CAUTION
• When large spills occur in the area of the circuit boards, 110 volt cables and motors, immediately unplug the bed
power cord from the wall socket. Remove the patient from the bed and clean up the fluid. Have maintenance
completely check the bed. Fluids can affect the operational capabilities of any electrical product. DO NOT put
the bed back into service until it is completely dry and has been thoroughly tested for safe operation.
• Preventative maintenance should be performed at a minimum of annually to ensure all bed features are functioning
properly.
• Close attention should be given to safety features including, but not limited to safety side latching mechanisms,
frayed electrical cords and components, all electrical controls return to off or neutral position when released,
caster braking systems, no controls or cabling entangled in bed mechanisms, leakage current 300 μA (microamps)
maximum, scale and bed exit systems calibrated properly.
• Because individual beds may have different options, footboards should not be moved from one bed to another.
Mixing footboards could result in unpredictable bed operation.
• The lockout buttons on the footboard lock the Fowler, Gatch and Bed Up/Down functions and prevent motion of
the bed. It is the responsibility of attending medical personnel to determine whether these functions should be
locked and to use the buttons accordingly.
• The weight of the I.V. bags should not exceed 40 pounds.
• Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse
Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the
potential for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full
down position to prevent the interference from causing the scale system to weigh inaccurately
• When attaching equipment to the frame, ensure it will not impede normal operation. For example: hooks on
hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, etc.
• The use of a mattress overlay may reduce the effectiveness of the siderail.
• I.V. Poles should not be used as a bed push/pull device. The cleanliness and integrity of both ground chains must
be maintained to minimize static build up and discharge.
• Do not add or remove weight when the bed exit system is armed.
• Zoom and battery backup beds must have their brake set in order for the bed to communicate with the iBed locator.
Failure to set brake could result in loss of location information.

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 Safety Tips and Guidelines

ZOOM® OPTION
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the Zoom option.

WARNING
• The 3002 Patient Transport Frame is intended for use by trained hospital personnel only. Failure to properly train
personnel could result in injury.
• USE CAUTION while maneuvering the unit with the drive wheel activated. Always ensure there are no obstacles
near the unit while the drive wheel is activated. Injury to the patient, user or bystanders or damage to the frame
or surrounding equipment could occur if the unit collides with an obstacle.
• Use caution when transporting the unit down halls, through doors, in and out of elevators, etc. Damage to the
siderails or other parts of the unit could occur if the unit comes in contact with walls or door frames.
• Put the drive wheel in the neutral position and release the brakes before pushing the unit manually. Do not attempt
to push the unit manually with the drive wheel engaged. The unit will be difficult to push and injury could result.
• If unanticipated motion occurs, unplug the power cord from the wall socket, push the battery power on/off switch
to the ”OFF” position (the LED will not be illuminated) and actuate the drive wheel pedal to the neutral position.
• The power save mode is activated after one hour on battery power with no motion release switch activation.
Functions including Bed Exit, Scale and Motion will cease to operate when the unit enters the power save mode.
Injury to the patient could occur if proper patient monitoring protocol is not observed.
• Always unplug the power cord and push the battery power on/off switch to the “OFF” position before service or
cleaning. When working under the frame, always place blocks under the litter frame to prevent injury in case the
Bed Down switch is accidently activated.
• Due to the weight the battery adds to the bed (approximately 50 pounds), additional force is required to move the
bed. Caution should be used when transporting this bed. Additional assistance should be used when necessary.
Failure to use caution while transporting this bed may result in injury to the user.
• Battery posts, terminals and related accessories contain lead and lead compounds, chemicals known to the State
of California to cause cancer and birth defects or other reproductive harm. Wash hands after handling.
• Do not modify the 3002 Patient Transport Frame. Modifying the unit can cause unpredictable operation resulting in
injury to the patient or operator. Modifying the unit will also void its warranty.

CAUTION
• To avoid damage while transporting the bed, verify the I.V. pole is at a low enough height to allow it to safely pass
through door openings and under light fixtures.
• The battery tray assembly weighs 50 pounds. Take care when removing the two hex head screws securing it to the
base frame or personal injury could result.

iBED AWARENESS OPTION

In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the iBed Awareness option.

WARNING
• The optional iBed Awareness system only indicates the siderail position, it does NOT indicate if the siderail is
locked. It is the caregiver’s responsibility to ensure that the siderails are locked after every move and also before
leaving a patient in the room.
• The optional iBed Awareness system indicator lights are only an aid to the caregiver, and in no way replace the
caregiver’s responsibility of checking on patients. Caregivers should not rely on the lights to perform their duties.
• Before arming the optional iBed Awareness system, the nurse must physically verify that the siderails are locked.

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 Safety Tips and Guidelines

iBED AWARENESS OPTION (CONTINUED)

CAUTION
• If the optional iBed Awareness system is being used, ensure the bed is in the desirable state (iBed Awareness ON
and with the light green) before leaving the room.
• If the optional iBed Awareness system is being used and the iBed Awareness is alerting, do not turn off iBed
Awareness as the display information to troubleshoot the bed will get lost.
• If the optional iBed Awareness system is being used, use of accessories that cover the center and side alert lights
at the footboard are not recommended.

iBED® WIRELESS OPTION

In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the iBed® Wireless option.

WARNING
• The optional iBed® Wireless function provides remote information of bedside information to aid the caregiver. In
no way does this option replace the caregiver’s responsibility of checking on patients. Caregivers should not rely
only on the remote information to perform their duties.
• The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate
location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote
information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be re-
mapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the
room / location information is changed after initial installation.
• Line of sight between iBed Locator and the head end of bed must be free of obstruction at all times. Any line
of sight interference could impede communication and cause the room / location information not to be available.
• iBed® Wireless compatible footboard must be used for all iBed® Wireless beds. Some iBed® Wireless functionality
will be lost if an older version of the footboard is used.
• iBed® Wireless functionality shall be verified after installation. Failure to do may result loss of remote information
or wrong remote information. At a minimum, verify iBed locator communication with bed in all bed positions, and
iBed® Wireless communication with the wireless access point.
• iBed Locators must be installed more than 71” apart from one another in the same room, such as in a semi-private
room with more than one bed. Failure to do so could result in a bed communicating with the other adjacent iBed
Locator, thus providing incorrect bed location information.

CAUTION
Wireless bed only transmits bed information and not nurse call information. The wireless bed is not intended to replace
the existing nurse call system.

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 Setup Procedures

SETUP PROCEDURES

It is important that the Secure II Bed is working properly before it is put into service. The following list will help ensure
that each part of the bed is tested.

• Plug the bed into a properly grounded, hospital grade wall receptacle and ensure the ”Power” LED light at the foot
end of the bed comes on.

WARNING
The Secure II is equipped with a hospital grade plug for protection against shock hazard. It must be plugged directly into
a properly grounded three prong receptacle. Grounding reliability can be achieved only when a hospital grade receptacle
is used.

• Plug the optional interface cable into the 37 pin connector under the litter frame at the head end of the bed, and
into the ”Patient Station”, ”Head Wall”, ”Docker Station”, or equivalent (whichever applies). Test the interface cable
to verify it is functioning properly.

WARNING
Use only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly which
may result in patient or user injury.

• Ensure the siderails raise, lower and store smoothly and lock in the up position and in the intermediate position
when lowered (page 19).
• Ensure that all four casters lock when the brake pedal is engaged (and 17).
• Raise the back up to approximately 600. Squeeze the CPR release handle and ensure the back will drop with
minimal effort.

NOTE
Ensure that the ”Brake Not Set” LED located on the outside of the head end siderails and the footboard control panel
(Non-LBS option only) or ”Brake” LED located on the outside of the footboard control panel (LBS option only) come
on when the brakes are disengaged.
• Run through each function on the footboard control panel to ensure that each function is working properly
(page 22).
• Run through each function on both head end siderails to ensure that each is working properly (page 19).
• Activate the motion stop system to ensure it is functioning properly; press and hold the BED DOWN key. As the
bed lowers, lift up on the motion interrupt pan and ensure the downward motion stops. Release the pan and allow
the downward motion to continue.

NOTE
The bed’s upward motion or other functions are not disrupted by the motion stop system.
• If the bed is equipped with the Nurse Call option, verify it is functioning properly prior to patient use.

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 Setup Procedures

ZOOM® OPTION

If your bed is equipped with the Zoom drive wheel option, run through the setup procedures on page 16 and continue
with the procedures listed below.

• Plug the power cord into a properly grounded, hospital grade wall receptacle. The 12 volt batteries that provide
power to the drive wheel and backup power to the unit functions will charge whenever the power cord is plugged
into the wall socket. The batteries require approximately 10 hours of charging time before the bed is put into
service.
• Unplug the power cord from the wall socket. Push the battery power switch located on the lower left corner of the
head end to the “ON” position. Again, verify each function on the footboard and siderails is operating properly.
• With the battery power switch in the “ON” position and the brakes engaged, ensure the “Release Brakes”LED on
the head end control panel is illuminated.
• With the battery power switch in the “ON” position and the drive wheel in the neutral position (not touching the
floor), ensure the “Engage Drive Wheel” LED on the head end control panel is illuminated.
• Run through the operation of the drive wheel (page 35) to ensure it is operating properly.

If any problems are found during bed setup, contact Stryker Customer Service at (800) 327−0770.

iBED® WIRELESS OPTION

In order for your bed to be capable of receiving a wireless connection the iBed Locator needs to be installed on the
wall at the head end of the bed. The iBed Locator communicates with the IR Module installed in your bed. For detailed
instructions on mounting the 5212 iBed Locator refer to the instruction sheet (part number 5212-009-101) packaged
with your optional 5212 iBed Locator Installation kit.

If any problems are found during the iBed Locator Installation, contact Stryker Technical Support at (800) 327−0770.

WARNING
The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate location
information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote information.
Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be re-mapped to the new
room / location in which it is moved to. iBed Locator re-mapping will also be required if the room / location information
is changed after initial installation.

The wireless connection settings need to be loaded before the device will communicate with the iBed Server application.
Reference the iBed Server Installation and Configuration Manual (5212-009-001).

Note
iBed® Wireless will not send iBed Locator information unless the brake is set (Battery Backup and Zoom®
options only).

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 Base Operation Guide

BRAKE PEDAL OPERATION

WARNING
Always apply the caster brakes when a patient is getting on or off the bed. Push on the bed to ensure the brakes are
securely locked. Always engage the brakes unless the bed is being moved. Injury could result if the bed moves while
a patient is getting on or off the bed.

To activate the brakes, push down once on one of the pedals

located at the midpoint of the bed on both sides (identified by
the label at right). The pedal will remain in the lowered position,
indicating the brakes are engaged. To disengage the brakes,
push down once and the pedal will return to the upper position.

NOTE
There are LED lights on the outside of the head end siderails and on the foot end control panel that will blink when the
brakes are not engaged only if the bed is plugged into a wall socket (page 57 and 23) The brakes will still operate
properly when the bed is not plugged in.

STEER PEDAL OPERATION (BEDS WITHOUT THE ZOOM DRIVE WHEEL OPTION)

When the bed is moved, the steer caster helps guide the bed along a straight line and helps the bed pivot around
corners.

To activate the steer caster, move the pedal located at the head
end of the bed to your left as shown on the label.

NOTE
For proper ”tracking” of the steer caster, push the bed approximately 10 feet to allow the wheels to face the direction
of travel before engaging the steer pedal. If this is not done, proper ”tracking” will not occur and the bed will be dif-
ficult to steer.

WARNING
Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal is
activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when the steer
pedal is activated may cause injury to the user.

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 Litter Operation Guide

CPR EMERGENCY RELEASE

When quick access to the patient is needed, and the Fowler is raised, squeeze one of the two red release handles and
the Fowler can be quickly guided down to a flat position.

NOTE
The handle can be released at any time to stop the Fowler from lowering.

FOOT PROP USAGE

A
To prop the foot end of the Knee Gatch up, grasp the end of
the Knee Gatch and lift upward, allowing the foot prop (A)
to engage at the desired height. To release the prop, swing
the prop (A) toward the head end of the bed to disengage
the hinge and lower the foot end.

WARNING
To avoid injury while cleaning or servicing under the foot
section, secure the foot section with string or bungee cords
or hold it up out of the way.

FRACTURE FRAME USAGE

A standard fracture frame can be mounted on the bed
using the IV sockets located on all four corners of the bed. FOOT END
I.V. poles can be used in conjunction with a fracture frame
if the I.V. pole adaptor sockets are purchased.

WARNING
Use only retractable traction or fracture frames. Failure to use a retractable frame may result in injury to the patient and/
or damage to the equipment.

FOLEY BAG HOOKS USAGE

The standard Foley bag hooks are found at two locations on both sides of the frame; under the frame below the seat
section and at the extreme foot end of the frame. The optional isolated Foley bag hooks are located at the foot end of
the bed on top of the lift header. The patient weight reading on the scale system will not be affected when the optional
isolated Foley bag hooks are used.

PATIENT RESTRAINT STRAP LOCATIONS

The bed has 12 locations for installing patient restraint straps on the litter top, 6 on each side of the bed.

WARNING
Improperly adjusted restraint straps can cause serious injury to a patient. The clinician must use her/his judgement to
determine proper use of restraint straps and restraint strap locations. Clean Velcro AFTER EACH USE. Saturate Velcro
with disinfectant and allow disinfectant to evaporate. (Appropriate disinfectant for nylon Velcro should be determined by
the hospital.)

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 Litter Operation Guide

POSITIONING SIDERAILS

NOTE
• The siderails can be locked at two heights (intermediate & full up). The foot end siderails on a Short Bed do not
have an intermediate position.
• The siderails can slide to the side of the bed when not in use. To remove the rail from the tucked position, grasp
the top of the rail and pull outward.
• To engage the head end siderail, grasp the rail and swing it upward to full height. When the siderail is being raised,
it does not lock in the intermediate position. To lower the siderail, push in the yellow release handle (A) and rotate
the siderail until it locks in the intermediate position. To lower the siderail fully, push in the yellow release handle
(A) again and rotate the siderail until it is completely lowered.
• To engage the foot end siderail, the same procedure is required as for the head end siderail, however, the siderail
swings toward the foot end of the bed.

WARNING
Be sure the siderail is locked securely into position.
Siderails are not intended to keep patients from exiting
the bed. They are designed to keep a patient from
inadvertently rolling off the bed. Proper restraint methods
should be utilized to ensure the patient remains in the
bed. The siderails are not intended to be used as a
push device.

To disengage the rail, push in the yellow release handle

(A) and swing the rail down to the desired height. Store
the siderails slid.

A
SIDERAIL CONTROL PANEL LIGHTS
The bed is equipped with lights to illuminate the head end siderail control panel and the red nurse call switches. Both
can be activated at the footboard control panel. Three settings are available for the control panel lights: low, medium
and high intensity. When all lights are off, push the siderail control light button at the footboard once to turn on both
the control lights and the nurse call light at the siderail. Push again to change from low to medium setting, and a third
time to change to the high setting. The nurse call light intensity is not affected. Pushing the button a fourth time will turn
off the siderail control panel lights and pushing it a fifth time will turn off the red nurse call light as well (page 22).

NOTE
The purpose of the red nurse call light on the siderails is to ensure the patient immediately knows which button to
push to contact the nurse station. Turning the red light off may compromise this ability, especially in a darkened room.

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 Litter Operation Guide

OPERATING I.V. POLES

A
To use the 2-Stage Permanently Attached I.V. pole:

Note
The 2-stage permanently attached I.V. pole is an option and may have been C
installed at either the head, foot or both ends. The choice was made at the
time the unit was purchased.

1. Lift and pivot the pole from the storage position and push down until it
rests in the receptacle. B

2. To raise the height of the pole, pull up on the telescoping portion (A) until
it locks into place at its fully raised position.
3. Rotate the I.V. hangers (B) to desired position and hang I.V. bags.
4. To lower the I.V. pole turn the latch (C) clockwise until section (A) lowers.

CAUTION
The weight of the I.V. bags should not exceed 40 pounds.

WARNING
To avoid pinching your fingers, place the I.V. pole in the upright position before
using the drive handle.

To use the “Removable” IV pole:

1. Install the pole at any of the four receptacles on the bed top (located on
all four corners of the frame).
2. To raise the height of the pole, turn knob (A) counterclockwise and pull
up on the telescoping portion (B) of the pole and raise it to the desired
height.
3. Turn knob (A) clockwise to tighten the telescoping portion in place.

CAUTION
The weight of the I.V. bags should not exceed 40 pounds.

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 Litter Operation Guide

NIGHT LIGHT USAGE

The bed is equipped with two night lights to illuminate the floor area
around the bed. There is a switch under the litter thigh section on the
patient’s left side that turns both lights on and off.

NOTE
The night lights have a sensor so the lights will turn off, even when
the switch is on, if the light in the room is bright enough so a night
light is not necessary.

NURSE CALL BACKUP BATTERY (OPTIONAL EQUIPMENT)

• To prevent a low battery condition when the bed is not plugged in, position the cord out switch at the head end
of the bed to the off position. The switch is identified by the label shown below. If the switch is not positioned
as shown below and the bed power cord and pendant cord are unplugged, the life of the backup battery will be
significantly reduced.
• If the power light (located on the footboard) is flashing, the Nurse Call battery needs to be replaced. The battery is
located on the patient’s left side at the head end of the bed. No tools are required to replace the battery. Unplug
the bed power cord from the wall socket and replace the battery.

USING THE 110 VOLT OUTLET (OPTIONAL EQUIPMENT)

• The 110V outlet has its own power cord that must be plugged into a properly grounded three prong wall receptacle
different from the wall receptacle the bed power cord is plugged into.
• If the equipment plugged into the bed outlet is not receiving power, check the circuit breakers located on the litter
frame under the head section. Reset, if necessary.

WARNING
• Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by
equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not
exceed 300uA. Grounding continuity should be checked periodically.
• To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or
receptacle.
• Do not use the optional 110V outlet for life sustaining equipment.

CPR BOARD USAGE (OPTIONAL EQUIPMENT)

If the bed is equipped with the optional CPR board, it is stored on the bed’s head board. To remove it, pull it away from
the head board and lift it out of storage position. If the CPR board option was not purchased, the head board can also
be removed and used as an emergency CPR board.

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 Footboard Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

FOOTBOARD CONTROL PANEL GUIDE

1. Push repeatedly for low, medium and high settings for the siderail control panel lights. Pushing a fourth and fifth
time will turn off the siderail lights and the red nurse call light respectively (page 19).

NOTE
The intent of the red nurse call light on the siderails is to ensure the patient immediately knows which button to push
to contact the nurse station. Turning the red light off may compromise this ability, especially in a darkened room.

2. Push to lock out all bed motions. The MOTION lock icon and the “BED MOTION LOCKED” LED will light. Push
again to unlock.
3. Push to lock out Back Rest controls at both siderails. The HEAD lock icon will light. Push again to unlock.
4. Push to lock out Knee Gatch controls at both siderails. The KNEE lock icon will light. Push again to unlock.
5. Push to lock out bed height movement at both siderails. The UP/DOWN lock icon will light. Push again to
unlock.
6. Push to raise bed height.
7. Push to lower bed height.
8. Push to lower head end/raise foot end of bed (Trendelenburg position).
9. Push to lower foot end/raise head end of bed (Reverse Trendelenburg position).

CAUTION
Individual beds may have different options therefore, footboards should not be moved from one bed to another. Mixing
footboards could result in unpredictable bed operation.

1. Push to raise Fowler.
2. Push to raise Knee Gatch.
3. Push to lower Fowler.
4. Push to lower Knee Gatch.
• This panel is optional equipment.

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 Footboard Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

LED DISPLAY PANEL GUIDE

The LED Display Panel is located at the foot end of the bed, under the Control Panel.

”POWER” − will light when the bed is plugged into the wall receptacle. Will blink if the 9V Nurse Call battery needs
to be replaced.
”BED MOTION LOCKED” − will light when the Bed Motion Lock has been activated.
”BRAKE NOT SET” − will blink when the brakes have not been set.
”BED EXIT ON” − will light when the Bed Exit function has been activated (optional equipment).

FUNCTION LOCKOUT SYSTEM USAGE

1. To lock out the bed movement functions on the siderails and prevent the patient from changing the positioning of
the bed, push the ”HEAD”, ”KNEE” and/or ”UP/DOWN” switches in the ”Siderail Control Lockouts” module on the
footboard control panel.

NOTE
The footboard controls for these motions are not affected by the lockout switches.
The ”padlock” symbol on the control panel will be lighted when that function is locked out.

2. To lock out the entire bed motion for all switches on the bed (siderails and footboard), push the ”ON/OFF”
switch in the ”Bed Motion Lock” module on the footboard control panel.

CAUTION
The lockout buttons on the footboard lock the Fowler, Gatch and Bed Up/Down functions and prevent motion of the bed.
It is the responsibility of attending medical personnel to determine whether these functions should be locked and to use
the buttons accordingly.

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 Footboard Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

CHAPERONE® BED EXIT (OPTIONAL EQUIPMENT)

For beds with a scale system:

NOTE
If the weigh system is in use, it will switch to ”off” when the “ARM” key is pressed.

1. Before putting the patient on the bed, the weigh system must be zeroed for the Bed Exit System to function
properly (see page 28 for instructions on zeroing the weigh system).
2. Put the patient on the bed and push the “ARM” key to activate the Bed Exit function. The ”ARMED” light will come
on .
3. To deactivate Bed Exit, push the ”DISARM” key. The ”ARMED” and ”BED EXIT ON” lights will turn off.

For beds without a scale system:

1. Before putting the patient on the bed, press and hold the ”ARM” and the ”DISARM” keys together until the
”ARMED” light begins to flash.
2. Release the ”ARM” and the ”DISARM” keys and do not touch the bed until the ”ARMED” light stops flashing.
3. Put the patient on the bed and push the ”ARM” key to activate the Bed Exit function. The ”ARMED” light will
come on.
4. To deactivate Bed Exit, push ”DISARM”. The ”ARMED” and ”BED EXIT ON” lights will turn off.

WARNING
The Bed Exit System is intended only to aid in the detection of a patient exiting the bed. It is NOT intended to replace
patient monitoring protocol. It signals when a patient is about to exit. Adding or subtracting objects from the bed after
arming the bed exit system may cause a reduction in the sensitivity of the bed exit system. To avoid possible injury and
to assure proper operation when using a powered mattress replacement system such as XPRT, do not initialize (“arm”)
bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and position resulting from a
dynamic therapy mattress may adversely affect bed exit system performance.

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 Footboard Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

CHAPERONE® BED EXIT WITH ZONE CONTROL (OPTIONAL EQUIPMENT)

For Beds with a Scale System:

NOTE
If the weigh system is in use, it will switch to ”off” when Bed Exit is armed.

1. Before putting the patient on the bed, the weigh system must be zeroed for the Bed Exit System to function
properly (see page 28 for instructions on zeroing the weigh system).
2. Put the patient on the bed and push and release the ”ARM/DISARM” key (top light will come on).
3. The Bed Exit system with Zone Control will automatically select the first zone. To change the zone, push and hold
the “SELECT ZONE” key until the light indicating the desired zone comes on.
4. To deactivate Bed Exit, push the ”ARM/DISARM” key. The selected zone light and ”BED EXIT ON” lights will turn
off.

For Beds without a Scale System:

1. Before putting the patient on the bed, press and hold the ”ARM/DISARM” and the ”SELECT ZONE” keys together
for 5 seconds. The top light will begin to flash.
2. Release the ”ARM/DISARM” and the ”SELECT ZONE” keys and do not touch the bed until the top light stops
flashing.
3. Put the patient on the bed and push and release the ”ARM/DISARM” key (top light will come on).
4. The Bed Exit system with Zone Control will automatically select the first zone. To change the zone, push and hold
the “SELECT ZONE” key until the light indicating the desired zone comes on.
5. To deactivate Bed Exit, push the ”ARM/DISARM” key. The selected zone light and ”BED EXIT ON” light will turn
off.

WARNING
To avoid possible injury and to assure proper operation when using a powered mattress replacement system such as
XPRT, do not initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and
position resulting from a dynamic therapy mattress may adversely affect bed exit system performance.

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 Footboard Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

CHAPERONE® BED EXIT WITH ZONE CONTROL (OPTIONAL EQUIPMENT) (CONTINUED)

CHAPERONE® ZONE SETTINGS

The first zone (top indicator light) is the traditional Bed Exit zone. The patient can move around the bed freely but
cannot fully exit the bed or the alarm will sound.

The second zone (middle indicator light) is more restrictive than the first zone. When the zone is selected, the bed
measures the location of the patient’s center of gravity. If the patient’s center of gravity moves from the original
location more than 6.5 inches to either side or 13 inches toward the head or foot, an alarm will sound.

The third zone (bottom indicator light) is the most restrictive zone. When the zone is selected, the bed measures the
location of the patient’s center of gravity. If the patient’s center of gravity moves from the original location more than
1 inch to either side or 1 inch toward the head or foot, an alarm will sound.

NOTE
All zone dimensions are ± .5 inches.

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

SCALE SYSTEM CONTROL PANEL GUIDE (OPTIONAL)

NOTE
This panel is optional equipment.

1. LCD − displays patient weight. Trendelenburg angle is displayed when the scale is not active.
2. Press to zero bed (page 29). Also press to scroll while Menu Mode is active.
3. Press to enter and exit the Menu Mode.
4. Press when adding or removing equipment to the bed (page 30).
5. Press to turn scale system on and off. Also press to scroll while Menu Mode is active.
6. Press to change weight from pounds to kilograms or back (page 30). Also press while using the Menu Mode.

NOTE
If weight is displayed, SCALE ON/OFF must be pressed to turn off the scale before the Trend or Fowler angle will
display.

CAUTION
Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse
Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the potential
for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full down position
to prevent the interference from causing the scale system to weigh inaccurately.

WARNING
To avoid malfunction, the Optional Scale System should not be used adjacent to or stacked with other equipment. If
adjacent or stacked use is necessary, the Optional Scale System should be observed to verify normal operation in the
configuration in which it will be used.

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

SCALE SYSTEM CONTROL PANEL GUIDE (CONTINUED)

WARNING (CONTINUED)
To avoid possible injury and to assure proper operation when using model number 2750, 2920, 2950 or 2981 mattress:
• Confirm proper scale system operation following mattress installation. For best results, secure the therapy mattress
power cord to prevent damage to the cord or interference with the bed frame and the scale system.
• Do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn Assist active. Patient motion
and position resulting from the dynamic therapy mattress may adversely affect scale system performance.
• Do no initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and
position resulting from the dynamic therapy mattress may adversely affect bed exit system performance.
• When using an XPRT (2950), Position PRO (2920), ComfortGel (2850) or Symmetric Aire (2750) mattress, extra
caution and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.

For more detailed operating instructions, see the following Operation Sections:

1. Preparing The Bed For Patient Stay/Zeroing the Bed - page 29

2. Activating the Scale System and Displaying Patient Weight - page 29
3. Adding or Removing Items During a Patient’s Stay - page 30
4. Converting the Patient’s Weight - page 30
5. Displaying the Weight Log - page 31
6. Viewing Patient Weight In Gain/Loss Mode - page 32
7. Changing the Numerical Value Of Displayed Weight - page 33

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

PREPARING THE BED FOR PATIENT STAY / ZEROING THE SCALE SYSTEM

NOTE
Do not zero the bed while a patient is in bed. If this should occur, remove the patient and zero the bed again. If Bed
Exit is armed, it must be disarmed before the scales can be zeroed.

Prepare the bed for the patient’s stay by adding/removing linens, pillows, etc.

• Press and release The scale monitor will read:

“LET GO FOR SCALE”

“WEIGHING”
“XXX.X LB”

• Press and hold The scale monitor will read:

“HOLD TO ZERO WT.”

“RELEASE TO ZERO”

• Release The scale monitor will now read:

“DO NOT TOUCH BED”

“0.0 LB”

The bed is now ready for the patient.

NOTE
If there is a problem with a load cell or another component of the scale system, the system will try to zero for 30 sec-
onds, and the scale monitor will read:
“UNABLE TO ZERO”
“TRY AGAIN”

If the problem continues, after 3 attempts at zeroing, the scale system will lock and the scale monitor will read:

“Scale Sys. Error”

“Call for service”

Unplug the bed power cord from the wall socket and plug it back in. If the problem continues, call a service technician.

ACTIVATING THE SCALE SYSTEM AND DISPLAYING PATIENT WEIGHT

• Press and release The scale monitor will read:

“LET GO FOR SCALE”

“WEIGHING”
“XXX.X LB”

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

ADDING OR REMOVING ITEMS DURING A PATIENT’S STAY

• If it is necessary to add or remove items (monitors, pumps, etc.) during the patient’s stay, press and release

to activate the scale system. After the scale monitor reads: “XXX.X LB”, press and hold

The scale monitor will read: “HOLD TO START”

“RELEASE TO START”

• Release The scale monitor will read: “DO NOT TOUCH BED”
“ADD/REMOVE EQUIP.”

• Add or remove the equipment and press The scale monitor will read: “RELEASE TO FIN.”

• Release The scale monitor will read: “DO NOT TOUCH BED”
“XXX.X LB”

The weight displayed will be that of the patient only.

• If the CHANGE EQUIPMENT function is started but not finished, after approximately 45 seconds the monitor will
read: “HIT CH. EQ. TO END”

• Press The scale monitor will read: “RELEASE TO FIN.”

• Release The scale monitor will read: “DO NOT TOUCH BED”
“XXX.X LB”

CONVERTING THE PATIENT’S WEIGHT

• Press and release The scale monitor will read: ”WEIGHT NOW KGS”
”XXX.X KG”

• Repeat the procedure to return to pounds. The display will read: ”WEIGHT NOW LBS”
”XXX.X LB”

• If the unit of measurement has been locked, the display will read: “UNITS ARE LOCKED”

Note
A service technician must be called to unlock the unit of measurement.

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

DISPLAYING THE WEIGHT LOG

• To display a list of the previous 10 weight readings, press to activate the scale system.
The scale monitor will read: “LET GO FOR SCALE”
“XXX.X LB”

• Press to enter the Menu Mode. The scale monitor will read: “ FOR OPTIONS”

• Press or to scroll through the menu options. The scale monitor will read:

“SHOW WEIGHT LOG”

“PUSH ENTER”

• Press The scale monitor will read: “ WEIGHT LOG”

• Press or to scroll through the weight log. The scale monitor will read: “1. 0.0 LB”

• A weight reading is logged each time the button is pressed and the bed is in the scale mode for at least
15 seconds.

The first weight reading displayed (1.) is the most recent. If the change in the patient’s weight since the last reading
was taken is less than .2 pounds, the log will not update. Zeroing the scale system clears the weight log.

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

VIEWING PATIENT WEIGHT IN GAIN / LOSS MODE

• To view the patient’s weight and to begin totaling the amount of weight the patient has gained or lost, press

to activate the scale system. The scale monitor will read: “LET GO FOR SCALE”

• Press to enter the Menu Mode. The scale monitor will read: “ FOR OPTIONS”

• Press or to scroll through the menu options. The scale monitor will read:
“START GAIN/LOSS”
“PUSH ENTER”

• Press The scale monitor will read: “DO NOT TOUCH BED”
“XXX.X LB G XX.X”

• To exit Gain/Loss mode, press to enter the Menu Mode. The scale monitor will read:

“ FOR OPTIONS”

• Press to to scroll through the menu options. The scale monitor will read:
“QUIT GAIN/LOSS”
“PUSH ENTER”

• Press The scale monitor will read: “XXX.X LB“

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 Scale System Operation Guide
(Applies to Non-iBed Awareness Option / iBed® Wireless Option Beds)

CHANGING THE NUMERICAL VALUE OF DISPLAYED WEIGHT

• To decrease the numerical value of the displayed weight, press to activate the scale system.

The scale monitor will read: “LET GO FOR SCALE”

“XXX.X LB”

• Press to enter the Menu Mode. The scale monitor will read: “ FOR OPTIONS”

• Press or to scroll through the menu options. The scale monitor will read:
“CHNG. PTNT. WGT.”
“PUSH ENTER”

• Press The scale monitor will read: “HOLD TO INC.

TO DEC.”

• Press to decrease the displayed weight or to increase the displayed weight.

• Once the desired weight is displayed, press The scale monitor will read: “XXX.X LB”

NOTE
If one of the load cells is malfunctioning or overloaded, the scale monitor will read: “Scale Sys. Error”
“Call for service”
Call a service technician.

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 Optional Pendant Operation Guide

Press to turn on Press to activate

the TV/Radio. Nurse Call.

Press to increase
Press to turn
the volume of
on room lights.
the TV/Radio.

Press to decrease Press to turn on

the volume of reading lights.
the TV/Radio.

Press to raise Press to raise

head section. knee section.

Press to lower Press to lower

head section. knee section.

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 Zoom™ Option Operation Guide

DRIVE WHEEL OPERATION

1. Unplug the power cord from the wall socket

and secure the cord sufficiently to prevent
entanglement while the unit is in motion. The
drive wheel will not operate if the power cord is
plugged into the wall socket.
2. Activate the power to the drive wheel by placing
the battery power switch located at the left side
of the head end of the litter in the “ON” position.
The LED will illuminate.
3. Engage the drive wheel by rotating the pedal
located at the head end to the left as shown
on the label. To place the drive wheel in the
neutral position, rotate the pedal to the right.
4. Release the brakes. The drive system will not
function while the brakes are engaged. The
“Release Brakes” LED on the head end control
panel will be illuminated if the brakes are
engaged while the battery power switch is on.

WARNING
When maneuvering the unit with the drive wheel activated, always ensure there are no obstacles near the unit while the
drive wheel is activated. Injury to the patient, user or bystanders or damage to the unit or surrounding equipment could
occur if the unit collides with an obstacle. Be aware when transporting the unit down halls, through doors, in and out of
elevators, etc. Damage to the siderails or other parts of the unit could occur if the unit comes in contact with walls or
door frames.

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 Zoom™ Option Operation Guide

DRIVE WHEEL OPERATION (CONTINUED)

5. Grasp the drive handle at the two raised grip areas. Squeeze either of the motion release switches (A) located
under the handle to enable the movement of the drive wheel. Either or both switches will enable movement but
both switches must be released to stop movement.

6. While continuing to squeeze the switch(es), push the handle away from you or pull the handle toward you to
initiate motion in that direction. The forward speed will increase proportionally to the distance the drive handle
is moved. I.E. the farther forward the drive handle is pushed, the faster the unit will move.
To stop motion, remove your hands from the switches and the handle.

NOTE
The drive wheel does not pivot. The unit cannot be moved directly sideways with the drive wheel engaged. With the
drive wheel pedal in the neutral position and the unit’s brakes released, the unit can be moved in any direction including
sideways.

Driving a Zoom® equipped unit over liquids or slick surfaces could decrease the traction of the drive wheel.

WARNING
Put the drive wheel in the neutral position and release the brakes before pushing the unit manually. Do not attempt to
push the unit manually with the drive wheel engaged. The unit will be difficult to push and injury could result.

CAUTION
When attaching equipment to the frame, ensure it will not impede normal operation. For example: hooks on hanging
equipment must not actuate control buttons, equipment must not hide the nurse call button, etc.

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 Zoom™ Option Operation Guide

HEAD END CONTROL PANEL OPERATION

1 3 5
UP

K NE E B ACK

2 4 6
DOWN

7 ENGAGE DRIVE WHEEL 8 RELEASE BRAKES

9 PLUG BED IN TO CHARGE

1. Press and hold to raise the litter.

2. Press and hold to lower the litter.
3. Press to raise the Knee section.
4. Press to lower the Knee section.
5. Press to raise the Back section.
6. Press to lower the Back section.
7. The “Engage Drive Wheel” LED will be illuminated whenever the battery power switch is on and the drive
wheel pedal is in the neutral position. The light will go off when the drive wheel is in the drive position.
8. The “Release Brakes” LED will be illuminated whenever the bed’s brakes are engaged while the battery
power switch is on. The light will go off when the brakes are disengaged.
9. The “Plug Bed In To Charge” LED will be illuminated while the battery power switch is on if the battery level
is low. Plug the bed power cord into the wall socket to charge the batteries.

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 Zoom™ Option Operation Guide

BATTERY CHARGING AND OPERATION

NOTE
The bed may be equipped with a battery backup option without the Zoom® drive wheel.

1. The unit has two 12 volt batteries to provide power to the drive wheel and backup power to the unit functions if the
power cord is unplugged from the wall socket. Neither the unit functions nor the drive wheel will operate properly
if the batteries are not sufficiently charged. The batteries require approximately 10 hours of charging time when
they are fully discharged.
2. The batteries are charging whenever the power cord is plugged into a properly grounded, hospital grade wall
socket. When the unit is stationary, the power cord should be plugged into a wall socket whenever possible.

NOTE
The battery will operate under slightly decreased power until it has run through 10−15 cycles of usage and recharging.

1. The “Plug Bed In To Charge” LED on the Head End Control Panel will be illuminated while the battery power switch
is on if the battery level is low (see page 36). Plug the power cord into a wall socket to charge the batteries.
2. After one hour on battery power with no motion release switch activation, the unit will enter power save mode and
none of the unit’s powered functions will operate. Squeeze either of the motion release switches located under
the drive handle to enable the unit functions.

NOTE
The three LEDs on the Head End Control Panel may still be illuminated when the unit is in power save mode. The
Battery Power LED located at the left side of the head end of the unit will be illuminated when the unit is in power save
mode.

WARNING
The power save mode is activated after one hour on battery power with no motion release switch activation. Functions
including Bed Exit, Scale and Motion will cease to operate when the unit enters the power save mode. Injury to the
patient could occur if proper patient monitoring protocol is not observed.

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 Optional iBed Awareness Operation Guide

The iBed Awareness system is intended to serve as a secondary monitoring system, informing the operator via a visual
or audible alert when a preset condition changes.

• When the iBed Awareness is turned “On”, the system has the ability to automatically monitor the following:
- Brake Set/Not Set
- Siderail Position
• Additionally, when the bed is in low height and/or Chaperone® Bed Exit system is armed, the system has the ability
to monitor these features when iBed Awareness is turned “On”.

FOOTBOARD CONTROL PANEL BUTTONS

LOCKS MOTION BED EXIT SCALE iBed / MENU

2 6 8 10 12 14 18 20 22 24

1 3 4 5 7 9 11 13 15 16 17 19 21 23 25

Button Name Button Name Button Name

1 Bed Motion Lock 9 Bed Down 17 Bed Exit Zone Control

2 Fowler 30+ Lock 10 Fowler Up 18 Scale

3 Patient Fowler Lock 11 Fowler Down 19 Scale Zero

4 Patient Gatch Lock 12 Gatch Up 20 iBed On/Off

Patient Bed Up/
5 13 Gatch Down 21 Menu
Down Lock
6 Trend 14 Cardiac Chair 22 Menu Up

7 Reverse Trend 15 CPR Drop 23 Menu Down

Exit
8 Bed Up 16 Bed Exit Arm/Disarm 24
X
Enter
25
P

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 Optional iBed Awareness Operation Guide

FOOTBOARD CONTROL PANEL FUNCTIONS

2 6 8 10 12 14

1 3 4 5 7 9 11 13 15

Button Name Function

Locks all motion on bed. The Bed Motion Lock button will illuminate
1 Bed Motion Lock
when activated.
Places bed at 300 and locks Fowler below 300. The Fowler 30+ button
2 Fowler 30+ Lock
will illuminate when activated.
Locks out Fowler control at all locations (Siderail, Pendant, Headend)
3 Patient Fowler Lock with the exception of the operator controls located on the Footboard.
LOCKS

The Patient Fowler Lock will illuminate when activated.

Locks out Gatch control at all locations (Siderail, Pendant, Headend,
Footboard). The Patient Gatch Lock will illuminate light when activated.
4 Patient Gatch Lock This function also prevents the auto contour of the Gatch when motion
is used. Note: Auto contour is the feature of the bed that when fowler
is actuated, Gatch automatically moves with the Fowler.
Locks out Bed Height control at all locations (Siderail, Pendant,
Patient Bed Up/ Headend) with the exception of the operator controls located on the
5
Down Lock Footboard. The Patient Bed Up/Down Lock button will illuminate light
when activated.
6 Trendelenburg Lowers head end and raises foot end of bed.
Reverse
7 Lowers foot end and raises head end of bed
Trendelenburg
8 Bed up Raises bed.
9 Bed Down Lowers bed.
MOTION

10 Fowler Up. Raises Fowler.

11 Fowler Down Lowers Fowler.
12 Gatch Up Raises Gatch.
13 Gatch Down Lowers Gatch.
When activated, the knee will raise, the Fowler will raise or lower to
14 Cardiac Chair approximately 520 degrees and the bed will tilt to approximately -120
Reverse Trendelenburg (foot end down).
Activates electronic CPR function; flattens litter and puts bed in low
15 CPR Drop
height.

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 Optional iBed Awareness Operation Guide

FOOTBOARD CONTROL PANEL FUNCTIONS (CONTINUED)

18 20 22 24

16 17 19 21 23 25

Button Name Function

Activates BED EXIT system. The selected zone graphic will illuminate
BED EXIT

16 Bed Exit Arm/Disarm when activated. When Bed Exit is in alarm mode, press “Arm/Disarm”
to turn Bed Exit “Off”.

17 Zone Control Changes the Zone.

SCALE

18 Scale Turns Scale system ON/OFF.

19 Zero Zeroes Bed.

20 iBed On/Off Turns iBed Awareness system ON/OFF.

21 Menu Access MENU selections.

iBED/MENU

22 Menu Up Scroll Up through menu.

23 Menu Down Scroll Down through menu.

Exit Exits or Escapes from menu selection; also used to Save and/or
24
X Cancel operations.
Enter
25 Selects menu item; also used to Save and/or Cancel operations.
P

Note
iBed Awareness options populated with Chaperone® Bed Exit features without Zone Control will not have button 17.

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 Optional iBed Awareness Operation Guide

LED INDICATORS: FOOTBOARD

The LEDs inform the operator of various product conditions as listed below.

L N
C
M

B D E G

Button Name: Function LED Indicator

Bed Motion Lock LED: LED is illuminated if Bed Motion is locked; blinking if
B AMBER
motion is attempted when lock is “On”.
Fowler 30+ Lock LED: LED is illuminated if Fowler 30+ is locked; blinking if
C AMBER
locked and motion is attempted; flashing if lock condition is violated by CPR.
Patient Control Fowler Lock LED: LED is illuminated if the Patient Fowler Lock
D AMBER
is “On”.
Patient Control Gatch Lock LED: LED is illuminated if the Patient Gatch Lock
E AMBER
is “On”.
Patient Control Bed Up/Down Lock LED: LED is illuminated if the Patient Bed
G AMBER
Up/Down Lock is “On”.
L Zone 1 LED: LED is illuminated when Bed Exit is “On” and Zone 1 activated. AMBER
M Zone 2 LED: LED is illuminated when Bed Exit is “On” and Zone 2 activated. AMBER
N Zone 3 LED: LED is illuminated when Bed Exit is “On” and Zone 3 activated. AMBER

Note
iBed Awareness options populated with Chaperone® Bed Exit features without Zone Control will not have items
M or N.

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 Optional iBed Awareness Operation Guide

LED INDICATORS: DASHBOARD

A F H K I P R S

Button Name: Function LED Indicator

A Bed Motion Lock LED: LED is illuminated when Bed Motion Lock is activated. AMBER

Patient Control Lock LED: LED is illuminated when any of the Patient Control
F AMBER
(Fowler, Gatch, Bed Up/Down) Lock buttons are activated.
Low Height LED: LED is illuminated when bed is in low height. The LED will
H blink if the iBed Awareness system is “On”, the low height is being monitored, AMBER
and the bed is not in low height.
Bed Exit LED: LED is illuminated when the Bed Exit is armed. The LED will
I AMBER
blink if the Bed Exit is turned Off while the iBed Awareness system is turned On.
Brake LED: LED is illuminated when the brake is set, and will blink if the brake
K AMBER
is not set.
P Bed Zero LED: LED is illuminated if Bed Zero is successful. AMBER
Siderail LED: LED is illuminated if iBed Awareness system is “On”. The LED
R AMBER
will blink when siderail state has changed.
S Power LED: LED is illuminated when bed has power. GREEN

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www.stryker.com 3002-509-001 REV B 43
 Optional iBed Awareness Operation Guide

DISPLAY SCREENS

There are 4 types of display screens listed by priority below with one being the highest.

Screen Type Priority

Bed Exit Alarm Message 1
Alarm Indications
Brake Alarm Message 2
iBed Awareness Alert Messages 3
Messages
Conditional Message 4
Menus Main Menu 5
Status Screen Default Screen 6
A. Power Up
• The initialization screen shown in Figure 1 will be displayed on power up.
B. Status Screen (without iBed Wireless option)
• Figure 2a shows an example of the default “Status” Screen.
• Information on this screen includes the ‘Fowler Angle’ and the
‘Trend Angle’ values.
• If this screen is inactive for 60 seconds, the Backlighting will
be reduced.
C. Status Screen (with iBed Wireless option)
• Figure 2b shows an example of the default “Status” Screen.
Figure 1
• Information on this screen includes the WiFi and iBed Locator
connection status, ‘Fowler Angle’ and the ‘Trend Angle’
values.
• If this screen is inactive for 60 seconds, the Backlighting will
be reduced.

230 -120
Icons
X
Figure 2a
Not
Wireless
Connected;
Connectivity Connected
Trying to
Status
Connect
Signal
None Low Good Excellent
Strength Level
X < -90
230 300.6lbs -120
Signal -90 dB ≤ -71 dB ≤
dB or X ≥ -57 dB
Strength, X X < -71 dB X < -57 dB
X = 0 dB Figure 2b

D. Message Screen
• As required message screens are provided during alarm conditions and user interaction with the bed.
E. Main Menu
• The Menu screen provides of list of available features accessible to the operator.

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 Optional iBed Awareness Operation Guide

DISPLAY SCREENS (CONTINUED)

Main Menu Screen

• The Main Menu contains selectable product features to the caregiver.

• There are eight features listed in the main menu as ordered below:
1. Weight Log (Weight Log is the Default Selection)
2. Gain/Loss
3. Change Equip. (Change Equipment)
4. Change Ptnt. Wgt. (Change Patient Weight)
5. Scale Units (Change Scale Units)
6. Backlight (Backlighting)
7. Advanced Options
8. Exit Menu
• To select a feature, press the “Menu Up” and “Menu Down” button to scroll to the desired feature and press
the “Enter/P” button.

1. Weight Log

• This feature provides the operator with up to 10 of the last weights

logged by the scale system as shown in Figure 3.

Figure 3

2. Gain/Loss

• This feature provides information to the caregiver on the weight gain or

loss of the patient.

To enable: Hold Enter to Enable

• Select “Gain/Loss” in the menu then press the “Enter/P” button,
Figure 4 will be displayed.
• When “Release Button” message flashes on the display, release Figure 4
the “Enter/P” button; “Do Not Touch Bed” message will flash on
the display.
• When Gain/Loss is On, “Gain/Loss Enable” message displays.

NOTE: Refer to Figure 5

• The base represents the scale weight when the gain/loss feature was
enabled.
• The second piece of information represents the “Gain” or the “Loss” Figure 5
and the weight difference between the current displayed weight and the
saved base weight.
•
NOTE: Refer to Figure 6
• If the Gain or the Loss exceeds 99.9 lb, then the system will display ‘---’
instead of a value.

Figure 6

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 Optional iBed Awareness Operation Guide

DISPLAY SCREENS (CONTINUED)

Main Menu (Continued)

3. Change Equipment

The change equipment feature allows the operator to add or remove item
from the product without affecting the patient weight.
Hold to
To Change Equipment:
• Select “Change Equip.” in the menu then press the “Enter/P” button,
Change Equipment
Figure 7 will be displayed.
• When “Release to Start” message displays on the screen, release
the “Enter/P” button; “Do Not Touch Bed” message will flash on Figure 7
display.
• Figure 8 will display when the system is ready to change equipment.
• Press the “Enter/P” button to Add/Remove equipment or press the
“Exit/X” button to cancel operation.
• If “Enter/P” is pressed to Add/Remove Equipment then the
message “Do Not Touch Bed” will flash on the display.
• If “Exit/X” is pressed, “Operation Canceled” message will
display. Figure 8
• Figure 9 will be displayed when the system completes the change
equipment adjustment.

Equipment
Changed
4. Change Patient Weight

The change patient feature allows the operator to add or remove weight from Figure 9
the patient weight.

To Change Patient Weight:

• Select “Change Pnt. Wgt.” in the menu.
• Press and hold the “Enter/P” button, Figure 10 will be displayed.
• When “Release Button” message displays on the screen, release
the “Enter/P” button; “Do Not Touch Bed” message will flash on
Hold to Change
display.
• When the system is ready to change patient weight the following Patient Weight
information will be displayed:
- Allow used to Change patient Weight using arrow button;
- Display the new patient weight; Figure 10
- Press” Enter/P” when done;
- Press “Exit/X” to cancel operation.
• If “Enter/P” is pressed, the message “Do Not Touch Bed” will flash on the display.
• If “Exit/X” is pressed, “Patient Weight Changed” message will display.

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 Optional iBed Awareness Operation Guide

DISPLAY SCREENS (CONTINUED)

Main Menu (Continued)

5. Scale Units

• The Change Scale Units feature allows the operator to select the unit of
value (lb or kg) for the scale information that is presented on the display.
• When the change scale units is selected, Figure 11 is displayed.
• This screen will highlight the current scale unit setting.
• To change the scale unit setting, scroll to the desired setting and press
the “Enter/P” button.
• The default setting is “Pounds [lb]”
Figure 11

6. Backlight

• When the backlight feature is selected the display will change to the backlight selection screen as shown in
Figure 12.
• This screen will highlight the current backlight setting.
• Five settings are available for the backlight; Off, Low, Medium, High, and
Nurse Call Only.
• To change the backlight setting; scroll to the desired setting and press
the “Enter/P” Button; “Save Successful” message will display.
• The default setting is “Low”.
Figure 12

7. Advanced Options

The advanced menu items include:

1. Choose Exit Alarm
2. Brake Alarm
3. Bed Status Alarm
Awareness Alarm (iBed® Wireless Option)
4. Status to N/C
5. Exit Menu

Choose Exit Alarm

The caregiver can choose between 10 exit alarms.

To Select Alarm:
• Select “Choose Exit Alarm” from the menu.
• Scroll through the 10 Tone Patterns listed in the menu. A sample alarm will sound for each Tone Pattern
highlighted.
• Select desired Tone Pattern and Press “Enter/P”
• “Save Successful” message will be displayed.

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 Optional iBed Awareness Operation Guide

DISPLAY SCREENS (CONTINUED)

Main Menu / Advanced Options (Continued)

Brake Alarm

The caregiver can enable or disable a brake alarm feature. If the brakes are not engaged and the bed is
plugged in an audible alarm will occur. This feature is only available on non-Zoom beds.

To Enable/Disable Brake Alarm:

• Select “Brake Alarm” from the menu.
• Use the Up and Down Arrow buttons to select enable or disable the alarm.
• Press “Enter/P” to save the alarm state.
• “Save Successful” message will be displayed.

Bed Status Alarm (iBed Awareness Audible Alarm)

Awareness Alarm (iBed® Wireless Option) (iBed Awareness Audible Alarm)

The caregiver can enable or disable an audible alarm for iBed Awareness alert states.

To Enable/Disable Alarm:
• Select the applicable alarm option from the menu.
• Select “On” to Enable or “Off” to disable and then press “Enter/P”
• “Save Successful” message will be displayed.

Status Nurse Call (iBed Awareness Priority Signal)

The caregiver can enable or disable a priority signal alarm through the Nurse call system based on an iBed
Awareness alarm state.

To Enable/Disable Alarm:
• Select “Status to N/C” from the menu.
• Select “On” to Enable or “Off” to disable and then press “Enter/P”
• “Save Successful” message will be displayed.

8. Exit Menu

Exits Main Menu screen and returns display to the default Status Screen.

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 Optional iBed Awareness Operation Guide

IBED AWARENESS FUNCTIONALITY

• The iBed Awareness provides functionality that will monitor status conditions on the product and produce an alert
if the state had changed.
• When the system is turned “On”, it monitors each of the siderail positions and brake automatically. If the bed is in
Low Height and/or Bed Exit is armed, the system will also monitor these features when bed status is turned “On”.
• In the event of a power loss, the iBed Awareness system will operate in the last known condition when power is
restored.
• iBed Awareness will not be able to be turned “On” if any system error conditions exist that impede the function of
the iBed Awareness system. The system errors that affect this feature include the four side rail sensors and the
scale system. For details on error codes, refer to the Maintenance Manual.

IBED AWARENESS LIGHT BAR

A light bar, located centrally on the front of the footboard, will illuminate and indicate the state of the iBed Awareness
system.

Features
• When the iBed Awareness system is “On” the light bar turns green.
• If an alert state on the iBed Awareness system is triggered, the light bar will change to the alert state and
flash AMBER.
• During an alert state, an AMBER dashboard LED associated with the alert will blink on the footboard and the
display screen will show the details of the alert state.

IBED AWARENESS SIDE LEDS

LEDs, located on each side of the bed near the foot end, will provide an indication of an alert state.

Features

• If an alert state on the iBed Awareness system is triggered, the side LEDs will change to the alert state and
blink AMBER.
• During an alert state, an AMBER dashboard LED associated with the alert will blink on the footboard and the
display screen will show details of the alert state.

IBED AWARENESS BUTTON

The iBed control button is used to turn the iBed Awareness system “On” and “Off”.

Features
When the button is pressed the iBed Awareness system will save information based on the current state of the product
and based on the system rules.

Turning on the iBed Awareness system

1. Press the iBed On/Off button.
2. The following message will be displayed on the screen: “Bed Status On”.

Turning off the iBed Awareness system

1. Press and hold the iBed On/Off button.
2. The following message will be displayed on the screen: “Bed Status Off”.

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 Optional iBed Awareness Operation Guide

IBED AWARENESS MONITORING AND ALARMS

Low Height
• If the low height state changes:
1. The low height LED on the dashboard blinks and the display screen flashes between Figure 13 message
and Figure 14 message.

Figure 13 Figure 14

Brakes

• If the brake state changes:

1. The brake LED on the dashboard blinks and the display screen flashes between Figure 15 message and
Figure 16 message.

Figure 15 Figure 16

Siderails

• If the siderail state changes:

1. The siderail LED on the dashboard blinks and the display screen flashes between Figure 17 message and
Figure 18 message.

Figure 17 Figure 18

Note
The arrow pointing to the siderail in Figure 17 and 18 will change depending on the siderail position in alarm.

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 Optional iBed Awareness Operation Guide

IBED AWARENESS MONITORING AND ALARMS (CONTINUED)

Bed Exit
• If the bed exit is disarmed:
1. The bed exit LED on the dashboard blinks and the display screen flashes between Figure 19 message
and Figure 20 message.

Figure 19 Figure 20

Additional Alarm Conditions

• If an audible alarm is required, the caregiver can set the bed status alarm to “On” through the Advanced
Options Menu in the Main Menu.
• If the caregiver would like to set the bed status alarm to the Nurse Call Station, the “Status to N/C” must be
turned “On” through the Advanced Options Menu in the Main Menu.

Note
• By default these two advanced options are turned “Off”.

IBED AWARENESS LOCKS

Fowler 30+ Lock button

• The Fowler 30+ Lock is a dual purpose button. It positions the bed’s fowler 300 to the horizontal and locks
any Fowler motion below 300.
• When the Fowler 30+ button is pressed, the bed will reposition only if it is below 300 and Figure 21 will be
displayed.
• Once the bed reaches its final position (Trend Angle = 00, Fowler Angle = 300), Figure 22 will be displayed.
• If the button is not held until the final position is reached Figure 23 will be displayed.
• If bed is put in CPR position manually or by pressing the CPR button, Figure 24 will be displayed.

Figure 21 Figure 22

Lock Violation, Turn

Off Lock or Raise
Fowler
Figure 23 Figure 24

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 Optional iBed Awareness Operation Guide

IBED AWARENESS LOCKS (CONTINUED)

Bed Motion Lock

• If Bed Motion lock button is pressed Figure 25 will be displayed.

• If Bed Motion lock button is pressed when already “on” then Figure 26 will be displayed.

Figure 25 Figure 26

• If Motion is attempted when lock is “On”, Figure 27 and 28 are displayed.

Note: CPR Drop button overrides locks.

Figure 27 Figure 28

Patient Control Locks

• If the Patient Control lock button is pressed Figure 25 as shown above will be displayed.
• If the Patient Control lock button is pressed when already “on” then Figure 26 as shown above will be
displayed.

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52 3002-509-001 REV B www.stryker.com
 Optional Infrared (IR) Module

2 3

Item Name Function

Provides infrared communications with the iBed
1 IR (Infrared) Lens
Locator.
Provides connection status for IR (infrared)
communications with iBed Locator.

Slow Flash - attempting to connect to iBed Locator.

2 iBed Locator Connection LED Solid LED - iBed Locator connected.
Rapid Flash - Error condition detected.
OFF - iBed Locator is not trying to connect. This
occurs only on ZOOM® and Battery Backup beds when
the brake is released.
Provides connection status for WiFi (wireless)
communications with wireless access point.

3 Wireless (WiFi) Connection LED Slow Flash - WiFi attempting to connect.

Solid LED = WiFi connected.
Rapid Flash - WiFi was not connected after 6 minutes
and timed out.

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 Optional iBed Locator

The Optional iBed Locator component provides iBed Locator ID and battery status information to the IR Module.
Installation and operational procedures for the Optional iBed Locator are located in the iBed Locator Instructions For
Use manual (5212-009-101).

Item Name Function

1 IR (Infrared) Lens Provides Infrared communications with the iBed IR Module.

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54 3002-509-001 REV B www.stryker.com
 Preventative Maintenance
Beds require an effective maintenance program, we recommend checking these items annually. Use this sheet for
your records. Keep on file.

CHECKLIST
_____ All fasteners secure (reference all assembly prints).
_____ Engage brake pedal and push on the bed to ensure all casters lock securely.
_____ Inspect the brake assembly (Brake Cam, Brake Plate Body, Brake Ratchet Spring and Brake Bar) for
degradation or signs of wear at the foot end and head end of the bed. Ensure brake assembly components
are functioning properly.
_____ “Brake Not Set” LED on the footboard (iBed Awareness option only) blinks when brakes are not engaged.
_____ “Brake” LED on the footboard (iBed Awareness option only) blinks when brakes are not engaged.
_____ Locking steer caster engages and disengages properly.
_____ Siderails move, latch and stow properly.
_____ CPR release working properly.
_____ Optional foot prop intact and working properly.
_____ I.V. pole working properly.
_____ Foley bag hooks intact.
_____ Optional CPR board not cracked or damaged and stores properly.
_____ No cracks or splits in head and footboards.
_____ No rips or cracks in mattress cover.
_____ All functions on head end siderails working properly (including LEDs).
_____ All functions on footboard working properly (including LEDs).
_____ Scale and Bed Exit system calibrated properly.
_____ Motion Interrupt switches working properly.
_____ Night light working properly.
_____ Power cord not frayed.
_____ No cables worn or pinched.
_____ All electrical connections tight.
_____ All grounds secure to the frame.
_____ Ground impedance not more than 100 mΩ (milliohms).
_____ Current leakage not more than 300 μA (microamps).
_____ Apply grease to the bed grease points including the fowler clutch and brake cam.
_____ Engage drive wheel and ensure it is operating properly (Zoom option).
_____ Motion release switches working properly (Zoom option).
_____ Confirm Head End Control Panel functionality (Zoom option).
_____ Confirm battery powered functionality (Zoom option).
_____ Ensure ground chains are clean, intact, and have at least two links touching the floor.
_____ Check Fowler angle for accuracy 00 - 600 (iBed Awareness option).
_____ Siderail switches working properly (iBed Awareness option).
_____ iBed Awareness Light Bar LEDs working properly (iBed Awareness option).
_____ iBed Awareness Side Indicator LEDs working properly (iBed Awareness option).
_____ Inspect footboard control labeling for signs of degradation (iBed Awareness option).
_____ Check labels as specified in the Operations and Maintenance manuals for legibility, proper adherence and
integrity.
_____ Wireless connection to access point is working properly.
_____ Bed properly connects to the iBed Locator.
_____ Confirm iBed® Wireless Module and IR Module are intact and footboard icons are displaying
(iBed® Wireless Option).
Bed Serial Number:

Completed by: _______________________________________ Date: ___________________

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www.stryker.com 3002-509-001 REV B 55
 Siderail Operation Guide

INSIDE SIDERAIL FUNCTION GUIDE

Function Display

Patient’s Left Rail Patient’s Right Rail

1. Push to raise Fowler. 1. Push to raise Knee Gatch.

2. Push to lower Fowler. 2. Push to lower Knee Gatch.
3. Push to raise Knee Gatch. 3. Push to raise Fowler.
4. Push to lower Knee Gatch. 4. Push to lower Fowler.

Optional Nurse Call Optional TV / Radio

1. Push to activate Nurse Call. 1. Push to turn TV or radio on

and to select a channel.
Note 2. Push to increase volume.
Yellow LED will light when button 3. Push to decrease volume.
is pushed.
Red LED will light with Nurse
Station acknowledgment.

This panel is optional equipment. This panel is optional equipment.

Optional Lights Optional SMTV

Channel/Volume
1. Push to turn the room light
on. 1. Push to change TV channel
2. Push to turn the bed over- up.
head light on. 2. Push to change TV channel
down.
3. Push to mute TV volume.
This panel is optional equipment. Push again to turn the sound
back on.
4. Push to display the closed
captioning. Push again
to turn off the closed
captioning.

This panel is optional equipment.

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 Siderail Operation Guide

OUTSIDE SIDERAIL FUNCTION GUIDE

Function Display

Optional Patient’s Optional Patient’s

Left Rail Right Rail

1. Push to raise Fowler. 1. Push to raise Knee Gatch.

2. Push to lower Fowler. 2. Push to lower Knee Gatch.
3. Push to raise Knee Gatch. 3. Push to raise Fowler.
4. Push to lower Knee Gatch. 4. Push to lower Fowler.

Raise/Lower Bed Optional Nurse Call

1. Push to raise bed height. 1. Push to activate Nurse Call.

2. Push to lower bed height.

This panel is optional equipment.

Optional Cardiac Chair

Brake Not Set LED
1. Push to activate the Cardiac
1. LED will blink when the Chair function.
brakes are not set. 2. The Knee will raise.
3. The back will raise or lower to
approximately 520
4. The bed will tilt to ap-
proximately −120 reverse
Trendelenburg (foot end down).
5. For Short Beds it will tiltl approximatley −100.
6. Release the button to stop bed movement; hold
the button until movement stops to complete the
function.

This panel is optional equipment.

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 Product Labels

Part Name/Number Product Label

Bed Exit
3006-508-109
(Optional)

Bed Exit with Zone Control

3006-508-106
(Optional)

Scale System
3006-508-107
(Optional)

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58 3002-509-001 REV B www.stryker.com
 Product Labels

Part Name/Number Product Label

Awareness Status
3006-508-108
(Optional)

WiFi Capable Wi-Fi

3003-508-105 Capable

Wi-Fi
Capable
WiFi CPU Cover
3003-300-105 CPU P/N
3003-408-900
ONL Y

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www.stryker.com 3002-509-001 REV B 59
 Cleaning

Hand wash all surfaces of the bed with warm water and mild detergent. DRY THOROUGHLY. Do not steam clean or
hose off the Secure II Bed. Do not immerse any part of the bed. Some of the internal parts of the bed are electric
and may be damaged by exposure to water.

Suggested cleaners for bed surfaces:

• Quaternary Cleaners (active ingredient − ammonium chloride)

• Phenolic Cleaners (active ingredient − o−phenylphenol)
• Chlorinated Bleach Solution (5.25% − less than 1 part bleach to 100 parts water)

Avoid over saturation and ensure the product does not stay wet longer than the chemical manufacturer’s guidelines
for proper disinfecting.

CAUTION
SOME CLEANING PRODUCTS ARE CORROSIVE IN NATURE AND MAY CAUSE DAMAGE TO THE PRODUCT IF USED
IMPROPERLY. If the products described above are used to clean Stryker patient care equipment, measures must be
taken to insure the beds are wiped with a damp cloth soaked in clean water and thoroughly dried following cleaning.
Failure to properly rinse and dry the beds will leave a corrosive residue on the surface of the bed, possibly causing
premature corrosion of critical components. Failure to follow the above directions when using these types of cleaners
may void this product’s warranty.

For mattress cleaning instructions, please see the tag on the mattress, or contact the mattress manufacturer.

Clean Velcro AFTER EACH USE. Saturate Velcro with disinfectant and allow disinfectant to evaporate. (Appropriate
disinfectant for nylon Velcro should be determined by the hospital).

Virex® TB is not an approved cleaning agent for this product. Do not use for bed cleaning.

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60 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 3002-300-896 (Reference Only)

A
B

Item Recycling/Material Code Important Information Qty

A (3002-407-950) CPU Board 1
A (3003-407-900) CPU Board (iBed Awareness Option Only) 1
A (3003-408-900) CPU Board (iBed® Wireless Option Only) 1
B (0059-157-000) Power Supply 1

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www.stryker.com 3002-509-001 REV B 61
 Recycling Passport

Assembly Part number: Reference Only)

3001-400-040 (Left)
3001-400-045 (Right)

Left Siderail Shown

Assembly Part number: 3001-400-035 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3001-400-930) Siderail Inner PCB, Left 1
(3001-400-930) Siderail Inner PCB, Right 1
B (3001-400-910) Siderail Outer PCB 1

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62 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 3001-303-045 (Reference Only)

Head End, Patient Left Side

Item Recycling/Material Code Important Information Qty

A (3000-303-871) Battery 9V 1

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 Recycling Passport

Assembly Part number: 3001-314-012 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3001-314-920) Pendant Port PCB 1

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64 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 3001-500-028 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3001-500-930) Footboard PCB 1

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www.stryker.com 3002-509-001 REV B 65
 Recycling Passport

Assembly Part number: 3004-553-011 (iBed Awareness) (Reference Only)

3004-554-011 (iBed® Wireless) (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3003-500-900) Footboard PCB iBed Awareness Option 1
A (3003-502-900) Footboard PCB iBed® Wireless Option 1

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66 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 3002-507-030 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3001-507-910) Scale Keypad 1

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 Recycling Passport

Assembly Part number: 3002-508-030 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3002-508-900) Bed Exit Board 1

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68 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 3001-508-030 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (3001-508-910) Bed Exit 1
Keypad Assembly

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www.stryker.com 3002-509-001 REV B 69
 Recycling Passport

Assembly Part number: 5212-300-053 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (5212-300-930) 1
IR Module PCB Assembly

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70 3002-509-001 REV B www.stryker.com
 Recycling Passport

Assembly Part number: 5212-300-012 (Reference Only)

Item Recycling/Material Code Important Information Qty

A (5212-300-910) 1
Wireless Module PCB Assembly

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www.stryker.com 3002-509-001 REV B 71
 EMC Information

MEDSURG BED, MODEL 3002 SECURE II

Guidance and Manufacturer’s Declaration - Electromagnetic Immunity

The MedSurg Bed, Model 3002 Secure II is suitable for use in the electromagnetic environment specified below. The
customer or the user of the MedSurg Bed, Model 3002 Secure II should ensure that it is used in such an environment.
Electromagnetic
Immunity Test IEC 60601 Test Level Compliance Level
Environment Guidance
Electrostatic Discharge (ESD) +6 kV contact +6 kV contact Floors should be wood,
IEC 61000-4-2 +8 kV air +8 kV air concrete, or ceramic tile.
If floors are covered with
synthetic material, the relative
humidity should be at least
30%.
Electrostatic fast +2 kV for power +2 kV for power Main power quality should be
Transient/burst supply lines supply lines that of a typical commercial or
IEC 61000-4-4 +1 kV for input/ +1 kV for input/ hospital environment.
output lines output lines
Surge +8 kV differential mode +8 kV differential mode Main power quality is that of
IEC 61000-4-5 +2 kV common mode +2 kV common mode a typical commercial and/or
hospital environment.
Voltage dips, voltage <5%Ut (95% dip in Ut) for <5%Ut (95% dip in Ut) Main power quality should be
variations and short 0.5 cycle for 0.5 cycle that of a typical commercial
interruptions on power supply 40%Ut (60% dip in Ut) for 40%Ut (60% dip in Ut) and/or hospital environment. If
input lines 5 cycles for 5 cycles the user of the MedSurg Bed,
IEC 61000-4-11 70%Ut (30% dip in Ut) for 70%Ut (30% dip in Ut) Model 3002 Secure II requires
25 cycles. for 25 cycles. continued operation during
<5% Ut (>95% dip in Ut) <5% Ut (>95% dip in Ut) power main interruptions,
for 5 sec. for 5 sec. it is recommended that the
device be powered from an
uninterrupted power supply or
a battery.
Power frequency (50/60 Hz) 3 A/m 3 A/m Power frequency magnetic
magnetic field fields should be at levels
IEC 61000-4-8 characteristic of a typical
location in a typical commercial
and/or hospital environment.
Note: UT is the a.c. mains voltage prior to applications of the test level.

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 EMC Information

MEDSURG BED, MODEL 3002 SECURE II (CONTINUED)

Recommended separation distances between portable and mobile RF

communications equipment and the MedSurg Bed, Model 3002 Secure II.
The MedSurg Bed, Model 3002 Secure II is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the MedSurg Bed, Model 3002 Secure II can help prevent
electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications
equipment (transmitters) and the MedSurg Bed, Model 3002 Secure II as recommended below, according to the
maximum output power of the communications equipment.
Rated maximum output Separation distance according to frequency of transmitter
power of transmitter
W m
150 kHz to 80 MHz 80 MHz to 800 MHz 8000 MHz to 2.5 GHz
d=1.2 d=1.2 d=2.3

0.01 1.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

Note 1
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

Note 2
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.

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 EMC Information

MEDSURG BED, MODEL 3002 SECURE II (CONTINUED)

The MedSurg Bed, Model 3002 Secure II is suited for use in the electromagnetic environment specified below. The
customer or the user of the MedSurg Bed, Model 3002 Secure II should ensure that it is used in such an environment.
Compliance
Immunity Test IEC 60601 Test Level Electromagnetic Environment - Guidance
Level
Portable and mobile RF communications
equipment should be used no closer to any
part of the MedSurg Bed, Model 3002 Secure
II, including cables, than the recommended
separation distance calculated from the
equation appropriate for the frequency of the
transmitter.

Recommended Separation Distance

Conducted 3 Vrms 3 Vrms
RF 150 kHz to 80 MHz d=1.2
IEC 61000-4-6

Radiated RF 3 V/m 3 V/m

IEC 61000-4-3 80 MHz to 2.5 GHz d=1.2

d=2.3
800 MHz to 2.5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according to
the transmitter manufacturer and d is the rec-
ommended separation distance in metres (m).

Field strengths from fixed RF transmitters,

as determined by an electromagnetic site
survey,a should be less than the compliance
level in each frequency range.b

Interference may occur in the vicinity of

equipment marked with the following symbol:

Note 1
At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location in which the MedSurg Bed, Model 3002 Secure
II is used exceeds the applicable RF compliance level above, the MedSurg Bed, Model 3002 Secure II should be
observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary,
such as reorienting or relocating the MedSurg Bed, Model 3002 Secure II.

b
Over the frequency range 150 kHz to 80 MHz, field strengths are less than 3 V/m.
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 EMC Information

MEDSURG BED, MODEL 3002 SECURE II (CONTINUED)

Guidance and Manufacturer’s Declaration - Electromagnetic Emissions

The MedSurg Bed, Model 3002 Secure II is intended for use in an electromagnetic environment specified below. The
customer or the user of the MedSurg Bed, Model 3002 Secure II should ensure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment
Group 1,
The MedSurg Bed, Model 3002 Secure II uses RF energy
without iBed Wireless option
RF Emissions only for its internal function. Therefore, its RF emissions
CISPR 11 are very low and are not likely to cause any interference
Group 2,
in nearby electronic equipment.
with iBed Wireless option
The MedSurg Bed, Model 3002 Secure II is suitable
for use in all establishments other than domestic and
RF Emissions
Class A those directly connected to the public low voltage power
CISPR 11
supply network that supplies buildings used for domestic
purposes.

Harmonic Emissions
Class A
IEC 61000-3-2

Voltage Fluctuations
Flicker Emissions Complies
IEC 61000-3-3

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 Warranty

LIMITED WARRANTY

Stryker Medical Division, a division of Stryker Corporation, warrants to the original purchaser the Secure II Med-Surg
Bed to be free from defects in material and workmanship for a period of one (1) years after date of delivery. Stryker’s
obligation under this warranty is expressly limited to supplying replacement parts and labor for, or replacing, at its
option, any product which is, in the sole discretion of Stryker, found to be defective. If requested by Stryker, products
or parts for which a warranty claim is made shall be returned prepaid to the factory. Any improper use or any alteration
or repair by others in such manner as in Stryker’s judgment affects the product materially and adversely shall void this
warranty. Any repair of Stryker products using parts not provided or authorized by Stryker shall void this warranty. No
employee or representative of Stryker is authorized to change this warranty in any way.

Stryker Medical Bed products are designed for a 15 year expected service life under normal use, conditions, and with
appropriate periodic maintenance as described in the maintenance manual for each device. Stryker warrants to the
original purchaser that the welds on its Bed products will be free from structural defects for the expected 15 year life
of the Bed product as long as the original purchaser owns the product.

Stryker Medical optional components and/or accessories are warranted as follows:

• iBed® Wireless Components: Ten (10) years service life under normal use and proper care

This statement constitutes Stryker’s entire warranty with respect to the aforesaid equipment. Stryker makes no
other warranty or representation, either expressed or implied, except as set forth herein. There is no warranty
of merchantability and there are no warranties of fitness for any particular purpose. In no event shall Stryker be
liable here under for incidental or consequential damages arising from or in any manner related to sales or use of
any such equipment.

TO OBTAIN PARTS AND SERVICE

Stryker products are supported by a nationwide network of dedicated Stryker Field Service Representatives. These
representatives are factory trained, available locally, and carry a substantial spare parts inventory to minimize repair
time. Simply call your local representative, or call Stryker Customer Service USA at 1-800-327−0770, Canada
1-888-233-6888.

SERVICE CONTRACT COVERAGE

Stryker has developed a comprehensive program of service contract options designed to keep your equipment
operating at peak performance at the same time it eliminates unexpected costs. We recommend that these programs
be activated before the expiration of the new product warranty to eliminate the potential of additional equipment
upgrade charges.

A Service Contract helps to:

• Ensure equipment reliability

• Stabilize maintenance budgets
• Diminish downtime
• Establish documentation for JCAHO
• Increase product life
• Enhance trade-in value
• Address risk management and safety

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 Warranty

SERVICE CONTRACT PROGRAMS

Stryker offers the following service contract programs:

Service Agreement Options * Premium Complete Standard

Annually scheduled preventative maintenance X X
All parts X X
All labor and travel X X
Unlimited emergency service calls X X
Priority one contact: two hour phone response X X
Most repairs completed within 3 days X X
JCAHO documentation X X X
On-site record of PM & emergency service X X
Factory-trained Stryker service technician X X X
Stryker authorized parts used X X X
Service during regular business hours (8−5) X X X

* Does not include maintenance due to abuse or for any disposable items. Stryker reserves the right to change options without notice.

Stryker Medical also offers personalized service contracts.

Pricing is determined by age, location, model and condition of product.

For more information on our service contracts,

please call your local representative.

RETURN AUTHORIZATION

Merchandise cannot be returned without approval from the Stryker Customer Service Department. An authorization
number will be provided which must be printed on the returned merchandise. Stryker reserves the right to charge
shipping and restocking fees on returned items. Special, modified, or discontinued items not subject to return.

DAMAGED MERCHANDISE

ICC Regulations require that claims for damaged merchandise must be made with the carrier within fifteen (15) days of
receipt of merchandise. Do not accept damaged shipments unless such damage is noted on the delivery receipt at
the time of receipt. Upon prompt notification, Stryker will file a freight claim with the appropriate carrier for damages
incurred. Claim will be limited in amount to the actual replacement cost. In the event that this information is not
received by Stryker within the fifteen (15) day period following the delivery of the merchandise, or the damage was not
noted on the delivery receipt at the time of receipt, the customer will be responsible for payment of the original invoice
in full. Claims for any short shipment must be made within thirty (30) days of invoice.

INTERNATIONAL WARRANTY CLAUSE

This warranty reflects U.S. domestic policy. Warranty outside the U.S. may vary by country. Please contact your local
Stryker Medical representative for additional information.

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www.stryker.com 3002-509-001 REV B 77
 UNITED STATES
Stryker Medical
3800 E. Centre Ave.,
Portage, Michigan USA
49002

EC REP

European Representative
Stryker France S.A.S.
ZAC – avenue Satolas Green
69881 MEYZIEU Cedex
France

2011/12 3002-509-001 REV B www.stryker.com