Stryker InTouch FL27 series User manual

Operations Manual
InTouch®Critical Care Bed
InTouch®Intensivpflegebett
Letto per terapia intensiva InTouch®
InTouch®-bed voor kritieke zorg
Κρεβάτι εντατικής θεραπείας InTouch®
Model/Modell/Modello/Μοντέλο FL27 (2131/2141)
Version 2.5
2012/04 B.22131-309-005 REV B www.stryker.com
For parts or technical assistance call:
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Voor onderdelen of technische bijstand belt u:
Για εξαρτήματα ή τεχνική βοήθεια καλέστε:
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Canada/Kanada/Καναδάς: 1-888-233-6888
Bedienungsanleitung
Manuale d’uso
Gebruikshandleiding
Εγχειρίδιο λειτουργιών
REF
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EASTERN EUROPE
Stryker SA - Export Business
Grand-Rue 90
P.O. Box 1567
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
AUSTRALIA
Stryker Australia
8 Herbert Street
St Leonards NSW 2065
Australia
Phone: [phone]
Fax: [phone]
AUSTRIA
Stryker-Howmedica Osterreich GmbH
Millenium Tower
Handelskai 94-96
120 Wien
Austria
Phone: [phone]
Fax: [phone]
BELGIUM
NV Stryker SA
Ikaros Business Park- Fase III
Ikaroslaan 12
1930 Zaventem, Brussels
Belgium
Phone: [phone]
Fax: [phone]
DENMARK
Stryker Denmark
Filial of Stryker AB
Postbox 772
1532 Copenhagen
Denmark
Phone: [phone]
Fax: [phone]
NORWAY
Stryker Norway
Norsk Fillial
Nedre Vollgate 3
0158 Oslo
Norway
Phone: [phone]
Fax: [phone]
POLAND
Stryker Polska Sp. ZO.O
Kolejowa 5/7
01-217 Warsawa
Poland
Phone: [phone]
Fax: [phone]
PORTUGAL
Stryker Portugal Produtos
Medicos, LTDA.
Avenida Marechal Gomes
da Costa, 35
1800-255 Lisboa
Portugal
Phone: [phone]
Fax: [phone]
ROMANIA
Stryker Osteonics Romania S.R.L.
19, Leonida Str.
District 2
7000 Bucharest
Romania
Phone: [phone]
Fax: [phone]
SOUTH AFRICA
Stryker Osteonis PTY. LTD.
3 Susan Street
Strydom Park
Johannesburg, 2194 - South Africa
Mailing Address:
P.O. Box 48039
2129 Roosevelt Park
Johannesburg, South Africa
Phone: [phone]
Fax: [phone]
SPAIN
Stryker Iberia SL
c/Sepulveda n17
28108 Alcobendas
Madrid
Spain
Phone: [phone]
Phone: [phone]
Fax: [phone]
SWEDEN
Stryker AB/Scandinavia
Box 50425
SE-204 14 Malmo
Sweden
Phone: [phone]
Fax: [phone]
UK/IRELAND
Stryker UK Limited
Stryker House
Hambridge Road
Newbury, Berkshire
RG14 5EG, England
Phone: [phone]
Phone: [phone]
Fax: [phone]
FINLAND
Stryker AB, Finland
PO 80 Makelankatu 2
00501 Helsinki
Finland
Phone: [phone]
Fax: [phone]
FRANCE
Stryker France S.A.S
ZAC - Avenue de Satolas Green
69330 Pusignan
France
Phone: [phone]
Fax: [phone]
GERMANY
Stryker Howmedica GmbH
Dr. Homer Stryker Platz 1
47228 Duisburg
Germany
Phone: [phone]
Fax: [phone]
GREECE
Stryker Hellas EPE
455 Messogion ave
153 43 Agia Paraskevi
Athens, Greece
Phone: [phone]
Fax: [phone]
ITALY
Stryker Italia SrL
Via Ghisalba 15B
00188 Roma
Italy
Phone: [phone]
Fax: [phone]
MIDDLE EAST / NORTH AFRICA
Stryker Osteonics SA
Twin Towers
11th Floor, Suite 1101 & 1102
P.O. Box 41446
Baniyas Road
Dubai, Deira, UAE
Phone: [phone]
Fax: [phone]
NEDERLANDS
Stryker Nederlands BV
(P.O. Box 13, 4180 BA Waardenburg)
4181 CD Waardenburg
The Nederlands
Phone: [phone]
Fax: [phone]
EUROPE HEADQUARTERS
Stryker SA
Cite-Centre, Grand-Rue 90
P.O. Box 1568
1820 Montreux, Switzerland
Phone: [phone]
Fax: [phone]
International Addresses

www.stryker.com 2131-309-005 REV B 1-1
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Table of Contents
Symbols and Definitions ...................................................................1-4
Warning / Caution / Note Definition........................................................1-5
Introduction ............................................................................1-6
Intended Use ........................................................................1-6
Brief Product Description and Intended Use Statement .........................................1- 6
Product Illustration ....................................................................1-7
Specifications .......................................................................1-8
Specifications (Continued) ..............................................................1-9
Summary of Safety Precautions ............................................................1-10
Optional Zoom®Drive System (Model 2141 Only) ............................................1-12
Setup Procedures.......................................................................1-13
Optional XPRT™ Therapy Mattress ......................................................1-14
Optional PositionPRO™ Patient Repositioning Mattress Option ..................................1-14
Applying the linens ...............................................................1-15
Optional Zoom®Drive System (Model 2141 Only) ............................................1-15
Modes of Operation .....................................................................1-16
Powering the Bed....................................................................1-16
Modes of Operation with the Battery .....................................................1-16
Base Operation Guide ...................................................................1-17
Brake / Drive / Neutral Operation ........................................................1-17
Electronic Mode .................................................................1-17
Manual Mode ...................................................................1-17
Litter Operation Guide ...................................................................1-18
CPR Emergency Release ..............................................................1-18
Lowering the Fowler During a Power Failure.............................................1-18
Foley Bag Hooks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-18
Patient Restraint Locations.............................................................1-18
Nurse Call Usage....................................................................1-19
Auxiliary Power Outlet Usage ...........................................................1-19
Head and Footboard Operation .........................................................1-19
Positioning the Siderails ...............................................................1-20
Bed Positioning .....................................................................1-21
Siderail Operation Guide..................................................................1-22
Siderail Motion Control Panel, Nurse Control ...............................................1-22
Bed Positioning Descriptions ...........................................................1-23
Siderail Brake/Motion Control Panel, Nurse Control...........................................1-2 4
Optional Pendant Control ..............................................................1-25
Footboard Operation Guide................................................................1-26
Control Panel.......................................................................1-26
System Message Indicator Lights ........................................................1-27
Main Menu: Patient Information .........................................................1-2 8
Patient Information, New Patient .....................................................1-29
Patient Information, Configure .......................................................1-29
Main Menu: Bed Controls .............................................................1-30
Main Menu: Scale ..................................................................1-31

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Table of Contents
Footboard Operation Guide (Continued)
Zero Button.....................................................................1-33
Weight History Button .............................................................1-3 4
Change Weight Button.............................................................1-35
Gain or Loss Button ..............................................................1-36
Main Menu: Bed Exit.................................................................1-38
Main Menu: Support Surfaces ..........................................................1-40
Air Mattress Options ..............................................................1-40
XPRT™ Mattress Specifications......................................................1-40
InTouch® integrated with the XPRT™ Mattress ..........................................1-40
PositionPRO™ Mattress Specifications.................................................1-41
Interaction Between InTouch® and PositionPRO™ ........................................1-41
Specific PositionPRO™ Functionality on the InTouch® .....................................1- 41
Main Menu: Options .................................................................1-42
Time Setup Button ...............................................................1-43
Smart TV Button (Optional) .........................................................1-43
Language Button.................................................................1-43
Advanced Options Button ..........................................................1-44
History Button ...................................................................1-45
Nurse Control Backlight Button ......................................................1-47
Maintenance Button ..............................................................1-47
Main Menu: Lockouts ................................................................1-48
Main Menu: iBed ...................................................................1-49
iBed, Awareness .................................................................1-49
iBed, Protocol Reminder™..........................................................1-50
iBed, Protocol Reminder™ (Continued) ................................................1-51
iBed, Head of Bed (HOB) History.....................................................1-52
iBed, Bed Height History ...........................................................1-52
iBed, Calculator .................................................................1-53
iBed, Converter..................................................................1-53
iBed, Translations ................................................................1-54
iBed, Documentation..............................................................1-55
iBed, The Braden Scale for Predicting Pressure Sore Risk ..................................1-56
iBed, Sound Therapy™ ............................................................1-57
ZOOM®Drive Operations (Model 2141) .......................................................1-58
Using the Zoom®Drive (Model 2141)......................................................1-58
Optional Bed Accessories.................................................................1-59
Bed Extender - FA64234-XXX..............................................................1-60
Permanent I.V. Pole - FA64221/FA64238 ......................................................1-61
Dual Head End Permanent I.V. Pole - FA64202 .................................................1-63
Line Management System (Accessory Clip) - FA64210............................................1-65
Monitor Tray - FA64214...................................................................1-66
Upright Oxygen Bottle Holder - FA64187 ......................................................1-68
Right Fit Oxygen Bottle Holder - FA64203 .....................................................1-69
Pendant with Motion Control Only - FA64209...................................................1-70

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Table of Contents
Optional Bed Accessories (Continued)
Pendant with Motion Control/Nurse Call - FA64194 ..............................................1-71
Pendant with Motion Control/Smart TV - FA64195 ...............................................1-72
Pendant with Motion Control/NC/Smart TV - FA64193 ............................................1-73
Pendant Clip - FA64186 ..................................................................1-74
Traction Sleeve - FA64215 through FA64219 ...................................................1-75
Wall Saver - FA64208....................................................................1-76
X-Ray Cassette Holder - FA64205...........................................................1-77
Cleaning..............................................................................1-78
Bed Cleaning.......................................................................1-78
Mattress Care ......................................................................1-78
Preventative Maintenance.................................................................1-79
Checklist ..........................................................................1-79
Recycling Passports .....................................................................1-80
Warranty .............................................................................1-96
Limited Warranty ....................................................................1-96
To Obtain Parts and Service ...........................................................1-96
Service Contract Coverage ............................................................1-96
Service Contract Programs ............................................................1-97
Return Authorization..................................................................1-97
Damaged Merchandise ...............................................................1-97
International Warranty Clause...........................................................1-97

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Symbols and Definitions
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
Protection from liquid splash
IPX4
Alternating Current
1.6 SYMBOLS
6.3A 250V
1.6 SYMBOLS
10A 250V
~
Safe Working Load
Medical Equipment approved by the Canadian Standards Association with Respect to Electric Shock,
Fire, Mechanical and Other Specified Hazards.
Potential Equalization
Protective Earth Terminal
Dangerous Voltage
Fuse Rating for Beds with the 100V~ or 120V~ Electric System
Fuse Rating for Beds with the 200V~ or 220V~ or 240V~ Electric System
Warning/Caution, consult accompanying documentation
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.
Manufacturer
Model Number

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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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INTENDED USE
This manual is designed to assist you with the operation of Stryker InTouch® Critical Care Bed Model FL27 (2131/2141).
Carefully read this manual thoroughly before using the equipment or beginning maintenance on it. To ensure safe
operation of this equipment, it is recommended that methods and procedures be established for educating and training
staff on the safe operation of this bed.
This Operations Manual is an integral part of the bed and should be included if the bed is sold or transferred.
BRIEF PRODUCT DESCRIPTION AND INTENDED USE STATEMENT
INTENDED MEDICAL INDICATIONS: InTouch is an AC-powered adjustable hospital bed designed to position patients
for procedures, therapy, and recovery in healthcare environment, transport patients between bays and procedural
rooms, provide patient security, measure and display patient weight, allow patients to alert caregiver when the patient
requires emergency assistance or any assistance to improve comfort levels, and monitor patient position to alert
caregiver of a deliberate exit or potential fall. The bed has thirty-nine prerecorded clinical phrases in 24 languages and
offers music therapy.
INTENDED PATIENT POPULATION: The intended patient population is acute-care human patients. The safe working
load (i.e. the sum of the patient, the mattress, and accessory weight) for InTouch is 550lbs (250kg). This bed is not
intended for use with patients 35 inches or less and/or patients that weigh less than 50 pounds.
INTENDED PART OF THE BODY: InTouch is intended to support a patient. It is intended to be used with a sleep surface.
The Frame can come in contact with human skin but a patient should never be on the frame without a support surface.
INTENDED USER PROFILE: InTouch is intended for use in Acute Care settings. These settings may include critical
care, step down, progressive care, med/surg, sub-acute care, and post anesthesia care unit (PACU) or other locations
as prescribed. Intended operators are health care professionals (nurses, nurse aids, doctors) which can use all bed
operations (e.g., bed motion functions, nurse call, siderail communications, bed exit, therapy options), patient and
bystander, which can use bed motion functions, nurse call & siderail communications, and trained professionals for
installation, service, and calibration.
INTENDED CONDITION OF USE AND EXPECTED LIFE: Stryker Medical Bed products are designed for a 10 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 10 year life of the Bed product as long as the original purchaser
owns the products.
The product is intended to be used in a healthcare environment, including hospitals, surgery centers, long term acute
care centers, and rehabilitation centers. The intended environmental conditions are 10 to 40 degrees Celsius and
30 to 75% RH. The product is compatible with 35” x 84” surfaces, the facility nurse call system, standard Med-Surg
equipment, and the facility infrastructure. InTouch is intended to be used with a 6”-8.5” sleep surface; asleep surface
or overlay greater than 6” that offers therapeutic value may be used with, patient supervision.
Introduction

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Nurse Control
Panel
Casters
ZOOM®Drive Wheel
(Model 2141 only)
(Under base -
not shown)
Siderails
Footboard
Control Panel
Footboard
Nurse Call
Foley Bag
Hooks
CPR Emergency
Release Pedal
Manual
Backup
Siderail
Release
Levers
Brake Control
Panel
Headboard
InTouch®
Screen
PRODUCT ILLUSTRATION
Introduction

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Introduction
SPECIFICATIONS
Safe Working Load
Note: Safe Working Load indicates the
sum of the patient, mattress and accessory
weight.
550 lbs 249 kg
Bed Weight 750 lbs 340.2 kg
Overall Bed Length 90” 228,6 cm
Overall Bed
Width
Siderails Up 42” 106,7 cm
Siderails Down 40” 102,9 cm
Base Under Bed Clearance 5” 12,7 cm
Litter Patient Surface
• Width
• Length
• Length (with Optional Bed Extender)
35”
84”
90”
88,9 cm
213,4 cm
228,6 cm
Seat Section
• Depth 18.5” 47 cm
Foot Section
• Length
• Angle 29”
0° to 50°
73,7 cm
0° to 50°
Fowler Section
• Length
• Width
• Angle
36”
34” to 35”
0° to 70°
91,4 cm
86,4 cm - 88,9 cm
0° to 70°
Gatch Section
• Length
• Width
• Angle
18”
34” to 35”
0° to 15°
45,7 cm
86,4 cm - 88,9 cm
0° to 15°
Cardiac Chair
• Standard Cardiac Chair Position
• Enhanced Cardiac Chair Position Head: 65°, Seat: 17°, Foot: 30°, Trend: 3°
Head: 70°, Seat: 19°, Foot: 47°, Trend: 3°
Fowler Length 36.5” 92,7 cm
Bed Lift
System
Height (high) to top of litter 33” 83,8 cm
Height (low) to top of litter 16” 40,6 cm
Trendelenburg/Reverse Trendelenburg 12°
Bed Lift Time 35 seconds maximum from lowest to highest position
Scale System Capacity 550 lbs 249 kg
Accuracy:
• For weight from 100 lb to 550 lb
• For weight from 100 lb to 550 lb
• For weight under 100 lb
• For weight under 100 lb
+/- 2% when in Trendelenburg or Reverse Trendelenburg
+/- 2% when Flat
+/- 2 lb when in Trendelenburg or Reverse Trendelenburg
+/- 2 lb when Flat
CPR System Speed to level bed from any position
• Fowler
• Foot and Seat
15 seconds
60 seconds
Drive System Speed (Optional ZOOM®Drive)
• Forward
• Backwards 3.6 mph
2.5 mph
5.8 km/h
4.0 km/h

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Introduction
SPECIFICATIONS (CONTINUED)
Mattress
Recommended Mattress Size
•With Bed Extender DM64196
(PositionPRO) (35” x 6” x 4”)
•With Bed Extender DM64197
(XPRT™) (35” x 6” x 5.5”)
35” x 84” x 6” 88,9 cm x 213,4 cm x 15,2 cm
35” x 90” x 4” 88,9 cm x 228,6 cm x 10,1 cm
35” x 90” x 5.5” 88,9 cm x 228,6 cm x 13,9 cm
Recommended Air Mattress Size
•With Bed Extender DM64196
(PositionPRO) (35” x 6” x 4”)
•With Bed Extender DM64197
(XPRT™) (35” x 6” x 5.5”)
35” x 84” x 6” - 8.5” 88,9 cm x 213,4 cm x
15,2 cm - 21,6 cm
35” x 90” x 4” 88,9 cm x 228,6 cm x 10,1 cm
35” x 90” x 5.5” 88,9 cm x 228,6 cm x 13,9 cm
Maximum
Current
Consumption
Without Optional Auxiliary Outlet
(120VAC Only) 4.8 Amps
With Optional Auxiliary Outlet(s)
(120VAC Only) 9.8 Amps
Environmental
Conditions
Storage
• Ambient Temperature
• Relative Humidity
• Atmospheric Pressure
-40°F to 158°F
10 to 100%
500 to 1060 hPa
-40°C to 70°C
Operating
• Ambient Temperature
• Relative Humidity
• Atmospheric Pressure
• Scale Accuracy
50°F to 104°F
30 to 75%
700 to 1060 hPa
18 °C to 25 °C
10°C to 40°C
64 °F to 77 °F
Electrical
Requirements
All electrical requirements meet CSA
C22.2 No. 601.1, UL 60601-1 and IEC
60601-1.60601-2-38 specifications.
100V~, 50-60Hz, 7.5A - Two 250V, 10A Fuses
120 ± 10% Vac, 50/60Hz - Two 250V, 10A Fuses
120V~, 50-60Hz, 4.0A (9.8A with 120V Optional Auxiliary
Outlet) - Two 250V, 10A Fuses
200V~, 50-60Hz, 3.2A -Two 250V, 6.3A Fuses
220V~, 50-60Hz, 2.9A -Two 250V, 6.3A Fuses
240V~, 50-60Hz, 2.7A -Two 250V, 6.3A Fuses
Battery
12 V, 17.6 Ahr, Sealed Lead-Acid Battery (Part Number QDF9188)
3.0 V 220mAh Lithium Battery, Size 20mm - Varta Int. CR2032
Coin Cell PC Battery Holder, Size 20mm - MDP Int. BA2032
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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Before operating the bed, it is important to read and understand all information in this manual. Carefully read and
strictly follow the safety guidelines listed below.
Note
To ensure safe operations of the bed, methods and procedures must be established for educating and training hospital
staff on the intrinsic risks associated with the usage of electric beds.
WARNING
• To prevent permanent damage to this unit, the unit must reach room temperature prior to conducting any setup
and/or unit operations.
• The Weigh system is intended to assist in the monitoring of the patient’s weight variation. Under no circumstances
should its reading be used as sole reference for medical treatment.
• Preventative maintenance should be performed at least once a year to ensure all bed features are functioning
properly.
• This bed is not intended for pediatric use, i.e, for any patient measuring 35 inches (88,9 cm) or less.
• This bed is equipped with a hospital grade plug for protection against shock hazard. It must be plugged directly
into a properly grounded receptacle. Grounding reliability can be achieved only when a hospital grade receptacle
is used.
• Shock Hazard - Improper handling of the power cord may result in damage to the power cord and potential shock
hazards. If damage has occurred to the power cord, immediately remove the bed from service and contact the
appropriate maintenance personnel. Failure to do so could result in serious injury or death.
• Serious injury can result if caution is not used when operating the bed. Operate the bed only when all people and
equipment are clear of the electrical and mechanical systems.
• Always apply the brakes when a patient is on the bed or entering/exiting the bed. Serious injury could result if the
bed moves while a patient is getting on or off the bed. Once the brake pedal is engaged, push on the bed to ensure
the brakes are securely applied. Do the same test when using the electrical brake.
• To help reduce the number and severity of a potential fall when the patient is unattended, keep the siderails in the
fully raised position and the sleep surface horizontal in its lowest position, unless his/her medical condition dictates
otherwise. When raising the siderails, be sure that you hear the “click” that signals the locked condition. Pull firmly
on the siderail to ensure it is locked into position.
• When the sleep surface sections are articulated, ensure that all the patient’s limbs are within the raised siderails
to avoid patient injury.
• When a patient’s condition requires greater safety measures for his/her security, use the lockout controls in the
footboard control panel to inhibit the siderail functions or remove any optional pendant control and install protective
pads on the siderails.
• Siderails, with or without their padded covers, are not intended to serve as restraint devices to keep patient from
exiting the bed. Siderails are designed to keep a patient from inadvertently rolling off the bed. It is the responsibility
of the attending medical personnel to determine the degree of restraint necessary to ensure a patient will remain
safely in bed. Failure to use the siderails properly could result in serious patient injury.
• To reduce risk of injury, ensure the sleep surface is horizontal and in the lowest position with the siderails fully
raised and locked when moving the bed with a patient in it.
• To avoid injury to the patient and/or user, do not attempt to move the bed laterally with the steer mode engaged.
The steer wheel cannot swivel.
• The CPR emergency pedal is for emergency use only. When activating the CPR pedal, all people and equipment
must be removed from the area below and around the head, thigh and foot sections of the bed or serious personal
injury and/or equipment damage could occur.
• The manual backup brake is for emergency use only. It should not be used for any other situation than an
emergency or it might get overused when the time comes to use it for an emergency.
• Possible fire hazard exists when this bed is used with oxygen administering equipment other than nasal, mask type
or half bed-length tent type. Unplug the bed power cord from the wall when oxygen administering equipment is used.
When using a half bed-length tent type, ensure that the siderails are outside the oxygen tent and that the tent does
not extend below the mattress support level.
Summary of Safety Precautions

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• The Bed Exit system (optional) is intended only to aid in the detection of a patient exiting the bed. It is not intended
to replace patient monitoring protocol. The Bed Exit system signals when a patient is about to exit the bed. The
addition or removal of equipment with the Bed Exit system armed must be done using the “Adding or Removing
Equipment with the System Armed” procedure, otherwise the sensitivity of the system may be affected and the
readings of the patient’s movements in the bed be erroneous.
• The Weigh system as well as the Bed Exit system must be adjusted if accessories are added when either system
is in function.
• The maximum load capacity of the Monitor Tray is 40 lbs (18kg).
• The maximum load capacity of the tubular support is 150 lbs (68 kg).
• The Bed Exit system is not designed to be used with patients weighing less than 50 lbs (23 kg).
• Do not route the power cord between the mattress and the bed frame.
• Do not attach the power cord to any moving parts of the bed frame.
• The power cord could be pinched and may cause electrical shock if a bed extender is used.
• Do not sit on the bed extender. This may cause the bed to flip.
• Do not steam clean, hose off or ultrasonically clean the bed. Do not immerse any part of the bed. The internal
electrical parts may be damaged by exposure to water. Hand wash regularly all surfaces of the bed with warm
water and a mild detergent. Wipe cleaned surfaces dry to avoid build-up of cleaning substance. Inspect the
mattress after each use. Discontinue use if any cracks or rips, which may allow fluid to enter the mattress, are
found in the mattress cover. Failure to properly clean the mattress, or dispose of it if defective, may increase the
risk of exposure to pathogenic substances and may bring about diseases to the patient and user.
• Always unplug the bed power cord from the wall socket when servicing or cleaning the bed. When working under
the bed with the bed in the high position, always apply the brakes and place blocks under the Bed Lift levers to
prevent injury in case the Bed Down switch is accidentally pressed.
• Improperly adjusted restraint straps can cause serious injury to a patient. It is the responsibility of the attending
medical personnel to determine proper use of the restraint straps and restraint strap locations. Stryker is not
responsible for the type and/or use of restraint straps on any of Stryker’s products.
• Use only hospital grade electric equipment consuming 5A or less with the auxiliary power outlet (optional). The
use of standard electric equipment may bring the current leakage to a level unacceptable for hospital equipment.
• 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 InTouch® bed. Modifying the unit can cause unpredictable operation resulting in injury to the
patient or user. Modifying the unit will also void this warranty.
CAUTION
• The weight of the I.V. bags should not exceed 22 lbs (10 kg).
• The mattress thickness should not exceed 6 inches (15,24 cm).
• When using a mattress thicker than 6 inches (15,24 cm) or a mattress overlay, extra caution and/or patient
supervision may be required to reduce the likelihood of occurence of a patient fall.
• Preventative maintenance should be performed at least once a year to ensure all bed features are functioning
properly. Ensure that any bed malfunction is promptly reported to your service personnel for immediate attention.
• When large fluid spills occur in the area of the circuit boards, 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 have an adverse effect on operational capabilities of any electrical product.
DO NOT put the bed back into service until it is completely dried and has been thoroughly tested for safe operation.
Ensure, among other things, that the plastic components being used as covers for the siderail mechanism arms
and the foot end casing are removed and that the parts they cover are thoroughly dried.
• 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.)
Summary of Safety Precautions
WARNING (CONTINUED)

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Summary of Safety Precautions
OPTIONAL ZOOM®DRIVE SYSTEM (MODEL 2141 ONLY)
In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped
with the ZOOM®.
WARNING
• The 2141 InTouch® Bed 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 brake before pushing the unit manually. For 2141 models;
push the Brake Off button to disengage drive wheel (ZOOM®) 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” (0) position (the LED will not be illuminated), actuate the drive wheel pedal to the neutral position
and call maintenance.
• 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” (0) position before service
or cleaning. When working under the frame, always support the litter frame to prevent injury in case the Bed Down
switch is accidently activated.
• To avoid damage to the siderail mechanisms, do not move the bed using the raised siderails. Move the bed using
the handles integrated to the boards.
• 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.
• When servicing use only identical replacement parts provided by Stryker.
• 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 ensure
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.
Note
• Throughout this Operations Manual, the words “right” and “left” refer to the right and left sides of a patient lying
on his/her back on the bed.
• The addition of accessories affects the motion of the bed.
• The iBed option is only used as an informational feature and is not supposed to replace normal patient monitoring
protocol.
WARNING (CONTINUED)

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Setup Procedures
It is important to ensure that the bed is working properly before it is put into service. The following list will help
ensure that each part of the bed is checked.
• Install the foot and headboards on the bed. Insert the footboard carefully so that the footboard fit in smoothly.
CAUTION
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.
• Plug the power cord to the bed connector at the head end of the bed and into a properly grounded hospital grade
wall socket.
• Turn the battery power switch to the “ON” (1) position (located below the litter surface at patient right side).
• Set the time and date through the touch screen (see page 42 for procedure).
WARNING
This bed is equipped with a hospital grade plug for protection against shock hazard. It must be plugged directly into a
properly grounded receptacle. Grounding reliability can be achieved only when a hospital grade receptacle is used.
• To test the manual backup brake (located on the patients right side only), flip the manual backup brake pedal
outward and depress down fully on the foot end side of the pedal. The word BRAKE in red will be visible in the
clear window located on the base next to the pedal and the Brake symbol will be flashing on the footboard control
panel. The brakes should now be applied.
• To test the electric brake; engage the brake by pressing the brake button on the siderail or footboard control panel.
Try moving the bed to ensure the brakes are applied. Press the Neutral or Brake button on the siderail control panel
or on the footboard to disengage the brake.
• For Model 2141 Beds only: On the patient’s right side of the bed, flip the manual backup brake pedal outward and
depress down fully on the head side of the pedal. The letter D in GREEN should be visible in the clear window
located on the base next to the pedal. The ZOOM®Drive wheel should now be engaged. Depress down fully on
the center of the pedal until the letter N in BLUE is visible in the clear window. The ZOOM®Drive wheel should
now be disengaged.
• Ensure that the siderails raise, lock in the fully raised position and lower smoothly.
• Run through each control on the footboard.
• Verify the scale system and the Bed Exit system for proper operation.
• Run through each control on both inner and outer control panels of the head siderails. If the bed is equipped with
the optional Communication Pendant, plug the provided cable to the 37-pin connector located at the head end of
the bed and into the proper wall socket.
• Raise the bed completely and activate the Trendelenburg function. Ensure the head end lowers to the full down
position. See “Nurse Control” illustration on page 20. Level the bed using the Bed Lift system controls.
• Raise the bed completely and activate the reverse Trendelenburg function. Ensure the foot end lowers to the full
down position. See “Nurse Control” illustration on page 20. Level the bed using the Bed Lift system controls.
• Verify functionality of the CPR emergency release: raise the fowler up then depress down on the CPR pedal
located on either side of the bed at the head end of the bese. The fowler will lower towards a flat position until
the pedal is released.
• Ensure the Knee Gatch (if raised) also starts flattening when the Fowler is completely down. Following the
complete lowering of the Fowler, wait approximately 30 seconds (the time for the Fowler control motor to reset)
and verify that the motor has indeed reset by raising the Fowler fully up using the “Fowler Up” control.
• Verify the following optional equipment for proper operation: 120V aux-
iliary outlet, night light, emergency crank operation, etc.
To prevent permanent damage to this unit, the unit must reach room temperature prior to conducting any setup
and/or unit operations.

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Setup Procedures
OPTIONAL XPRT™ THERAPY MATTRESS
If your bed is equipped with the XPRT™ Therapy Mattress option, perform the following setup procedures to install
the Mattress. For graphic representation of the setup procedures, refer to the XPRT™ Therapy Mattress Operations
Manual.
1. Place mattress over bed litter with printed logo at head end of the bed.
2. Fold back foot end section of mattress.
3. Place foot box on foot end of bed litter.
4. Connect the two (2) color coded connectors on the foot box to the corresponding color coded connectors on the
mattress. Connect black connection on foot box to cable adapter 2950-001-180 and then to the bed frame.
5. Turn the locking collars clockwise to secure the connections.
6. Connect the other end of the black connector to the bed (left side of litter at foot end behind the accessory
outlet).
7. Connect the air line from the mattress to the corresponding fitting on the foot box.
8. Fasten the two (2) retaining clips to the two (2) D-Rings on the foot box.
9. Lower the foot section of mattress over the foot box. Attach the mattress to the bed frame using the mattress tie-
downs.
10. Apply linens utilizing the “D” rings for the flat sheet.
11. To secure linens, to mattress, thread four corners through D-Rings attached to mattress.
12. To ensure proper therapy, do not pull linens taut. The linens should remain loose and wrinkly on the surface of
the mattress.
13. Plug the mattress power cord into a properly grounded, hospital grade receptacle.
Note
The InTouch® bed will detect when the mattress has been connected as well as what type of mattress it is. This will
be shown on the InTouch® screen.
WARNING
• Do not route the power cord between the mattress and the bed frame.
• Do not attach the power cord to any moving parts of the bed frame.
• The power cord could be pinched and may cause electrical shock if a bed extender is used.
OPTIONAL POSITIONPRO™ PATIENT REPOSITIONING MATTRESS OPTION
If your bed is equipped with the Position PRO™ Patient Repositioning Mattress option, perform the following setup
procedures to install the mattress. For graphic representation of the setup procedures, refer to the Position PRO™
Mattress Operations Manual.
1. Place the mattress onto the bed.
2. Flip the foot section towards the head end.
3. Place the control box (upside down) into the opening in the foot section.
4. Connect outer transparent tubes to manifold, matching the color coding.
5. Connect tilt sensor cables.
a. Align the white dots.
b. Twist clockwise to fasten.
6. Connect pendant cable.
7. Connect power cord (4’) and turn the switch to on.
Note: The switch is hidden under the power cord.
8. Fasten straps over the power cord.
9. Install the power cord in the two (2) retaining clips.
10. Fasten the three (3) retaining straps.
11. Carefully rotate the foot end control box and the mattress into the flat position.

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OPTIONAL POSITIONPRO™ PATIENT REPOSITIONING MATTRESS OPTION (CONTINUED)
CAUTION
Gently lower the foot end section to not damage the control box.
12. Fasten the retaining straps to secure the mattress to the bed frame (four (4) straps total).
13. Connect the power cord to the 110V outlet on the bed.
Applying the linens
1. Apply the linens using the “D” rings for the flat sheet.
2. To effectively use the “Turn Assist”, do not pull linens taut. Linens should remain loose and wrinkly on surface of
the mattress.
WARNING
Ensure that you have always access to the CPR straps.
OPTIONAL ZOOM®DRIVE SYSTEM (MODEL 2141 ONLY)
If your bed is equipped with the Optional ZOOM®Drive System, run through the preceding setup procedures and
continue with the procedures listed below.
• 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 (refer to page 57) to ensure it is operating properly.
• On both sides of the bed, flip the manual backup brake pedal outward and depress down fully on the head side of
the pedal. The letter D in GREEN should be visible in the clear window located on the base next to the pedal. The
ZOOM® drive (2141 Model only) should now be engaged. Depress down fully on the center of the pedal until the
letter N in BLUE is visible in the clear window. The ZOOM®drive should now be disengaged.
Setup Procedures

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POWERING THE BED
When the bed power switch is turned off or in the event of a power failure, the settings of the lockout controls and the
calibration data of the Scale and the Bed Exit (optional) systems are preserved.
Note
The bed is provided with batteries which will charge themselves while the bed is connected to the wall socket. When
the “Battery Low” light is on you must connect the bed to make sure the battery will be recharged. Also, make sure the
battery disconnect switch is turned on.
WARNING
Shock Hazard - Improper handling of the power cord may result in damage to the power cord and potential shock
hazards. If damage has occurred to the power cord, immediately remove the bed from service and contact the appropriate
maintenance personnel. Failure to do so could result in serious injury or death.
MODES OF OPERATION WITH THE BATTERY
A power outage to the boards will initiate the battery mode. During the operation in the battery mode, the system will
set itself in the following modes:
Sleep Mode:
Alarm Mode before Dead Mode:
Dead Mode:
Normal Mode:
Power Up Mode:
This mode occurs as a result of the absence of electricity and no activity has been
detected from the control panels for 5 minutes. Also, after 1 hour with no activity
when the bed is on DC power, the touch screen turns off and the sleep mode
occurs.
The Alarm Mode before Dead Mode occurs if, while the system is in the Sleep
Mode, the Bed Exit is activated and if there is no activity in regards to the control
panels of the bed for a period of 4 hours or the batteries are weak.
The Dead Mode is activated if, while the bed is in the Sleep Mode, the Bed Exit is
not activated and there is no activity on the control panels for a period of 1 hour
or the batteries are weak. This mode is also activated after 15 minutes if, while the
system is in the Alarm Mode before Dead Mode, the power is not back and there is
no activity on the control panels.
This is activated under the following conditions:
1. The power is back or if any sign of activity is detected back on the control
panels.
2. The touch screen is no longer in the calibration state.
If the power supply is back (that is, the bed is plugged back to the wall socket or
the power outage is over), the system will exit the Dead Mode to go to the Power Up
Mode if the batteries no longer have power and need to be recharged. The system
then goes to the Initialization Mode which goes back to the Normal Mode.
Modes of Operation
Note
The time needed to charge both batteries completely is approximately 8 hours.