Stryker PositionPRO Series User manual

2016/10 G.2 2920-109-001 REV G www.stryker.com
Operations Manual
PositionPRO® Patient Repositioning Support
Surface
Standalone with pendant or integrated with FL27 InTouch® CC
Model Beds
2920

sample text

www.stryker.com 2920-109-001 REV G
Symbols
Operating instructions/Consult instructions for use
General warning
Caution
Catalogue number
Serial number
Manufacturer
Safe working load
~
Alternating current
Dangerous voltage
Protective earth ground
IPX4 Protection from liquid splash
Type B equipment providing a particular degree of protection against electric shock, particularly
regarding allowable leakage current and reliability of the protective earth connection.
Class II Per Rule 9- PositionPRO is considered an active therapeutic device intended to be used
to administer or withdraw energy to or from the body.
Medical Equipment Recognized by Underwriters Laboratories LLC With Respect to Electric
Shock, Fire, and Mechanical Hazards only in accordance with UL 60601-1: 2003 and CAN/CSA-
C22.2 No. 601.1-M90 updates 1 and 2.
In accordance with European Directive 2012/19/EU 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. Contact your local distributor for disposal information.
Wash by hand
Do not dry-clean
Allow to completely air dry
Do not tumble dry
Do not iron

2920-109-001 REV G www.stryker.com
Symbols
Chlorinated bleach
For US Patents see www.stryker.com/patents
Do not stack more than 1 high

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Table of Contents
Warning/Caution/Note Definition ..................................................................................................................3
Summary of safety precautions..............................................................................................................3
Introduction..............................................................................................................................................5
Product description..............................................................................................................................5
Indications for use...............................................................................................................................5
Expected service life............................................................................................................................6
Contraindications ................................................................................................................................6
Specifications.....................................................................................................................................6
Contact information .............................................................................................................................7
Serial number location .........................................................................................................................7
Product illustration...............................................................................................................................8
Date of manufacture............................................................................................................................8
Installation...............................................................................................................................................9
Operation .............................................................................................................................................. 13
Applying the linens ............................................................................................................................ 13
Positioning the patient........................................................................................................................ 13
Activating CPR.................................................................................................................................. 14
Resetting CPR with the optional pendant control ...................................................................................... 14
Starting and stopping max inflate with the optional pendant control.............................................................. 15
Locking and unlocking the optional pendant control.................................................................................. 15
Adjusting firmness with the optional pendant control................................................................................. 16
Starting and stopping turn assist with the optional pendant control............................................................... 17
Alarming call maintenance with the optional pendant control ...................................................................... 19
Resetting CPR with the optional InTouch footboard .................................................................................. 19
Starting and stopping max inflate with the optional InTouch footboard .......................................................... 19
Locking and unlocking with the optional InTouch footboard ........................................................................ 19
Adjusting firmness with the optional InTouch footboard ............................................................................. 20
Starting and stopping turn assist with the optional InTouch footboard ........................................................... 21
Alarming call maintenance with the optional InTouch footboard .................................................................. 23
Transferring a patient to and from the support surface.............................................................................. 23
Transporting a patient ........................................................................................................................ 24
Managing incontinence and drainage .................................................................................................... 24
Cleaning................................................................................................................................................ 25
Cleaning the control box ..................................................................................................................... 25
Cleaning the pendant ......................................................................................................................... 25
Disinfecting............................................................................................................................................ 27
Preventive maintenance ........................................................................................................................... 28
Top cover replacement....................................................................................................................... 28
Fire barrier replacement ..................................................................................................................... 28
Quick reference replacement parts............................................................................................................. 30
EMC information ..................................................................................................................................... 31
Warranty ............................................................................................................................................... 35
Warranty exclusion and damage limitations ............................................................................................ 35

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Table of Contents
To obtain parts and service ................................................................................................................. 35
Return authorization........................................................................................................................... 35
Damaged product.............................................................................................................................. 35
International warranty clause............................................................................................................... 35

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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 product 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: Provides special information to make maintenance easier or important instructions clearer.
Summary of safety precautions
Carefully read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
• Always make sure that the operator has access to the CPR straps.
• Do not stick needles into a support surface through the support surface cover. Holes may allow body fluids to enter
the inside (inner core) of the support surface and could cause cross-contamination, product damage, or product
malfunction.
• Do not use fitted sheets with this support surface.
• Always center the patient on the support surface before starting functions. Check the patient frequently for proper
positioning and to make sure that the support surface maintains proper inflation.
• Always make sure that the tubing and wiring that is connected to the patient is long enough, stabilized, and secure
during Lateral Rotation or Turn Assist.
• Do not extubate or intubate patients during Lateral Rotation or Turn Assist. The rotation functions could interfere
with the performance of the ancillary devices.
• Always secure the support surface anchoring straps to the bed frame.
• Always raise the bed siderails before starting Turn Assist.
• Do not leave the patient unattended during Turn Assist.
• Do not exceed the safe working load of the bed frame when supporting both the patient and the support surface.
Excess weight could cause unpredictable safety and performance of this product.
• Always deflate the support surface before beginning CPR.
• Do not arm bed exit with Lateral Rotation or Turn Assist active. The patient motion and position that results from the
support surface may adversely affect bed exit system performance.
• Do not use dynamic mattress systems for stroke victims without a physician’s order.
• Do not turn a patient with unstable fractures, unstable spinal cord injuries, or those in skeletal traction.
• Always monitor the patient condition at regular intervals for patient safety.
• Do not immerse support surface or foot box in cleaning or disinfectant solutions. To avoid the risk of product
damage or patient injury.
• Do not allow fluid to pool on the support surface or foot box. Fluids can cause degradation of components and may
cause unpredictable safety and performance of this product.

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Warning/Caution/Note Definition
Summary of safety precautions (Continued)
WARNING (CONTINUED)
• Always inspect support surface covers (top and bottom) for tears, punctures, excessive wear, and misaligned
zippers each time the covers are cleaned. If compromised, the support surface cover should be removed from
service immediately and replaced to prevent cross-contamination.
• Always perform preventative maintenance more frequently based on the usage level of the product. The life of the
support surface can be adversely affected by an increase in usage which may include more frequent cleaning and
disinfection.
• Always allow the control box to completely dry before you place the support surface on top of it.
• Always disinfect the support surface between patients, to avoid the risk of cross-contamination and infection.
• Always make sure that you wipe each product with clean water and thoroughly dry each product after cleaning.
Some cleaning agents are corrosive in nature and may cause damage to the product if you use them improperly. If
you do not properly rinse and dry the product, a corrosive residue may be left on the surface of the product that
could cause premature degradation of critical components. Failure to follow these cleaning instructions may void
your warranty.
• Always unplug the product power cord before cleaning or disinfecting to avoid the risk of shock.
CAUTION
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in
this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
• Always lower the foot end section gently to avoid the risk of damage to the control box.
• Do not allow sharp objects to come into contact with the support surface that could puncture tear or cut the cover.
• Always secure all patient lines and tubing together before starting Turn Assist to prevent pulling, removal, or
breakage.
• Do not iron, dry-clean, or tumble dry the support surface covers.
• Do not power wash the support surface as this may cause malfunction and damage the product.
• Always make sure that the support surface cover is completely dry before storing, adding linens or placing a patient
on the surface. Drying the product aids in preventing the performance of the product from being impaired.
• Do not over expose the covers to higher concentration disinfectant solutions as these may degrade the covers.
• Do not use accelerated hydrogen peroxides or quaternaries that contain glycol ethers as they may damage the
cover.

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Introduction
This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating
or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or
maintenance of this product.
CAUTION
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in
this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
Notes
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current
product information available at the time of printing. There may be minor discrepancies between your product and
this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770.
Product description
PositionPRO® is a powered pressure relief support surface with low air loss (LAL) intended for medical purposes.
PositionPRO consists of multiple air cells filled and emptied by an integrated control unit to provide changes in the
distribution of body weight for pressure relief. PositionPRO offers turn assist. See the specifications page for
compatible frames.
Indications for use
PositionPRO is intended to assist in the prevention and treatment of pressure injures (including stages 1,2,3,4,
unstageable injury, and deep tissue injury) that are associated with immobile, critically ill, injured or hospitalized human
patients.
Use PositionPRO with a mattress cover at all times. The support surface is intended to support a patient’s full body.
PositionPRO is for patient use in acute care settings, which includes critical care, step down, progressive care,
med/surg, sub acute care, and post anesthesia care unit (PACU). The patient is under the care of a physician. The
typical operator is a healthcare professional. PositionPRO is not suitable for use in the presence of a flammable
anesthetic mixture with air or with oxygen or nitrous oxide.
PositionPRO is not intended to:
• support a patient in a prone position
• be used in a home health position
• be used as a sterile product
• include a measuring function
PositionPRO is not recommended for patients with the following conditions:
• unstable fractures
• skeletal traction
• agitated patients
• severe hemoptysis
• for whom a head-down position is contraindicated, such as a head injury
• bleeding disorders
• rib fractures / fractures
• predisposed to pathological fractures

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Introduction
Indications for use (Continued)
• for whom the techniques increased dyspnea or wheezing
• who are hemodynamically unstable
Expected service life
PositionPRO has a five year expected service life under normal use, conditions, and with appropriate periodic
maintenance.
Contraindications
Patients with spinal cord injuries
Specifications
Model Pendant 2920-100-000 DH29201005 with Dartex Cover
DH29201015 with Nylon Cover
Integrated 2920-500-000 DH29201010 with Dartex Cover
DH29201020 with Nylon Cover
Dimensions Mattress 35” x 84” x 7” 88.9 cm x 213.4 cm x 17.8
cm
Weight Complete system 63 lb 28.6 kg
Mattress 29 lb 13.1 kg
Pendant 1 lb 0.45 kg
Pump Box 33 lb 15 kg
Safe working load Stationary 500 lb 226.8 kg
Default 22 mmHg, optimal
pressure relief
200 lb 90.7 kg
Turn Assist 300 lb 136.1 kg
Power cord 15 foot, 16 AWG cord with hospital grade plug for use with wall outlet
4 foot, 16 AWG cord with hospital grade plug for use with accessory outlet
Over current protection 2 fuses 5 x 20 mm, 5 AMP Slo-Blo, 250 VAC
120VAC; 50-60Hz, 1AMP; Two 250V, 5A Fuses
Output flow rate 12.5 LPM (0.4 SCFM) minimum @ 30mmHg
Current leakage 300 uA Maximum
Classification Class 1 Grounded Equipment
Class 2, FDA and Health Canada
Continuous operation- Not suitable for use in the presence of flammable anesthetic
mixture with air or with oxygen or nitrous oxide. Suitable for continuous duty.
Medical equipment: Classified with respect to electric shock, mechanical hazards only,
in accordance with UL60601-1 CAN/CSA C22.2 No. 601.1.-M90.
Electromagnetic compatibility, meets EN 60601-1-2, 2001 (CISPR II classified as Class
A, Group 1 ISM equipment)

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Introduction
Specifications (Continued)
Flammability standards USA 16 CFR 1632, USA 16 CFR 1633, CALTB 129, Boston BFD IX-11
Method 27.7-1979 of CAN 2-4.2 M77
Compatible frames 84” x 35” flat deck frames GoBed II®, Secure 3®, InTouch®, and Epic II®
Stryker reserves the right to change specifications without notice.
Environmental conditions Operation Storage and transportation
Temperature
104°F
(40°C)
50°F
(10°C)
158 °F
(70 °C)
-40°F
(-40°C)
Contact information
Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
To view your operations or maintenance manual online, see https://techweb.stryker.com/.
Have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical
Support. Include the serial number in all written communication.
Serial number location
A

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Introduction
Product illustration
A
B
C
D
E
F
G
H
Figure 1: Product illustration
ACPR straps E Handles
B D rings F Head end
CFoot box GIntegration cable
D Foot end H Power cord
Date of manufacture
The year of manufacture is the first four digits of the serial number.

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Installation
This section explains how to install the support surface and the control box. The support surface is either equipped with
a standalone pendant control option or integrated with InTouch FL27 Critical Care Bed option. The differences are
noted in the appropriate installation steps.
1. Position the support surface onto the bed.
2. Flip the foot section toward the head end.
3. Turn the control box upside down and place the control box into the opening in the foot section of the support
surface (Figure 2 on page 9).
Figure 2: Insert the foot box
4. Match the outer transparent tubes colors to the manifold colors and connect them (Figure 3 on page 9) (Green,
Blue, Red, White, Black Yellow).
Figure 3: Connect tubes by color
5. Connect the tilt sensor cables.
a. Align the white dots on the tilt sensor cable connectors.
b. Twist the tilt sensor cables clockwise to fasten (Figure 4 on page 10).

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Installation
Figure 4: Connect the tilt sensor cables
6. Connect the pendant cable (Figure 5 on page 10).
Note: The pendant cable for the InTouch FL27 bed is QDF27-1534.
Figure 5: Connect the pendant cable
7. Connect the power cord (4 in. or 15 in.) and turn the switch to the ON or 1 position.
Note: The switch is under the power cord.
8. Fasten the straps over the power cord.
9. Install the power cord in the two retaining clips (Figure 6 on page 10).
Figure 6: Retaining clips
10. Fasten the three retaining straps.

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Installation
11. Carefully rotate the foot end control box and support surface into the flat position (Figure 7 on page 11).
CAUTION
Always lower the foot end section gently to avoid the risk of damage to the control box.
Figure 7: Installation complete and ready to flip
12. Fasten all four of the retaining straps to secure the support surface to the bed frame (Installation on page 9Figure 9
on page 11).
Figure 8: Strap locations
Figure 9: Fasten the retaining straps
13. Install the clip for the pendant standalone optional control in one of the two locations listed below (Figure 10 on
page 11) and (Figure 11 on page 12).
a. Siderails
Figure 10: Pendant on siderails
b. Footboard

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Installation
Figure 11: Pendant on footboard
Note: Always plug the hospital grade three-prong plug into a properly grounded receptacle to protect against
shock hazard. Grounding reliability can be achieved only when a hospital grade receptacle is used.
14. Connect the power cord to the power source.
15. Calibrate the bed following the procedures in the InTouch maintenance manual.

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Operation
Applying the linens
WARNING
• Always make sure that the operator has access to the CPR straps.
• Do not stick needles into a support surface through the support surface cover. Holes may allow body fluids to enter
the inside (inner core) of the support surface and could cause cross-contamination, product damage, or product
malfunction.
• Do not use fitted sheets with this support surface.
To apply the linens:
1. Apply the linens using the “D” rings for the flat sheet.
2. Thread the four linen corners through the “D” rings (c) attached to the support that are surface to secure the linens
(a) to the mattress (b).
Figure 12: Apply linens
Note: Do not pull the linens tight. Keep the linens loose and as smooth as possible on top of the support surface to
effectively use the Turn Assist and Lateral Rotation functions.
Positioning the patient
WARNING
• Always center the patient on the support surface before starting functions. Check the patient frequently for proper
positioning and to make sure that the support surface maintains proper inflation.
• Always make sure that the tubing and wiring that is connected to the patient is long enough, stabilized, and secure
during Lateral Rotation or Turn Assist.
• Do not extubate or intubate patients during Lateral Rotation or Turn Assist. The rotation functions could interfere
with the performance of the ancillary devices.
• Always secure the support surface anchoring straps to the bed frame.
• Always raise the bed siderails before starting Turn Assist.
• Do not leave the patient unattended during Turn Assist.
• Do not exceed the safe working load of the bed frame when supporting both the patient and the support surface.
Excess weight could cause unpredictable safety and performance of this product.
• Always deflate the support surface before beginning CPR.

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Operation
Positioning the patient (Continued)
CAUTION
• Do not allow sharp objects to come into contact with the support surface that could puncture tear or cut the cover.
To position the patient:
1. Place the patient in the center of the support surface, aligning the patient’s head toward the head board.
2. Check the patient frequently during Turn Assist and Lateral Rotation for proper positioning and support surface
inflation.
Activating CPR
When CPR is activated, the manifold bladder deflates, the pump is off and all of the valves are energized. CPR
activation is detected by a fast drop of pressure in a short period of time.
WARNING
Always make sure that the operator has access to the CPR straps.
Pull the red CPR strap (Figure 13 on page 14) that is located on the left and right side of the head end of the mattress.
You can activate one or either of the straps.
Note: The CPR visual alarm LED turns red. The CPR alarm LED continues to flash to indicate that a hazardous situation
has been detected. The CPR alarm LED will continue to flash until you reset the alarm.
Figure 13: CPR Strap
Resetting CPR with the optional pendant control
When you activate the CPR, the pendant CPR LED starts flashing red without an audible alert.
To reset the CPR:
1. Reinsert the red CPR straps by pulling down on the strap.
2. Press the Stop button and the Increase Firmness (+) button simultaneously to reset the CPR alarm. The support
surface will begin to reinflate.

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Operation
Resetting CPR with the optional pendant control (Continued)
A
Button Name Function
AStop and Firmness Increase (+) Press both buttons at the same time
to reset the CPR.
Starting and stopping max inflate with the optional pendant control
To start Max Inflate:
Press the Max Inflate button to inflate the air bladders to the maximum level to aid in patient boosts and patient
transfers.
To stop Max Inflate:
Press the Max Inflate button to stop inflation.
Note: If Max Inflate has been on longer than 30 minutes, the alarm will sound, and the support surface will return to the
default firmness setting.
Locking and unlocking the optional pendant control
To Lock:
Press the Lock button to prevent options from being selected on the pendant after you have activated the functions.
To Unlock:
Press the Unlock button to allow the selection of options.
Note: When selected, the lock icon LED illuminates red.

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Operation
Locking and unlocking the optional pendant control (Continued)
AB
C
Button Name Function
A Max Inflate Inflates the support surface to
maximum pressure (60 mmHg)
BStop Press once to return to previous
firmness setting
CLock Out / Unlock
Press to lock all pendant functions
Press again to unlock all pendant
functions.
Adjusting firmness with the optional pendant control
You can adjust the support surface firmness settings for patient comfort. The product has five levels of firmness
settings that range from 14 mmHg to 30 mmHg. The default of 22 mmHg provides optimal pressure relief for patients up
to 200 lb. For average sized patients, 18-22mmHg is recommended.
Notes
• For larger patients, higher settings are recommended.
The increase firmness (+) and decrease firmness (-) buttons are inactive when Turn Assist or Max Inflate is active.