Stryker GLIDE 3061 Operation And Maintenance Manual
STRYKER GLIDE™
Lateral Patient Transfer System
Model 3061
Operations/Maintenance Manual
For Parts or Technical Assistance:
USA: 1-800-327-0770 (option 2)
Canada: 1-888-233-6888
2008/05 3061-009-001 REV A www.stryker.com
Table of Contents
Introduction...............................................................................4
Intended Use ..........................................................................4
Product Description .....................................................................4
Product Illustration ......................................................................4
Specifications .........................................................................5
Warning / Caution / Note Definition ..........................................................6
Symbols .................................................................................7
Requirements By Symbol For Patient Transfer and Mattress Inflations .................................7
Summary of Safety Precautions................................................................8
Operation Guide ..........................................................................10
Selecting Appropriate Mattress Size ........................................................10
Positioning Mattress Underneath The Patient ................................................. 10
Connecting The Air Supply ...............................................................11
Transfer Of Patient From Stretcher To Bed ...................................................12
Preventative Maintenance ...................................................................13
Maintenance Checklist ..................................................................13
Cleaning................................................................................14
Routine Care: Mattress .................................................................14
Routine Care: Protective Sheet ...........................................................14
Routine Care: Blower Unit ...............................................................15
Disinfection ..........................................................................15
Blood Contamination ................................................................... 15
Troubleshooting Guide......................................................................16
Service Information ........................................................................ 17
Hose Replacement.....................................................................17
Power Cord Replacement ............................................................... 17
ON/OFF Switch Replacement ............................................................. 17
Upper Housing Replacement..............................................................18
Blower Assembly Replacement ............................................................18
Quick Reference Replacement Parts List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
3060-000-028 Replacement Part List (Regular) ................................................19
3060-000-032 Replacement Part List (Large)..................................................19
3060-000-046 Replacement Part List (Bariatric)................................................19
Blower Unit Assembly, Standard - 3060-400-110 ...................................................20
Blower Base with Feet - 3060-001-125 ..........................................................22
Hose Assembly, Standard - 3060-001-127........................................................23
Hose Assembly, Optional 25’- 3060-045-002 .....................................................24
Mattress Assemblies .......................................................................25
Tote Assembly - 3060-001-041 ...............................................................26
Warranty................................................................................27
Limited Warranty ......................................................................27
To Obtain Parts and Service ..............................................................27
Return Authorization....................................................................27
Damaged Merchandise..................................................................27
EMC Information ..........................................................................28
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Introduction
INTENDED USE
This manual is designed to assist you with the safe operation and maintenance of the GLIDE™. 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
GLIDE™.
PRODUCT DESCRIPTION
The GLIDE™ includes one model for use in the United States and Canada. The GLIDE™ transfers a patient on a soft
nylon mattress designed with hundreds of tiny perforations on the underside. The air supply attaches to the mattress
and pumps air out through the tiny perforations on the underside of the mattress The continuous air flow helps to reduce
friction between the sleep surface and the GLIDE™ Matt allowing the operator to transfer the patient with ease.
PRODUCT ILLUSTRATION
Extended Pull
Handles
Blower Assembly
Hose Assembly
Stryker GLIDE™ Matt
Patient Centering Straps
Extended Pull
Handles
Hose
Connection
Air Hose
Retention
Strap
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Introduction
SPECIFICATIONS
Mattress
3061-110-028
Regular (width x length)• 28” x 78” 71,1 cm x 198,1 cm
Weight (including protective cover)• 3.5 lbs. 1.6 kg
Patient Capacity Limit•
Weight Limit• 500 lbs. 226.8 kg
Width Limit• 28” 71 cm
Nylon, Polyurethane under coated, water resistant, anti-static, non-latex•
3061-110-032
Large (width x length)• 32” x 78” 81,3 cm x 198,1 cm
Weight (including protective cover)• 5 lbs. 2.3 kg
Patient Capacity Limit•
Weight Limit• 700 lbs. 317.5 kg
Width Limit• 32” 81,3 cm
Nylon, Polyurethane under coated, water resistant, anti-static, non-latex•
3061-110-046
Bariatric (width x length)• 46” x 80” 116,8 cm x 198,1 cm
Weight (including protective cover)• 6.5 lbs. 2.9 kg
Patient Capacity Limit•
Weight Limit• 1000 lbs. 453.6 kg
Width Limit• 46” 116,8 cm
Nylon, Polyurethane under coated, water resistant, anti-static, non-latex•
Protective Sheet
3061-120-028 34” x 79” 86,4 cm x 200,1 cm
3061-120-032 36” x 79” 91,4 cm x 200,1 cm
3061-120-046 54” x 82” 137,2 cm x 208,3 cm
Air Supply / Power Requirements
Domestic
3060-001-210 (US / CAN)
Duty Cycle 30 seconds ON / 1 minute OFF for 5 cycles followed by a 30 minute rest period.
Product Compliance
Electrical
Weight 8.5 lbs. 3.9 kg
IEC/EN 60601-1
UL 60601-1
CAN/CSA-C22.2 No 601.1-M90
IEC/EN 60601-1-2:2001
120 VAC, 50/60 Hz, 12Amps
Power Cord - ST 2-16 Type w/NEMA 115P
Polarized Plug
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Introduction
SPECIFICATIONS (CONTINUED)
Environmental Conditions Operation Storage and Transportation
30 0C
Ambient Temperature
Relative Humidity
(Non-Condensing)
Atmospheric Pressure
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.
10 0C
(50 0F)
30%
700 hPa
(86 0F)
-25 0C
(-13 0F)
75%
10%
1060 hPa
500 hPa
60 0C
(140 0F)
95%
1060 hPa
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 serous 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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Symbols
~
Warning / Caution - Consult accompanying documentation
Maximum Safe Working Load
Maximum Patient Width
Alternating Current
Class II Equipment: Equipment in which protection against electric shock does not rely on basic insulation
only, but in which additional safety precautions such as double insulation or reinforced insulation are
provided, there being no provision for protective earthing or reliance upon installation conditions.
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.
O
I
IPX0
Indicates Power Off position on black power rocker switch
Indicates Power On position on black power rocker switch
No protection against harmful ingress of water.
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.
REQUIREMENTS BY SYMBOL FOR PATIENT TRANSFER AND MATTRESS INFLATIONS
Patient must be centered on mattress
prior to starting inflation process.
Patient Support Platform must be
at a position of zero Trendelenburg
prior to starting inflation process.
Patient Support Platform brakes
must be set to “ON” prior to starting
inflation process.
Patient must be secured on the
mattress prior to starting inflation
process.
A minimum of two caregivers
is required when transferring a
patient.
Patient Support Platform siderails
must be in the “UP” position prior
to starting inflation process or
transferring a patient.
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Summary of Safety Precautions
WARNINGS
Never leave patient unattended while the GLIDE™ mattress is inflated and air supply is on.•
The GLIDE™ equipment is not suitable for use in the presence of a flammable anesthetic mixture with air, oxygen •
or nitrous oxide.
Mattress must be oriented so that white symbols are pointing upwards.•
The GLIDE™ is not to be used as an air mattress for patient stays with the blower on.•
Do not place and operate the GLIDE™ blower unit in close proximity to uncontainable fluids or biomass.•
Medical electrical equipment requires special precautions regarding EMC and needs to be installed and put into •
service according to the EMC information provided on page 28 to prevent equipment malfunction. Portable and
mobile RF communication equipment can affect Medical Electrical Equipment.
The GLIDE™ is not to be used in the presence of flammable anesthetics.•
The GLIDE™ is not to be used in oxygen rich environments or hyperbaric chambers•
The GLIDE™ is not to be used in the presence of open sources of ignition such as cigarettes, etc…•
Patient straps are used to center patient on the product during inflation and deflation. They are not intended to be •
safety restraint straps that keep the patient on the stretcher or bed.
The GLIDE™ blower and mattress are not to be used as a patient warmer.•
The GLIDE™ blower is not to be used with other manufacturers air transfer mattresses.•
The GLIDE™ air transfer mattress is not to be used with other manufacturing blowers. •
Patient is to be centered before and during inflation.•
Patient support surface (i.e. stretcher, bed, operating table, etc…) must be at 0˚ trendelenburg or level to prevent the •
patient moving under their own weight. The patient support surface should be level with one another.
When using the GLIDE™ side rails must be raised to act as guards to stop the patients movement during a •
transfer.
When using the GLIDE™ for transfers between products that have a transfer gap greater than three inches, the •
transfer bridge must be used. The transfer bridge is not meant to support a patient load. The transfer bridge is
meant to ease transfer of a patient from one patient support surface (i.e. stretcher, bed, etc.) to another. Always
insure that the patient support surfaces and their respective transfer gaps are adequate to support the patient.
The GLIDE™ is to be used with a minimum of two care givers. Care givers need to be positioned so that they can •
control positioning of patient.
The GLIDE™ must be centered under patient without any bunching present. Bunching will cause patient to be •
pushed / lifted off center.
The GLIDE™ can only be used on transfers between fixed patient support surfaces. Mobile surfaces need the •
brakes applied to make them a fixed surface.
Stow accessories such as the Stryker pop-up push handles before beginning a transfer using the GLIDE™.•
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Summary of Safety Precautions
CAUTIONS
Do not operate air supply motor near equipment that is sensitive to electromagnetic interference.•
There is a weight limit on the mattress, the bed, gurney or other surface that the mattress is being used on. Adhere •
to all weight limits as stated in accompanying documentation.
Insert hose into matt and secure with Velcro strap.•
Inspect mattress for seam failures.•
Do not leave the GLIDE™ mattress under patients susceptible to decubitus ulcers.•
Do not leave patients laying on the buckles of the centering straps. •
To avoid malfunction, this product should not be used adjacent to or stacked with other equipment. If stacked use is •
necessary, this product should be observed to verify normal operation in the configuration in which it will be used.
The mattress size is specified in two ways; by the weight of the patient and by the physical size of the patient. •
Selection of an inappropriately sized matt may reduce the overall transfer performance of the Glide or may cause
harm to the patient or the caregiver.
Note
Maximum leakage current shall not exceed 100 micro amps on air supply enclosure and 100 micro amps on air •
mattress.
No automatic pressure relief exists on device. •
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Operation Guide
Operating the GLIDE™ is a three step process; positioning the mattress under patient, connecting air supply, then
transferring patient from stretcher to bed. See detailed instructions below.
SELECTING APPROPRIATE MATTRESS SIZE
The mattress size is specified in two ways; by the weight of the patient and by the physical size of the patient. Selection
of an inappropriately sized mattress may reduce the overall transfer performance of the Glide or may cause harm to the
patient or the caregiver.
The selection of the appropriate size matt is characterized as follows:
28” mattress is appropriate for patients up to a weight of 500 lbs. and a maximum width of 28”.•
32” mattress is appropriate for patients up to a weight of 700 lbs. and a maximum width of 32”.•
46” • mattress is appropriate for patients up to a weight of 1000 lbs. and a maximum width of 46”.
Selection of the appropriate size mattress is determined by comparing the width of the patient to the width of the deflated
mattress. The width of the patient shall not exceed the width of the deflated mattress at any point along its length.
POSITIONING MATTRESS UNDERNEATH THE PATIENT
Note
The GLIDE™ is to be used with a minimum of two caregivers. Caregivers need to be positioned so that they •
can control positioning of the patient.
If soiling is possible, place protector sheet on top of mattress, dull side down, before it is positioned underneath •
the patient.
1. Roll the mattress lengthwise towards center from one side such that the side with the perforations will be against
the bed, not the patient.
2. Place the mattress under the patient using a “log-rolling” technique.
Note: Ensure the patient’s head is located at the same end as the “HEAD” label on the mattress topside.
a. Roll the patient onto their side toward the attendant, (the bed sheet can be used to help with the log roll).
b. Place the rolled edge of the mattress against the patient.
c. Roll the patient back towards the opposite side enough to unroll the mattress as you would when changing a
bed sheet.
d. Center the patient on the mattress.
3. Attach the two patient centering straps in gentle contact with the patient. Straps need not be tight.
Note: Do not pull on the patient centering straps to transfer the patient.
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