model_1080_fluoroscopy_stretcher_operations_manual_.pdf
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Fluoroscopy Stretcher
1080
Operations Manual
2017/07 A.1
1080-109-001 REV A
www.stryker.com
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sample text
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Symbols
Operating instructions
General warning
Caution
Warning; crushing of hands
No pushing
Do not store the oxygen bottle
Catalogue number
Serial number
Batch code
For US Patents see www.stryker.com/patents
CE mark
EC REP
Manufacturer
Date of manufacture
Safe working load
Lubricate
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sample text
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Table of Contents
Warning/Caution/Note Definition ..................................................................................................................2
Summary of safety precautions ....................................................................................................................3
Introduction..............................................................................................................................................4
Product description..............................................................................................................................4
Indications for use ...............................................................................................................................4
Expected service life............................................................................................................................4
Contraindications ................................................................................................................................4
Specifications.....................................................................................................................................5
Product illustration...............................................................................................................................6
Contact information .............................................................................................................................6
Serial number location .........................................................................................................................7
Date of manufacture ............................................................................................................................7
Operation ................................................................................................................................................8
Applying and releasing the brakes ..........................................................................................................8
Raising or lowering the litter...................................................................................................................8
Positioning the product in Trendelenburg/Reverse Trendelenburg .................................................................9
Raising or lowering the siderails .............................................................................................................9
Raising or lowering the pneumatic Fowler backrest .................................................................................. 10
Accessories ........................................................................................................................................... 11
Attaching the footboard/chart holder ..................................................................................................... 11
Positioning the two-stage permanently attached IV pole option ................................................................... 11
Positioning the three-stage permanently attached IV pole option ................................................................. 12
Attaching and positioning the removable IV pole ...................................................................................... 13
Attaching the upright oxygen bottle holder .............................................................................................. 14
Locating the patient restraint strap tie-ins ............................................................................................... 15
Cleaning................................................................................................................................................ 16
Cleaning the product.......................................................................................................................... 16
Cleaning the mattress ........................................................................................................................ 16
Remove iodine.................................................................................................................................. 17
Special instructions ........................................................................................................................... 17
Disinfecting............................................................................................................................................ 18
Disinfecting the product ...................................................................................................................... 18
Disinfecting the mattress .................................................................................................................... 18
Preventive maintenance ........................................................................................................................... 20
Warranty ............................................................................................................................................... 21
Warranty exclusion and damage limitations ............................................................................................ 21
To obtain parts and service ................................................................................................................. 21
Return authorization........................................................................................................................... 21
Damaged product.............................................................................................................................. 21
International warranty clause ............................................................................................................... 21
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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.
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Summary of safety precautions
Carefully read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
•
•
Always apply the brakes when a patient is getting on the product or off the product or when the product is not
moving. Push on the product to make sure that the brakes are locked. Injury could result if the product moves while
a patient is getting on the product or off the product.
Always remove any devices that may be in the way before you raise or lower the litter.
•
Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended
on the product. Do not leave the product at a higher height.
•
Always lock the siderails in the full up position with the sleep surface horizontal in the lowest position when you
transport a patient.
•
•
Always keep the patient’s limbs away from the siderail spindles when you lower the siderail.
Do not allow the siderails to lower on their own.
•
Always keep hands and fingers clear of the Fowler backrest release handles and the Fowler backrest frame when
you lower the Fowler backrest.
•
Always use caution when you raise a pneumatic Fowler backrest while a patient is on the product. Use proper lifting
techniques and get help, if necessary.
•
•
Do not use the IV pole as a push/pull device. Product damage may occur.
Do not place objects that exceed 40 lb (18 kg) in the upright oxygen bottle holder.
•
Always use caution when you attach restraint straps. Patient or operator injury may occur. Physical restraints, even
if secured, may result in serious harm to patients and operators, including entanglement, entrapment, physical injury,
or death.
•
Always attach restraint straps or devices only at the identified attachment points of the product. Failure to do so
may result in patient or operator injury. Do not attach restraints straps to the siderail.
•
Always refer to the applicable state and federal restrictions and regulations and the appropriate facility protocols
before you use any restraint strap or device.
•
•
Do not clean, service, or perform maintenance while the product is in use.
Do not immerse the mattress in cleaning or disinfectant solutions. Excess moisture could cause product
malfunction that results in product damage or patient injury.
Do not allow fluid to pool on the mattress. Fluids can cause corrosion of components and may cause the safety and
performance of this product to become unpredictable.
Always inspect mattress covers for tears, punctures, excessive wear, and misaligned zippers every time you clean
the covers. Remove and replace a damaged mattress immediately to prevent cross-contamination.
•
•
•
Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may
void this product’s warranty.
•
Always disinfect the mattress between patients. Failure to do so could result in cross-contamination and infection.
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.
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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
The Stryker Model 1080 Fluoroscopy Stretcher is a wheeled stretcher that consists of a platform mounted on a wheeled
frame to transport patients in a horizontal position within a healthcare facility by health professionals or trained
representatives of the user facility. The device has a U-shaped base and full-length C-arm access to enhance imaging
capabilities. The device has siderails, supports for fluid infusion equipment, and various options and accessories that
assist with the support and position of the patient during imaging or procedures requiring fluoroscopic X-ray system and
transport of the patient.
Indications for use
The Stryker Model 1080 Fluoroscopy Stretcher is a wheeled device that provides support and positioning of a patient
during transport, imaging, or interventional procedures, especially those requiring the use of a general-purpose
fluoroscopic X-ray system, within healthcare facilities. The device has full-length C-arm access that offers flexibility
during imaging and a dual pneumatic backrest that helps to provide access for imaging without the need to reposition
the patient. The stretcher may be used for minor procedures and short-term stay, typical of existing stretcher
applications, including outpatient clinical evaluation, treatment, minor procedures, and outpatient recovery.
The Fluoroscopy Stretcher is for use in all acute care hospitals and medical outpatient services.
The Fluoroscopy Stretcher has a safe working load up to 500 lb (225 kg).
The Fluoroscopy Stretcher is not for long-term inpatient treatment and recovery.
Expected service life
The Fluoroscopy Stretcher has a 10 year expected service life under normal use conditions and with appropriate
periodic maintenance.
Contraindications
None known.
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Introduction
Specifications
500 lb
225 kg
87 in.
220.9 cm
High
32.75 in.
83.2 cm
Low
23.5 in.
59.7 cm
30.5 in.
77.4 cm
Safe working load indicates the sum of the patient, mattress and
accessory weight
Overall length
Height
Overall width
Litter positioning
Dual backrest operation
0°-90°
Trendelenburg/Reverse Trendelenburg
±8°
Patient surface
26 in. x 84 in.
66 cm x 213.4 cm
Siderails
13 in. x 55 in.
33 cm x 139.5 cm
Fluoroscopy window
27.5 in. x 66 in.
69.9 cm x 167.6 cm
Caster diameter/width
6 in.
15 cm
C-arm access width
54 in.
137.2 cm
Stryker reserves the right to change specifications without notice.
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Introduction
Product illustration
F
G
H
K
K
A
B
E
C
J
D
A
Brake/steer pedal
F
IV pole
B
Bumper
G
Pneumatic backrest
C
Caster
H
Pneumatic backrest release handle
D
Foot end hydraulic release pedal
J
Pump pedal
E
Head end hydraulic release pedal
K
Siderail
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.
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Introduction
Serial number location
A
Date of manufacture
The year of manufacture is the first 2 digits of the serial number.
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Operation
Applying and releasing the brakes
WARNING
Always apply the brakes when a patient is getting on the product or off the product or when the product is not moving.
Push on the product to make sure that the brakes are locked. Injury could result if the product moves while a patient is
getting on the product or off the product.
To apply the brakes, push down on the brake/steer pedal (A) (Figure 1 on page 8). Push on the product to make sure
that the brakes work.
To release the brakes, push up on the brake/steer pedal (B).
To put the brake/steer pedal in the neutral position, put the brake/steer pedal (C) straight.
B
C
A
Figure 1: Brake pedal
Raising or lowering the litter
WARNING
Always remove any devices that may be in the way before you raise or lower the litter.
To raise the litter, press down on the pump pedal (C) (Figure 2 on page 9).
To lower the head end, push down on the hydraulic release pedal (B) at either end of the product.
To lower the foot end, push down on the hydraulic release pedal (A) at either end of the product.
To lower the entire litter, push down on both hydraulic release pedals (A and B) together.
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Operation
Raising or lowering the litter (Continued)
D
D
A
B
C
B
A
C
Figure 2: Raising or lowering the litter
Positioning the product in Trendelenburg/Reverse Trendelenburg
WARNING
Always remove any devices that may be in the way before you raise or lower the litter.
To lower the head end of the litter (Trendelenburg), press down on the hydraulic release pedal (B) at either end of the
product (Figure 2 on page 9).
To lower the foot end of the litter (Reverse Trendelenburg), press down on the hydraulic pedal (A) at either end of the
product.
Raising or lowering the siderails
WARNING
•
Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended
on the product. Do not leave the product at a higher height.
•
Always lock the siderails in the full up position with the sleep surface horizontal in the lowest position when you
transport a patient.
•
•
Always keep the patient’s limbs away from the siderail spindles when you lower the siderail.
Do not allow the siderails to lower on their own.
To raise the siderails, use two hands to grasp the siderail. Raise the siderail until the release latch clicks into place. Pull
on the siderail to make sure that the siderail is locked.
To lower the siderails, pull up on the release latch. Guide the siderail to the lowest position.
Note: Do not use siderails as restraint devices to keep the patient from exiting the product. The siderails keep the
patient from rolling off the product. The operator must determine the degree of restraint necessary to make sure that the
patient is safe.
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Operation
Raising or lowering the pneumatic Fowler backrest
WARNING
•
Always keep hands and fingers clear of the Fowler backrest release handles and the Fowler backrest frame when
you lower the Fowler backrest.
•
Always use caution when you raise a pneumatic Fowler backrest while a patient is on the product. Use proper lifting
techniques and get help, if necessary.
To raise the Fowler backrest, squeeze the red Fowler backrest release handle. Pull the Fowler backrest up to the
desired position.
To lower the Fowler backrest, squeeze the red Fowler backrest release handle. Push the Fowler backrest down to the
desired position.
Note: You can operate the Fowler backrest from both ends of the product litter. This allows the patient to be reversed
on the product when taking X-rays.
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Accessories
These accessories may be available for use with your product. Confirm availability for your configuration or region. Call
Stryker Customer Service: 1-800-327-0770.
Name
Part number
Footboard/chart holder
1080-134-000
IV pole, 2-stage permanent, foot end
1080-112-000
IV pole, 2-stage permanent, head end
1080-110-000
IV pole, removable
0390-025-010
Oxygen bottle holder, upright
1020-130-000
Restraint strap, ankle
0946-043-001
Restraint strap, chest
1010-058-000
Restraint strap, full package
1010-077-000
Restraint strap, wrist
0946-044-000
Restraint strap, body-chest
0390-019-000
Attaching the footboard/chart holder
WARNING
Always use caution if the defibrillator tray/foot extender, footboard/chart holder, or upright oxygen bottle holder is
attached to avoid pinching your fingers when you position the foot end push handle option.
To attach the footboard/chart holder, insert the footboard/chart holder pins into the sockets at the foot end of the
product.
Note: Do not use the footboard/chart holder as a push/pull device. Product damage may occur.
Positioning the two-stage permanently attached IV pole option
WARNING
Do not use the IV pole as a push/pull device. Product damage may occur.
You can purchase the product with the two-stage IV pole option permanently attached at the head end, foot end, or both
ends of the product. The IV pole is equipped with a telescopic pole that extends to provide a second height position. You
can fold and store the IV pole when not in use.
To position the two-stage IV pole (Figure 3 on page 12):
1.
2.
3.
4.
5.
Lift and pivot the pole from the storage position.
Push the IV pole down until the IV pole locks in place.
To raise the height of the IV pole, pull up on the telescoping portion (A) until the pole locks in place at the fully
raised position.
Rotate the IV hangers (B) to the desired position and hang the IV bags.
To lower the IV pole, hold the telescoping portion of the IV pole, turn the latch (C), and lower the telescoping portion.
Notes
• Do not hang IV bags that exceed 40 lb (18 kg) on the IV pole.
• Always make sure that the IV pole is at a low height to pass safely through door openings when you transport a
patient.
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Accessories
Positioning the two-stage permanently attached IV pole option (Continued)
A
B
A
C
Figure 3: Positioning the 2 stage permanently attached IV pole
Positioning the three-stage permanently attached IV pole option
WARNING
Do not use the IV pole as a push/pull device. Product damage may occur.
You can purchase the product with the three-stage IV pole option permanently attached at the head end, foot end, or
both ends of the product. The IV pole is equipped with a telescopic pole that extends to provide a second and third
height position. You can also fold and store the IV pole when not in use.
To position the three-stage IV pole (Figure 4 on page 13):
1.
2.
3.
4.
5.
6.
7.
Lift and pivot the pole from the storage position.
Push the IV pole down until the pole locks in place.
To raise the height of the IV pole, pull up on the telescoping portion (A) until the pole locks into place at the fully
raised position.
For a higher IV pole, pull up on section (B). Release section (B) at any desired height to lock the pole in place.
Rotate the IV hangers (C) to the desired position and hang the IV bags.
To lower the IV pole, push up on the yellow portion of the grip (D) while holding on to section (B) until the pole
lowers.
Turn the latch (E) and lower the IV pole telescoping portion.
Notes
• Do not hang IV bags that exceed 12 lb (5 kg) total for all bags on the IV pole.
•
•
12
Do not hang IV bags that exceed 9.3 lb (4.2 kg) on a single IV hanger.
Always make sure that the IV pole is at a low height to allow the pole to pass safely through door openings
when you transport a patient.
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Accessories
Positioning the three-stage permanently attached IV pole option (Continued)
C
B
D
A
E
Figure 4: Positioning the three-stage permanently attached IV pole
Attaching and positioning the removable IV pole
WARNING
Do not use the IV pole as a push/pull device. Product damage may occur.
To attach and position the removable IV pole (Figure 5 on page 14):
1.
2.
3.
Insert the IV pole into a socket at the head end or foot end of the product.
Turn the knob (A) counterclockwise and pull up on the telescoping portion (B) until you reach the desired height.
Turn the knob (A) clockwise to lock the telescoping portion in place.
Notes
• Do not hang IV bags that exceed 40 lb (18 kg) on the IV pole.
•
Always make sure that the IV pole is at a low height to pass through door openings when you transport a patient.
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Accessories
Attaching and positioning the removable IV pole (Continued)
B
A
Figure 5: Removable IV pole
Attaching the upright oxygen bottle holder
WARNING
•
•
Do not place objects that exceed 40 lb (18 kg) in the upright oxygen bottle holder.
Always use caution if the defibrillator tray/foot extender, footboard/chart holder, or upright oxygen bottle holder is
attached to avoid pinching your fingers when you position the foot end push handle option.
The upright oxygen bottle holder supports an oxygen bottle in a vertical position.
To attach the upright oxygen bottle holder:
1.
2.
14
Insert the support bar into any of the IV sockets.
Insert the cotter pin through the hole in the support bar to secure the bottle holder to the product.
Note: Do not use the upright oxygen bottle holder as a push/pull device.
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Accessories
Locating the patient restraint strap tie-ins
WARNING
•
Always use caution when you attach restraint straps. Patient or operator injury may occur. Physical restraints, even
if secured, may result in serious harm to patients and operators, including entanglement, entrapment, physical injury,
or death.
•
Always attach restraint straps or devices only at the identified attachment points of the product. Failure to do so
may result in patient or operator injury. Do not attach restraints straps to the siderail.
•
Always refer to the applicable state and federal restrictions and regulations and the appropriate facility protocols
before you use any restraint strap or device.
There are eight patient restraint strap tie-in locations on the litter assembly for attaching patient restraint straps (Figure
6 on page 15).
Figure 6: Restraint strap tie-in locations
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Cleaning
Cleaning the product
WARNING
Do not clean, service, or perform maintenance while the product is in use.
Recommended cleaning method
1.
2.
3.
4.
5.
Follow the cleaning solution manufacturer’s dilution recommendations.
Hand wash all surfaces of the product with warm water and mild detergent.
Avoid over-saturation and make sure that the product does not stay wet longer than the detergent manufacturer’s
guidelines for proper cleaning.
Dry thoroughly. Do not replace the mattress on the product until the product is dry.
Check functionality before you return the product to service.
• Raise and lower the product
• Lock and unlock the brake/steer pedal in both positions
• Latch and unlatch the siderails
• Raise and lower the Fowler backrest
• Raise and lower the gatch
• Make sure all components have proper lubrication
• Make sure all labels are intact
Notes
• 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 corrosion of critical components. Failure to follow these cleaning
instructions may void your warranty.
•
Do not steam clean, power wash, hose off, or ultrasonically clean the product. Use of these methods of
cleaning is not recommended and may void the product’s warranty.
•
•
Clean the base hood.
Clean the bottom of the brake pads to prevent wax or floor remnant buildup.
Cleaning the mattress
WARNING
•
Do not clean, service, or perform maintenance while the product is in use.
•
Do not immerse the mattress in cleaning or disinfectant solutions. Excess moisture could cause product
malfunction that results in product damage or patient injury.
Do not allow fluid to pool on the mattress. Fluids can cause corrosion of components and may cause the safety and
performance of this product to become unpredictable.
Always inspect mattress covers for tears, punctures, excessive wear, and misaligned zippers every time you clean
the covers. Remove and replace a damaged mattress immediately to prevent cross-contamination.
Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may
void this product’s warranty.
•
•
•
The life of the mattress can be affected by an increase in frequency of usage, which might include more frequent
cleaning and disinfection.
1.
2.
16
Use a clean, soft cloth to wipe down the entire mattress with a mild soap and water solution to remove foreign
material.
Wipe down the mattress with a clean, dry cloth to remove any excess liquid or cleaning agents.
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Cleaning
Cleaning the mattress (Continued)
3.
4.
5.
Rinse and dry covers after cleaning.
Disinfect as needed with a hospital grade disinfectant after cleaning has been completed (Disinfecting the mattress
on page 18).
Check functionality before you return the product to service.
• Raise and lower the product
• Lock and unlock the brake/steer pedal in both positions
• Latch and unlatch the siderails
• Raise and lower the Fowler backrest
• Raise and lower the gatch
• Make sure all components have proper lubrication
• Make sure all labels are intact
Notes
• Do not iron, dry-clean, or tumble dry the mattress, as this will cause malfunction and damage the product.
•
The mattress cover must be completely dry before you store, add linens, or place a patient on the mattress to
prevent impairment of the product performance.
•
•
Avoid over-exposure to alcohol or hydrogen peroxide. The cover material will swell.
Do not allow liquid to seep into the zipper area and watershed cover barrier. Fluids allowed to come in contact
with the zipper may leak into the mattress which could impair the product performance.
Remove iodine
1.
2.
3.
4.
Make a solution of 1 to 2 tablespoons of sodium thiosulfate in a pint of warm water. Use the solution to wipe down
the stained area.
Clean the stain as soon as possible after the stain occurs.
If stains are not immediately removed, allow solution to soak or stand on the mattress before you wipe the mattress.
Rinse the mattresses which have been exposed to the solution with clear water before you return the mattresses to
service.
Note: Failure to follow these directions when you use these types of cleaners may void this product’s warranty.
Special instructions
Velcro®
Saturate with disinfectant, rinse with water, and allow the
solution to evaporate.
Solids or stains
Use neutral soaps and warm water. Do not use harsh
cleansers, solvents, or abrasive cleaners.
Hard-to-clean spots
Use standard household cleansers or vinyl cleansers and
a soft bristle brush on troublesome spots or stains. Presoak dried-on soil.
Laundering
Laundering is not recommended. Laundering may
substantially decrease the useful life of the mattress.
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Disinfecting
Disinfecting the product
WARNING
•
Do not clean, service, or perform maintenance while the product is in use.
•
Do not steam clean, hose off, or ultrasonically clean the product. Use of these methods of cleaning is not
recommended and may void the product’s warranty.
Recommended disinfectants
•
•
•
•
Quaternaries (active ingredient - ammonium chloride)
Phenolic disinfectant (active ingredient - o-phenylphenol)
Chlorinated bleach solution (5.25% bleach diluted 1 part bleach to 100 parts water which equals 520 ppm available
chlorine (40 mL of a 5.25% bleach solution per 4000 mL water))
70% isopropyl alcohol
Recommended disinfection method
1.
2.
3.
4.
5.
6.
Follow the disinfectant solution manufacturer’s dilution recommendations.
Hand wash all surfaces of the product with a disinfectant solution.
Avoid over-saturation and make sure that the product does not stay wet longer than the chemical manufacturer’s
guidelines for proper disinfecting.
Dry thoroughly. Do not replace the mattress on the product until the product is dry.
Disinfect the Velcro® after every use. Saturate the Velcro® with disinfectant, rinse with water, and allow the
disinfectant to evaporate (appropriate disinfectant is determined by the facility).
Check functionality before you return the product to service.
• Raise and lower the product
• Lock and unlock the brake/steer pedal in both positions
• Latch and unlatch the siderails
• Raise and lower the Fowler backrest
• Raise and lower the gatch
• Make sure all components have proper lubrication
• Make sure all labels are intact
Note: Some cleaning agents are corrosive in nature and may cause damage to the product if you use them
improperly. If you do not rinse and dry the product well, a corrosive residue may be left on the surface of the
product that could cause premature corrosion of critical components. Failure to follow these cleaning instructions
may void your warranty.
Disinfecting the mattress
These instructions provide recommended disinfecting methods for the mattress.
WARNING
Always disinfect the mattress between patients. Failure to do so could result in cross-contamination and infection.
Recommended disinfectants:
• Quaternaries (active ingredient - ammonium chloride)
• Phenolic disinfectant (active ingredient - o-phenylphenol)
• Chlorinated bleach solution (5.25% bleach diluted 1 part bleach to 100 parts water which equals 520 ppm available
chlorine (40 mL of a 5.25% bleach solution per 4000 mL water))
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Disinfecting
Disinfecting the mattress (Continued)
•
70% isopropyl alcohol
1.
2.
3.
Make sure that the mattress has been thoroughly cleaned and dried before you apply disinfectants.
Wipe down the mattress with a clean, dry cloth to remove any excess liquid or disinfectant.
Care must be taken to thoroughly rinse and dry covers after disinfection.
Notes
• The mattress cover must be completely dry before you store or add linens. Failure to remove excess
disinfectant could cause degradation of the cover material.
•
•
•
Some cleaning agents are corrosive in nature and may cause damage to the product if you use them
improperly. If you do not rinse and dry the product well, a corrosive residue may be left on the surface of the
product that could cause premature corrosion of critical components. Failure to follow these cleaning
instructions may void your warranty.
Frequent or prolonged exposure to higher concentrations of disinfectant solutions may prematurely age the
cover fabric.
The use of accelerated hydrogen peroxides or quaternaries that contain glycol ethers may damage the cover.
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Preventive maintenance
Remove product from service before you perform the preventive maintenance inspection. Check all items listed during
annual preventive maintenance for all Stryker Medical products. You may need to perform preventive maintenance
checks more often based on your level of product usage. Service only by qualified personnel.
Note: Clean and disinfect the exterior of the mattress before inspection, if applicable.
Inspect the following items:
All welds
All fasteners are secure
Brake mechanism works
Steer function works
Siderails raise, lower, and latch
Casters lock when you apply the brakes
Casters secure and swivel
Casters are free of wax or debris
Fowler backrest raises, lowers, and latches
Skins are not cracked
Trendelenburg/Reverse Trendelenburg raises and lowers from all locations
IV pole is intact (optional)
Oxygen bottle holder is intact and is in good working condition (optional)
Body restraints are not torn and can be adjusted and latched
Accessories and mounting hardware are in good working condition
No rips, tears, or cracks in the mattress cover
Velcro® on the mattress is in good condition
Velcro® on litter is in good condition; replace if necessary (0381-024-007)
Ground chain is intact
No leaks at hydraulic connections
Hydraulic jacks holding
Hydraulic drop rate is set
Hydraulic oil level is sufficient
Lubricate where required, including the brake adjuster assembly, brake cam, and pump bar pivot brackets
Product serial number:
Completed by:
Date:
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Warranty
Stryker Medical, a division of Stryker Corporation, warrants to the original purchaser the Stryker Model 1080
Fluoroscopy Stretcher, to be free from defects in material and workmanship for a period of one year 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, product 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 a 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 stretchers have a 10 year expected service life under normal use, conditions, and with appropriate
periodic maintenance as described in the maintenance manual for each device.
The above noted warranty periods apply only to the original purchaser of the Fluoroscopy Stretcher and begin on the
date of delivery to such original purchaser.
Warranty exclusion and damage limitations
The express warranty set forth herein is the only warranty applicable to the product. Any and all other warranties,
whether express or implied, including any implied warranty of merchantability or fitness for a particular purpose
are expressly excluded by Stryker. In no event shall Stryker be liable for incidental or consequential damages.
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 at 1-800-327-0770.
Return authorization
Product cannot be returned without prior approval from the Stryker Customer Service Department. An authorization
number will be provided which must be printed on the returned product. Stryker reserves the right to charge shipping
and restocking fees on returned product. Special, modified, or discontinued products are not subject to return.
Damaged product
ICC Regulations require that claims for damaged product must be made within fifteen (15) days of receipt of the product.
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. Claims 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 product, 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 within thirty (30) days of
receipt. Claims for any incomplete shipments 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. Contact your local Stryker
Medical representative for additional information.
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