Camilla
Camilla
Camilla
Operations Manual
SYMBOLS
Safe Working Load indicates the sum of the patient, mattress, and accessory weight
Do not push/pull
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.
This manual is designed to assist you with the operation of the Stryker Model 747/748 Transport Stretcher. 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 stretcher.
PRODUCT DESCRIPTION
The Stryker Model 747/748 Transport Stretcher is a general purpose patient transport and treatment stretcher.
The Stryker Model 747/748 Transport Stretcher is a non-powered, wheeled device which consists of a platform mounted
on a wheeled frame that is designed to support patients in a horizontal position. The device has siderails and has the
option available to support the temporary or permanent placement of I.V. poles. A stretcher provides the operator a
method of transporting patients within a healthcare facility. Some stretchers may also be used for minor procedures
and short-term stay (treatment and recovery).
SPECIFICATIONS
CONTACT INFORMATION
Contact Stryker Customer Service or Technical Support at: (800) 327-0770 or (269) 324-6500.
Stryker Medical
3800 E. Centre Avenue
Portage, MI 49002
USA
Please 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.
Carefully read and strictly follow the warnings and cautions listed on this page.
Service only by qualified personnel. See the maintenance manual for additional information.
WARNING
• Always apply the brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure that the
brakes are securely locked. Always engage the brakes unless the stretcher is being moved. Injury could result if
the stretcher moves while a patient is getting on or off the stretcher.
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height
in a raised position could increase the chance of patient falls and injury.
• Make sure that the brakes are completely released before attempting to move the unit. Attempting to move the unit
with the brakes engaged could result in injury to the user and/or patient.
• After raising the siderails, pull firmly on the siderail to ensure that it is securely locked into the fully raised position.
Siderails are not intended to serve as a patient restraint device to keep patients from exiting the unit. Siderails are
intended to keep a patient from inadvertently rolling off the unit. It is the responsibility of the attending medical
personnel to determine the degree of restraint necessary to ensure that a patient will remain in place. Failure to
utilize the siderails properly could result in patient injury.
• When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the siderail
spindles or injury could occur.
• During patient transfer, keep patient and operator extremities away from collapsed siderails or injury could occur.
• Operation of the pneumatic fowler is a manual procedure. Use caution when raising the fowler while a patient is
on the stretcher. Use proper lifting techniques and get additional assistance, if necessary. Failure to use proper
lifting techniques could cause injury to the operator.
• Keep hands/fingers clear of the area around the fowler release handle and the fowler frame when lowering the
fowler. Injury could result if care is not taken when lowering the fowler.
• If the stretcher is equipped with the optional foot end push handles, use caution while the foot extension/defibrillator
tray is installed to avoid pinching your fingers.
• To avoid the risk of injury to the patient or user or damage to the I.V. pole while transporting the stretcher, make sure
that the I.V. caddy is securely tightened on the I.V. pole.
CAUTION
• Do not modify this stretcher. Modifying the unit can cause unpredictable operation resulting in injury to the patient
or operator. Modifying the unit will also void its warranty.
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
• To avoid injury or damage to the equipment, do not allow the siderail to lower on its own.
• The push handles were designed for use while transporting the stretcher. Avoid using other parts of the stretcher
as push/pull devices because damage could occur.
• The weight capacity of the base hood is 60 lb. Do not sit or stand on the base hood. Injury or damage to the
equipment could occur.
• Do not step on the base hood.
• Do not use the cutout for the oxygen bottle holder on the base hood for the storage of oxygen bottles or patient
belongings.
• To avoid damage, do not put items weighing more than 30 lb. on the defibrillator tray.
• Do not use the defibrillator tray as a push/pull device because equipment damage could occur.
• If the stretcher is equipped with the optional foot end I.V. pole, the I.V. pole must be in the raised position when the
foot extension/defibrillator tray is installed. If the I.V. pole is not raised, the foot extension will not function properly
and injury could occur.
• To avoid damage, do not put items weighing more than 30 lb. on the defibrillator tray/foot extender.
• Do not use the defibrillator tray/foot extender as a push/pull device because equipment damage could occur.
• Do not use the footboard/chartholder as a push/pull device because equipment damage could occur.
• Always store the I.V. caddy when not in use to avoid damaging it when the unit is moved.
• To avoid damage, do not put items weighing more than 30 lb. on the serving tray.
• Do not use the serving tray as a push/pull device because equipment damage could occur.
• To avoid damage, the weight of the I.V. bags should not exceed 40 lb.
• To avoid damage while transporting the stretcher, verify that the I.V. pole is at a low enough height to allow it to
safely pass through door openings and under light fixtures.
• Do not use the I.V. pole as a push/pull device because equipment damage could occur.
• To avoid damage, the weight of the I.V. bags should not exceed 12 lb. while the weight of any one item attached to
each stage of the three-stage permanently attached I.V. pole should not exceed 9.3 lb.
• To avoid damage, do not put items weighing more than 40 lb. in the upright oxygen bottle holder.
• Do not use the upright oxygen bottle holder as a push/pull device because equipment damage could occur.
• Before returning the unit to service after cleaning, ensure that the unit is functioning properly by verifying that all
labels are intact, raise/lower the stretcher height, brake/steer pedal locks properly in both positions, latch/unlatch
the siderails, raise/lower the fowler and gatch, and check all components for proper lubrication.
• Some cleaning products are corrosive in nature and may cause damage to the product if used improperly. If the
products suggested above are used to clean Stryker patient handling equipment, measures must be taken to
ensure that the stretcher is wiped with a damp cloth soaked in clean water and thoroughly dried following cleaning.
Failure to properly rinse and dry the stretcher will leave a corrosive residue on the surface of the stretcher, 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
• Clean the base hood storage area regularly.
• The bottom of the brake pads should be cleaned regularly to prevent wax or floor remnant buildup.
Make sure that the unit is working properly before it is put into service. The following list will ensure that each part of
the unit is checked.
1. Fully depress the brake pedal of the stretcher to set the four wheel brakes and verify that all four casters are
locked (page 10).
2. Raise and lower the hydraulic lift system (page 11).
3. Raise the unit completely and activate the Trendelenburg function. Ensure that the head end lowers to the lowest
position (page 12).
4. Raise the unit completely and activate the reverse Trendelenburg function. Ensure that the foot end lowers to the
lowest position (page 12).
5. Activate the fifth wheel to ensure that it is operating properly (page 13).
6. Ensure that the siderails raise and lower smoothly and lock securely when fully raised (page 14).
7. Raise and lower the fowler (head end) (page 16).
CAUTION
Do not modify this stretcher. Modifying the unit can cause unpredictable operation resulting in injury to the patient or
operator. Modifying the unit will also void its warranty.
For user convenience, a brake/steer control pedal is located on both ends of the stretcher as shown in Figure 1.
WARNING
Always apply the brakes when a patient is getting on or off the stretcher. Push on the stretcher to ensure that the brakes
are securely locked. Always engage the brakes unless the stretcher is being moved. Injury could result if the stretcher
moves while a patient is getting on or off the stretcher.
To engage the brakes on the foot end, push down on the brake (red) side of pedal (A).
To engage the brakes on the head end, push down on the brake (red) side of pedal (B).
To release the brakes on the foot end, push down on the steer (green) side of pedal (A).
To release the brakes on the head end, push down on the steer (green) side of pedal (B).
Note: Your stretcher may be equipped with optional side control brake and steer functions (C) in addition to the
standard head end (A) and foot end (B) controls. The side control brakes operate the same as the head end and foot
end brakes.
A C
B
Head End
C
Figure 1: Brake System
Note: The bottom of the brake pads should be cleaned regularly to prevent wax or floor remnant buildup.
To operate the base controls, see Figure 2 to locate which pedals are used for what operation.
CAUTION
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
To raise the litter height, pump pedal (A) repeatedly until the desired height is achieved.
To lower both ends of the litter together, depress the center of pedal (B).
To lower only the head end of the litter, depress the side of pedal (B) closest to the head end.
To lower only the foot end of the litter, depress the side of pedal (B) closest to the foot end.
WARNING
• Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight could cause
the litter surface to tip up, possibly causing patient injury.
• Leave the stretcher height in the lowest position when the patient is left unattended. Leaving the stretcher height in
a raised position could increase the chance of patient falls and injury.
B A
Head End
B A
Figure 2: Stretcher Base Controls - Side Control
A B
Litter height must first be raised in order to achieve a Trendelenburg or reverse Trendelenburg position.
CAUTION
• To avoid damage, remove any equipment that may be in the way before raising or lowering the litter height.
• Do not raise the unit (hydraulics on base) with a patient lift under the stretcher.
For Trendelenburg positioning (head down), depress the side of pedal (B) closest to the head end (see Figure 2 on
page 11).
For reverse Trendelenburg positioning (foot down), depress the side of pedal (B) closest to the foot end (see Figure
2 on page 11).
Note: The higher the litter is before pedal (B) is activated, the greater the Trendelenburg or reverse Trendelenburg
angle will be. (Maximum Trendelenburg angle is +18°. Maximum reverse Trendelenburg angle is -18°.)
WARNING
Make sure that the brakes are completely released before attempting to move the unit. Attempting to move the unit with
the brakes engaged could result in injury to the user and/or patient.
The fifth wheel guides the stretcher along a straight line during transport and pivots the stretcher around corners.
To operate the fifth wheel, push the steer (green) side of any brake/steer pedal to the lowest position (see Figure 1
on page 10).
To disengage the fifth wheel, push the brake (red) side of any brake/steer pedal to the neutral position (see Figure 1
on page 10).
Raising and lowering the siderails safely is a two-handed operation. Use one hand to hold and position the siderail and
the other hand to operate the siderail latch.
To raise the siderails, pull up on the siderail (A) and raise it to the highest position until the latch (B) engages.
WARNING
After raising the siderails, pull firmly on the siderail to ensure that it is securely locked into the fully raised position.
Siderails are not intended to serve as a patient restraint device to keep patients from exiting the unit. Siderails are
intended to keep a patient from inadvertently rolling off the unit. It is the responsibility of the attending medical personnel
to determine the degree of restraint necessary to ensure that a patient will remain in place. Failure to utilize the siderails
properly could result in patient injury.
Figure 3: Siderails
To lower the siderails, pull up on the latch (B) and guide the siderail to the lowest position.
WARNING
• When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the siderail
spindles or injury could occur.
• During patient transfer, keep patient and operator extremities away from collapsed siderails or injury could occur.
CAUTION
To avoid injury or damage to the equipment, do not allow the siderail to lower on its own.
Make sure that the siderail latching mechanism is working properly at all times. If it is not, see the stretcher maintenance
manual for ”Siderail Latch Adjustment”.
To use the push handles, pivot the handles up and push down until they are locked into position.
To store the push handles, lift the handles up and pivot them down to store in the handle rests.
CAUTION
The push handles were designed for use while transporting the stretcher. Avoid using other parts of the stretcher as
push/pull devices because damage could occur.
To raise the fowler, squeeze the red fowler handle (A) for pneumatic assist until the fowler has reached the desired
angle.
To lower the fowler, squeeze the red fowler handle (A) and push down until the fowler has reached the desired angle.
WARNING
• Operation of the pneumatic fowler is a manual procedure. Use caution when raising the fowler while a patient is
on the stretcher. Use proper lifting techniques and get additional assistance, if necessary. Failure to use proper
lifting techniques could cause injury to the operator.
• Keep hands/fingers clear of the area around the fowler release handle and the fowler frame when lowering the
fowler. Injury could result if care is not taken when lowering the fowler.
If the pneumatic fowler is difficult to operate, see the stretcher maintenance manual for ”Pneumatic Fowler Adjustment”.
You can store items in the base hood (A) as shown in Figure 6.
CAUTION
• The weight capacity of the base hood is 60 lb. Do not sit or stand on the base hood. Injury or damage to the
equipment could occur.
• Do not step on the base hood.
• Do not use the cutout for the oxygen bottle holder on the base hood for the storage of oxygen bottles or patient
belongings.
The accessories listed below can be purchased and installed on the Model 747/748 Transport Stretcher.
Footboard/Chartholder 1105-045-500 20
CAUTION
• To avoid damage, do not put items weighing more
than 30 lb. on the defibrillator tray.
• Do not use the defibrillator tray as a push/pull device
because equipment damage could occur.
CAUTION
• If the stretcher is equipped with the optional foot end
I.V. pole, the I.V. pole must be in the raised position
when the foot extension/defibrillator tray is installed.
If the I.V. pole is not raised, the foot extension will D
not function properly and injury could occur.
• To avoid damage, do not put items weighing more
than 30 lb. on the defibrillator tray.
• Do not use the defibrillator tray/foot extender as a
push/pull device because equipment damage could
occur.
WARNING
Figure 7.2: Foot Extension/
If the stretcher is equipped with the optional foot end push Defibrillator Tray - Foot End
handles, use caution while the foot extension/defibrillator
tray is installed to avoid pinching your fingers.
Return To Table of Contents
CAUTION
Do not use the footboard/chartholder as a push/pull device
because equipment damage could occur.
CAUTION
Always store the I.V. caddy when not in use to avoid damaging it when the unit is moved.
WARNING
To avoid the risk of injury to the patient or user or damage to the I.V. pole while transporting the stretcher, make sure that
the I.V. caddy is securely tightened on the I.V. pole.
To use the optional serving tray, pull out on either end of the serving tray to extend it to the proper width to fit on top
of the stretcher siderails as shown in Figure 9.1.
To store the serving tray in the optional serving tray holder/foot board, push in both ends of the serving tray and
slide it into holder as shown in Figure 9.2.
Figure 9.1: Serving Tray Figure 9.2: Serving Tray - Foot End
CAUTION
• To avoid damage, do not put items weighing more than 30 lb. on the serving tray.
• Do not use the serving tray as a push/pull device because equipment damage could occur.
Note: The two-stage permanently attached I.V. pole is an option and may have been installed at either the head, foot
or both ends of the stretcher. The choice was made at the time that the stretcher was purchased.
B A
A
C
C
CAUTION
• To avoid damage, the weight of the I.V. bags should not exceed 40 lb.
• To avoid damage while transporting the stretcher, verify that the I.V. pole is at a low enough height to allow it to
safely pass through door openings and under light fixtures.
• Do not use the I.V. pole as a push/pull device because equipment damage could occur.
Note: The three-stage permanently attached I.V. pole is an option and may have been installed at either the head,
foot or both ends of the stretcher. The choice was made at the time that the stretcher was purchased.
A
E C
C
B
D
A B
E
Figure 11.2: I.V. Pole Latch Detail
Figure 11.1: I.V. Pole Figure 11.3: I.V. Pole Grip Detail
CAUTION
• To avoid damage, the weight of the I.V. bags should not exceed 12 lb. while the weight of any one item attached to
each stage of the three-stage permanently attached I.V. pole should not exceed 9.3 lb.
• To avoid damage while transporting the stretcher, verify that the I.V. pole is at a low enough height to allow it to
safely pass through door openings and under light fixtures.
• Do not use the I.V. pole as a push/pull device because equipment damage could occur.
To install and use the siderail pads, tuck the siderail pad between the mattress
and siderail. Then, attach the Velcro® straps around the top of the siderail to
secure the pad to the siderail.
Figure 12.1: Removable I.V. Pole
STRETCHER CLEANING
These instructions are intended to provide recommended cleaning methods for the Stryker Model 747/748 Transport
Stretcher. Follow hospital protocol for cleaning procedures and frequency.
• R emove the mattress prior to washing the unit; do not wash the mattress with the stretcher.
• Wipe the unit with cleaning solution and water per manufacturer’s recommended dilution.
• Dry thoroughly. Do not replace the mattress on the stretcher until the unit is completely dry.
CAUTION
efore returning the unit to service after cleaning, ensure that the unit is functioning properly by verifying that all labels
B
are intact, raise/lower the stretcher height, brake/steer pedal locks properly in both positions, latch/unlatch the siderails,
raise/lower the fowler and gatch, and check all components for proper lubrication.
DO NOT STEAM CLEAN, PRESSURE WASH, HOSE OFF OR ULTRASONICALLY CLEAN THE STRETCHER.
Using these methods of cleaning are not recommended and may void this product’s warranty.
RECOMMENDED CLEANERS
Avoid over saturation and ensure that the product does not stay wet longer than the chemical manufacturer’s guidelines
for proper disinfecting.
CAUTION
Some cleaning products are corrosive in nature and may cause damage to the product if used improperly. If the products
suggested above are used to clean Stryker patient handling equipment, measures must be taken to ensure that the
stretcher is wiped with a damp cloth soaked in clean water and thoroughly dried following cleaning. Failure to properly
rinse and dry the stretcher will leave a corrosive residue on the surface of the stretcher, 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.
MATTRESS CLEANING
These instructions are intended to provide recommended cleaning methods for stretcher mattresses. Follow hospital
protocol for cleaning procedures and frequency.
• Hand-wash all surfaces of the mattress with warm water and mild detergent cleaner.
• Dry thoroughly.
• Apply disinfectant solution either by spray, solution or pre-impregnated wipes (do not soak mattress).
• Clean per hospital protocol for mattresses.
• Wipe up excess disinfectant.
• Rinse with clean water.
• Allow surface to dry.
RECOMMENDED DISINFECTANTS
When used in concentrations recommended by the manufacturer, diluted bleach, diluted phenolic, or diluted quaternary
germicidal disinfectants are recommended. Chlorine Bleach, typically 5.25% Sodium Hypochlorite, should be used at
a dilution ratio of 1 part bleach to 10 parts water.
These products are NOT considered mild detergents. They are corrosive in nature and may cause damage to your
stretcher mattress if used improperly. Mattresses must be rinsed with clean water and dried thoroughly after using
corrosives such as quaternary, phenolic, or chlorine bleach. Failure to properly rinse and dry the mattress leaves a
corrosive residue on the surface, likely causing premature corrosion.
Iodophor type disinfectants are not recommended for use because staining may result.
The following table lists the recommended cleaner types for each mattress cover material (see definitions below):
Vinyl Mattress Cover Polyurethane Mattress Cover
Recommended Phenolics Quaternary, Quat/Isopropyl
Acceptable Quaternary, Chlorine Bleach (1:10) Chlorine Bleach (1:10)
Not Recommended Quat/Isopropyl Phenolics
Quaternary Cleaners: identified by ingredients containing the phrase “…yl ammonium chloride”
Quat/Isopropyl Cleaners: identified by a quaternary ingredient above plus isopropyl alcohol
Phenolic Cleaners: identified by ingredients containing the suffix “-phenol”
Chlorine Bleach: known generically as “Sodium Hypochlorite”
SPECIAL INSTRUCTIONS
Velcro To clean and disinfect, saturate with disinfectant, rinse with water, and allow it to evaporate.
Soils or Stains Use neutral soaps and warm water. Do not use harsh cleansers, solvents or abrasive cleaners.
Hard-To-Clean Spots Use standard household/vinyl cleansers and a soft bristle brush on troublesome spots or
stains. Pre-soak heavy, dried-on soil.
Laundering Laundering is NOT RECOMMENDED. Laundering may substantially decrease the useful
life of the mattress.
DO NOT STEAM CLEAN, PRESSURE WASH, HOSE OFF OR ULTRASONICALLY CLEAN MATTRESSES.
Using these methods of cleaning are not recommended and may void this product’s warranty.
1. Make a solution of 1−2 tablespoons Sodium Thiosulfate in a pint of warm water and use it to wipe the stained area.
Clean the stain as soon as possible after it occurs. If stains are not immediately removed, allow solution to soak
or stand on the surface before wiping.
2. Rinse surfaces which have been exposed to the solution with clear water before returning mattress to service.
Note: Failure to follow the above directions when using these types of cleaners may void this product’s warranty.
At a minimum, preventative maintenance should be performed annually. A preventative maintenance program should
be established for all Stryker Medical equipment. Preventative maintenance may need to be performed more frequently
based on the usage level of the product.
LIMITED WARRANTY
Stryker Medical Division, a division of Stryker Corporation, warrants to the original purchaser of the Stryker Model
747/748 Transport Stretcher to be free from defects in material and workmanship for a period of one (1) 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, products or parts for which a warranty claim is made shall be returned prepaid to the factory. Any improper
use or any alteration or repair by others in such manner as in Stryker’s judgment affects the product materially and
adversely shall void this warranty. Any repair of Stryker products using parts not provided or authorized by Stryker shall
void this warranty. No employee or representative of Stryker is authorized to change this warranty in any way.
Stryker Medical Stretcher 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 Stretcher products will be free from structural defects for the expected
10 year life of the Stretcher product as long as the original purchaser owns the product.
This statement constitutes Stryker’s entire warranty with respect to the aforesaid equipment. Stryker makes no
other warranty or representation, either expressed or implied, except as set forth herein. There is no warranty
of merchantability and there are no warranties of fitness for any particular purpose. In no event shall Stryker be
liable here under for incidental or consequential damages arising from or in any manner related to sales or use of
any such equipment.
Warranty does not include any disposable items, I.V. poles (except for Stryker permanently attached poles), mattresses,
batteries, or damage resulting from abuse.
Stryker products are supported by a nationwide network of dedicated Stryker Field Service Representatives. These
representatives are factory trained, available locally, and carry a substantial spare parts inventory to minimize repair
time. Simply call your local representative, or call Stryker Customer Service USA at 1-800-327-0770.
Stryker has developed a comprehensive program of service contract options designed to keep your equipment operating
at peak performance at the same time it eliminates unexpected costs. We recommend that these programs be activated
before the expiration of the new product warranty to eliminate the potential of additional equipment upgrade charges.
* Replacement parts and labor for products under PM contract will be discounted.
** Does not include any disposable items, I.V. poles (except for Stryker permanently attached poles), mattresses, batteries, or damage resulting from
abuse.
RETURN AUTHORIZATION
Merchandise cannot be returned without approval from the Stryker Customer Service Department. An authorization
number will be provided which must be printed on the returned merchandise. Stryker reserves the right to charge
shipping and restocking fees on returned items. Special, modified, or discontinued, items not subject to return.
DAMAGED MERCHANDISE
ICC Regulations require that claims for damaged merchandise must be made with the carrier within fifteen (15) days of
receipt of merchandise. Do not accept damaged shipments unless such damage is noted on the delivery receipt at
the time of receipt. Upon prompt notification, Stryker will file a freight claim with the appropriate carrier for damages
incurred. Claim will be limited in amount to the actual replacement cost. In the event that this information is not received
by Stryker within the fifteen (15) day period following the delivery of the merchandise, or the damage was not noted on
the delivery receipt at the time of receipt, the customer will be responsible for payment of the original invoice in full.
Claims for any short shipment must be made within thirty (30) days of invoice.
This warranty reflects U.S. domestic policy. Warranty outside the U.S. may vary by country. Please contact your local
Stryker Medical representative for additional information.
EC REP
European Representative
Stryker France
ZAC Satolas Green Pusignan
Av. De Satolas Green
69881 MEYZIEU Cedex
France