Camilla Stryker 660 Manual
Camilla Stryker 660 Manual
Camilla Stryker 660 Manual
Model 660
Operations Manual
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2, 3
Operating Base Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4, 5
Raising And Lowering Litter Height . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Trendelenburg/Reverse Trendelenburg Positioning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Applying The Brake System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Operating the Big Wheel Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Using Siderails . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Operating The Fowler/Knee Gatch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Operating Optional 2–Stage Permanently Attached I.V. Pole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Operating Optional 3–Stage Permanently Attached I.V. Pole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Operating Optional Tethered I.V. Pole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Using The Optional X–Ray Cassette Holder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Operating Optional Heel Stirrups . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Operating Optional Foot Extension/Defibrillator Tray . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Preventative Maintenance Checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16, 17
Limited Warranty
Obtaining Parts and Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Supplemental Warranty Coverage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Return Authorization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Freight Damage Claims . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Introduction
INTRODUCTION
This manual is designed to assist you with the operation of the Model 660 Atlas Stretcher. Read it thoroughly
before using the equipment or beginning any maintenance on it.
SPECIFICATIONS
Maximum Weight Capacity 660 pounds
Overall Bed Length \ Width 83” \ 34.5”
Minimum \ Maximum Bed Height 22” \ 31”
Fowler Angle 0 to 90°
Knee Gatch Angle 0 to 35_
Trendelenburg \ Reverse Trendelenburg +16 to –16°
WARNING
The personal safety of the patient or user may be involved. Disregarding this information could result in injury
to the patient or user.
CAUTION
These instructions point out special procedures or precautions that must be followed to avoid damaging the
equipment.
NOTE
This provides special information to make maintenance easier or important instructions clearer.
WARNING
Patients should be discouraged from sitting directly on the ends of the stretcher. Excessive weight will cause
the litter surface to tip up, possibly causing patient injury.
Always apply the caster brakes when a patient is getting on or off the stretcher. Push on the stretcher to en-
sure 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.
2
Introduction
Before operating this stretcher, it is important to read and understand all information in this manual. Carefully
read and strictly follow the warnings listed on this page.
WARNING
Be sure to move any equipment that may be in the way before raising or lowering the litter height.
Always apply the caster brakes when a patient is getting on or off the stretcher. Push on the stretcher to en-
sure 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. If brakes do not hold proper-
ly, refer to your stretcher maintenance manual for a brake adjustment procedure.
When lowering the siderail to the collapsed position, keep extremities of patients and staff away from the side-
rail spindles.
Do not allow siderail to lower on its own.
Keep fingers/hands clear of area around Fowler release handle and Fowler frame when lowering. Injury could
result if care is not taken when lowering the Fowler.
If pneumatic system appears to be difficult to operate, refer to the stretcher maintenance manual for “Pneu-
matic Fowler Adjustment”
The weight of the I.V. bags should not exceed 40 pounds.
3
Stretcher Operation
HEAD END
D C
A
B
4
Stretcher Operation
HEAD END
B C
A
5
Stretcher Operation
CAUTION
Be sure to move any equipment that may be in the way before raising or lowering the litter height.
To raise the litter height, pump pedal (A) repeatedly until the desired height is achieved (see page 4).
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 (see page 4).
CAUTION
Be sure to move any equipment that may be in the way before raising or lowering the litter height.
To raise the litter height, pump pedal (A) repeatedly until the desired height is achieved (see page 5).
To lower both ends of the litter simultaneously, depress pedal (B) and (C) together using the same foot. To
lower only the head end of the litter, depress pedal (B). To lower only the foot end of the stretcher, depress
pedal (C) (see page 5).
CAUTION
Be sure to remove any equipment that may be in the way before lowering the stretcher.
For Trendelenburg positioning (head down), depress the side of pedal (B) closest to the head end of the
stretcher (see page 4).
For Reverse Trendelenburg positioning (foot down), depress the side of pedal (B) closest to the foot end.
NOTE
The higher the litter is before pedal (B) is activated, the greater the trend. or reverse trend. angle will be.
(Maximum trend. angle is +16_. Maximum reverse trend. angle is –16_).
CAUTION
Be sure to remove any equipment that may be in the way before lowering the stretcher.
For Trendelenburg positioning (head down), depress pedal (B) (see page 5).
For Reverse Trendelenburg positioning (foot down), depress pedal (C) (see page 5).
6
Stretcher Operation
NOTE
For user convenience, the brake/steer pedal is located on both ends of the stretcher.
WARNING
Always apply the caster brakes when a patient is getting on or off the stretcher. Push on the stretcher to en-
sure the brakes are securely locked. Always engage the brakes unless the stretcher is being moved. If
brakes do not hold properly, refer to your stretcher maintenance manual for a brake adjustment procedure.
The stretcher may move, resulting in injury to the patient, if excessive force is applied. Use caution while
entering or exiting the stretcher or using the stretcher as a support.
To engage the brakes on the head (non–control) end, push fully down on the left side of pedal (E) (see illustra-
tion on page 5).
To engage the brakes on the foot (control) end, push fully down on the right side of pedal (D) (see illustration
on page 5).
NOTE
Your stretcher may be equipped with optional side control brake and steer functions in addition to the standard
head and foot end controls. The side control brakes operate the same as the head and foot end versions.
They are indicated by a label on each side of the stretcher base.
RIGHT SIDE
LEFT SIDE
7
Stretcher Operation
When the brake/steer pedal is in the neutral or brake position, the Big Wheel is elevated approxi-
mately 1” and the stretcher rests on the four casters.
NOTE
The two Big Wheels do not pivot. The stretcher cannot be moved directly sideways with the Big
Wheel activated. With the pedal in the neutral position, the stretcher can be moved in any direction
including sideways.
When the brake/steer pedal is in the steer position, the foot end casters are elevated approximate-
ly 1/4” and the stretcher rests on the two head end casters and the two Big Wheels. This provides
increased mobility and ease of steering the stretcher.
8
Stretcher Operation
NOTE
Raising and lowering the siderails is a two–
handed operation. Use one hand to hold and A
position the siderail and the other hand to op-
erate the siderail latch.
WARNING
When lowering the siderail to the collapsed A
position, keep the extremities of patients and
staff away from the siderail spindles or injury
could occur.
B
To raise siderails: Pull up on the siderail (A) A B
and raise it to the full up position until the latch HEAD END
(B) engages.
A
To lower siderails: Pull up on the latch (B) and
guide the siderail to the full down position.
NOTE
The latches (B) are colored red for easy identi-
fication.
WARNING
To avoid injury or damage to the equipment, Do
not allow the siderail to lower on its own.
B
B
NOTE
There is a dual siderail latch option available
where there are latches on both ends of the
stretcher.
LATCH DETAIL
9
Stretcher Operation
Squeeze handle (A) for pneumatic assist in lifting the Fowler to the desired height. Remove your hands from
the handle when the desired height is reached.
To lower, squeeze handle (A) and push down on the Fowler until it has reached the desired height. Remove
your hands from the handle when the desired height is reached.
WARNING
Keep hands/fingers clear of the area around the Fowler release handle and Fowler frame when lowering the
Fowler. Injury could result if care is not taken when lowering the Fowler.
FOOT END
10
Stretcher Operation
A
B
C
A
NOTE
The 2–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 the stretcher was purchased.
CAUTION
11
Stretcher Operation
C
E
B
B
D
NOTE
The 3–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 the stretcher was purchased.
To use the 3–stage permanently attached I.V. pole:
1. Lift and pivot the pole from the storage position and push down until it is locked into the receptacle.
2. To raise the height of the pole, pull up on the telescoping portion (A) until it locks into place at its fully raised
position.
3. For a higher I.V. pole, pull up on section (B). Release section (B) at any desired height and it will lock
into place.
4. Rotate the I.V. hangers (C) to the desired position and hang the I.V. bags.
5. To lower the I.V. pole, push up on the red portion of grip (D) while holding onto section (B) until it lowers.
Turn latch (E) clockwise until section (A) lowers.
CAUTION
12
Stretcher Operation
NOTE
The tray position can be adjusted, from the patient’s
head to the buttocks area, by loosening the knob on the A
front of the tray, sliding the tray to the desired position, and
re–tightening the knob to hold the position.
13
Stretcher Operation
1. To use the optional heel stirrups, turn the handle (A) on the
lock screw located under the litter frame and swing the
stirrup assembly into position. Tighten the handle (A) to
hold the assembly in place.
2. Loosen knob (B) and pull out the extension tube (C) to the
desired length. Tighten knob (B).
3. Loosen knob (D) and raise or lower the stirrup (E) to the
A
desired height. Tighten knob (D).
C B
WARNING
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 D
properly and injury could occur.
If the stretcher is equipped with the optional foot end
push handles, use caution while the foot extension/defi-
brillator tray is installed to avoid pinching your fingers.
FOOT END
14
Preventative Maintenance
CHECKLIST
NOTE
Preventative maintenance should be performed at a minimum of annually. A preventative maintenance pro-
gram 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.
15
Preventative Maintenance
CLEANING
Model 660 stretchers are designed to be power–washable. The unit may show some signs of oxidation or
discoloration from continuous washing. However, no degradation of the stretcher’s performance characteris-
tics or functionality will occur due to power washing as long as the proper procedures are followed.
DO NOT STEAM CLEAN THE UNIT. Use a maximum water temperature of 180_F/68_C. Maximum air dry
temperature (cart washers) is 240_F/115_C. Water pressure – 1500 psi/130.5 bar. If a hand held wand is
being used to wash the unit, the pressure nozzle must be kept a minimum of 24 inches/.61m from the unit.
Stretchers must have maintenance performed after a minimum of every fifth washing. Refer to the mainte-
nance manual for specific lubrication instructions.
Failure to comply with these instructions may invalidate any/all warranties.
16
Preventative Maintenance
CLEANING (CONTINUED)
In general, when used in those concentrations recommended by the manufacturer, either phenolic type or
quaternary type disinfectants can be used. Iodophor type disinfectants are not recommended for use be-
cause staining may result. The following products have been tested and have been found not to have a harm-
ful effect WHEN USED IN ACCORDANCE WITH MANUFACTURERS RECOMMENDED DILUTION.*
*MANUFACTURER’S
TRADE NAME DISINFECTANT MANUFACTURER RECOMMENDED
TYPE DILUTION
A33 Quaternary Airwick (Professional Products Division) 2 ounces/gallon
A33 (dry) Quaternary Airwick (Professional Products Division) 1/2 ounce/gallon
Beaucoup Phenolic Huntington Laboratories 1 ounce/gallon
Blue Chip Quaternary S.C. Johnson 2 ounces/gallon
Elimstaph Quaternary Walter G. Legge 1 ounce/gallon
Franklin Phenomysan F2500 Phenolic Purex Corporation 1 1/4 ounce/gallon
Franklin Sentinel Quaternary Purex Corporation 2 ounces/gallon
Galahad Phenolic Puritan Churchill Chemical Company 1 ounce/gallon
Hi–Tor Quaternary Huntington Laboratories 1/2 ounce/gallon
LPH Phenolic Vestal Laboratories 1/2 ounce/gallon
Matar Phenolic Huntington Laboratories 1/2 ounce/gallon
Omega Quaternary Airwick (Professional Products Division) 1/2 ounce/gallon
Quanto Quaternary Huntington Laboratories 1 ounce/gallon
Sanikleen Quaternary West Chemical Products 2 ounces/ gallon
Sanimaster II Quaternary Service Master 1 ounce/gallon
Vesphene Phenolic Vestal Laboratories 1 1/4 ounce/ gallon
Quaternary Germicidal Disinfectants, used as directed, and/or Chlorine Bleach products, typically 5.25% So-
dium Hypochlorite in dilutions ranging between 1 part bleach to 100 parts water, and 2 parts bleach
to 100 parts water are not considered mild detergents. These products are corrosive in nature and
may cause damage to your stretcher if used improperly. If these types of products are used to clean
Stryker patient handling equipment, measures must be taken to insure the stretchers are rinsed with clean
water and thoroughly dried following cleaning. Failure to properly rinse and dry the stretchers will leave a cor-
rosive residue on the surface of the stretcher, possibly causing premature corrosion of critical components.
NOTE
Failure to follow the above directions when using these types of cleaners may void this product’s warranty.
17
Warranty
Limited Warranty:
Stryker Medical Division, a division of Stryker Corporation, warrants to the original purchaser that its products
should 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. Stryker
warrants to the original purchaser that the frame and welds on its beds will be free from structural defects
for as long as the original purchaser owns the bed. If requested by Stryker, products or parts for which a
warranty claim is made shall be returned prepaid to Stryker’s factory. Any improper use or any alteration or
repair by others in such manner as in Stryker’s judgement 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 are designed for a 10 year expected life under normal use conditions and appropri-
ate periodic maintenance as described in the maintenance manual for each device.
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 HEREUNDER FOR INCIDENTAL OR CONSEQUENTIAL DAMAGES ARISING FROM OR IN ANY
MANNER RELATED TO SALES OR USE OF ANY SUCH EQUIPMENT.
18
Warranty
* Replacement parts and labor for products under PM contract will be discounted.
** Does not include any disposable items, I.V. poles (except for Stryker HD permanent poles), mattresses, or damage re-
sulting from abuse.
Return Authorization:
Merchandise cannot be returned without approval from the Stryker Customer Service Department. An autho-
rization 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.
19
European Representative
Stryker EMEA RA/QA Director
Stryker France
ZAC Satolas Green Pusignan
Av. De Satolas Green
69881 MEYZIEU Cedex
France