Camilla Stryker 660Z Servicio
Camilla Stryker 660Z Servicio
Camilla Stryker 660Z Servicio
Model 660Z
MAINTENANCE MANUAL
PREVENTIVE MAINTENANCE
MAINTENANCE PROCEDURES
INTENDED USE
This product is intended to be used as a general purpose patient transport and treatment stretcher.
SPECIFICATIONS
Maximum Weight Capacity 660 pounds
Overall Bed Length \ Width 84” \ 34.5”
Minimum \ Maximum Bed Height 22” \ 36”
Fowler Angle 0 to 90°
Trendelenburg \ Reverse Trendelenburg +15 to −15°
Electrical Requirements − Power Source 115 VAC, 60 Hz, 3.0 Amps
Battery Voltage 24 V, 31 Ah
Noise 61 decibels
Water Protection IPX5
Mode of Operation Continuous
Environmental Conditions for Storage and Transport −20_ C − +70_ C
10% − 100% Relative Humidity
Atmospheric Pressure − 500 − 1060 hPa (14.76
inHg − 31.30 inHg)
Ambient Temperature in Charge Mode Not to exceed 28_ C
Stryker reserves the right to change specifications without notice.
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.
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
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.
Serious injury can result if caution is not used when operating the unit. Operate the unit only when all persons
are clear of the electrical and mechanical systems.
USE CAUTION while maneuvering the unit with the drive wheel activated. Always ensure there are no ob-
stacles near the unit while the drive wheel is activated. Injury to the patient, users or bystanders or damage
to the stretcher frame or surrounding equipment could occur if the unit collides with an obstacle.
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.
Ensure the brakes are completely released prior to attempting to move the unit. Attempting to move the unit
with the brakes actuated could result in injury to the user and/or patient.
Do not attempt to push the unit manually with the drive wheel engaged and the “ON/DRIVE − OFF/MANUAL”
switch in the ON position. The unit will be difficult to push and injury could result.
If unanticipated motion occurs, unplug the power cord from the wall socket and rotate the “ON/DRIVE − OFF/
MANUAL” switch to the OFF position.
Leave the stretcher litter in the lowest position when the patient is unattended. Leaving the litter in a raised
position could increase the chance of patient falls and injury.
Leave the siderails fully up and locked when the patient is unattended. After raising the siderails, pull firmly
on the siderail to ensure it is securely locked into the up position. Siderails are not intended to serve as a
patient restraint device to keep patients from exiting the unit. Siderails are designed 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 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 side-
rail spindles.
To avoid personal injury or damage to the equipment, do not allow the 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.
WARNING
Hand wash all surfaces of the frame with warm water and mild detergent. Dry thoroughly. DO NOT STEAM
CLEAN, PRESSURE WASH, HOSE OFF OR ULTRASONICALLY CLEAN. Using these methods of cleaning
is not recommended and may void this product’s warranty. Inspect the mattress cover after each use. Dis-
continue use if any cracks or rips are found in the cover which may allow fluids to enter the mattress. Exposure
to fluids may cause injury to patient and/or user.
If large fluid spills occur in the area of the circuit boards or motors, immediately unplug the power cord from
the wall socket and rotate the “ON/DRIVE − OFF/MANUAL” switch to the OFF position. Remove the patient
from the unit and clean up the fluid. Have maintenance completely check the unit. Fluids can short out con-
trols and may cause the unit to operate erratically or make some functions completely inoperable. Compo-
nent failure caused by fluids could even cause the unit to operate unpredictably and could cause injury to the
patient. DO NOT put the unit back into service until it is completely dry and has been thoroughly tested for
safe operation.
Preventative maintenance should be performed at a minimum of annually to ensure all features are function-
ing as designed. Close attention should be given to safety features including, but not limited to:
Safety side latching mechanisms Caster braking systems
Leakage current 300 microamps max. No controls or cabling entangled in frame mechanisms
Frayed electrical cords and components All controls return to off or neutral position when released
Danger: Explosion hazard. Equipment not suitable for use in the presence of a flammable anesthetic mixture
with air or with oxygen or nitrous oxide.
Caution: Possible fire hazard when oxygen administering equipment of other than the nasal mask or 1/2 bed
length tent type is used. Oxygen tent should not extend below mattress support level.
Always unplug the power cord and rotate the “ON/DRIVE − OFF/MANUAL” switch to the OFF position before
service or cleaning.
Remove the batteries if the equipment is placed in storage or will remain idle for an extended period of time.
Each battery weighs 25 pounds. To avoid personal injury, use caution when removing the two batteries.
Battery posts, terminals and related accessories contain lead and lead compounds, chemicals known to the
State of California to cause cancer and birth defects or other reproductive harm. Wash hands after han-
dling. Properly dispose of batteries when required.
The Model 660Z Stretcher is not intended for pediatric use or for patients under 50 pounds.
The Model 660Z Stretcher is intended for use by trained hospital personnel only.
Service only by qualified personnel. Refer to maintenance manual.
Do not modify the Model 660Z Stretcher. Modifying the unit can cause unpredictable operation resulting in
injury to the patient or operator. Modifying the unit will also void its warranty.
It is important that the Model 660Z Stretcher is working properly before it is put into service. The following
list will help ensure that each part of the unit is checked.
S Plug the power cord into a properly grounded, hospital grade wall receptacle. The 12 volt batteries that
provide power to the drive wheel and back−up power to the unit functions will charge whenever the power
cord is plugged into the wall socket. The batteries require approximately 6 hours of charging time before
the stretcher is put into service.
WARNING
The Model 660Z Stretcher is equipped with a hospital grade plug for protection against shock hazard. It must
be plugged directly into a properly grounded three−prong receptacle. Grounding reliability can be achieved
only when a hospital grade receptacle is used.
S Depress the pedal at either end of the stretcher fully to set the four wheel brakes and verify all four casters
are locked.
S Ensure the siderails raise and lower smoothly and lock securely in the full up position.
S Run through the operation of the drive wheel to ensure it is operating properly.
~ Alternating Current
Class 1 Equipment: equipment in which protection against electric shock does not rely
on BASIC INSULATION only, but which includes an additional safety precaution in that
means are provided for the connection of the EQUIPMENT to the protective earth con-
ductor in the fixed wiring of the installation in such a way that ACCESSIBLE METAL
PARTS cannot become live in the event of a failure of the BASIC INSULATION.
Internally powered.
IPX5
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.
* 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.
Serial No.:
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.
*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.
In the text, the words “right” and “left” refer to the right and left sides of a patient lying face up on the bed.
MAINTENANCE CONTENTS
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet Standard Screwdriver
Side Cutters
1. Remove the litter from the stretcher (see page 3−2 for procedure).
2. Using a 1/2” socket with extension and a 3/8” drive ratchet, remove the two hex head screws holding the
jack base to the stretcher base frame.
3. Remove the two hex head screws holding the jack reservoir clamp to the base frame and remove the
clamps.
4. Lift straight up on the pump connecting rod and disconnect the pump piston from the connecting rod.
5. Disconnect the pump pedal swivel from the release pedal mounting plate.
6. Remove the head end release rod from the release valve assembly.
7. Using a 1/2” socket with extension and a 3/8” drive ratchet, remove the two hex head screws holding the
jack base to the stretcher base frame.
8. Lift out the jack assembly.
9. To reinstall the jack, install the bolts on the jack and reservoir clamp but do not tighten them fully.
10. Reinstall the pump connecting rod and release rod.
11. Depress the pump pedal fully (to the floor). This will properly locate the jack onto the base frame.
12. Tighten the bolts on the jack and reservoir clamp.
13. Pump up the litter and apply weight to verify the jacks hold and do not drift.
NOTE
The jack descent rate is set at the factory and adjustment is not recommended.
1. Remove the litter from the stretcher (see page 3−2 for procedure).
2. Using a 1/2” socket with extension and a 3/8” drive ratchet, remove the kep nut securing the plastic battery
cover to the batteries.
3. Disconnect the battery cables.
4. Remove the batteries and set them aside.
5. Using a 1/2” socket with extension and a 3/8” drive ratchet, remove the hex head screw on each side of
the battery tray.
6. Push the battery connectors back through the battery tray.
7. Remove the battery tray and set it aside.
8. Using a 1/2” socket with extension and a 3/8” drive ratchet, remove the two hex head screws holding the
jack base to the stretcher base frame.
9. Remove the two hex head screws holding the jack reservoir clamp to the base frame and remove the
clamps.
10. Lift straight up on the pump connecting rod and disconnect the pump piston from the connecting rod.
11. Push the pump piston back through the oversized hole on the pump connecting rod.
12. Disconnect the release pedal swivel and remove the foot end release rod from the release valve.
13. Lift out the jack assembly.
14. To reinstall the jack, install the bolts on the jack and reservoir clamp but do not tighten them fully.
15. Reinstall the pump connecting rod and release rod.
16. Depress the pump pedal fully (to the floor). This will properly locate the jack onto the base frame.
17. Tighten the bolts on the jack and reservoir clamp.
18. Pump up the litter and apply weight to verify the jacks hold and do not drift.
NOTE
The jack descent rate is set at the factory and adjustment is not recommended.
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet
NOTE
The internal components of the electrical enclosure are not user serviceable. Return the entire assembly for
service (see page 1−7 for return authorization guidelines).
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet
1. Remove the litter from the stretcher (see page 3−2 for procedure).
2. Put the base brake/steer pedal in the steer position.
3. Remove the rue ring cotter and clevis pin holding the brake rod drive link to the brake rod at the head
end of the stretcher base.
4. Remove the rue ring cotter and clevis pin from the cam arm weldment.
5. Pull on the brake pedal at the head end of the stretcher to separate the brake rod from the cam arm as-
sembly.
6. Repeat steps 3 and 4 to remove the foot end brake rod.
7. Using a1/2” socket with extension, and a 3/8” drive ratchet, remove the two hex washer head cap screws
holding the cam arm assembly to the housing on the stretcher base frame.
8. Using a1/2” socket with extension, and a 3/8” drive ratchet, remove the two hex washer head cap screws
at the foot end of the stretcher holding the Zoomr carriage assembly to the stretcher base frame.
9. Under the base frame, remove the rue ring cotter and clevis pin holding the lift fork weldment to the Zoomr
undercarriage.
10. Disconnect the motor cable.
11. Remove the Zoomr carriage assembly.
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet
Required Tools:
1/2” Socket w/Extension 3/8” Drive Ratchet
1. Using a 1/2” socket and a 3/8” drive ratchet, remove the two hex head screws threaded through the cam
arm assembly into the housing on the stretcher base frame.
2. Using a 1/2” socket and a 3/8” drive ratchet, remove the nylock nut and carriage bolt threaded vertically
through the cam arm assembly into the housing on the stretcher base frame.
3. Pull on the left side of the cam arm assembly and lift it off the base frame.
Required Tools:
Needle Nose Pliers
1. Remove the cotter pins and clevis pins holding the brake rods to the cam arm weldment in the center of
the base.
2. Remove the cotter pins and clevis pins holding the brake rods to the brake rod drive links.
3. Remove the brake rods.
Required Tools:
9/16” Socket w/Extension 3/8” Drive Ratchet Needle−Nose Pliers
1. Using needle−nose pliers, unhook the extension springs from the top of the base caster tubes.
2. Remove the plastic caster covers.
3. While putting pressure on the caster carriage bolt, use a 9/16” socket and a 3/8” drive ratchet to remove
the caster nut on both sides of the stretcher.
4. Remove the casters.
5. Remove the brake rod (see procedure on page 3−7).
6. Remove the cotter pin from the clevis pin in the center of the brake ring weldment.
7. Remove the cotter pin from the bearing pivot support.
8. Remove the 3/4” nylock hex nut from the bearing pivot support.
9. Remove the drive link assembly.
10. Pull the brake ring down and out away from the stretcher base frame.
Required Tools:
None
1. Manually disengage the release pedal swivel (item J on page 5−20) from the release pedal assembly.
2. To increase the release rod engagement with the release valve, turn the release pedal swivel clockwise
on the threaded release rod.
3. To decrease the release rod engagement with the release valve, turn the release pedal swivel counter-
clockwise on the threaded release rod.
NOTE
If the pedal swivel assembly is threaded too far onto the release rod, the release valve will be partially acti-
vated and the jack will drift.
Required Tools:
7/16” Socket w/Extension 3/8” Drive Ratchet T−40 & T−27 Torx Sockets
1/2” Wrench
1. If the unit is equipped with an IV Pole, remove the nut and bolt holding the IV pole in the socket and remove
the IV pole.
2. Lift straight up on the display cover to separate the Velcro holding it on and remove the cover.
3. Remove the two hex head cap screws holding the belly tray to the underside of the base plate and remove
the tray.
4. Remove the two hex head cap screws and the two hex washer head screws fastening the PCB box as-
sembly to the base plate.
5. Carefully lift up on the PCB box assembly to expose the load cell cable, signal coil cord and left and right
handle connections.
6. Disconnect the cables and lift out the PCB box.
Required Tools:
7/16” Socket w/Extension 3/8” Drive Ratchet T−40 & T−27 Torx Sockets
1/2” Wrench 9/16” Socket
1. Remove the PCB box assembly to gain access to the load cell (see procedure above).
2. Disconnect the load cell cable at the handle PCB assembly
3. Remove the two hex head cap screws holding the load cell to the base plate.
4. Remove the external retaining ring from the handle cross bar.
5. Slide the handle cross bar from left to right.
6. Remove the load cell.
Required Tools:
Small Phillips Screwdriver
1. Remove the three pan head screws holding the halves of the handle grip together and remove the covers.
2. Carefully pull out the light pipe assembly and disconnect the handle switch cable from the handle exten-
sion cable.
3. Remove the handle pivot pin and external retaining ring securing the handle to the handle pivot.
4. Remove the handle.
In the parts lists, the words “right” and “left” refer to the right and left sides of a patient lying face up on the
stretcher.
DETAIL C
Cam Hanger
Bracket HEAD END
1040−010−320
1040−060−050 or Cord
1040−060−060 Clamp
See Detail D
DETAIL B
HEAD END
See Detail E
DETAIL E
FOOT END
See Detail F
DETAIL F
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 0005−040−000 Carriage Bolt 1 W 0081−330−000 Radial Bearing 1
B 0011−447−000 Washer 2 X (page 5−16) Base Ass’y/Std. Brakes 1
C 0013−038−000 Ext. Tooth Lock Washer 2 Y (page 5−7) Brake Rod Assembly 2
D 0014−007−000 Washer 1 Z (page 5−19) Base Ass’y/Dual Hyd. 1
E 0014−101−000 Wave Washer 1 AA (page 5−8) Cam Arm Assembly 1
F 0016−036−000 Nylock Hex Nut 2 AB 1040−006−031 Cam Arm Weldment 1
G 0021−166−000 Set Screw 2 AC (page 5−10) Overtravel Spring Ass’y 1
H 0023−288−000 Hex Washer Hd. Screw 12 AD 1040−010−027 Trend Limiter 2
J 0023−290−000 Hex Washer Hd. Screw 2 AE 1040−010−801 Comm. Coil Cord Cable 1
K 0023−305−000 Hex Washer Hd. Screw 1 AG 1040−010−831 Bezel 1
L 0026−273−000 Clevis Pin 4 AH (page 5−11) Zoom Carriage Assembly 1
M 0027−020−000 Rue Ring Cotter 4 AJ 1210−201−335 Red Brake Label 2
N 0029−007−000 Dual Lock 4 AK 1210−201−336 Green Steer Label 2
O 0029−009−000 Dual Lock 4 AL 1210−301−653 Cover w/Counterweight 2
R 0038−111−000 Cable Tie 4 AM 1040−010−008 Cord Ring 2
T 0042−020−000 Lock Collar 2 AN 1040−010−092 Scrunut 2
U 0081−329−000 Flange Bushing 3
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 0011−447−000 Washer 1 J 0081−240−000 Flange Bearing 4
B 0016−036−000 Nylock Hex Nut 1 L 1040−007−003 Fork Tray 1
D 0026−330−000 Clevis Pin 1 M 1040−007−005 Lift Fork Weldment 1
E 0026−331−000 Clevis Pin 2 N 1040−007−011 Spring Shaft 1
F 0027−020−000 Rue Ring Cotter 1 P 1040−007−013 Lift Spring Collar 1
G 0027−022−000 Rue Ring Cotter 2 Q 1040−007−014 Lift Spring Adjustable Collar 1
H 0038−496−000 Compression Spring 1 R 1040−007−031 Fork Sleeve Bushing 1
Battery Cable
1040−010−810
1040−010−836
1040−010−837
1040−010−808
TO MOTOR
1040−010−838
Bar Code
1040−010−807
NEGATIVE TERMINAL
BLACK CABLE
POSITIVE
TERMINAL
RED CABLE
SEE DETAIL A
DETAIL A
SEE DETAIL C
SEE DETAIL B
DETAIL C
Set Part Number Brake/Drive Label, Brake/Drive Label, Lift/Lower Label, Left Lift/Lower Label, Right
Foot End Head End
RED 1040−010−011 1040−010−012 1040−010−013 1040−010−014
1040−010−025
PURPLE 1040−010−111 1040−010−112 1040−010−113 1040−010−114
1040−010−125
GREEN 1040−010−211 1040−010−212 1040−010−213 1040−010−214
1040−010−225
GRAY 1040−010−311 1040−010−312 1040−010−313 1040−010−314
1040−010−325
TEAL 1040−010−411 1040−010−412 1040−010−413 1040−010−414
1040−010−425
PINK 1040−010−511 1040−010−512 1040−010−513 1040−010−514
1040−010−525
BLUE 1040−010−611 1040−010−612 1040−010−613 1040−010−614
1040−010−625
NOTE
All base hood department labels are quantity of two.
LITTER BUMPERS
NOTE
All litter bumpers are quantity of two.
Female IEC
to Control Box Male Plug Cord
HEAD END
HEAD END
1040−050−001 or
1040−150−001 (no I.V.)
See Detail A
WIRE ROUTING
DETAIL A
See Detail A
WIRE ROUTING
DETAIL A
page 5−40
Siderail−to−Litter Assembly, Fold−to−Head
HEAD END
FOOT END
HEAD END
page 5−43
Siderail−to−Litter Assembly, Fold−to−Foot
HEAD END
FOOT END
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 0003−359−000 Hex Hd. Cap Screw 4 L 1001−226−045 Latch Spacer 2
B 0007−070−000 Truss Hd. Mach. Screw 2 M 1001−226−161 Dual Latch Cable Ass’y 2
C 0016−118−000 Nylock Nut 6 N 1001−226−142 Latch Pin 2
D 1001−226−147 Dual Latch Pivot 1 P 0038−222−000 Extension Spring 2
E 1001−226−170 Dual Latch Pivot 1 R 1001−226−158 Latch Cover 2
G 1001−226−046 Latch Pivot, Right 1 S 1001−226−047 Latch Pivot, Left 1
H 0052−017−000 Nylon Washer 2 T 1001−226−157 Dual Latch Wldmt., Left 1
J 1001−226−156 Dual Latch Wldmt., Right 1 W 0059−767−000 Cable Clamp 2
HEAD END
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 1001−001−036 Hole Plug 2 H 0016−118−000 Hex Nut 8
B 1211−231−025 Trip Bar Pivot 2 J 0004−455−000 But. Hd. Cap Screw 2
C 1501−031−013 Fowler Tube 1 K 0037−064−000 Grommet Bumper 2
D 1510−231−012 Fowler Skin (Fiberresin) 1 L 0007−070−000 Truss Hd. Mach. Screw 4
E 1711−131−014 Pneu. Pivot Bar Wldmt. 1 M 0025−172−000 Blind Rivet 7
F 1711−231−018 Trip Bar Weldment 1 N 1211−131−030 Handle Grip 2
G 1711−231−029 Gas Spring Mount Wldmt. 1 P 0004−135−000 But. Hd. Cap Screw 2
HEAD END
HEAD END
FOOT END
HEAD END
FOOT END
HEAD END
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 0946−039−004 Tray 1 J 0946−039−003 Support Tube 2
B 0926−039−016 Crosstube 3 K 0926−001−082 Label 1
C 0025−055−000 Rivet 4 L 1010−050−021 Long Strap 1
D 0926−039−009 Cover 1 N 0946−001−283 Label 1
E 0018−006−000 Umbrella Nut 6 P 0926−039−015 Holder 2
F 0029−008−000 Dual Lock 6 R 0002−044−000 Rd. Hd. Mach. Screw 2
H 0029−010−000 Dual Lock 6 S 0002−105−000 Rd. Hd. Mach. Screw 6
Label Detail
Label Detail
Item Part No. Part Name Qty. Item Part No. Part Name Qty.
A 0008−049−000 Socket Hd. Shoulder Bolt 4 M 1010−050−050 Knob 2
B 0014−020−000 Nylon Washer 2 N 1010−050−057 “Max. Weight” Label 4
C 0014−021−000 Nylon Washer 2 P 1010−050−205 Cushion Assembly 1
D 0016−028−000 Fiberlock Nut 4 R 1010−050−218 Foot & Tray Board 1
E 0037−052−000 Rubber Bumper 2 S 1010−050−225 Pivot Frame Weldment 1
F 0038−133−000 Spring 2 T 1010−050−242 Pin Lock 1
H 0052−017−000 Spacer 4 W 1010−050−246 Base Mounting Ass’y 1
J 1010−050−017 Specification Label 1 Y 1010−050−248 Lower Pin Lock 1
K 1010−050−019 “Push/Pull” Label 1 Z 1010−050−250 Pin Adjuster 1
L 1010−050−021 Long Strap 1 AB 0721−031−065 Hole Plug 2
* If the stretcher has the crank Knee Gatch option, (2) 0003−355−000 and (2) 0003−358−000 replace (4)
0003−359−000.
A
View
A−A
6.5” (Ref.)
2”
(Ref.)
Base Hood