stryker Prime Series Stretcher Instruction Manual

: June 12, 2024
: stryker

Table of Contents

Prime Series Stretcher
Product Information
Symbols
Warning/Caution/Note Definition
WARNING
CAUTION
Note

Prime Series Stretcher

Product Information

The product is a Stryker medical device, model number 1125. It
is designed to assist with patient care and can be used for various
medical procedures. The product has been manufactured according to
European medical device standards and bears the CE mark. The
manufacturer is Stryker, and the date of manufacture is indicated
in the manual. The product has a safe working load capacity, which
is specified in the manual. It operates on both direct and
alternating current.

Symbols

Refer to instruction manual/booklet
Consult instructions for use
General warning
Caution
Warning; crushing of hands
Warning; non-ionizing radiation
No pushing
Do not store the oxygen bottle
Catalogue number
Serial number
Lot (batch) code
For US Patents see www.stryker.com/patents
CE mark
Authorized representative in the European Community
Manufacturer
Date of manufacture
Importer
Safe working load
Maximum patient weight
Mass of equipment with safe working load
Direct current
Alternating current
Dangerous voltage
Potential equalization
Protective earth ground
Protection from water jets
Type B applied part
MR Unsafe
This way up
Keep dry
Fragile, handle with care
Stacking limit by number

Warning/Caution/Note Definition

The words WARNING, CAUTION, and NOTE have 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.

Summary of Safety Precautions

Always read and strictly follow the warnings and cautions listed
in the manual. Service should only be performed by qualified
personnel.

Product Usage Instructions

Introduction

This manual provides assistance with the operation and
maintenance of the Stryker product. Before operating or maintaining
the product, it is important to read this manual thoroughly.
Additionally, methods and procedures should be set in place to
educate and train staff on the safe operation and maintenance of
the product.

Pinch Points

The manual contains information about pinch points that should
be taken into consideration during the operation and maintenance of
the product. Care should be taken to avoid injury or damage.

Setup

Refer to the corresponding section in the manual for detailed
instructions on setting up the product for use. Follow the provided
instructions carefully to ensure proper installation and
configuration.

Operation

Refer to the corresponding section in the manual for detailed
instructions on operating the product. Follow the provided
instructions carefully to ensure safe and effective use of the
product.

Option

If the product has additional optional features or functions,
refer to the “Option” section in the manual for instructions on how
to utilize those features. Follow the provided instructions
carefully to maximize the benefits of the product.

Scale System Option

If the product includes a scale system option, refer to the
“Scale System Option” section in the manual for instructions on how
to use this feature. Follow the provided instructions carefully to
ensure accurate measurements.

Please note that these usage instructions are a summary. For
complete and detailed instructions, refer to the specific sections
of the manual mentioned above.

Prime Series® Stretcher
Operations Manual 1125
with Zoom® Motorized Drive

1125-309-005 Rev AB.0

2021-12

Symbols

Refer to instruction manual/booklet Consult instructions for use General warning Caution Warning; crushing of hands Warning; non-ionizing radiation

No pushing

Do not store the oxygen bottle Catalogue number Serial number Lot (batch) code For US Patents see www.stryker.com/patents CE mark Authorized representative in the European Community European medical device

Manufacturer

Date of manufacture

Importer

Safe working load

1125-309-005 Rev AB.0

~
IPX5
87VL
MR

Maximum patient weight
Mass of equipment with safe working load Direct current
Alternating current
Dangerous voltage
Potential equalization
Protective earth ground Protection from water jets Type B applied part
Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1: 2005 and CAN/ CSA-C22.2 No. 60601-1:08. *For Prime X option, Associated Equipment of X-ray Equipment IEC 60601-2-54 In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic Equipment (WEEE) as amended, this symbol indicates that the product should be collected separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor for disposal information. Ensure infected equipment is decontaminated prior to recycling.
MR Unsafe
This way up
Keep dry

Fragile, handle with care Stacking limit by number

1125-309-005 Rev AB.0

Table of Contents
Warning/Caution/Note Definition ……………………………………………………………………………………………………..3 Summary of safety precautions …………………………………………………………………………………………………3 Pinch points ……………………………………………………………………………………………………………………6
Introduction ………………………………………………………………………………………………………………………………..7 Product description ………………………………………………………………………………………………………………..7 Indications for use ………………………………………………………………………………………………………………….7 Clinical benefits……………………………………………………………………………………………………………………..8 Contraindications …………………………………………………………………………………………………………………..8 Expected service life……………………………………………………………………………………………………………….8 Disposal/recycle…………………………………………………………………………………………………………………….8 Specifications ……………………………………………………………………………………………………………………….8 Product illustration – Prime ……………………………………………………………………………………………………..11 Product illustration – Prime X option ………………………………………………………………………………………….12 Applied parts – electric litter option ……………………………………………………………………………………………13 Applied parts – Prime X option …………………………………………………………………………………………………13 Contact information ………………………………………………………………………………………………………………13 Serial number location …………………………………………………………………………………………………………..14
Setup ………………………………………………………………………………………………………………………………………15 Operation …………………………………………………………………………………………………………………………………16
Applying and releasing the brakes ……………………………………………………………………………………………16 Prime base controls………………………………………………………………………………………………………………17 Raising the non- electric litter …………………………………………………………………………………………………..17 Lowering the non- electric litter…………………………………………………………………………………………………17 Raising the electric litter option ………………………………………………………………………………………………..18 Lowering the electric litter option ……………………………………………………………………………………………..18 Positioning the product in Trendelenburg …………………………………………………………………………………..18 Positioning the product in Reverse Trendelenburg ……………………………………………………………………….19 Transporting a patient without Big Wheel …………………………………………………………………………………..19 Transporting a patient with Big Wheel ……………………………………………………………………………………….20 Transporting a patient with Zoom Motorized Drive ……………………………………………………………………….20 Charging Zoom Motorized Drive battery …………………………………………………………………………………….23 Transporting a patient manually without Zoom Motorized Drive wheel ………………………………………………24 Raising the siderail ……………………………………………………………………………………………………………….24 Lowering the siderail……………………………………………………………………………………………………………..25 Positioning the product with the siderail patient control panel – electric litter option- Prime only ……………….25 Operator control panel – electric litter option – Prime only ……………………………………………………………….26 Locking and unlocking the patient control panel lockout – electric litter option – Prime only……………………..27 Raising or lowering the Fowler backrest – non-electric litter …………………………………………………………….27 Raising or lowering the Fowler backrest – electric litter option………………………………………………………….28 Raising or lowering the Gatch – non-electric litter – Prime only …………………………………………………………29 Raising or lowering the Gatch – electric litter option – Prime only………………………………………………………29 Positioning the recovery chair – Prime only …………………………………………………………………………………29 Storing objects in the base hood………………………………………………………………………………………………30 Hanging devices with the pump rack option ………………………………………………………………………………..30 Extending or retracting the power cord with the retractable cord reel option – electric lift option or electric litter
option ……………………………………………………………………………………………………………………31 Scale system option ……………………………………………………………………………………………………………..31
Scale icon/button identification ………………………………………………………………………………………….32 Weighing a patient………………………………………………………………………………………………………….32 Locking the scale unit of measure ………………………………………………………………………………………33 Arming or disarming the Chaperone option …………………………………………………………………………..33 Setting the Chaperone option alert pattern……………………………………………………………………………33 Setting the Chaperone option alert volume …………………………………………………………………………..34 Charging the scale system battery pack option – electric litter option or electric litter option with
Chaperone option – Prime only ………………………………………………………………………………34 Replacing the batteries for the scale system option – non-electric litter ………………………………………..34 Accessories and parts …………………………………………………………………………………………………………..35 Attaching the defibrillator tray ……………………………………………………………………………………………37 Converting the defibrillator tray/foot extender to a defibrillator tray ……………………………………………..38 Converting the defibrillator tray/foot extender to a foot extender ………………………………………………..38

1125-309-005 Rev AB.0

1 EN

Attaching the footboard/chart holder……………………………………………………………………………………39 Attaching the IV caddy …………………………………………………………………………………………………….39 Positioning or stowing the foot supports – Prime only ………………………………………………………………40 Positioning the two-stage permanently attached IV pole ………………………………………………………….41 Positioning the three-stage permanently attached IV pole ………………………………………………………..42 Attaching and positioning the removable IV pole ……………………………………………………………………43 Attaching the upright oxygen bottle holder ……………………………………………………………………………44 Extending or stowing the serving tray holder/footboard ……………………………………………………………44 Attaching the siderail pads ……………………………………………………………………………………………….45 Locating the patient restraint strap tie-ins …………………………………………………………………………….45 Positioning the upright X-ray cassette holder – Prime X option …………………………………………………..45 Positioning the lateral X-ray cassette holder – Prime X option ……………………………………………………46 Inserting or removing X-ray cassettes – Prime X option ……………………………………………………………47 Cleaning ………………………………………………………………………………………………………………………………….49 Cleaning the product …………………………………………………………………………………………………………….49 Cleaning the mattress……………………………………………………………………………………………………………49 Remove iodine ………………………………………………………………………………………………………………50 Special instructions…………………………………………………………………………………………………………50 Disinfecting ………………………………………………………………………………………………………………………………51 Disinfecting the product …………………………………………………………………………………………………………51 Disinfecting the mattress………………………………………………………………………………………………………..51 Preventive maintenance ………………………………………………………………………………………………………………53 EMC information ………………………………………………………………………………………………………………………..55

EN 2

1125-309-005 Rev AB.0

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.
Summary of safety precautions
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING · Always allow the product to reach room temperature before you set up the product or test functional operations.
Permanent product damage may occur. · Always operate the product when all operators are clear of the mechanisms. · Always use care when you handle the power cord. Entanglement, damage to the power cord, or potential shock hazards
may occur. If the power cord is damaged, immediately remove the product from service and contact the appropriate maintenance personnel. · Do not use the Prime Series stretcher with Zoom Motorized Drive in the MR (Magnetic Resonance Imaging) environment. The Prime Series stretcher with Zoom Motorized Drive is MR Unsafe. · Always plug the product directly into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade outlet. This product is equipped with a hospital grade plug to protect against electric shock hazard. · Always apply the brakes when a patient is getting on the product or off the product or when the product is not moving. Injury could result if the product moves while a patient is getting on the product or off the product. · Always position the patient in the center of the product. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do not leave the product at a higher height. · Always remove any devices that may be in the way before you raise or lower the litter. · Do not sit on the end of the product. The product may tip. · Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you transport a patient. · Do not use the Prime Series stretcher with Zoom Motorized Drive in the MR environment. The Prime Series stretcher with Zoom Motorized Drive is MR (Magnetic Resonance Imaging) Unsafe. · Always unplug the power cord from the wall outlet before you transport a patient or clean the product. · Do not attempt to push the product manually with the drive wheel engaged and the On/Drive-Off/Manual switch in the On position. The product will be difficult to push and injury may occur. · Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option. · Always lock the siderails in the full up position with the sleep surface flat and in the lowest position when you transport a patient. · Always keep the patient’s limbs away from the siderail spindles when you raise or 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.

1125-309-005 Rev AB.0

3 EN

· Always use caution when you raise a the Fowler backrest while a patient is on the product. Use proper lifting techniques and get help, if necessary.
· Always keep hands and fingers clear of the foot end push handles when you lower the Gatch.
· Always keep device lines on the pump rack away from the Gatch handles.
· Always make sure that devices on the pump rack can pass safely through door openings.
· Do not lift the product by the pump rack.
· Always unplug the power cord from the wall outlet before you transport or clean the product.
· Always use the retractable cord reel to store the power cord inside the base when you transport the product.
· Do not use the scale system option or electric lift option or electric litter option adjacent to or stacked with other devices. If adjacent or stacked use is necessary, the scale system option or electric lift option or electric litter option should be observed to make sure that all devices are operating normally in the configuration in which they will be used.
· Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray. Always strap down all devices that you place on the defibrillator tray.
· 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.
· Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray/foot extender. Always strap down all devices that you place on the defibrillator tray.
· Always secure the IV pole to the IV caddy when you transport the product.
· Always store the IV caddy when not in use to avoid product damage.
· Do not sit on the foot supports. This may cause the product to tip.
· Always clear your fingers from the mechanisms when you operate the foot supports.
· Always stow the foot supports when you transport a patient with the product.
· Always tighten the foot supports before you use the foot supports.
· Do not operate the scale system with the foot supports. Inaccurate readings may occur.
· Do not operate the Chaperone option with the foot supports. Inaccurate readings may occur.
· 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.
· Do not place objects that exceed 30 lb (14 kg) on the serving tray.
· 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 restraint 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.
· Always take protective measures when you use the upright or lateral X-ray cassette holder. The X-ray cassette holder does not protect against radiation.
· Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use Prime X option with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered radiation.
· Always follow the Positioning the upright X-ray cassette holder – Prime X option instructions to insert the X-ray cassette.
· Always use caution when you take X-rays with the Fowler backrest in the upright position or when you use a lateral cassette.
· Always follow the Positioning the lateral X-ray cassette holder – Prime X option instructions to insert the X-ray cassette.
· Always unplug the power cord and turn the On/Drive – Off/Manual switch to the Off position before service or cleaning.
· Do not steam clean, pressure wash, hose off, or ultrasonically clean the product.
· 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 to prevent cross-contamination.

EN 4

1125-309-005 Rev AB.0

· Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may void the product’s warranty.
· 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.
· 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.
· Always disconnect the plug from the wall outlet to isolate the Prime Series stretcher with Zoom Motorized Drive from the supply mains.
· Always position the Prime Series stretcher with Zoom Motorized Drive to allow for access to the wall outlet.
· Do not use the hydraulics on the base to raise the product with a patient lift under the product.
· Do not apply the steer pedal when Big Wheel is resting on a threshold or other raised area. The force required to apply Big Wheel will be higher than normal which may cause product damage.
· Always immediately unplug the power cord from the wall outlet and turn the On/Drive-Off/Manual switch to the Off position if large fluid spills occur in the area of the circuit boards or motors. Fluids can short out controls and may cause the product to operate erratically or may make some functions inoperable. Component failure caused by fluids may also cause the product to operate unpredictably and could cause injury to the patient. Do not put the product back into service until it is dry and has been tested for safe operation.
· Remove the batteries if the equipment is placed in storage or will remain idle for an extended period of time. Each battery weighs 25 lb. Use caution when removing the batteries to avoid injury.
· 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 your hands after handling. Properly dispose of batteries when required.
· The weight capacity of the Gatch is 200 lb (90.7 kg).
· Always make sure that the Gatch prop rod is secure before use.
· Do not sit or stand on the Gatch.
· Always use caution when you attempt to lower the Gatch while the product is unpowered. Gravity may cause a rapid drop of the Gatch.
· Do not place objects that exceed 60 lb (27 kg) in the base hood.
· Do not sit, step, or stand on the base hood.
· The weight capacity of the pump rack is 40 lb (18 kg).
· Do not use the pump rack as a push/pull device. Product damage may occur.
· Do not use the scale for patients under 50 lb.
· Do not use the scale system reading as a reference for medical treatment.
· Always raise the IV pole before you attach the defibrillator tray/foot extender to the product. If you do not raise the IV pole, the foot extender will not operate.
· Do not use the IV pole as a push/pull device. Product damage may occur.
· 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.
· Do not use abrasive cleaners to clean the display enclosure for the scale system option. Do not allow cleaning solutions or other fluids to pool on the display unit. Wipe dry all surfaces after spills or cleaning.
· The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation.
· The emissions characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment, for which CISPR 11 class B is normally required, this equipment might not offer adequate protection to radio frequency communication services. The user might need to take mitigation measures, such as relocating or reorienting the equipment.
· Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be used no closer than 12 inches (30 cm) to any part of the Prime stretcher, including cables specified by the manufacturer.

1125-309-005 Rev AB.0

5 EN

· Avoid stacking or placing other equipment adjacent with other equipment to prevent improper operation of the products. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they are operating properly.
Pinch points
Figure 1 Prime X option

EN 6

1125-309-005 Rev AB.0

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.
Note · 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 1125 Prime Series® stretcher with Zoom® Motorized Drive is a powered wheeled stretcher that consists of a platform mounted on a wheeled frame that is designed to support patients in a horizontal position. The stretcher provides a method of transporting patients within the interior of a healthcare facility by health professionals or trained representatives of the facility. The Prime Series stretcher with Zoom Motorized Drive features an electric drive system which aids the health professional or trained representative by assisting stretcher movement and maneuverability in various healthcare facilities. The device can be manually pushed by the user in the event of power loss to Zoom Motorized Drive. The device has siderails and has the option available to support the temporary or permanent placement of IV poles, along with various other options and accessories to assist with the transport of the patient.
Indications for use
The Stryker Model 1125 Prime Series stretcher with Zoom Motorized Drive is an electromechanical stretcher that provides a healthcare professional or trained representative greater maneuverability in steering and moving the stretcher with significantly less force.
The Prime Series stretcher may be used as a short-term outpatient clinical evaluation, treatment, minor procedure, and short-term outpatient recovery platform. The stretcher may include use in, but is not limited to:
· Emergency Department (ED)
· Trauma area
· Post-Anesthesia Care Unit (PACU)
The Prime Series stretcher may be used for minor procedures and short-term stay (treatment and recovery). See the specifications table for the intended environmental conditions.
The Stryker Prime Series stretcher has not been evaluated for compliance to bed standard BS EN 50637. This product is not intended for use for short term stay with pediatric patients or adult patients with atypical anatomy in markets that recognize this bed standard for market authorization.
The Prime Series stretcher has a safe working load up to 700 lb (318 kg) and is intended to be used with all patients, including those mildly to critically ill. The stretcher may also be used to transport deceased patients within an enclosed healthcare facility.
The Prime X® option provides an articulating radiographic patient support surface and a platform below the patient support surface for X-ray cassette placement. The Prime X option is intended to allow the capture of clinical X-rays (AP full body, optional full body lateral, and optional upright chest) when used with a medical X-ray system.

1125-309-005 Rev AB.0

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Clinical benefits
Patient transport, facilitate treatment, and diagnostic

Contraindications
The Prime Series stretcher with Zoom Motorized Drive is not intended for home healthcare or domestic use or those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes.
The Prime Series stretcher with Zoom Motorized Drive with Prime X option is not intended for use with a mattress with a thickness greater than four inches and is not compatible for use with a C-Arm.

Expected service life
The Prime Series stretcher and the Prime Series stretcher with Prime X option have a 10 year expected service life under normal use conditions and with appropriate periodic maintenance.

Disposal/recycle
Always follow the current local recommendations and/or regulations governing environmental protection and the risks associated with recycling or disposing of the equipment at the end of its useful life.

Specifications

Prime Series 26 in. width

Prime Series 30 in. width

Prime X option 30 in. width

Note – Safe working load indicates the sum of the patient, mattress, and accessory weight

700 lb

318 kg

700 lb

318 kg

700 lb

318 kg

Maximum patient weight Weight of product standard configuration Weight of product with all options/ accessories
Overall length
Overall width (siderails up)
Overall width (siderails down)

675 lb

306 kg

675 lb

306 kg

675 lb

306 kg

415 lb

188 kg

435 lb

197 kg

435 lb

197 kg

465 lb

211 kg

485 lb

220 kg

485 lb

220 kg

86 in. (± .5 in.)
34 in. (± 1 in.)
30.25 in. (± .5 in.)

218.4 cm (± 86 in. (± .5 1.27 cm) in.)

86.4 cm

38 in. (± 1 in.)

76.8 cm

30.5 in. (± .5 in.)

218.4 cm (± 86 in. (± .5 218.4 cm (±

1.27 cm)

in.)

1.27 cm)

96.5 cm

38 in. (± 1 in.)

96.5 cm

77.5 cm

30.5 in. (± .5 in.)

77.5 cm

EN 8

1125-309-005 Rev AB.0

Prime Series 26 in. width

Prime Series 30 in. width

Prime X option 30 in. width

Minimum/maximum height

23 in. / 34 in. (± 1 in.)

58 cm / 86 cm (±2.54 cm)

23 in. / 34 in. (± 1 in.)

58 cm / 86 cm (±2.54 cm)

23 in. / 34 in. (± 1 in.)

58 cm / 86 cm (±2.54 cm)

Fowler backrest angle

0° to 90° (± 5°)

Gatch height

5.5 in. (14 cm) minimum

Not applicable

Trendelenburg/Reverse Trendelenburg

+16°/-16°

2.5 in. nominal

6.4 cm

2.5 in. nominal

6.4 cm

2.5 in. nominal

6.4 cm

Minimum clearance

1.75 in. under the hydraulic jacks

4.5 cm

1.75 in. under the hydraulic jacks

4.5 cm

1.75 in. under the hydraulic jacks

4.5 cm

0.75 in. under Zoom 1.9 cm wheels

0.75 in. under Zoom wheels

1.9 cm

0.75 in. under Zoom 1.9 cm wheels

Electrical requirements

100 VAC, 50 Hz, 4A 120 VAC, 60 Hz, 4A 240 VAC, 50/60 Hz, 4A

Battery type

2 x 12 VDC 31Ah battery (2 x 12 VDC) lead acid gel cell battery

Battery voltage

24 VDC

Attenuation equivalent (aluminum equivalence)

Not applicable

Maximum value allowed is 1.7 mm Al

Scale system option weight operating range

50 lb (22.7 kg) to 700 lb (318 kg)

Scale system option accuracy

±3 lb (1.3 kg) for weights less than 100 lb (45 kg) and ±3% for weights greater than or equal to 100 lb (45 kg)*

*To meet the scale system option accuracy claim, the patient surface must be in the flat position (Fowler backrest and Gatch down) and the product cannot exceed 5 degrees of Trendelenburg/Reverse Trendelenburg.

Electric options Electrical requirements Duty cycle

Optional electric litter (available on Prime only)
120 VAC, 60 Hz, 4A 240 VAC, 50 Hz, 4A 240 VAC, 50/60 Hz, 4A
Continuous operation with intermittent loading is 1 min. ON/20 min. OFF

Optional scale system Battery type Battery voltage

Non-electric litter (available on Prime and Prime X option)
4 x AA battery (4 x 1.5 VDC) alkaline type (LR6)
6.0 VDC

1125-309-005 Rev AB.0

9 EN

Optional scale system Battery type Battery voltage

Optional electric litter 1 x rechargeable lithium ion battery pack (0058-135-000) 10.8 VDC, 2.4Ah

Optional scale system with Chaperone® (stretcher exit)
Battery type
Battery voltage

Optional electric litter 1 x rechargeable lithium ion battery pack (0058-134-000) 10.8 VDC, 4.8Ah

Stryker reserves the right to change specifications without notice.
Note – This product is not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.

Environmental conditions
Temperature

Operation
50 °F (10 °C)

100 °F (38 °C)

Charging
50 °F (10 °C)

82 °F (28 °C)

Storage and transportation

-4 °F (-20 °C)

140 °F (60 °C)

Relative humidity

75% 30%

95% 10%

Atmospheric pressure

700 hPa

1060 hPa

700 hPa

1060 hPa

500 hPa

1060 hPa

Note – The scale system option (non-electric litter/electric litter option) operation temperature range is 61 °F (16 °C) to 79 ° F (26 °C).
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
In accordance with the European REACH regulation and other environmental regulatory requirements, the components that contain declarable substances are listed.

Description Gel cell battery assembly Battery assembly

Number 1040-020-007 1040-010-870

Substance of very high concern (SVHC) chemical name
Lead
Lead

EN 10

1125-309-005 Rev AB.0

Product illustration – Prime
Q A

B
C

J D
E
FG
I H

Figure 2 Product illustration – Prime

Zoom handle

BackSmart® siderail

Base hood storage

Pump pedal

Uni-lower pedal

Big Wheel

Bumper, integrated

Caster with integrated wheel cover

Brake/steer pedal

Hydraulic release pedal

Pump pedal

Siderail latch

Gatch release handle

BackSmart foot end operator control panel, optional

BackSmart scale system option

Patient control panel lockout, optional

Siderail patient control panel, optional

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11 EN

Product illustration – Prime X option A

B
C
D

L
K J

E F
G I
H

Figure 3 Product illustration – Prime X option

Zoom handle

Patient surface with Clearview Technology® deck

Cassette tray

BackSmart siderail

Pump pedal

Uni-lower pedal

Bumper, integrated

Caster with integrated wheel cover

Brake/steer pedal

Siderail latch

Pump rack, optional

BackSmart scale system option

EN 12

1125-309-005 Rev AB.0

Applied parts – electric litter option

Figure 4 Type B applied parts – electric litter option
Applied parts – Prime X option

Contact information

Figure 5 Type B applied parts – Prime X option

Contact Stryker Customer Service or Technical Support at: 1-800-327-0770.

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Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA Note – The user and/or the patient should report any serious product-related incident to both the manufacturer and the Competent authority of the European Member State where the user and/or patient is established. 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.
Serial number location
A
Figure 6 Serial number location

EN 14

1125-309-005 Rev AB.0

Setup
To unpack your product, see the unpacking instructions that are attached to the product inside of the shipping crate.
WARNING · Always allow the product to reach room temperature before you set up the product or test functional operations.
Permanent product damage may occur. · Always operate the product when all operators are clear of the mechanisms. · Always use care when you handle the power cord. Entanglement, damage to the power cord, or potential shock hazards
may occur. If the power cord is damaged, immediately remove the product from service and contact the appropriate maintenance personnel. · Do not use the Prime Series stretcher with Zoom Motorized Drive in the MR (Magnetic Resonance Imaging) environment. The Prime Series stretcher with Zoom Motorized Drive is MR Unsafe. · Always plug the product directly into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade outlet. This product is equipped with a hospital grade plug to protect against electric shock hazard.
CAUTION · Always disconnect the plug from the wall outlet to isolate the Prime Series stretcher with Zoom Motorized Drive from
the supply mains. · Always position the Prime Series stretcher with Zoom Motorized Drive to allow for access to the wall outlet.
Make sure that the product is working before you put the product into service.
1. Apply the brake. Push on the product to make sure that all four casters are locked. 2. Release the brake. Push on the product to make sure that all four casters are unlocked. 3. Raise and lower the litter with the hydraulic lift system. 4. Raise the product to the highest position and put the product in the Trendelenburg position. Make sure that the head end
lowers to the full down position. 5. Raise the product to the highest position and put the product in the Reverse Trendelenburg position. Make sure that the
foot end lowers to the full down position. 6. Apply Big Wheel and make sure that the product raises and you can guide the product with the front casters and Big
Wheel. 7. Apply Zoom Motorized Drive. Make sure that you can push the product forward and backward with the push handles. 8. Make sure that the siderails raise, lower, and lock in place. 9. Raise and lower the manual Fowler backrest (head end). 10. Raise and lower the manual Gatch (foot end).
For product with the electric litter option:
1. Complete the setup checklist above. 2. Plug the product into a grounded, hospital grade wall outlet. Make sure that the LED lights illuminate on the lockout
keypad. 3. Make sure that each function on the siderail patient control panel option works. 4. Make sure that each function on the foot end operator control panel option works. 5. Raise and lower the electric Fowler backrest (head end). 6. Raise and lower the electric Gatch (foot end).
For product with the scale system option – electric litter option (with or without Chaperone option):
1. Complete the setup checklist above. 2. Charge the batteries.

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15 EN

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. 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 (red) side of the brake/steer pedal. Push on the product to make sure that the brakes work. To release the brakes, push down on the steer (green) side of the brake/steer pedal.
A
A
Figure 7 Operating the brake/steer pedal Note – Do not push down on the center of the brake/steer pedal. Always push down on the outer side (A) of the brake/steer pedal (Figure 7).

EN 16

1125-309-005 Rev AB.0

Prime base controls

D D

A CA

A C

A BD

Figure 8 Prime base controls and label
Raising the non-electric litter
WARNING · Always position the patient in the center of the product. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always remove any devices that may be in the way before you raise or lower the litter. · Do not sit on the end of the product. The product may tip.
CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product.
To raise the litter, press down on the pump pedal (A) until you achieve the desired height (Prime base controls (page 17)).

Lowering the non-electric litter
WARNING · Always position the patient in the center of the product. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always remove any devices that may be in the way before you raise or lower the litter. · Do not sit on the end of the product. The product may tip.

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CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product.
To lower the entire litter, press down on the center of the uni-lower pedal (C) (Prime base controls (page 17)).
To lower the head end of the litter, press down on the pedal (B) or on side of the uni-lower pedal (C) closest to the head end of the product.
To lower the foot end of the litter, press down on the pedal (D) or press down on the side of the uni-lower pedal (C) closest to the foot end of the product.

Raising the electric litter option
WARNING · Always position the patient in the center of the product. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always remove any devices that may be in the way before you raise or lower the litter. · Do not sit on the end of the product. The product may tip.
CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product.
To raise the electric litter, press down on the pump pedal (A) until you achieve the desired height (Prime base controls (page 17)).

Lowering the electric litter option
WARNING · Always position the patient in the center of the product. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always remove any devices that may be in the way before you raise or lower the litter. · Do not sit on the end of the product. The product may tip.
CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product.
To lower the entire electric litter, press on the center of the uni-lower pedal (C) (Prime base controls (page 17)).
To lower the head end of the litter, press down on the pedal (B) or push down on the side of the uni-lower pedal (C) closest to the head end of the product.
To lower the foot end of the litter, press down on the pedal (D) or push down on the side of the uni-lower pedal (C) closest to the foot end of the product.

Positioning the product in Trendelenburg
WARNING – Always remove any devices that may be in the way before you raise or lower the litter.
CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product. To position the product in the Trendelenburg position (head down), raise the litter to the highest height (Raising the nonelectric litter (page 17) or Raising the electric litter option (page 18)). Note – Raise the litter to the highest height for a greater Trendelenburg angle.

EN 18

1125-309-005 Rev AB.0

To lower the head end of the product, push down on the head end or foot end release pedal (D) or push down on the side of the uni-lower pedal (C) closest to the head end (Prime base controls (page 17)). To lower the product from Trendelenburg position, push down on the head end and foot end release pedals (B and D) at the same time or push down on the center of the uni-lower pedal (C) until the litter is flat.
Positioning the product in Reverse Trendelenburg
WARNING – Always remove any devices that may be in the way before you raise or lower the litter.
CAUTION – Do not use the hydraulics on the base to raise the product with a patient lift under the product.
To position the product in the Reverse Trendelenburg position (foot down), raise the litter to the highest height (Raising the non-electric litter (page 17) or Raising the electric litter option (page 18)). Note – Raise the litter to the highest height for a greater Trendelenburg angle. To lower the foot end of the product, push down on the head end or foot end release pedal (B) or push down on the side of the uni-lower pedal (C) closest to the foot end (Prime base controls (page 17)). To lower the product from Reverse Trendelenburg position, push down on the head end and foot end release pedals (B and D) at the same time or push down on the center of the uni-lower pedal (C) until the litter is flat.
Transporting a patient without Big Wheel
WARNING · Always position the patient in the center of the product. · Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
To transport a patient without Big Wheel: 1. Put the brake/steer pedal (A) in the neutral position (Figure 9).
A

Figure 9 Transporting without Big Wheel
2. Lower the litter to the lowest position. 3. For Model 1125 only, make sure that the On/Drive-Off/Manual switch is in the Off position. 4. Unplug the power cord from the hospital grade wall outlet if your product is equipped with the electric lift option or
electric litter option. 5. Use the push handles to push the product. 6. Apply the brakes to lock the product in place.

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Note · Always make sure that the brake is released before you move the product to avoid operator or patient injury. · With the product in the neutral position, Big Wheel (B) is elevated and the product rests on all four casters (C) (Figure
9). In this position, you can move the product in any direction, including sideways.
Transporting a patient with Big Wheel
WARNING · Always position the patient in the center of the product. · Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
CAUTION – Do not apply the steer pedal when Big Wheel is resting on a threshold or other raised area. The force required to apply Big Wheel will be higher than normal which may cause product damage.
To transport a patient with Big Wheel: 1. Raise the siderails to the highest position. Pull on each siderail to make sure it is latched. 2. Lower the litter to the lowest position. 3. For Model 1125 only, make sure that the On /Drive-Off/Manual switch is in the Off position. 4. Unplug the power cord from the hospital grade wall outlet if your product is equipped with the electric lift option or
electric litter option. 5. Put the brake/steer pedal (A) in the steer position (Figure 10).
A

Figure 10 Transporting with Big Wheel
6. Use the push handles to push the product. 7. Apply the brakes to lock the product in place.
Note · Always make sure that the brake is released before you attempt to move the product. Attempting to move the product
with the brakes applied may result in operator or patient injury. · The Big Wheel (B) does not pivot. You cannot move the product sideways when you apply Big Wheel. · When you apply Big Wheel (B), the product is raised and the foot end casters (C) are elevated. The product rests on the
head end casters and Big Wheel makes the product easier to steer (Figure 10).
Transporting a patient with Zoom Motorized Drive
WARNING · Always position the patient in the center of the product.

EN 20

1125-309-005 Rev AB.0

· Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you transport a patient.
· Do not use the Prime Series stretcher with Zoom Motorized Drive in the MR environment. The Prime Series stretcher with Zoom Motorized Drive is MR (Magnetic Resonance Imaging) Unsafe.
· Always operate the product when all operators are clear of the mechanisms.
CAUTION – Always immediately unplug the power cord from the wall outlet and turn the On/Drive-Off/Manual switch to the Off position if large fluid spills occur in the area of the circuit boards or motors. Fluids can short out controls and may cause the product to operate erratically or may make some functions inoperable. Component failure caused by fluids may also cause the product to operate unpredictably and could cause injury to the patient. Do not put the product back into service until it is dry and has been tested for safe operation. To transport a patient with Zoom Motorized Drive: 1. Unplug the power cord from the wall outlet.
Note – The drive function will not operate if the power cord is plugged into the wall outlet. 2. Put the brake/steer pedal (A) in the steer position (Figure 11).
A B
Figure 11 On/Drive-Off/Manual switch 3. Lower the litter to the lowest position. 4. Turn the On/Drive-Off/Manual switch (B) to the ON position. 5. Check the two LEDs on the drive handle to see if the product is ready for use. If the green LED is on, the product is
ready for use. If the amber LED is on, the product is not ready for use. Make sure that the pedal is in the steer position, the power cord is not plugged in, and the power switch is in the ON position. 6. If the drive handles are in the stowed position, pull the handles up to the raised position and then push down on the handles to lock them in the use position (Figure 12).

1125-309-005 Rev AB.0

21 EN

A
Figure 12 Zoom handles in the raised position 7. Grasp the drive handles at the two raised grip areas. Squeeze one or both of the motion release switches (A) under the
handles to move the product (Figure 13). Note – You can use either motion release handle to start movement, but you must release both motion release handles to stop movement.
Figure 13 Zoom operation 8. Push the handles away from you or pull the handles toward you to move the product in the desired direction. As you
push or pull, the product will adjust the speed in proportion to the amount of force that you apply to the drive handles. When the desired speed is reached, relax the force to maintain the speed. 9. Push or pull the handles again to increase or decrease the speed of the product. 10. Release both handles to stop the product. Note – The drive wheel does not pivot. You cannot move the product directly sideways when the drive wheel is applied. With the drive wheel in the neutral position and the brakes released, you can move the product in any direction, including sideways. 11. Apply the brakes to lock the product in place. 12. Stow the drive handles by lifting up on the handles. Push the handles into the stowed position (Figure 14).

EN 22

1125-309-005 Rev AB.0

B
Figure 14 Zoom handles in the stowed position Note · Use caution when you move the product with the drive wheel applied. Make sure that there are no obstacles near the
product while the drive wheel is applied. Injury to patient, operator, or bystander or damage to the product or surrounding equipment could occur if the product collides with an obstacle. · Always make sure that the brake is released before you attempt to move the product. Attempting to move the product with the brakes applied may result in operator or patient injury. · If unanticipated motion occurs, turn the On/Drive-Off/Manual switch to the Off position. Unplug the power cord from the wall outlet.
Charging Zoom Motorized Drive battery
CAUTION · Remove the batteries if the equipment is placed in storage or will remain idle for an extended period of time. Each
battery weighs 25 lb. Use caution when removing the batteries to avoid injury. · 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 your hands after handling. Properly dispose of batteries when required.
Two 12 volt batteries are required to power the drive wheel. The drive wheel will not operate properly if the batteries are not sufficiently charged. When fully discharged, the batteries require approximately 8 hours of charging time to recharge (Figure 15). Plug the power cord into a grounded, hospital grade wall outlet whenever possible to maintain the battery charge levels. The battery power gauge is located at the head end of the litter (Figure 15). The six LEDs illuminate individually to indicate the level of battery power that is available to the product. As the batteries are charging, the LEDs will flash in succession until all are flashing to indicate that the batteries are fully charged.

1125-309-005 Rev AB.0

23 EN

Figure 15 Battery power gauge
Transporting a patient manually without Zoom Motorized Drive wheel
WARNING · Always unplug the power cord from the wall outlet before you transport a patient or clean the product. · Do not attempt to push the product manually with the drive wheel engaged and the On/Drive-Off/Manual switch in the On
position. The product will be difficult to push and injury may occur. · Always position the patient in the center of the product. · Always lock the siderails in the full up position with the sleep surface horizontal and in the lowest position when you
transport a patient.
CAUTION – Do not apply the steer pedal when Big Wheel is resting on a threshold or other raised area. The force required to apply Big Wheel will be higher than normal which may cause product damage.
To transport a patient manually without Zoom Motorized Drive wheel: 1. Raise the siderails to the highest position. Pull on each siderail to make sure it is latched. 2. Unplug the power cord from the wall outlet. 3. Turn the On /Drive-Off/Manual switch to the Off position. 4. Put the brake/steer pedal in the steer position.
Note – You can now move the product with Big Wheel for easier manual transportation. 5. Use the push handles to push the product. 6. Apply the brakes to lock the product in place.
Note · Always make sure that the brake is released before you move the product to avoid operator or patient injury. · When you apply Big Wheel, the product is raised and the foot end casters are elevated. The product rests on the
head end casters and Big Wheel to make the product easier to steer.
This manual transport option allows you to move the product with the assistance of Big Wheel without the power assistance of Zoom Motorized Drive wheel.
Raising the siderail
WARNING · Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always lock the siderails in the full up position with the sleep surface flat and in the lowest position when you transport a
patient. · Always keep the patient’s limbs away from the siderail spindles when you raise or lower the siderail. · Do not allow the siderails to lower on their own.
To raise the siderail: 1. Use two hands to grasp the siderail. 2. Lift the siderail toward the foot end of the product until the yellow release latch clicks into place. Pull on the siderail to
make sure that the siderail is latched.

EN 24

1125-309-005 Rev AB.0

Note · There is a dual siderail release latch option available with latches on both ends of the product. · 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 how much restraint is needed to make sure that the patient is safe. · You can use the foot end of the siderail top rail as a push/pull device. · Siderails only lock in the full up position.
Lowering the siderail
WARNING · Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option. · Always put the product in the lowest position with the siderails up and latched when you leave a patient unattended. Do
not leave the product at a higher height. · Always lock the siderails in the full up position with the sleep surface flat and in the lowest position when you transport a
patient. · Always keep the patient’s limbs away from the siderail spindles when you raise or lower the siderail. · Do not allow the siderails to lower on their own.
To lower the siderail: 1. Use one hand to grasp the siderail. 2. Use the other hand to pull up on the yellow release latch. 3. Lift and guide the siderail toward the head end of the product until the yellow release latch clicks into place. Pull on the
siderail to make sure that the siderail is latched.
Note · There is a dual siderail release latch option available with latches on both ends of the product. · 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 how much restraint is needed to make sure that the patient is safe. · You can use the foot end of the siderail top rail as a push/pull device. · Siderails only lock in the full up position.
Positioning the product with the siderail patient control panel – electric litter option- Prime only
WARNING – Always operate the product when all operators are clear of the mechanisms.
Use the siderail patient control panel to position the Fowler backrest and Gatch (Figure 16).
Healthcare professionals must instruct patients how to operate the patient controls.
Note · Always plug the power cord into a grounded, hospital grade wall outlet. · The siderail patient control panel is positioned in a staggered location on each side of the product for easy patient
access. · Each siderail has backlit controls to allow the patient to position the Fowler backrest and Gatch. When the product is
plugged in and the patient control panel is unlocked, the white buttons are illuminated.

1125-309-005 Rev AB.0

25 EN

CD DC

Fowler down

Fowler up

Gatch up

Gatch down

Figure 16 Siderail patient control panel
Lowers the Fowler (head section) Raises the Fowler (head section) Raises the Gatch (foot section) Lowers the Gatch (foot section)

Operator control panel – electric litter option – Prime only
WARNING – Always operate the product when all operators are clear of the mechanisms. Use the operator control panel to adjust the position of the patient on the product (Figure 17). Note – Always plug the power cord into a grounded, hospital grade wall outlet.

AB CD

Fowler up

Fowler down

Gatch up

Gatch down

Figure 17 Operator control panel – electric litter option
Raises the Fowler backrest Lowers the Fowler backrest Raises the Gatch Lowers the Gatch

EN 26

1125-309-005 Rev AB.0

Locking and unlocking the patient control panel lockout – electric litter option Prime only
WARNING – Always operate the product when all operators are clear of the mechanisms.
To lock the siderail patient control panel, press Unlock/Lock (A) once (Figure 18). Note – The lock icon (C) illuminates amber when the patient controls are locked. To unlock the siderail patient control panel, press Unlock/Lock (A) a second time. Note – The unlock icon (B) illuminates green when the patient controls are unlocked. Note · Always plug the power cord into a grounded, hospital grade wall outlet. · You can lock the patient control panel to prevent the patient from moving the backrest and the Gatch. · The siderail patient control panel is not backlit when you lock the patient control panel.

A BC
Figure 18 Patient control panel lockout
Raising or lowering the Fowler backrest – non-electric litter
WARNING · Always operate the product when all operators are clear of the mechanisms. · 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 the Fowler backrest while a patient is on the product. Use proper lifting techniques
and get help, if necessary.
To raise the Fowler backrest, squeeze one or both of the Fowler backrest release handles (A) and pull the Fowler backrest up to the desired position (0° to 90°) (Figure 19).
Note – The Lift Assist® backrest uses patient weight to assist in patient positioning. The Lift Assist backrest also helps to keep the patient from sliding toward the foot end of the product when you raise the Fowler backrest.
To lower the Fowler backrest, squeeze one or both of the Fowler backrest release handles (A) and push the Fowler backrest down to the desired position (90° to 0°) (Figure 19).

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Figure 19 Raising or lowering the Fowler backrest (Prime / Prime X)
Raising or lowering the Fowler backrest – electric litter option
WARNING · Always operate the product when all operators are clear of the mechanisms. · 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 the Fowler backrest while a patient is on the product. Use proper lifting techniques
and get help, if necessary.
To raise the Fowler backrest, press the up button on the Fowler backrest side of the siderail patient control panel (Positioning the product with the siderail patient control panel – electric litter option- Prime only (page 25)) or foot end operator control panel (Operator control panel – electric litter option – Prime only (page 26)) until the Fowler backrest has reached the desired angle (0° to 70°).
Note – The Lift Assist backrest uses patient weight to assist in patient positioning. The Lift Assist backrest also helps to keep the patient from sliding toward the foot end of the product when you raise the Fowler backrest.
To lower the Fowler backrest, press the down button on the Fowler backrest side of the siderail patient control panel (Positioning the product with the siderail patient control panel – electric litter option- Prime only (page 25)) or foot end operator control panel (Operator control panel – electric litter option – Prime only (page 26)) until the Fowler backrest has reached the desired angle (70° to 0°).
Note – Always plug the power cord into a grounded, hospital grade wall outlet.
Healthcare professionals must instruct patients how to operate the patient controls.

EN 28

1125-309-005 Rev AB.0

Raising or lowering the Gatch – non-electric litter – Prime only
WARNING – Always keep hands and fingers clear of the foot end push handles when you lower the Gatch.
CAUTION · The weight capacity of the Gatch is 200 lb (90.7 kg). · Always make sure that the Gatch prop rod is secure before use. · Do not sit or stand on the Gatch.
To raise the non-electric Gatch, pump the Gatch pump handle to the left until you achieve the desired position (see Product illustration – Prime litter). Lift up on the end of the Gatch and secure the prop rod in the bracket. To release the prop rod, lift up on the end of the Gatch, swing the prop rod toward the head end of the product, and lower the foot end. To lower the Gatch, pull the Gatch release handle until you achieve the desired position (see Product illustration – Prime litter). Note – You cannot raise the Gatch manually if the product has the electric litter option.
Raising or lowering the Gatch – electric litter option – Prime only
WARNING · Always keep hands and fingers clear of the foot end push handles when you lower the Gatch. · Always operate the product when all operators are clear of the mechanisms.
CAUTION · The weight capacity of the Gatch is 200 lb (90.7 kg). · Do not sit or stand on the Gatch. · Always use caution when you attempt to lower the Gatch while the product is unpowered. Gravity may cause a rapid
drop of the Gatch.
To raise the Gatch, press up on the Gatch side of the siderail patient control panel or the foot end operator control panel. To lower the Gatch, press down on the Gatch side of the siderail patient control panel or on the foot end operator control panel. Note – Always plug the power cord into a grounded, hospital grade wall outlet. Healthcare professionals must instruct patients how to operate the patient controls.
Positioning the recovery chair – Prime only
WARNING – Always operate the product when all operators are clear of the mechanisms.

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To place the product in the recovery chair position (Figure 20):

Figure 20 Recovery chair (Model 1115 shown)
1. Raise the Fowler backrest to a seated position (Raising or lowering the Fowler backrest – non-electric litter (page 27) or Raising or lowering the Fowler backrest – electric litter option (page 28)).
Note – To position the recovery chair, the product must have the Lift Assist backrest option and the Gatch option. 2. Raise the Gatch to the full up position (Raising or lowering the Gatch – non-electric litter – Prime only (page 29) or
Raising or lowering the Gatch – electric litter option – Prime only (page 29)). 3. Raise the litter to the highest height (Raising the non-electric litter (page 17) or Raising the electric litter option (page
18)). 4. Place the product into the Reverse Trendelenburg position (Positioning the product in Reverse Trendelenburg (page
19)). 5. Reverse steps to lower the product to the flat position.
Storing objects in the base hood
CAUTION · Do not place objects that exceed 60 lb (27 kg) in the base hood. · Do not sit, step, or stand on the base hood.
You can store patient belongings in the base hood. Do not use the oxygen bottle holder cutout to store oxygen bottles or patient belongings.
Hanging devices with the pump rack option
WARNING · Always keep device lines on the pump rack away from the Gatch handles. · Always remove any devices that may be in the way before you raise or lower the litter. · Always make sure that devices on the pump rack can pass safely through door openings. · Do not lift the product by the pump rack.

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CAUTION · The weight capacity of the pump rack is 40 lb (18 kg). · Do not use the pump rack as a push/pull device. Product damage may occur.
You can store or hang additional devices on the pump rack that is located on the foot end of the product. Note – You must select the pump rack option at the time of purchase.
Extending or retracting the power cord with the retractable cord reel option electric lift option or electric litter option
WARNING · Always unplug the power cord from the wall outlet before you transport or clean the product. · Always use the retractable cord reel to store the power cord inside the base when you transport the product.
To extend the power cord, pull the power cord out from the retractable cord reel (A) to the desired length (Figure 21).
A

Figure 21 Retractable cord reel
To retract the power cord: 1. Unplug the power cord from the wall outlet. 2. Tug lightly on the power cord. 3. Guide the power cord into the retractable cord reel.

Scale system option
WARNING – Do not use the scale system option or electric lift option or electric litter option adjacent to or stacked with other devices. If adjacent or stacked use is necessary, the scale system option or electric lift option or electric litter option should be observed to make sure that all devices are operating normally in the configuration in which they will be used.
CAUTION – Do not use the scale for patients under 50 lb.
The scale system option is available for products with or without the electric litter option. The scale system option has a battery backup option. The standby icon indicates when the product is using the battery backup.

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The Chaperone option allows you to set zone controls to alert an operator when a patient may be attempting to exit the product. The Chaperone option is available for products with the electric litter option and the scale system option. The scale system option with Chaperone option has a battery backup option. The standby icon indicates when the product is using the battery backup.
Raise the foot end push handles before you attempt to operate the scale system option.
Use the scale system control panel to operate the scale system option (Scale icon/button identification (page 32)).
Do not touch the product while you weigh or zero the scale system option.
The patient must remain still while the system is weighing. If the patient is moving, the scale system will try for 20 seconds to get a stable weight or zero value before displaying the error message ( ).
The error ( ) appears in the display if there is a loose connection or if the scale is not operating. If you attempt to operate the scale again and the error appears, contact Stryker Technical Support.
Note – To meet the scale system accuracy claim, the patient surface must be in the flat position (Fowler backrest and Gatch down) and the product cannot exceed 5 degrees of Trendelenburg/Reverse Trendelenburg.

Scale icon/button identification

Item A

Icon/button

Name Stand by icon

Zone 1 icon

Description
Illuminates green when you plug the power cord into a wall outlet.
Illuminates amber when you unplug the power cord from the wall outlet. Battery backup functionality will turn on.
The patient can move freely, but the alarm sounds when the patient attempts to leave the product.

Zone 2 icon

The patient can move with limited movement. The alarm sounds when

the patient approaches the siderails or moves toward the foot end.

Arm/Disarm button Arms and disarms the Chaperone option (stretcher exit). See Arming

or disarming the Chaperone option (page 33).

Weigh button

Weighs the patient. See Weighing a patient (page 32).

lb/kg button

Changes the displayed unit of measure. See Locking the scale unit of

measure (page 33).

Zero button

Zeros the scale settings. See Locking the scale unit of measure (page

33).

Weighing a patient
CAUTION – Do not use the scale system reading as a reference for medical treatment. EN 32

1125-309-005 Rev AB.0

1. Raise the foot end push handles before you operate the scale system option. 2. Press and hold Zero until rel displays on the screen to zero the scale. 000.0 flashes and then stops flashing.
Note – The scale is not ready for use until the 000.0 stops flashing. 3. Place the patient on the product. 4. Press lb/kg to select the unit of measure (lb or kg). 5. Press Weigh to obtain the patient’s weight.
Note – The patient’s weight displays for 40 seconds.
Locking the scale unit of measure
1. Press and hold Weigh, lb/kg, and Zero until diag displays. 2. Press lb/kg or Zero to toggle to Unit Loc. 3. For scale without Chaperone, press and hold lb/kg and Zero until rel displays to select Unit Loc. 4. For scale with Chaperone, press and hold lb/kg and Zero to select Unit Loc. 5. Press lb/kg or Zero to toggle to lb, kg, or Any. 6. Press and release lb/kg and Zero. Only and the selected unit of measure displays.
Note – Only will not appear if you select Any. 7. Press and hold Weigh until quit displays. 8. Press and hold Zero until rel displays. 000.0 flashes and then stops flashing.
Note – The scale is not ready for use until the 000.0 stops flashing.
Arming or disarming the Chaperone option
When armed, the Chaperone option monitors the patient’s position on the product. To arm and disarm the Chaperone option: 1. With the patient on the product, press Arm/Disarm.
Note – This arms Zone 1. Zone 1 illuminates amber when applied. 2. To arm Zone 2, press Arm/Disarm twice within 3 seconds.
Note – This arms Zone 2. Zone 2 illuminates amber when applied. 3. To disarm the Chaperone option, press and hold Arm/Disarm.
Note – You must zero the scale before you arm the Chaperone option. Note – If the patient moves outside of the limits of the selected zone, an amber light flashes, Alrt flashes in the scale system option display, and a sound alarm is triggered.
Setting the Chaperone option alert pattern
To change the Chaperone option alert pattern: 1. Press and hold both Arm/Disarm and Weigh together for approximately 6 seconds. Ignore all display messages until
Ptrn appears on the display (Scale icon/button identification (page 32)). 2. Release the Arm/Disarm and Weigh buttons.
Note – The pattern setting P (1-10) appears on the display. 3. Press Arm/Disarm or Weigh to scroll through the pattern options.
Note – A brief sample of the pattern plays as you scroll through the pattern options.

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4. Press and hold both Arm/Disarm and Weigh together for 6 seconds until set appears on the display to save your selected pattern.
5. Release Arm/Disarm and Weigh.
Note – The pattern setting you selected appears on the display. A brief sample of the pattern confirms your pattern setting.
Setting the Chaperone option alert volume
To change the Chaperone option alert volume: 1. Press and hold both Zero and lb/kg together until vol appears on the display (Scale icon/button identification (page
32)). 2. Release Zero and lb/kg.
Note – The volume levels L (1-4) appear on the display. 3. Press Zero or lb/kg to scroll through the volume levels.
Note – A brief sample of the volume plays as you scroll through the volume levels. 4. Press and hold both Zero and lb/kg together for 6 seconds until set appears on the display to save your selected
volume level. 5. Release Zero and lb/kg.
Note – The volume level you selected appears on the display. A brief sample of the volume level confirms your volume level setting.
Charging the scale system battery pack option – electric litter option or electric litter option with Chaperone option – Prime only
The scale system with the electric litter option requires one 10.8V Li-ION battery pack (0058-135-000 without the Chaperone option; 0058-134-000 with the Chaperone option). Recharge the battery pack when the battery charge indicator displays one unit remaining. This prevents the scale system option from shutting down due to drained batteries.
To recharge the scale system Li-ION battery pack, plug the power cord into a grounded, hospital grade wall outlet. The battery pack fully charges in approximately three hours.
Note – Always plug the product into a grounded, hospital grade wall outlet when not in use. This helps the battery to maintain a sufficient charge and maximizes product performance while on battery power.
Replacing the batteries for the scale system option – non-electric litter
Replace the batteries when the battery charge indicator displays one unit remaining. This prevents the scale system option from shutting down due to drained batteries.
When the display flashes Lo batt, the batteries are at their lowest charge and the scale system option is disabled.
Tools required:
· Phillips screwdriver · Four AA batteries (Alkaline type (LR6))
To replace the batteries: 1. Using a Phillips screwdriver, the screws that hold the battery compartment cover to the display assembly. 2. Remove and discard all four AA batteries.
Note – Always dispose of old batteries in accordance with local regulations. 3. Place four new AA batteries as indicated in the battery holder.
Note – Never mix old batteries with new batteries.

EN 34

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4. Use the screws removed in step 1 to reinstall the battery compartment cover on the display assembly.

Accessories and parts

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 Defibrillator tray Defibrillator tray/foot extender Footboard/chart holder Heel pad assembly IV caddy HAVASUTM IV pole, removable IV pole, head end, left IV pole, head end, right IV pole, three-stage, foot end, left, 26″ IV pole, three-stage, foot end, right, 26″ IV pole, three-stage, foot end, left, 30″ IV pole, three-stage, foot end, right, 30″ IV pole, three-stage, foot end, left, 30″ (Prime X option) IV pole, three-stage, foot end, right, 30″ (Prime X option) IV pole, three-stage, head end, left, 26″ IV pole, three- stage, head end, right, 26″ IV pole, two-stage, foot end, left, 26″ IV pole, two-stage, foot end, right, 26″ IV pole, two-stage, foot end, left, 30″ IV pole, two-stage, foot end, right, 30″ IV pole, two-stage, foot end, left, 30″ (Prime X option) IV pole, two-stage, foot end, right, 30″ (Prime X option) IV pole, two-stage, head end, left, 30″ IV pole, two-stage, head end, right, 30″ Mattress, ComfortGel SETM, fire barrier, 26″ Mattress, ComfortGel SE, fire barrier, 30″ Mattress, ComfortGel SE, without fire barrier, 26″ Mattress, ComfortGel SE, without fire barrier, 30″ Mattress, Enhanced Comfort, 3″ x 26″

Part number 1105-045-200 1105-045-400 1105-045-500 1105-045-022 0785-155-000 0390-025-010 1125-060-145 1125-060-140 1105-035-644 1105-035-639 1105-035-344 1105-035-339 1105-035-364 1105-035-361 1125-035-642 1125-035-637 1105-035-640 1105-035-643 1105-035-340 1105-035-343 1105-035-362 1105-035-363 1125-035-338 1125-035-341 1805-034-601 1805-034-301 1805-034-600 1805-034-300 0785-034-613

1125-309-005 Rev AB.0

35 EN

Name

Part number

Mattress, Enhanced Comfort, 3″ x 30″

0785-034-313

Mattress, Enhanced Comfort, 4″ x 26″

0785-034-623

Mattress, Enhanced Comfort, 4″ x 30″

0785-034-323

Mattress, IsoFlex SETM, fire barrier, 30″

1806-034-300

Mattress, IsoFlex SE, without fire barrier, international, 30″ 1806-034-301

Mattress, Ultra Comfort, 4″ x 26″

0785-034-603

Mattress, Ultra Comfort, 4″ x 30″

0785-034-303

Mattress, Ultra Comfort, 5″ x 26″

0785-034-633

Mattress, Ultra Comfort, 5″ x 30″

0785-034-333

Mattress, Ultra Comfort SETM, 4″ x 26″

1704-034-600

Mattress, Ultra Comfort SE, fire barrier, international, 4″ x 1704-034-601 26″

Mattress, Ultra Comfort SE, 3″ x 30″

1703-034-300

Mattress, Ultra Comfort SE, fire barrier, 3″ x 30″

1703-034-301

Mattress, Ultra Comfort SE, 4″ x 30″

1704-034-300

Mattress, Ultra Comfort SE, fire barrier, 4″ x 30″

1704-034-301

Oxygen bottle holder, upright

1115-130-000

Pump bar option, 26″

1105-045-065

Pump bar option, 30″

1105-045-035

Restraint strap package

0785-045-010

Restraint strap, ankle

0785-045-020

Restraint strap, body

0785-045-015

Restraint strap, wrist

0946-044-000

Restraint strap, chest

1010-058-000

Serving tray

1105-045-700

Serving tray holder/footboard

1105-045-800

Siderail pads

1001-052-000

X-ray cassette holder, lateral

1105-045-100

X-ray cassette holder, upright

1105-045-300

Electrical components
Name Actuator, Fowler Actuator, Gatch Battery, Li-ION Smart battery pack (scale only)

Number 1008-012-020 1008-014-020 0058-135-000

EN 36

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Name

Number

Battery, Li-ION Smart battery pack (scale and Chaperone) 0058-134-000

Board, DC control PCB assembly

1008-116-800

Board, non-lift AC assembly

1008-002-800

Board, lift control PCB assembly

1008-002-810

Board, scale control assembly (scale only)

1008-237-850

Board, scale and Chaperone control assembly

1008-237-840

Capacitor, 440 VAC, 35 MFD

0059-087-000

Keypad, scale control (non-electric litter)

1008-037-820

Keypad, siderail control, left

1008-011-017

Keypad, siderail control, right

1008-011-016

Keypad, operator control

1008-015-800

Load cell (scale system option)

1008-037-057

Motor, pump

1008-002-015

Power cord, standard

1028-146-060

Power cord, international, Type, E

1125-060-170

Power cord, international, Type, F

1125-060-180

Power cord, international, Type, G

1125-060-160

Power cord, international, Type, I

1125-060-200

Scale box assembly (non-electric litter)

1070-237-020

Transformer Transformer, international

1008-014-857 1008-014-877

Attaching the defibrillator tray
WARNING · Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray. Always strap down all devices that you
place on the defibrillator tray. · 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 defibrillator tray: 1. Insert the defibrillator tray pins into the sockets at the foot end of the product. 2. Use the strap to secure devices to the defibrillator tray.
Note · Do not use the defibrillator tray as a push/pull device. Product damage may occur. · Always raise the foot end push handles when you use accessories (such as the defibrillator tray/foot extender,
footboard/chart holder, upright oxygen bottle holder) or the accessories will not function.

1125-309-005 Rev AB.0

37 EN

Converting the defibrillator tray/foot extender to a defibrillator tray
WARNING · Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray/foot extender. Always strap down all
devices that you place on the defibrillator tray. · 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.
CAUTION – Always raise the IV pole before you attach the defibrillator tray/foot extender to the product. If you do not raise the IV pole, the foot extender will not operate.
To convert the defibrillator tray/foot extender to a defibrillator tray: 1. Pull out the top knob (A) (Figure 22). 2. Pivot the defibrillator tray (B) until the tray is flat over the foot end of the product. Release the top knob (A). Make sure
that the defibrillator tray is locked in place. 3. Use the strap to secure devices to the defibrillator tray.
Note · Do not use the defibrillator tray/foot extender as a push/pull device. Product damage may occur. · Do not attach items to the foot extender.
B

Figure 22 Defibrillator tray/foot extender
Converting the defibrillator tray/foot extender to a foot extender
WARNING · Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray/foot extender. Always strap down all
devices that you place on the defibrillator tray. · 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.
CAUTION – Always raise the IV pole before you attach the defibrillator tray/foot extender to the product. If you do not raise the IV pole, the foot extender will not operate.
To convert the defibrillator tray/foot extender to a foot extender (Figure 22): 1. Pull out the top knob (A).

EN 38

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2. Pivot the defibrillator tray (B) until the tray locks against the foot extender. 3. Pull out the bottom knob (D) while you hold the defibrillator tray/foot extender assembly. 4. Lower the foot extender (C) until the foot extender is flat. 5. Release the bottom knob (D). Push on the foot extender to make sure that the foot extender is locked in place.
Note · Do not use the defibrillator tray/foot extender as a push/pull device. Product damage may occur. · Do not attach items to the foot extender.
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.
Attaching the IV caddy
WARNING · Always secure the IV pole to the IV caddy when you transport the product. · Always store the IV caddy when not in use to avoid product damage.
To attach the IV caddy (Figure 23): 1. Lift the IV caddy out of the storage tray or from the storage clip. 2. Pivot the IV caddy to the desired position. 3. Turn the knob (A) counterclockwise to loosen the pole clamp (C). 4. Pivot the knob (A) away from the arm connection assembly (B). 5. Open the clamp (C). 6. Place the IV pole into the clamp (C). 7. Close the clamp (C) around the IV pole and pivot the knob (A) into position. 8. Turn the knob (A) clockwise to tighten the knob. 9. Reverse steps to disconnect the IV caddy from the product.
To store the IV caddy, place the IV caddy in the storage tray or secure the caddy in the storage clip.

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39 EN

Figure 23 IV caddy
Positioning or stowing the foot supports – Prime only
WARNING · Do not sit on the foot supports. This may cause the product to tip. · Always clear your fingers from the mechanisms when you operate the foot supports. · Always stow the foot supports when you transport a patient with the product. · Always tighten the foot supports before you use the foot supports. · Do not operate the scale system with the foot supports. Inaccurate readings may occur. · Do not operate the Chaperone option with the foot supports. Inaccurate readings may occur.
To position or stow the foot supports: 1. Loosen the knee knob (A) at the top of the foot supports to adjust the side-to-side angle of the foot supports (Figure 24). 2. Tighten the knee knob (A) to lock the foot supports in the desired position.

CA B

Figure 24 Positioning the foot supports
3. Loosen the leg knob (B) on the side of the foot supports to adjust the length. 4. Tighten the leg knob (B) to lock the foot supports in the desired position. 5. Flip the foot supports (C) up before you position the patient. 6. Reverse steps to stow the foot supports (Figure 25).

EN 40

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AC CA
B B
Figure 25 Stowing the foot supports
You cannot purchase the following options and accessories if you select the foot support: · Foot end push handles · Defibrillator tray · Defibrillator tray/foot extender · Serving tray holder/footboard · Footboard/chart holder · Foot end IV poles Note · Do not use the foot supports to store patient belongings. · Do not use the foot supports as a push/pull device. Product damage may occur. · Always apply the brakes when you use the foot supports to avoid instability. · Do not use the backrest or Gatch with the foot supports.
Positioning the two-stage permanently attached IV pole
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 26): 1. Lift and pivot the pole from the storage position. 2. Push the IV pole down until the IV pole locks in place. 3. 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. 4. Rotate the IV hangers (B) to the desired position and hang the IV bags. 5. To lower the IV pole, hold the telescoping portion of the IV pole, turn the latch (C), and lower the telescoping portion.
Note · 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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41 EN

B A
A
C
Figure 26 Positioning the 2 stage permanently attached IV pole
Positioning the three-stage permanently attached IV pole
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 27): 1. Lift and pivot the pole from the storage position. 2. Push the IV pole down until the pole locks in place. 3. 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. 4. For a higher IV pole, pull up on section (B). Release section (B) at any desired height to lock the pole in place. 5. Rotate the IV hangers (C) to the desired position and hang the IV bags. 6. 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. 7. Turn the latch (E) and lower the IV pole telescoping portion.
Note · Do not hang IV bags that exceed 12 lb (5 kg) total for all bags on the IV pole. · 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.

EN 42

1125-309-005 Rev AB.0

C
B
D
A E
Figure 27 Positioning the three-stage permanently attached IV pole
Attaching and positioning the removable IV pole
CAUTION · Do not use the IV pole as a push/pull device. Product damage may occur. · 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. To attach and position the removable IV pole (Figure 28): 1. Insert the IV pole into a socket at the head end or foot end of the product. 2. Turn the knob (A) counterclockwise and pull up on the telescoping portion (B) until you reach the desired height. 3. Turn the knob (A) clockwise to lock the telescoping portion in place.

1125-309-005 Rev AB.0

43 EN

B A

Figure 28 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. Insert the support bar into any of the IV sockets. 2. 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. Product damage may occur.
Extending or stowing the serving tray holder/footboard
WARNING – Do not place objects that exceed 30 lb (14 kg) on the serving tray.
To fit the serving tray on the siderail, pull out on both sides of the serving tray and position the tray over the siderails. To stow the serving tray: 1. Remove the serving tray from the siderails. 2. Push in the sides of the serving tray. 3. Store the serving tray in the footboard.
Note – Do not use the serving tray/footboard as a push/pull device. Product damage may occur.

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1125-309-005 Rev AB.0

Attaching the siderail pads
To attach the siderail pads: 1. Tuck the siderail pad between the mattress and the siderail. 2. Fasten the Velcro® straps around the top of the siderail to secure the siderail pad.
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 restraint 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 29 or Figure 30).

Figure 30 Prime X option restraint strap locations

Figure 29 Prime restraint strap locations
Note – Restraint straps are Type B applied parts.
Positioning the upright X-ray cassette holder – Prime X option
WARNING · Always take protective measures when you use the upright or lateral X-ray cassette holder. The X-ray cassette holder
does not protect against radiation. · Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use Prime X
option with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered radiation. · Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option. · Always follow the Positioning the upright X-ray cassette holder – Prime X option instructions to insert the X-ray cassette.

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The X-ray cassette holder attaches to the Fowler backrest weldment to support X-ray cassettes. You can take X-rays while a patient is on the product. You can also adjust the cassette’s position before you take an X-ray. To position the X-ray cassette holder: 1. Apply the brakes. Push on the product to make sure that the brakes are working. 2. Raise the Fowler backrest section to full height. 3. Insert the lower retainer guides (A) under the Fowler backrest weldment bar (Figure 31). 4. Raise the cassette holder until the retainer guides latch onto the Fowler backrest weldment. Make sure that the cassette
holder is secure.
C
C
B

Figure 31 X-ray cassette holder
5. Insert an X-ray cassette from either side of the cassette holder or pull the slider release arrow (B) to release the cassette holder from the Fowler, position the cassette, and secure the cassette holder in the Fowler backrest weldment.
6. To adjust the height of the cassette, loosen the knob (E) and move the cassette support rail (D) up or down until you reach the desired height.
7. Tighten the knob (E) to secure the cassette support rail in place. 8. When the X-ray process is complete, pull up on the slider release arrow (B) to release the cassette holder from the
Fowler backrest weldment. 9. Remove the X-ray cassette from the cassette holder. 10. Close and stow the cassette holder.
Positioning the lateral X-ray cassette holder – Prime X option
WARNING · Always take protective measures when you use the upright or lateral X-ray cassette holder. The X-ray cassette holder
does not protect against radiation. · Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use Prime X
option with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered radiation.

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· Always use caution when you take X-rays with the Fowler backrest in the upright position or when you use a lateral cassette.
· Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with Prime X option. · Always follow the Positioning the lateral X-ray cassette holder – Prime X option instructions to insert the X-ray cassette.
To position the lateral X-ray cassette holder: 1. Apply the brakes. Push on the product to make sure that the brakes are working.
D
B

C A

B C

Figure 32 Lateral X-ray cassette holder
2. Press down on the yellow release button (A) to open the lateral cassette holder (Figure 32). 3. Slide the flat base (B) between the mattress and the patient platform. 4. Position the lateral cassette holder in the desired location. 5. Place the X-ray cassette in the cassette canal (C). 6. Pull up on the cassette hook (D) to adjust the height of the arm to fit over the X-ray cassette to hold the cassette in
place. 7. Reverse steps to remove the cassette and stow the lateral cassette holder.

Inserting or removing X-ray cassettes – Prime X option

WARNING · Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use Prime X
option with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered radiation. · Always use caution when you take X-rays with the Fowler backrest in the upright position or when you use a lateral cassette.
Prime X option provides both an articulating radiographic support surface and a platform below the patient support surface for X-ray cassette placement. Working with medical X-ray systems, the radiographic support surface allows the capture of clinical X-rays (AP full body, optional full body lateral, and optional upright chest) while the patient is on the product. You can insert cassettes from the head end, foot end, and either side of the product.
To insert an X-ray cassette:
1. Center the patient on the product with the position indicator labels located on all sides of the product (Figure 33).
2. Insert an X-ray cassette below the patient surface. Use the cassette guides to assist in positioning the X-ray cassette.

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Figure 33 Inserting or removing X-ray cassettes on Prime X option
Note · Do not use a mattress with a thickness greater than four inches with the Prime X option. · Do not use a C-Arm with Prime X option. Prime X option is not compatible with a C-Arm.

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Cleaning
Cleaning the product
WARNING · Always unplug the power cord and turn the On/Drive – Off/Manual switch to the Off position before service or cleaning. · Do not steam clean, pressure wash, hose off, or ultrasonically clean the product.
CAUTION – Do not use abrasive cleaners to clean the display enclosure for the scale system option. Do not allow cleaning solutions or other fluids to pool on the display unit. Wipe dry all surfaces after spills or cleaning.
These instructions provide recommended cleaning methods for Model 1125 Prime Series Stretcher.
Recommended cleaning method: 1. If the product is equipped with the electric lift option or electric litter option, unplug the power cord from the wall outlet
before you transport or clean the product. 2. Remove the mattress from the product. 3. Follow the cleaning solution manufacturer’s dilution recommendations. 4. Dry the product. Do not place the mattress on the product until the product is dry.
Note · Direct skin contact with visibly soiled, permeable material may increase the risk of infection. · Clean the base hood storage area. · Clean the bottom of the brake pads to prevent wax or floor remnant buildup. · 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.
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 to prevent cross-contamination. · Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may void
the 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.
Recommended cleaning method: 1. Use a clean, soft cloth to wipe down the entire mattress with a mild soap and water solution to remove foreign material. 2. Wipe down the mattress with a clean, dry cloth to remove any excess liquid or cleaning agents. 3. Rinse and dry covers after cleaning. 4. Disinfect as needed with a hospital grade disinfectant after cleaning has been completed (see Disinfecting the
mattress).

1125-309-005 Rev AB.0

49 EN

Note
· 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.
· 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.

Remove iodine
1. 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.
2. Clean the stain as soon as possible after the stain occurs. 3. If stains are not immediately removed, allow solution to soak or stand on the mattress before you wipe the mattress. 4. 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® Solids or stains Hard-to-clean spots
Laundering

Saturate with disinfectant, rinse with water, and allow the solution to evaporate.
Use neutral soaps and warm water. Do not use harsh cleansers, solvents, or abrasive cleaners.
Use standard household cleansers or vinyl cleansers and a soft bristle brush on troublesome spots or stains. Pre-soak dried-on soil.
Laundering is not recommended. Laundering may substantially decrease the useful life of the mattress.

EN 50

1125-309-005 Rev AB.0

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) that contain less than 3% glycol ether · 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. Follow the disinfectant solution manufacturer’s dilution recommendations. 2. Hand wash all surfaces of the product with a disinfectant solution. 3. Avoid over-saturation and make sure that the product does not stay wet longer than the chemical manufacturer’s
guidelines for proper disinfecting. 4. Dry the product. Do not place the mattress on the product until the product is dry. 5. 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). 6. 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 · Direct skin contact with visibly soiled, permeable material may increase the risk of infection. · 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
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) that contain less than 3% glycol ether

1125-309-005 Rev AB.0

51 EN

· 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. Make sure that the mattress is clean and dry before you apply disinfectants.
2. Wipe down the mattress with a clean, dry cloth to remove any excess liquid or disinfectant.
3. Rinse and dry covers after disinfection.
Note · The mattress cover must be 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.

EN 52

1125-309-005 Rev AB.0

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 fasteners are secure Siderails move and latch Casters lock when you apply the brake pedal Casters are secure and swivel Casters are free of wax and debris Brake mechanism works Steer function works Check for cracks Fowler backrest raises, lowers, and latches Gatch raises, lowers, and latches (option) Trendelenburg/Reverse Trendelenburg operates from all locations Ground chain intact No leaks at hydraulic connections Hydraulic jacks hold Lubricate where required Body restraints work (option) IV pole is intact and adjusts and latches in all positions (option) Oxygen bottle holder is intact and operates (option) No rips or cracks in the mattress cover Accessories and mounting hardware are in good condition Battery powered functionality (option) Cables are not worn or pinched (option) Power cord and plug are free of damage (option) All electrical connections are tight (option) All grounds secure to the frame (option) Ground impedance not more than 200 m (milliohms) (option) (Max: test points include electronics enclosure and motor chassis mounted to the base of the product) Current leakage not more than 300 µA (microamps) (per UL 60606-1-1) (option) Batteries charged (scale system option) Display housing is intact and not damaged (scale system option) Load cells are intact and not damaged (scale system option) Foot support knee knob mechanism functions (option) Foot support leg knob mechanism functions (option) Foot support extends to the full extended position and stops in the correct position (option) Foot support self-tapping screws (6) are secured and are not stripped (option)

1125-309-005 Rev AB.0

53 EN

Scale calibrated. Recalibrate, if necessary (scale system option) Upright X-ray cassette holder is working (Prime X option) No damage to the Fowler backrest skin and foot skin (Prime X option) No damage to the head and foot trays (Prime X option) Bolt and nut through each Fowler backrest pivot are not loose (Prime X option) No excessive play in the drive handles Press the handle switches and make sure that the product does not move unless the handles are pushed forward or pulled back Press the handle switches and make sure that the product moves forward and backward
Product serial number: Completed by:
Date:

EN 54

1125-309-005 Rev AB.0

EMC information
CAUTION
· The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation.
· The emissions characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment, for which CISPR 11 class B is normally required, this equipment might not offer adequate protection to radio frequency communication services. The user might need to take mitigation measures, such as relocating or reorienting the equipment.

Guidance and manufacturer’s declaration – electromagnetic emissions

The electric lift option, electric litter option, or scale system option is intended for use in an electromagnetic environment specified below. The operator of the electric lift option, electric litter option, or scale system option should make sure that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment

RF Emissions CISPR 11

Group 1

The electric lift option, electric litter option, or scale system option uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF Emissions CISPR 11
Harmonic Emissions IEC 61000-3-2
Voltage Fluctuations Flicker Emissions IEC 61000-3-3

Class A Class A Complies

The electric lift option, electric litter option, or scale system option is suitable for use in all establishments other than domestic and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes.

Applies to electric lift option or electric litter option only.
CAUTION · Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should
be used no closer than 12 inches (30 cm) to any part of the Prime stretcher, including cables specified by the manufacturer. · Avoid stacking or placing other equipment adjacent with other equipment to prevent improper operation of the products. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they are operating properly.

Recommended separation distances between portable and mobile RF communications equipment and the electric lift option, electric litter option, or scale system option.
The electric lift option, electric litter option, or scale system option is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the electric lift option, electric litter option, or scale system option can help prevent electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the electric lift option, electric litter option, or scale system option as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter W
0.01

Separation distance according to frequency of transmitter m

150 kHz to 80 MHz D=(1.2) (P) 0.12

80 MHz to 800 MHz D=(1.2) (P) 0.12

800 MHz to 2.7 GHz D=(2.3) (P) 0.23

1125-309-005 Rev AB.0

55 EN

0.1

0.38

0.73

1.2

2.3

3.8

7.3

100

For transmitters rated at a maximum output power not listed above, the recommended separation distance (D) in meters (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

Note 1 – At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

Note 2 – These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

Guidance and manufacturer’s declaration – electromagnetic immunity

The electric lift option, electric litter option, or scale system option is intended for use in the electromagnetic environment specified below. The customer or the user of the electric lift option, electric litter option, or scale system option should assure that it is used in such an environment.

Immunity test

IEC 60601 test level

Compliance level

Electromagnetic environment guidance

Electrostatic Discharge (ESD) IEC 61000-4-2

±8 kV contact ±15 kV air

Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Electrostatic fast transient/ burst IEC 61000-4-4
Surge IEC 61000-4-5
Voltage dips, voltage variations and short interruptions on power supply input lines IEC 61000-4-11*

±2 kV for power supply lines ±1 kV for input/output lines

Mains power quality should be that of a typical commercial or hospital environment.

±1 kV line(s) to line(s) ±2 kV line(s) to earth

Mains power quality should be that of a typical commercial or hospital environment.

0% UT for 0.5 cycle at 0°, 45°, 90°, 135°, 180°, 225°, 270°, and 315°
0% UT for 1 cycle
70% UT (30% dip in UT) for 25 cycles
0% UT for 250 cycles

Mains power quality should be that of a typical commercial or hospital environment. If the user of the electric lift option or electric litter option requires continued operation during power mains interruptions, it is recommended that the device be powered from an uninterrupted power supply or a battery.

Power frequency (50/60 Hz) 30 A/m magnetic field IEC 61000-4-8

30 A/m

Note: Ut is the AC mains voltage before application of the test level.

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

*Applies to the electric lift option or electric litter option only.

EN 56

1125-309-005 Rev AB.0

Guidance and manufacturer’s declaration – electromagnetic immunity

The electric lift option, electric litter option, or scale system option is intended for use in the electromagnetic environment specified below. The customer or user of the electric lift option, electric litter option, or scale system option should assure that it is used in such an environment.

Immunity test

IEC 60601 test level Compliance level

Electromagnetic environment guidance

Portable and mobile RF communications equipment should be used no closer to any part of the electric lift option, electric litter option, or scale system option, including cables, than the recommended separation distance calculated from the equation appropriate for the frequency of the transmitter.

Recommended separation distance

D=(1.2) (P)

Conducted RF IEC 61000- 4-6*
Radiated RF IEC 61000-4-3

3 Vrms 6 Vrms in ISM and amateur radio bands 150kHz to 80MHz
3 V/m 80 MHz to 2.7 GHz

3 Vrms
6 Vrms in ISM and amateur radio bands
3 V/m

D=(1.2) (P)
80 MHz to 800 MHz
D=(2.3) (P)
800 MHz to 2.7 GHz
where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and D is the recommended separation distance in meters (m).

Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey a, should be less than the compliance level in each frequency range b.

Interference may occur in the vicinity of equipment marked with the following symbol:

Note 1: At 80 MHz and 800 MHz, the higher frequency range applies. Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. Note 3: The ISM (industrial, scientific and medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the electric lift option, electric litter option, or scale system option is used exceeds the applicable RF compliance level above, the electric lift option, electric litter option, or scale system option should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the electric lift option, electric litter option, or scale system option.
b Over the frequency range 150 kHz to 80 MHz, field strengths are less than 3 V/m.
*Applies to electric litter option only.

1125-309-005 Rev AB.0

57 EN

Lehátko Prime Series®
Pírucka pro obsluhu 1125
s motorizovaným pohonem Zoom®

1125-309-005 Rev AB.0

2021-12

Symboly

Prostudujte si pírucku / brozuru s pokyny Pectte si návod k pouzití Obecné varování Upozornní Varování; rozdrcení rukou Varování; neionizující záení

Netlacte

Neskladujte kyslíkovou láhev Katalogové císlo Sériové císlo Císlo sarze Patenty USA viz www.stryker.com/patents Znacka CE Zplnomocnný zástupce pro Evropské spolecenství Evropský zdravotnický prostedek

Výrobce

Datum výroby

Dovozce

Bezpecná pracovní zátz

1125-309-005 Rev AB.0

~
IPX5
87VL
MR

Maximální hmotnost pacienta
Hmotnost výrobku vcetn bezpecné pracovní zátze Stejnosmrný proud
Stídavý proud
Nebezpecné naptí
Ekvalizace potenciálu
Ochranné uzemnní Ochrana proti silnému proudu vody Pílozná cást typu B
Zdravotnické vybavení klasifikované spolecností Underwriters Laboratories Inc., pouze pokud jde o nebezpecí zásahu elektrickým proudem, nebezpecí pozáru nebo mechanická nebezpecí, podle norem ANSI/AAMI ES60601-1:2005 a CAN/CSA-C22.2 c. 60601-1:08. *Pro volitelný doplnk Prime X viz Píslusenství RTG zaízení, IEC 60601-2-54 Podle smrnice Evropského parlamentu a Rady 2012/19/EU o odpadních elektrických a elektronických zaízeních (OEEZ) ve znní pozdjsích pedpis tento symbol oznacuje, ze výrobek se musí sbírat k recyklaci oddlen. Nelikvidujte s bzným netídným odpadem. Informace o likvidaci si vyzádejte od místního distributora. Ped recyklací zajistte dekontaminaci infikovaných prostedk.
Není bezpecné pro vysetení MR
Touto stranou nahoru
Uchovávejte v suchu

Kehké, manipulujte opatrn Limit stohování podle poctu

1125-309-005 Rev AB.0

Obsah
Definice varování/upozornní/poznámky …………………………………………………………………………………………..3 Pehled bezpecnostních opatení ………………………………………………………………………………………………3 Místa, kde hrozí skípnutí …………………………………………………………………………………………………..6
Úvod ………………………………………………………………………………………………………………………………………… 7 Popis výrobku ……………………………………………………………………………………………………………………….7 Indikace k pouzití …………………………………………………………………………………………………………………..7 Klinické pínosy……………………………………………………………………………………………………………………..8 Kontraindikace ………………………………………………………………………………………………………………………8 Ocekávaná zivotnost ………………………………………………………………………………………………………………8 Likvidace / recyklace ………………………………………………………………………………………………………………8 Technické parametry ………………………………………………………………………………………………………………8 Obrázek výrobku Prime……………………………………………………………………………………………………….11 Ilustrace produktu moznost Prime X ……………………………………………………………………………………….12 Pílozné cásti elektricky ovládaná lozná plocha nosítek (volitelný doplnk)………………………………………13 Pílozné cásti volitelný doplnk Prime X…………………………………………………………………………………..13 Kontaktní informace ……………………………………………………………………………………………………………..13 Umístní sériového císla………………………………………………………………………………………………………..14
Píprava …………………………………………………………………………………………………………………………………..15 Provoz …………………………………………………………………………………………………………………………………….16
Zabrzdní a odbrzdní brzd ……………………………………………………………………………………………………16 Ovládání podvozku Prime ………………………………………………………………………………………………………17 Zvýsení nosítek bez elektrického mechanismu ……………………………………………………………………………17 Snízení nosítek bez elektrického mechanismu ……………………………………………………………………………17 Zvýsení elektricky ovládané lozné plochy nosítek (volitelný doplnk)………………………………………………..18 Snízení volitelné elektricky ovládané lozné plochy nosítek……………………………………………………………..18 Umístní výrobku do Trendelenburgovy polohy …………………………………………………………………………..19 Umístní výrobku do obrácené Trendelenburgovy polohy ……………………………………………………………..19 Peprava pacienta bez pouzití kola Big Wheel …………………………………………………………………………….19 Peprava pacienta za pouzití kola Big Wheel ………………………………………………………………………………20 Peprava pacienta za pouzití motorizovaného pohonu Zoom ………………………………………………………….21 Dobíjení baterie motorizovaného pohonu Zoom…………………………………………………………………………..23 Peprava pacienta rucn bez pouzití kola motorizovaného pohonu Zoom ………………………………………….24 Zvednutí postranice………………………………………………………………………………………………………………24 Spustní postranice………………………………………………………………………………………………………………25 Nastavení polohy výrobku s ovládacím panelem pro pacienta na postranici varianta s elektricky ovládanou
loznou plochou nosítek pouze Prime…………………………………………………………………………..25 Ovládací panel pro obsluhu volitelná elektricky ovládaná lozná plocha nosítek pouze Prime ……………..26 Zablokování a odblokování funkcí ovládacího panelu pro pacienta volitelná elektricky ovládaná lozná
plocha nosítek pouze Prime ……………………………………………………………………………………..27 Zvednutí nebo snízení zádové cásti nosítka bez elektrického mechanismu ……………………………………..27 Zvednutí nebo snízení zádové cásti varianta s elektricky ovládanou loznou plochou nosítek ……………….28 Zvedání a sklápní podkolenní cásti nosítka bez elektrického mechanismu pouze Prime………………….29 Zvedání a sklápní podkolenní cásti nosítka s elektrickým mechanismem pouze Prime……………………29 Poloha zotavovacího kesla pouze Prime ………………………………………………………………………………..30 Ukládání pedmt do krytu podvozku ………………………………………………………………………………………30 Zavsování zdravotnických prostedk pi pouzití volitelné konzoly pro pumpu …………………………………..31 Vytazení a zatazení napájecího kabelu pomocí volitelného navijáku na kabel pouze u volitelného
elektrického zvedacího mechanismu nebo volitelné elektricky ovládané lozné plochy nosítek ………………………………………………………………………………………………………………….. 31 Systém váhy (volitelný doplnk) ………………………………………………………………………………………………32 Identifikace ikon/tlacítek váhy ……………………………………………………………………………………………32 Vázení pacienta …………………………………………………………………………………………………………….33 Uzamknutí mrné jednotky na váze ……………………………………………………………………………………33 Aktivace a deaktivace funkce Chaperone …………………………………………………………………………….33 Nastavení alarm pro funkci Chaperone………………………………………………………………………………34 Nastavení hlasitosti alarmu pro funkci Chaperone ………………………………………………………………….34 Nabíjení sady baterií systému váhy (volitelný doplnk) elektricky ovládaná lozná plocha nosítek
(volitelný doplnk) nebo elektricky ovládaná lozná plocha nosítek s funkcí Chaperone (volitelný doplnk) pouze Prime ……………………………………………………………………………………….34 Výmna baterií volitelného systému váhy nosítka bez elektrického mechanismu ………………………..35

1125-309-005 Rev AB.0

1 CS

Doplky a soucásti ……………………………………………………………………………………………………………….35 Pipevnní desky pro defibrilátor………………………………………………………………………………………..38 Pemna desky pro defibrilátor / nozní nástavec v desku pro defibrilátor ……………………………………..38 Pemna desky pro defibrilátor / nozní nástavec v nozní nástavec……………………………………………..39 Pipevnní dolní pelesti / drzáku dokument …………………………………………………………………………40 Pipevnní IV podstavce ………………………………………………………………………………………………….40 Nastavení nebo ulození oprek pro nohy pouze Prime………………………………………………………….40 Umístní dvoudílného trvale pipevnného IV stojanu …………………………………………………………….42 Umístní trojdílného trvale pipevnného IV stojanu ……………………………………………………………….42 Pipevnní a úprava polohy snímatelného IV stojanu………………………………………………………………43 Pipojení svislého drzáku kyslíkové láhve …………………………………………………………………………….44 Vytazení nebo odstranní drzáku servírovacího podnosu / dolní pelesti ………………………………………44 Pipevnní podlozek postranice …………………………………………………………………………………………45 Umístní vázání pro pacientské upínací pásy ……………………………………………………………………….45 Umístní svislého drzáku RTG kazety volitelný doplnk Prime X …………………………………………….45 Umístní bocního drzáku RTG kazety volitelný doplnk Prime X…………………..

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stryker Prime Series Stretcher Instruction Manual

Prime Series Stretcher

Product Information

Symbols

Warning/Caution/Note Definition

WARNING

CAUTION

Note

Summary of Safety Precautions

Product Usage Instructions

Introduction

Pinch Points

Setup

Operation

Option

Scale System Option

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