Stryker SV2 User manual

2017/08 KK-7500 REV 02 www.stryker.com
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Operations Manual
SV2 Electric Hospital Bed
7500

sample text

2017/08 KK-7500 REV 02 www.stryker.com
SV2 Electric Hospital Bed
7500
Operations Manual

sample text

www.stryker.com KK-7500 REV 02
English
EN
Symbols
Refer to instruction manual/booklet
Operating instructions / Consult instructions for use
General warning
Caution
Warning; crushing of hands
Warning; crushing of feet
Do not insert lift pole
Headboard and footboard orientation
Do not store items under the bed.
Gatch positioning
Catalogue number
Serial number
CE mark
Manufacturer
Mass of equipment with safe working load
Safe working load
Maximum patient weight
Adult patient

KK-7500 REV 02 www.stryker.com
English
EN
Symbols
Direct current
~
Alternating current
Dangerous voltage
Unit provides terminal for connection of a potential equalization conductor. The potential
equalization conductor provides direct connection between the unit and potential equalization
busbar of the electrical installation.
Protective Earth terminal
IPX4 Protection from liquid splash
Type B applied part
In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic
Equipment (WEEE), this symbol indicates that the product must not be disposed of as
unsorted municipal waste, but should be collected separately. Contact your local distributor
for disposal information. See the maintenance manual for servicing instructions and
recyclable components.

www.stryker.com KK-7500 REV 02 1-1
English
EN
Table of Contents
Warning/Caution/Note Definition ...............................................................................................................1-3
Summary of safety precautions.................................................................................................................1-4
Pinch points....................................................................................................................................1-7
Introduction...........................................................................................................................................1-8
Product description...........................................................................................................................1-8
Indications for use............................................................................................................................1-8
Expected service life.........................................................................................................................1-9
Contraindications .............................................................................................................................1-9
Warranty ........................................................................................................................................1-9
Specifications..................................................................................................................................1-9
Product illustration.......................................................................................................................... 1-12
Applied parts................................................................................................................................. 1-13
Contact information ........................................................................................................................ 1-13
Serial number location .................................................................................................................... 1-14
Setup................................................................................................................................................. 1-15
Operation ........................................................................................................................................... 1-16
Plugging or unplugging the battery cable............................................................................................. 1-16
Plugging or unplugging the product.................................................................................................... 1-17
Charging the battery ....................................................................................................................... 1-17
Storing the battery long term............................................................................................................. 1-18
Storing the power cord .................................................................................................................... 1-18
Transporting the product.................................................................................................................. 1-19
Applying or releasing the brakes........................................................................................................ 1-19
Applying or releasing steer lock......................................................................................................... 1-21
Applying or releasing the fifth wheel (option)........................................................................................ 1-22
Activating and resetting the CPR release............................................................................................. 1-23
Removing or replacing the headboard ................................................................................................ 1-23
Removing or replacing the footboard.................................................................................................. 1-24
Raising or lowering the lower leg section............................................................................................. 1-25
Raising or lowering the siderails ........................................................................................................ 1-26
Nurse control panel (outside siderail) (option) ...................................................................................... 1-27
Patient control panel (inside siderail) (option)....................................................................................... 1-28
Patient control pendant (option) ........................................................................................................ 1-30
Nurse control pendant..................................................................................................................... 1-31
Extending the bed extender (option)................................................................................................... 1-32
Installing the bed extender bolster mattress ......................................................................................... 1-33
Extending or retracting the linen tray (option) ....................................................................................... 1-34
Inserting or removing a cassette from the X-ray cassette holder (option) ................................................... 1-34
Accessories........................................................................................................................................ 1-36
Installing the IV pole........................................................................................................................ 1-36
Adjusting the IV pole ....................................................................................................................... 1-37
Installing the lifting pole................................................................................................................... 1-37
Installing the lifting pole handle ......................................................................................................... 1-38

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Table of Contents
Installing the oxygen bottle holder...................................................................................................... 1-39
Installing the Foley bag basket.......................................................................................................... 1-39
Cleaning............................................................................................................................................. 1-41
Preparing the product for cleaning..................................................................................................... 1-41
Cleaning....................................................................................................................................... 1-41
Cleaning the siderails...................................................................................................................... 1-42
Disinfecting......................................................................................................................................... 1-43
Preventive maintenance ........................................................................................................................ 1-44
EMC information.................................................................................................................................. 1-46

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www.stryker.com KK-7500 REV 02 1-3
Warning/Caution/Note Definition
The words WARNING,CAUTION, and NOTE carry special meanings and should be carefully reviewed.
WARNING
Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe
potential serious adverse reactions and safety hazards.
CAUTION
Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the
user or patient or damage to the product or other property. This includes special care necessary for the safe and
effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or
misuse.
Note: Provides special information to make maintenance easier or important instructions clearer.

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Summary of safety precautions
Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel.
WARNING
• Only use the input voltage and frequency as rated on the product.
• Always allow the product to reach room temperature before you begin setup or test functional operations, to
prevent permanent product damage.
• Do not use this product if it has identifiable failures, defects, malfunctions, or damage.
• Do not use this product under any conditions if use would cause injury to the operator or patient.
• Only operate the product when all operators are clear of the mechanisms.
• Do not attach the power cord to any parts of the product.
• Always unplug the power cord and call maintenance if unanticipated motion occurs.
• Do not store items under the bed.
• Do not use the bed without the litter covers.
• To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth.
• Always store the power cord to avoid the risk of entanglement, damage to the power cord, or potential shock
hazards. If the power cord is damaged, remove the product from service and contact the appropriate maintenance
personnel.
• Always allow enough clearance between the head end of the product and the adjacent wall, so you can unplug the
power cord from the wall outlet during an emergency.
• Always store the power cord before transporting the product.
• Always disconnect the power cord from the wall outlet if you detect overheating of the battery, control cables, or
pendants. Do not use the product again until it has been inspected, serviced, and confirmed to work as intended by
authorized maintenance personnel.
• Always replace the battery after it surpasses its expected service life.
• Do not open a dead battery.
• Do not throw the battery into a fire.
• Do not spill liquid onto the battery or submerge the battery in liquid.
• Always unplug the battery cable from the control box before you store the product for a long period of time.
• Always lock the siderails in the full up position with the sleep surface horizontal in the lowest position when
transporting a patient.
• Always keep limbs, hands, fingers, and other body parts clear of mechanisms and gaps.
• Always make sure that there are no obstacles near the product. Injury to the patient, operator, bystanders or
damage to the frame or surrounding equipment could occur if you collide with an obstacle.
• Do not attempt to move the product laterally. This may cause the product to tip.
• Do not move the product after you apply the brakes.
• Always apply the brakes when a patient is getting into or out of the product to avoid instability.
• Always apply the brakes when the patient is unattended.
• Always make sure that all persons and equipment are away from the area below and around the backrest before
you activate the CPR release. The CPR release is for emergency use only.
• Always properly orient the headboard when replacing the headboard to avoid entrapment.
• Always properly orient the footboard when replacing the footboard to avoid entrapment.
• Always make sure that all persons and equipment are away from the area below and around the leg rest before you
lower the lower leg section.
• Always lock the siderails unless a patient’s condition requires extra safety measures.
• Always lock the siderails in the full up position when the patient is unattended.

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Summary of safety precautions
WARNING (CONTINUED)
• Do not use siderails as restraint devices to keep the patient from exiting the product. The operator must determine
the degree of restraint necessary to make sure that the patient is safe.
• Do not sit on the siderails.
• Always lock bed motion controls when the patient is unattended.
• Never store the nurse control panel within the patient’s reach.
• Do not sit on the bed extender. This may cause the product to tip.
• Always lock the bed extender before you place weight on the bed extender.
• Always retract the linen tray (option) before you put the product in motion.
• Always retract the linen tray (option) when not in use.
• Do not use the product for X-ray procedures if it does not have the radiolucent backrest (option).
• Do not use accessories to support patient limbs or other body parts.
• Do not clean, service, or perform maintenance while the product is in use.
• Always power off and unplug the power cord before cleaning, servicing, or performing maintenance.
• Always power off the product and unplug the power cord from the wall outlet when large spills occur near the circuit
boards, cables, and motors. Remove the patient from the product, clean up the fluid, and have service personnel
inspect the product. Fluids can cause unpredictable operation and decreased functionality of any electrical product.
Do not return the product to service until it is completely dry and has been thoroughly tested for safe operation.
• Do not spray cleaners directly onto the battery, control boxes, actuators, cables, or other electric equipment.
• Do not use abrasive powder, steel wool, or similar materials that may damage the product surface.
• Do not use Virex®TB for product disinfecting.
• Do not use acid-based chemicals or flammable chemicals, such as gasoline, diesel, or acetone for cleaning
purposes.
• The cleaners and disinfectants must not be highly alkaline or acidic (pH value 6-8).
• Do not directly spray or saturate the siderail control panel, patient control pendant, or nurse control pendant with
cleaners.
• Do not use sharp objects to clean the siderail control panel.
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.
• To minimize the risk of any electromagnetic interference, the product design follows the standard IEC 60601-1-2.
To avoid problems, use the bed in accordance with the EMC/EMI requirements in the EMC section of this
operations manual.
• Portable RF communications equipment (including peripherals such as antenna cables and external antennas)
should be used no closer than 30 cm (12 in.) to any part of the SV2, including cables specified by the manufacturer.
Otherwise, degradation of the performance of this equipment could result.
• Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in
improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify
that they are operating normally.

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Summary of safety precautions
CAUTION (CONTINUED)
• Use of accessories, transducers, and cables other than those specified or provided by the manufacturer of this
equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this
equipment and result in improper operation.
• Do not place objects into any gaps of the product.
• Always plug the product into a wall outlet (regulated AC-power source) when not in use to maintain a sufficient
battery charge and to maximize product performance while operating on battery power.
• Always replace batteries that have corrosion at the terminals, display cracking, have expanded or bulging sides, or
no longer can maintain a full charge.
• Only use authorized batteries when replacing the batteries. Use of unauthorized batteries may lead to unpredictable
system performance.
• Do not place or store heavy objects on the product.
• Do not squeeze or pinch the power cord in the bed frame.
• Do not use the siderails as a push or pull device. Always move the product using the integrated handles in the
headboard and footboard.
• Always remove the patient lift pole before transporting the product.
• Do not use the IV pole as a push or pull device.
• Always make sure that the IV pole is at a low height during transport.
• Always apply the brake to prevent unintended movement.
• Do not apply the brake pedal to stop a moving product.
• Always hang the nurse control pendant onto a foot end siderail or the linen tray (option) before removing the
footboard.
• Do not raise the lower leg section while the bed extender is in use. This is to avoid the situation where the product
does not support the lower legs of a taller patient.
• Always place the patient control pendant safely on the mattress while the pendant is in use.
• Always hang the patient control pendant onto the siderail when the pendant is not in use.
• Do not squeeze or pinch the pendant cord in the bed frame.
• Always place the nurse control pendant onto the footboard.
• Do not remove the footboard after you extend the bed extender.
• The safe working load of the linen tray is 15 kg.
• Only use authorized accessories for this product. The use of unauthorized accessories may result in product
damage or injury to the operator or patient. Stryker is not responsible for any damage or injury that may result from
the misuse of the product or the use of unauthorized accessories.
• Always make sure that accessories are locked into position.
• Do not allow accessories to interfere with mechanical or electric mechanisms of the product.
• Do not use the lifting pole as a push or pull device.
• Do not use the oxygen bottle holder as a push or pull device.
• Always turn the oxygen bottle holder in toward the bed before transporting a patient.
• Do not strike the oxygen bottle holder while transporting a patient.
• The safe working load of each Foley hook is 2 kg.
• Do not steam clean, pressure wash, ultrasonically clean, or immerse any part of the product in water. Exposure to
water may damage the internal electric parts. These methods of cleaning are not recommended and may void this
product’s warranty.

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Summary of safety precautions
CAUTION (CONTINUED)
• Always make sure that you wipe each product with clean water and thoroughly dry each product after cleaning.
Some cleaning products are corrosive in nature and may cause damage to the product if you use them improperly.
If you do not properly rinse and dry the product, you may leave a corrosive residue on the surface of the product
that could cause premature corrosion of critical components. Failure to follow these cleaning instructions may void
your warranty.
Pinch points
Figure 1-1: SV2 pinch points

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Introduction
This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating
or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or
maintenance of this product.
CAUTION
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in
this manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable
operation resulting in injury to patient or operator. Modifying the product also voids its warranty.
Notes
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current
product information available at the time of printing. There may be minor discrepancies between your product and
this manual. If you have any questions, contact Stryker Customer Service or Technical Support at + 90 (352) 321
43 00 (pbx).
Product description
SV2 is an AC-powered bed with a battery backup system. SV2 is for patients to receive treatment for extended periods
of time at hospitals and care centers. SV2 has four electrical actuators that allow it to adjust to numerous positions,
including CPR, Trendelenburg, Reverse Trendelenburg, and chair positions. SV2 is equipped with retractable siderails,
removable headboard and footboard, and options and accessories that assist with the care of the patient.
SV2 is an electromechanical MedSurg and ICU bed with DC-powered actuators and controls to adjust the patient sleep
surface. The patient sleeping surface consists of four sections: the backrest, seat, upper leg section, and lower leg
sections. Siderails are split, with two siderails on the head end, and two siderails on the foot end. The siderails secure in
the full up position. When unlatched, siderails open outside and move to the lowest position.
You can actuate electromechanical functions with the siderail control panel, patient control pendant, and nurse control
pendant. The control box consists of logic controls and a power supply that power and control signals to all four
actuators via a distribution box. The siderail control panels, patient control pendant, and nurse control pendant controls
are also controlled by the control box via distribution box.
The bed is equipped with two pairs of actuators (four actuators total). The first pair below the litter surface control the
backrest down and up functions, and upper leg down and up functions. The second pair of actuators below the
undercarriage control the litter down and up functions, Trendelenburg, and Reverse Trendelenburg.
Additional bed mechanisms allow for manual CPR, knee gatch motion, and bed length extension. The bed is also
equipped with brake and steer control for the casters. Casters help in emergency or non-emergency intra-hospital
transport of a patient on the bed.
Indications for use
SV2 is for use by human adult patients in a MedSurg and ICU setting requiring the support of a hospital bed. Use this
product with a patient sleep surface.
Operators for the bed include healthcare professionals (such as nurses, nurse aides, and medical doctors), service or
maintenance personnel, patients, and bystanders who can use bed motion functions.
SV2 is for use in medical, surgical, and critical care healthcare environments, including hospitals, institutions and clinics.
The SV2 bed frame, litter mounted accessories, and mattresses can come in contact with human skin.

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Introduction
Indications for use (Continued)
The SV2 bed frame is not intended to be used with an oxygen tent, in the presence of flammable anesthetics, or to
support more than one individual at a time.
Expected service life
SV2 has a ten year expected service life under normal use conditions and with appropriate periodic maintenance.
The battery has a one year expected service life under normal use conditions.
The casters have a two year expected service life under normal use conditions.
The optional fifth wheel has a two year expected service life under normal use conditions.
Contraindications
None known.
Warranty
Warranty may vary by country. Contact your local Stryker Medical representative for additional information.
Specifications
Safe working load
Note: Safe working load indicates the sum of
the patient, mattress, and accessory weight
250 kg
Maximum patient weight 215 kg
Product weight 160 kg
Overall product
size
Length 2200 mm (±10 mm)
Length (with bed extender - option) 2510 mm (±10 mm)
Width 990 mm (±10 mm)
Product height
(without mattress)
Low 375 mm (+15 / -25 mm)
High 755 mm (±10 mm)
Under product clearance 150 mm
Caster size (single and optional dual-casters) 150 mm
Product angle indicator 0° - 15°
Backrest angle indicator 0° - 90°
Backrest angle 0° - 60°

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Introduction
Specifications (Continued)
Trendelenburg/Reverse Trendelenburg 0° - 12°
Gatch angle 0° - 30°
Electrical requirements
Battery 24 VDC, 10 amps, Model BA1812
Control box 100-240 VAC, 50 Hz - 60 Hz nominal, 5 amps
Electrical
classification
Class 1 when product is plugged into mains power
Internally powered when the product is unplugged
Duty cycle 2 mins of actuation and 18 mins idle
Class I Equipment: Equipment that protects against electrical shock and does not solely rely on basic insulation, but
which includes an additional safety precaution that is provided for the connection of the equipment to the protective
earth conductor in the fixed wiring of the installation that accessible metal parts cannot become live in the event of a
failure of basic insulation.
Compatible mattresses
7002-2-012 2000 mm x 860 mm x 120 mm
7002-2-014 2000 mm x 860 mm x 140 mm
7002-2-512 2000 mm x 860 mm x 120 mm
7002-2-514 2000 mm x 860 mm x 140 mm
7002-5-012 2000 mm x 860 mm x 120 mm
7002-5-014 2000 mm x 860 mm x 140 mm
7002-5-512 2000 mm x 860 mm x 120 mm
7002-5-514 2000 mm x 860 mm x 140 mm
7002-5-712 2000 mm x 860 mm x 120 mm
Environmental conditions Operation Storage and transportation
Temperature
(38 °C)
(5 °C)
(50 °C)
(-10 °C)
Relative humidity
90%
20%
90%
20%
Atmospheric pressure
1060 hPa
800 hPa
1060 hPa
800 hPa

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Introduction
Specifications (Continued)
Specifications listed are approximate and may vary slightly from product to product or by power supply fluctuations.
Stryker reserves the right to change specifications without notice.
Standards applied
IEC 60601-1:2012 Medical electrical equipment - Part 1: General requirements
for basic safety and essential performance
IEC 60601-1-2:2014
Medical electrical equipment - Part 1-2: General
requirements for basic safety and essential performance -
Collateral standard: Electromagnetic compatibility -
Requirements and tests
IEC 60601-2-52:2009 + A1:2015 Medical electrical equipment - Part 2-52: Particular
requirements for the basic safety and essential performance
of medical beds
IEC 60601-2-54:2009 + A1:2015*
*Only applicable when the product is equipped with
the radiolucent backrest option
Medical electrical equipment - Part 2-54: Particular
requirements for the basic safety and essential performance
of X-ray equipment for radiography and radioscopy
WARNING
Only use the input voltage and frequency as rated on the product.
CAUTION
• To minimize the risk of any electromagnetic interference, the product design follows the standard IEC 60601-1-2.
To avoid problems, use the bed in accordance with the EMC/EMI requirements in the EMC section of this
operations manual.
• Portable RF communications equipment (including peripherals such as antenna cables and external antennas)
should be used no closer than 30 cm (12 in.) to any part of the SV2, including cables specified by the manufacturer.
Otherwise, degradation of the performance of this equipment could result.
• Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in
improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify
that they are operating normally.
• Use of accessories, transducers, and cables other than those specified or provided by the manufacturer of this
equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this
equipment and result in improper operation.

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EN
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Introduction
Product illustration
A
BC
D
E
F
G
H
I
J
K
L
M
P
O
R
S
T
Q
N
U
V
AAccessory sleeve LLinen tray (option)
B Backrest M Lower leg section
C Backrest indicator N Roller bumper
DBed angle indicator O Seat section
EBed extender (option) P Siderails
FBrake/steer pedal QSiderail control panel (Inside siderail) (option)
GCasters (Dual-wheel casters optional) RSiderail control panel (Outside siderail) (option)
H CPR release S Siderail latch
IFoley hooks TUpper leg section
J Footboard U Nurse control pendant (option)
K Headboard V Patient control pendant (option)

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Introduction
Applied parts
Figure 1-2: Type B applied parts
Contact information
Contact your Stryker Customer Service:
Stryker Medical International
Kayseri Serbest Bölge Şubesi
2. Cad. No:17 38070
Kayseri, Turkey
E-mail : [email protected]
Phone : + 90 (352) 321 43 00 (pbx)
Fax: + 90 (352) 321 43 03
www.mukametal.com
Have the serial number (A) of your product available. Include the serial number in all written communication.

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Introduction
Serial number location
A