Secure II Medsurg Bed Model 3002 Operations Manual Rev B Dec 2011

Table of Contents Symbols and Definitions ... 6 Warning/Caution/Note Definition ... 7 Introduction... 8 Intended Use – Styker 3002 Secure® II... 8 Intended Use – iBed® Wireless with iBed Awareness... 8 Specifications... 8 Mattress Specifications... 9 Bed Illustration ... 10 Safety Tips and Guidelines ... 11 Safety Tips and Guidelines... 11 Zoom® Option ... 13 iBed Awareness Option... 13 iBed® Wireless Option... 14 Setup Procedures... 15 Zoom® Option ... 16 iBed® Wireless Option... 16 Base Operation Guide... 17 Brake Pedal Operation ... 17 Steer Pedal Operation (Beds without the Zoom Drive Wheel Option) ... 17 Litter Operation Guide... 18 CPR Emergency Release ... 18 Foot Prop Usage... 18 Fracture Frame Usage ... 18 Foley Bag Hooks Usage ... 18 Patient Restraint Strap Locations... 18 Positioning Siderails... 19 Siderail Control Panel Lights... 19 Operating I.V. Poles ... 20 Night Light Usage... 21 Nurse Call Backup Battery (Optional Equipment)... 21 Using the 110 Volt Outlet (Optional Equipment) ... 21 CPR Board Usage (Optional Equipment) ... 21 Footboard Operation Guide... 22 Footboard Control Panel Guide ... 22 LED Display Panel Guide ... 23 Function Lockout System Usage... 23 Chaperone® Bed Exit (Optional Equipment)... 24 Chaperone® Bed Exit With Zone Control (Optional Equipment)... 25 Chaperone® Zone Settings ... 26 Scale System Operation Guide ... 27 Scale System Control Panel Guide (Optional) ... 27 Preparing The Bed For Patient Stay / Zeroing The Scale System... 29 Activating The Scale System And Displaying Patient Weight... 29

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Table of Contents Scale System Operation Guide (Continued) Adding Or Removing Items During A Patient’s Stay ... 30 Converting The Patient’s Weight... 30 Displaying The Weight Log ... 31 Viewing Patient Weight In Gain / Loss Mode ... 32 Changing The Numerical Value Of Displayed Weight... 33 Optional Pendant Operation Guide... 34 Zoom™ Option Operation Guide... 35 Drive Wheel Operation ... 35 Head End Control Panel Operation ... 37 Battery Charging And Operation ... 38 Optional iBed Awareness Operation Guide... 39 Footboard Control Panel Buttons... 39 Footboard Control Panel Functions... 40 LED Indicators: Footboard... 42 LED Indicators: Dashboard ... 43 Display Screens... 44 Main Menu Screen... 45 iBed Awareness Functionality... 49 iBed Awareness Light Bar... 49 iBed Awareness Side LEDs... 49 iBed Awareness Button... 49 iBed Awareness Monitoring and Alarms... 50 Low Height... 50 Brakes... 50 Siderails... 50 Bed Exit... 51 Additional Alarm Conditions... 51 iBed Awareness Locks ... 51 Fowler 30+ Lock button ... 51 Bed Motion Lock ... 52 Patient Control Locks ... 52 Optional Infrared (IR) Module... 53 Optional iBed Locator... 54 Preventative Maintenance ... 55 Checklist ... 55 Inside Siderail Function Guide... 56 Outside Siderail Function Guide ... 57 Product Labels ... 58 Cleaning... 60

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Table of Contents Recycling Passport ... 61 EMC Information... 72 Warranty... 76 Limited Warranty... 76 To Obtain Parts and Service... 76 Service Contract Coverage... 76 Service Contract Programs... 77 Return Authorization... 77 Damaged Merchandise... 77 International Warranty Clause... 77

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Symbols and Definitions Warning, consult accompanying documentation

Safe Working Load Symbol

Dangerous Voltage Symbol

~

Alternating Current

Direct Current

Protective Earth Terminal

Potential Equalization Symbol Type B Equipment: equipment providing a particular degree of protection against electric shock, particularly regarding allowable leakage current and reliability of the protective earth connection. Class 1 Equipment: equipment in which protection against electric shock does not rely on BASIC INSULATION only, but which includes an additional safety precaution in that means are provided for the connection of the EQUIPMENT to the protective earth conductor in the fixed wiring of the installation in such a way that ACCESSIBLE METAL PARTS cannot become live in the event of a failure of the BASIC INSULATION. Mode of Operation: Continuous

IPX4

Protection from liquid splash Medical Equipment Classified by Underwriters Laboratories Inc. with Respect to Electric Shock, Fire, Mechanical and Other Specified Hazards Only in Accordance with UL 60601−1, First Edition (2003) and CAN/CSA C22.2 No. 601.1−M90 with updates 1 and 2 and IEC 60601-1 (1998) with Amendment 1 (1991) and Amendment 2 (1995). In accordance with European Directive 2002/96/EC on Waste Electrical and Electronic Equipment, this symbol indicates that the product must not be disposed of as unsorted municipal waste, but should be collected separately. Refer to your local distributor for return and/or collection systems available in your country. Non-ionizing radiation; i.e. RF transmitter (WiFi) This icon means the iBed Locator is connected.

X

This icon means the iBed Locator is not connected. This icon means the Network is connected.

X

This icon means the Network is not connected.

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Symbols and Definitions WARNING/CAUTION/NOTE DEFINITION The words Warning, Caution and Note carry special meanings and should be carefully reviewed.

WARNING Alerts the reader about a situation, which if not avoided, could result in death or serious injury. It may also describe potential serious adverse reactions and safety hazards.

CAUTION Alerts the reader of a potentially hazardous situation, which if not avoided, may result in minor or moderate injury to the user or patient or damage to the equipment or other property. This includes special care necessary for the safe and effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or misuse. Note This provides special information to make maintenance easier or important instructions clearer.

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Introduction This manual is designed to assist you with the operation of the Model 3002 Secure® II MedSurg Bed. Read it thoroughly before using the equipment.

INTENDED USE – STYKER 3002 SECURE® II This device is an AC-powered adjustable hospital bed intended for medical purposes that consists of a bed with a built-in motor and remote controls that can be operated by the patient to adjust the height and surface contour of the bed. The device includes movable and latchable siderails.

INTENDED USE – iBED® WIRELESS WITH iBED AWARENESS The intended use for the iBed® Wireless (with iBed Awareness) is to assist clinical staff to monitor bed parameters on specific Stryker beds. The desired bed parameters will be set by clinicians at the bedside. The iBed® Wireless software is intended to be used only with specifically enabled Stryker beds that have been verified and validated with the iBed® Wireless software, and is not intended to provide bed status information for non-Stryker beds. The iBed® Wireless software is not intended to communicate any patient status information, nor to permanently store any type of data. The iBed® Wireless with iBed Awareness System is not intended to provide automated treatment decisions or as a substitute for professional healthcare judgment. The iBed® Wireless with iBed Awareness System is not a replacement or substitute for vital signs monitoring or alert equipment. All patient medical diagnosis and treatment are to be performed under direct supervision and oversight of an appropriate health care professional.

SPECIFICATIONS Safe Working Load Note: Safe Working Load indicates the sum of the patient, mattress, and accessory weight. Scale System Capacity (optional equipment). Loads weighing up to Scale System Accuracy (optional equipment)

227 kg

Standard Beds with Zoom® Option Short Beds w/Zoom® Option

500 lbs 227 kg ± 2 pounds at 0° - ± 10° Trendelenburg for patients weighing 100 pounds or less ± 2% of the total patient weight at 0° - ± 10° Trendelenburg for patients weighing greater than 100 pounds 93” x 42.5” 236 cm x 108 cm 93” x 40” 236 cm x 101.6 cm 93” x 42.5” 236 cm x 108 cm 93” x 36” 236 cm x 92 cm 85” x 42.5” 216 cm x 108 cm 85” x 36” 216 cm x 92 cm 95” x 42.5” 241 cm x 108 cm 95” x 40” 241 cm x 101.6 cm 87” x 42.5” 221 cm x 108 cm 87” x 36” 221 cm x 92 cm 84” x 35” 213 cm x 89 cm 76” x 35” 193 cm x 89 cm 16” to 30” ±0.5 41 cm to 76 cm 19.75” x 30” 50 cm x 76 cm 20.5” x 30” 52 cm x 76 cm

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Overall Length/ Standard Bed (Inside Width US and Canada) Standard Bed (Outside US and Canada) Short Bed (Inside US and Canada) Zoom® Bed (Inside US and Canada) Zoom® Short Bed (Inside US and Canada)

Siderails Up Siderails Down Siderails Up Siderails Down Siderails Up Siderails Down Siderails Up Siderails Down Siderails Up Siderails Down

Patient Sleep Surface - Standard Bed Patient Sleep Surface - Short Beds Bed Height to Top of Seat Litter - 6” Casters

500 lbs

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Introduction SPECIFICATIONS (CONTINUED) Litter Platform to Top of Siderail

Full Up Head End Siderail Full Up Foot End Siderail Outside US/Canada Head End Siderail Outside US/Canada Foot End Siderail Space Between Siderails (Full Up) Outside the US and Canada Knee Gatch Angle Fowler Angle Trendelenburg/Reverse Trendelenburg Non-Zoom Trend Rev. Trend Zoom® Trend Rev. Trend Electrical Requirements - all electrical requirements meet UL 2601 specifications. Wireless Radio (iBed® Wireless Option)

Outlet Option iBed® Wireless (Optional Wireless Connection)

iBed Locator (Wall Module) IR Module (Bed) WiFi Module (Bed)

• • • •

15.75” 40 cm 15.25” 38.7 cm 15” 38.1 cm 14” 35.5 cm 9.75” 24.7 cm 9.125” (8”) 23.1 cm 0° to 40° 0° to 60° 12° ± 1° -10° ± 1° 10° ± 1° -10° ± 1° 115 VAC, 60 Hz, 8.0 A Optional: 230 VAC, 50/60 Hz, 4.0 A 802.11 b/g, 2.4 GHz • Minimum Operational Signal Strength: -65 dB • Supported Securities: WEP WPA-PSK (TKIP) WPA2-PSK (CCMP/AES) • Supports IPv4 and DHCPv4 110 VAC, 60 Hz, 10.0 A (not available with Zoom® Option) Uses infrared based Stryker proprietary communication scheme. Uses infrared based Stryker proprietary communication scheme. Communication is line of sight based. Communication scheme used is IEEE 802.11 b/g (2.4 GHz Band)

MATTRESS SPECIFICATIONS Thickness Width Length ILD

6” >= 35” >= 84” 80 lbs

15.2 cm >= 88.9 cm >= 213.4 cm 36.3 kg

The above stated mattress specifications assist in ensuring the product conforms to HBSW and IEC specifications. Stryker reserves the right to change specifications without notice. Specifications listed are approximate and may vary slightly from unit to unit or by power supply fluctuations.

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Bed Illustration

HEAD END PATIENT’S RIGHT

CPR Release Handle

PATIENT’S LEFT

I.V. and Fracture Frame Mount

Footboard Control Panel

Steer Pedal

Siderail Release Handle Brake Pedal Foley Bag Hooks (Standard)

FOOT END I.V. and Fracture Frame Mount (Behind Foot Board)

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Safety Tips and Guidelines SAFETY TIPS AND GUIDELINES Before operating the Secure Bed, it is important to read and understand all information in this manual. Carefully read and strictly follow the safety guidelines listed on this page. It is important that all users have been trained and educated on the inherent hazards associated with the usage of electric beds.

WARNING • • •

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•

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Danger: Explosion hazard. Do not use in the presence of flammable anesthetics. Always apply the caster brakes when a patient is getting on or off the bed. Always keep the caster brakes applied when a patient is on the bed (except during transport). After the brake pedal is applied, push on the bed to ensure the brakes are locked. Serious injury could result if the bed moves while a patient is getting in or out of bed. Ensure the brakes are completely released prior to attempting to move the unit. Attempting to move the unit with the brakes actuated could result in injury to the user and/or patient. Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal is activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when the steer pedal is activated may cause injury to the user. The Secure II Bed is not intended for use with patients less than two years of age. Serious injury can result if caution is not used when operating the unit. Operate the unit only when all persons are clear of the electrical and mechanical systems. To help reduce the number and severity of falls by patients, always leave the bed in the lowest position when the patient is unattended. When attaching equipment to the frame, ensure it will not impede normal frame operation. For example: hooks on hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, etc. Use only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly which may result in patient or user injury. The Secure II is equipped with a hospital grade plug for protection against shock hazard. It must be plugged directly into a properly grounded three prong receptacle. Grounding reliability can be achieved only when a hospital grade receptacle is used. When using the manual override shaft to manually actuate bed functions, always unplug the bed power cord from the wall socket to avoid injury in the event of a sudden return of power to the bed. When raising the siderails, listen for the ”click” that indicates the siderail has locked in the up position. Pull firmly on the siderail to ensure it is locked into position. Siderails are not intended to be a patient restraint device. It is the responsibility of attending medical personnel to determine the degree of restraint and the siderail positioning to ensure a patient will remain safely in bed. The Bed Exit System is intended only to aid in the detection of a patient exiting the unit. It is NOT intended to replace patient monitoring protocol. The bed exit system signals when a patient is about to exit. Adding or subtracting objects from the frame after zeroing the weigh system may cause a reduction in the sensitivity of the bed exit system. Always unplug the bed power cord from the wall socket and push the battery power on/off switch to the“OFF” position before servicing or cleaning the bed. When working under the bed with the bed in the high position, always place blocks under the litter frame and apply the brakes to prevent injury in case the Bed Down switch is accidently pressed. The CPR emergency release on the Short Bed frame may require assistance to lower the back when the back is in the highest position. Attempting to lower the back in this position without assistance may result in injury to the operator. Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not exceed 300uA. Grounding continuity should be checked periodically.

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Safety Tips and Guidelines WARNING (CONTINUED) • • • •

To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or receptacle. Do not use the optional 110V outlet for life sustaining equipment. To avoid pinching your fingers, place the I.V. pole in the upright position before using the drive handle. When using any mattress and/or mattress overlay that increases the overall height greater than 6” extra caution and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.

To avoid possible injury and to assure proper operation when using a powered mattress replacement system such as XPRT: • Confirm proper scale system operation following mattress installation. For best results, secure the therapy mattress power cord to prevent damage to the cord or interference with the bed frame and the scale system. • Do not zero bed scales or weigh patient with Percussion, Vibration, Rotation or Turn Assist active. Patient motion and position resulting from the dynamic therapy mattress may adversely affect scale system performance. • Do no initialize (“arm”) bed exit with Percussion, Vibration, Rotation or Turn Assist active. The patient motion and position resulting from the dynamic therapy mattress may adversely affect bed exit system performance. • When using an XPRT Therapy Mattress extra caution and/or operator supervision is required to help reduce the likelihood of a patient fall occurring.

CAUTION •

• •

• •

• •

• • • • •

When large spills occur in the area of the circuit boards, 110 volt cables and motors, immediately unplug the bed power cord from the wall socket. Remove the patient from the bed and clean up the fluid. Have maintenance completely check the bed. Fluids can affect the operational capabilities of any electrical product. DO NOT put the bed back into service until it is completely dry and has been thoroughly tested for safe operation. Preventative maintenance should be performed at a minimum of annually to ensure all bed features are functioning properly. Close attention should be given to safety features including, but not limited to safety side latching mechanisms, frayed electrical cords and components, all electrical controls return to off or neutral position when released, caster braking systems, no controls or cabling entangled in bed mechanisms, leakage current 300 μA (microamps) maximum, scale and bed exit systems calibrated properly. Because individual beds may have different options, footboards should not be moved from one bed to another. Mixing footboards could result in unpredictable bed operation. The lockout buttons on the footboard lock the Fowler, Gatch and Bed Up/Down functions and prevent motion of the bed. It is the responsibility of attending medical personnel to determine whether these functions should be locked and to use the buttons accordingly. The weight of the I.V. bags should not exceed 40 pounds. Scale function may be affected by siderail/caster interference. With the litter fully lowered or lowered in Reverse Trendelenburg, the siderails tucked under the litter in the storage position and the casters turned, there is the potential for interference between the siderail and the caster. Raise the siderails when lowering the litter to the full down position to prevent the interference from causing the scale system to weigh inaccurately When attaching equipment to the frame, ensure it will not impede normal operation. For example: hooks on hanging equipment must not actuate control buttons, equipment must not hide the nurse call button, etc. The use of a mattress overlay may reduce the effectiveness of the siderail. I.V. Poles should not be used as a bed push/pull device. The cleanliness and integrity of both ground chains must be maintained to minimize static build up and discharge. Do not add or remove weight when the bed exit system is armed. Zoom and battery backup beds must have their brake set in order for the bed to communicate with the iBed locator. Failure to set brake could result in loss of location information.

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Safety Tips and Guidelines ZOOM® OPTION In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped with the Zoom option.

WARNING • •

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The 3002 Patient Transport Frame is intended for use by trained hospital personnel only. Failure to properly train personnel could result in injury. USE CAUTION while maneuvering the unit with the drive wheel activated. Always ensure there are no obstacles near the unit while the drive wheel is activated. Injury to the patient, user or bystanders or damage to the frame or surrounding equipment could occur if the unit collides with an obstacle. Use caution when transporting the unit down halls, through doors, in and out of elevators, etc. Damage to the siderails or other parts of the unit could occur if the unit comes in contact with walls or door frames. Put the drive wheel in the neutral position and release the brakes before pushing the unit manually. Do not attempt to push the unit manually with the drive wheel engaged. The unit will be difficult to push and injury could result. If unanticipated motion occurs, unplug the power cord from the wall socket, push the battery power on/off switch to the ”OFF” position (the LED will not be illuminated) and actuate the drive wheel pedal to the neutral position. The power save mode is activated after one hour on battery power with no motion release switch activation. Functions including Bed Exit, Scale and Motion will cease to operate when the unit enters the power save mode. Injury to the patient could occur if proper patient monitoring protocol is not observed. Always unplug the power cord and push the battery power on/off switch to the “OFF” position before service or cleaning. When working under the frame, always place blocks under the litter frame to prevent injury in case the Bed Down switch is accidently activated. Due to the weight the battery adds to the bed (approximately 50 pounds), additional force is required to move the bed. Caution should be used when transporting this bed. Additional assistance should be used when necessary. Failure to use caution while transporting this bed may result in injury to the user. Battery posts, terminals and related accessories contain lead and lead compounds, chemicals known to the State of California to cause cancer and birth defects or other reproductive harm. Wash hands after handling. Do not modify the 3002 Patient Transport Frame. Modifying the unit can cause unpredictable operation resulting in injury to the patient or operator. Modifying the unit will also void its warranty.

CAUTION • •

To avoid damage while transporting the bed, verify the I.V. pole is at a low enough height to allow it to safely pass through door openings and under light fixtures. The battery tray assembly weighs 50 pounds. Take care when removing the two hex head screws securing it to the base frame or personal injury could result.

iBED AWARENESS OPTION In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped with the iBed Awareness option.

WARNING •

• •

The optional iBed Awareness system only indicates the siderail position, it does NOT indicate if the siderail is locked. It is the caregiver’s responsibility to ensure that the siderails are locked after every move and also before leaving a patient in the room. The optional iBed Awareness system indicator lights are only an aid to the caregiver, and in no way replace the caregiver’s responsibility of checking on patients. Caregivers should not rely on the lights to perform their duties. Before arming the optional iBed Awareness system, the nurse must physically verify that the siderails are locked.

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Safety Tips and Guidelines iBED AWARENESS OPTION (CONTINUED)

CAUTION • • •

If the optional iBed Awareness system is being used, ensure the bed is in the desirable state (iBed Awareness ON and with the light green) before leaving the room. If the optional iBed Awareness system is being used and the iBed Awareness is alerting, do not turn off iBed Awareness as the display information to troubleshoot the bed will get lost. If the optional iBed Awareness system is being used, use of accessories that cover the center and side alert lights at the footboard are not recommended.

iBED® WIRELESS OPTION In addition to the previous warnings and cautions, all of the following warnings and cautions apply to units equipped with the iBed® Wireless option.

WARNING •

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• • •

•

The optional iBed® Wireless function provides remote information of bedside information to aid the caregiver. In no way does this option replace the caregiver’s responsibility of checking on patients. Caregivers should not rely only on the remote information to perform their duties. The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be remapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the room / location information is changed after initial installation. Line of sight between iBed Locator and the head end of bed must be free of obstruction at all times. Any line of sight interference could impede communication and cause the room / location information not to be available. iBed® Wireless compatible footboard must be used for all iBed® Wireless beds. Some iBed® Wireless functionality will be lost if an older version of the footboard is used. iBed® Wireless functionality shall be verified after installation. Failure to do may result loss of remote information or wrong remote information. At a minimum, verify iBed locator communication with bed in all bed positions, and iBed® Wireless communication with the wireless access point. iBed Locators must be installed more than 71” apart from one another in the same room, such as in a semi-private room with more than one bed. Failure to do so could result in a bed communicating with the other adjacent iBed Locator, thus providing incorrect bed location information.

CAUTION Wireless bed only transmits bed information and not nurse call information. The wireless bed is not intended to replace the existing nurse call system.

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Setup Procedures SETUP PROCEDURES It is important that the Secure II Bed is working properly before it is put into service. The following list will help ensure that each part of the bed is tested. •

Plug the bed into a properly grounded, hospital grade wall receptacle and ensure the ”Power” LED light at the foot end of the bed comes on.

WARNING The Secure II is equipped with a hospital grade plug for protection against shock hazard. It must be plugged directly into a properly grounded three prong receptacle. Grounding reliability can be achieved only when a hospital grade receptacle is used. •

Plug the optional interface cable into the 37 pin connector under the litter frame at the head end of the bed, and into the ”Patient Station”, ”Head Wall”, ”Docker Station”, or equivalent (whichever applies). Test the interface cable to verify it is functioning properly.

WARNING Use only a Stryker supplied interface cable. Use of any other cable may cause the bed to function improperly which may result in patient or user injury. • • •

Ensure the siderails raise, lower and store smoothly and lock in the up position and in the intermediate position when lowered (page 19). Ensure that all four casters lock when the brake pedal is engaged (and 17). Raise the back up to approximately 600. Squeeze the CPR release handle and ensure the back will drop with minimal effort.

NOTE Ensure that the ”Brake Not Set” LED located on the outside of the head end siderails and the footboard control panel (Non-LBS option only) or ”Brake” LED located on the outside of the footboard control panel (LBS option only) come on when the brakes are disengaged. • Run through each function on the footboard control panel to ensure that each function is working properly (page 22). • Run through each function on both head end siderails to ensure that each is working properly (page 19). • Activate the motion stop system to ensure it is functioning properly; press and hold the BED DOWN key. As the bed lowers, lift up on the motion interrupt pan and ensure the downward motion stops. Release the pan and allow the downward motion to continue.

NOTE The bed’s upward motion or other functions are not disrupted by the motion stop system. • If the bed is equipped with the Nurse Call option, verify it is functioning properly prior to patient use.

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Setup Procedures ZOOM® OPTION If your bed is equipped with the Zoom drive wheel option, run through the setup procedures on page 16 and continue with the procedures listed below. •

• • • •

Plug the power cord into a properly grounded, hospital grade wall receptacle. The 12 volt batteries that provide power to the drive wheel and backup power to the unit functions will charge whenever the power cord is plugged into the wall socket. The batteries require approximately 10 hours of charging time before the bed is put into service. Unplug the power cord from the wall socket. Push the battery power switch located on the lower left corner of the head end to the “ON” position. Again, verify each function on the footboard and siderails is operating properly. With the battery power switch in the “ON” position and the brakes engaged, ensure the “Release Brakes”LED on the head end control panel is illuminated. With the battery power switch in the “ON” position and the drive wheel in the neutral position (not touching the floor), ensure the “Engage Drive Wheel” LED on the head end control panel is illuminated. Run through the operation of the drive wheel (page 35) to ensure it is operating properly.

If any problems are found during bed setup, contact Stryker Customer Service at (800) 327−0770.

iBED® WIRELESS OPTION In order for your bed to be capable of receiving a wireless connection the iBed Locator needs to be installed on the wall at the head end of the bed. The iBed Locator communicates with the IR Module installed in your bed. For detailed instructions on mounting the 5212 iBed Locator refer to the instruction sheet (part number 5212-009-101) packaged with your optional 5212 iBed Locator Installation kit. If any problems are found during the iBed Locator Installation, contact Stryker Technical Support at (800) 327−0770.

WARNING The iBed Locator must be correctly associated or mapped to the room / location in order to provide accurate location information. Failure to properly map the iBed Locator to the room / location will yield incorrect remote information. Additionally, if an iBed Locator is to be moved after it has been installed and mapped, it must be re-mapped to the new room / location in which it is moved to. iBed Locator re-mapping will also be required if the room / location information is changed after initial installation.

The wireless connection settings need to be loaded before the device will communicate with the iBed Server application. Reference the iBed Server Installation and Configuration Manual (5212-009-001).

Note iBed® Wireless will not send iBed Locator information unless the brake is set (Battery Backup and Zoom® options only).

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Base Operation Guide BRAKE PEDAL OPERATION WARNING Always apply the caster brakes when a patient is getting on or off the bed. Push on the bed to ensure the brakes are securely locked. Always engage the brakes unless the bed is being moved. Injury could result if the bed moves while a patient is getting on or off the bed.

To activate the brakes, push down once on one of the pedals located at the midpoint of the bed on both sides (identified by the label at right). The pedal will remain in the lowered position, indicating the brakes are engaged. To disengage the brakes, push down once and the pedal will return to the upper position.

NOTE There are LED lights on the outside of the head end siderails and on the foot end control panel that will blink when the brakes are not engaged only if the bed is plugged into a wall socket (page 57 and 23) The brakes will still operate properly when the bed is not plugged in.

STEER PEDAL OPERATION (BEDS WITHOUT THE ZOOM DRIVE WHEEL OPTION) When the bed is moved, the steer caster helps guide the bed along a straight line and helps the bed pivot around corners.

To activate the steer caster, move the pedal located at the head end of the bed to your left as shown on the label.

NOTE For proper ”tracking” of the steer caster, push the bed approximately 10 feet to allow the wheels to face the direction of travel before engaging the steer pedal. If this is not done, proper ”tracking” will not occur and the bed will be difficult to steer.

WARNING Do not attempt to move the foot end of the bed laterally when the steer pedal is activated. When the steer pedal is activated, the steer caster at the foot end of the bed cannot swivel. Attempting to move the bed laterally when the steer pedal is activated may cause injury to the user.

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Litter Operation Guide CPR EMERGENCY RELEASE When quick access to the patient is needed, and the Fowler is raised, squeeze one of the two red release handles and the Fowler can be quickly guided down to a flat position.

NOTE The handle can be released at any time to stop the Fowler from lowering.

FOOT PROP USAGE To prop the foot end of the Knee Gatch up, grasp the end of the Knee Gatch and lift upward, allowing the foot prop (A) to engage at the desired height. To release the prop, swing the prop (A) toward the head end of the bed to disengage the hinge and lower the foot end.

A

WARNING To avoid injury while cleaning or servicing under the foot section, secure the foot section with string or bungee cords or hold it up out of the way.

FRACTURE FRAME USAGE A standard fracture frame can be mounted on the bed using the IV sockets located on all four corners of the bed. I.V. poles can be used in conjunction with a fracture frame if the I.V. pole adaptor sockets are purchased.

FOOT END

WARNING Use only retractable traction or fracture frames. Failure to use a retractable frame may result in injury to the patient and/ or damage to the equipment.

FOLEY BAG HOOKS USAGE The standard Foley bag hooks are found at two locations on both sides of the frame; under the frame below the seat section and at the extreme foot end of the frame. The optional isolated Foley bag hooks are located at the foot end of the bed on top of the lift header. The patient weight reading on the scale system will not be affected when the optional isolated Foley bag hooks are used.

PATIENT RESTRAINT STRAP LOCATIONS The bed has 12 locations for installing patient restraint straps on the litter top, 6 on each side of the bed.

WARNING Improperly adjusted restraint straps can cause serious injury to a patient. The clinician must use her/his judgement to determine proper use of restraint straps and restraint strap locations. Clean Velcro AFTER EACH USE. Saturate Velcro with disinfectant and allow disinfectant to evaporate. (Appropriate disinfectant for nylon Velcro should be determined by the hospital.)

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Litter Operation Guide POSITIONING SIDERAILS NOTE • • •

•

The siderails can be locked at two heights (intermediate & full up). The foot end siderails on a Short Bed do not have an intermediate position. The siderails can slide to the side of the bed when not in use. To remove the rail from the tucked position, grasp the top of the rail and pull outward. To engage the head end siderail, grasp the rail and swing it upward to full height. When the siderail is being raised, it does not lock in the intermediate position. To lower the siderail, push in the yellow release handle (A) and rotate the siderail until it locks in the intermediate position. To lower the siderail fully, push in the yellow release handle (A) again and rotate the siderail until it is completely lowered. To engage the foot end siderail, the same procedure is required as for the head end siderail, however, the siderail swings toward the foot end of the bed.

WARNING Be sure the siderail is locked securely into position. Siderails are not intended to keep patients from exiting the bed. They are designed to keep a patient from inadvertently rolling off the bed. Proper restraint methods should be utilized to ensure the patient remains in the bed. The siderails are not intended to be used as a push device.

To disengage the rail, push in the yellow release handle (A) and swing the rail down to the desired height. Store the siderails slid. A

SIDERAIL CONTROL PANEL LIGHTS The bed is equipped with lights to illuminate the head end siderail control panel and the red nurse call switches. Both can be activated at the footboard control panel. Three settings are available for the control panel lights: low, medium and high intensity. When all lights are off, push the siderail control light button at the footboard once to turn on both the control lights and the nurse call light at the siderail. Push again to change from low to medium setting, and a third time to change to the high setting. The nurse call light intensity is not affected. Pushing the button a fourth time will turn off the siderail control panel lights and pushing it a fifth time will turn off the red nurse call light as well (page 22).

NOTE The purpose of the red nurse call light on the siderails is to ensure the patient immediately knows which button to push to contact the nurse station. Turning the red light off may compromise this ability, especially in a darkened room.

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Litter Operation Guide OPERATING I.V. POLES A

To use the 2-Stage Permanently Attached I.V. pole:

Note C

The 2-stage permanently attached I.V. pole is an option and may have been installed at either the head, foot or both ends. The choice was made at the time the unit was purchased.

1. 2. 3. 4.

Lift and pivot the pole from the storage position and push down until it rests in the receptacle. To raise the height of the pole, pull up on the telescoping portion (A) until it locks into place at its fully raised position. Rotate the I.V. hangers (B) to desired position and hang I.V. bags. To lower the I.V. pole turn the latch (C) clockwise until section (A) lowers.

B

CAUTION The weight of the I.V. bags should not exceed 40 pounds.

WARNING To avoid pinching your fingers, place the I.V. pole in the upright position before using the drive handle.

To use the “Removable” IV pole: 1. 2.

3.

Install the pole at any of the four receptacles on the bed top (located on all four corners of the frame). To raise the height of the pole, turn knob (A) counterclockwise and pull up on the telescoping portion (B) of the pole and raise it to the desired height. Turn knob (A) clockwise to tighten the telescoping portion in place.

CAUTION The weight of the I.V. bags should not exceed 40 pounds.

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Litter Operation Guide NIGHT LIGHT USAGE The bed is equipped with two night lights to illuminate the floor area around the bed. There is a switch under the litter thigh section on the patient’s left side that turns both lights on and off.

NOTE The night lights have a sensor so the lights will turn off, even when the switch is on, if the light in the room is bright enough so a night light is not necessary.

NURSE CALL BACKUP BATTERY (OPTIONAL EQUIPMENT) •

•

To prevent a low battery condition when the bed is not plugged in, position the cord out switch at the head end of the bed to the off position. The switch is identified by the label shown below. If the switch is not positioned as shown below and the bed power cord and pendant cord are unplugged, the life of the backup battery will be significantly reduced. If the power light (located on the footboard) is flashing, the Nurse Call battery needs to be replaced. The battery is located on the patient’s left side at the head end of the bed. No tools are required to replace the battery. Unplug the bed power cord from the wall socket and replace the battery.

USING THE 110 VOLT OUTLET (OPTIONAL EQUIPMENT) • •

The 110V outlet has its own power cord that must be plugged into a properly grounded three prong wall receptacle different from the wall receptacle the bed power cord is plugged into. If the equipment plugged into the bed outlet is not receiving power, check the circuit breakers located on the litter frame under the head section. Reset, if necessary.

WARNING •

• •

Only use equipment with the following electrical specs: 110 VAC; 10A; 60Hz. Maximum total load drawn by equipment used in this receptacle outlet must not exceed 10A. The total system chassis risk current should not exceed 300uA. Grounding continuity should be checked periodically. To avoid risk of electrical shock, unplug all power cords before opening the service compartment, junction box or receptacle. Do not use the optional 110V outlet for life sustaining equipment.

CPR BOARD USAGE (OPTIONAL EQUIPMENT) If the bed is equipped with the optional CPR board, it is stored on the bed’s head board. To remove it, pull it away from the head board and lift it out of storage position. If the CPR board option was not purchased, the head board can also be removed and used as an emergency CPR board.

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