Pegasus Healthcare
Atlas Model 9002 Operating and Product Care Instructions Issue 6 April 2009
Operating and Product Care Instructions
24 Pages
Preview
Page 1
TM
Atlas
(Model 9002)
Operating and Product Care Instructions
LFT16889 Issue 6 April 2009
Contents SECTION
Page No.
ATLAS 9002 Contents... 2 Foreword ... 3 Product Identification ... 4 Important Safety Information... 5 Product Description ... 6-7 Preparing Bedframe For Use... 6 Introduction ... 7 Product Description - Function... 7-17 Familiarisation ... 8 Manual Controls ... 9-11 Programmable Option (Auto-Turn) ... 12 CPR / Reanimation... 12 Manual Turn... 12 Siderails ... 13 Bedframe Operation ... 14 Turning ... 14-16 Emergency Procedures... 16-17
The vertical and horizontal lines printed in the margins adjacent to the text / illustrations in these instructions are for Pegasus Ltd. use only and should be disregarded by the reader. Some of the information contained in these instructions may become outdated, due to improvements made to the product in the future. If you have, any questions regarding these instructions please contact Pegasus Ltd. or their approved dealer. The policy of Pegasus Ltd. is one of continuous development, and therefore Pegasus Ltd. reserves the right to change specifications without notice.
Alarms and Fault Finding ... 18
Pegasus Ltd. strongly advise and warn that only Pegasus Company designated parts, which are designed for the purpose, should be used on equipment and other appliances supplied by Pegasus Ltd., to avoid injuries attributable to the use of inadequate parts.
Cleaning / Infection Control ... 20
Accessories / Options... 19
User Maintenance ... 21-22 Technical Specification ... 23 Contact Information... 24
Unauthorised modifications on any Pegasus Ltd. equipment may affect its safety and are in breach of any warranty on it. Pegasus Ltd. will not be held responsible for any accidents, incidents or lack of performance that occur as a result of any unauthorised modification to it’s product. The Pegasus Company’s condition of sale makes specific provision confirming no liability in such circumstances.
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Foreword All references to the patient in these instructions refer to the person being cared for, and reference to the carer refer to the person who operates the bedframe.
Your PEGASUS ATLAS 9002 is part of a series of quality products designed especially for hospitals. We are dedicated to serving your needs and providing the best products available along with training that will bring your staff maximum benefit from every Pegasus product.
References to left and right of the bedframe are taken from the patient’s perspective. References to left and right for the control panel are taken when facing the control panel.
Please contact us if you have any questions about the operation or maintenance of your Pegasus equipment.
Before using your PEGASUS ATLAS 9002, familiarise yourself with the various parts and controls, please read this manual thoroughly in its entirety before using your PEGASUS ATLAS 9002.
The expected operational life of your PEGASUS ATLAS 9002 bedframe is 10 (ten) years from the date of manufacture, providing the following conditions are adhered to: -
Information in the manual is crucial to the proper operation and maintenance of the equipment, and will help protect your product and ensure that the equipment performs to your satisfaction. Some of the information in this booklet is important for your safety and must be read and understood to help prevent possible injury. If there is anything in the manual that is confusing or difficult to understand, please call Pegasus Ltd or their appointed distributor (the telephone number appears on the last page of this manual).
Conditions
• The bedframe is cared for and serviced in accordance with recommended, published “Operating and Product Care Instructions” (LFT16889) and the “Service Procedure” (LFT16954).
• The guidelines for product care, must begin on first use of the bedframe by the customer.
Symbols used adjacent to the text in these instructions: -
• The equipment is used for its intended purpose only and is operated within the published limitations.
Danger: Means:- electrical hazard warning, failure to understand and obey this warning may result in electrical shock.
• Only Pegasus designated spare parts should be used, as published in “Spare Parts” manual (LFT16950).
Warning: Means:- failure to understand and obey this warning may result in injury to you or to others.
The expected life for consumable products, such as batteries and fuses is dependent upon the care and usage of the equipment concerned.
Caution: Means:- failure to follow these instructions may cause damage to all or parts of the system or equipment. Note: Means:- this is important information for the correct use of this system or equipment. This product has been designed and manufactured to provide you with trouble free use, however, this product does contain components that with regular use are subject to wear.
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Product Identification When making contact with Pegasus Customer Service always have the following information to hand:
•
The correct Name or Model number.
•
The Serial Number of the Product.
Both can be found on the identification label. IDENTIFICATION LABEL: The label detailing the model and serial number is located on the PEGASUS ATLAS 9002 bedframe at the head end, to the centre (from the patient’s perspective) of the top frame assembly.
References to left and right of the bedframe in these instructions are as viewed from the patient’s perspective when lying on their back. Pegasus contact details are located on the rear of this manual.
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Important Safety Information PLEASE READ THIS SECTION PRIOR TO USING ANY PEGASUS SUPPLIED PRODUCT. The PEGASUS ATLAS 9002 bedframe must be used in accordance with these ‘Operating and Product Care Instructions’ (LFT16889).
WARNINGS: Only personnel trained or formally approved by Pegasus in operation and maintenance of Pegasus bedframes may perform maintenance; modification or repair work on any Pegasus supplied product. Unqualified personnel attempting to work on Pegasus bedframes risk serious injury to themselves and others, and possibly death by electrocution. When operating the bedframe functions ensure there is sufficient clearance (approximately 190mm) to prevent contact with walls, equipment etc. During any operation involving bedframe section movement, ensure that both patient and attending staff are positioned so as to avoid entrapment. Ensure the mains (power supply) cable is not trapped or twisted and is routed suitably to avoid crushing or entrapment when connected to the PEGASUS ATLAS 9002 bedframe. Do not place any objects or accessories on the bedframe base assembly as damage may occur during normal operation. All siderails and accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security. For patient safety, siderails should be fitted and raised when manoeuvring the bedframe. In accordance with MHRA guidelines, there must be a minimum of 220mm clearance between the top of the siderail and the uncompressed mattress / overlay combination top surface. When moving the bedframe ensure the mains (power supply) cable is disconnected from the mains outlet socket and suitably stowed to avoid any damage whilst moving the PEGASUS ATLAS 9002 bedframe. Ensure there is sufficient clearance to allow free movement of the mattress platform in all modes of operation with any required accessories fitted. Make sure all patient connected items, ventilator tubes, IV sets and catheter tubes have adequate length to accommodate intended movement of the bedframe. Only move the PEGASUS ATLAS 9002 bedframe when in the horizontal and level position. Ensure that a suitable number of staff are available to control the bedframe particularly on inclines or when transporting patients. Do not move the PEGASUS ATLAS 9002 on an incline greater than 10°.
CAUTIONS: Materials and procedures used for cleaning may be subject to local health and safety regulations (e.g. OSHA / COSHH Regulations) - these ‘Operating and Product Care Instructions’ (LFT16889) must be followed at all times. If spares are required only recommended Pegasus spare parts must be used (most of these spare parts will be found in the ‘Spare Parts List’ manual [LFT16950]). The fitting of spares not supplied or recommended by Pegasus, may invalidate any warranties, alter functionality and specification. Any unauthorised modifications on any Pegasus bedframes may affect its safety and are in breach of any warranties. Pegasus will not be held responsible for any accidents, incidents or lack of performance that occur as a result of any unauthorised modification to it’s product. It is not recommended that the mains supply connection is made via multiple portable socket outlets. Where it is essential to the layout of the facility that a multiple portable socket outlet is required. This should not be laid on the floor or other location where it may become wet, cause a trip hazard or be crushed by the PEGASUS ATLAS 9002 bedframe. When connecting equipment after transportation or storage, inspect the mains (power supply) cable visually for any signs of damage. If evident, do not use equipment and contact Pegasus or local qualified electrician for repair. Pegasus systems are designed to comply with all relevant electrical safety, manufacturing and performance standards published by UL, IS0, IEE & BSI.
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Product Description PREPARING BEDFRAME FOR USE: Do not overload the PEGASUS ATLAS 9002 bedframe beyond the approved safe working load of 216kg (including patient, mattress, bedding, and all accessories mounted to the bedframe). Plug the bedframe into a suitable electrical outlet. The bedframe is to be run using mains supply to ensure the Battery Back-up is maintained at full charge. The Battery Back-up is for emergency or transport use only. It will give a minimum of 10 full movements (raise and lower) of the electrical functions. Running the bedframe on partially charged batteries may cause the system to fail. The maximum period of Actuator motor operation is 2 minutes in each 20 minutes. Prior to proceeding with bedframe operation, operators should familiarise themselves with the location and function of the controls detailed in the Product Description / Function Section of these instructions. During Trendelenburg and Reverse Trendelenburg operations, the tilting movement of the mattress platform will also tilt the foot panels. Ensure there is sufficient clearance to prevent contact with walls, equipment, siderails, accessories etc. During any operation involving bedframe section movement, ensure that both patient and attending staff are positioned so as to avoid entrapment. Ensure there is sufficient clearance to allow free movement of the mattress platform in all modes of operation with any required accessories fitted. Ensure any patient connected items, ventilator tubes, IV giving sets and catheter tubes have adequate length to accommodate intended movement of the bedframe. Do not disconnect the bedframe from the mains supply even when not in use.
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Product Description INTRODUCTION: ™
PEGASUS ATLAS
Tilt and Turn Bedframe (Model 9002)
Figure 1
™
The PEGASUS ATLAS 9002 tilt and turn frame offers carers and users the ultimate in assistance for the repositioning and management of immobile or heavy patients in a care environment. Developed in conjunction with leading multi-disciplinary professionals, the frame can help reduce the incidence of back injury associated with manual handling. Key System Components: 1. Control Panel Assembly. 2. Mattress (supplied with spare waterproof cover SCM18218). 3. Brake System. 4. CPR (located under bedframe). 5. Siderails (not shown).
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Product Description - Functions FAMILIARISATION: Prior to operating the bedframe with a patient on board, operators should familiarise themselves with the location and function of the controls detailed below. Bedframe Movement There are horseshoe shaped levers on both foot end Castors; each lever has three positions: The levers are linked so that when either lever position is changed the other lever will move to the same position. STEER FREE BRAKE
STEER FREE BRAKE
STEER FREE BRAKE
Brake: With the lever in the down position, three Castors are locked against rotation and sideways movement. Free: All Castors are free to rotate and move in any direction.
Steer: The left-hand head end Castor is fixed in the dead-ahead position; all other Castors are free to move in any direction.
Prepare the bedframe for operation 1. Place the bedframe at the position required, ensure the Castors are in the brake position, the bedframe is horizontal and then plug the bedframe into a suitable electrical outlet. 2. Plug the Remote Control Handset (if supplied) into the Remote Control Socket at the side of the Control Box. If Remote Control Handset is not supplied, fit the blue Anti-static Cap into the Remote Socket.
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Product Description - Functions MANUAL CONTROLS: Control Panel Functions
Figure 2 1. CPR /Reanimation Button. 2. Mains Power Indicator. 3. Reverse Trendelenburg Button. 4. Trendelenburg Button. 5. Bedframe Raise / Lower and Trendelenburg / Reverse Trendelenburg Lockout Switch. 6. Bedframe Height Raise Button. 7. Bedframe Height Lower Button. 8. Turn Right Button and Interlock Indicator. 9. Turn Left Button and Interlock Indicator. 10. Turn Lockout Switch. 11. Backrest Raise Button. 12. Backrest Lower Button and Interlock Indicator. 13. Backrest Lockout Switch (locked and unlocked with a key).
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Product Description - Functions Bedframe Height Raise / Lower
Backrest Raise / Lower
Press and hold the appropriate button to raise or lower the bedframe. Movement stops when the button is released or when upper limit (815mm) or lower limit (595mm) is reached.
Press and hold the appropriate button to raise or lower Backrest. The Backrest stops when the limit is reached (65°); the Backrest is lowered to its lowest setting or when the button is released.
Trendelenburg Trendelenburg
/
If the bedframe is not level the Backrest will not raise, and one of the small amber LED’s next to the Manual-Turn buttons will illuminate. This advises the carer which function must be operated to return the bedframe to the level position. The LED’s go out when the button is released.
Reverse
Press and hold the appropriate button to achieve Trendelenburg or Reverse Trendelenburg position. This function stops when the limit is reached or when the button is released. The maximum angle of incline – Trendelenburg 12º, Reverse Trendelenburg 12º.
Mains Power Indicator When the bedframe is connected to the mains supply, the green LED will be illuminated. When removed from the power supply the LED is extinguished and the Battery Backup system will be available (No visual indication is present for battery operation as this is for emergency use only).
Manual-Turn Left / Right Press and hold the appropriate button to turn the patient onto right or left-hand side. The Manual-Turn function stops when the button is released or the limit is reached (45°). The Manual-Turn utility does not function if the Backrest is raised or if the Turn Lockout Switch is in the locked position. When the Backrest is raised, pressing either Turn button will illuminate the small amber LED located in the Backrest lower button. This indicates that the Backrest must be lowered to its lowest position before the ManualTurn function will operate. When turning the bedframe all Siderails and Accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security.
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The Battery Back-up will only provide sufficient power for 10 complete operations. CPR / Reanimation Press and hold the CPR / Reanimation button to move the bedframe into the CPR / Reanimation position. The bedframe will level and go to maximum height. This is the secondary method of achieving the CPR / Reanimation position, for the primary method (see page 16).
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Product Description - Functions Lockout Switches
Remote Control Handset (optional accessory)
All bedframe movement functions can be locked via the Control Panel. The functions are locked by turning the Lockout Switches 45° anticlockwise and can be unlocked by turning the Switches 45° clockwise.
The Remote Control Handset has function pushbuttons to correspond with the same pushbuttons on the main control panel: (see figure 3). 1. 2. 3. 4.
The Lockout Switch for the Backrest raise / lower function, is operated with a Key Switch for additional safety. The Key is turned in the same (45°) directions as above.
Bedframe Height Raise / Lower. Reverse Trendelenburg / Trendelenburg. Manual-Turn Left / Right. Backrest Raise / Lower.
Turn Indicator When using the Manual-Turn buttons, use the Spirit Level (Turn) Indicator (left), to obtain the required position. To level the bedframe press the appropriate Turn button. When the bedframe approaches the level position a green LED, next to the Spirit Level Indicator will illuminate. Remove finger from Turn button immediately if you wish to raise the Backrest. Should the bedframe have the Backrest raised when shutdown occurs, lower the Backrest as detailed in ‘Emergency Procedures: CPR/Reanimation’ section (see page 16).
Figure 3 The position and setting of the Lockout Switches apply to the Remote Control Handset as well as the main Control Box. Hence, any functions lockedout on the Control Panel will also be locked-out on the Handset.
Should the bedframe be in a turned position when shutdown occurs (Battery Back-up exhausted), return to the level position as detailed on page 17 ‘Manual (override) Turn: no power available’. The bedframe cannot be manually moved from the Trendelenburg or Reverse Trendelenburg (tilt) positions. In the event of total shut down.
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Product Description - Functions When the programme is running the decimal point in the corner of the displays will illuminate in turn, in a clockwise movement through each of the displays.
Auto-Turn Option
The programme can be stopped at any time by pressing the Stop Turn button. When the button is pressed 3 ‘beeps’ will be heard and 1 minute later the display will switch off.
CPR/Reanimation: Cardio Pulmonary Resuscitation is an emergency procedure performed on a patient who is having a cardiac arrest. The primary method of operation is by using the CPR/Reanimation handles at either side of the bedframe see figure 10. The secondary method of achieving the CPR/Reanimation position is by using the pushbutton on the control panel (see figure 11 on page 16). Manual (Override) Turn The bedframe is equipped with a Manual (override) Turn operation. This function levels the bedframe in the event of total power failure (both loss of mains and battery power), further details are explained on page 17.
Figure 4 If fitted, the programmable option (Auto-Turn) Front Panel allows the carer to pre-programme the bedframe to perform specific set movements over a period of time. The left and right limits of movements are set using the ‘up’ and ‘down’ arrow buttons below the appropriate indicator. Maximum 45° - Minimum 0°. The angle of movement for each time the bedframe moves is set using the ‘minus’ and ‘plus’ buttons below the indicator for degrees per move. In incremental steps of 5°, 10°, 15° and 20°. The time interval between moves is set using the ‘minus’ and ‘plus’ buttons below the indicator for minutes between moves. In incremental steps of 15, 30, 45, 60, 75 and 90 minutes. Once the specific parameters have been set, pressing the Start Turn button will allow the bedframe to begin its programmed movement. The Control Panel will bleep 3 times, and the bedframe will start to turn.
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Product Description - Functions SIDERAILS: Each Siderail fits into two Removable Brackets fitted on each side of the bedframe (mattress platform). Two Knob operated Locking Pins on each of the Brackets allow raising and lowering of the Siderails and tilting of the Siderails outwards to a maximum of 20° for patient security when the bedframe is turned. All Siderails and Accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security. For patient safety Siderails should be fitted when maneuvering the bedframe. Raising and Lowering When the Siderail is in the lowered position do not attempt to tilt them.
Figure 6
Figure 5 Tilting The Siderails can only be tilted when they are raised (see figure 6).
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Product Description - Functions BEDFRAME OPERATION: Setting Up
Sitting the Patient up in the Bedframe
Prior to proceeding with bedframe operation, operators should familiarise themselves with the location and function of the controls detailed in the appropriate sections of this manual. 1.
2.
Prior to raising the Backrest, ensure the bedframe level indicator reads 0° by operating the respective Turn button and ensure that the green level LED illuminates prior to pressing the Backrest raise button.
Place the bedframe at the position required, ensure that the wheels are in the full lock position and the bedframe is horizontal. Ensure there is sufficient clearance to allow free movement of the mattress platform in all modes of operation with any required accessories fitted.
3.
Ensure any patient connected items such as ventilator tubes, IV tubes and catheter tubes, have adequate length to accommodate intended movement of the bedframe.
4.
Plug the bedframe into a suitable electrical outlet.
1.
Raise the patient to the desired position by pressing the Backrest raise button.
2.
If the Backrest does not raise, check the Backrest Lockout Switch position.
3.
If the bedframe is not level the Backrest will not raise and one of the small amber LED’s next to the left and right Turn buttons will be illuminated. This advises which function must be operated to return the bedframe to the level position. The LED’s go out when the button is released.
TURNING:
5.
Power Available
Plug the Remote Control Handset (if supplied) into the Remote Control Socket at the side of the Control Box.
When turning an obese patient, care must be exercised to prevent the patient’s abdomen from putting weight against the Siderails. In these circumstances, it is advisable to limit the logroll turn to less than 45°.
The bedframe is only to be run using mains supply to ensure the Battery Backup is maintained at full charge. The Battery Back-up is for emergency use only.
6.
1.
Ensure the patient is positioned down the centre of the bedframe.
Do not disconnect the bedframe from the mains supply even when not in use.
2.
Place pillows beneath the patient’s calves to raise their heels clear of the bedframe surface.
Running the bedframe on partially charged batteries may cause the system to fail.
3.
Place a second pillow between the patient’s thighs / knees.
4.
To reduce sliding and shear in patients it may be useful to place a pillow along the patient’s side from the armpit to the hip.
5.
If turn is to be greater than 30°, place the Siderails in the full 20° tilted position (this is not necessary if the turn is to be 30° or less).
Prepare bedframe to receive patient, lower the bedframe to its lowest position, or if patient is mobile, to a comfortable height, then lower the appropriate Siderail for patient access.
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Product Description - Functions 6.
Advise the patient of the proposed bedframe movement to lessen the patients apprehension.
When the bedframe is first powered up, only the decimal points on the Auto-Turn panel will be illuminated.
7.
For Manual-Turn, operate the left and right Turn buttons as necessary to turn the patient to the required position.
To turn on the programmable option press any key on the Front Panel and the display will illuminate.
8.
When manual turning, use the Spirit Level Indicator (see figure 7, below), to ensure required position is attained.
Use the controls to set the parameters required – left and right Turn limits, ‘Degrees Per Move’ and ‘Minutes Between Moves’. When these are set, press the Start Turn button. If the bedframe is not already level, it will go to the level position. Once the bedframe is level it will perform the first programmed movement. The decimal points will rotate around the displays in a clockwise direction, showing that the programme has been set and is running. After one minute the displays will become dim (although will remain readable). If an alarm sounds 5 times whilst the Start Turn button is pressed. Check to see if the small amber LED on the Backrest lower button is illuminated. If this is illuminated, the Backrest is not fully down and the Programmable Turn will not function. In addition, the decimal points will not be illuminated. Lower the Backrest fully down and press the Start Turn button again to commence the programmed turn.
Figure 7 Auto-Turn Option
There are 3 pre set programmes built in to the bedframe. These are selected by pressing the ‘Prog’ button. Each time the ‘Prog’ button is pressed the parameters of the next pre set programme will be displayed. To select one of these pre set programmes press the Start Turn button when the selected pre set programme is displayed.
LEFT TURN LIMIT
RIGHT TURN LIMIT
DEGREES PER MOVE
MINUTES BETWEEN MOVES
1 2 3
5 25 45
5 25 45
5 10 20
15 45 15
30 seconds before a move, that has been programmed, is due to commence the minutes between moves display will flash. After the move is completed, the display will revert to the dim setting.
Figure 8
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PROG.
The parameters of each pre set programme are as shown below.
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Product Description - Functions If any button is pressed on the programmable option Front Panel, whilst the programme is running 5 bleeps will occur to indicate to the carer that a programme is already running. The only exception is the Stop Turn button when the bedframe movement will cease, but there will be no alarm. If a button is pressed on the manual control front panel, the programmed movement will cease and there will be a continuous audible alarm until the alarm cancel button (see figure 9, below) is pressed.
Figure 10 1.
Depress either of the CPR Handles either side of the bedframe to attain the CPR/Reanimation position as shown in figure 10. Hold in CPR Handles in position until the bedframe movement stops. This will automatically move the bedframe to a level position at the maximum height.
2.
On completion, replace the Retaining Strap over the CPR Handle.
3.
Releasing the CPR Handle will cause the bedframe movement to halt in it’s current position.
Figure 9 In the event of a power failure with a programmed Turn option is running, there will be a continuous audible alarm and the programme will cease. The alarm can be silenced using the alarm cancel button. The manual controls will continue to work utilising the Battery Back-up for a minimum of 10 operations. EMERGENCY PROCEDURES:
CPR/Reanimation:
Secondary operation
Cardio Pulmonary Resuscitation is an emergency procedure performed on a patient who is having a cardiac arrest.
method
of
CPR/Reanimation
The primary method of operation is by using the CPR/Reanimation Handles at either side of the bedframe (see figure 10). The secondary method of achieving the CPR / Reanimation position is by using the pushbutton on the Control Panel (see figure 11). Figure 11 Primary operation
method
of
CPR/Reanimation Press and hold to move the bedframe to the CPR/Reanimation position i.e. the bedframe is level and at it’s maximum height. If the programmed option is running it will instantly cease and the alarm will sound continuously. The alarm can be silenced with the alarm cancel button (figure 9).
If raised, the Backrest can drop sharply. Ensure nothing can get trapped under the Backrest. A Retaining Strap is fitted over each CPR/Reanimation Handle. Slide the strap off the CPR Handle before operation.
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Product Description - Functions 4.
MANUAL (OVERRIDE) TURN: No Power Available
Reconnect the bedframes main power cable into the electrical outlet for normal operation.
The Manual (override) Turn must only be used when the mains supply and battery power have failed. The Crank Handle is stowed under the right-hand side of the bedframe (mattress platform).
Figure 12 1.
Push the Knob to disengage Drive Motor.
2.
Fit Crank Handle into Manual (override) Turn Drive, ensuring that it is fully engaged.
3.
Turn the Crank Handle until bedframe is in position required, then remove Crank Handle. Do not turn bedframe beyond the 45° maximum angle as mechanical damage to the bedframe can occur.
To return to normal operation: 1.
Insert the Crank Handle.
2.
Pull the Knob to engage the Drive Motor (the Crank Handle may have to be turned slightly to enable the Knob to pull out fully, allowing the gears to mesh correctly).
3.
Remove the Crank Handle and replace in its stowage position (see note above). Do not leave the Crank Handle engaged while the bedframe is in normal operating mode.
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Alarms and Fault Finding Alarms An alarm may sound from the Actuator Control Box positioned at the left-hand side of the bedframe base or the Auto-Turn Panel (if fitted). Fault Finding SYMPTOM
ACTION
The power light is not Check mains supply is present. present on the Control Check the bedframe is plugged into the mains supply. Check the mains plug Fuse. Box. Check green LED is illuminated on the Actuator Control Box. The bedframe does Check that the Backrest is not raised and the Turn Interlock Switch is closed. Check the Turn Lockout Switch is set to the unlocked position. not Turn left or right. Check Cable Connectors for security. The Backrest does not Check to see if the small amber LED’s illuminate, when pressing the Backrest raise button in either right or left Turn button (indicating that the bedframe is not raise. level). If either LED is illuminated, press the corresponding Turn button until bedframe is level (the green LED next to Spirit Level Indicator illuminates when bedframe is level). Check that the Backrest Lockout Switch is in the unlocked position. Alarms sound when Stop any bedframe operations. any button is pressed. Reconnect the bedframe to the mains supply (when the supply is connected, the Alarms sound batteries will re-charge automatically). Normal operation can now be resumed. continuously Auto-Turn will only function with mains power supply connected. Auto-Turn Option Fitted The bedframe will not If the Backrest is raised check the LED backrest lower button – if the LED is Auto-Turn and alarm illuminated press Backrest lower button. sounds 5 times. An audible alarm can Press the alarm cancel button to cancel alarming. Then remove power from be heard and all bedframe for 10 seconds and reconnect. displays are lit. Mains failure whilst Restore power to the bedframe. If desired restart Auto-Turn program. Auto-Turn program running.
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Accessories / Options Description
Part number
Additional Waterproof Mattress Cover Replacement Mattress Headboard Footboard (standard size) Footboard (extended height) Telescopic Siderails (including Brackets to fit) Skull Traction (excluding Weights) Lower Limb Traction IV Pole (double hook, height adjustable) Remote Control Handset Arm Rest
SCM18218 SA9090 SA9000 SA9001 SA9071 SA9006 SA9085 SA9004 SA9052 SA9011 SA9012
Other Accessories may be available on request.
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Infection Control and Cleaning Infection Control Infection control and cleaning must be carried out in accordance with your local Infection Control Policy. Cleaning Guidelines Ensure the system is disconnected from the mains electricity supply before cleaning. Do not immerse the Remote Control Handset in water.
Figure 13 Mattress Care Turn the mattress head to foot between patients or monthly, whichever is more frequent.
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