Pegasus Healthcare
Atlas Model 9002 Operating and Product Care Instructions Issue 3 Sept 2004
Operating and Product Care Instructions
24 Pages
Preview
Page 1
Atlas
TM
(Model 9002)
Operating and Product Care Instructions
LFT16889 Issue 3 September 2004
Contents SECTION
Page No.
ATLAS 9002 Contents ... 2 Forward ... 3 General Information... 4 Important Safety Information ... 5 Preparing Bedframe For Use ... 6 Product Description / Function ... 7-13 Introduction ... 7 Familiarisation ... 8 Manual Controls ... 9-11 Remote Control ... 11 Programmable Option ... 12 CPR / Reanimation... 12 Manual Turn... 12 Side Rails ... 13
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 Some of the information contained in these instructions may become outdated, due to improvements made to the product in the future.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.
Setting Up / Operation ... 14-17 Bedframe Operation ... 14 Turning ... 14-16 Emergency Procedures... 16-17
The policy of Pegasus Ltd. is one of continuous development, and therefore Pegasus Ltd. reserves the right to change specifications without notice. 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.
Alarms and Fault Finding ... 18 Cleaning / Infection Control ... 19
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 un-authorised modification to it’s product.
Accessories ... 20 Technical Specification ... 21
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.
Thank you for purchasing Pegasus equipment Your PEGASUS ATLAS 9002 is part of a series of quality products designed especially for hospitals.
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.
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.
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.
Please contact us if you have any questions about the operation or maintenance of your Pegasus equipment.
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).
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: Conditions
• The bedframe is cared for and serviced in accordance with recommended, published “Operating and Product Care Instructions” (LFT16889) the “Preventive Maintenance Schedule” (LFT16953) and the “Service Procedure” (LFT16954).
Symbols used adjacent to the text in these instructions: Danger: Means:- electrical hazard warning, failure to understand and obey this warning may result in electrical shock
• The guidelines for product care, must begin on first use of the bedframe by the customer.
• The equipment is used for its intended purpose only and is operated within the published limitations.
Warning: Means:- failure to understand and obey this warning may result in injury to you or to others.
• Only Pegasus designated spare parts should be used, as published in “Spare Parts” manual (LFT16950).
Caution: Means:- failure to follow these instructions may cause damage to all or parts of the system or equipment.
The expected life for consumable products, such as batteries and fuses is dependent upon the care and usage of the equipment concerned.
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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General Information 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 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 patients 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 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 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 any trailing mains (power supply) cable’s are not trapped, twisted and are routed suitably to avoid crushing or entrapment when connected to the Atlas 9002 bedframe. All side rails and accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security. For patient safety, side rails should be fitted when manoeuvring 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 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 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 Atlas 9002 on an incline greater than 10%.
CAUTIONS: Materials used for cleaning procedures may be subject to localised health and safety regulations (e.g. OSHA / COSHH Regulations) - the ‘Operating and Product Care Instructions’ (LFT16889) must be followed at all times. Materials / parts used for maintenance and repair may be subject to any local regulations – the ‘Spare Parts‘ manual (LFT16950) must be used to order any required replacement parts. If spares are required only recommended Pegasus spare parts must be used (most of these spare parts will be found in the ‘Spare Parts’ manual). 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 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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Preparing the 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, side rails, 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 and Function 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 Box 2. Mattress 3. Brake System 4. CPR (located under bedframe) 5. Side Rails (not shown)
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Product Description and Function 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 wheels; 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. S TE E R FREE BRAKE
S TE ER F RE E B RAK E
S TE ER F RE E B RA K E
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 wheels are in the brake position, the bedframe is horizontal and then plug the bedframe into a suitable electrical outlet. 2. Plug the remote control (if supplied) into the remote control socket at the side of the control box. If remote is not supplied, fit the blue antistatic cap into the remote socket.
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Product Description and Function 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 and Function 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. 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.
Trendelenburg Trendelenburg
/
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 back-up system will be available (No visual indication is present for battery operation as this is for emergency use only). The battery back-up will only provide sufficient power for 10 complete operations.
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 manual ‘Turn’ function will operate. When turning the bedframe all side rails and accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security.
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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 and Function 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 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 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 as well as the main control box. Hence, any functions locked-out 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 and Function 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.
Programmable 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 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 and Function SIDE RAILS: Each side rail 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 side rails and tilting of the side rails outwards to a maximum of 20° for patient security when the bedframe is turned. All side rails and accessories must be securely fixed to the bedframe. For patients safety, these must be checked regularly for security. For patient safety side rails should be fitted when maneuvering the bedframe. Raising and Lowering When the side rail is in the lowered position do not attempt to tilt them.
Figure 6
Figure 5 Tilting The side rails can only be tilted when they are raised (see figure 6).
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Setting Up / Operation 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.
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.
5.
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. 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: Power Available
Plug the remote control (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 side rails. In these circumstances, it is advisable to limit the log-roll 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.
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 side rails 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 side rail for patient access.
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Setting Up / Operation 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 Programmable 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 10
15 45 45
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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Setting Up / Operation 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 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: Cardio Pulmonary Resuscitation is an emergency procedure performed on a patient who is having a cardiac arrest.
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.
Secondary operation
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). Primary operation
method
of
CPR/Reanimation
Figure 11 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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Setting Up / Operation 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 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 TABLE 1 SYMPTOM
ACTION
The power light is not Check the bedframe is plugged into the mains supply. present on the control Check the mains plug fuse. box. The bedframe does Check that the backrest is not raised. not ‘Turn’ left or Check the ‘Turn’ lockout switch position. right. The backrest does not Check to see if the interlock LED’s illuminate in either right or left ‘Turn’ raise. button (indicating that the bedframe is not 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. Programmable Option Fitted The bedframe will not This signifies the Auto ‘Turn’ is already selected – no action is required. Auto ‘Turn’ and alarm If the backrest is raised check the LED backrest lower button – if the LED is sounds 5 times. illuminated press backrest lower button. 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. A continuous audible Refer to ‘Service Procedure’ Manual (LFT16954) for further details. alarm is present. TABLE 2 These alarms only relate to the actuator back-up batteries. Should these batteries fail, the bedframe cannot be operated. SYMPTOM ACTION Alarms sound when Stop any bedframe operations. any button is pressed. Alarms sound Reconnect the bedframe to the mains supply (when the supply is connected, the batteries will re-charge automatically). Normal operation can now be resumed. continuously
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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 in water.
Figure 13 Mattress Care Turn the mattress head to foot between patients or monthly, whichever is more frequent.
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Accessories ACCESSORIES: Item Number 1 2 3 4 5 6 7 8
Description
Part number
Additional Waterproof Mattress Cover Headboard Footboard Skull Traction (excluding weights) IV Rod (double hook, height adjustable) Patient’s Mirror Remote Control Balkan Beam
MAT13495 SA9000 SA9001 SA9005 SA9002 SA9057 SA9059 SA9059
Other accessories may be available on request.
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