User Manual - Mobility Hire
Contents
1. When moving the patient to a sitting or more upright position the pressure may need to be increased to provide added support and to avoid bottoming out A It is important to return to the original pressure setting when the patient returns to the supine position A Wait a minimum of 12 minutes between pressure adjustment and patient assessment it may take a full cycle for the system to adjust CPR Function Rapid deflation of the mattress may be required for emergency treatment or system deflation Firmly pull the release CPR tag from the side of the mattress to rapidly deflate the entire system To re inflate the system after the CPR tag has been pulled replace the CPR tag ensuring all sealing connectors are firmly attached see image opposite and restart the control unit Wait for the mattress system to reach optimal pressure Aa bottoming out test must be performed after mattress inflation following rapid deflation A Re inflation settings could be different to setting prior to deflation Ensure correct pressure setting is selected 10 OPERATION To gain access to the sealing connectors unzip the top cover past the CPR tag Use of Incontinence Products Incontinence products such as sheets or pads can be used with this system However product performance is likely to reduce due to the patient experiencing less pressure relief when using these aids If incontinence products are to be used it2. C Alarm Mute Button Silences the audible alarm The audible alarm will resume after 20 minutes if cause of failure is unresolved The audible alarm also sounds when the power is switched off press alarm mute to silence D A S Button Selecting alternating mode cyclically inflates and deflates the cells in sequence Selecting static mode fully inflates all cells with no dynamic alternation Static mode will automatically revert to alternation mode after 1 hour for patient safety E Pressure Buttons Press to increase or decrease the pressure setting There are 8 available pressure settings from soft to firm 18mmHg to 60mmHg 6mmbg per step The green LED s illuminate to indicate which of the 8 settings is operational W m F Max Button Pressing the max button facilitates rapid inflation to the maximum pressure setting 6OmmHg the orange static LED will illuminate After 20 minutes the system automatically reverts back to the previous pressure setting for patient safety If this function requires cancellation prior to the system automatically switching back to the previous setting either the max or A S buttons can be pressed G Control Unit Lock Unlock Button Pressing for at least 2 seconds locks the control unit settings an audible tone sounds and an amber LED illuminates to indicate the system is locked When locked only the alarm mute
3. is recommended that regular patient skin checks are performed to ensure skin integrity is maintained 11 Release the first press stud between the side former and the side of the base cover Reattach the press stud after the connectors are re sealed Push together keeping both halves parallel to each other Static Mode Patients should always be nursed on the mattress in alternating mode but the static mode maybe selected for short intervals if a patient is finding it difficult to tolerate the alternating mode This could occur if for example the patient is in pain nauseated or perhaps having difficulty in getting off to sleep When static is selected all cells inflate at the pressure at which the mattress is set thereby offering anon moving surface The digital control system will return to alternating mode after one hour if not manually selected by the user This is a safety mechanism to ensure patients are not left on a constantly inflated surface It should be used only after assessing the risk to the patient s skin To select static mode depress the A S button the static LED will illuminate The pressure canbe adjusted to suit using the pressure adjustment functions on the front of the control unit OPERATION System Removal 1 Turn off the control unit by pressing the power button for at least 2 seconds and unplug the mains cable 2 Remove the air connection handle from the contro
4. all four sealing connectors are firmly fitted to the control unit and the air hoses Check the CPR tag is attached and both sealing connectors are firmly secure Check all air hoses along the inside of the mattress each should be firmly connected Check each air cell is securely attached to its connecting air pipe 4 Check all cells pipes and hoses for any air leakage 5 Switch on power 13 TROUBLESHOOTING Alarm Fault Alarm LED audible alarm Cause Pressure too high Solution Reset the alarm turn off power and press the alarm mute button Disconnect the air hoses to reduce pressure reconnect when pressure has decreased Check for twists in the air hoses between mattress and control unit Switch on power Alarm LED Alternating Reset the alarm turn off power and press the ee mode failure no alarm mute button alternation Disconnect the air hoses to reduce pressure audible alarm reconnect when pressure has decreased Switch on power Alarm LED Power down Press the alarm mute button to silence the audible audible alarm alarm Check the mains cable is firmly plugged into a wall socket and the control unit Check the mains power is switched on to ensure socket is working plug in a lamp or other fused electrical device Check the mains plug fuse 8A then check the control unit fuse 1A see section Maintenance A Do not try to open the control unit Openin
5. inspections If there are any signs of damage or the system is not performing as it should withdraw it from service until the system has been repaired and is fit for use again Air Filter Replacement See service manual for control unit air filter maintenance and replacement A Good filter maintenance is critical to maintain an optimal operating system Failure to keep the filters clean will result in system downtime and increase repair costs It is recommended that the air filter be replaced annually Replacement air filters are available please see contact information on rear cover Fuse Replacement Control Unit Ale 16 Switch off the power supply to the control unit Remove the mains cable from the control unit Insert a small flat head screwdriver into the groove in the fuse holder and turn anti clockwise quarter turn Remove the used fuse from the fuse holder clip and discard Insert a new fuse into the fuse holder clip Push fuse holder into the control unit against the force of the spring and turn clockwise with the screwdriver quarter turn TECHNICAL SPECIFICATION Control System Cycle Time Supply Voltage Fuse Rating Power Rating Standards No of Cells Cell Height Alternating therapy Maximum patient weight Mattress Replacement Dimensions Control Unit Dimensions Cell material Base material Cover material Hose Connection Emergency CPR Mode of Operation Operating S
6. lasting and reliable service Please ensure that you understand all the instructions if you have any questions concerning the operation and maintenance of the mattress please contact your supplier who will provide you with expert professional advice Harmony XL Mattress System A The box contains an assembled mattress system consisting of A Harmony XL Alternating Dynamic System B Digital Control Unit N aE C Power Cord D Carry Bag E User Manual SAFETY PRECAUTIONS In General Control Unit A Do not use this equipment in the presence of flammable anaesthetics A Keep away from sources of heat and naked flames A Bed frames used with the systems can vary greatly depending on the specific healthcare setting i e hospitals nursing homes home care etc It is the responsibility of the carer to carry out the necessary risk assessments to ensure the safety of the patient This includes but is not limited to the appropriate use of side rails to prevent falls and or patient entrapment A Minimise articles e g bedding between the mattress surface and patient and secure bed sheets loosely so as not to affect the alternating cell movement A The control unit is tested and CE marked in line with Medical Device Directive 93 42 EEC A Only plug into a mains socket using the mains cable supplied with the system A Exposure of the control unit to any liquid while it is plugged in could res
7. Cin i HARMONY XL Dynamic Mattress Replacement System User Instructions CONTENTS Important Notice Before operating this medical equipment it is important to read this manual and understand the operating instructions and safety precautions Failure to do so could result in injury and or damage to the product If you have any questions please see contact information on rear cover CE INTRODUCTION ccssccseseeeeereeeeteeseees 4 SAFETY PRECAUTIONG scsseeeeeee 5 PRODUCT OVERVIEW cssecseeeseeeees 6 INSTALLATION eccsseeeeeeseeeeeeeeeeseeneeeees 7 OPERATION ic ccnnecnccecescstceeesnecsncessscnteeenien 9 Control Unit Panel eee 9 Mattress FUNCTION eee eeeeeees 10 Use of Incontinence Products 11 Static MOE ssciciecrevserecvvacserervens 11 Removal amp Transport Function 12 Mains Supply Power Failure 12 TROUBLESHOOTING cccccseetseeees 13 CLEANING eseceeceeseseeeeeeeeseeneeeeseeeeneees 15 MAINTENANCE cccsseseeeeteeseeeeeeeeeee 16 TECHNICAL SPECIFICATION 20000 17 WARRANTY INFORMATION 0025 23 INTRODUCTION Harmony XL Dynamic Mattress Replacement System Thank you for choosing a Harmony XL Dynamic Mattress Replacement System This user manual should be read carefully before using the mattress as it contains important information regarding safe operation and maintenance in order to provide long
8. an be repositioned according to individual needs the maximum patient weight limit is 220kg 35 Stone Mattress This system includes three static head cells to provide static support for optimum user comfort while air pressure in the other cells is alternated over a 12 minute cycle This provides regular periods of pressure reduction to aid blood and lymphatic flow to vulnerable tissue Control Unit The control unit provides the air supply to the mattress e Itis controlled via a touch panel with integrated digital display The alarm sounds when low pressure is detected or when power is interrupted The alarm mute function silences the alarm for a maximum of 20 minutes the alarm resumes if the cause of failure is not resolved The alarm will sound for up to two hours following an interruption to power e The control unit includes a back up battery for the audible alarm This battery is continuously re charged and will last the life time of the product Functions on the control panel adjust the 8 comfort level settings e When a fault condition exists a warning LED is illuminated with an audible alarm The visible and audible alarm function has a number of indications depending on the cause of the failure see Troubleshooting section If the mains cable becomes detached the alternation sequence is suspended and the mattress cells remain inflated and or deflated based on the current cycle The audible a
9. and lock unlock buttons remain operational Pressing again for at least 2 seconds unlocks the control unit alarm sounds and amber LED extinguishes The control unit will automatically unlock in the event of a power failure OPERATION Mattress Function Establishing Pressure supine patient With the patient lying supine face upwards use the functions to establish the best setting for effective support and comfort Before changing or lowering the pressure ensure the system is working effectively by performing a bottoming out test Once the system has been set for the patient re check after approximately 20 30 minutes to ensure the patient is comfortable and that the unit is functioning correctly Bottoming Out Test When altering the pressure setting ensure the patient is not bottoming out insufficiently supported by the air cells 1 Ensure the system is in alternation mode 2 With the patient lying in a supine position unzip top cover just past the sacral buttocks region 8 Slide a hand along a deflated cell under the patient s sacral area The inner static cell will remain inflated but a hand should slide easily between patient and static cell 4 Ifahand can pass under the sacral area the patient is adequately supported and pressure can be lowered as required 5 Repeat bottoming out test if pressure has been lowered Establishing Pressure upright position
10. ence may occur in the vicinity of equipment marked with the following symbol NOTE 1 At80MHzand 800 MHz the higher frequency range applies NOTE2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people a Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the Hamony XL is used exceeds the applicable RF compliance level above the Harmony XL should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the HarmonyXL b Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m 21 TECHNICAL SPECIFICATION Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM for ME EQUIPMENT or ME SYSTEM that are not LIFE SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the Harmony XL Alternating Control Unit The Harmony XL is intended for use in an electro
11. ferent pressure setting illumination sequences The signals and corresponding pressure setting LED displays are illustrated below Alarm Fault Cause Control unit does not The control operate no display unit may not be LED s illuminate attached toa power socket or a fuse may need replacing Solution ais Check the mains cable is firmly plugged into a wall socket and the control unit Check the mains power is switched on to ensure socket is working plug in a lamp or other fused electrical device Check the mains plug fuse 8A then check control unit fuse 1A see Section Maintenance A Do not try to open the control unit Opening the unit could cause personal injury or equipment damage Alarm LED Initial failure e within 50 minutes audible alarm Reset the alarm turn off power and press the alarm mute button Check the handle is intact ensuring all four sealing connectors are firmly fitted to the control unit and the air hoses Check the CPR tag is attached and all sealing connectors are firmly secure Check all air hoses along the inside of the mattress each should be firmly connected Check each air cell is securely attached to its connecting air pipe 4 Check all cells pipes and hoses for any air leakage 5 Switch on power Alarm LED Pressure too low audible alarm Reset the alarm turn off power and press the alarm mute button Check the handle is intact ensuring
12. g the unit could cause personal injury or equipment damage Patient is sinking or bottoming out The pressure may be set too low for the patient s weight Increase the pressure setting by pressing the button To check effective system performance conduct a bottoming out test as described previously A If the above actions fail to rectify the problem please contact your local authorised service provider or Sidhil Limited 14 CLEANING Infection Control Routine cleaning for infection control must be carried out in accordance with your local infection control policy or regulatory body Cleaning the Control Unit A Disconnect the mains cable from the power socket before attempting to clean the control unit A Do not immerse the power unit in water A Ensure the mains cable and power unit are dry before use The control unit can be cleaned by wiping down with a damp cloth soaked in a sodium hypochlorite solution 1000 ppm available chlorine and dried with a clean dry cloth A The power unit is not IP rated therefore care should be taken to ensure only a damp cloth is used Cleaning the Mattress Before attempting to clean the mattress the top cover should be checked for physical signs of damage that may lead to strike through ingress of fluid through cover This is achieved by unzipping the top cover and looking for signs of staining to the white underside Any evidence of strike throu
13. gh will require a new cover to be fitted to the system A The cover must not be reused if strike through is evident 15 Wipe down with a disposable soft cloth moistened with a mild detergent and diluted in warm water 40 C dry thoroughly before use Wipe down with a solution of Sodium Hypochlorite or similar up to 1 000ppm Chlorine dry thoroughly before use A In extreme cases 10 000ppm Chlorine can be used but the following process must be adhered to 1 Wipe cover down using cold water 2 Clean with Chlorine solution 3 Finally wipe cover again using cold water The top cover may also be decontaminated using Ethylene Oxide or the Draeger method Additional infection control and routine cleaning must be carried out in accordance with your local infection control policy Do not use Phenol based cleaning agents e g Stericol Hycoline Clearsol etc Mattress Cover Cleaning Instructions Machine Wash at 71 C Do Not Iron Do Not Bleach Do Not Dry Clean Tumble Dry on Low Heat O x ME If the above washing instructions are not followed the warranty will be invalidated MAINTENANCE Only authorised service personnel or Sidhil service engineers should carry out repairs or service activities Failure to do so may result in the product warranty becoming void The mattress system must be serviced once yearly as a minimum Sidhil also recommends that the carer performs frequent visual and operational
14. l unit and disconnect the CPR tag 3 Place the control unit and mains cable on top of the mattress and detach the mattress from the bed frame 4 Once air has been released from all cells roll up the mattress and return all items to the carry bag for safe keeping Mains Supply Power Failure If it is known there is to be a power cut in advance follow the instructions detailed under the heading Transport Function prior to the power going off In the event of an unplanned power cut 1 Remove the air connection handle from the control unit and seal with the attached transport cap 2 Turn off the control unit A Mattress will stay inflated under normal conditions for up to 30 hours Transport Function 1 Before patient transport switch modes from alternating to static and wait for 12 minutes for all cells to inflate 2 Remove the air connection handle from the control unit sealing with the attached transport cap see image below 3 Turn off the control unit A Mattress will stay inflated under normal conditions for up to 30 hours 12 TROUBLESHOOTING The red alarm LED flashes and an audible alert sounds to indicate the control unit or mattress pressure has failed The LED will remain illuminated until appropriate pressure is restored The audible alarm can be silenced by pressing the alarm mute button The system has five different alarm signals identified by five dif
15. larm will sound INSTALLATION Any damaged or missing components should be reported to your supplier as soon as possible System Installation Control Unit Activation The following describes the procedures for initial system set up a Remove all covers sheets and mattress from the bed A b On a standard bed position the mattress on top of the bed frame top cover facing upwards and air hoses at the foot of the bed for control unit positioning c Attach to the bed by securing the adjustable straps loosely under each section of the bed x3 A On a profiling bed secure the adjustable straps around the moveable sections of the bed frame d To avoid any risk of damage to the mattress ensure there are no sharp objects which may come in contact with it A Check that the attachment of the mattress does not interfere with the movement or operation of the bed e Ensure the CPR tag sealing connectors are pushed firmly onto the air pipes Position the control unit by hanging the hooks over the foot board or place unit on the floor under the bed with the front facing upwards Ensure the rear of the unit is not obstructed by carpet rugs etc Itis advisable to place the unit on a firm surface ame Attach the air connector handle to the control unit Ensure air hoses do not kink between frame and control unit Insert mains cable into the control
16. magnetic environment in which radiated RF disturbances are controlled The customer or the user of the Harmony XL can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the Harmony XL as recommended below according to the maximum output power of the communications equipment Rated maximum Separation distance according to frequency of output power of transmitter m transmitter W 150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 167 P d 1 167yP d 2 333yP For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be estimated using the equation applicable to the frequency of the transmitter where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE1 At80MHzand 800 MHz the separation distance for the higher frequency range applies NOTE2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 22 WARRANTY INFORMATION Sidhil Ltd guarantees this product is free from defects in material and workmanship under normal use for two 2 years from the date of purchase from Sidhil Ltd and its subsidiary companies or its authorised dealers All implied warranties including but not limited to those implied warra
17. nties of fitness and merchantability are limited in the total duration of one year from date of purchase Proof of purchase must be presented with any claim Except as provided herein Sidhil Ltd product warranty does not cover damage caused by misuse or abuse accident the attachment of any unauthorised accessory alteration to the product or any other conditions whatsoever that are beyond the control of Sidhil Ltd Sidhil Ltd and its subsidiary companies shall have no liability or responsibility to customer or any other person or entity with respect to any liability loss or damage caused direct or indirectly by use or performance of the product or arising out of any breach of this warranty including but not limited to any damages resulting from inconvenience loss of time property revenue or profit or any indirect special incidental or consequential damages even if Sidhil Ltd or their subsidiary companies or authorised dealers has been advised of the possibility of such damages In the event of a product defect during the warranty period you should contact Sidhil Ltd or their authorised dealer who will at its option unless otherwise provided by law a correct the defect by product repair without charge for parts and labour b replace the product with one of the same or similar design or c refund the purchase price All replaced parts and products on which refund is made become the property of Sidhil Ltd New or reconditioned parts and prod
18. sary A o a SN Serial number z 18 TECHNICAL SPECIFICATION Declaration electromagnetic emissions for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture s declaration electromagnetic emission The Harmony XL is intended for use in the electromagnetic environment specified below The customer or the user of the Harmony XL should ensure that it is used in such an environment Compliance Emission test RF emissions CISPR 114 RF emission CISPR 11 Harmonic emissions IEC 61000 3 2 Voltage fluctuations flicker emissions IEC 61000 3 3 19 Electromagnetic environment guidance The Harmony XLuses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment The Harmony XL is suitable for use in all establishments including domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes TECHNICAL SPECIFICATION Declaration electromagnetic immunity Guidance and manufacture s declaration electromagnetic immunity The Harmony XL is intended for use in the electromagnetic environment specified below The customer or the user of the Harmony XL should ensure that it is used in such an environment Immunity test Electrostatic discharge ESD IEC 61000 4 2 Electrical fast
19. terruptible power supply or a battery Power frequency magnetic fields should be at levels characteristic of a typical location in atypical commercial or hospital environment TECHNICAL SPECIFICATION Declaration electromagnetic immunity for ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Guidance and manufacture s declaration electromagnetic immunity The Harmony XLis intended for use in the electromagnetic environment specified below The customer or the user of the Harmony XL should ensure that it is used in such an environment Immunity IEC 60601 Compliance Electromagnetic environment guidance test test level level Conducted Portable and mobile RF communications equipment RF 150 kHz to should be used no closer to any part of the CT515 IEC 61000 80 MHz including cables than the recommended separation 4 6 distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 167 P Radiated RF swm d 1 167 P 80 MHz to 800 MHz 80 MHz to IEC 61000 2 5GHz 4 3 Where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and dis the recommended separation d 2 333yP 800 MHz to 2 5 GHz distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interfer
20. torage Transport Environment Classification IEC60601 1 Digital micro controller 12 minutes 230V 50Hz 0 2A for Control Unit Mains Plug 3AMP Control Unit 1AMP x1 25VA CE marked in line with Medical Devices Directive 93 42 EEC 21 cells which includes 3 static head cells 18 alternating cells incl 7 narrow heel cells with cell in cell function 2 side bolsters 265mm ABC pattern 220kgs 35 Stone Length 2190mm 20mm Width 880mm 20mm Height 270mm 10mm Weight 13 4kgs Height 270mm Width 290mm Depth 120mm Weight 4 5kgs 210D PA TPU Dartex TC 185S PU Dartex Silver 3 Biocompatible PU knitted PES two way stretch Push on connector handle Rapid release tag Non continuous Air humidity 30 to 75 10 to 70 Ambient temperature 10 C to 40 C 10 C to 60 C Class Il equipment Type B applied part IPXO Not category AP APG equipment Avai product specifications are subject to change without notice 17 TECHNICAL SPECIFICATION Definition of Symbolys Used The following symbols may appear in this manual on the Control Unit or on its accessories Some of the symbols represent standards and compliances associated with the Control Unit and its use Caution Consult accompanying documents Class II equipment Manufacturer Type B applied part DISPOSAL Do not dispose of this product as unsorted municipal waste Collection of such waste separately for special treatment is neces
21. transient burst IEC 61000 4 4 Surge IEC 61000 4 5 Voltage dips short interruptions and voltage variations on power supply input lines EC 61000 4 11 Power frequency 50Hz magnetic field IEC 61000 4 8 NOTE IEC 60601 test level 6 kV contact 8 kV air 2 kV for power supply lines 1 kV line s to line s lt 5 U gt 95 dip in U for 0 5 cycle 40 U_ 60 dip in U for 5 cycles 70 U 30 dip in UT for 25 cycles lt 5 U gt 95 dip in U for 5 sec Compliance level 6 kV contact 8 kV air 2kV for power supply lines 1 kV differential mode lt 5 U gt 95 dip in U for 0 5 cycle 40 U 60 dip in U for 5 cycles 70 U 80 dip in U for 25 cycles lt 5 U gt 95 dip in U for 5 sec U is the a c mains voltage prior to application of the test level 20 Electromagnetic environment guidance Floors should be wood concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the Harmony XL requires continued operation during power mains interruptions it is recommended that the Harmony XL be powered from an unin
22. ucts may be used in the performance of warranty service Repaired or replaced parts and products are warranted for the remainder of the original warranty period You will be charged for repair or replacement of the product made after the expiration of the warranty period This warranty does not cover a damage or failure by or attributes to acts of God abuse accident misuse improper or abnormal usage failure to follow instructions improper installation or maintenance alterations lightning or other incidence of excess voltage or current b any repairs other than those provided by a Sidhil Ltd authorised technician c consumables such as fuses d cosmetic damage e transportation shipping or insurance costs or f costs of product removal installation setup service adjustment or re installation This limited two year warranty gives you specific legal rights and you may also have other rights Sidhil Ltd cannot be held responsible for any injury or incident which relates to the use of the Dynamic Mattress range in conjunction with accessories manufactured by companies other than Sidhil Ltd All products carry the CE mark in accordance with EC Directive on Medical Devices 93 42 EEC Sidhil has a policy of continual product improvement and reserves the right to amend specifications covered in this brochure No part of this brochure may be reproduced without the written approval of Sidhil Ltd 23 CONTACT INFORMATION Tel 01422 233000 Fa
23. ult in a severe electrical hazard A Only use fuses that have the same specified rating Using fuses with higher ratings could result in damage and or injury See Technical Specification A the control unit is a precision electronic product Use care when handling or transporting Dropping or other sudden impacts may result in damage to the unit A Do not open the control unit risk of electrical shock Do not attempt to repair or service the control unit Repairs and service should be conducted by suitably trained personnel If the control unit is not functioning properly or has been damaged unplug the unit and take it out of service immediately See contact information on rear cover for repair and service information A Do not place any objects or items such as blankets on or over the control unit A The mains cable to the control unit should be correctly positioned to avoid a tripping hazard and or damage to the cable It is recommended to place the cable under the bed frame and attach it to a mains socket by the head end of the bed PRODUCT OVERVIEW Alternating Mattress System See Technical Specification The Harmony XL Dynamic Mattress Replacement System is intended to provide comfort and pressure relief to patients vulnerable to pressure damage It is designed for use on both standard and profiling bed frames Ideally patients allocated to this system will have some degree of independent mobility or c
24. unit plug into a mains socket Press the power button for at least two seconds to activate the control unit The pressure LED s will flash indicating the system has activated The system will be ready for use in a maximum of 50 minutes When initial inflation is complete the 4th pressure LED and the alternating mode LED will illuminate to indicate the system is ready for use system automatically defaults to alternating mode at start up Once inflated ensure the straps that attach the mattress to the bed frame are secure and hold the mattress in place adjust as necessary Once the mattress is fully inflated the bedding can be replaced Secure sheets loosely enough to ensure they do not interfere with cell alternation INSTALLATION To attach the handle to the control unit 1 Depress the lever on the top of the handle 2 Aligning the ports on the handle with those on the control box firmly push the handle into position 3 Release the lever ensuring this has engaged onto the catch connected to the control box To remove the handle from the control unit 1 Depress the lever on the top of the handle 2 Pull the handle away from the control unit OPERATION Control Unit Panel A Power Button Turns system on off by pressing for at least two seconds B Alarm LED The red LED flashes and an audible alarm sounds when a fault condition has arisen in the control unit or mattress
25. x 01422 233010 Email sales sidhil com www sidhil com Sidhil Business Park Holmfield Halifax HX2 9TN A member of the Siddall amp Hilton Ltd Group of Companies 3 UKAS QUALITY MANAGEMENT CE 93 42 EEC Certificate No FM14550 INSTRUC HARMONYXL 05 08 2011 REV3
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