Quattro Fusion User Manual
Contents
1. Tallev QUATTRO FUSION Matiress Replacement System User Guidelines BE Explanation of Label Svmbols and Statements CE W Intertek O Im U A Caution Refer to instructions of use booklet Medical Devices Directive 93 42 EEC North America ETL listed Class II Equipment Double Insulated Do not dispose of with the normal household waste please refer to www tallevgroup com for further details Manufacturer Date of Manufacture Fragile handle with care 4 WARNING CAUTION IP21 Protect from heat and radioactive sources Temperature limitation Humidity limitation Atmospheric pressure limitation Suitable for connection to type BF applied parts This is a statement that alerts the user to the possibility of serious injury or other adverse reactions with the use or misuse of the device This is a statement that alerts the user to the possibility of a problem with the system associated with its use or misuse Operating Instructions IP Ingress Protection 2 Protection against fingers or other object not greater than 80mm in length and 12mm in diameter 1 Protection from vertically dripping water Contents Page EXPLANATION OF LABELS SVMBOLS AND STATEMENTS 1 INTRODUCTION 2 CAUTIONS AND WARNINGS INFORMATION 8 INSTALLATION AND USER GUIDELINES 5 CARE AND MAINTENANCE 8 FAULT FINDING 10 SPECIFICATIONS 12 EMI EMC STATEMENT AND MANUFACTURER S2. any product without prior notice in line with a policy of continual product development Our standard terms and conditions apply 12 Notes EMI EMC Statement and Manufacturer s Declaration This equipment has been tested and found to comply with the limits of EN 60601 1 2 These limits are designed to provide reasonable protection against harmful interference in both a medical and residential environment This equipment generates uses and can radiate radio frequency energy and if not used in accordance with manufacturer s instructions may cause harmful interference to radio communications However there is no guarantee that interference will not occur in a particular installation If this equipment does cause harmful interference to radio or television reception or other equipment which can be determined by turning the equipment off and on the user is encouraged to try to correct the interference by one of the following measures e Reorient or relocate the receiving antenna e Increase the separation between the equipment e Connect the equipment to an outlet on a circuit different from that to which the receiver or equipment was connected The equipment having been tested to operate within the limits of electromagnetic compatibility Immunity to interference from nearby sources radiating radio frequency energy Sources exceeding these limits may give rise to operation faults Where possible the system will sense the interfe
3. Reset power unit by system requires pressing inspection MUTE button 11 Specifications POWER UNIT Construction Dimensions Weight Mains Cable Electricity Supply Rated Input Fuse Rating IP Rating Cycle Time MATTRESS Construction Number of Cells Mode of Operation Dimensions Weight ABS Plastic 335mm 13 2 x 233mm 9 2 x 165mm 6 5 3 4 kg 7 5 Ibs 5 metres 16 5 For the USA only a hospital grade attachment plug with a 15A NEMAP 5 15 configuration and 18AWG hospital grade flexible cord is to be used as Supplied by Talley 230V 5OHz CE marked 120V 7 6OHz cETLus listed 230V 6OHz 9 4 VA T500mA 250V HRC ceramic 5 x 20 mm IP21 16 minutes continuous FOAM FRAME Combustion modified polyether foam RX33190 HEAD SECTION Combustion modified visco elastic foam VC50055 CELLS PU film encasing combustion modified visco elastic foam VC50055 inner cells COVER PU coated stretch 240g m Polyamide with PU coated stretch 215g m Polyamide non slip base 14 Static foam Active 1 in 4 cell cycle Continuous Low Pressure 1970mm x 880mm x 170mm 14 5kg UK standard size approx max top surface inflated 15mm Talley products are manufactured to comply with International and National safety standards Talley design and manufacture products to conform to the requirements of ISO9001 ISO13485 and Directive 93 42 EEC Talley reserves the right to modify the specification of
4. 2 5GHz d 2 3 VP 0 01 0 01 0 01 0 01 0 12 0 12 0 12 0 12 0 12 0 12 0 12 0 12 0 23 0 23 0 23 0 23 0 1 0 1 0 1 0 1 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 Note At 80MHz and 800MHz the separation distance for the higher frequency range applies Note These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people This medical device is compliant with IEC 60601 1 3rd edition Medical electrical equipment safety and essential performance IEC 60601 1 11 Home healthcare environment USER MANUAL PART NUMBER 50 02 07 217 2 Talley Group Limited A FI Premier Wav Abbev Park Industrial Estate iG V V Romsey Hampshire S051 9DQ England T ses EE yy al ey TEL 44 0 1794 503500 KE eg gt FAX 44 0 1794 503555 BVA ATTAN e Il 3 ke cele oR eLo an E MAIL sales talleygroup com 03 2015
5. DECLARATION 14 Introduction Thank you for choosing to use a Talley pressure area care product effective for the prevention and management of pressure ulcers The QUATTRO FUSION mattress replacement system combines the comfort and pressure reducing properties of visco elastic foam with the clinically proven pressure relieving benefits of a 1 in 4 active alternating air pressure cycle all in the same mattress Used alone the mattress provides comfort and pressure care for patients at elevated risk of pressure damage Once the power unit is connected the mattress provides all the benefits associated with an alternating air pressure mattress with a choice of either active 1 in 4 cell cycle therapy or continuous low pressure therapy Designed for the prevention and treatment of pressure ulcers within all care environments the versatile QUATTRO FUSION is suitable for patients at all risk levels providing the ability to step up or down according to the level of patient care required throughout their treatment Cautions and Warnings AN CONTRAINDICATIONS FOR USE Alternating pressure therapy should not be used for patients with unstable fractures gross oedema burns or an intolerance to motion There are no special skills required to operate the system The medical professional is responsible for applying his her best medical judgment when using this system Select correct setting for therapy required Care should be taken not to accid
6. afety hazard when handling To protect the covers mattresses should be packed in minimum 200 micron clear polythene MANUFACTURER S GUARANTEE The QUATTRO FUSION power unit and mattress are covered by a 24 month manufacturer s guarantee The intended design life is 5 years if fully serviced Fault Finding The power unit can be reset by pressing the MUTE button once This also silences the sounder and clears the message from the display screen All systems have a fault log that records the last 5 faults via the DATA display mode If problems reoccur contact Talley AC FAIL fault indicates a mains power failure a sounder will be heard if power is interrupted e g power unit switched off power cut disconnection of mains lead Press MUTE or re connect to power supply ROTOR SYSTEM fault indicates the automatic sequential cycle has stopped or there is a fault in the system Switch power off press MUTE button then switch power on again If the fault re occurs contact Talley LOW PRESSURE fault indicates pressure has fallen below the minimum allowable levels Check that the hose is connected to the power unit correctly Check that the internal cells are connected and that no cell is punctured Press the MUTE button to clear the message and to silence the sounder If the fault re occurs contact Talley EMI fault indicates that the unit detects the pressure sensor amplifier is adversely affected by external RF fields This wil
7. ation of button functions except MUTE as indicated bv L on the displav screen Press and hold the MUTE UNLOCK button until power unit beeps if further button operation is needed i e change of therapv mode or comfort setting 11 Place the carrv bag and user manual in a safe place for future use OPERATION BUTTONS The operation buttons on the face of the power unit provide the following functions THERAPV MODE Pressing the THERAPY MODE button will toggle between ACTIVE 1 in 4 alternating air pressure cycle and CONTINUOUS LOW PRESSURE therapy modes The selected therapy mode is shown on the display screen The default mode is ACTIVE therapy To switch to CONTINUOUS LOW PRESSURE mode press THERAPY MODE button for 2 seconds until an audible tone is heard The system will then display PLEASE WAIT and requires approximately 2 minutes to initialise posture and therapy are constantly maintained at optimum levels in response to patient weight movement and position Equalisation of cell pressure automatically takes place at each stage of the 1 in 4 cycle again to ensure precise pressure and therapy is provided The automatic default comfort setting is MEDIUM However if the patient prefers a firmer or softer mattress increase or decrease the comfort control setting accordingly using the UP and DOWN arrow buttons SOFT MEDIUM FIRM The comfort setting is shown on the display screen Check periodically to ensure patient support and com
8. cer prevention program not solely relied upon for this purpose The above warnings cautions and any safety considerations should be observed on a routine and regular basis not only upon installation Installation and User Guidelines 10 Remove any existing mattress from the bed frame the QUATTRO FUSION is intended to completely replace the bed mattress Place the mattress on the bed frame bed base Ensure the printed cover is uppermost and the mattress hose can exit at the foot end on the right hand side if required The mattress is now ready to use as a static foam mattress If using as a powered mattress suspend the power unit from the foot board of the bed having first adjusted the hanger brackets as instructed at the rear of the unit Alternatively the power unit may be placed on the floor The mattress air supply hose can be found at the foot end of the mattress under the mattress cover Unzip the cover to locate it re zipping the cover close to the air supply hose once it has been removed from the mattress interior Attach the mattress air supply hose to the power unit by matching up the button on the mattress hose connector with the alignment notch on the power unit connection port and pushing together Fig 1 Ensure that this has been correctly clicked into place otherwise a leak may occur Plug the smaller end of the power lead into the left hand side of the power unit and the other end into mains outlet in wal
9. dures the MAX INFLATE mode inflates the mattress to maximum static pressure for a period of 15 minutes After pressing the MAX INFLATE button to inflate mattress the svstem displavs PLEASE WAIT followed bv READV and a b second audible tone when maximum pressure is achieved and MAX INFLATE is shown on the displav screen After 15 minutes the svstem automaticallv returns to the Active mode of operation MAXIMUM USER WEIGHT GUIDELINES 250kg 39 stone max CPR FACILITV Fig 2 For rapid deflation of the powered mattress press the button on the mattress hose connector and pull the mattress hose away from the power unit to disconnect The QUATTRO FUSION can be used on profiling bed frames slatted frames in filled frames and divans Back rests or pillows for Support should be placed beneath the mattress to allow uninterrupted body contact with the mattress surface When a bottom sheet is added to the mattress ensure that it is left loose to allow the mattress surface to conform with the patient s body as much as possible Avoid using fitted sheets The use of incontinence sheets excessive bedding beneath the patient may reduce the pressure relieving effect of the mattress To remove air from the mattress when dismantling the system use the CPR facility as described above Care should be taken when raising and lowering bed safety side rails in order to avoid possible interference with the mattress air supply hose A ga
10. ectrostatic Floors should be wood concrete or ceramic tile If floors discharge ESD Ni ay 7 ay iad are covered with synthetic material the relative humidity IEC 61000 4 2 should be at least 30 alae ees IEC 2 kV For mains supply lines 2 kV For mains supply lines Mains supply quality for the mains adapter should be 61000 4 4 1kV For input output lines 1kV For input output lines that of a typical commercial and or hospital environment Surge i l Mains supplv qualitv for the mains adapter should be IEC61000 4 5 tik aint Orne A TKV PRIE MOINE that of a typical commercial and or hospital environment lt 5 Ur gt 95 Ur for 0 5 cycle lt 5 Ur gt 95 Ur for 0 5 cycle Mains power quality should be that of a typical f commercial and or hospital environment If the user of interruptions and 40 Ur 60 dip in Ur for 5 cycles 40 Ur 60 dip in Ur for 5 cycles the QUATTRO requires continued operation during voltage variations 70 Ur 30 dip in Ur for 25 cycles 70 Ur 30 dip in Ur for 25 cycles POwer mains interruption it is recommended that the On mains Supp pele aly y gi d QUATTRO be powered from an uninterruptible power Voltage dips short IEC 61000 4 11 gt 5 Ur gt 95 dip in Ur for 5secs gt 5 Ur gt 95 dip in Ur for 5 secs supply or battery Mains frequency Mains frequency magnetic fields should be at levels 50 60Hz magnetic 3 A m 3 A m characteristic of a typical
11. ently change pressures once set as the efficiency of the therapy may be reduced This could also be caused by pets pests or children The electricity supply is of the type indicated on the power unit Check the mains lead is free from damage and is positioned so as not to cause an obstruction or injury e g strangulation Ensure the mains lead or pump cannot become trapped or crushed e g via raising or lowering of bed or bed rails or any other moving object The power unit must only be used with a suitable approved cord and plug set as supplied by Talley The system is not used in the presence of flammable anaesthetics Suitable for continuous use Not suitable for sterilisation Do not position the power unit to make it difficult to disconnect the power supply plug or mattress Do not place device on or near a heat source Do not use with hot water bottles or electric blankets The materials used in the manufacture of all components of the system comply with the required fire safety regulations Talley advice against smoking whilst the system is in use to prevent the accidental secondary ignition of associated items which may be flammable such as bed linen Do not allow sharp objects to penetrate the mattress material Do not modify the mattress or power unit in any way Do not store in damp conditions Not for use in an oxygen enriched environment Not for use in an outdoor environment Intended for home healthcare u
12. fort COMFORT CONTROL Air pressure is regulated within each of the cells throughout the cycle so that support DATA i Pressing the DATA button at anv time switches the displav into DATA mode Use the up and down arrow buttons to scroll through the product data and user information set Pressing the DATA button again returns the displav to the previous mode NB Used for accessing information oniv does not affect mode of operation MUTE UNLOCK Press to silence the sounder and to clear the message from the displav screen The power unit will automaticallv lock 2 minutes after the last button operation when running to prevent the inadvertent operation of button functions except MUTE as indicated bv L on the displav screen Press and hold the MUTE UNLOCK button until the power unit beeps if further button operation is needed i e comfort setting The power unit will lock again 2 minutes after the last button operation NB After power failure switching the power off pressing MUTE cancels the svstem s previous settings When power returns the default setting of ACTIVE mode comfort setting 3 is invoked Note that previous settings are automaticallv cancelled if the duration between switch off and switch on is greater than 12 seconds If power returns before a period of 12 seconds has passed and the MUTE button has not been pressed the svstem will return to the previous mode of operation MAX INFLATE Necessarv for some nursing proce
13. is will help prevent any possible long term compatibility issues associated with disinfectant residues Alternatively disinfection may be achieved by laundering at temperatures not exceeding 65 C for 10 minutes or 73 C for 3 minutes which may include a chlorine rinse Do not use abrasive cleaners phenol disinfectants solvents or alcohol based cleansers e g Dettol Phenicol Hibiscrub Clearsol Stericol Hycoline as these will destroy the cover materials Do not iron Ensure that the mattress cover is thoroughly dried before remaking the bed or placing in storage INTERIOR COMPONENTS Check air cells and mattress interior for signs of damage or contamination e g staining or evidence of fluid ingress The frequency of these checks should be at each decontamination process i e between patients or patient occupancy or weekly for longer term patients Care should be taken to avoid puncturing air cells with objects such as needles scalpels pat slides acrylic nails etc The individual cells can also be wiped clean with a mild antiseptic solution All cells are replaceable and can be obtained easily from Talley Do not immerse the mattress in water or wet the foam components POWER UNIT Alwavs disconnect the power unit from the electricitv supplv before carrving out maintenance repairs servicing or cleaning Check all electrical connections and power lead for signs of excessive wear The power unit can be wiped down with de
14. l Ensure that the mains lead and tubing cannot become trapped in the bed frame the mattress includes cable management loops for routing of the mains lead Switch the power on at the outlet and at the side of power unit adjacent to the power lead entry The system will display STARTING then INITIALISING whilst the mattress inflates this will take approximately 2 minutes is not disconnected from the power unit If this is done the power unit must be switched off MUTE button pressed when the sounder is heard the mattress connector re engaged and the power unit restarted If UNCALIBRATED is displayed when switched on the system will continue to operate but should be recalibrated as soon as possible 1 Note It is important that during the INITIALISING phase the mattress connector Allow the mattress to inflate before positioning the patient on the mattress If however the patient is already in situ having been using the foam mattress without power the mattress will still inflate and there is no need to disturb the patient Once inflated the system will automatically default to ACTIVE mode CONTINUOUS LOW PRESSURE therapy can be selected via the THERAPY MODE button please see THERAPV MODE on page 6 The comfort setting can be adjusted using the up and down arrow buttons see COMFORT CONTROL on page 6 NB The power unit will automaticallv lock 2 minutes after last button operation when running to prevent inadvertent oper
15. l clear when interference ceases OTHER FAULTS PUMP OR TRIAC fault indicates a pump control failure or an open pump coil fault Should this occur contact Talley 10 UNCALIBRATED contact Talley for recalibration If you have any queries relating to this system please contact Talley or your local authorised dealer LOW PRESSURE FAULT ROTOR PUMP or SYSTEM TRIAC FAULT FAULT AC FAIL FAULT Indicates mains power failure Silence sounder by pressing MUTE button XI Check mattress air supply hose is correctly attached to power unit i e mattress hose connector is correctly aligned with power unit connector and has clicked into place Reset power unit by pressing MUTE button Reset power unit by pressing MUTE button eal If fault persists If fault persists power unit requires power unit requires Reconnect to power inspection inspection supply to continue using mattress Check air cells and tubing are intact MATTRESS NOT INFLATING no sounder UNCALIBRATED FAULT Reset power unit by Check that mains pressing power is connected MUTE button indicated by illuminated LCD display and allow at least 2 minutes for mattress to inflate The system will Caused by external continue to operate RF fields Fault will but contact Talley for clear when recalibration as soon interference ceases as possible If fault persists
16. location in a typical commercial field IEC61000 4 8 and or hospital environment Note Ur is the A C mains voltage prior to application of the test level Guidance and Manufacturer s Declaration Electromagnetic Immunity IEC 60601 1 2 Immunity IEC 60601 Compliance Electromagnetic Environment Guidance Test Test Level Level Portable and mobile RF communications equipment should be used no closer to any part of the QUATTRO including cables than the recommended separation distance calculated from the equation appropriate to the frequency of the transmitter Recommend separation distance Conducted RF 3M MS 80 MHz d 124P IEC 61000 4 6 3 V rms d 1 2 VP 80 MHz to 800 MHz 3 Vim d 2 3 WP 800 MHz to 2 5 GHz Radiated RF 3 V m where P is the maximum output power rating of the transmitter in watts W according to the 80 MHz l IEC 61000 4 3 25 GHz transmitter manufacturer and d is the recommended separation survey should be less than the compliance level in each frequency range distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site e Interference may occur in the vicinity of equipment marked with the following symbol A Note1 At 80 MHz and 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
17. nforms to this IEC60601 1 2 standard for immunity and emission Nevertheless special precautions need to be observed e The QUATTRO needs to be installed and put into service according to the EMC information below e The QUATTRO is intended for use in the electromagnetic environment specified in the tables below The user of the QUATTRO should assure that it is used in such environment In general although the QUATTRO complies too the EMC standards it can be affected by portable and mobile RF communications equipment Such as mobile telephones e The QUATTRO should not be used adjacent to or stacked with other equipment In case adjacent or stacked use is necessary the QUATTRO should be observed to verify normal operation Guidance and Manufacturer s Declaration Electromagnetic Emissions IEC 60601 1 2 Emissions Test Compliance Electromagnetic environment guidance RF emissions CISPR 11 Class B The QUATTRO systems are suitable for use in all establishments including domestic establishments and those directly connected to the public low voltage pump supply network that supplies buildings Voltage fluctuations flicker emissions 61000 3 3 Complies used for domestic purposes Harmonics emissions 61000 3 2 Class A 14 Guidance and Manufacturer s Declaration Electromagnetic Immunitv IEC 60601 1 2 Immunitv Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance El
18. p of 2 5cm on either side of the mattress should not be exceeded when side rails are deployed Care and Maintenance AN COVER Always keep the mattress cover as clean as is practicable The material is waterproof and vapour permeable Inspect top cover for signs of damage or wear which could result in the contamination of the interior e g tears holes damage to seams or zips underside staining etc The frequency of these checks should be at each decontamination process i e between patients or patient occupancy or weekly for longer term patients Care should be taken to avoid puncturing cover with objects such as needles scalpels pat slides acrylic nails etc The cover may be removed and cleaned in accordance with The Revised Healthcare Cleaning Manual June 2009 subject to the following action Following the use of a detergent and or disinfectant solution the mattress cover should be rinsed with clean water using a clean cloth and allowed to dry Frequent or prolonged exposure to high concentrations of aggressive disinfectant solutions will reduce the useful life of the mattress cushion cover Where high concentration disinfectants e g gt 10 000ppm chlorine releasing agent e g Haztab or bleach or combined cleaning chlorine releasing agent e g Chlorcleam Actichlor and detergent solutions are used to remove blood or other body fluids mattresses cushions should be thoroughly rinsed with clean water to remove any residues Th
19. people 4 Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile 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 electro magnetic site survey should be considered If the measured field strength in the location in which the QUATTRO is used exceeds the applicable RF compliance level above the QUATTRO should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the QUATTRO gt Over the frequency range 150 kHz to 80MHz field strengths should be less than 3 V m Recommended Separation Distance Between Portable and Mobile RF Communications Equipment and the QUATTRO The QUATTRO is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The user of the QUATTRO can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the QUATTRO as recommended below according to the maximum output power of the communications equipment Output Power of Transmitter in Separation distance according to frequency of transmitter in Meters m Watts W 150 kHz to 80 MHz d 1 2 P 80 MHz to 800 MHz d 1 2 P 800 MHz to
20. rence and if it is of short duration transparently take countermeasures whilst operating near normally or failing this will issue a warning and take measures for the continued safely of the user Further increased levels of energy may cause the system to stop operating continuously generate random faults or continuous resets Try to ascertain the source of the interference by turning nearby or Suspect equipment off and see if the interference effects stop In any such event the user is encouraged to try to correct the interference by one of the following measures e Have the interfering equipment repaired or replaced Reorient or relocate the interfering equipment Increase the separation between the equipment and the possible source of the interference Connect the equipment to an outlet on a circuit different from that to which the interfering equipment was connected Information regarding Electro Magnetic Compatibility EMC according to IEC60601 1 2 clause 6 8 With the increased number of electronic devices such as PC s and mobile telephones medical devices in use may be susceptible to electromagnetic interference from other devices The EMC Electro Magnetic Compatibility standard IEC60601 1 2 defines the levels of immunity to these electromagnetic interferences From the other hand medical devices must not interfere with other devices IEC60601 1 2 also defines the maximum levels of emissions for these medical devices The QUATTRO co
21. se and professional healthcare facilitv environments where operators with medical training are continuallv available when patients are present The power unit is intended to be hung over the bed s footboard Wireless equipment such as mobile phones should be kept at least 10 feet or 3 3 meters away from the equipment Do not connect to any other medical device or equipment Risk of fire if incorrect fuse used The mattress and pump should be cleaned between patient use please refer Care and Maintenance section for all warnings and cautions Mattress must be properly set up as directed Check periodically to ensure patient support and comfort adjusting the Comfort Control setting if desired All hoses must be free of kinks twists properly connected and positioned so as not to cause an obstruction or injury In order for the alternating air pressure mattress to operate effectively please avoid placing objects on the surface that may obstruct the movement of air between the cells For the same reason please discourage people from sitting on the edge or on the end of the mattress whilst it is in use Do not use bleach chlorine releasing agents in concentrations over 1000 ppm solvents or alcohol based cleansers e g Phenicol Hibiscrub Clearsol Stericol Hycoline as these will destroy the matress material Do not place heavy objects on the surface of foam mattresses when not in use The system is used as part of a pressure ul
22. t parts lists and other information necessary for Talley an authorised dealer or a competent electrical engineer to repair or service the system Talley s standard terms and conditions apply to all sales A copy is available on request For service maintenance and any questions regarding this or any other product please contact Talley It is the customer s responsibility to ensure the following prior to collection e the system is cleaned of any obvious contaminants e contamination status is documented e assistance is given to Talley personnel to bag the equipment if the mattress has been in a known or suspected infectious environment TRANSPORT AND STORAGE Handle with care Please report instances of damage or impact to Talley Service Department Transport 25 C without relative humidity control and 70 C ata relative humidity up to 93 non condensing An atmospheric pressure range of 700 hPa to 1 060 hPa Suitable for all standard modes of transport when in the correct packaging OPERATIONAL CONDITIONS A temperature range of 5 C to 40 C A relative humidity range of 15 to 93 non condensing and Operational Atmospheric Pressure 700 hPa to 1060 hPa Suitable for pollution degree 2 Operational altitude lt 2 000 m IP Rating IP21 pump only TRANSPORTATION OF MATTRESS SYSTEM The mattress should be transported flat and not rolled Mattresses should not be stored more than 6 high as this can potentially be a s
23. tergent or disinfectant solution or wipe Do not use solvents Unsuitable for sterilisation Dispose of the pump mattress in accordance with the local regulations including WEEE requirements In line with the MHRA Medical Device Alert MDA 2013 019 Talley advises customers to use pH neutral high level disinfectant cleaning products to sanitise reusable medical devices to prevent damage to materials and the degradation of plastic surfaces after prolonged use The use of inappropriate cleaning and detergent materials on medical equipment could damage surfaces and may compromise the ability to decontaminate medical devices adequately or may interfere with device function Talley recommends the use of TECcare CONTROL antimicrobial wipes and fluid to clean and decontaminate all products it supplies to health and social care facilities TECcare CONTROL products provide class leading broad spectrum high level disinfection with an exceptional safety profile Being pH neutral TECcare CONTROL can be universally used on all hard and soft surfaces without any detrimental effect TECcare CONTROL is CE marked for cleaning medical equipment SERVICING Talley recommend that all power units should be serviced every two years or as indicated by the hours to service display The unit contains no user serviceable parts and should only be serviced by either Talley or an authorised dealer Talley will make available on request service manuals componen
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