Instructions for Use
Contents
1. Do not use Phenol based solutions or abrasive compounds or pads during the decontamination process as these will damage the surface coating Avoid immersing electrical parts in water during the cleaning process Do not spray cleaning solutions directly onto the pump Do not immerse the tubeset in water To clean Clean all exposed surfaces and remove any organic debris by wiping with a cloth moistened with a simple neutral detergent and water Do not allow water or cleaning solutions to collect on the surface of the pump Chemical Disinfection We recommend a chlorine releasing agent such as sodium hypochlorite at a strength of 1 000ppm available chlorine this may vary from 250ppm to 10 000ppm depending on local policy and contamination status Wipe all cleaned surfaces with the solution then wipe using a cloth moistened with water and dry thoroughly Alcohol based disinfectants strength 70 may be used as an alternative Ensure the product is dry before storage If an alternative disinfectant is selected from the wide variety available we recommend that suitability for use is confirmed with the chemical supplier prior to use Caution Garments are single patient use and hence cannot be cleaned or reused 8 Routine Maintenance Flowtron Excel System Maintenance Servicing Service Period Flowtron Excel Pump General Care Maintenance and Inspection Serial Labels The equipment has been designed2. ENVIRONMENTAL INFORMATION Temperature Range Condition Operating 10 C to 40 C 50 F to 104 F Relative Humidity 30 to 75 non condensing Atmospheric Pressure 700 hPa to 1060 hPa Storage and Transport Long Term 10 C to 40 C 50 F to 104 F 20 to 95 non condensing 700 hPa to 1060 hPa Storage and Transport Short Term 20 C to 50 C 4 F to 122 F 20 to 95 non condensing 500 hPa to 1060 hPa If the pump is stored in conditions outside of the Operating ranges it should be allowed time to stabilise at normal operating conditions before use 13 Symbols The operator must read this document P E f Instructions for Use enn oni Do not dispose of in before use the malhs Suppl domestic refuse Note This symbol is blue PPY on the product label With respect to electric shock fire and mechanical hazards only Power in accordance with CAN Connects to the CSA C22 2 No 60601 1 mains supply CAN CSA C22 2 No 60601 1 2008 2008 MEDICAL EQUIPMENT Refer to this document Instructions for Use for a description of the Serial Number Model number product classification 3rd Edition Refer to this document Instructions for Use for a description of the Double Insulated product classification 2nd Edition Manufacturer This symbol is accompanied by the name and the address of the m
3. 16 AUSTRALIA ArjoHuntleigh Pty Ltd 78 Forsyth street O Connor AU 6163 Western Australia Tel 61 89337 4111 Free 1 800 072 040 Fax 61 89337 9077 BELGIQUE BELGI ArjoHuntleigh NV SA Evenbroekveld 16 B 9420 ERPE MERE T l Tel 32 0 53 60 73 80 Fax 32 0 53 60 73 81 E mail info arjohuntleigh be CANADA ArjoHuntleigh Canada Inc 1575 South Gateway Road Unit C MISSISSAUGA ON L4W 5J1 Tel T l 1 905 238 7880 Free 1 800 665 4831 Institutional Free 1 800 868 0441 Home Care Fax 1 905 238 7881 E mail info canada arjohuntleigh com CESKA REPUBLIKA ARJO Hospital Equipment s r o Hlinky 118 CZ 603 00 BRNO Tel 420 549 254 252 Fax 420 541 213 550 DANMARK ArjoHuntleigh A S Vassingeradvej 52 DK 3540 LYNGE Tel 45 49 13 84 86 Fax 45 49 13 84 87 E mail info dk arjohuntleigh com DEUTSCHLAND ArjoHuntleigh GmbH Peter Sander Strasse 10 D 55252 MAINZ KASTEL Tel 49 0 6134 186 0 Fax 49 0 6134 186 160 E mail info de arjohuntleigh com EAAAAA C Psimitis Co Ltd Dimitriou Andr 59 GR 16121 KAISARIANI ATTIKIS Tn 21 0724 36 68 g 21 0721 55 53 ESPANA ArjoHuntleigh Ib rica S L Ctra de Rub 88 1 planta A1 08173 Sant Cugat del Vall s ES BARCELONA 08173 Tel 34 93 583 11 20 Fax 34 93 583 11 22 E mail info es arjohuntleigh com FAR EAST ARJO Far East Limited Unit 3A 4 F Block B Hoi Luen Industrial Centre 55 Hoi Yuen Road
4. Kwun Tong Kowloon HONG KONG Tel 852 2508 9553 Fax 852 2508 1416 FRANCE ArjoHuntleigh SAS 2 Avenue Alcide de Gasperi BP 133 59436 RONCQ CEDEX T l 33 0 3 20 28 13 13 Fax 33 0 3 20 28 13 14 E mail info france arjohuntleigh com INTERNATIONAL ArjoHuntleigh International Ltd ArjoHuntleigh House Houghton Hall Park Houghton Regis UK DUNSTABLE LU5 5XF Tel 44 0 1582 745 800 Fax 44 0 1582 745 866 E mail international ArjoHuntleigh com ITALIA ArjoHuntleigh S p A Via di Tor Vergata 432 00133 ROMA ITALIA Tel 39 0 6 87426211 Fax 39 0 6 87426222 E mail Italy promo arjohuntleigh com NEDERLAND ArjoHuntleigh Nederland BV Biezenwei 21 4004 MB TIEL Postbus 6116 4000 HC TIEL Tel 31 0 344 64 08 00 Fax 31 0 344 64 08 85 E mail info nl arjohuntleigh com NORGE ArjoHuntleigh Norway AS Ryenstubben 2 NO 0679 OSLO Tel 47 22 08 00 50 Faks 47 22 08 00 51 E mail post arjo no POLSKA ArjoHuntleigh Polska Sp z 0 0 ul Ks Piotra Wawrzyniaka 2 PL 62 052 KOMORNIKI Poznan Tel 48 61 662 15 50 Fax 48 61 662 15 90 E mail arjo arjohuntleigh com www arjohuntleigh com PORTUGAL ArjoHuntleigh em Portugal MAQUET Portugal Lda Distribudor Exclusivo Rua Poeta Bocage n 2 2G 1600 233 Lisboa Portugal Tel 351 214 189 815 Fax 351 214 177 413 E mail Portugal arjohuntleigh com SUISSE SCHWEIZ ArjoHuntleigh AG Fabrikstrasse 8 Postfach
5. 4614 Hagendorf T l Tel 41 0 61 337 97 77 Fax 41 0 61 311 97 42 SUOMI ArjoHuntleigh OY Vanha Porvoontie 229 FI 01380 VANTAA Puh 358 9 4730 4320 Faksi 358 9 4730 4999 SVERIGE ARJO Scandinavia AB Verkstadsvagen 5 Box 61 SE 241 21 ESLOV Tel 46 0 413 645 00 Fax 46 0 413 645 83 E mail kundservice arjohuntleigh com UNITED KINGDOM ArjoHuntleigh UK ArjoHuntleigh House Houghton Hall Park Houghton Regis UK DUNSTABLE LU5 5XF Tel 44 0 1582 745 700 Fax 44 0 1582 745 745 E mail sales admin ArjoHuntleigh com USA ArjoHuntleigh Inc 2349 W Lake Street Suite 250 Addison IL 60101 Tel 1 630 307 2756 Free 1 800 323 1245 Institutional Free 1 800 868 0441 Home Care Fax 1 630 307 6195 E mail us info ArjoHuntleigh com OSTERREICH ArjoHuntleigh GmbH Dorrstrasse 85 AT 6020 INNSBRUCK Tel 43 0 512 204 160 0 Fax 43 0 512 204 160 75 ARJOHUNTLEIGH GETINGE GROUP www arjohuntleigh com ArjoHuntleigh AB Verkstadsvagen 5 241 38 Esl v SWEDEN GETINGE GROUP is a leading global provider of products and systems that contribute to quality enhancement and cost efficiency within healthcare and life sciences We operate under the three brands of ArjoHuntleigh GETINGE and MAQUET ArjoHuntleigh focuses on patient mobility and wound management solutions GETINGE provides solutions for infection control within healthcare and contamination prevention within life sciences MAQUE
6. additional measures may be necessary such as reorientating or relocating the pump gt Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m 15 Recommended separation distances between portable and mobile RF communications equipment and the pump The pump is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the pump can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the pump as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter Rated maximum m output power of transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz d 1 2 P d 1 2 P d 2 3 P For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres 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 80 MHz and 800 MHz 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
7. showing the desired output pressure when the garments are inflated Visually recheck the display at regular intervals If necessary the pressure can be adjusted during the active inflation period by rotating the pressure control knob until the desired pressure is displayed To confirm the calibration accuracy of the pressure control and display perform the following check each time the pump is turned on During normal operation when the pressure display reads H the pointer on the pressure control knob should be located within the 40 mmHg arc on the front panel Ay If the display reads 40 but the control knob is not within the 40 mmHg arc the pump should not be used and referred to service for recalibration 7 Decontamination The following processes are recommended but should be adapted to comply with the local or national guidelines Decontamination of Medical Devices which may apply within the Healthcare Facility or the country of use If you are uncertain you should seek advice from your local Infection Control Specialist The Flowtron Excel pump should be routinely decontaminated between patients and at regular intervals while in use as is good practice for all reusable medical devices WARNING Remove the electrical supply to the pump by disconnecting the mains power cable from the mains power supply before cleaning Protective clothing should always be worn when carrying out decontamination procedures Caution
8. ARJOHUNTLEIGH FLOWTRON EXCEL A Instructions for Use C 0086 with people in mind Contents General Safety e u se ee oes A ee ee d Ee ees iii Introduction 2 2 20 aaa ee bee eee eee eee ee eee 1 About this Manual seses ederrera A ahd aoe eA Le 1 IntendedsUse aif eel a da 1 About Flowtron ExcCel cece eee ee eee a A 1 Clinical Applications sssssssssnnnnnnnnnnnnnunnnnnnann nna 3 Indications Sos ca e a Aa a ee SL ab PR 3 GontraindicationS ss 2 edce ene bate dd woe Pete s 3 GAUT OMS rss E A AS A a ed ate 3 Guidelines and Recommendations 0 00 eee eee ee eee 4 System Set UP cai a See ee ee 5 Installing the PUMP cric 2 3 content SA6G9 24 30 25 6 A 5 Garment ADPICALION seal cds curp dae ass 5 Garment Removal 0000 do dae 5 To Use Only One Garment 0 0 ee eee eens 5 Pre UsSe Check io a te al A Sade e a Sl dD Ko LS 6 Op ration rata a hehe ae eee were elas ee bet da 7 SAND asia RARA ARANA AA Ne ee ee Ve s 7 SHU DOWN usa a a ia ate 7 Pressure Adjustment lt asma radera tl eee ed s eet ot eet eee ee uk 8 Pressure Qutp t Check ss tapers E AAA ee Aa R A 8 Adjusting the Output Pressure s 1 11222 suala kaka aa 8 System Calibration Check 0 00 ce eee sansa aran 8 Decontamination 2 2 2 22 A A A ae Ad iS 9 Routine Maintenance anninunnnnnnnnnnnnnnnnnnnnnnnnn nna 10 Flowtron Excel System 0oooooooooooec
9. IFU before calling a service engineer or contacting your local ArjoHuntleigh sales office I Loss of mains power will halt therapy Turn the power switch to the off 0 position Turning the power off will stop the patient therapy ES Ifitis required to completely isolate the pump from the mains power remove the plug from the mains power socket Disconnect and remove the garment s as required IS Garments are for single patient use only Do not use the garments on a different patient after treatment 6 Pressure Adjustment Pressure Output Check Adjusting the Output Pressure System Calibration Check The pressure control mechanism is located on the front of the pump and ranges from 30 60mmHeg The pressure exerted by the garments on the leg can be adjusted by turning this knob Turning the knob clockwise increases the pressure counterclockwise decreases the pressure IES The recommended pressure setting is 40 mmHg Alternatively use the pressure prescribed by the treating physician The Flowtron Excel pump pressure monitoring system is independent of the pressure control and delivery system providing added reliability and safety The digital display indicates the actual pressure that is delivered to the garments and provides immediate and continuous feedback regarding pump performance The pressure display is used for the following functions After turning the pump on check that the pressure display is
10. T specializes in solutions therapies and products for surgical interventions and intensive care 247933EN_01 07 2012
11. anufacturer Guidance and manufacturer s declaration electromagnetic emissions The pump is intended for use in the electromagnetic environment specified below The customer or the user of the pump should assure that it is used in such an environment Emissions Test Compliance Electromagnetic environment guidance RF emissions Group 1 The pump uses RF energy only for its internal function therefore its RF emissions are very low CISPR 11 and are not likely to cause any interference in nearby electronic equipment RF emissions Class A The pump is suitable for use in all establishments other than domestic and those directly connected CISPR 11 to the public low voltage power supply network that supplies buildings used for domestic Harmonic emissions Aa Voltage fluctuations Complies flicker emissions IEC 61000 3 2 14 Guidance and manufacturer s declaration electromagnetic immunity The pump is intended for use in the electromagnetic environment specified below The customer or the user of the pump should assure that it is used in such an environment Immunity IEC 60601 Test Compliance Electromagnetic environment guidance Test Level Level Portable and mobile RF communications equipment should be used no closer to any part of the pump including cables that the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommend
12. d ensure that the compression stockings are properly measured applied and worn by the patient Any compression stocking used should be routinely checked to ensure continued proper fit and application in addition to assessing the condition of the skin Where appropriate patients should be instructed in the proper use of the system the purpose of therapy and that any problems should be reported to the nursing staff The Flowtron Excel system should be applied to the patient pre operatively prior to the induction of anaesthesia The system should be used continuously for no less than 72 hours post operatively or until the patient becomes fully ambulatory If the garment cannot be applied to the operative limb during surgery it may be applied to the limb once the patient reaches the recovery unit In the non surgical patient the system should be initiated immediately the risk of DVT formation is identified 3 System Set Up Installing the Pump Attach the pump to the bed frame using the bed bracket or place the pump on the floor under the bed Garment Application 1 2 I Garment Removal 1 Check that the mains power switch on the pump is in the off 0 position Remove the garments from the packaging and unfold Garments are for single patient use only Do not use the garments on a different patient after treatment Place the back of the patient s leg in the centre section of the garment with the connecto
13. ed separation distance Conducted RF 3 Vrms d 1 2VP IEC 61000 4 6 150 kHz to 80 MHz d 1 2VP 80 MHz to 800 MHz Radiated RF 3 V m d 2 3VP 800 MHz to 2 5 GHz IEC 61000 4 3 80 MHz to 2 5GHz where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres 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 Interference may occur in the vicinity of equipment marked with the following symbol CY Note At 80 MHz and 800 MHz 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 4Field 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 pump is used exceeds the applicable RF compliance level above the pump should be observed to verify normal operation If abnormal operation is observed
14. essible at all times To disconnect the pump completely from the electricity supply remove the plug from the mains power socket e Disconnect the pump from the mains power socket before cleaning and inspecting Keep the pump away from sources of liquids and do not immerse in water e Do not use the pump in the presence of uncontained flammable liquids or gasses e Only the pump and garment insert combination as indicated by ArjoHuntleigh should be used The correct function of the product cannot be guaranteed if incorrect pump and garment combinations are used e The Flowtron Excel system is NOT intended for use in the Home Healthcare Environment e g private dwellings or nursing homes Caution applicable to the USA market only US Federal law restricts this device to sale by or on the order of a physician Precautions For your own safety and the safety of the equipment always take the following precautions e Do not expose the system to naked flames such as cigarettes etc e Do not store the system in direct sunlight e Do not use phenol based solutions to clean the system e Make sure the system is clean and dry prior to use or storage Electromagnetic Compatibility EMC This product complies with the requirements of applicable EMC Standards Medical electrical equipment needs special precautions regarding EMC and needs to be installed in accordance with the following instructions e The use of accessories not speci
15. fied by the manufacturer may result in increased emissions by or decreased immunity of the equipment affecting its performance e Portable and mobile radio frequency RF communications equipment e g mobile cell phones can affect medical electrical equipment iii e If this equipment needs to be used adjacent to other electrical equipment normal operation must be checked before use e For detailed EMC information contact ArjoHuntleigh service personnel Expected Service Life The Flowtron Excel pump has an expected service life of seven years To maintain the condition of the pump have the pump serviced regularly according to the schedule recommended by ArjoHuntleigh Do NOT use unapproved accessories or attempt to modify disassemble or otherwise misuse the Flowtron Excel system Failure to observe this caution could result in injury or in extreme cases death Environmental Protection Incorrect disposal of this equipment and its component parts particularly batteries or other electrical components may produce substances that are hazardous to the environment To minimise these hazards contact ArjoHuntleigh for information on correct disposal Design Policy and Copyright and are trademarks belonging to the ArjoHuntleigh group of companies As our policy is one of continuous improvement we reserve the right to modify designs without prior notice The content of this publication may not be copied either whole or in par
16. inked causing a blocked Check hoses for kinks or tube obstructions Hose disconnected at pump Check the hose connection at pump outlet Single garment attached Press single leg button if only one without pressing single leg garment to be used button Pump failure DO NOT USE PUMP Call the service engineer No displays 1 Power failure 1 Check mains power supply no indications Check power cable no operation 2 Fuse blown 2 Call the service engineer Red LED on the Single Internal electronic fault DO NOT USE PUMP Leg mode button Call the service engineer flashes approximately 4 times per second Alarm Cancel After a fault has been corrected the alarm can be cancelled by two methods 1 Switch the pump off then on again 2 Allow the pump to run until it senses a normal inflation it will then reset itself Continue to watch the display for approximately one minute after reset If no flashing messages reappear the fault has been cleared IS If the troubleshooting procedures do not return the system to normal performance stop using the system immediately and call the service engineer II 10 Accessories GARMENTS AND TUBING Description Garment Part No Standard Calf Garment DVT10 Circumference up to 43cm 17 Calf Garment Sterile DVT10S Circumference up to 43cm 17 Large Calf Garment DVT20 Circumference up t
17. n and connection to the pump is essential 2 Garments should be positioned in such a way that they do not create any potential for constant pressure points on the patient s limb Additional care should be taken when placing the garments on any deformed leg or on legs with significant oedema 3 When used for DVT prevention continuous external pneumatic compression is recommended until the patient is fully ambulatory Uninterrupted use of the Flowtron Excel system is encouraged 4 Garments should be removed immediately if the patient experiences tingling numbness or pain and the physician notified 5 The Flowtron Excel system should be USED WITH CAUTION on patients with e Insensitive extremities e Diabetes e Impaired circulation e Fragile or impaired skin I These are guidelines only and should not replace clinical judgement and experience Guidelines and Recommendations General Recommendations DVT Prophylaxis While using the system the patient s limbs should be checked during every shift and more often if the patient has known circulatory or skin problems or is diabetic Clinical judgment should be used to determine if the patient s skin condition requires additional measures or if the treatment should be discontinued and alternative modalities used ArjoHuntleigh does not recommend the use of compression stockings with its system If these are ordered by the physician the clinician shoul
18. nual part No SERO019 available from your local ArjoHuntleigh sales office Carry Handle Pressure Display ARJOHUNTLEIGH o Single Leg L ja mode button Garment and indicator Twa 40 TAN Connectors S py mmHg Pressure Control Mains Power Switch Flowtron Excel Pump Front View 2 Clinical Applications Indications Contraindications Cautions The primary application of the Flowtron Excel system is for the prevention of Deep Vein Thrombosis DVT when combined with an individualised monitoring programme These systems represent one aspect of a DVT strategy if the patient s condition changes the overall therapy regimen should be reviewed by the prescribing clinician The above are guidelines only and should not replace clinical judgement The Flowtron Excel system should not be used in the following conditions 1 Severe arteriosclerosis or other ischaemic vascular diseases 2 Known or suspected acute Deep Vein Thrombosis DVT or phlebitis 3 Severe congestive cardiac failure or any condition where an increase of fluid to the heart may be detrimental Pulmonary embolism 5 Any local condition in which the garments would interfere including gangrene recent skin graft dermatitis or untreated infected leg wounds If you are unsure of any contraindications refer to the patient s physician before using the device 1 Proper garment applicatio
19. o 58cm 23 Standard Thigh Garment DVT30 Circumference up to 71cm 28 Thigh Garment Sterile DVT30S Circumference up to 71cm 28 Large Thigh Garment DVT40 Circumference up to 89cm 35 Extra Large Calf Garment DVT60 Circumference up to 71cm 28 Calf Garment L501 M Circumference up to 43cm 17 Thigh Garment L503 M Circumference up to 71cm 28 Connector Tubing L550 Length 150cm 60 Connector Tubing L552 12 Length 300cm 118 11 Technical Specification Model Flowtron Excel Part Numbers UK AUS KSA USA 247003 UK 247003AU AUS 247008 247001 Supply Voltage 230 V 220 V 120 V Supply Frequency 50 Hz 60 Hz 60 Hz Power Input 35 VA MAX 35 VA MAX 35 VA MAX Size 133 x 152 x 275 mm Weight 2 7 kg Case Material Fire Retardant ABS Plastic Plug Fuse Rating 5A BS1362 UK ONLY Pump Fuse Rating F500 mAH 250 V Degree of protection against electric shock Type BF Class Il Double Insulated with Functional Earth Degree of protection against liquid ingress IPXO No protection Mode of operation Continuous Cycle or Therapy Modes 60 seconds total 12 seconds inflation 48 seconds deflation Pressure Range 30 60 mmHg 4 mmHg
20. orenr ee 10 Flowtron Excel PUMP iaa A A hae 10 Serial Labels runa nf ht th e a te O e A a 10 Tro bl shooting oered aaie A a i 11 Alarm Ganceliz ta 2446 te Soe te eee be eee eee e a e a 11 ACCOSSOMOS sensi Sn ts bY A oe a ee a Se eee ae 12 Garments and Tubing es vse cick Ciow dhe bee eek Lee eee bales 12 Technical Specification 22nvsnssnnanannnnnnnnnnnnnnnnnua 13 PUN Pin banal is dei s pd Oe acts 13 i ii General Safety Before you connect the system pump to a mains socket read carefully all the installation instructions contained within this manual The system has been designed to comply with regulatory safety standards including e EN60601 1 1990 A13 1996 and IEC 60601 1 1988 A2 1995 e UL60601 1 UL2601 1 and CAN CSA C22 2 No 601 1 M90 e EN60601 1 2006 and IEC 60601 1 2005 e AAMI ANSI ES60601 1 2006 and CAN CSA C22 2 No 60601 1 2008 Safety Warnings It is the responsibility of the care giver to ensure that the user can use this product safely e Make sure that the mains power cable and tubeset or air hoses are positioned to avoid causing a trip or other hazard and are clear of moving bed mechanisms or other possible entrapment areas e Electrical equipment may be hazardous if misused There are no user serviceable parts inside the pump The pump s case must only be removed by authorised technical personnel No modification of this equipment is allowed e The mains power socket plug must be acc
21. r tubing pointing downwards towards the foot Starting with the side of the garment that does not have the Velcro tabs wrap securely against the leg While holding the garment against the leg wrap the tabs over the top Ensure that the garment is close fitting and has no creases or folds The connector tubing should be pointing towards the patient s heel Make sure the tubing assembly is connected to the garment connector on the pump Connect the garment connector to the tubing assembly Ensure that a sharp click is heard Pull lightly to confirm proper connection Repeat steps 3 to 6 for the second garment if used To disconnect a garment press on the tubing assembly snap lock connector and pull the garment connector away from the tubing assembly To Use Only One To use only one garment connect a single garment to Garment either connector I The snap lock connectors on the pump are self sealing and do not require unused garments to be attached I Velcro is a registered trademark of VELCRO USA Inc 5 4 Pre Use Check Before powering on the Flowtron Excel system ensure that The pressure control knob has been set to the mid position marked 40 mmHg Garments have been applied to the patient s legs correctly close fitting and without creases or folds There are no kinks in the tubing The pump is connected to the mains power supply but not switched on All tubing connections a
22. re secure The system has been arranged so that the power cable and garment tubing do not pose a trip or strangulation hazard 5 Operation Start Up Shut Down Connect the pump to the mains power supply using the power cable provided Turn the mains power switch to the on 1 position and it will illuminate green The pump performs a two second self test cycle where the pressure display LEDs and alarm are tested The pump then proceeds directly to the inflation cycle The garments will inflate alternately The first garment inflates for approximately 12 seconds and is deflated for approximately 48 seconds The second garment if used inflates 30 seconds after the first garment has deflated and follows the same inflation deflation cycle If a single garment is attached press the Single Leg button 1 to prevent the alarm system from indicating a fault The system responds with a beep and the red LED on the button illuminates Is Ifthe Single Leg button 1 is pressed while two garments are connected the system will automatically reset to two garment operation after two single garment inflation cycles Verify that the pressure display is indicating the desired output pressure prescribed by the physician Refer to section Pressure Adjustment on page 8 for specific pressure setting instructions ts Ifthe operation or performance of the pump changes during use refer to Troubleshooting on page II of this
23. t without the consent of ArjoHuntleigh ArjoHuntleigh 2012 iv 1 Introduction About this Manual Intended Use About Flowtron Excel This manual is your introduction to the Flowtron Excel system You must read and fully understand this manual before using the system Use this manual to initially set up the system and keep it as a reference for day to day routines and as a guide to maintenance If you have any difficulties in setting up or using the Flowtron Excel system contact your local ArjoHuntleigh sales office listed at the end of this manual The intended use of this product is to prevent Deep Vein Thrombosis DVT The garments are single use only It is not for use in the home healthcare environment The Flowtron Excel system should be used as part of a prescribed plan of care refer to Indications on page 3 The Flowtron Excel pump operates on a 60 second automatically timed cycle consisting of approximately 12 seconds of inflation followed by approximately 48 seconds of deflation The Flowtron Excel system may be used on patients at risk of developing deep vein thrombosis and in conjunction with systemic interventions e g anticoagulation drugs for the high risk patient The Flowtron Excel is intended for use ONLY in Professional Healthcare Facilities e g hospitals or physicians offices A full technical description of the Flowtron Excel system can be found in the Service Ma
24. to be maintenance free between service periods ArjoHuntleigh will make available on request service manuals component parts lists and other information necessary for ArjoHuntleigh trained personnel to repair the system ArjoHuntleigh recommend that the Flowtron Excel pump is serviced every 12 months by an ArjoHuntleigh authorised service agent Check all electrical connections and power cable for signs of excessive wear Check the tubeset and connectors for any damage In the event of the pump being subjected to abnormal treatment e g immersed in water or dropped the unit must be returned to an authorised service centre The serial number for the pump is on the label on the back of the pump case Quote this serial number when requesting service 10 9 Troubleshooting The Flowtron Excel system features an audible and visual alarm If a problem occurs the system will sense the fault and briefly flash a message on the front panel pressure display If the same fault continues for 10 successive inflations the audible alarm will sound and a flashing message will remain on the pressure display until corrective action is completed C The exception to this is an F fault which will alarm immediately Problem Corrective Action Hose disconnected at garment Check the hose connection at garment end Garment leak Check garment and replace if faulty Low pressure Call the service engineer Hose k
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