Arjo Flowtron ACS900 User manual

Flowtron ACS900
526933ZH-t Rev F 06/2019
INSTRUCTIONS FOR USE
EN •ZH-T
ἧ䓐婒㖶

Design Policy and Copyright
® and ™ are trademarks belonging to the Arjo group of companies.
© Arjo 2019.
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 part without the
consent of Arjo.
姕妰㓧䫾␴䇰㪲
® ␴!™ 堐䣢䚠ㅱ⓮㧁Ⱄ㕤!Arjo 普⛀℔⎠ˤ
© Arjo 2019.
⚈㛔℔⎠⮎㕥㊩临㓡忚󰶔㓧䫾炻㓭ᾅ䔁嬲㚜姕妰󰶔㪲⇑炻ỮᶵḰḳ󱂑忂䞍ˤ
㛒䴻!Arjo ⎴シ炻ᶵ⼿⮵㛔↢䇰䈑忚埴ℐ悐ㆾ悐ấ墯墥ˤ
WARNING
To avoid injury, always read this Instructions for Use and accompanied documents
before using the product.
Mandatory to read the Instructions for Use
警告
為避免造成傷害，使用本產品前請務必閱讀本使用手冊和隨附文件。
使用者務必閱讀本使用手冊

Contents
General Safety .........................................................................................................4
Introduction .............................................................................................................6
About this Manual .....................................................................................................6
Intended Use .............................................................................................................6
About the Flowtron ACS900 System .........................................................................6
Pump: Front View ......................................................................................................7
Pump: Rear View ......................................................................................................7
Clinical Applications ...............................................................................................8
Indications .................................................................................................................8
Contraindications ......................................................................................................8
Cautions ....................................................................................................................9
Guidelines and Recommendations ...........................................................................10
Controls, Alarms and Indicators ............................................................................11
Control Panel with Typical LCD Screen View in Run Mode ......................................11
LCD Screen Icons .....................................................................................................12
LED Indicators on the Pump Case ............................................................................15
Operation .................................................................................................................16
General .....................................................................................................................16
Installing the Pump ....................................................................................................16
Start Up .....................................................................................................................16
Standby Screens .......................................................................................................17
Starting Therapy ........................................................................................................18
Stopping Therapy ......................................................................................................21
Switching Off the Pump .............................................................................................21
Warnings/Alarms .......................................................................................................23
Settings Adjustment ..................................................................................................24
Cleaning and Disinfection ......................................................................................25
Routine Maintenance ..............................................................................................26
Flowtron ACS900 System .........................................................................................26
Serial Labels .............................................................................................................26
Troubleshooting ......................................................................................................27
General .....................................................................................................................27
Troubleshooting Table ..............................................................................................27
Accessories .............................................................................................................33
Technical Specification ..........................................................................................34
Pump Specification ...................................................................................................34
Electromagnetic Compatibility ...................................................................................35
Symbols ....................................................................................................................38

目錄
一般安全須知 .............................................................................................................40
簡介 ...........................................................................................................................42
關於此手冊 ................................................................................................................42
設計用途 ....................................................................................................................42
關於 Flowtron ACS900 系統 ......................................................................................42
加壓機：前視圖 .........................................................................................................43
加壓機：後視圖 .........................................................................................................44
臨床應用 ....................................................................................................................45
適應症 .......................................................................................................................45
禁忌症 .......................................................................................................................45
注意事項 ....................................................................................................................46
指南與建議 ................................................................................................................47
控制器、警報與警示器 ..............................................................................................48
在運行模式下的獨特 LCD 螢幕控制面板 ...................................................................48
LCD 螢幕圖示 ............................................................................................................49
加壓機外殼上的 LED 指示燈 .....................................................................................52
操作 ...........................................................................................................................53
概述 ...........................................................................................................................53
安裝加壓機 ................................................................................................................53
啟動 ...........................................................................................................................53
待機螢幕 ....................................................................................................................54
開始治療 ....................................................................................................................55
停止治療 ....................................................................................................................59
關閉加壓機 ................................................................................................................59
警告 /警報 .................................................................................................................60
設定調整 ....................................................................................................................61
清潔和消毒 ................................................................................................................62
例行維護 ....................................................................................................................63
Flowtron ACS900 系統 ..............................................................................................63
序號標籤 ....................................................................................................................63
疑難排解 ....................................................................................................................64
概述 ...........................................................................................................................64
疑難排解表 ................................................................................................................64
配件 ...........................................................................................................................69
技術規格 ....................................................................................................................70
加壓機規格 ................................................................................................................70
電磁相容性 ................................................................................................................71
符號 ...........................................................................................................................74

4
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:
• EN60601-1:2006/A1:2013 and IEC 60601-1:2005/A1:2012
• ANSI/AAMI ES 60601-1(2005)+AMD(2012) and CAN/CSA C22.2 No.60601-1
(2008)+(2014).
Safety Warnings
• It is the responsibility of the caregiver to ensure that the user can use this product
safely.
• 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.
• 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.
• The mains power socket/plug must be accessible at all times. To disconnect the
pump completely from the electricity supply, remove the plug from the mains
power socket.
• 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.
• Do not use the pump in the presence of uncontained flammable liquids or gasses.
• Only the pump and garment combination as indicated by Arjo should be used. The
correct function of the product cannot be guaranteed if incorrect pump and
garment combinations are used.
• The Flowtron ACS900 system is intended for use only in hospitals and other health
care facilities, under the supervision of an appropriately qualified clinical
professional. The Flowtron ACS900 system should be used as part of a prescribed
plan of care.
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:
• Do not expose the system to open flames, such as cigarettes, etc.
• Do not store the system in direct sunlight.
• Do not use phenol-based solutions to clean the system.
• Make sure the system is clean and dry prior to use or storage.
• If a serious incident occurs in relation to this medical device, affecting the user, or the
patient then the user or patient should report the serious incident to the medical device
manufacturer or the distributor. In the European Union, the user should also report the
serious incident to the Competent Authority in the member state where they are located.

5
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:
• The use of accessories not specified by the manufacturer may result in increased
emissions by, or decreased immunity of, the equipment, affecting its performance.
• Portable and mobile radio frequency (RF) communications equipment (for example
mobile/cell phones) can affect medical electrical equipment.
• If this equipment needs to be used adjacent to other electrical equipment, normal
operation must be checked before use.
• For detailed EMC information contact Arjo service personnel.
Expected Service Life
The 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 your Arjo
distributor.
Do NOT use unapproved accessories or attempt to modify, disassemble or otherwise misuse
the system. Failure to observe this caution could result in injury, or in extreme cases, death.
End of Life Disposal
• Garment material or any other textiles, polymers or plastic materials etc. should be sorted
as combustible waste.
• Pump units have electrical and electronic components should be disassembled and
recycled per Waste of Electrical and Electronic Equipment (WEEE) or in accordance with
local or national regulation.
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 Arjo for information on correct disposal.

6
1. Introduction
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About the Flowtron
ACS900 System
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7
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Pump: Front View
Pump: Rear View
LCD Screen
LED Indicators
Garment Tubeset Connector 1
Control Buttons
Connectors
Tubeset Connector 2
(Blue Button)
(Orange Button)
Swing-out
Bed-Hooks
Mains Power Cord
Tubeset Retention Clips
Mains Power Cord Retention Clip
Power Button
Swing-out
Bed-Hooks
Integral Carry Handle
Mains Power
LED Indicator
Integral Tube and
Cable Management
System
Cord
(on underside)
USB Port
(refer to Service
Manual SER0026)

8
2. Clinical Applications
Indications 7KHLQWHQGHGXVHRIWKHFlowtron$&6V\VWHPLVWR
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The type of garment used on an individual patient
must be specified by a physician.
Contraindications
Uniform & Sequential
Calf and Calf & Thigh
Garments
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9
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If you are unsure of any contraindications refer to
the patient’s physician before using the device.
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 7KHSDWLHQW¶VVNLQVKRXOGEHLQVSHFWHGIUHTXHQWO\
GXULQJHYHU\VKLIW
Many patients are at risk for pressure ulcers on the
heel. Use of the foot garments does not negate the
necessity for heel protection and appropriate skin
care.
 &OLQLFDOMXGJHPHQWLVUHTXLUHGWRGHWHUPLQHLIWKH
SDWLHQWVVNLQFRQGLWLRQUHTXLUHVDGGLWLRQDO
SURWHFWLYHPHDVXUHVRULIWKHWKHUDS\VKRXOGEH
GLVFRQWLQXHGDQGDQDOWHUQDWLYHPRGDOLW\XVHG
 *DUPHQWVVKRXOGEHUHPRYHGLPPHGLDWHO\LIWKH
SDWLHQWH[SHULHQFHVWLQJOLQJQXPEQHVVRUSDLQDQG
WKHSK\VLFLDQQRWLILHG

10
 :KHQXVHGIRU'97SUHYHQWLRQFRQWLQXRXV
H[WHUQDOSQHXPDWLFFRPSUHVVLRQLVUHFRPPHQGHG
XQWLOWKHSDWLHQWLVIXOO\DPEXODWRU\8QLQWHUUXSWHG
XVHRIWKHV\VWHPLVHQFRXUDJHG
 7KHV\VWHPVKRXOGEH86(':,7+&$87,21
RQSDWLHQWVZLWK
 ,QVHQVLWLYHH[WUHPLWLHV
 'LDEHWHV
 ,PSDLUHGFLUFXODWLRQ
 )UDJLOHRULPSDLUHGVNLQ
These are guidelines only and should not replace
clinical judgement and experience.
Guidelines and Recommendations
General
Recommendations
 7KHV\VWHPVKRXOGEHLQLWLDWHGLPPHGLDWHO\RQFHWKH
ULVNRI'97IRUPDWLRQLVLGHQWLILHGDQGWKHSODQRI
FDUHKDVEHHQSUHVFULEHG
 ,IFRPSUHVVLRQVWRFNLQJVDUHRUGHUHGE\WKH
SK\VLFLDQWKHFOLQLFLDQVKRXOGHQVXUHWKDWWKH
FRPSUHVVLRQVWRFNLQJVDUHSURSHUO\PHDVXUHG
DSSOLHGDQGZRUQE\WKHSDWLHQW$Q\FRPSUHVVLRQ
VWRFNLQJXVHGVKRXOGEHURXWLQHO\FKHFNHGWRHQVXUH
FRQWLQXHGSURSHUILWDQGDSSOLFDWLRQLQDGGLWLRQWR
DVVHVVLQJWKHFRQGLWLRQRIWKHVNLQ
 :KHUHDSSURSULDWHSDWLHQWVVKRXOGEHLQVWUXFWHGLQ
WKHSURSHUXVHRIWKHV\VWHPWKHSXUSRVHRIWKHUDS\
DQGWKDWDQ\SUREOHPVVKRXOGEHUHSRUWHGWRWKH
QXUVLQJVWDII
 )RUVXUJLFDOSDWLHQWVWKHV\VWHPVKRXOGEHDSSOLHGWR
WKHSDWLHQWSUHRSHUDWLYHO\SULRUWRWKHLQGXFWLRQRI
DQDHVWKHVLD
 7KHV\VWHPVKRXOGEHXVHGFRQWLQXRXVO\IRUQROHVV
WKDQKRXUVSRVWRSHUDWLYHO\RUXQWLOWKHSDWLHQW
EHFRPHVIXOO\DPEXODWRU\
 ,IWKHJDUPHQWFDQQRWEHDSSOLHGWRWKHRSHUDWLYH
OLPEGXULQJVXUJHU\LWPD\EHDSSOLHGWRWKHOLPE
RQFHWKHSDWLHQWUHDFKHVWKHUHFRYHU\XQLW

11
3. Controls, Alarms and Indicators
Control Panel with Typical LCD Screen View in Run Mode
Power Button
and Mains Indicator
7RVZLWFKWKHSXPSRQ
 &RQQHFWWKHSXPSWRPDLQVSRZHUDQGWKHSXPSZLOO
UXQLWVLQWHUQDOGLDJQRVWLFWHVWVDQGJRWR6WDQGE\
UHIHUWR³6WDQGE\6FUHHQV´RQSDJH 
 ,IWKHSXPSLVDOUHDG\FRQQHFWHGWRPDLQVSRZHU
SUHVVDQGKROGWKH3RZHUEXWWRQIRUDSSUR[LPDWHO\
VHFRQGVDQGWKHSXPSZLOOJRGLUHFWO\WR6WDQGE\
 ,IWKHSXPSLVQRWFRQQHFWHGWRPDLQVSRZHUSUHVV
DQGKROGWKH3RZHUEXWWRQIRUDSSUR[LPDWHO\
VHFRQGVDQGWKHSXPSZLOOUXQLWVLQWHUQDOGLDJQRVWLF
WHVWVDQGJRWR6WDQGE\
7KH0DLQVLQGLFDWRUDERYHWKH3RZHUEXWWRQVKRZVWKH
PDLQVSRZHUVWDWXVRIWKHSXPS
 ([WLQJXLVKHGPDLQVSRZHULVGLVFRQQHFWHG
 ,OOXPLQDWHGJUHHQPDLQVSRZHULVFRQQHFWHGWRWKH
SXPS
7RVZLWFKRIIWKHSXPSSUHVVDQGKROGWKH3RZHUEXWWRQ
IRUDSSUR[LPDWHO\VHFRQGV7KHQ
 ,IWKHSXPSLVFRQQHFWHGWRPDLQVSRZHUWKH/&'
VFUHHQEDFNOLJKWZLOOEHH[WLQJXLVKHGDQGRQO\WKH
PDLQVSRZHUDQGEDWWHU\LQGLFDWLRQLFRQVZLOOEH
GLVSOD\HG5HOHDVHWKHEXWWRQ
 ,IWKHSXPSLVQRWFRQQHFWHGWRPDLQVSRZHUWKH
SXPSZLOOSRZHUGRZQDQGWKH/&'VFUHHQZLOOEH
EODQN5HOHDVHWKHEXWWRQ
Mains Indicator
Right Control Button
Power Button
LCD Screen
Left Control Button Middle Control Button

12
Middle Control Button :KHQWKHSXPSLVLQ6WDQGE\DQGRQHRUWZRJDUPHQWV
DUHFRQQHFWHGSUHVVWKLVEXWWRQWRSXWWKHSXPSLQWRWKH
5XQPRGHDQGVWDUWWKHUDS\WKH/('LQGLFDWRUVRQWKH
IURQWDQGXQGHUVLGHRIWKHFDVHZLOOEHLOOXPLQDWHGJUHHQ
7RVWRSWKHWKHUDS\DQGSXWWKHSXPSLQWR6WDQGE\SUHVV
DQGKROGWKLVEXWWRQIRUDSSUR[LPDWHO\VHFRQGVXQWLO
WKH6WDQGE\VFUHHQLVGLVSOD\HGDQGWKHQUHOHDVHWKH
EXWWRQ7KH/('LQGLFDWRUVRQWKHIURQWFDVHZLOOEH
H[WLQJXLVKHG
Left Control Button ,IDQDXGLEOHDODUPVRXQGVGXULQJWKHUDS\SUHVVWKLV
EXWWRQWRPXWHWKHDXGLEOHDODUP
Only certain alarms can be muted.
Refer to “Troubleshooting” on page 27 for details
of the various alarm conditions and possible
corrective actions to rectify the faults.
:KHQWKHSXPSLVLQ6WDQGE\SUHVVWKLVEXWWRQWR
FKDQJHWKHDODUPYROXPHUHIHUWR³7R&KDQJHWKH
$XGLEOH$ODUP9ROXPH6HWWLQJ´RQSDJH 
Right Control Button 3UHVVWKLVEXWWRQWRUHVHWWKHSDWLHQWUXQKRXUV7KLVFDQ
EHGRQHHLWKHUDWSRZHUXSDIWHUWKHSXPSKDVLQLWLDOLVHG
RULIWKHWKHUDS\LVVWRSSHGDQGWKHSXPSLVLQ6WDQGE\
UHIHUWR³5HVHWWLQJWKH3DWLHQW5XQ+RXUV´RQSDJH 
LCD Screen Icons 7KLVVFUHHQVKRZVWKHSRVLWLRQDQGGHVFULSWLRQRIDOO
SRVVLEOHLFRQVZKLFKFDQEHGLVSOD\HG7KHDFWXDOLFRQV
ZKLFKZLOOEHGLVSOD\HGZLOOGHSHQGRQWKHSXPSVWDWXV
SDWLHQWWKHUDS\DQGZKHWKHUDIDXOWKDVEHHQGHWHFWHG
Garment Mains Power
Battery Level
Pressure
Indication
Not Connected
Mains Power
Connected
Indication
High Temperature
Warning/Alarm
Hardware Fault/
Patient
Run Hours
Wait/
Initialising
Start/Stop
Therapy
Kinked/
Blocked Tube
Low Pressure/
Leak
Audible
Audible
Audible Alarm
Volume
Garment Type
and Inflation
Indication
Alarm
Indication
Alarm Status
Tubeset
Connector
Number
Alarm
Muted
Service Required

13
Garment Type and
Inflation Indication
7KHVHVKRZZKLFKJDUPHQWW\SHLVFRQQHFWHGWRHDFK
WXEHVHWDQGZKHQHDFKJDUPHQWLVEHLQJLQIODWHG
A garment connected but not inflated is shown as an
outline on the leg icon. When it is inflated, the
garment outline is filled in black.
Tubeset Connector
Number
7KHJDUPHQWFRQQHFWRURQWKHHQGRIHDFKWXEHVHWKDVD
SXVKEXWWRQZKLFKLVFRORXUFRGHGDQGKDVDQXPEHU
PDUNHGRQLWEOXH³´RURUDQJH³´7KHQXPEHUV
FRUUHVSRQGZLWKWKH³´DQG³´RQWKHOHIWVLGHRIWKH
/&'VFUHHQDGMDFHQWWRWKHOHJLFRQV
Start/Stop Therapy 7KHLFRQDERYHWKH0LGGOH&RQWUROEXWWRQFKDQJHV
EHWZHHQ5XQDQG6WDQGE\PRGHVDVIROORZV
Garment Pressure
Indication
7KHGHIDXOWWDUJHWLQIODWLRQSUHVVXUHIRUHDFKJDUPHQWLV
DVIROORZV
 )RRW PP+J
 8QLIRUPFDOIDQGFDOIWKLJK PP+J
 6HTXHQWLDOFDOIDQGFDOIWKLJK PP+J
Garment Connected and
Not Inflated
Connected and
Inflated
Foot
Uniform (DVT) Calf
(or Calf & Thigh)
Sequential (Tri Pulse) Calf
(or Calf & Thigh)
Start Therapy icon. In normal operation, this
icon is displayed when the pump is in
Standby and at least one garment is
connected. Press the button to start therapy.
Stop Therapy icon. In normal operation, this
icon is displayed when the pump is in Run
mode. Press the button to stop therapy.

14
Mains Power
Indication
Battery Indication :KHQWKHSXPSLVFRQQHFWHGWRWKHPDLQVSRZHUVXSSO\
 ,IWKHEDWWHU\LVIXOO\FKDUJHGWKHLQGLFDWRUZLOOEH
VWDWLFDQGVKRZ³IXOO´
 ,IWKHEDWWHU\LVQRWIXOO\FKDUJHGWKHLQGLFDWRUZLOO
VFUROOIURP³%DWWHU\(PSW\´WRWKHFXUUHQWEDWWHU\
FDSDFLW\IRUH[DPSOH³%DWWHU\ò)XOO´WRLQGLFDWH
WKDWWKHSXPSLVEHLQJFKDUJHG
:KHQWKHSXPSLV127FRQQHFWHGWRWKHPDLQVSRZHU
VXSSO\WKHLQGLFDWRULVVWDWLFDQGVKRZVWKHDSSUR[LPDWH
FKDUJHUHPDLQLQJLQWKHEDWWHU\
If the pump is not connected to the mains power
supply and the battery is fully charged and in good
condition, the pump will continue to operate
normally for approximately 12 hours for calf and
calf and thigh garments, and for approximately 6
hours for foot garments.
The battery has a service life of 5 years
(approximately 600 charge cycles). It is not user
replaceable and must be replaced as part of the
service procedure.
Wait/Initialising 7KLVLVDURWDWLQJVHJPHQWFLUFXODULFRQZKLFK
LQGLFDWHVWKDWWKHSXPSLVLQLWLDOLVLQJDIWHUSRZHUXS
Patient Run Hours 7KLVVKRZVWKHWRWDOSXPSUXQWLPHLQKRXUV5HIHUWR
³5HVHWWLQJWKH3DWLHQW5XQ+RXUV´RQSDJH WRFOHDU
WKHSDWLHQWUXQKRXUV
This is the pump run time since the patient run hours
was last reset.
The pump is connected to the mains power
supply.
The pump is NOT connected to the mains
power supply.
Battery Empty Battery ¼ Full
Battery ½ Full Battery ¾ Full
Battery Full

15
Audible Alarm Status :KHQDQDODUPZKLFKLVDEOHWREHPXWHGLVVKRZQRQ
WKH/&'VFUHHQWKLVLFRQLVVKRZQWRLQGLFDWHWKDWWKH
DODUPFDQQRZEHPXWHG
:KHQWKHSXPSLVLQ6WDQGE\WKLVLFRQLQGLFDWHVWKDWWKH
DODUPYROXPHFDQEHFKDQJHGUHIHUWR³7R&KDQJHWKH
$XGLEOH$ODUP9ROXPH6HWWLQJ´RQSDJH 
Audible Alarm Muted 7KLVLFRQLQGLFDWHVWKDWWKHDXGLEOHDODUPKDVEHHQ
PXWHG
Warning and Alarm
Indications
7KHIROORZLQJILYHLFRQVLQGLFDWHWKDWDIDXOWKDVEHHQ
GHWHFWHGLQWKHV\VWHP5HIHUWR³7URXEOHVKRRWLQJ´RQ
SDJH IRUDOLVWRIIDXOWFRQGLWLRQVWKHFRUUHVSRQGLQJ
ZDUQLQJDQGDODUPLQGLFDWLRQVDQGSRVVLEOHFRUUHFWLYH
DFWLRQVWRUHFWLI\WKHIDXOWV
LED Indicators on the
Pump Case
7KHUHDUHDGGLWLRQDO/('LQGLFDWRUVRQWKHSXPSWR
VKRZSXPSVWDWXVDQGDODUPV
 7ZRVHWVRQWKHIURQWRIWKHSXPS
 2QHVHWRQWKHXQGHUVLGHRIWKHSXPS
7KHLUVWDWXVLVDVIROORZV
Alarm detected which may cause an
interruption in therapy.
Low pressure or garment leak.
Kinked or blocked tubeset.
High temperature.
Hardware fault detected or periodic service
required.
LED Colours Pump Status Warnings/Alarms
Extinguished Off or Standby - -
Green Run • No fault detected.
• Warning only detected.
Yellow Run Fault detected with full audible and visual alarm.

16
4. Operation
General 7KHVHLQVWUXFWLRQVFRYHUWKHURXWLQHRSHUDWLRQRIWKH
V\VWHP2WKHURSHUDWLRQVVXFKDVPDLQWHQDQFHDQG
UHSDLUVKRXOGRQO\EHFDUULHGRXWE\VXLWDEO\TXDOLILHG
SHUVRQQHO
5HIHUWR³&RQWUROV$ODUPVDQG,QGLFDWRUV´RQSDJH 
IRUDGHVFULSWLRQRIWKHFRQWUROVLQGLFDWRUVDQG/&'
VFUHHQ
If the operation or performance of the pump
changes during use, refer to “Troubleshooting” on
page 27 of this IFU before calling a service
engineer or contacting your local Arjo sales office.
Installing the Pump  7KHSXPSVKRXOGEHSODFHGIHHWGRZQRQDQ\
FRQYHQLHQWKRUL]RQWDOVXUIDFHRUDOWHUQDWLYHO\
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Mains Power Connected Mains Power Disconnected

17
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The Start Therapy icon does not appear until at least
one garment is connected to a tubeset connector.
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Garments are for single patient use only. Do not use
the garments on multiple patients.
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Major Revision
Minor Revision

18
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A garment connected but not inflated is shown as an
outline on the leg icon. When it is inflated, the
garment outline is filled in black.
The same garment outline is used for both calf and
calf & thigh garments.
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Tubeset
Connector 1
Tubeset
Connector 2
No garment connected
Foot garment
Tubeset
Connector 1
Tubeset
Connector 2
Sequential (Tri Pulse) calf or
calf & thigh garment
No garment connected
Tubeset
Connector 1
Tubeset
Connector 2
Uniform (DVT) calf or calf &
thigh garment
Uniform (DVT) calf or calf &
thigh garment
Tubeset
Connector 1
Tubeset
Connector 2
Foot garment
Uniform (DVT) calf or calf &
thigh garment