System One User Manual - Discount Medical Supply
Contents
1. REMstar RESPIRONICS 2009 Respironics Inc and its affiliates All rights reserved Table of Contents Intended OS sc 2 ulvejgcii seeni A EAEE R A E N EEA a GE 2 WV AUTH S erriei n e E E A E A AR E N RRA 2 S Up R EE T RE SE S 3 Comtrraindications E EE E E 3 Sync A E E E EAE E E 3 System CONTEMES sstart EET 4 VEON A EN E O O E E O T E 4 eeepc 5 Installing I PeMinl rre e 6 Connecting the Breathing Circuit siscsssssccssssssvasssssessenessscaiesostsassosscveccsonsastsltgesaetescedasascosipaaeuuseassnsacbadipeaessadesoniates 6 Where to Place the Device Supplying AC Power tothe D evice erret ttes tete tita reaR doses tesi eben 7 Navigating the D evice Screeri nep eon etes pete eire eee deve A NE 7 Ki igrDLAUIBIS em 7 DeinR l cc 8 Setup SCHESM M Q 8 n 9 Device Alerts Troubleshooting eese m 13 ll m 14 Traveling With Acum 15 Cleaning the Device P 15 Cleaning or Replacing the Filtets si sissscsssussnssasestsssaescsecoisussouasissusscossnsstuesavsaiesabensssdsebustozendessssasgseerdisavsbeassasa4s 15 e ADM2. M 15 Service Nhreljel m 16 DisPOSal ais E 17 How to Contact Resplrohies o ncitrretcttt n isttstto mestiere petro ER En Rug aes EUR EHE De pee b de M EDM Res ai 17 i2Mieiiniuii 18 limited Warranty caeci EE rti rebat eet esi bt epu etr EEE ee eus Back Page User Manual CAUTION U S federal law restricts this device to sale by or on the order of a physician Intended Use The Respironics REMstar system delivers positive airway pressure therapy for the treatment of Obstructive Sleep Apnea in spontaneously breathing patients weighing over 30kg 66 Ibs It is for use in the home or hospital institutional environment Important The device is to be used only on the instruction of a licensed physician Your home care provider will make the correct pressure settings according to your health care professional s prescription Several accessories are available to make your OSA treatment with the REMstar system as convenient and comfortable as possible To ensure that you receive the safe effective therapy prescribed for you use only Respironics accessories Warnings A warning indicates the possibility of injury to the user or the operator This manual serves as a reference The instructions in this manual are not intended to supersede the health care professional s instructions regarding the use of the device The operator should read and
3. If Ramp has not been prescribed for you discuss this feature with your home care provider to see if they will change your prescription If your provider has enabled Ramp but the feature still does not work check the CPAP setting on your Active Display screen If CPAP is set to the minimum setting 4 0 cm H O or the starting pressure is the same as the prescribed pressure the Ramp feature will not work Make sure that the ramp time setting is gt 0 The airflow is much warmer than usual The air filters may be dirty The device may be operating in direct sunlight or near a heater Clean or replace the air filters The temperature of the air may vary somewhat based on your room temperature Make sure that the device is properly ventilated Keep the device away from bedding or curtains that could block the flow of air around the device Make sure the device is away from direct sunlight and heating equipment If using the humidifier with the device check the humidifier settings Refer to the humidifier instructions to make sure the humidifier is working properly If the problem continues contact your home care provider User Manual 13 Accessories There are several accessories available for your REMstar system such as a humidifier or a modem Contact your home care provider for additional information on the available accessories When using optional accessories always follow the instructions enclos
4. User Manual 9 Device Alerts High Priority These alerts require immediate operator response The alert signal consists of a high priority sound which is a continuous two beep pattern indicated in the following table as e e Additionally the backlights on the buttons will provide a high priority flashing pattern consisting of a continuous bright to off two flash pattern indicated in the following table as 00 00 Medium Priority These alerts require prompt operator response The alert signal consists of a medium priority sound which is a continuous one beep pattern indicated in the following table as Additionally the backlights on the buttons will provide a medium priority flashing pattern consisting of a continuous bright to dim one flash pattern indicated in the following table as 0 Alert Summary Table The following table summarizes the alerts ALERT Service Required AUDIBLE INDICATOR VISUAL INDICATOR 00 00 Screen displays Service required indicating that service is required Device AcTION The device enters the Safe state in which the device power remains on but the airflow is disabled PossiBLE Cause Device failure PaTiENT ACTION Press either the wheel or ramp button to silence the alert Remove the power supply cord from the device to remove power Plug the cord back into the device s power inlet to restore power If the alert continues to occur contact
5. Power Cord and Battery Adapter Cable Use of any other system may cause damage to the device Contraindications When assessing the relative risks and benefits of using this equipment the clinician should understand that this device can deliver pressures up to 20 cm H O In the event of certain fault conditions a maximum pressure of 30 cm H O is possible Studies have shown that the following pre existing conditions may contraindicate the use of CPAP therapy for some patients Bullous Lung Disease Pathologically Low Blood Pressure Bypassed Upper Airway Pneumothorax Pneumocephalus has been reported in a patient using nasal Continuous Positive Airway Pressure Caution should be used when prescribing CPAP for susceptible patients such as those with cerebral spinal fluid CSF leaks abnormalities of the cribriform plate prior history of head trauma and or pneumocephalus Chest 1989 96 1425 1426 The use of positive airway pressure therapy may be temporarily contraindicated if you exhibit signs of a sinus or middle ear infection Not for use with patients whose upper airways are bypassed Contact your health care professional if you have any questions concerning your therapy Symbol Key The following symbols may appear on the device and power supply User Manual SYMBOL DEFINITION SYMBOL DEFINITION EN Separate collection for electrical and electronic l Corisult acesmpanying ee forze equipment per EC Directive 2002 9
6. Valve must be placed in line with the patient circuit after the oxygen source Failure to use the pressure valve could result in a fire hazard Do not connect the device to an unregulated or high pressure oxygen source Donotuse the device in the presence of a flammable anaesthetic mixture in combination with oxygen or air or in the presence of nitrous oxide Do not use the device near a source of toxic or harmful vapors Do not use this device if the room temperature is warmer than 35 C 95 F If the device is used at room temperatures warmer than 35 C 95 F the temperature of the airflow may exceed 43 C 109 F This could cause irritation or injury to your airway Do not operate the device in direct sunlight or near a heating appliance because these conditions can increase the temperature of the air coming out of the device Contact your health care professional if symptoms of sleep apnea recur If you notice any unexplained changes in the performance of this device if it is making unusual or harsh sounds if it has been dropped or mishandled if water is spilled into the enclosure or if the enclosure is broken disconnect the power cord and discontinue use Contact your home care provider Repairs and adjustments must be performed by Respironics authorized service personnel only Unauthorized service could cause injury invalidate the warranty or result in costly damage Periodically inspect electrical cords and cabl
7. in such an environment IMMUNITY TEST IEC 60601 Test LeveL COMPLIANCE LeveL Conducted RF 3 Vrms 3 Vrms IEC 61000 4 6 150 kHz to 80 MHz Radiated RF 3 V m IEC 61000 4 3 80 MHz to 2 5 GHz 3 V m ELECTROMAGNETIC ENVIRONMENT GUIDANCE Portable and mobile RF communications equipment should be used no closer to any part of the device including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 12 P d 1 2 P d 223 P 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 meters m 80 MHz to 800 MHz 800 MHz to 2 5 GHz 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 1 NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies objects and people NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures 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
8. screen displays the total therapy hours for the device the total blower hours and the total number of days used when the sessions were greater than 4 hours since the device was last reset by the home care provider This screen also displays a compliance number used by your home care provider to validate that the data provided by you is the data taken from this screen This setting only appears if your provider has enabled this feature Compliance VIC Visual Inspection Check This screen displays the start date and the total number of days used when the sessions were greater than 4 hours This screen also displays a check code number used by your home care provider to validate that the data provided by you is the data taken from this screen This setting only appears if your provider has enabled this feature Therapy hours The device is capable of recognizing the difference between the time the patient is actually receiving therapy and the time when the blower is simply running This screen displays the average amount of time the patient is actually receiving therapy on the device over a 7 day and 30 day time frame provided the device has at least 7 or 30 days of data respectively If the device has only 5 days of data to use for the calculation the 5 day average value will be seen under the 7 day display Days gt 4 This screen displays the cumulative number of device therapy sessions that exceeded 4 hours over a 7 day and 30 day time frame
9. 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 device is used exceeds the applicable RF compliance level above the device should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the device b Over the frequency range 150 kHz to 80 MHz the field strengths should be less than 3 V m User Manual 19 Recommended Separation Distances between Portable and Mobile RF Communications Equipment and This Device The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and this device as recommended below according to the maximum output power of the communications equipment Rateb Maximum Power SEPARATION DisTANCE ACCORDING TO FREQUENCY OF TRANSMITTER OUTPUT OF TRANSMITTER M Ww 150 kHz To 80 MHz 80 MHz ro 800 MHz 800 MHz ro 2 5 GHz dz 1 2 dP dz 1 2 4P dz 2 3 JP 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 12 12 23 10 3 8 3 8 73 100 12 12 23 For transmitters rated at a maximum output power not listed abo
10. transitions the provider set a patient reminder scheduled provider from on to off to pop up at a particular time to Alert present for remind you to replace your mask 6 minutes or until change your filters etc Check user acknowledges your mask a new one may be available Call your provider is the default message The provider may change the message Instant Message single beep Home care Only displayed when Message from Your home care provider may provider will therapy is off the provider send an instant message Contact supply text to be your home care provider with any displayed questions SD Card Prescription single beep Screen displays Alert present for n a Card status can be checked in Accepted SD card inserted 30 seconds or until Status menu prescription user acknowledges accepted SD Card Prescription single beep 09 Alert present for Prescription Contact your home care provider Rejected Screen displays 30 seconds or until missing or for correct prescription SD card inserted user acknowledges incorrect prescription rejected SD Card Inserted e o 09 Alert present until SD card Alert is present until card is Incorrectly Screen displays action is taken inserted removed Remove SD card and SD card inserted incorrectly reinsert correctly If the alert incorrectly continues to occur contact your home care provider SD Card Full e o 09 Alert present until SD card is f
11. 6 EC DC Power Class Il Double Insulated IPX1 Drip Proof Equipment Do not disassemble Type BF Applied Part a For Indoor Use Only System Contents Your REMstar system includes the following items Device Side cover panel User manual SD card Carrying case Reusable gray foam filter Flexible tubing Disposable ultra fine filter optional Power cord and power supply Humidifier optional Note If any of these items are missing contact your home care provider System Overview The REMstar is a CPAP Continuous Positive Airway Pressure device designed for the treatment of Obstructive Sleep Apnea OSA CPAP maintains a constant level of pressure throughout the breathing cycle When prescribed for you the device provides a special feature to help make your therapy more comfortable The ramp function allows you to lower the pressure when you are trying to fall asleep The air pressure will gradually increase until your prescription pressure is reached You also have the option of not using the ramp feature at all Several accessories are also available for use with your REMstar device Contact your home care provider to purchase any accessories not included with your system SD Card Accessory Slot Air Outlet Port Power Inlet Filter Area This figure illustrates some of the device features described in the following table Device FEATURE DESCRI
12. PTION Air Outlet Port Connect the flexible tubing here conical 22 mm SD Card Accessory Slot If applicable insert the optional accessory SD card here SD Card Cover If applicable the optional accessories such as a Link Module or Modem can be installed here Refer to the instructions supplied with the accessory When not using an accessory this cover must be in place on the device Power Inlet Connect the power cord here Filter Area A reusable gray foam filter must be placed in the filter area to screen out normal household dust and pollens An optional white ultra fine filter can also be used for more complete filtration of very fine particles Side Cover If using a humidifier with the device this side cover can be easily removed with the release tab before attaching the humidifier Refer to the humidifier manual When not using a humidifier this cover must be in place on the device 4 User Manual Controls Buttons Humidifier Icon amp Number Settings 1 __LCD Display Screen Control Wheel Push Button _ Ramp Button This figure shows the primary control buttons on the device described in the following table FEATURE DESCRIPTION Display Screen Shows therapy settings patient data and other messages The startup screen is shown temporarily when the unit is first powered Humidifier Icon This Icon lights up when the optional humidifier is attached Th
13. e Accuracy Pressure Increments 4 0 to 20 0 cm H O in 0 5 cm H O increments Pressure Stability Static Dynamic Dynamic lt 10 cm H O 2 10 0 to 20 cm H O Device 0 5 cm H O lt 0 5 cm H O lt 1 0 cm H O Device w Humidifier 0 5 cm H O lt 0 5 cm H O lt 1 0 cm H O Maximum Flow Rate Test pressures cm H O 4 0 8 0 12 0 16 0 20 0 Measured pressure at the patient 3 37 7 03 11 44 14 99 18 98 connection port cm H O Average flow at the patient 57 65 91 27 123 90 129 20 115 44 connection port l min Noise Sound Pressure Level 30 dB A This measurement applies to the therapy device with or without the optional Humidifier Sound Power Level 38 dB A 16 User Manual Disposal Separate collection for electrical and electronic equipment per EC Directive 2002 96 EC Dispose of this device in accordance with local regulations How to Contact Respironics To have your device serviced contact your home care provider If you need to contact Respironics directly call the Respironics Customer Service department at 1 800 345 6443 or 1 724 387 4000 You can also use the following address Respironics Inc 1001 Murry Ridge Lane Murrysville PA 15668 User Manual 17 EMC Information Guidance and Manufacturer s Declaration Electromagnetic Emissions This device is intended for use in the electromagnetic environment specified below The user of this device
14. e does not require routine servicing WARNING If you notice any unexplained changes in the performance of this device if it is making unusual or harsh sounds if it has been dropped or mishandled if water is spilled into the enclosure or if the enclosure is broken disconnect the power cord and discontinue use Contact your home care provider User Manual 15 Specifications Environmental Operating Temperature 5 to 35 C 41 to 95 F Storage Temperature 20 to 60 C 4 F to 140 F Relative Humidity operating amp storage 15 to 95 non condensing Atmospheric Pressure 101 to 77 kPa 0 2286 m 0 7500 ft Physical Dimensions 18 x 14 x 10 cm 7 Lx 5 5 W x 4 H Weight Device with power supply Approximately 1 53 kg 3 37 Ibs Standards Compliance This device is designed to conform to the following standards IEC 60601 1 General Requirements for Safety of Medical Electrical Equipment EN ISO 17510 1 Sleep Apnea Breathing Therapy Devices EN 60601 1 2 Electromagnetic Compatibility IEC 60601 1 Classification Type of Protection Against Electric Shock Class Il Equipment Degree of Protection Against Electric Shock Type BF Applied Part Degree of Protection against Ingress of Water device amp AC power supply Drip Proof IPX1 Mode of Operation Continuous Electrical AC Power Consumption 100 240 VAC 50 60 Hz 2 1 A DC Power Consumption 12 VDC 5 0 A Fuses There are no user replaceable fuses Pressur
15. e humidifier number settings are only visible when the humidifier is attached and therapy is active Please refer to the humidifier user manual for more information Control Wheel Push Button Turn the wheel to toggle between options on the screen Press the wheel to choose an option Primary function is to turn airflow on off Ramp Button When the airflow is on this button allows you to activate or restart the ramp function This button lights up when therapy is active or during specific alerts User Manual Installing the Air Filters CAUTION A properly installed undamaged gray foam filter is required for proper operation The device uses a gray foam filter that is washable and reusable and an optional white ultra fine filter that is disposable The reusable filter screens out normal household dust and pollens while the optional ultra fine filter provides more complete filtration of very fine particles The gray reusable filter must be in place at all times when the device is operating The ultra fine filter is recommended for people who are sensitive to tobacco smoke or other small particles A reusable gray foam filter is supplied with the device A disposable ultra fine filter is available as an accessory If your filter is not already installed when you receive your device you must at least install the reusable gray foam filter before using the device To install the filter s 1 If you are using the white disposabl
16. e metal object and bonding oneself by means of a wrist strap to the equipment or system or to earth Before operating the device ensure that the SD card cover is replaced whenever any of the accessories such as the Link Module or Modem are not installed Refer to the instructions that came with your accessory Condensation may damage the device If this device has been exposed to either very hot or very cold temperatures allow it to adjust to room temperature operating temperature before starting therapy Do not operate the device outside of the operating temperature range shown in the Specifications Do not use extension cords with this device Do not place the device directly onto carpet fabric or other flammable materials Do not place the device in or on any container that can collect or hold water A properly installed undamaged reusable foam inlet filter is required for proper operation Tobacco smoke may cause tar build up within the device which may result in the device malfunctioning Dirty inlet filters may cause high operating temperatures that may affect device performance Regularly examine the inlet filters as needed for integrity and cleanliness Never install a wet filter into the device You must ensure sufficient drying time for the cleaned filter When DC power is obtained from a vehicle battery the device should not be used while the vehicle s engine is running Damage to the device may occur Only use a Respironics DC
17. e ultra fine filter insert it into the filter area first mesh side facing in towards the device 2 Insert the required gray foam filter into the filter area after the ultra fine filter Note If you are not using the white disposable filter simply insert the gray foam filter into the filter area Connecting the Breathing Circuit To use the system you will need the following accessories in order to assemble the recommended circuit Respironics interface nasal mask or full face mask with integrated exhalation port or Respironics interface with a separate exhalation device such as the Whisper Swivel II Respironics 1 83 m 6 ft flexible tubing Respironics headgear for the mask WARNING If the device is used by multiple persons such as rental devices a low resistance main flow bacteria filter should be installed in line between the device and the circuit tubing to prevent contamination To connect your breathing circuit to the device complete the following steps 1 Connect the flexible tubing to the air outlet on the side of the device Note If required connect a bacteria filter to the device air outlet and then connect the flexible tubing to the outlet of the bacteria filter Note The bacteria filter is recommended to protect the patient care provider and equipment from the transference of a virus or bacteria through the breathing circuit Note When using the bacteria filter the device performance may be affected Howev
18. ed with the accessories CAUTION Pins of connectors should not be touched Connections should not be made to these connectors unless ESD precautionary procedures are used Precautionary procedures include methods to prevent build up of electrostatic charge e g air conditioning humidification conductive floor coverings non synthetic clothing discharging one s body to the frame of the equipment or system or to earth or a large metal object and bonding oneself by means of a wrist strap to the equipment or system or to earth Adding a Humidifier You can use the Heated humidifier or the Passover humidifier with your device They are available from your home care provider A humidifier may reduce nasal dryness and irritation by adding moisture to the airflow CAUTION For safe operation the humidifier must always be positioned below the breathing circuit connection at the mask and the air outlet on the device The humidifier must be level for proper operation Note Refer to the humidifier s instructions for complete setup information Using the SD Card The REMstar system comes with an SD card inserted in the SD card slot on the back of the device to record information for the home care provider Your home care provider may ask you to periodically remove the SD card and send it to them for evaluation Note The SD card does not need to be installed for the device to work properly The SD card records device usage information for your home care pr
19. emove and problem may contact your home care provider reinsert exist with the SD card or it is inserted incorrectly Modem Making Call single beep Modem will Alert present for 30 Refer to If modem is making call while display its own seconds after call modem therapy is active alert for call icon on the device sequence or until instruction sequence is not displayed Refer to modem user acknowledges manual instruction manual Modem Unsuccessful single beep 09 Alert present for Refer to No action needed Call Modem will 30 seconds or until modem display its own user acknowledges instruction icon on the device manual Refer to modem instruction manual 12 User Manual Troubleshooting The table below lists some of the problems you may experience with your device and possible solutions to those problems PROBLEM Nothing happens when you apply power to the device The backlights on the buttons do not light Why IT HAPPENED There s no power at the outlet or the device is unplugged What ro Do If you are using AC power check the outlet and verify that the device is properly plugged in Make sure there is power available at the outlet Make sure the AC power cord is connected correctly to the power supply and the power supply cord is securely connected to the device s power inlet If the problem continues to occur contact your home care provider Return both the device and power supply to your pro
20. er the device will remain functional and deliver therapy 2 Connect the tubing to the mask Refer to the instructions that came with your mask 3 Attach the headgear to the mask if necessary Refer to the instructions that came with your headgear Where to Place the Device Place the device on a firm flat surface somewhere within easy reach of where you will use it at a level lower than your sleeping position Make sure the filter area on the back of the device is not blocked by bedding curtains or other items Air must flow freely around the device for the system to work properly Make sure the device is away from any heating or cooling equipment e g forced air vents radiators air conditioners CAUTION Do not place the device directly onto carpet fabric or other flammable materials CAUTION Do not place the device in or on any container that can collect or hold water 6 User Manual Supplying AC Power to the Device CAUTION Condensation may damage the device If this device has been exposed to either very hot or very cold temperatures allow it to adjust to room temperature operating temperature before starting therapy Do not operate the device outside of the operating temperature range shown in the Specifications WARNING Be sure to route the power cord to the outlet in a way that will prevent the cord from being tripped over or interfered with by chairs or other furniture WARNING This device is activated when the power co
21. es for damage or signs of wear Discontinue use and replace if damaged To avoid electrical shock always unplug the power cord from the wall outlet before cleaning the device DO NOT immerse the device in any fluids If the device is used by multiple persons such as rental devices a low resistance main flow bacteria filter should be installed in line between the device and the circuit tubing to prevent contamination Besure to route the power cord to the outlet in a way that will prevent the cord from being tripped over or interfered with by chairs or other furniture Using this device at an incorrect altitude setting could result in airflow pressures higher or lower than the prescribed setting Always verify the altitude setting when travelling or relocating and adjust the system accordingly This device is activated when the power cord is connected Note Please see the Limited Warranty section of this manual for information on warranty coverage 2 User Manual Cautions A Caution indicates the possibility of damage to the device Pins of connectors should not be touched Connections should not be made to these connectors unless ESD precautionary procedures are used Precautionary procedures include methods to prevent build up of electrostatic charge e g air conditioning humidification conductive floor coverings non synthetic clothing discharging one s body to the frame of the equipment or system or to earth or a larg
22. foam filter at least once every two weeks and replace it with a new one every six months The white ultra fine filter is disposable and should be replaced after 30 nights of use or sooner if it appears dirty DO NOT clean the ultra fine filter CAUTION Dirty inlet filters may cause high operating temperatures that may affect device performance Regularly examine the inlet filters as needed for integrity and cleanliness 1 If the device is operating stop the airflow Disconnect the device from the power source 2 Remove the filter s from the enclosure by gently squeezing the filter in the center and pulling it away from the device 3 Examine the filter s for cleanliness and integrity 4 Wash the gray foam filter in warm water with a mild detergent Rinse thoroughly to remove all detergent residue Allow the filter to air dry completely before reinstalling it If the foam filter is torn replace it Only Respironics supplied filters should be used as replacement filters 5 If the white ultra fine filter is dirty or torn replace it 6 Reinstall the filters inserting the white ultra fine filter first if applicable CAUTION Never install a wet filter into the device You must ensure sufficient drying time for the cleaned filter Cleaning the Tubing Clean the tubing daily Disconnect the flexible tubing from the device Gently wash the tubing in a solution of warm water and a mild detergent Rinse thoroughly Air dry Service The devic
23. g and adjust the system accordingly Auto on You can enable this feature if you want the device to automatically turn the airflow on whenever you apply the interface mask to your airway Auto off You can enable this feature if you want the device to automatically turn the airflow off whenever you remove the interface mask from your airway Mask alert You can enable or disable the mask alert setting If chis feature is enabled the mask alert will appear on the display screen when a significant mask leak is detected and an audible alert will sound Refer to the Device Alerts section for more information about the mask alert LED backlight You can enable or disable the LED backlight for the humidifier icon and settings on the device User Manual Info Screen From the Home screen highlight the Info option and press the wheel The following Info screen will appear The user cannot change settings in the Info menu Note These screens are only for reference Your home care provider may periodically ask you for this information Compliance VIC Therapy hours Days gt 4 Back Info Screen Note The screen will only show 4 lines at a time As you rotate the wheel to toggle over different options the screen will slide up and down accordingly Status This displays information sent from a peripheral SD card modem etc If two peripherals are attached two lines will appear with corresponding icons Phone in This
24. m the Home screen highlight the Setup option and press the wheel The following Setup screen will appear The user can change settings in the Setup menu Back Humidifier 012345 Ramp start 4 0 CPAP pres Altitude 1 2 3 Auto on on off Auto off on off Mask alert on off LED backlight on off Back Setup Screen Note The screen will only show 4 lines at a time As you rotate the wheel to toggle over different options the screen will slide up and down accordingly If the text is too long to completely fit on the screen it will scroll horizontally across the screen when highlighted Humidifier This displays the humidifier setting This will only display if the humidifier is attached Please refer to the humidifier manual if using a humidifier Ramp Start This displays the ramp starting pressure You can increase or decrease the ramp starting pressure in 0 5 cm H O increments This is only available if Ramp time has been set to gt 0 and CPAP pressure gt 4 cm H O Altitude This screen allows you to modify the altitude adjustment setting 1 less than 2500 ft 762 m 2 2500 to 5000 ft 762 m to 1524 m 3 5001 to 7500 ft 1525 m to 2286 m Note Elevations over 7500 ft 2286 m may affect the accuracy of the pressure Warning Using this device at an incorrect altitude setting could result in airflow pressures higher or lower than the prescribed setting Always verify the altitude setting when travelling or relocatin
25. nstructions supplied with the mask 4 Turn the wheel to toggle between the three options Highlight Therapy Press the wheel to turn on the airflow and begin therapy The Therapy screen will appear which will show the current pressure setting being delivered 5 Make sure that no air is leaking from your mask into your eyes If necessary adjust the mask and headgear until the air leak stops See the instructions provided with your mask for more information Note A small amount of mask leak is normal and acceptable Correct large mask leaks or eye irritation from an air leak as soon as possible 6 If you are using the device in a bed with a headboard try placing the tubing over the headboard This may reduce tension on the mask 7 Press the wheel again to turn off therapy and return to the Home screen User Manual 7 Ramp Feature The device is equipped with an optional ramp feature that your home care provider can enable or disable This feature reduces the air pressure when you are trying to fall asleep and then gradually increases ramps the pressure until your prescription setting is reached allowing you to fall asleep more comfortably If ramp is enabled on your device after you turn on the airflow press the RAMP button on the top of the device You can use the RAMP button as often as you wish during the night Note If the ramp feature is disabled nothing will happen when you press the RAMP button Setup Screen Fro
26. on by Respironics Inc Service Respironics Inc disclaims all liability for economic loss loss of profits overhead or consequential damages which may be claimed to arise from any sale or use of this product Some states do not allow the exclusion or limitation of incidental or consequential damages so the above limitation or exclusion may not apply to you This warranty is given in lieu of all other express warranties In addition any implied warranties including any warranty of merchantability or fitness for the particular purpose are limited to two years Some states do not allow limitations on how long an implied warranty lasts so the above limitation may not apply to you This warranty gives you specific legal rights and you may also have other rights which vary from state to state To exercise your rights under this warranty contact your local authorized Respironics Inc dealer or contact Respironics Inc at 1001 Murry Ridge Lane Murrysville Pennsylvania 15668 8550 1 724 387 4000 Respironics Inc 312 Alvin Drive New Kensington PA 15068 USA REF 1066941 1066937 JR 9 9 2009 EN DOM
27. ovider You can refer to the Device Alerts section in this manual for more information on the SD card Contact your provider if you have any questions about the SD card Adding Supplemental Oxygen Oxygen may be added at the mask connection Please note the warnings listed below when using oxygen with the device WARNINGS When using oxygen with this system the oxygen supply must comply with local regulations for medical oxygen When using oxygen with this system a Respironics Pressure Valve must be placed in line with the patient circuit after the oxygen source Failure to use the pressure valve could result in a fire hazard When using oxygen with this system turn the device on before turning on the oxygen Turn the oxygen off before turning the device off This will prevent oxygen accumulation in the device Do not connect the device to an unregulated or high pressure oxygen source Supplying DC Power to the Device The Respironics DC Power Cord can be used to operate this device in a stationary recreational vehicle boat or motor home The Respironics DC Battery Adapter Cable when used with the DC Power Cord enables the device to be operated from a 12 VDC free standing battery CAUTION When DC power is obtained from a vehicle battery the device should not be used while the vehicle s engine is running Damage to the device may occur CAUTION Only use a Respironics DC Power Cord and Battery Adapter Cable Use of any other system may ca
28. rd is connected IMPORTANT If you are using your device with a humidifier refer to the instructions included with your humidifier for details on how to power the device and humidifier Complete the following steps to operate the device using AC power 1 Plug the socket end of the AC power cord included into the power supply also included 2 Plug the pronged end of the AC power cord into an electrical outlet that is not controlled by a wall switch 3 Plug the power supply cord s connector into the power inlet on the back of the device 4 Ensure that all connections are secure IMPORTANT To remove AC power disconnect the power supply cord from the electrical outlet WARNING Periodically inspect electrical cords and cables for damage or signs of wear Discontinue use and replace if damaged CAUTION Do not use extension cords with this device Navigating the Device Screens Turn the wheel to toggle between options and settings on the screen Press the wheel to choose an option or setting that is highlighted If you choose Back on any screen it will take you back to the previous screen Note The screens shown throughout this manual are examples only Actual screens may vary slightly Examples are for reference only Starting the Device 1 Supply power to the device 2 The Home screen will appear shown below Home Screen 3 Put on your mask assembly Note If you are having trouble with your mask refer to the i
29. should make sure it is used in such an environment Emissions TEsT COMPLIANCE ELECTROMAGNETIC ENVIRONMENT GUIDANCE RF emissions Group 1 The device uses RF energy only for its internal function Therefore its RF emissions CISPR 11 are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class B The device is suitable for use in all establishments including domestic establishments CISPR 11 and those directly connected to the public low voltage power supply network Harmonic emissions Class A IEC 61000 3 2 Voltage fluctuations Flicker emissions Complies IEC 61000 3 3 Guidance and Manufacturer s Declaration Electromagnetic Immunity This device is intended for use in the electromagnetic environment specified below The user of this device should make sure it is used in such an environment IMMUNITY TEST Electrostatic Discharge ESD IEC 61000 4 2 IEC 60601 Test LeveL 6 kV contact 8 kV air CoMPLIANCE LEVEL X6 kV contact X8 kV air ELECTROMAGNETIC ENVIRONMENT GUIDANCE Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 3076 Electrical fast Transient burst 2 kV for power supply lines 1 kV for input output lines 2 kV for supply mains 1 kV for input output lines Mains power quality should be that of a typical home or hospital environmen
30. t 2 kV common mode IEC 61000 4 4 Surge 1 kV differential mode 1 kV differential mode Mains power quality should be that of a typical IEC 61000 4 5 home or hospital environment 2 kV for common mode Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 lt 5 UL gt 95 dip in U_ for 0 5 cycle 40 U 60 dip in U for 5 cycles 70 U 30 dip in U for 25 cycles lt 5 U gt 95 dip in U for 5 sec 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 U for 25 cycles lt 5 U gt 95 dip in U_ for 5 sec Mains power quality should be that of a typical home or hospital environment If the user of the device requires continued operation during power mains interruptions it is recommended that the device be powered from an uninterruptible power supply or a battery Power frequency 50 60 Hz magnetic field IEC 61000 4 8 3 A m 3 Alm Power frequency magnetic fields should be at levels characteristic of a typical location in a typical hospital or home environment NOTE U is the a c mains voltage prior to application of the test level User Manual Guidance and Manufacturer s Declaration Electromagnetic Immunity This device is intended for use in the electromagnetic environment specified below The user of this device should make sure it is used
31. ull Alert is present until card is Screen displays action is taken removed Card status can be SD card full checked in the Status menu Remove SD card and replace SD Card Remove single beep 09 Alert present for SD card has No action needed Screen displays 30 seconds or until been removed SD card user acknowledges removed SD Card Data single beep Screen displays Alert present until n a Only displayed immediately after Activity Data activity Do user acknowledges therapy is turned off when data is not remove card or data activity complete transferring to the card User Manual 11 AUDIBLE VISUAL Device AcTION PossiBLE PATIENT ACTION INDICATOR INDICATOR Cause SD Card Corrupt e o 09 Alert present until A problem Choose yes to reformat Screen displays action is taken exists with the the card Screen displays Corrupt card SD card The Reformatting do not remove inserted reformat data may be card card corrupted If you choose no the alert will disappear and the card will not be reformatted Note Any information on the card will be lost when reformatted Contact your home care provider with any questions SD Card Remove ee 09 Alert present until Device cannot Remove SD card and reinsert and Reinsert Screen displays action is taken read the If the alert continues to occur SD card error SD card A replace with another card or r
32. understand this entire manual before using the device This device is not intended for life support The device should be used only with masks and connectors recommended by Respironics or with those recommended by the health care professional or respiratory therapist A mask should not be used unless the device is turned on and operating properly The exhalation port s associated with the mask should never be blocked Explanation of the Warning The device is intended to be used with special masks or connectors that have exhalation ports to allow continuous flow of air out of the mask When the device is turned on and functioning properly new air from the device flushes the exhaled air out through the mask exhalation port However when the device is not operating enough fresh air will not be provided through the mask and exhaled air may be rebreathed When using oxygen with this system the oxygen supply must comply with local regulations for medical oxygen When using oxygen with this system turn the device on before turning on the oxygen Turn the oxygen off before turning the device off This will prevent oxygen accumulation in the device Explanation of the Warning When the device is not in operation and the oxygen flow is left on oxygen delivered into the tubing may accumulate within the device s enclosure Oxygen accumulated in the device enclosure will create a risk of fire When using oxygen with this system a Respironics Pressure
33. use damage to the device Refer to the instructions supplied with the DC Power Cord and adapter cable for information on how to operate the device using DC power 14 User Manual Traveling with the System When traveling the carrying case is for carry on luggage only The carrying case will not protect the system if it is put through checked baggage For your convenience at security stations there is a note on the bottom of the device stating that it is medical equipment It may be helpful to bring this manual along with you to help security personnel understand the REMstar device If you are traveling to a country with a line voltage different than the one you are currently using a different power cord or an international plug adaptor may be required to make your power cord compatible with the power outlets of the country to which you are traveling Contact your home care provider for additional information Cleaning the Device WARNING To avoid electrical shock always unplug the power cord from the wall outlet before cleaning the device DO NOT immerse the device in any fluids 1 Unplug the device and wipe the outside of the device with a cloth slightly dampened with water and a mild detergent Let the device dry completely before plugging in the power cord 2 Inspect the device and all circuit parts for damage after cleaning Replace any damaged parts Cleaning or Replacing the Filters Under normal usage you should clean the gray
34. ve 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 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 20 User Manual Limited Warranty Respironics Inc warrants that the system shall be free from defects of workmanship and materials and will perform in accordance with the product specifications for a period of two 2 years from the date of sale by Respironics Inc to the dealer If the product fails to perform in accordance with the product specifications Respironics Inc will repair or replace at its option the defective material or part Respironics Inc will pay customary freight charges from Respironics Inc to the dealer location only This warranty does not cover damage caused by accident misuse abuse alteration water ingress and other defects not related to material or workmanship The Respironics Inc Service department shall examine any devices returned for service and Respironics Inc reserves the right to charge an evaluation fee for any returned device as to which no problem is found after investigati
35. vider so they can determine if the problem is with the device or power supply If you are using DC power make sure your DC power cord and battery adaptor cable connections are secure Check your battery It may need recharged or replaced If the problem persists check the DC cord s fuse following the instructions supplied with your DC cord The fuse may need to be replaced If the problem still occurs contact your home care provider The airflow does not turn on There may be a problem with the blower Make sure the device is powered correctly Make sure Therapy is highlighted when pressing the control wheel to start airflow If the airflow does not turn on there may be a problem with your device Contact your home care provider for assistance The device s display is erratic The device has been dropped or mishandled or the device is in an area with high Electromagnetic Interference EMI emissions Unplug the device Reapply power to the device If the problem continues relocate the device to an area with lower EMI emissions away from electronic equipment such as cellular phones cordless phones computers TVs electronic games hair dryers etc If the problem still occurs contact your home care provider for assistance The Ramp feature does not work when you press the Ramp button Your home care provider did not prescribe Ramp for you or your CPAP pressure is already set to the minimum setting
36. your home care provider Mask Alert e o 09 Alert present until The breathing Turn off airflow Check your Screen displays action is taken circuit is breathing circuit connections Mask alert disconnected and reconnect the tubing if it has or there is a come loose Make sure your large air leak mask is on properly before you restart the airflow If the alert continues to occur contact your home care provider to have your mask checked You may need a mask refitting Auto Off single beep Screen displays The airflow shuts The mask has Put your mask back on and turn Auto off off and the device been removed the airflow on to resume therapy enters the Standby state approximately 45 60 seconds after detection Alert present for 30 seconds or until user acknowledges Humidifier Alert none 09 Only displayed when Humidifier Alert is present for 12 minutes or Humidifier LED both the humidifier failure until the condition is fixed Turn icon will flash and therapy is on off airflow and reconnect the humidifier to the device according to the humidifier instructions DAA If the alert continues to occur contact your home care provider 10 User Manual ALERT AUDIBLE VISUAL Device AcTION PossiBLE PATIENT ACTION INDICATOR INDICATOR Cause Patient Reminder single beep Screen displays Only displayed when Message from Your home care provider may message from the therapy
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