Respironics 1116426 Continuous Positive Airway Pressure Device User Manual

Respironics Inc. Continuous Positive Airway Pressure Device

User Manual

Auto CPAPCPAPUser manualDreamStation Go
Table of contents1. Safety Information .................................................................................. 1Intended use .............................................................................................................................1Warnings ....................................................................................................................................1Cautions .................................................................................................................................... 4Contraindications ................................................................................................................... 6Safety Symbols Glossary ...................................................................................................... 62. System Overview .................................................................................. 10System Contents ....................................................................................................................10Accessories .............................................................................................................................. 10System Diagram ......................................................................................................................113. Therapy Device ..................................................................................... 12Where to Place Your Device ............................................................................................... 12Supplying AC Power to Your Device ................................................................................. 12Starting the Device ................................................................................................................ 13Navigating the Device Screens .......................................................................................... 14Therapy On Menu Navigation Settings ........................................................................... 15 Ramp Feature ................................................................................................................. 15Therapy O Menu Navigation Settings ........................................................................... 16 My Info .............................................................................................................................. 16 My Comfort ...................................................................................................................... 17 My Device ........................................................................................................................ 18 My Support ......................................................................................................................19 Check Mask Fit .............................................................................................................. 20 Pairing Therapy Device to Bluetooth®-enabled Mobile Device ...................... 21Device Pop-Up Messages ...................................................................................................224. Tubing .....................................................................................................25Tubing Types ...........................................................................................................................25Connecting the Tubing to Your Device ............................................................................25Changing Your Tube Type ....................................................................................................26Cleaning the Tubing ..............................................................................................................27Tubing Device Pop-Up Messages .....................................................................................275. Filter ........................................................................................................28Filter Types ..............................................................................................................................28Installing or Replacing the Filter ...................................................................................... 29Filter Device Pop-Up Messages ....................................................................................... 296. Accessories .......................................................................................... 30Using the USB Port and the Micro USB Port ................................................................ 30Using the microSD Card ....................................................................................................... 31
microSD card Device Pop-Up Messages ........................................................................327. Battery Pack ..........................................................................................33Indicators and Buttons on the Battery Pack ..................................................................33Preparing the Battery Pack for First Use and Recharging .........................................35Attaching the Battery Pack to the Device ......................................................................35Disconnecting the Battery Pack ........................................................................................378. Care and Maintenance ........................................................................ 38Caring for the Therapy Device or Battery Pack .............................................................38Caring for the Reusable Filter ............................................................................................389. Troubleshooting .................................................................................. 40Tips and Tricks ....................................................................................................................... 40Contacting Customer Service .............................................................................................4210. Additional Notes.................................................................................43Traveling with the System ...................................................................................................43Airline Travel ...........................................................................................................................43Altitude Compensation ........................................................................................................43Adding Supplemental Oxygen...........................................................................................43Service ......................................................................................................................................43Additional Notices .................................................................................................................44Specications..........................................................................................................................45Disposal ................................................................................................................................... 48EMC Information ................................................................................................................... 48Limited warranty .........................................................................................52
1Intended useThe Philips Respironics DreamStation Go systems deliver positive airway pressure therapy for the treatment of Obstructive Sleep Apnea in spontaneously breathing patients weighing over 30 kg (66 lbs.). It is for use in the home or hospital/institutional environment.ImportantThis device is to be used only on the instruction of a licensed physician. Your supplier will make the correct pressure settings according to your health care professional’s prescription. Several accessories are available to make your Obstructive Sleep Apnea (OSA) treatment with the DreamStation Go system as convenient and comfortable as possible. To ensure that you receive the safe, eective therapy prescribed for you, use only Philips Respironics accessories. WarningsA warning indicates the possibility of injury to the user or operator.Device usage This device is not intended for life support. Personnel qualicationsThis manual serves as a reference. The instructions in this manual are not intended to supersede your health care professional’s instructions regarding the use of the device. The operator should read and understand this entire manual before using the device. Operating and storage temperaturesDo not use this device if the room temperature is warmer than 95˚ F (35˚ C) because the temperature of the airow may exceed 109˚ F (43˚ C). This could cause thermal irritation or injury to the patient’s airway. Do not use the device while positioned in a warm place, such as direct sunlight or near a heating appliance. These conditions can increase the temperature of the airow and could cause thermal irritation or injury to the patient’s airway. Bacteria lter If the device is used by multiple persons in a hospital environment (such as rental devices), a low-resistance, main ow bacteria lter should be installed in-line between the device and the circuit tubing to prevent contamination.If the device is used on multiple users, discard and replace the bacteria lter each time the device is used on a dierent person. 1. Safety Information
2 1. Safety InformationPatient circuits and tubingThe device should be used only with masks and connectors recommended by Philips 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 ow of air out of the mask. When the device is turned on and functioning properly, new air from the device ushes 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. If you are using a full face mask (a mask covering both your mouth and your nose), the mask must be equipped with a safety (entrainment) valve. Do not pull or stretch the tubing. This could result in circuit leaks.Inspect the tubing for damage or wear. Discard and replace the tubing as necessary.Improperly functioning deviceIf you notice any unexplained changes in the performance of the device, if it is making unusual sounds, if water is spilled into the enclosure, or if the enclosure is cracked or broken, discontinue use and contact your supplier.Power cord 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.This device is activated when the power cord is connected.Use only power cords supplied by Philips Respironics for this device. Use of power cords not supplied by Philips Respironics may cause overheating or damage to the device.To avoid strangulation hazards, ensure that all cords connected to the device and battery pack are properly routed.
31. Safety InformationAccessories Do not use any accessories, detachable parts, and materials not recommended by Philips Respironics. Incompatible parts or accessories can result in degraded performance.The USB charging port is designed only for use in charging a mobile device, such as a cell phone. Ensure there are no additional accessories attached to the mobile device while connected to this charging port.Use of accessories, transducers and cables other than those specied or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation. Oxygen When using oxygen with this system, the oxygen supply must comply with local regulations for medical oxygen.Do not connect the device to an unregulated or high pressure oxygen source.When using oxygen with this system, a Philips Respironics pressure valve must be placed in-line with the patient circuit between the device and the oxygen source. The pressure valve helps to prevent the back ow of oxygen from the patient circuit into the device when the unit is o. Failure to use the pressure valve could result in a re hazard.Oxygen supports combustion. Oxygen should not be used while smoking or in the presence of an open ame.Do not use the device in the presence of a ammable anesthetic mixture in combination with oxygen or air, in the presence of nitrous oxide, or in an oxygen-enriched environment.Do not use the device near a source of toxic or harmful vapors.When using oxygen with this system, turn the device on before turning on the oxygen. Turn the oxygen o before turning the device o. This will prevent oxygen accumulation in the device. Explanation of the Warning: When the device is not in operation and the oxygen ow 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 re.EMC Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation.The Health Industry Manufacturers Association recommends that a minimum separation of six inches be maintained between a wireless phone and a pacemaker to avoid potential interference with the pacemaker. The DreamStation Go on-board Bluetooth communication should be considered a wireless phone in this regard.
4 1. Safety InformationCare and MaintenancePeriodically inspect electrical cords, cables, tubing, and accessories for damage or signs of wear. Discontinue use and replace if damaged.Repairs and adjustments must be performed by Philips Respironics-authorized service personnel only. Unauthorized service could cause injury, invalidate the warranty, or result in costly device damage. Contact your supplier for maintenance.Do not attempt to modify the device or battery pack in any way.Periodically check battery pack charge status and recharge if depleted.To avoid electrical shock, always unplug the power cord from the wall outlet before caring for the device. DO NOT immerse the device in any uids.Do not submerge the battery pack in water or any other liquid.Choking This device contains small parts which could result in a choking hazard.Nebulization Nebulization or humidication can increase the resistance of breathing system lters and the operator must monitor the breathing system lter frequently for increased resistance and blockage to ensure the delivery of the therapeutic pressure.General Contact your health care professional if symptoms of sleep apnea recur. CautionsA caution indicates the possibility of damage to the device.US Federal CautionU.S. federal law restricts this device to sale by or on the order of a physician. EMC Medical electrical equipment needs special precautions regarding EMC and needs to be installed according to EMC information. Contact your supplier regarding EMC installation information.Mobile RF CommunicationsPortable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 in.) to any part of the [ME EQUIPMENT or ME SYSTEM], including cables specied by the manufacturer. Otherwise, degradation of the performance of this equipment could result.Device usage Before operating the device, ensure that both end caps are attached whenever any of the accessories such as the battery pack is not installed.Ensure that the therapy device is properly secured if it is being used in a portable environment.
51. Safety InformationElectrostatic Discharge (ESD)Pins of connectors shall not be touched and connections shall not be made without special precautions. Precautionary procedures include methods to prevent build-up of electrostatic charge (e.g., air conditioning, humidication, conductive oor coverings, non-synthetic clothing), discharging one’s body to the frame of the equipment or system or to earth. It is recommended that all individuals that will handle this device understand these precautionary procedures at a minimum as part of their training.Condensation Condensation may damage the device. If the 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 Specications section later in this manual.Filters A properly installed, undamaged Philips Respironics reusable lter or disposable, ne lter is required for proper operation.Clogged inlet lters may cause high operating temperatures that may aect device performance. Regularly examine the inlet lters as needed for integrity and to check for accumulated debris.Never install a wet lter into the device. You must ensure sucient drying time for the rinsed lter.Make sure the air inlet holes on the side of the device are not blocked by bedding, curtains, or other items. Air must ow freely around the device for the system to work properly.Battery Pack Do not expose the battery pack to extreme temperatures (see the Specications section for temperature specications). If the battery pack becomes very hot or very cold, allow it to come to room temperature before using.There are no user-serviceable parts inside of the battery pack; therefore, do not attempt to disassemble or repair it.Extension cords Do not use extension cords with this device.Device placementDo not place the device in or on any container that can collect or hold water.Do not place the device directly onto carpet, fabric, or other ammable materials.Tobacco use Tobacco smoke may cause tar build-up within the device, which may result in the device malfunctioning.
6 1. Safety InformationContraindicationsWhen assessing the relative risks and benets of using this equipment, the clinician should understand that this device can deliver pressures up to 20 cm H2O. In the event of certain fault conditions, a maximum pressure of 40 cm H2O 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 uid (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.Safety Symbols GlossaryThe following symbols may appear on the device and accessories:Symbol Title and Meaning ReferenceOperator’s manual; operating instructionsConsult instructions for use.IEC 60878ISO 7000-1641Symbol 5.4.3, ISO 15223-1Approved for airline use. RTCA/DO-160G section 21, category MAC power (Alternating current)Indicates on the rating plate that the equipment is suitable for alternating current only; to identify relevant terminals.IEC 60417-5032Separate collection for electrical and electronic equipment.EC Directive 2012/19/EU
71. Safety InformationSymbol Title and Meaning ReferenceLi Ion Battery -Bluetooth® symbolIndicates the device has Bluetooth capabilities.-IP22 Drip proof equipmentProtection against ingress of solid foreign objects ≥ 12.5 mm diameter. Protection against ingress of water with harmful eects dripping (15° tilted).-Non-ionizing electromagnetic radiationIndicates that the equipment includes RF transmitters.IEC 60878IEC 60417-5140Caution, consult accompanying documents. IEC 60878Symbol 5.1.2, ISO 15223-1Prescription deviceCaution: U. S. federal law restricts this device to sale by or on the order of a physician.-Electrostatic sensitive devices (ESD warning symbol)Attention – Observe precautions for handling electrostatic sensitive devices.IEC 60878IEC 60417-5134Serial connectionIdenties a connector for a serial data connection.IEC 60878IEC 60417-5850Class II equipment (Double Insulated)To identify equipment meeting the safety requirements specied for Class II equipment.IEC 60878IEC 60417-5172Keep away from sunlightIndicates the medical device needs protection from light sources.IEC 60878ISO 7000-0624Symbol 5.3.2, ISO 15223-1Type BF applied partTo identify a type BF applied part complying with IEC 60601-1.IEC 60878IEC 60417-5333
8 1. Safety InformationSymbol Title and Meaning ReferenceDo not disassemble. -For indoor use onlyEquipment is designed primarily for indoor use.IEC 60878IEC 60417-5957ManufacturerIndicates the medical device manufacturer.IEC 60878ISO 7000-3082Symbol 5.1.1, ISO 15223-1Date of manufactureIndicates the date when the medical device was manufactured.IEC 60878ISO 7000-2497Symbol 5.1.3, ISO 15223-1Reorder numberIndicated the manufacturer’s catalogue number so the medical device can be identied.ISO 7000-2493Symbol 5.1.6, ISO 15223-1Serial numberIdentify the manufacturer’s serial number for the medical device.IEC 60878ISO 7000-2498Symbol 5.1.7, ISO 15223-1Keep dryIndicates the medical device that needs to be protected from moisture.IEC 60878ISO 7000-0626Symbol 5.3.4, ISO 15223-1Fragile, handle with careIndicates the medical device can be broken or damaged if not handled carefully.IEC 60878ISO 7000-0621Symbol 5.3.1, ISO 15223-1Humidity limitationIndicates the range of humidity to which the medical device can be safely exposed.IEC 60878ISO 7000-2620Symbol 5.3.8, ISO 15223-1Temperature limitIndicates the storage temperature limits to which the medical device can be safely exposed.IEC 60878ISO 7000-0632Symbol 5.3.7, ISO 15223-1
91. Safety InformationISO 7000:2014, Graphical symbols for use on equipment – Registered symbolsISO 7010:2011+A1:2012+A2:2012+A3:2012+A4:2013+A5:2014+A6:2014, Graphical symbols -- Safety colours and safety signs -- Registered safety signs (not currently FDA recognized)EN 15986:2011, Symbols for medical devices containing phthalates (not currently FDA recognized)ISO 15223-1:2012, Medical devices—Symbols to be used with medical devices labels - General requirementsIEC 60417:2002 DB, Graphical symbols for use on equipmentIEC/TR 60878:2015, Graphical symbols for electrical equipment in medical practice
10 The DreamStation Go CPAP is a Continuous Positive Airway Pressure therapy device designed for the treatment of Obstructive Sleep Apnea (OSA). Your supplier will choose the appropriate pressure settings for you.Several accessories are also available for use with your device. Contact your supplier to purchase any accessories not included with your system.System ContentsYour DreamStation Go system may include the following items: • Device • microSD Card (optional)• User Manual • Disposable Fine Filter (optional)• Reusable Filter • Battery Pack (optional)• 12 mm Micro-exible Tubing (12 Type)• 6 ft. (1.83 m) Power Cord NoteIf any of these items are missing, contact your supplier.AccessoriesThe following accessories are available for your DreamStation Go system:• 6 ft. (1.83 m) Serial Communication Cable (with ferrites)• 10 ft. (3.04 m) Power Cord• Small Travel Kit • Medium Travel Kit• 15 mm Standard Tubing (15 Type) • 22 mm Performance Tubing (22 Type)• Bacteria Filter • Pressure Valve (for use with supplemental oxygen)NoteYour mobile device charging cable should not be longer than 6 ft (1.83 m).2. System Overview
112. System OverviewSystem DiagramThe gure above illustrates some of the device features, described in the following table.# Feature Description1Therapy on/o button Starts and stops the airow for therapy.2Display Touchscreen This is the User Interface for the therapy device.3 Ambient Light Sensor Detects room light levels and adjusts brightness of the display screen.4 Air Outlet Port Connect the tubing here.5 Serial Connector Access the serial connector here. 6 AC Power Inlet Connect the power cord here.7Battery Pack Access This end cap slides o for access to the battery pack connection.8 microSD Card Access the microSD card here.9 Mobile Charging Port Access the USB charging port here for mobile device usage.10 Filter Access Access the lter here. 12345678910
12 Where to Place Your DevicePlace the device on a rm, at surface somewhere within easy reach of where you will use it. The device should sit at a level lower than your sleeping position. Make sure the device is away from any heating or cooling equipment (e.g., forced air vents, radiators, air conditioners).Note When positioning the device, make sure that the power cable is accessible because removing power is the only way to turn o the device.Supplying AC Power to Your DeviceComplete the following steps to operate the device by plugging the AC power cord into an electrical outlet.1. Plug the power cord connector into the power inlet on the back of the device.2. Plug the pronged end of the AC power cord into an electrical outlet that is not controlled by a wall switch.3. Make sure that all connections are secure.3. Therapy Device
133. Therapy DeviceStarting the Device1. Ensure power is supplied to the device. Tap anywhere on the display screen to wake up the device.# Feature1 Therapy on/o button2Display Touchscreen2. Put on your mask assembly. Refer to the instructions supplied with the mask.3. Tap the therapy button on top of the device to turn on airow and begin thera-py. The current delivered pressure will display on the screen. The therapy button is only for therapy.4. A small amount of mask leak is normal and acceptable. Correct large amount of mask leaks or eye irritation by adjusting your mask headgear. See the instructions provided with your mask for more information, or refer to the Check Mask Fit sec-tion.5. Tap the therapy button again to turn o the therapy. To turn o therapy when the display screen is o, place and hold a nger on the display screen for three sec-onds. Alternatively, tap anywhere on the display screen to wake up the display and then tap the therapy button to turn o therapy.Notes• 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. • During therapy, if there is a power loss, the device will return to the home screen once power is restored. You may resume therapy as needed.12
143. Therapy DeviceNavigating the Device ScreensThe User Interface (UI) on this device allows you to adjust the device settings and view information about your therapy. The UI consists of the display screen and the touch panel. Swipe left or right on the touch panel to scroll through the menu options on the display screen.To adjust a setting:1. Swipe the touchscreen until you nd your desired menu option.2. Tap the desired menu option.3. Swipe the touchscreen until you nd the sub-menu option and tap to select that setting.4. Swipe the touchscreen to change the setting.5. Tap the icon or tap the up arrow in the upper left corner of the display to save the setting, and return to the previous menu option.Notes• The swipe icon on any screen indicates to swipe the display left or right to perform an action.• The t ap icon on any screen indicates to press the display to perform an action.• Tapping the down arrow on the display when the down arrow appears on any screen will take you to a sub-menu with more menu options. Tapping the up arrow when the up arrow appears on any sub-menu will return you back to the main menu.• The screens shown throughout this manual are examples for reference only. Actual screens may vary based upon device model and supplier settings.
153. Therapy DeviceTherapy On Menu Navigation SettingsWhile the device is delivering therapy, you can adjust or view the following settings. # Feature Description1 Therapy pressure Displays the current delivered pressure.2 Ramp Feature The device is equipped with an optional ramp feature that your supplier can enable or disable.Ramp FeatureThis 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 airow, tap the Ramp ( ) icon on the display. You can use the ramp feature as often as you wish.When you tap the Ramp icon, the therapy screen will change to reect the ramp in pressure, and the numbers within the blue circle will reect the gradual increase in pressure.Your device has two ramp modes. Your supplier will select the one that is most appropriate for you. The standard ramp mode increases pressure at a steady rate. Alternately, the SmartRamp mode maintains a constant lower pressure until the device detects that you require more pressure.12
163. Therapy DeviceTherapy O Menu Navigation SettingsFrom the Home screen, you can scroll between the following four options: Battery My Info My Comfort My Device My SupportBattery This menu is visible when the battery pack is connected. See Chapter 7, Battery Pack for details.My Info This menu provides summary statistics of your therapy use.My Comfort This menu contains comfort settings that you can adjust as needed.My Device This menu contains device settings that you can change.My Support This menu contains information that your supplier may direct you to read to them so they can better assist you over the phone.My Info When you select My Info, you will be able to view the following screens. You cannot change settings in the My Info menu. These screens are only for reference. Your supplier may periodically ask you for this information. If any of the below options are not visible, your supplier did not enable those options.Icon Text DescriptionTherapy HoursThis screen displays the amount of time the user is actually receiving therapy on the device for the most recent 1-day time frame.AHI AHI This screen displays the nightly Apnea/Hypopnea indices (AHI) value for the most recent 1 day time frame.
173. Therapy DeviceIcon Text DescriptionMask Fit Displays the value “100% minus Large Leak”. Large Leak is the percentage of time that the mask leak was so high that it is no longer possible for the device to identify respiratory events with statistical accuracy. Displays the value for the most recent 1 day.My Comfort When you select My Comfort, you will be able to view the following screens. You can change the settings in the setup menu. These screens will only display if they are available and enabled on your device. If any of the below options are not visible, your supplier did not enable those options. If a lock icon is displayed on this screen, it indicates that your supplier has locked this setting and you cannot change it.Icon Text DescriptionRamp This displays the ramp starting pressure. You can increase or decrease the ramp starting pressure in 0.5 cm H2O increments. Ramp time When you set the ramp time, the device increases the pressure from the value set on the ramp screen to the therapy pressure setting over the length of time specied here. Flex This allows you to adjust the level of air pressure relief that you feel when you exhale during therapy. Your supplier can enable or disable this feature. When your supplier enables Flex, a level will already be set for you on the device. You can increase or decrease the setting from 1 to 3. The setting of “1” provides a small amount of pressure relief, with higher numbers providing additional relief.Mask type This setting allows you to adjust the level of air pressure relief based on the specic Philips Respironics mask. Each Philips Respironics mask may have a “System One” resistance control setting. Contact your supplier if you cannot nd this resistance setting for your mask.
183. Therapy DeviceIcon Text DescriptionTube type This setting allows you to select the correct tubing type that you are using with the device. You can choose (12) for the Philips Respironics 12 tubing type, (15) for the Philips Respironics 15 tubing type, or (22) for the Philips Respironics 22 tubing type. Note: The 12 type and 15 type tubing are identied on the cu with the tubing identier symbol: “12” or “15”. The 22 tubing type does not have any identier on the cu.Check mask tThis feature allows you to check the t of your mask prior to starting therapy. This is done by measuring the amount of leak.My Device When you select My Device, you will be able to view the following screens. You can change the settings in the setup menu. These screens will only display if they are available and enabled on your device. If any of the below options are not visible, your supplier did not enable those options.Icon Type DescriptionTherapy RingThis setting controls the therapy button LED light ring during therapy. The LED light ring will remain on during therapy if you select Light On. The LED light ring will fade with the display backlight if you select Light Dims.Language This feature allows you to choose which language to display on the interface.Bluetooth This feature allows you to turn Bluetooth o and on. Also, it allows you to clear the pairing with a compatible Bluetooth device.Time This setting allows you to adjust the time. The default setting is Greenwich Mean Time, but you may adjust the time in 30 minute increments to match your local time zone.Note: This time setting should not be used as a clock function on the device. It is to align your therapy data for your supplier’s data reports.
193. Therapy DeviceMy Support When you select My Support, you will be able to view the following screens. You cannot change settings in the support menu. These screens are only for reference. Your supplier may periodically ask you for this information. If any of the below options are not visible, your supplier did not enable those options.Icon Text DescriptionDevice Info This screen displays your therapy device information: serial number, model, and software version.Performance CheckYour device is equipped with a self-diagnostic tool called “Performance Check.” This tool can evaluate your device for certain errors. It also allows you to share key device settings with your supplier. Use Performance Check when directed to by your supplier. At conclusion of the scan, the screen displays a green checkmark if no issue is detected. If device displays a red “X,” please contact your supplier for assistance.Phone-In This screen displays the total therapy hours and total blower hours for the device, and a compliance check number used by your supplier to validate that data provided by you is the data taken from this screen.
203. Therapy DeviceCheck Mask FitThe optional Check Mask Fit feature can be enabled or disabled by your supplier. This feature allows you to check the t of your mask prior to starting therapy. 1. Put on your mask assembly. Refer to your mask instructions if needed. 2. Navigate to the Check Mask Fit screen under My Comfort and tap the display to initi-ate the check.3. The device will deliver a test pressure while the screen counts down 40 seconds. 4. After the test is complete, the screen will either display a green checkmark or a red “X”. The green checkmark indicates that there is an appropriate amount of leak. The red “X” indicates that the leak may aect device performance, however, the device will remain functional and deliver therapy.NoteIf you choose to try to improve your mask fit, you can stop therapy, adjust the fit of your mask, and rerun the Check Mask Fit feature. Refer to the instructions that came with your mask and headgear for the proper fitting procedure.
213. Therapy DevicePairing Therapy Device to Bluetooth®-enabled Mobile DeviceYour device may have Bluetooth wireless technology, which is one method by which you can transfer your therapy device’s data to DreamMapper. DreamMapper is a mobile and web-based system designed to help you enhance your sleep therapy experience.Notes• You can only pair your therapy device to one mobile device at any given time.• Pairing works best when your therapy device and mobile device are in the same room.• The current version of DreamMapper will guide you through these instructions.• After initiating pairing, you will have 30 seconds to complete the setup. After this time, it will be cancelled automatically.Follow the steps below to manually pair to your mobile phone or tablet.1. Install DreamMapper on your mobile device.2. With your therapy device powered up and the blower o, initiate Bluetooth Setup from the DreamMapper mobile app.3. The therapy device will appear as PR BT XXXX (XXXX will be the last four digits of the serial number listed on the bottom of your therapy device or in My Support settings).4. Your mobile device will require you to conrm pairing via one of these two meth-ods: —Enter a PIN codeThe following icon will appear on your therapy device screen with Pair?: Swipe left or right to select “yes,” and tap the display to conrm your setting. Your therapy device will display a 6 digit PIN. Enter this PIN on your mobile device to complete pairing. —Confirm a PIN codeThe following icon will appear on your therapy device screen with a 6-digit PIN and Pair?: Verify that the PIN is the same on both the therapy device and the mobile device. If so, swipe the therapy device’s display to select “yes” and tap the display to select. Then, accept on the mobile device to complete pairing.
223. Therapy DeviceDevice Pop-Up MessagesDevice pop-ups are messages that show up on the user interface screen. Additional pop-up messages are contained in each chapter.The following summary table summarizes the messages:Condition Icon Description Possible CauseActionTime Prompts to set the time.n/a Set the time on the device.Sleep Progressn/a Shows a three night summary of therapy.n/a Tap the display to acknowledge and clear the message.Change AcceptedConrms acceptance of prescription change or device upgrade.n/a Tap the display to acknowledge and clear the message.Pair?: 123456 Yes/NoPrompts to accept or decline pairing to a Bluetooth compatible device. This device can be identied by the digits displayed.n/a Swipe the display to accept pairing (Yes), or decline (No), then tap the display to conrm selection. The pop-up will timeout after 30 seconds and the pairing will be cancelled if you do not select Yes.
233. Therapy DeviceCondition Icon Description Possible CauseActionBluetooth LE PasskeyPrompts to accept or decline pairing to a Bluetooth compatible device before displaying the pairing passkey.n/a If you selected Yes to accept pairing, the Bluetooth LE Passkey will display a passkey on the screen. Enter the passkey on your mobile device to pair. The pop-up will timeout after 30 seconds and the pairing will be cancelled if you do not use the passkey.Patient MessageMessage from your supplier.n/a Tap the display to acknowledge and clear the message.Change RejectedA prescription or settings change was rejected.Change missing or incorrect.Contact your supplier.Service RequiredIndicates an error which enters device into “Safe State.” This allows power to remain on but airow is disabled.Device error Disconnect device from power. Reattach power cord to restore power. If the alert continues to occur, contact your supplier.Automatic O Displayed when therapy ends due to automatic o function.The mask has been removed.Put your mask back on, conrm good t, and turn airow on to resume therapy.Loading Language and RebootingDisplayed when a new language is selected from the menu.n/a No action needed. Times out when complete.
243. Therapy DeviceCondition Icon Description Possible CauseActionBusy Displayed when the device is temporarily inaccessible due to data communication.n/a No action needed.Software UpgradePrompts to update the device for software changes.n/a Choose between “Yes”/”No” when asked to upgrade the software. If “yes” is selected, the upgrade will be made. Do not remove from power. If you select “no”, the message will be cleared.
25Tubing TypesThere are three dierent types of tubing that you may use with your DreamStation Go therapy device. You must select the tube type on your device.12 tubing type 15 tubing type 22 tubing typeThe 12 tubing type will have a “12” identied on the tubing cu (as shown in the image above). The 15 tubing type will have a “15” identied on the tubing cu (as shown in the image above). The 22 tubing type does not have any number or symbol on the tubing cu (as shown in the image above).Connecting the Tubing to Your DeviceTo connect the tubing to your device, you will need the following Philips Respironics accessories:• Nasal or full face mask (interface) with built-in exhalation, or a nasal or full face mask (interface) with a separate exhalation device attached (such as the Whisper Swivel II)• Flexible tubing, 6 ft. (1.83 m)• Mask headgear 12154. Tubing
26 4. TubingFollow these steps to connect tubing to your device:1. Insert the 12, 15 or 22 tubing type cu into the air outlet port on your therapy device.2. Connect the tubing to your mask. For proper placement and positioning, refer to the instructions that came with your mask.NoteYou may use a standard tube with a bacteria lter. If required, connect a bacteria lter to the device air outlet, and then connect the exible tubing to the outlet of the bacteria lter. When using the bacteria lter, the device performance may be aected. However, the device will remain functional and deliver therapy.Changing Your Tube TypeChange your tube type by navigating to My Comfort -> Tube Type. Swipe left or right to switch between tube types.For more information on navigation or selection, please refer to Chapter 3, Navigating the Device Screens or My Comfort.
274. TubingCleaning the TubingClean the tubing before rst use and daily.1. Disconnect the exible tubing from the device. 2. Gently wash the tubing in a solution of warm water and a mild detergent. 3. Rinse thoroughly. 4. Air dry. Inspect the tubing for damage or wear. Discard and replace as necessary.Tubing Device Pop-Up MessagesDevice pop-ups are messages that show up on the user interface screen.Condition Icon Description Possible CauseActionLow leak: Check mask and tubeBlocked airwayBlockage at tube or maskCheck tube is not crushed or folded, such that airow is restricted. Check mask is attached properly and without any obstruction.
28Filter TypesYou may use either a reusable lter that is washable, or a disposable, ne lter. Reusable Filter Disposable Fine FilterThe reusable lter screens out normal household dust and pollen. The reusable lter is supplied with your device. The disposable, ne lter provides more complete ltration of ne particles. The disposable, ne lter is recommended for people who are sensitive to tobacco smoke or other small particles. The disposable, ne lter is sold separately. The disposable, ne lter contains Philips Respironics branding in the media (shown in the image above). DO NOT rinse the disposable, ne lter.When using the disposable, ne lter, the device performance may be aected. However, the device will remain functional and deliver therapy.5. Filter
295. FilterInstalling or Replacing the FilterOne of the lters must be in place at all times to operate the device. If a lter is not already installed in the device, you must at least install the reusable lter before using your device. The device has an automatic air lter reminder. Every 30 days, your device will display a message reminding you to check your lters and replace them as needed.NoteThe lter reminder is a message only. The device does not detect the performance of the lters, nor does it recognize when a lter has been replaced.Follow these steps to install/replace a lter into your device: 1. If replacing an existing lter, pull out the old lter assembly.2. Insert a dry, reusable lter or a new, disposable, ne lter into the lter access on the device.Filter Device Pop-Up Messages Device pop-ups are messages that show up on the user interface screen. Condition Icon Description Possible CauseActionInlet blocked. Check lter.Blocked airwayBlockage at device inlet.Check device air inlet is not obstructed. Check air lter(s) are installed properly; replace if needed.
30There are several accessories available for your DreamStation Go system, such as a microSD card, a travel kit or a battery pack. The device also comes with a USB port and a micro USB port. The travel kit is available for convenient portability while traveling with your device. Contact your supplier for additional information on the available accessories. When using optional accessories, always follow any instructions enclosed with the accessories.Using the USB Port and the Micro USB PortThe DreamStation Go device comes with a USB port and a micro USB port. The USB port may be used to charge your mobile devices. The micro USB port may be used by your supplier to extract therapy data. Remove the cover over each port to access.USB Port Micro USB Port6. Accessories
316. AccessoriesUsing the microSD CardThe DreamStation Go system may come with a microSD card inserted in the microSD card slot on the side of the device to record information for your supplier. Your supplier may ask you to periodically remove the microSD card and send it to them for evaluation.You will use the lter to remove the microSD card.Turn o therapy and follow these steps to remove the microSD card: 1. Remove the lter from the device. Refer to the Installing or Replacing the Filter section in Chapter 5 of this manual.2. Use the end of the lter to push in on the microSD card. This will push the microSD card out of the device.
32 6. AccessoriesmicroSD Card Device Pop-Up MessagesDevice pop-ups are messages that show up on the user interface screen. Condition Icon Description Possible Cause ActionData Activity: Do not remove microSD cardmicroSD card read/write underway.n/a No action needed. Message will clear when the microSD card activity is nished.microSD card removedIndicates microSD card has been removed from therapy device and not reinserted before the start of the current therapy session.microSD card was not reinserted into device.Reinsert microSD card, or click to clear alert.microSD card error: Remove and reinsertmicroSD card error detected.Device cannot read the microSD card. A problem may exist with the microSD card or it was ejected during a writing activity, or it was inserted incorrectly.Remove microSD card and reinsert. If message reappears, contact your supplier for a replacement card.microSD card fullmicroSD card is full. microSD card is full.Remove microSD card and replace with a new card from your supplier.
33Indicators and Buttons on the Battery Pack# Feature1 Push Button2 LED Display3 AC Power Inlet• Push Button - The push button is located on the LED display of the battery pack.• LED Display - The battery pack uses one green LED light to indicate the battery pack charge status when the battery pack is charging while not connected to the therapy device (standalone charging). The LED will be in one of the three modes:* Steady when the battery pack is fully charged* Blinking when charging* O when connected to the therapy device1237. Battery Pack
347. Battery Pack• Battery Pack Charge Indicator During Therapy - The display touchscreen shows the current battery pack charge status in the lower right hand corner when the pack is connected and therapy is active (shown below). A fully charged battery pack is indicated by four charge bars. The white charge bars disappear as the battery pack charge decreases. Depending on your settings, mask leak and environmental conditions, a fully charged battery pack typically lasts 8 hours. For further information, speak with your supplier.• Battery Pack Charge Indicator When Therapy Is Not Active - The display touchscreen will show the battery charge percentage when the battery is connected to the therapy device but not in use (shown below). This screen will appear in your main menu selections.• Battery Pack State of Charge Alert - The display touchscreen will display a battery with a question mark in the center (shown below) when the charge level cannot be determined.
357. Battery Pack• Battery Pack Fault Alert - The display touchscreen will show a battery with an X inside (shown below) when a battery fault is detected. Preparing the Battery Pack for First Use and Recharging1. Remove the battery pack from the packaging. 2. Plug the end of the AC power cord into the battery pack. 3. Plug the AC power cord into an AC outlet. The battery pack will begin to charge au-tomatically. 4. Once the battery pack is fully charged, it is ready for use with the DreamStation Go therapy device.Notes• Periodically charge the battery pack if not used regularly.• Retain your packaging in case you ever need to return your battery pack to Philips Respironics.• Before using the battery pack for the rst time, you must plug it in until it is fully charged. This may take up to 5 hours.Attaching the Battery Pack to the DeviceAfter charging, your battery pack is ready to use. It can either be disconnected from the AC outlet and used as an external battery pack (standalone mode), or remain plugged into the AC outlet for a continuous, fully charged battery pack (uninterruptible power supply (UPS) mode). To use the battery pack in UPS mode, follow the below steps: 1. Keep the battery pack plugged into the power source and connected to an AC outlet. This will allow you to use the battery pack continuously without losing any charge.
367. Battery Pack2. Remove the battery pack end cap on the therapy device. 3. Slide the battery pack onto the device where the end cap was. Make sure the bat-tery pack latches onto the therapy device.4. Attach the AC power cord to the battery pack and then to the AC outlet.To use the battery pack in standalone mode, follow these steps: 1. Make sure the battery pack is fully charged. Disconnect the power cord from the AC outlet and disconnect the power cord from the therapy device. It can now be used with your therapy device as an external battery pack. 2. Remove the battery pack end cap on the therapy device.3. Slide the battery pack onto the device where the end cap was. Make sure the bat-tery pack latches onto the therapy device.4. Momentarily push the battery pack push button to wake up the battery pack.
377. Battery PackNotes• The rst time you charge your battery pack, it must be fully charged in accordance with the Preparing the Battery Pack for First Use and Recharging section. After the rst charge is complete, the battery pack will charge while connected in UPS mode.• To preserve battery life in UPS mode, the battery pack stops charging when it reaches full charge. The battery will start charging again when it depletes to 90% charge status.• When the battery pack is used in standalone mode and the therapy device enters standby mode, the therapy device automatically shuts down the battery pack to preserve battery charge.Disconnecting the Battery Pack1. Disconnect the power cord.2. Hold the battery pack push button down for 5 seconds, or the battery pack will shut o within 30 minutes when not in use.3. The power down pop-up message will appear and the therapy device will power down and go dark.4. You can now disconnect the battery pack. Disengage the battery pack by sliding the latch on the back of the pack, and pulling the battery pack away from the therapy device.5. Replace the battery pack end cap on the therapy device.
38Caring for the Therapy Device or Battery PackEvery two weeks of use, inspect your device or battery pack to see if it needs care. 1. To avoid electrical shock, make sure that the device and battery pack are discon-nected from all outlets and power sources. Remove any cables attached to the device or battery pack.2. Wipe the outside of the device or battery pack with a cloth slightly dampened with water.3. Allow the device or battery pack to dry completely before reconnecting it to a power source, battery pack, device or cable.NoteInspect the device, battery pack, and all circuit parts (lter, tube and mask) for damage, such as cracks, tears or broken pieces. Replace any damaged parts.Caring for the Reusable FilterUnder normal usage, you should rinse the reusable lter at least once every two weeks and replace it with a new one every six months.The disposable, ne lter should be replaced after 30 nights of use, or sooner if it appears clogged. DO NOT rinse the ne lter.Follow these steps to rinse the reusable lter: 1. If the device is operating, stop the airow. Disconnect the device from the power source. 2. Remove the lter from the device. Refer to the Installing or Replacing the Filter section in Chapter 5.3. Take the reusable lter to a sink, turn it upside down (tabs down), and run warm tap water through the white middle portion of the lter to rinse away any debris.4. Shake the lter to remove as much water as possible.5. Allow the lter to air dry completely before reinstalling it. If the lter is damaged, replace it.6. Reinstall the lter into the lter access area on the device. Refer to the Installing or Replacing the Filter section in Chapter 5.8. Care and Maintenance
398. Care and MaintenanceNotes• Only Philips Respironics supplied lters should be used as replacement lters.• Replace the disposable, ne lter if it is damaged or has accumulated debris.
40Tips and TricksYour device is equipped with a self-diagnostic tool called Performance Check. This tool can evaluate your device for certain errors. It also allows you to share diagnostic information with your supplier. Use Performance Check when directed by your supplier.The table below lists some of the problems you may experience with your device and possible solutions to those problems.Contact customer service for assistance if none of the below troubleshooting tips work for you.Problem Why it happened What to doNothing happens when you apply power to the device. The backlights on the buttons do not light.There’s no power at the outlet or the device is unplugged.• If you are using AC power: Check the outlet and verify that the device is properly plugged in, and that there is power available at the outlet. Make sure the AC power cord is connected correctly to the device’s power inlet.• If you are using the battery pack: Make sure your battery pack is securely connected to your device. If the battery pack has been exposed to extreme temperatures, allow the battery back to cool or warm to room temperature. Check to see if your battery pack needs charged or replaced.The airow does not turn on.There may be a problem with the blower.• Make sure the device is powered correctly. • Make sure the home screen appears on the user interface.• Press the therapy button on top of the device to start airow. If the airow does not turn on, there may be a problem with your device.9. Troubleshooting
419. TroubleshootingProblem Why it happened What to doThe device’s display is erratic.The device has been dropped or mishandled, or the device is in an area with several electronic devices.Unplug the device. Reapply power to the device. If the problem continues, relocate the device to an area away from electronic equipment (such as cellular phones, cordless phones, computers, TVs, electronic games, hair dryers, etc.).The Ramp feature does not work when you press the Ramp button.Your supplier did not enable Ramp for you, or your therapy pressure is already set to the minimum setting.• If ramp has not been enabled for you, discuss this feature with your supplier.• If your supplier has enabled ramp, but the feature still does not work, check the current pressure setting on the therapy screen. If the therapy pressure is set to the minimum setting (4.0 cm H2O), or the ramp starting pressure is the same as the therapy pressure, the ramp feature will not work. Make sure that the ramp time setting is >0.The airow is much warmer than usual.The air lters may be dirty. The device may be operating in direct sunlight or near a heater. • Rinse or replace the air lter.• 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 ow of air around the device. • Make sure the device is away from direct sunlight and heating equipment.The airow pressure feels too high or too low.The tubing type setting may be incorrect.Make sure the tubing type setting (12, 15 or 22) matches the tubing that you are using (Philips Respironics 12, 15 or 22 tubing type).
42 9. TroubleshootingProblem Why it happened What to doI hear a leak or whistling sound coming from my therapy device (not related to mask leak).The therapy device air inlet may be obstructed.• Check therapy device air inlet is not obstructed, and lter has not accumulated excessive debris and is properly inserted.• Conrm that the device and tube are connected properly and not leaking.The battery pack LEDs will not light up while charging.Your battery pack may have been damaged.If the battery pack is completely depleted of charge, wait a few minutes for the LEDs to light up. If the LEDs still do not light up, replace your battery pack. If the battery pack has been exposed to extreme temperatures, allow the battery pack to cool or warm to room temperature.The battery pack LED is rapidly ashing.Your battery pack may have been damaged.If the battery pack has been exposed to extreme temperatures, allow the battery pack to cool or warm to room temperature. Unplug the battery pack from the power cord, then plug the power cord back into the battery pack. If the LED continues to rapidly ash, replace your battery pack.“Service Required” shown on display.A device error has occurred and placed the device into safe state.Disconnect power cord. Reattach the power cord to restore power. If the alert continues, contact your supplier.Contacting Customer ServiceShould you experience trouble with this equipment or require assistance setting up, using, or maintaining the device or accessories, please contact your supplier. If you need to contact Philips Respironics directly, call the Philips Respironics Customer Service department at 1-724-387-4000 or 1-800-345-6443. You can also use the following address:Respironics, Inc.1001 Murry Ridge Lane Murrysville, PA 15668
43Traveling with the SystemWhen traveling, the optional case is for carry-on luggage only. The optional 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 and is suitable for airline use. It may be helpful to bring this manual along with you to help security personnel understand the DreamStation Go device.If you are traveling to a country with a line voltage dierent than the one you are currently using, a dierent 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 supplier for additional information.Airline TravelThe device is suitable for use on airlines when the device is operating from an AC power source or battery pack.Altitude CompensationThis device automatically compensates for altitude up to 7,500 feet. No manual adjustment is necessary.Adding Supplemental OxygenOxygen can be added to the patient circuit.Notes• Refer to the pressure valve’s instructions for complete setup information.• When using oxygen with this system, turn the device on before turning on the oxygen. Turn the oxygen o before turning the device o. This will prevent oxygen accumulation in the device.• Do not connect the device to an unregulated or high pressure oxygen source.ServiceThe device does not require routine servicing.10. Additional Notes
4410. Additional NotesAdditional NoticesNotices:• The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by Philips Respironics is under license. Other trademarks and trade names are those of their respective owners.• The DreamStation Go Therapy Device transmits data between the therapy device and a mobile device, but it does not store any of your personal data. This connection between the therapy device and a mobile device is encrypted.• This device contains a FCC certied Bluetooth radio module (located on the main board). FCC ID: THO1116426• Use of non-original manufacturer-approved accessories may violate your local RF exposure guidelines and should be avoided.• This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio, TV reception, or other devices which can be determined by turning the equipment on and o, the user is encouraged to try to correct the interference by one or more of the following measures: Reorient or relocate the receiving antenna (on the radio, TV, or other device). Increase the separation between the equipment and receiver. Connect the equipment into an outlet on a circuit dierent from that to which the receiver is connected. Consult the dealer of the device for help.• Any changes or modications made to the device that are not expressly approved by Respironics may void the user’s authority to operate the equipment.
4510. Additional NotesSpecicationsEnvironmentalOperating TemperatureDevice: 5° to 35° C (41° to 95° F)Battery Pack: 5° to 35° C (41° to 104° F)Storage Temperature-20° to 60° C (-4° to 140° F)Relative Humidity (operating & storage)15 to 95% (non-condensing)Atmospheric Pressure: Device: 101 to 77 kPa (0 - 2286 m / 0 - 7500 ft)Battery Pack: 101 to 77 kPa (0 - 2286 m / 0 - 7500 ft)PhysicalDimensions Device: 150.8 x 150.8 x 58.8 mm (5.937” L x 5.937” W x 2.315” H)Battery Pack: 122 x 150.8 x 58.8 mm (4.803” L x 5.937” W x 2.315” H)Weight Device: Approximately 854 g (1.88 lb.)Battery Pack: Approximately 696 g (1.53 lb.)Service lifeThe expected service life of the DreamStation Go therapy device is 5 years.The expected service life of the battery pack is 3 years.Standards compliance This device is designed to conform to the following standards:• IEC 60601-1 General Requirements for Basic Safety and Essential Performance of Medical Electrical Equipment• ISO 80601-2-70 Sleep Apnea Breathing Therapy Equipment• EN 60601-1-2 Electromagnetic Compatibility• RTCA/DO-160G section 21, category M; Emission of Radio Frequency Energy
4610. Additional NotesIEC 60601-1 classicationType of Protection Against Electric ShockClass II Equipment/Internally PoweredDegree of Protection Against Electric ShockType BF Applied PartDegree of Protection against Ingress of WaterDevice: Drip Proof, IP22First characteristic numeral - 2 - Protection against ingress of solid foreign objects ≥ 12.5 mm diameter.Explanation: Protected against access to hazardous parts with a nger and protected against solid foreign objects of 12.5 mm diameter and greater.Second characteristic numeral - 2- Protection against ingress of water with harmful eects dripping (15° tilted).Explanation: Protected against vertically falling water drops when enclosure tilted up to 15°.Mode of Operation ContinuousElectricalAC Power Consumption 100–240 VAC, 50/60 Hz, 2.0-1.0 AFuses There are no user-replaceable fuses.USB Charging Port Output 5 VDC, 7.5 W (1.5 A)Electrical for the Battery PackRun Time > 8 hoursOutput voltage range 18-24.6 VDCBattery technology Lithium IonCapacity 62 WhInput voltage range 100-240 VAC, 50/60 Hz, 2.0-1.0 AOutput power (max continuous) 50WMinimum life cycle ≥ 70% of rated capacity after 500 cyclesRecharge time < 5 hours
4710. Additional NotesRadio SpecicationsOperating Frequency Range 2402 - 2480 MHzMaximum Output Power 4.0 dBmModulation GFSK, P/4 DQPSK, 8DQPSKIntake port ltersReusable Filter 100% Polyester88% Ecient @ 7-10 micron sizeFine Filter Blended Synthetic Fiber95% Ecient @ 0.5-0.7 micron sizeDeclared dual-number noise emissions values (in accordance with ISO 4871) Tube Size Sound Pressure Level (L)Uncertainty (K)Sound Power LevelUncertainty (K)12 (mm) tubing type 30.4 dB(A) 2 dB(A) 38.4 dB(A) 2 dB(A)15 (mm) tubing type 29.9 dB(A) 2 dB(A) 37.9 dB(A) 2 dB(A)22 (mm) tubing type 29.8 dB(A) 2 dB(A) 37.8 dB(A) 2 dB(A)NoteValues determined according to noise test code given in ISO 80601-2-70:2015, using the basic standards ISO 3744 and ISO 4871.Pressure AccuracyPressure Increments: 4.0-20.0 cmH2O (in 0.5 cmH2O increments)Maximum static pressure accuracy, according to ISO 80601-2-70:2015: Tube Type Pressure Accuracy12 (mm) tubing type 10 cmH2O ± 1.0 cmH2O15 (mm) tubing type and 22 (mm) tubing type10 cmH2O ± 0.5 cmH2OStatic pressure accuracy has a measurement uncertainty of 3.8%
4810. Additional NotesMaximum dynamic pressure variation, according to ISO 80601-2-70:2015: Tube Type 10 BPM 15 BPM 20 BPM12 (mm) tubing type ± 0.6 cmH2O ± 0.8 cmH2O ± 1.6 cmH2O15 (mm) tubing type and 22 (mm) tubing type ± 0.7 cmH2O ± 0.7 cmH2O ± 1.0 cmH2ODynamic pressure accuracy has a measurement uncertainty of 3.6%.Maximum Flow Rate (typical)Tube Type Flow Test pressures (cmH2O)4.0 8.0 12.0 16.0 20.012 (mm) tubing type Average ow at the patient connection port (l/min)90 119 112 106 9915 (mm) tubing type Average ow at the patient connection port (l/min)77 115 112 105 10622 (mm) tubing type Average ow at the patient connection port (l/min)80 121 127 121 109DisposalSeparate collection for electrical and electronic equipment per EC Directive 2012/19/EU. Dispose of this device in accordance with local regulations.EMC informationYour unit has been designed to meet EMC standards throughout its service life without additional maintenance. There is always an opportunity to relocate your DreamStation Go Therapy Device within an environment that contains other devices with their own unknown EMC behavior. If you believe your unit is aected by locating it closer to another device, simply separate the devices to remove the condition.Pressure and Flow AccuracyThe DreamStation Go Therapy Device is designed to perform within the pressure and owrate accuracies specied in the user manual. If you suspect that the pressure and/or ow rate accuracy is aected by EMC interference remove power and relocate the device to another area. If performance continues to be aected discontinue use and contact your supplier.Guidance and Manufacturer’s Declaration - Electromagnetic Emissions – This device is intended for use in the electromagnetic environment specied below. The user of this device should make sure it is used in such an environment.
4910. Additional NotesEmissions TEsT ComplianCE ElECTromagnETiC EnvironmEnT - guidanCERF emissionsCISPR 11 Group 1The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.RF emissionsCISPR 11Class BThe device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network.Harmonic emissionsIEC 61000-3-2 Class AVoltage uctuations/Flicker emissionsIEC 61000-3-3CompliesEmission of Radio Frequency EnergyRTCA/DO-160G Section 21Category M This device is suitable for use onboard commercial airplanes inside passenger cabin.Guidance and Manufacturer’s Declaration - Electromagnetic Immunity – This device is intended for use in the electromagnetic environment specied below. The user of this device should make sure it is used in such an environment.immuniTy TEsT iEC 60601 TEsT lEvElComplianCE lEvElElECTromagnETiC EnvironmEnT - guidanCEElectrostatic Discharge (ESD)IEC 61000-4-2±8 kV contact±15 kV air±8 kV contact±15 kV airFloors should be wood, concrete or ceramic tile. If oors are covered with synthetic material, the relative humidity should be at least 30%.Electrical fast Transient/burstIEC 61000-4-4±2 kV for power supply lines±1 kV for input-output lines±2 kV for supply mains±1 kV for input/output linesMains power quality should be that of a typical home or hospital environment.SurgeIEC 61000-4-5±1 kV dierential mode±2 kV common mode±1 kV dierential mode±2 kV for common modeMains power quality should be that of a typical home or hospital environment.
5010. Additional NotesimmuniTy TEsT iEC 60601 TEsT lEvElComplianCE lEvElElECTromagnETiC EnvironmEnT - guidanCEVoltage dips, short interruptions and voltage variations on power supply input linesIEC 61000-4-11<5% UT (>95% dip in UT) for 0.5 cycle at 45 degree increments<5% UT (>95% dip in UT) for 1 cycle70% UT (30% dip in UT) for 0.5 seconds <5% UT (>95% dip in UT) for 5 seconds<5% UT (>95% dip in UT) for 0.5 cycle at 45 degree increments<5% UT (>95% dip in UT) for 1 cycle70% UT (30% dip in UT) for 0.5 seconds<5% UT (>95% dip in UT) for 5 secondsMains 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 eldIEC 61000-4-830 A/m 30 A/m Power frequency magnetic elds should be at levels characteristic of a typical location in a typical hospital or home environment.NOTE: UT is the a.c. mains voltage prior to application of the test level.Guidance and Manufacturer’s Declaration - Electromagnetic Immunity – This device is intended for use in the electromagnetic environment specied below. The user of this device should make sure it is used in such an environment.
5110. Additional NotesImmunity Test IEC 60601 Test LevelCompliance Level Electromagnetic Environment - GuidanceConducted RFIEC 61000-4-6Radiated RFIEC 61000-4-33 Vrms150 kHz to 80 MHz6 VrmsAmateur Radio & ISM Bands between 150 kHz and 80 MHz10 V/m80 MHz to 2.7 GHzSpecial Telecommunication Bands between 300 MHz and 5.6 GHz3 Vrms150 kHz to 80 MHz6 VrmsAmateur Radio & ISM Bands between 150 kHz and 80 MHz10 V/mUp to 28 V/mPortable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended 30 cm separation distance.Interference may occur in the vicinity of equipment marked with the following symbol:
52Respironics, Inc., a Philips company, warrants that the system shall be free from defects of workmanship and materials and will perform in accordance with the product specications for a period of two (2) years for the therapy device and a period of one (1) year for the battery pack from the date of sale by Respironics, Inc. to the dealer. If the product fails to perform in accordance with the product specications, 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 investigation by Respironics, Inc. Service.This warranty is non-transferable by unauthorized distributors of Respironics, Inc. products and Respironics, Inc. reserves the right to charge dealers for warranty service of failed product not purchased directly from Respironics, Inc. or authorized distributors.Respironics, Inc. disclaims all liability for economic loss, loss of prots, 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 tness 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 specic 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 LaneMurrysville, Pennsylvania 15668-85501-724-387-4000Limited Warranty
11282391128239 R03 AD 3/7/2017 EN-DOM

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