AirCurve 10 User Guide July 2015
User guide English
3/10/2014 2:00:06 PM
Welcome The AirCurve™ 10 CS PaceWave™ is a positive airway pressure device that belongs to the adaptive servo-ventilator category.
WARNING • Read this entire guide before using the device. • Use the device according to the intended use provided in this guide. • The advice provided by your prescribing doctor should be followed ahead of the information provided in this guide.
AirCurve 10 CS PaceWave indications for use The AirCurve 10 CS PaceWave is indicated to stabilise the ventilation of adult patients exhibiting central sleep apnoea (CSA), mixed sleep apnoea and periodic breathing, with or without obstructive sleep apnoea. It is intended for home and hospital use. The humidifier is intended for single patient use in the home environment and re-use in a hospital/institutional environment.
Contraindications ASV therapy is contraindicated in patients with chronic, symptomatic heart failure (NYHA 2-4) with reduced left ventricular ejection fraction (LVEF ≤ 45%) and moderate to severe predominant central sleep apnea. Positive airway pressure therapy may be contraindicated in some patients with the following pre-existing conditions: •
severe bullous lung disease
pneumothorax or pneumomediastinum
pathologically low blood pressure, particularly if associated with intravascular volume depletion
cerebrospinal fluid leak, recent cranial surgery, or trauma.
Adverse effects You should report unusual chest pain, severe headache, or increased breathlessness to your prescribing physician. An acute upper respiratory tract infection may require temporary discontinuation of treatment. The following side effects may arise during the course of therapy with the device: •
drying of the nose, mouth, or throat
ear or sinus discomfort
At a glance The AirCurve 10 includes the following:
Power supply unit
SD card (already inserted).
Contact your care provider for a range of accessories available for use with the device including:
Air tubing (heated and non-heated): ClimateLineAir™, SlimLine™, Standard
Filter: Hypoallergenic filter, standard filter
Air10™ DC/DC converter (12V/24V)
SD card reader
Air10 oximeter adapter
Air10 USB adapter.
About your device
Air filter cover
SD card cover
Serial number and device number
About the control panel Start/Stop button
Press to start/stop therapy. Press and hold for three seconds to enter power save mode.
Turn to navigate the menu and press to select an option. Turn to adjust a selected option and press to save your change.
Press to return to the Home screen.
Different icons may be displayed on the screen at different times including: Ramp Time
No wireless connection
Wireless signal strength (green)
Wireless transfer not enabled (grey)
1. Place the device on a stable level surface. 2. Plug the power connector into the rear of the device. Connect one end of the power cord into the power supply unit and the other end into the power outlet. 3. Connect the air tubing firmly to the air outlet located on the rear of the device. 4. Connect the free end of the air tubing firmly onto the assembled mask. See your mask user guide for detailed information. Recommended masks are available on www.resmed.com. English
Starting therapy 1. Fit your mask. 2. Press Start/Stop or breathe normally if SmartStart is enabled. You will know that therapy is on when the Sleep Report screen is displayed. The pressure bar shows the inspiratory and expiratory pressures in green. The green bar will expand and contract as you breathe in and out.
The screen will go black automatically after a short period of time. You can press Home or the dial to turn it back on. If power is interrupted during therapy, the device will automatically restart therapy when power is restored. The AirCurve 10 device has a light sensor that adjusts the screen brightness based on the light in the room.
Stopping therapy 1. Remove your mask. 2. Press Start/Stop or if SmartStart is enabled, therapy will stop automatically after a few seconds. The Sleep Report now gives you a summary of your therapy session. Usage hours–Indicates the number of hours of therapy you received last session. Mask Seal–Indicates how well your mask sealed: Good mask seal. Needs adjusting, see Mask Fit.
If set by your care provider, you will also see: Events per hour–Indicates the number of apnoeas and hypopnoeas experienced per hour. More Info–Turn the dial to scroll down to view more detailed usage data.
Power save mode Your AirCurve 10 device records your therapy data. In order to allow it to transmit the data to your care provider, you should not unplug the device. However, you can put it into power save mode to save electricity. To enter power save mode: Press and hold Start/Stop for three seconds. The screen goes black.
To exit power save mode: Press Start/Stop once. The Home screen is displayed.
My Options Your AirCurve 10 device has been set up for your needs by your care provider, but you may find you want to make small adjustments to make your therapy more comfortable. Highlight My Options and press the dial to see your current settings. From here, you can personalise your options.
Ramp Time Designed to make the beginning of therapy more comfortable, Ramp Time is the period during which the pressure increases from a low start pressure to the prescribed treatment pressure. You can set your Ramp Time to Off or between 5 to 45 minutes. To adjust Ramp Time: 1. In My Options, turn the dial to highlight Ramp Time and then press the dial. 2. Turn the dial to adjust the ramp time to your preferred setting and press the dial to save the change.
Mask Fit Mask Fit is designed to help you assess and identify possible air leaks around your mask. To check Mask Fit: 1. Fit the mask as described in the mask user guide. 2. In My Options, turn the dial to highlight Run Mask Fit and then press the dial. The device starts blowing air. 3. Adjust the mask, mask cushion and headgear until you get a Good result.
To stop Mask Fit, press the dial or Start/Stop. If you are unable to get a good mask seal, talk to your care provider.
More options Your care provider may have given you access to personalise a few more options. Leak Alert
When Leak Alert is enabled, the device beeps if the mask leaks too much air or if you remove the mask during therapy.
When SmartStart is enabled, therapy starts automatically when you breathe into your mask. When you remove your mask, it stops automatically after few seconds.
This option shows your mask type setting. If you use more than one type of mask, adjust this setting when switching between masks.
Caring for your device It is important that you regularly clean your AirCurve 10 device to make sure you receive optimal therapy. The following sections will help you with disassembling, cleaning, checking and reassembling your device.
Disconnecting the air tubing
1. Hold the cuff of the air tubing and gently pull it away from the device. 2. Hold both the cuff of the air tubing and the swivel of the mask, then gently pull apart.
Cleaning You should clean the device weekly as described. Refer to the mask user guide for detailed instructions on cleaning your mask. 1. Wash the air tubing in warm water using mild detergent. Do not wash in a dishwasher or washing machine. 2. Rinse the air tubing thoroughly and allow to dry out of direct sunlight and/or heat. 3. Wipe the exterior of the device with a dry cloth.
Checking You should regularly check the air tubing and air filter for any damage. 1. Check the air tubing and replace it if there are any holes, tears or cracks. 2. Check the air filter and replace it at least every six months. Replace more often if there are any holes or blockages by dirt or dust.
To replace the air filter:
1. Open the air filter cover and remove the old air filter. The air filter is not washable or reusable. 2. Place a new air filter onto the air filter cover and then close it. Make sure the air filter is fitted at all times to prevent water and dust from entering the device.
Reconnecting the air tubing When the air tubing is dry, you can reconnect it to the device. 1. Connect the air tubing firmly to the air outlet located on the rear of the device. 2. Connect the free end of the air tubing firmly onto the assembled mask.
Therapy data Your AirCurve 10 device records your therapy data for you and your care provider so they can view and make changes to your therapy if required. The data is recorded and then transferred to your care provider wirelessly or via an SD card.
Data transmission Your AirCurve 10 device has the capability of wireless communication so that your therapy data can be transmitted to your care provider to improve the quality of your treatment. This is an optional feature that will only be available if you choose to benefit from it. It also allows your care provider to update your therapy settings in a more timely manner or upgrade your device software to ensure you receive the best therapy possible. The data is usually transmitted after therapy has stopped. In order to make sure that your data is transferred, leave your device connected to the mains power at all times and make sure that it is not in Airplane Mode. Notes:
Therapy data might not be transmitted if you use it outside of the country or region of purchase.
Devices with wireless communication might not be available in all regions.
SD card An alternative way for your therapy data to be transferred to your care provider is via the SD card. Your care provider may ask you to send the SD card by mail or to bring it in. When instructed by your care provider, remove the SD card. Do not remove the SD card from the device when the SD light is flashing.
To remove the SD card:
1. Open the SD card cover. 2. Push in the SD card to release it. Remove the SD card from the device. Place the SD card in the protective folder and send it back to your care provider. For more information on the SD card refer to the SD card protective folder provided with your device. Note: The SD card should not be used for any other purpose.
Travelling You can take your AirCurve 10 device with you wherever you go. Just keep the following in mind:
Use the travel bag provided to prevent damage to the device.
Make sure you have the appropriate power cord for the region you are travelling to. For information on purchasing, contact your care provider.
Travelling by plane Your AirCurve 10 device may be taken on board as carry-on luggage. Medical devices do not count toward your carry-on luggage limit. You can use your AirCurve 10 device on a plane as it meets the Federal Aviation Administration (FAA) requirements. Air travel compliance letters can be downloaded and printed from www.resmed.com. When using the device on a plane turn on Airplane Mode. To turn on Airplane Mode: 1. In My Options, turn the dial to highlight Airplane Mode and then press the dial. 2. Turn the dial to select On and then press the dial to save the change. The Airplane Mode icon is displayed at the top right of the screen.
Troubleshooting If you have any problems, have a look at the following troubleshooting topics. If you are not able to fix the problem, contact your care provider or ResMed. Do not try to open the device.
General troubleshooting Problem/possible cause
Air is leaking from around my mask Mask may be fitted incorrectly.
Make sure your mask is fitted correctly. See your mask user guide for fitting instructions or use the Mask Fit function to check your mask fit and seal.
Air pressure in my mask seems too high (it feels like I am getting too much air) Ramp may be turned off.
Use the Ramp Time option.
Air pressure in my mask seems too low (it feels like I am not getting enough air) Ramp may be in progress.
Wait for air pressure to build up or turn Ramp Time off.
My screen is black Backlight on the screen may have turned off. It turns off automatically after a short period of time.
Press Home or the dial to turn it back on.
Power may not be connected.
Connect the power supply and make sure the plug is fully inserted.
My therapy data has not been sent to my care provider Wireless coverage may be poor.
Make sure that the device is placed where there is coverage (ie, on your bedside table, not in a drawer or on the floor). The Wireless signal strength icon indicates good coverage when all bars are displayed, and poor coverage when fewer bars are displayed.
The No wireless connection icon is displayed on the top right of the screen. No wireless network available.
Make sure that the device is placed where there is coverage (ie, on your bedside table, not in a drawer or on the floor). If instructed to do so, send the SD card to your care provider. The SD card also contains your therapy data.
Device may be in Airplane Mode.
Turn off Airplane Mode, see Travelling by plane.
Data transfer is not enabled for your device.
Contact your care provider to enable the data transfer service.
My screen and buttons are flashing Software upgrade is in progress.
Software upgrade takes approximately 10 minutes to complete.
Device messages Device message/possible cause
High leak detected, connect your tubing Air tubing may not be connected properly.
Make sure the air tubing is firmly connected at both ends.
Mask may be fitted incorrectly.
Make sure your mask is fitted correctly. See your mask user guide for fitting instructions or use the Mask Fit function to check your mask fit and seal.
Tubing blocked, check your tubing Air tubing may be blocked.
Check the air tubing and remove any blockages. Press the dial to clear the message and then press Start/Stop to restart the device.
SD card error, remove your card and press Start to begin therapy SD card may not be inserted correctly.
Remove and reinsert the SD card.
Read only card, please remove, unlock and re-insert SD card SD card switch may be in the lock (read-only) position.
Move the switch on the SD Card from the lock position and then re-insert it. to the unlock position
System fault, refer to user guide, Error 004 Device may have been left in a hot environment.
Allow to cool before re-use. Disconnect the power supply and then reconnect it to restart the device.
Air filter may be blocked.
Check the air filter and replace it if there are any blockages. Disconnect the power supply and then reconnect it to restart the device.
Air tubing may be blocked.
Check the air tubing and remove any blockages. Press the dial to clear the message and then press Start/Stop to restart the device.
There may be water in the air tubing.
Empty the water from the air tubing. Disconnect the power supply and then reconnect it to restart the device.
All other error messages, for example, System fault, refer to user guide, Error 0XX An unrecoverable error has occurred on the device.
Contact your care provider. Do not open the device.
General warnings and cautions WARNING Make sure that you arrange the air tubing so that it will not twist around the head or neck. Make sure the power cord and plug are in good condition and the equipment is not damaged. Keep the power cord away from hot surfaces. If you notice any unexplained changes in the performance of the device, if it is making unusual sounds, if the device or the power supply are dropped or mishandled, or if the enclosure is broken, discontinue use and contact your care provider or your ResMed Service Centre. 10
Do not open or modify the device. There are no user serviceable parts inside. Repairs and servicing should only be performed by an authorised ResMed service agent. Beware of electrocution. Do not immerse the device, power supply or power cord in water. If liquids are spilled into or onto the device, unplug the device and let the parts dry. Always unplug the device before cleaning and make sure that all parts are dry before plugging it back in. Supplemental oxygen must not be used while smoking or in the presence of an open flame. Always make sure that the device is turned on and airflow generated before the oxygen supply is turned on. Always turn the oxygen supply off before the device is turned off, so that unused oxygen does not accumulate within the device enclosure and create a risk of fire. Do not perform any maintenance tasks while the device is in operation. The device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the device should be observed to verify normal operation in the configuration in which it will be used. The use of accessories other than those specified for the device is not recommended. They may result in increased emissions or decreased immunity of the device.
CAUTION Use only ResMed parts and accessories with the device. Non-ResMed parts may reduce the effectiveness of the treatment and/or damage the device. Use only vented masks recommended by ResMed or by the prescribing doctor with this device. Fitting the mask without the device blowing air can result in rebreathing of exhaled air. Make sure that the mask vent holes are kept clear and unblocked to maintain the flow of the fresh air into the mask. Be careful not to place the device where it can be bumped or where someone is likely to trip over the power cord. Blocking the air tubing and/or air inlet of the device while in operation could lead to overheating of the device. Keep the area around the device dry, clean and clear of anything (eg, clothes or bedding) that could block the air inlet or cover the power supply unit. Incorrect system setup may result in incorrect mask pressure reading. Ensure the system is correctly set up. Do not use bleach, chlorine, alcohol, or aromatic-based solutions, moisturising or antibacterial soaps or scented oils to clean the device, the water tub or air tubing. These solutions may cause damage or affect the humidifier performance and reduce the life of the products.
Technical specifications Units are expressed in cm H2O and hPa. 1 cm H2O is equal to 0.98 hPa. 90W power supply unit AC input range: DC output: Typical power consumption: Peak power consumption:
100–240V, 50–60Hz 1.0–1.5A, Class II 115V, 400Hz 1.5A, Class II (nominal for aircraft use) 24V 3.75A 53W (57VA) 104W (108VA)
Environmental conditions Operating temperature:
Operating humidity: Operating altitude: Storage and transport temperature: Storage and transport humidity:
+5°C to +35°C Note: The air flow for breathing produced by this therapy device can be higher than the temperature of the room. Under extreme ambient temperature conditions (40°C) the device remains safe. 10 to 95% relative humidity, non-condensing Sea level to 2,591 m; air pressure range 1013 hPa to 738 hPa -20°C to +60°C 5 to 95% relative humidity, non-condensing
Electromagnetic compatibility The AirCurve 10 complies with all applicable electromagnetic compatibility requirements (EMC) according to IEC60601-1-2:2007, for residential, commercial and light industry environments. It is recommended that mobile communication devices are kept at least 1 m away from the device. Information regarding the electromagnetic emissions and immunity of this ResMed device can be found on www.resmed.com, on the Products page under Service and Support. EN 60601-1:2006 classification Class II (double insulation), Type BF, Ingress protection IP22. Sensors Pressure sensor: Flow sensor:
Internally located at device outlet, analogue gauge pressure type, -5 to +45 cm H2O (-5 to +45 hPa) Internally located at device inlet, digital mass flow type, -70 to +180 L/min
Maximum single fault steady pressure Device will shut down in the presence of a single fault if the steady state pressure exceeds: 30 cm H2O (30 hPa) for more than 6 sec or 40 cm H2O (40 hPa) for more than 1 sec. Sound Pressure level measured according to EN ISO 17510-1:2009 (CPAP mode): SlimLine: 26.6 dBA with uncertainty of 2 dBA Standard: 26.6 dBA with uncertainty of 2 dBA Power level measured according to EN ISO 17510-1:2009 (CPAP mode): SlimLine: 34.6 dBA with uncertainty of 2 dBA Standard: 34.6 dBA with uncertainty of 2 dBA Declared dual-number noise emission values in accordance with ISO 4871:1996. Physical Dimensions (H x W x D): Air outlet (complies with ISO 5356-1:2004): Weight: Housing construction: Air filter Standard: Hypoallergenic:
116 mm x 205 mm x 150 mm 22 mm 1115 g Flame retardant engineering thermoplastic Material: Polyester non woven fibre Average arrestance: >75% for ~7 micron dust Material: Acrylic and polypropylene fibres in a polypropylene carrier Efficiency: >98% for ~7-8 micron dust; >80% for ~0.5 micron dust
Aircraft use ResMed confirms that device meets the Federal Aviation Administration (FAA) requirements (RTCA/DO-160, section 21, category M) for all phases of air travel. 12
Wireless module Technology used: 2G GSM It is recommended that the device is a minimum distance of 2 cm from the body during operation. Not applicable to masks, tubes or accessories Declaration of Conformity (DoC to the R&TTE Directive) ResMed declares that the AirCurve 10 device is in compliance with the essential requirements and other relevant provisions of Directive 1999/5/EC. A copy of the declaration of conformity (DoC) can be found on www.ResMed.com/ProductSupport. Operating pressure range ASV, ASVAuto: CPAP
4 to 25 cm H2O (4 to 25 hPa) 4 to 20 cm H2O (4 to 20 hPa)
Supplemental Oxygen Maximum flow:
15 L/min (CPAP, ASV); 4 L/min (ASVAuto)
Pneumatic flow path 1. Flow sensor 2. Blower 3. Pressure sensor 4. Mask 5. Air tubing 6. Side cover 7. Device 8. Inlet filter Design life Device, power supply unit: Cleanable humidifier: Air tubing:
5 years 2.5 years 6 months
General The patient is an intended operator. Air tubing Air tubing Material ClimateLineAir Flexible plastic and electrical components SlimLine Flexible plastic Standard Flexible plastic Heated air tubing temperature cut-out: 41°C
Length 2m 1.8 m 2m
Inner diameter 15 mm 15 mm 19 mm
Notes: The manufacturer reserves the right to change these specifications without notice. The electrical connector end of the heated air tubing is only compatible with the air outlet at the device end and should not be fitted to the mask. Do not use electrically conductive or antistatic air tubing. The temperature and relative humidity settings displayed are not measured values.
Displayed values Value Pressure sensor at air outlet: Mask pressure Flow derived values: Leak Tidal volume Respiratory rate Minute ventilation Value Pressure measurement: Mask pressure2 Flow and flow derived values1: Flow Leak2 Tidal volume2,3 Respiratory rate2,3 Minute ventilation2,3
4–25 cm H2O (4–25 hPa)
0.1 cm H2O (0.1 hPa)
0–120 L/min 0–4000 mL 0–50 BPM 0–30 L/min Accuracy1
1 L/min 1 mL 1 BPM 0.1 L/min
±[0.5 cm H2O (0.5 hPa) + 4% of measured value] ±6 L/min or 10% of reading, whichever is greater, at 0 to 150 L/min positive flow ±12 L/min or 20% of reading, whichever is greater, 0 to 60 L/min ±20% ±1.0 BPM ±20%
Results are expressed at ATPD (Ambient Temperature and Pressure, Dry). Accuracy may be reduced by the presence of leaks, supplemental oxygen, tidal volumes <100 mL or minute ventilation <3 L/min. 3 Measurement accuracy verified as per EN ISO 10651-6:2009 for Home Care Ventilatory Support Devices (Figure 101 and Table 101) using nominal ResMed mask vent flows. 2
Pressure accuracy Maximum static pressure variation at 10 cm H2O (10 hPa) according to EN ISO 17510-1:2009 Without humidification With humidification
Standard air tubing ± 0.5 cm H2O (± 0.5 hPa) ± 0.5 cm H2O (± 0.5 hPa)
SlimLine air tubing ± 0.5 cm H2O (± 0.5 hPa) ± 0.5 cm H2O (± 0.5 hPa)
Maximum dynamic pressure variation according to EN ISO 17510-1:2009 Device without humidification and Standard air tubing / Device with humidification and Standard air tubing Pressure [cm H2O (hPa)] 10 BPM 15 BPM 20 BPM 4 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 8 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 12 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 16 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 20 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 25 0.3 / 0.3 0.5 / 0.4 0.7 / 0.7 Device without humidification and SlimLine air tubing / Device with humidification and SlimLine air tubing 10 BPM 15 BPM 20 BPM Pressure [cm H2O (hPa)] 4 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 8 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 12 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 16 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 20 0.5 / 0.5 0.5 / 0.5 0.8 / 0.8 25
0.4 / 0.3
0.6 / 0.5
0.8 / 0.8
Symbols The following symbols may appear on the product or packaging. Read instructions before use. use.
Manufacturer. Catalogue number.
Indicates a warning or caution. European Authorised Representative.
Batch code. On / Off.
Protected against finger sized objects and against dripping water when tilted up to
15 degrees from specified orientation. equipment.
Follow instructions before
China pollution control logo 1.
Type BF applied part.
China pollution control logo 2.
(In the US, Federal law restricts these devices to sale by or on the order of a physician). Maximum water level. Atmospheric pressure limitation.
Use distilled water only.
Complies with RTCA DO-160 section 21, category M.
Environmental information This device should be disposed of separately, not as unsorted municipal waste. To dispose of your device, you should use appropriate collection, reuse and recycling systems available in your region. The use of these collection, reuse and recycling systems is designed to reduce pressure on natural resources and prevent hazardous substances from damaging the environment. If you need information on these disposal systems, please contact your local waste administration. The crossed-bin symbol invites you to use these disposal systems. If you require information on collection and disposal of your ResMed device please contact your ResMed office, local distributor or go to www.resmed.com/environment.
Servicing The AirCurve 10 device is intended to provide safe and reliable operation when operated in accordance with the instructions provided by ResMed. ResMed recommends that the AirCurve 10 device be inspected and serviced by an authorised ResMed Service Centre if there is any sign of wear or concern with device function. Otherwise, service and inspection of the products generally should not be required during their design life.
Limited warranty ResMed Ltd (hereafter 'ResMed') warrants that your ResMed product shall be free from defects in material and workmanship from the date of purchase for the period specified below. Product
Mask systems (including mask frame, cushion, headgear and tubing)-excluding single-use devices
Accessories-excluding single-use devices Flex-type finger pulse sensors Humidifier water tubs Batteries for use in ResMed internal and external battery systems
Clip-type finger pulse sensors
CPAP and bilevel device data modules Oximeters and CPAP and bilevel device oximeter adapters Humidifiers and humidifier cleanable water tubs Titration control devices CPAP, bilevel and ventilation devices (including external power supply units)
Battery accessories Portable diagnostic/screening devices This warranty is only available to the initial consumer. It is not transferable. If the product fails under conditions of normal use, ResMed will repair or replace, at its option, the defective product or any of its components. This Limited Warranty does not cover: a) any damage caused as a result of improper use, abuse, modification or alteration of the product; b) repairs carried out by any service organisation that has not been expressly authorised by ResMed to perform such repairs; c) any damage or contamination due to cigarette, pipe, cigar or other smoke; and d) any damage caused by water being spilled on or into an electronic device. Warranty is void on product sold, or resold, outside the region of original purchase. Warranty claims on defective product must be made by the initial consumer at the point of purchase. This warranty replaces all other expressed or implied warranties, including any implied warranty of merchantability or fitness for a particular purpose. Some regions or states do not allow limitations on how long an implied warranty lasts, so the above limitation may not apply to you. ResMed shall not be responsible for any incidental or consequential damages claimed to have resulted from the sale, installation or use of any ResMed product. Some regions or states do not allow the exclusion or limitation of incidental or consequential damages, 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 region to region. For further information on your warranty rights, contact your local ResMed dealer or ResMed office.
Further information If you have any questions or require additional information on how to use the device, contact your care provider.
ResMed Ltd DISTRIBUTED BY 1 Elizabeth Macarthur Drive ResMed Corp 9001 Spectrum Center Boulevard San Diego CA 92123 USA Bella Vista NSW 2153 Australia ResMed (UK) Ltd 96 Jubilee Ave Milton Park Abingdon Oxfordshire OX14 4RW UK See www.resmed.com for other ResMed locations worldwide. For patent and other intellectual property information, see www.resmed.com/ip. AirCurve, PaceWave, Air10, ClimateLine, HumidAir and SlimLine are trademarks of ResMed Ltd. AutoSet, SlimLine and ClimateLine are registered in U.S. Patent and Trademark Office. SD Logo is a trademark of SD-3C, LLC. © 2015 ResMed Ltd. 378195/1 2015-07