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The AirSense™ 10 AutoSet™ and AirSense 10 AutoSet for Her are ResMed's premium auto-adjusting pressure devices. The AirSense 10 Elite and AirSense 10 CPAP are ResMed's Continuous Positive Airway Pressure (CPAP) devices.
Read this entire guide before using the device.
In the US, Federal law restricts this device to sale by or on the order of a physician.
AirSense 10 AutoSet
The AirSense 10 AutoSet self-adjusting device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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.
AirSense 10 AutoSet for Her
The AirSense 10 AutoSet for Her self-adjusting device is indicated for the treatment of obstructive sleep apnea (OSA) in patients (female patients with mild to moderate OSA when using AutoSet for Her treatment mode) weighing more than 66 lb (30 kg). 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.
AirSense 10 Elite
The AirSense 10 Elite device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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.
AirSense 10 CPAP
The AirSense 10 CPAP device is indicated for the treatment of obstructive sleep apnea (OSA) in patients weighing more than 66 lb (30 kg). 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
Positive airway pressure therapy may be contraindicated in some patients with the following preexisting conditions:
• severe bullous lung disease
• pneumothorax
• pathologically low blood pressure
• dehydration
• 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:
The AirSense 10 includes the following:
Contact your care provider for a range of accessories available for use with the device including:
1 Air outlet
2 Air filter cover
3 Power inlet
4 Serial number and device number
5 Water tub
6 Screen
7 Adapter cover
8 SD card cover
Start/Stop button
Press to start/stop therapy.
Press and hold for three seconds to enter power save mode.
Dial
Turn to navigate the menu and press to select an option.
Turn to adjust a selected option and press to save your change.
Home button
Press to return to the Home screen.
Different icons may be displayed on the screen at different times including:
Ramp Time
Ramp Time Auto
Humidity
Humidifier warming
Humidifier cooling
Wireless signal strength (green)
Wireless transfer not enabled (gray)
No wireless connection
Airplane Mode
Do not overfill the water tub as water may enter the device and air tubing.
Recommended masks are available on www.resmed.com.
You will know that therapy is on when the Sleep Report screen is displayed.
The current treatment pressure is shown in green.
During ramp time the pressure is gradually increasing and you will see a spinning circle. Once the prescribed treatment pressure is reached, the entire circle will be green.
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 AirSense 10 device has a light sensor that adjusts the screen brightness based on the light in the room.
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.
Humidifier–Indicates if your humidifier is working properly:
Humidifier working.
Humidifier might be faulty, contact your care provider.
If set by your care provider, you will also see:
Events per hour–Indicates the number of apneas and hypopneas experienced per hour.
More Info–Turn the dial to scroll down to view more detailed usage data.
Your AirSense 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:
To exit power save mode:
Your AirSense 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 personalize your options.
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, 5 to 45 minutes or Auto. When Ramp Time is set to Auto, the device will detect when you have fallen asleep and then automatically rise to the prescribed treatment pressure.
To adjust Ramp Time:
The humidifier moistens the air and is designed to make therapy more comfortable. If you are getting a dry nose or mouth, turn up the humidity. If you are getting any moisture in your mask, turn down the humidity.
You can set the Humidity Level to Off or between 1 and 8, where 1 is the lowest humidity setting and 8 is the highest humidity setting.
To adjust the Humidity Level:
If you continue to get a dry nose or mouth, or moisture in your mask, consider using ClimateLineAir heated air tubing. ClimateLineAir together with Climate Control delivers more comfortable therapy.
Mask Fit is designed to help you assess and identify possible air leaks around your mask.
To check Mask Fit:
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.
There are some more options on your device which you can personalize.
Pressure Relief* | When Pressure Relief is enabled, you may find it easier to breathe out. This can help you get used to therapy. |
SmartStart* | When SmartStart is enabled, therapy starts automatically when you breathe into your mask. When you remove your mask, it stops automatically after a few seconds. |
*When enabled by your care provider.
It is important that you regularly clean your AirSense 10 device to make sure you receive optimal therapy. The following sections will help you with disassembling, cleaning, checking and reassembling your device.
Regularly clean your tubing assembly, water tub and mask to receive optimal therapy and to prevent the growth of germs that can adversely affect your health.
1. Hold the water tub at the top and bottom, press it gently and pull it away from the device.
2. Open the water tub and discard any remaining water.
3. Hold the cuff of the air tubing and gently pull it away from the device.
4. Hold both the cuff of the air tubing and the swivel of the mask, then gently pull apart.
You should clean the device weekly as described. Refer to the mask user guide for detailed instructions on cleaning your mask.
You should regularly check the water tub, air tubing and the air filter for any damage.
When the water tub and air tubing are dry, you can reassemble the parts.
Your AirSense 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, if wireless network is available, or via an SD card.
Your AirSense 10 device is equipped with cellular communication. This allows your therapy data to be wirelessly transmitted to your care provider to enhance the quality of your treatment. It also allows therapy settings to be updated in a more timely manner or your device software to be upgraded. The Wireless signal strength icon displayed at the top right of your screen indicates the signal strength.
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 power outlet at all times and make sure that it is not in Airplane Mode.
Notes:
Please be aware that within the wireless network, the availability and quality of the network may be affected by terrain, buildings, and the weather. Wireless communication depends on network availability. Coverage is not available everywhere and varies by service.
An alternative way for your therapy data to be transferred to your care provider is via the SD card, if provided. 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, because data is being written to the card.
To remove the SD card:
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.
You can take your AirSense 10 device with you wherever you go. Just keep the following in mind:
Your AirSense 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 AirSense 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:
To turn on Airplane Mode:
The Airplane Mode icon is displayed at the top right of the screen.
Do not use the device with water in the water tub on a plane due to the risk of inhalation of water during turbulence.
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
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.
Humidity level may be set too low.
Adjust the Humidity Level. If you have ClimateLineAir heated air tubing, see the ClimateLineAir user guide.
Humidity level may be set too high.
Adjust the Humidity Level. If you have ClimateLineAir heated air tubing, see the ClimateLineAir user guide.
Air may be escaping through your mouth.
Increase the Humidity Level.
You may need a chin strap to keep your mouth closed or a full face mask.
Ramp may be turned off.
Use the Ramp Time option.
Ramp may be in progress.
Wait for air pressure to build up or turn Ramp Time off.
Backlight on the screen may have turned off.
It turns off automatically after a short period of time. Power may not be connected.
Press Home or the dial to turn it back on.
Connect the power supply and make sure the plug is fully inserted.
Device is cooling down.
Device blows a small amount of air in order to avoid condensation in the air tubing. It will stop automatically after 30 minutes.
Water tub may not be assembled correctly.
Check for damage and reassemble the water tub correctly.
Water tub may be damaged or cracked. Contact your care provider for a replacement.
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.
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.
Turn off Airplane Mode, see Traveling by plane.
Talk to your care provider about your settings.
Software upgrade takes approximately 10 minutes to complete.
Device messages
Water tub may not be inserted properly.
Make sure the water tub is correctly inserted.
Water tub seal may not be inserted properly.
Open the water tub and make sure that the seal is correctly inserted.
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.
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 may not be inserted correctly.
Remove and reinsert the SD card.
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.
Some parts of your device are designed to easily come off in order to avoid damage to the parts or the device. You can easily reassemble them as described below.
To insert the water tub seal:
To reassemble the water tub lid:
90W power supply unit AC input range: | 100–240V, 50–60Hz 1.0–1.5A, Class II 115V, 400Hz 1.5A, Class II (nominal for aircraft use) |
DC output: | 24V ![]() |
Typical power consumption: | 53W (57VA) |
Peak power consumption: | 104W (108VA) |
Environmental conditions Operating temperature: | +41°F to +95°F (+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 (104°F/40°C) the device remains safe. |
Operating humidity: | 10 to 95% relative humidity, non-condensing |
Operating altitude: | Sea level to 8,500' (2,591 m); air pressure range 1013 hPa to 738 hPa |
Storage and transport temperature: | -4°F to +140°F (-20°C to +60°C) |
Storage and transport humidity: | 5 to 95% relative humidity, non-condensing |
Electromagnetic compatibility
The AirSense 10 complies with all applicable electromagnetic compatibility requirements (EMC) according to IEC 60601-12:2014, 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/downloads/devices
Classification: IEC 60601-1:2005+/A1:2012
Class II (double insulation), Type BF, Ingress protection IP22.
Pressure sensor:
Internally located at device outlet, analog gauge pressure type, 0 to 40 cm H 2 O (0 to 40 hPa)
Flow sensor:
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 ISO 80601-2-70:2015 (CPAP mode):
SlimLine: 25 dBA with uncertainty of 2 dBA
Standard: 25 dBA with uncertainty of 2 dBA
SlimLine or Standard and humidification: 27 dBA with uncertainty of 2 dBA Power level measured according to ISO 80601-2-70:2015 (CPAP mode):
SlimLine: 33 dBA with uncertainty of 2 dBA
Standard: 33 dBA with uncertainty of 2 dBA
SlimLine or Standard and humidification: 35 dBA with uncertainty of 2 dBA
Declared dual-number noise emission values in accordance with ISO 4871:1996.
Physical - device and water tub Dimensions (H x W x D): | 4.57" x 10.04" x 5.91" (116 mm x 255 mm x 150 mm) |
Air outlet (complies with ISO 5356-1:2004): | 22 mm |
Weight (device and standard water tub): | 44 oz (1248 g) |
Weight (device and cleanable water tub): | 44 oz (1248 g) |
Housing construction: | Flame retardant engineering thermoplastic |
Water capacity: | To maximum fill line 380 mL |
Standard water tub - material: | Injection molded plastic, stainless steel and silicone seal |
Cleanable water tub - material: | Injection molded plastic, stainless steel and silicone seal |
Temperature Maximum heater plate: | 154°F (68°C) |
Cut-out: | 165°F (74°C) |
Maximum gas temperature: | ≤ 106°F (≤ 41°C) |
Air filter Standard: | Material: Polyester non woven fiber Average arrestance: >75% for ~7 micron dust |
Hypoallergenic: | Material: Acrylic and polypropylene fibers 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.
Wireless module Bands may not be available in all regions. | |
Technology used: | CDMA (USA only) 4G 3G 2G |
Frequencies: | CDMA (800/1900 MHz) 4G (700/850/1700/1900 MHz) 3G (850/900/1700/1900/2100 MHz) 2G (850/900/1800/1900 MHz) |
Max RF power output: | CDMA 24.5 dBm 4G 23.0 dBm 3G 24.0 dBm 2G 33.0 dBm |
FCC ID: 2ACHL-AIR104G, 2ACHL-AIR103G
IC: 9103A-AIR104G, 9103A-AIR103G
The AirSense 10 device complies with FCC Rules and Industry Canada rules.
The AirSense 10 device should be used at a minimum distance of 0.8" (2 cm) from the body during operation. Additional information regarding the FCC Rules and IC compliance for this device can be found on www.resmed.com/downloads/devices
Operating pressure range AutoSet, AutoSet For Her, Elite, CPAP | 4 to 20 cm H 2 O |
Supplemental oxygen Maximum flow: | 4 L/min |
Pneumatic flow path ![]() |
|
Design life Device, power supply unit: Cleanable water tub: Standard water tub, air tubing: | 5 years 2.5 years 6 months |
General The patient is an intended operator. |
Humidifier performance
Mask Pressure cm H 2 O (hPa) | RH output % at 63°F (17°C) ambient temperature | RH output % at 72°F (22°C) ambient temperature | Nominal system output AH1, BTPS 2 | |
Setting 4 | Setting 8 | Setting 4 | Setting 8 | |
4 | 85 | 100 | 6 | >10 |
10 | 85 | 100 | 6 | >10 |
20 | 85 | 90 | 6 | >10 |
|
Air tubing
Air tubing | Material | Length | Inner diameter |
ClimateLineAir | Flexible plastic and electrical components | 6'6" (2 m) | 0.6" (15 mm) |
ClimateLineAir Oxy | Flexible plastic and electrical components | 6'4" (1.9 m) | 0.75" (19 mm) |
SlimLine | Flexible plastic | 6' (1.8 m) | 0.6" (15 mm) |
Standard | Flexible plastic | 6'6" (2 m) | 0.75" (19 mm) |
Heated air tubing temperature cut-out: ≤ 106°F (≤ 41°C) |
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.
Air tubing resistance to flow and compliance information
Refer to the Air tubing compliance guide in ResMed.com.
Displayed values
Value | Range | Display resolution |
Pressure sensor at air outlet: Mask pressure Flow derived values: Leak | 4–20 cm H 2 0 (4–20 hPa) 0–120 L/min | 0.1 cm H 2 O (0.1 hPa) 1 L/min |
Value | Accuracy | |
Pressure measurement 1: | ||
Mask pressure 2 | ±[0.5 cm H 2 0 (0.5 hPa) + 4% of measured value] | |
Flow and flow derived values 1: | ||
Flow | ±6 L/min or 10% of reading, whichever is greater, at 0 to 150 L/min positive flow | |
Leak 2 | ±12 L/min or 20% of reading, whichever is greater, 0 to 60 L/min |
Measurement system uncertainties
In accordance with ISO 80601-2-70:2015 the measurement uncertainty of the manufacturer's test equipment is:
For measures of flow | ± 1.5 L/min or ± 2.7% of reading (whichever is greater) |
For measures of volume (< 100 mL) | ± 5 mL or 6% of reading (whichever is greater) |
For measures of volume (≥ 100 mL) | ± 20 mL or 3% of reading (whichever is greater) |
For measures of static pressure | ± 0.15 cm H2O (hPa) |
For measures of dynamic pressure | ± 0.27 cm H2O (hPa) |
For measures of time | ± 10 ms |
Note: ISO 80601-2-70:2015 stated accuracies and test results provided in this manual for these items already include the relevant measurement uncertainty from the table above.
Pressure accuracy
Maximum static pressure variation at 10 cm H 2 O (10 hPa) according to ISO 80601-2-70:2015 | ||||
Standard air tubing | SlimLine air tubing | |||
Without humidification | ± 0.5 cm H 2 O (± 0.5 hPa) | ± 0.5 cm H | 2 O (± 0.5 hPa) | |
With humidification | ± 0.5 cm H 2 O (± 0.5 hPa) | ± 0.5 cm H | 2 O (± 0.5 hPa) | |
Maximum dynamic pressure variation according to ISO 80601-2-70:2015 | ||||
Device without humidification and Standard air tubing / Device with humidification and Standard air tubing | ||||
Pressure [cm H2 O (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 | |
Device without humidification and SlimLine air tubing / Device with humidification and SlimLine air tubing | ||||
Pressure [cm H2 O (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 | |
Flow (maximum) at set pressures | ||||
The following are measured accordingly to ISO 80601-2-70:2015 at the end of the specified air tubing: | ||||
Pressure cm H2О(hPa) | AirSense 10 and Standard L/min | AirSense 10, humidification and Standard L/min | AirSense 10 and SlimLine L/min | AirSense 10, humidification and ClimateLineAir L/min |
4 | 180 | 143 | 162 | 151 |
8 | 168 | 135 | 151 | 142 |
12 | 157 | 136 | 140 | 135 |
16 | 144 | 134 | 128 | 121 |
20 | 131 | 123 | 117 | 109 |
The following symbols may appear on the product or packaging.
Read instructions before use.
Indicates a warning or caution.
Follow instructions before use.
Manufacturer.
European Authorized Representative.
Batch code.
Catalog number.
Serial number.
Device number.
On / Off.
Device weight.
Protected against finger sized objects and against dripping water when tilted up to 15 degrees from specified orientation.
Direct current.
Type BF applied part.
Class II equipment.
Humidity limitation.
Temperature limitation.
Non-ionising radiation.
China pollution control logo
1. China pollution control logo
2. Prescription only (In the US, Federal law restricts these devices to sale by or on the order of a physician).
Maximum water level.
Use distilled water only.
Operating altitude.
Atmospheric pressure limitation.
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 ResMed.com/environment.
The AirSense 10 device is intended to provide safe and reliable operation when operated in accordance with the instructions provided by ResMed. ResMed recommends that the AirSense 10 device be inspected and serviced by an authorized 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.
ResMed Pty 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 | Warranty period |
| 90 days |
| 6 months |
| 1 year |
| 2 years |
This warranty is only available to the initial consumer. It is not transferable.
During the warranty period, 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 organization that has not been expressly authorized 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 exposure to ozone, activated oxygen or other gases.
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.
Visit ResMed.com for the latest information on ResMed's Limited Warranty.
If you have any questions or require additional information on how to use the device, contact your care provider.
ResMed Pty Ltd
1 Elizabeth Macarthur Drive
Bella Vista NSW 2153 Australia
See ResMed.com for other ResMed locations worldwide.
Air10, AirSense, AutoSet, ClimateLine, HumidAir and SlimLine are trademarks and/or registered trademarks of the ResMed family of companies.
For patent and other intellectual property information, see ResMed.com/ip.
SD Logo is a trademark of SD-3C, LLC. © 2021 ResMed. 378947/1 2021-02
ResMed.com
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
Download ResMed AirSense 10 AutoSet, AutoSet for Her, Elite, CPAP Manual
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