Clinical guide
English
i
Contents
Welcome ...................................................................................................................................... 1
AirCurve 10 CS PaceWave indications for use ....................................................................... 1
Contraindications .................................................................................................................... 1
Adverse effects ...................................................................................................................... 1
At a glance ................................................................................................................................... 2
About the control panel .............................................................................................................. 3
Therapy information ................................................................................................................... 4
ASV therapy ............................................................................................................................ 4
ASV mode ........................................................................................................................ 4
ASVAuto mode ................................................................................................................. 4
Pressure Support .............................................................................................................. 4
Backup rate ...................................................................................................................... 5
CPAP mode ............................................................................................................................ 5
Leak management with VSync ............................................................................................... 5
Comfort features ......................................................................................................................... 5
Ramp ...................................................................................................................................... 5
Climate Control ....................................................................................................................... 6
Climate Control Auto ........................................................................................................ 6
Climate Control Manual .................................................................................................... 6
Setup ............................................................................................................................................ 7
Supplemental oxygen ............................................................................................................. 8
Antibacterial filters .................................................................................................................. 8
Accessing and exiting the Clinical Menu .................................................................................. 9
Adjusting the clinical settings ................................................................................................. 9
Setting the date and time ............................................................................................... 10
Settings menu ...................................................................................................................... 10
Therapy ........................................................................................................................... 10
Comfort .......................................................................................................................... 11
Accessories .................................................................................................................... 11
Options ........................................................................................................................... 12
Configuration .................................................................................................................. 12
Starting therapy ......................................................................................................................... 14
Stopping therapy ....................................................................................................................... 14
Viewing the Sleep Report ..................................................................................................... 14
Sleep Report screen parameters .......................................................................................... 15
Cleaning and Maintenance ....................................................................................................... 16
Disassembling ...................................................................................................................... 16
Cleaning ................................................................................................................................ 16
Checking ............................................................................................................................... 17
Reassembling ....................................................................................................................... 17
Reprocessing ............................................................................................................................. 18
Surface disinfection .............................................................................................................. 18
Reprocessing the air tubing .................................................................................................. 19
Disconnecting ................................................................................................................. 19
Decontaminating ............................................................................................................ 19
Disinfecting .................................................................................................................... 19
Inspecting ....................................................................................................................... 20
Reconnecting the air tubing ........................................................................................... 20
Packaging and storage ................................................................................................... 20
Reprocessing the humidifier and air outlet ........................................................................... 21
Disassembling ................................................................................................................ 21
ii
Decontaminating ............................................................................................................. 22
Disinfecting ..................................................................................................................... 22
Inspecting ....................................................................................................................... 23
Reassembling ................................................................................................................. 23
Packaging and storage .................................................................................................... 24
Data management and therapy compliance ........................................................................... 25
Remote monitoring ............................................................................................................... 25
SD card .................................................................................................................................. 25
Data storage .......................................................................................................................... 26
Software upgrade .................................................................................................................. 26
Managing patient care .............................................................................................................. 27
Patient menu ......................................................................................................................... 27
Therapy data .......................................................................................................................... 27
Travelling ............................................................................................................................... 27
Travelling by plane .......................................................................................................... 27
Troubleshooting......................................................................................................................... 28
General troubleshooting ........................................................................................................ 28
Device messages .................................................................................................................. 30
General warnings and cautions ................................................................................................ 31
Technical specifications ............................................................................................................ 32
Symbols................................................................................................................................. 36
Servicing ................................................................................................................................ 36
Limited warranty ................................................................................................................... 37
English 1
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, periodic breathing or Cheyne-Stokes Respiration
(CSR) that may or may not be associated with congestive heart failure. 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 or pneumomediastinum
pathologically low blood pressure, particularly if associated with intravascular volume depletion
dehydration
cerebrospinal fluid leak, recent cranial surgery, or trauma.
Adverse effects
Patients should report unusual chest pain, severe headache, or increased breathlessness to their
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
nosebleed
bloating
ear or sinus discomfort
eye irritation
skin rashes.
2
At a glance
The AirCurve 10 includes the following:
Device
HumidAir
™
humidifier
Air tubing
Power supply unit
Travel bag
SD card (already inserted).
A range of accessories are available for use with the device including:
Air tubing (heated and non-heated): ClimateLineAir
™
, SlimLine™, Standard
Side cover for use without the humidifier
Filter: Hypoallergenic filter, standard filter
Air10
™
DC/DC converter (12V/24V)
SD card reader
Air10 oximeter adapter
Air10 USB adapter.
Note: Make sure all parts and accessories used with the device are compatible. For compatibility
information, refer to www.resmed.com.
1 Air outlet 5 HumidAir humidifier
2 Air filter cover 6 Screen
3 Power inlet 7 Adapter cover
4 Serial number and device number 8 SD card cover
English 3
About the control panel
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
Wireless signal strength (green)
Humidity
Wireless transfer not enabled (grey)
Humidifier warming No wireless connection
Humidifier cooling
Airplane Mode
4
Therapy information
ASV, ASVAuto and CPAP mode are available on the AirCurve 10 CS PaceWave device.
ASV therapy
ResMed's ASV therapy targets the patient’s own recent Minute Ventilation (MV). It treats central
sleep apnoea and/or mixed apnoea and periodic breathing by automatically adjusting the pressure
support (PS) in a defined pressure range to maintain Minute Ventilation at the target.
The AirCurve 10 CS PaceWave device offers two different ASV modes:
ASV mode
ASVAuto mode.
ASV mode
In ASV mode, the expiratory positive airway pressure (EPAP) is fixed and can be manually adjusted
to eliminate obstructive events. The Pressure Support (PS) varies between the Min PS and the Max
PS to answer to the patient's need. Mandatory breaths are delivered at the patient’s recent
spontaneous breath rate, ie, the timed backup rate is automatically calculated to match the patient’s
needs and is applied appropriately in the case of an event.
ASVAuto mode
In addition to the functionality of the ASV mode, the device in ASVAuto mode automatically adjusts
the expiratory pressure in order to provide only the amount of pressure (EPAP) required to maintain
upper airway patency. The device analyses the state of the patient’s upper airway on a breath-bybreath basis and delivers expiratory pressure within the allowed range (Min EPAP and Max EPAP)
according to the degree of obstruction. EPAP is automatically adjusted depending on three
parameters: inspiratory flow limitation, snore, and obstructive apnoea.
Pressure Support
Pressure Support (PS) is defined as the difference between the peak pressure at the end of
inspiration, and the minimum pressure at the end of expiration (ie, the amplitude of the pressure
waveform delivered).
The AirCurve 10 CS PaceWave pressure support (Inspiration:Expiration and Expiration:Inspiration)
trigger points are set automatically based on measurement of the patient respiratory flow. The
AirCurve 10 CS PaceWave algorithm will automatically adjust pressure delivery to keep the patient’s
respiratory flow even.
ResMed recommends that the Max PS should be set to 15 cm H
2
O (15 hPa).
English 5
Backup rate
The AirCurve 10 CS PaceWave device uses breath phase mapping to provide a timed backup rate
that is synchronised with the patient’s own breathing. When the patient deviates from the
ventilatory target, the CS PaceWave device aims to stabilise the patient by adjusting Pressure
Support. If necessary, it will adjust the timed backup rate from one that matches the patient’s own
recent rate towards the built-in default 15 BPM backup rate.
CPAP mode
In CPAP mode, a fixed pressure is delivered.
Leak management with VSync
Using ResMed's VSync algorithm, the AirCurve 10 device monitors and compensates for leak by
continuously and automatically adjusting the baseline flow. This enables reliable delivery of therapy
pressure while maintaining patient-device synchrony.
Comfort features
Ramp
Designed to make the beginning of treatment more comfortable, ramp is available in all modes.
Note: Ramp is not recommended for patients exhibiting CSR during sleep onset.
In ASV and ASVAuto mode, the ramp time defines the period during which the expiratory pressure
increases linearly from a lower more comfortable start pressure (Start EPAP) to the minimum
treatment pressure (EPAP for ASV mode and Min EPAP for ASVAuto mode) before the autoadjusting algorithm commences.
During ramp, the pressure support is always at Min PS. After ramp, the pressure support modulates
within the PS range (Min PS and Max PS). In ASVAuto mode, the EPAP also modulates within the
EPAP range (Min EPAP and Max EPAP).
Note: If ramp is on (set between 5 min and 45 min), Start EPAP has to be set.
In CPAP mode, the pressure increases from a low pressure (Start Pressure) to the prescribed
treatment pressure.
6
Climate Control
Climate Control is an intelligent system that controls the humidifier and the ClimateLineAir heated
air tubing to deliver constant, comfortable temperature and humidity levels during therapy.
Designed to prevent dryness of the nose and mouth, it maintains the set temperature and relative
humidity during sleep. Climate Control can be set to either Auto or Manual and is only available
when the ClimateLineAir and the HumidAir humidifier are attached.
Climate Control Auto
Climate Control Auto is the recommended and default setting. Climate Control Auto is designed to
make therapy as easy as possible, so there is no need to change the temperature or humidity
settings.
The Tube Temperature is set to 27°C and Climate Control adjusts the humidifier output to maintain a
constant, comfortable humidity level of 85% relative humidity while protecting against rainout
(water droplets in the air tubing and mask).
Climate Control Manual
Designed to offer more flexibility and control over settings, Climate Control Manual lets the patient
adjust the temperature and humidity to the setting which is most comfortable for them.
In Climate Control Manual, the Tube Temperature and the Humidity Level can be set independently
however, rainout protection is not guaranteed. If rainout does occur, first try increasing the tube
temperature. If the air temperature becomes too warm and rainout continues, try decreasing the
humidity.
Tube Temperature
If the air in the mask feels too warm or too cold, the patient can adjust the temperature to find what
is most comfortable or turn it off completely. The Tube Temperature can be set to anywhere
between 16–30°C.
The temperature sensor located at the mask end of the ClimateLineAir heated air tubing enables the
system to automatically control the temperature of the air delivered to the patient. This ensures the
temperature of the air delivered to the patient does not fall below the set minimum temperature,
therefore maximising breathing comfort for the patient.
Humidity Level
The humidifier moistens the air and is designed to make therapy more comfortable. If the patient is
getting a dry nose or mouth, turn up the humidity. If the patient is getting moisture in their mask,
turn down the humidity.
The Humidity Level can be set to Off or between 1 and 8, where 1 is the lowest humidity setting
and 8 is the highest humidity setting.
For each humidifier setting, the Climate Control system delivers a constant amount of water vapour,
or absolute humidity (AH), to the patient’s upper airway.
Automatic adjustment
The humidifier and ClimateLineAir heated air tubing are controlled by the Climate Control algorithm
to deliver constant humidity and temperature outputs. The system adjusts automatically to changes
in:
ambient room temperature and humidity values
flow due to pressure changes
flow due to mask or mouth leak.
English 7
Setup
CAUTION
Do not overfill the humidifier as water may enter the device and air tubing.
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. Open the humidifier and fill it with water up to the maximum water level mark.
Do not fill the humidifier with hot water.
5. Close the humidifier and insert it into the side of the device.
6. Connect the free end of the air tubing firmly onto the assembled mask.
See the mask user guide for detailed information.
Recommended masks are available on www.resmed.com.
8
Supplemental oxygen
The AirCurve 10 device is designed to be compatible with up to 15 L/min of supplemental oxygen in
CPAP and ASV modes and up to 4 L/min in ASVAuto mode.
At a fixed rate of supplemental oxygen flow, the inhaled oxygen concentration will vary depending
on the pressure settings, patient breathing pattern, mask selection and the leak rate.
To connect supplemental oxygen to the device you need to connect an oxygen connector port. For
more information on how to set up the device with supplemental oxygen, refer to the user guide
supplied with that accessory.
Notes:
Adding oxygen may affect the delivered pressure and the accuracy of the displayed leak and
minute ventilation.
Before adding oxygen, familiarise yourself and your patient with the specific warnings relating to
the use of supplemental oxygen. These can be found at the end of this guide.
Antibacterial filters
Antibacterial filters increase resistance in the air circuit and may affect accuracy of displayed and
delivered pressure, particularly at high flows.
ResMed recommends using an antibacterial filter with a low impedance [eg, 2 cm H
2
O (2 hPa) at
60 L/min], such as PALL (BB50T), Air Safety Filter without Luer Port (4222/702) or Air Safety Filter
with Side Port 24966 (4222/701). If using the Air Safety Filter with Side Port, an Oxygen Connector
Port is required.
Note: When using the SlimLine air tubing above 20 cm H2O (20 hPa), the device optimum
performance may not be reached if used with an antibacterial filter. The device performance must
be checked prior to prescribing the SlimLine air tubing for use with an antibacterial filter.
English 9
Accessing and exiting the Clinical Menu
You can access, view and set parameters relating to a patient's therapy and device configuration in
the Clinical Menu.
To access the Clinical Menu:
Press and hold the dial and the Home button for three seconds.
The Home screen is displayed with an unlock icon
in the top right corner of the screen.
To exit the Clinical Menu:
Press and hold the dial and the Home button for three seconds.
Select Exit Clinical Menu from the Home screen.
The device will automatically exit the Clinical Menu after 20 minutes of inactivity.
Adjusting the clinical settings
1. Access the Clinical Menu, highlight Settings and press the dial.
The Settings menu is displayed.
2. Turn the dial to highlight the setting you want to adjust and then press the dial.
3. Turn the dial to adjust the setting and press the dial to save the change.
10
The settings can be changed in different ways depending on the type of screen:
Turn the dial to edit live in
the menu.
Turn the dial to change
the setting.
Select from a list of options.
Setting the date and time
Before you set up a new patient and start therapy for the first time, make sure you set the correct
local date and time on the device. If you set the date and time after starting therapy, you may lose
patient data.
1. In Settings menu, select Date and change the setting to the correct date.
2. Select Time and change it to the correct local time.
3. Make sure the correct local time and date has been applied.
The AirCurve 10 settings must be configured for each individual patient. The settings should be
periodically reassessed to ensure optimal therapy.
Settings menu
You set all parameters relating to a patient's therapy and device configuration in the Settings menu.
Note: Not all parameters are available in all regions. The default and range values may differ
between modes and regions.
The range of parameters in the Settings menu are expressed in cm H2O, where 1cm H2O is equal to
0.98 hPa. The units can be changed under Configuration.
Therapy
Parameter Description Mode Range
ASV ASVAuto CPAP
EPAP Sets the pressure to be delivered to
the patient when the device is
cycled into expiration.
4–15 cm H2O (4–15 hPa)
0.2 cm H
2
O (0.2 hPa) increments
English 11
Min EPAP Sets the minimum EPAP (minimum
expiratory pressure) delivered by
the device.
4–15 cm H2O (4–15 hPa)
Max EPAP Sets the maximum EPAP delivered
by the device.
Dependent on Min EPAP.
4–15 cm H2O (4–15 hPa)
Min PS Sets the minimum pressure support
delivered by the device
0–6 cm H2O (0–6 hPa)
Max PS Sets the maximum pressure support
delivered by the device.
Dependent on EPAP in ASV.
5–20 cm H2O (5–20 hPa)
Set Pressure Sets the fixed treatment pressure.
4–20 cm H2O (4–20 hPa), 0.2 cm
H
2
O (0.2 hPa) increments
Mask Select the type of mask used by the
patient. Refer to Mask Device
Compatibility List on
www.resmed.com.
Full Face / Nasal / Pillows
Comfort
Parameter Description Mode Range
ASV ASVAuto CPAP
Ramp Time Set the ramp time.
Off / 5–45 mins
Start Pressure Set the pressure at the start of
ramp, up to treatment pressure.
4–Set pressure, 0.2 cm H2O
(0.2 hPa) increments
Start EPAP Set the pressure at the start of
ramp, up to minimum treatment
pressure.
4–EPAP, 0.2 cm H2O (0.2 hPa)
increments
Start Pressure Set the pressure at the start of
ramp, up to treatment pressure.
4–Set pressure, 0.2 cm H2O
(0.2 hPa) increments
Climate Ctrl Available when humidifier is used
and ClimateLineAir heated air
tubing is connected.
Manual / Auto
Tube Temp. Set the minimum temperature of air
delivered by heated air tubing such
as ClimateLineAir.
Off / 60–86°F (16–30°C),
1° increments
Humidity Level Set the humidity level.
Off / 1–8
Accessories
Parameter Description Range
Tube Select the type of air tubing used by the patient. ClimateLineAir air tubing
is automatically detected when connected to the device.
SlimLine / Standard
AB filter Select Yes if you attach an antibacterial filter. No / Yes
12
Ext.
humidifier
Select Yes if you connect an external humidifier. No / Yes
View
oximeter
Displayed at all times when an oximeter is connected. 0-300 hrs
0-100% SpO
2
Options
Parameter Description Range
Essentials Set the level of access available to the patient. On / Plus
Leak Alert Enable / disable the Leak Alert feature. When enabled, leaks >40 L/min
(0.7 L/s) for >20 sec result in an audible alert and a high leak message is
displayed.
Off / On
SmartStart™ Enable / disable the SmartStart feature. If you enable the SmartStart
feature, the device will start automatically when the patient breathes into
the mask and then stop automatically when the patient removes the
mask.
Off / On
Reminders
Mask Set a recurring reminder to the patient to replace the mask. Off / 1– 24 mths, 1 month
increments
Humidifier Set a recurring reminder to the patient to replace the humidifier. Off / 1–24 mths, 1 month
increments
Tube Set a recurring reminder to the patient to replace the air tubing. Off / 1–24 mths, 1 month
increments
Filter Set a recurring reminder to the patient to replace the air filter. Off / 1–24 mths, 1 month
increments
Configuration
Parameter Description Selection
Language Set the display language.
(Not all languages available in all regions.)
English / Français / Español /
Português / Deutsch /
Italiano / Nederlands /
Svenska / Norsk / Dansk /
Suomi / Polski / Türkçe /
Русский / 简体中文 /
繁體中文
Date Set the current date.
If you set a new date that occurs in the past then an error message is
displayed. Before this change can be made, erase the compliance data
available under the Configuration menu.
DD Mmm YYYY
Time Set the current time.
If you set a new time that occurs in the past then an error message is
displayed. Before this change can be made, erase the compliance data
available under the Configuration menu.
24 hours
English 13
Press. Units Set the unit of pressure in which pressure is displayed. cm H2O / hPa
Temp. Units Set the temperature units. °F / °C
Restore
Defaults
Reset to default settings (except for language, date and time). Yes / No
Erase Data Erase all data stored on the device and the SD card. Settings, date, time
and device run hours are not affected.
Yes / No
About View Run Hours, SN, SW, provider, type, service and signal strength of
the device, CX number, humidifier and internal modem.
14
Starting therapy
1. Direct the patient to fit their mask.
2. Direct the patient to press Start/Stop, or if the SmartStart feature is enabled, direct them to
breathe into their mask.
Therapy will begin and 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 the patient breathes 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. Direct the patient to remove the mask.
2. Direct the patient to press Start/Stop, or if SmartStart is enabled, therapy will stop automatically
after a few seconds.
The Sleep Report now provides a summary of the therapy session.
Viewing the Sleep Report
The Sleep Report screen shows sleep quality and mask seal status for the most recent therapy
session. Turn the dial to scroll down to view more detailed usage data. The parameters displayed
will depend on the therapy mode.
English 15
Sleep Report screen parameters
Parameter Description
Usage hours Number of hours the device has been used during the last session.
Events (AHI) per hour Apnoeas and hypopnoeas measured per hour for one day. An apnoea is when the
respiratory flow decreases by more than 75% for at least 10 sec. A hypopnoea is when
the respiratory flow decreases to 50% for at least 10 sec. The Apnoea Index (AI) and
Apnoea-Hypopnoea Index (AHI) are calculated by dividing the total number of events
that occurred by the total mask-on therapy period in hours.
Mask Seal
Good—if the 70th percentile leak is less than 24 L/min.
Mask needs adjustment.
Humidifier
Humidifier attached and functional.
Humidifier fault; refer to troubleshooting section.
More Info
Period
Set the time interval covered by the Sleep Report.
The options are: 1 Day / 1 Week / 1 Month / 3 Months / 6 Months / 1 Year
Days Used Number of days the device has been used during the selected period or since the last
compliance data was reset.
Days 4hrs+ Number of days the device has been used for more than 4 hours during the selected
period or since the last compliance data was reset.
Avg. Usage Average number of hours per day the device has been used during the selected period.
Used Hrs Number of hours the device has been used during the selected period or since the last
compliance data reset.
Pressure Average inspiratory pressure during the selected period (95th percentile for each day;
average of 95
th
percentile values for periods >1 day).
Exp. Pressure Average expiratory pressure during the selected period (95
th
percentile for each day;
average of 95
th
percentile values for periods >1 day).
Leak Average of the 95
th
percentile values of leak during the selected period for days with
usage only.
AHI Apnoea-Hypopnoea Index—average AHI during the selected period. AHI and AI are
calculated for times of low leak only.
Total AI Apnoea Index—average total AI during the selected period.
AHI and Total AI: Central sleep apnoea detection (CSAD) is not active in ASVAuto and ASV modes. The ASV algorithm
eliminates central apnoeas. Therefore, any apnoeas reported by the device will be obstructive or indicative of a closed
airway.
16
Cleaning and Maintenance
It is important that the AirCurve 10 device is cleaned regularly to ensure optimal therapy. The
following sections will help with disassembling, cleaning, checking and reassembling the device.
Disassembling
1. Hold the humidifier at the top and bottom, press it gently and pull it away from the device.
2. Open the humidifier 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.
Cleaning
You should clean the device weekly as described. Refer to the mask user guide for detailed
instructions on cleaning the mask.
1. Wash the humidifier and air tubing in warm water using mild detergent.
2. Rinse the humidifier and 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.
Notes:
The humidifier may be washed in a dishwasher on the delicate or glassware cycle (top shelf
only). It should not be washed at temperatures higher than 65ºC.
Do not wash the air tubing in a dishwasher or washing machine.
Empty the humidifier daily and wipe it thoroughly with a clean, disposable cloth. Allow to dry out
of direct sunlight and/or heat.
English 17
Checking
You should regularly check the humidifier, air tubing and the air filter for any damage.
1. Check the humidifier:
Replace it if it is leaking or has become cracked, cloudy or pitted.
Replace it if the seal is cracked or torn.
Remove any white powder deposits using a solution of one part household vinegar to
10 parts water.
2. Check the air tubing and replace it if there are any holes, tears or cracks.
3. 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.
Reassembling
When the humidifier and air tubing are dry, you can reassemble the parts.
1. Connect the air tubing firmly to the air outlet located on the rear of the device.
2. Open the humidifier and fill it with room temperature water up to the maximum water level
mark.
3. Close the humidifier and insert it into the side of the device.
4. Connect the free end of the air tubing firmly onto the assembled mask.
18
Reprocessing
When the device is used for multiple patients, for example, in a sleep lab, clinic, hospital or at a
health care provider, the cleanable humidifier, air outlet and air tubing should be reprocessed
between each patient use.
If the cleanable humidifier or the air tubing are being used for a single user in the home, refer to the
cleaning instructions in this guide or in the User Guide.
Described here are ResMed’s recommended and validated procedures for cleaning and disinfecting
the cleanable humidifier, air outlet and air tubing. However, the steps for disinfection vary regionally
and each healthcare facility should consult its own procedures before carrying out those within this
guide.
WARNING
ResMed cannot give any assurance that deviations from the procedures listed in this guide,
and their effect on the performance of the product, will be acceptable.
When using detergents, disinfectants or sterilisation agents, always follow the
manufacturer's instructions.
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.
Surface disinfection
1. Wipe the exterior of the device including display, externally accessible ports, power supply unit
and accessories with a disposable cloth and mild detergent or alcohol disinfectant (see list
below).
2. Remove any excess disinfectant with a disposable dry cloth.
Agents recommended for surface disinfection and cleaning:
Warm water and mild detergent eg, Teepol
™
multipurpose detergent
Window cleaner or other premixed surface detergent
Methyl alcohol solution
70% Ethyl alcohol solution
70-90% Isopropanol solution
10% Bleach solution
Isopropyl wipes
CaviCide
™
Mikrozid
®
Actichlor
™
Plus
Terralin
®
.
Note: Agents may not be available in all regions.
English 19
Reprocessing the air tubing
Disconnecting
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.
Decontaminating
Before the disinfection process, each component must be cleaned and rinsed so no visible
contamination is present.
1. Clean all components with a soft bristled brush for one minute while soaking in detergent
solution (see table below). Pay particular attention to all crevices and cavities.
2. Run the detergent solution through the air tubing repeatedly until no contamination is visible.
3. Thoroughly rinse each component according to the detergent manufacturer's instructions.
ResMed has tested the following detergents according to the manufacturer’s instructions:
Detergent Water temperature SlimLine ClimateLineAir Standard
Alconox™ (diluted at 1%) Hot water (approx 60°C)
Warm water (approx 45 to 60°C)
Room temperature water (approx 21°C)
Neodisher MediZym™ (diluted
at 2.0%)
Warm water (approx 45 to 60°C)
Disinfecting
In the procedures below, only one disinfection process needs to be performed.
High level thermal
Part Validated number of cycles
Hot water: 75°C for 30 minutes OR 70°C for 100 minutes.
SlimLine 20
ClimateLineAir 10
Standard 100
1. Immerse the air tubing in a water bath.
Take care that no air bubbles are trapped inside the air tubing.
2. Increase the water bath temperature to 70°C for 100 minutes, or a maximum of 75ºC for
30 minutes. Higher temperatures may damage the tubing.
3. Air dry out of direct sunlight and/or heat.
20
High level chemical
Part Validated number of cycles
CIDEX® OPA Ortho-phthalaldehyde
0.55% for 12 minutes
SlimLine 100
ClimateLineAir 10
Standard 100
1. Soak the air tubing in a commercially available solution of a chemical sterilant.
Take care that no air bubbles are trapped inside the air tubing.
2. Thoroughly rinse the air tubing in drinking quality water (five litres per assembly) by immersing it
completely for a minimum of one minute in duration.
3. Repeat the rinse procedure two additional times using fresh water for a total of three rinses.
4. Air dry out of direct sunlight and/or heat.
Inspecting
Perform a visual inspection of the air tubing. If any visible deterioration is apparent (holes, tears or
cracks etc), the air tubing should be discarded and replaced. Slight discoloration may occur and is
acceptable.
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.
Packaging and storage
Store in a dry, dust-free environment away from direct sunlight.
Storage temperature: -20°C to 60°C.
English 21
Reprocessing the humidifier and air outlet
Disassembling
The following instructions provide guidance on how to correctly disassemble the cleanable
humidifier and the air outlet.
1. Remove the humidifier from the device, open it and discard any remaining water.
2. Hold the humidifier base and then fully open the humidifier lid and pull it away so that it easily
detaches from the base.
3. Remove the humidifier seal from the humidifier lid by pulling it away.
4. Locate the air outlet on the inside of the device.
5. Release the air outlet by pressing the clip located inside the device.
6. Remove the air outlet by pulling it out through the air outlet socket at the rear of the device.
22
Decontaminating
Before the disinfection process, each component must be cleaned and rinsed so no visible
contamination is present.
1. Clean all components with a soft bristled brush for one minute while soaking in detergent
solution (see table below). Pay particular attention to all crevices and cavities.
2. Thoroughly rinse each component according to the detergent manufacturer's instructions.
ResMed has tested the following detergents according to the manufacturer’s instructions:
Detergent Water temperature Cleanable
humidifier
Air outlet
Alconox (diluted at 1%) Hot water (approx 60°C)
Warm water (approx 45 to 60°C)
Room temperature water (approx 21°C)
Neodisher MediZym (diluted at
2.0%)
Warm water (approx 45 to 60°C)
Disinfecting
In the procedures below, only one disinfection process needs to be performed.
High level thermal
Part Validated number of cycles
Hot water: 90°C for 1 minute OR 75°C for 30 minutes OR 70°C for 100 minutes.
Due to specific regional requirements, ResMed cleanable humidifiers have been tested
for disinfection (100 cycles) at 93°C for 10 minutes
Cleanable humidifier 10
Air outlet 10
1. Soak the disassembled components in a hot water bath at pasteurizing temperature.
Take care that no air bubbles are trapped against the components.
2. Air dry out of direct sunlight and/or heat.
High level chemical
Part Validated number of cycles
CIDEX OPA Ortho-phthalaldehyde
0.55% for 12 minutes
Cleanable humidifier 10
Air outlet 10
1. Soak the disassembled components in a commercially available solution of a chemical sterilant.
Take care that no air bubbles are trapped against the components.
2. Thoroughly rinse the cleanable humidifier in drinking quality water (five litres per assembly) by
immersing it completely for a minimum of one minute in duration.
3. Repeat the rinse procedure two additional times using fresh water for a total of three rinses.
4. Air dry out of direct sunlight and/or heat.
English 23
Inspecting
Perform a visual inspection of all components. If any visible deterioration is apparent (cracking,
crazing, tears, etc), the humidifier should be discarded and replaced. Slight discoloration of the
silicone components may occur and is acceptable.
Reassembling
The following instructions provide guidance on how to correctly reassemble the air outlet and the
humidifier.
To reassemble the air outlet
1. Hold the air outlet with the seal pointing to the left and the clip pointing forward.
2. Make sure that the air outlet is correctly aligned and insert the air outlet into the socket. It will
click in place.
3. Check if the air outlet is inserted correctly as shown.
To insert the humidifier seal:
1. Place the seal into the lid.
2. Press down along all edges of the seal until it is firmly in place.
24
To reassemble the humidifier lid:
1. Insert one side of the lid into the pivot hole of the base.
2. Slide the other side down the ridge until it clicks into place.
Packaging and storage
Store in a dry, dust-free environment away from direct sunlight.
Storage temperature: -20°C to 60°C.
English 25
Data management and therapy compliance
For therapy management, the AirCurve 10 device stores patient therapy data on the device and has
the ability to transfer it remotely to the care provider. Data can then be accessed via ResMed's
AirView
™
therapy management solution.
The AirCurve 10 device also stores data on the SD card. This data can be transferred via an SD Card
Reader to ResMed's ResScan
™
therapy management system.
For more information on therapy management with AirView or ResScan, refer to the manuals
supplied with the software.
Remote monitoring
The AirCurve 10 device has wireless communication which has the ability to automatically transmit
summary and night profile data on a regular basis. It also allows you to change settings remotely.
The Wireless signal strength icon
displayed at the top right of the screen indicates the signal
strength. Advise the patient to check the signal strength on their device.
Notes:
Therapy data might not be transmitted if used outside of the country or region of purchase.
Devices with wireless communication might not be available in all regions.
SD card
Every AirCurve 10 device comes with an SD card already inserted and ready to be used. Once the
data is loaded into ResScan or AirView via the SD Card Reader, you can review and analyse data, as
well as update therapy settings and transfer them to the patient’s device via the SD card.
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.
Do not remove the SD card from the device when the SD light is flashing.
To insert the SD card:
1. Open the SD card cover.
2. Push the SD card into the device until it clicks.
The following message is briefly displayed: Preparing SD card, do not remove power or your
card.
26
Data storage
The AirCurve 10 device stores summary data such as AHI, Total Hours Used and Leak. Night profile
data such as snore and pulse rate are stored on the SD card and can be viewed with AirView and
ResScan. High resolution flow and pressure data are stored on the SD card.
Data can be transmitted to therapy management software either remotely via wireless
communication, or via SD card. The different ways of transmitting data are detailed in the table
below.
For more information on therapy management with AirView or ResScan, refer to the manuals
supplied with the software.
Type of data Transmission method Sessions stored
Wireless
communication
to AirView
SD card to
ResScan
SD Card to
AirView
(card-to-
cloud)
Summary data (compliance data)
365
Night profile data
Limited by usage and
SD card storage
capacity
High resolution flow and pressure data
(25 Hz - every 40 ms)
Night profile data are stored on the SD card and can be viewed via ResScan or AirView. Examples of
night profile data available are shown below.
Night profile data
Parameter Sampling rate
ResScan AirView
Apnoea or hypopnoea events aperiodic aperiodic
Flow limitation (flat to round) 1/2 Hz (2 sec) 1 min
Leak (L/sec) 1/2 Hz (2 sec) 1 min
Minute ventilation (L/min) 1/2 Hz (2 sec) 1 min
Pressure (cm H2O / hPa)
1/2 Hz (2 sec) 1 min
Snore (quiet to loud) 1/2 Hz (2 sec) 1 min
Pulse rate (beats/min)—if an oximeter adapter is attached 1 Hz (1 sec) 1 min
Oxygen saturation (SpO2)—if an oximeter adapter is attached 1 Hz (1 sec) 1 min
Software upgrade
The device has a software upgrade feature. When a software upgrade is in progress, the screen will
flash for approximately 10 minutes.
English 27
Managing patient care
The following section has been provided to assist you with managing your patients' care.
Patient menu
In the patient menu there are two types of access levels, Essentials and Essentials Plus.
Essentials is designed to make the device interaction and menu navigation easier for patients. It is a
simple choice for patients who do not want to worry about settings or menu navigation. It provides
access to the most important comfort features such as Ramp Time, Humidity Level (if humidifier
available) and Run Mask Fit.
However, by enabling Essentials Plus you can allow highly engaged patients to access additional
features for control over more of their therapy settings, including changing their mask type, EPR (if
available), SmartStart and Run Warmup (if humidifier available).
Essentials Plus can be enabled via the Settings menu. For more information on the patient menu,
see the User Guide.
Therapy data
The device has the ability to transmit a patient's compliance data remotely via wireless
communication.
If you wish to use wireless communication, advise patients to check the Wireless signal strength
icon
once they have the device set up at home. The icon will indicate the strength of coverage
by the number of bars displayed—the higher the number of bars, the stronger the signal.
Travelling
Patients can take their AirCurve 10 device wherever they go. Advise patients of the following:
Use the travel bag provided to prevent damage to the device.
Empty the humidifier and pack it separately in the travel bag.
Make sure the patient has the appropriate power cord for the region of travel. For information on
purchasing, contact your ResMed representative.
When using an external battery, turn off the humidifier in order to maximise battery life. Do this
by turning the Humidity Level to Off.
Travelling by plane
The AirCurve 10 device may be taken on board as carry-on luggage. Medical devices do not count
toward the carry-on luggage limit.
The AirCurve 10 device can be used 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:
Make sure the humidifier is completely empty and inserted into the device. The device will not
work without the humidifier inserted.
Turn on Airplane Mode (for instructions refer to the User Guide).
CAUTION
Do not use the device with water in the humidifier on a plane due to the risk of inhalation of
water during turbulence.
28
Troubleshooting
If there is a problem, try the following suggestions. If you are not able to fix the problem, contact
your local ResMed dealer or ResMed office. Do not open the device.
General troubleshooting
Problem/possible cause Solution
Air is leaking from around the mask
Mask may be fitted incorrectly. Make sure the mask is fitted correctly. See mask user guide
for fitting instructions or use the Mask Fit function to check
mask fit and seal.
The patient is getting a dry or blocked nose
Humidity level may be set too low. Adjust the Humidity Level.
If you have ClimateLineAir heated air tubing, see the
ClimateLineAir user guide.
There are droplets of water in the mask and air tubing
Humidity level may be set too high. Adjust the Humidity Level.
If you have ClimateLineAir heated air tubing, see the
ClimateLineAir user guide.
The patient is getting a very dry mouth
Air may be escaping through the patient's mouth. Increase the Humidity Level.
The patient may need a chin strap to keep the mouth closed
or a full face mask.
The patient feels that too much air is being delivered from the device
Ramp may be turned off. Use the Ramp Time option.
The patient feels that not enough air is being delivered from the device
Ramp may be in progress. Wait for air pressure to build up or turn Ramp Time off.
Ramp start pressure may be too low. Increase Ramp start pressure.
No display
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.
Therapy has stopped, but the device is still blowing air
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
20 minutes.
Humidifier is leaking
Humidifier may not be assembled correctly. Check for damage and reassemble the humidifier correctly.
English 29
Problem/possible cause Solution
Humidifier may be damaged or cracked. Replace the humidifier.
The patient's therapy data has not been transmitted
Wireless coverage may be poor. Advise the patient to place the device where there is
coverage (ie, on their 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.
Advise the patient that therapy data can be sent using the
SD Card.
Device may be in Airplane Mode. Turn off Airplane Mode, see Travelling by plane.
SmartStart is enabled, but the device does not automatically start when the patient breathes into their mask
Breath is not deep enough to trigger SmartStart. To start therapy, take a deep breath in and out through the
mask, before breathing normally.
Press Start.
There is excessive leak. Adjust the mask and headgear.
Air tubing may not be connected properly. Connect firmly at
both ends.
SmartStart is enabled, but the device does not automatically stop when the patient removes their mask
Incompatible mask being used. Only use equipment recommended by ResMed.
Contact ResMed or see www.resmed.com for more
information.
If the patient is using a nasal pillows mask with set pressure
less than 7 cm H
2
O (7 hPa), SmartStart will not work and
should be disabled.
30
Device messages
Device message/possible cause Solution
High leak detected, check your water tub, tub seal or side cover
Humidifier may not be inserted properly. Make sure the humidifier is correctly inserted.
Humidifier seal may not be inserted properly. Open the humidifier and make sure that the seal is correctly
inserted.
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 the mask is fitted correctly. See mask user guide
for fitting instructions or use the Mask Fit function to check
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.
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
to
the unlock position
and then re-insert it.
Date and time can not be set in the past
Date and time were not set before data was recorded.
Select Erase Data in Settings. Once the data is erased, set
the correct local date and time.
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 local ResMed dealer or ResMed office. Do not
open the device.
English 31
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.
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.
Do not place the device on its side as water might get into the device.
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 humidifier or air tubing. These
solutions may cause damage or affect the humidifier performance and reduce the life of
the products.
If you use the humidifier, always place the device on a level surface lower than the
patient's head to prevent the mask and air tubing from filling with water.
32
Do not overfill the humidifier as water may enter the device and air tubing.
Leave the humidifier to cool for ten minutes before handling to allow the water to cool and
to make sure that the humidifier is not too hot to touch.
Make sure that the humidifier is empty before transporting the device.
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: 100–240V, 50–60Hz 1.0–1.5A, Class II
115V, 400Hz 1.5A, Class II (nominal for aircraft use)
DC output: 24V
3.75A
Typical power consumption: 53W (57VA)
Peak power consumption: 104W (108VA)
Environmental conditions
Operating temperature: +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.
Operating humidity: 10 to 95% relative humidity, non-condensing
Operating altitude: Sea level to 2,591 m; air pressure range 1013 hPa to
738 hPa
Storage and transport temperature: -20°C to +60°C
Storage and transport humidity: 5 to 95% relative humidity, non-condensing
Electromagnetic compatibility
The AirCurve 10 complies with all applicable electromagnetic compatibility requirements (EMC) according to IEC60601-12:2007, 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: Internally located at device outlet, analogueue gauge
pressure type, -5 to +45 cm H
2
O (-5 to +45 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 H
2
O (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.
English 33
Physical - device and humidifier
Dimensions (H x W x D): 116 mm x 255 mm x 150 mm
Air outlet (complies with ISO 5356-1:2004): 22 mm
Weight (device and cleanable humidifier): 1248 g
Housing construction: Flame retardant engineering thermoplastic
Water capacity: To maximum fill line 380 mL
Cleanable humidifier - material: Injection moulded plastic, stainless steel and silicone seal
Temperature
Maximum heater plate: 68°C
Cut-out: 74°C
Maximum gas temperature:
41°C
Air filter
Standard: Material: Polyester non woven fibre
Average arrestance: >75% for ~7 micron dust
Hypoallergenic: 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.
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: 4 to 25 cm H
2
O (4 to 25 hPa)
CPAP 4 to 20 cm H
2
O (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. Humidifier
7. Device
8. Inlet filter
Design life
Device, power supply unit: 5 years
Cleanable humidifier: 2.5 years
Air tubing: 6 months
34
Humidifier performance
The following settings have been tested at 22°C ambient temperature:
Mask Pressure
cm H
2
O (hPa)
RH output % Nominal system output AH
1
, BTPS2
Setting 4 Setting 8 Setting 4 Setting 8
3 85 100 6 >10
4 85 100 6 >10
10 85 100 6 >10
20 85 90 6 >10
25 85 90 6 >10
1
AH - Absolute Humidity in mg/L
2
BTPS - Body Temperature Pressure Saturated
Air tubing
Air tubing Material Length Inner diameter
ClimateLineAir Flexible plastic and electrical components 2 m 15 mm
SlimLine Flexible plastic 1.8 m 15 mm
Standard Flexible plastic 2 m 19 mm
Heated air tubing temperature cut-out:
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.
Displayed values
Value Range Display resolution
Pressure sensor at air outlet:
Mask pressure 4–25 cm H2O (4–25 hPa) 0.1 cm H2O (0.1 hPa)
Flow derived values:
Leak 0–120 L/min 1 L/min
Tidal volume 0–4000 mL 1 mL
Respiratory rate 0–50 BPM 1 BPM
Minute ventilation 0–30 L/min 0.1 L/min
Value Accuracy
1
Pressure measurement:
Mask pressure2 ±[0.5 cm H2O (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
Tidal volume
2,3
±20%
Respiratory rate
2,3
±1.0 BPM
Minute ventilation
2,3
±20%
1
Results are expressed at ATPD (Ambient Temperature and Pressure, Dry).
2
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.
English 35
Pressure accuracy
Maximum static pressure variation at 10 cm H
2
O (10 hPa) according to EN ISO 17510-1:2009
Standard air tubing SlimLine air tubing
Without humidification ± 0.5 cm H2O (± 0.5 hPa) ± 0.5 cm H2O (± 0.5 hPa)
With humidification ± 0.5 cm H
2
O (± 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
Pressure [cm H
2
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
25 0.4 / 0.3 0.6 / 0.5 0.8 / 0.8
Flow (maximum) at set pressures
The following are measured accordingly to EN ISO 17510-1:2009 at the end of the specified air tubing:
Pressure
cm H
2
O (hPa)
AirCurve 10 and
Standard
L/min
AirCurve 10,
humidification and
Standard
L/min
AirCurve 10 and
SlimLine
L/min
AirCurve 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
25 120 115 96 84
36
Symbols
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 Authorised Representative. Batch code.
Catalogueue 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 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.
English 37
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 Warranty period
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
90 days
Batteries for use in ResMed internal and external battery systems
6 months
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
1 year
CPAP, bilevel and ventilation devices (including external power supply units)
Battery accessories
Portable diagnostic/screening devices
2 years
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.
ResMed.com
ResMed Ltd
1 Elizabeth Macarthur Drive
Bella Vista NSW 2153 Australia
DISTRIBUTED BY
ResMed Corp 9001 Spectrum Center Boulevard San Diego CA 92123 USA
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. Air10, AirCurve, AirView, ClimateLine, HumidAir, PaceWave, ResScan, SlimLine and SmartStart are trademarks of
ResMed Ltd. AutoSet, ClimateLine, ResScan, SlimLine and SmartStart are registered in U.S. Patent and Trademark Office. Actichlor is a
trademark of Ecolab US Inc. Alconox is a trademark of Alconox Inc. Cavicide is a registered trademark of Metrex Research, LLC. CIDEX is
a registered trademark of Advanced Sterilization Products, Division of Ethicon US, LLC. Mikrozid and Terralin are trademarks of Schülke &
Mayr GmbH. Neodisher MediZym is a trademark of Chemische Fabrik Dr Weigert GmbH & Co. KG. SD Logo is a trademark of SD-3C, LLC.
Teepol is a trademark of Shell Chemical Co. © 2014 ResMed Ltd. 378290/1 2014-09
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