ResMed Oxygen Equipment Stellar 100 User Guide

Stellar 100  
Stellar 150  
InvasIve and nonInvasIve  
ventIlators  
User Guide  
English  
Respiratory Care Solutions  
Making quality of care easy  
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Contents  
Indications for use  
Adverse effects  
1
1
Patient interface  
Humidification  
Internal battery  
ResMed USB stick  
Use on an aircraft  
Mobile use  
4
Remote Alarm  
Setting up for invasive use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5  
Starting therapy using oxygen  
Stopping therapy using oxygen  
Using the FiO2 monitoring sensor  
Stellar basics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10  
LCD screen  
10  
Starting therapy  
Stopping therapy  
Turning off the power  
Working with alarms  
Tailoring treatment setup options  
Using mask-fit  
12  
Using the menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15  
Setup menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16  
Setup menu: Clinical Settings (Mask Type)  
Setup menu: Alarm Settings (Alarm Volume)  
Setup menu: Options  
16  
16  
16  
17  
Setup menu: Configuration Menu  
Info menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18  
Event Summary  
Used Hours  
Device Information  
Reminders  
18  
18  
18  
18  
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Cleaning and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19  
Daily  
Weekly  
Monthly  
Replacing the air filter  
Disinfection  
Multipatient use  
Servicing  
20  
20  
21  
21  
22  
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22  
Alarm troubleshooting  
Other troubleshooting  
22  
25  
Technical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27  
Guidance and manufacturers declaration – electromagnetic emissions  
and immunity  
Symbols  
29  
31  
General warnings and cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32  
Limited warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34  
ii  
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Introduction  
Read the entire manual before using the device. This User Guide is for a non-clinician user,  
and does not contain all the information provided in the Clinical Guide.  
Indications for use  
The Stellar 100/150 is intended to provide ventilation for non-dependent, spontaneously  
breathing adult and paediatric patients (13 kg and above) with respiratory insufficiency, or  
respiratory failure, with or without obstructive sleep apnoea. The device is for noninvasive  
use, or invasive use (with the use of the ResMed Leak Valve). Operation of the device  
includes both stationary, such as in hospital or home, or mobile, such as wheelchair usage.  
Contraindications  
The Stellar is contraindicated in patients who are unable to endure more than brief  
interruptions in ventilation. The Stellar is not a life support ventilator.  
If you have any of the following conditions, tell your doctor before using this device:  
pneumothorax or pneumomediastinum  
pathologically low blood pressure, particularly if associated with intravascular volume  
depletion  
cerebrospinal fluid leak, recent cranial surgery or trauma  
severe bullous lung disease  
dehydration.  
The use of the Stellar or pulse oximetry (including XPOD) is contraindicated in an MRI  
environment.  
Adverse effects  
You should report unusual chest pain, severe headache or increased breathlessness to  
your prescribing physician.  
The following side effects may arise during the course of noninvasive ventilation with the  
device:  
drying of the nose, mouth or throat  
nosebleed  
bloating  
ear or sinus discomfort  
eye irritation  
skin rashes.  
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1
       
Stellar at a glance  
Handle  
H4i connector  
plug and AC  
connection  
Air outlet  
Oxygen inlet  
Air filter cover  
Infrared connection  
for humidifier  
XPOD pulse oximeter connection  
DC power socket  
AC power socket  
FiO sensor connection  
2
Data port for USB stick  
Power on/standby switch  
Remote alarm connection  
Data port for direct PC connection  
The Stellar comprises:  
• Stellar device • Hypoallergenic air filter • AC power cord • Carry bag • 2 m air tubing •  
ResMed USB stick • Low pressure oxygen connector.  
The following optional components are compatible with Stellar:  
• 3 m air tubing • SlimLine™ air tubing • Clear air tubing (disposable) • H4i™ heated  
humidifier • Antibacterial filter • Heat moisture exchanger filter (HMEF) • ResMed XPOD  
oximeter • Nonin™ pulse oximetry sensors • FiO2 monitoring kit (external cable, T-piece  
adapter) • FiO2 monitoring sensor • Stellar Mobility bag • ResMed Leak Valve • Tubing wrap.  
WARNING  
The Stellar should only be used with air tubing and accessories recommended by  
ResMed. Connection of other air tubing or accessories could result in injury or  
damage to the device.  
ResMed regularly releases new products. Please check the catalogue of ventilation  
2
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Patient interface  
Both masks and tracheostomy tubes can be used with Stellar. To set the patient interface  
type go to the Setup menu, select Clinical Settings, then Advanced Settings.  
For information on using masks, see the mask manual. For a full list of compatible masks  
Products page under Service & Support. If you do not have internet access, please  
contact your ResMed representative.  
Humidification  
A humidifier is recommended especially for patients experiencing dryness of the nose,  
throat or mouth. For information on using a humidifier as part of:  
noninvasive ventilation, see “Setting up for noninvasive use” on page 4.  
invasive ventilation, see “Setting up for invasive use” on page 5.  
Internal battery  
CAUTION  
Over time, the capacity of the internal battery will decrease. This depends on  
individual use and ambient conditions. As the battery degrades, it could lead to  
battery related alarms and or system errors. ResMed recommends the battery be  
tested after two years to assess the remaining battery life. Testing and replacement  
of the internal battery should only be performed by an authorised service agent.  
Note: The battery duration depends on the state of charge, the environmental conditions,  
the condition and age of battery, the device settings and the patient circuit configuration.  
In case of a mains power disruption, the device will operate using the internal battery if  
there is no external battery connected to the device. The internal battery will operate for  
approximately two hours under normal conditions (see “Technical specifications” on  
page 27). The power status of the battery is displayed on top of the LCD screen. Check the  
battery status regularly while operating the device with the internal battery and connect the  
device in time to mains power or alternatively to the external battery.  
Additionally the Internal battery use alarm will be displayed. Press the Alarm mute button  
to clear the alarm.  
To recharge the internal battery, connect the device to mains power. It can take up to three  
hours to fully recharge the internal battery, however this can vary depending on  
environmental conditions and if the device is in use.  
Maintenance  
The internal battery has to be discharged and recharged every six months.  
1
2
Remove the power cord while the Stellar is turned on (standy-by or in operation) and let  
the device operate with the internal battery to a charge level of 50%.  
Reconnect the power cord to the mains power. The internal battery will be fully recharged.  
Storing  
If the device is stored for a longer period the internal battery should be at the charge level  
of approximately 50% to increase the durability.  
Note: Check the charge level every six months, if necessary recharge the internal battery  
to a charge level of 50%.  
ResMed USB stick  
A ResMed USB stick may be used with the device either to help the clinician to monitor  
your treatment or to provide you with updated device settings. For more information, see  
“Data management” on page 19.  
Use on an aircraft  
ResMed confirms that the Stellar can be used during all phases of air travel without further  
testing or approval by the airline operator. See “Technical specifications” on page 27.  
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3
         
Mobile use  
The Stellar Mobility bag allows the Stellar to be used in mobile situations, eg, in a  
wheelchair. For setup and correct use, see the Stellar Mobility Bag User Guide. For  
extended mobile use, the ResMed Power Station II external power supply unit can be used  
as an additional power source. Limitations apply to the use of oxygen with the Stellar  
Mobility Bag. For more information, contact your local ResMed representative.  
Remote Alarm  
The Remote Alarm may be used to transfer audible and visual alarms by a direct cable  
connection. For more information on using the Remote Alarm, see the Remote Alarm user  
guide.  
Setting up for noninvasive use  
WARNING  
The air filter cover protects the device in the event of accidental liquid spillage  
onto the device. Ensure that the air filter and air filter cover are fitted at all times.  
Make sure that all the air inlets at the rear of the device and under the device and  
vents at the mask are unobstructed. If you put the device on the floor, make sure  
the area is free from dust and clear of bedding, clothes or other objects that could  
block the air inlets.  
Hoses or tubes must be non-conductive and antistatic.  
Do not leave long lengths of the air tubing or the cable for the finger pulse sensor  
around the top of your bed. It could twist around your head or neck while you are  
sleeping.  
CAUTION  
Be careful not to place the device where it can be bumped or where someone is  
likely to trip over the power cord.  
Make sure the area around the device is dry and clean.  
Notes:  
ResMed recommends using the AC power cord supplied with the unit. If a replacement  
power cord is required, contact your ResMed Service Centre.  
Place the device on a flat surface near the head of the bed.  
2
3
4
5
1
AC power cord  
AC locking clip  
1
2
3
Connect the power cord.  
Plug the free end of the power cord into a power outlet.  
Attach the H4i heated humidifier to the front of the Stellar.  
If the H4i is not in use, and if applicable, connect the antibacterial filter firmly onto the air  
outlet of the device (see “Attaching an antibacterial filter” on page 9).  
4
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Note: Other external humidifiers can be used for noninvasive setup. ResMed  
recommends using a breathing system (including antibacterial filter, air tubings, external  
humidifier) with an impedance of maximum 2 cm H2O at 30 L/min, 5 cm H2O at 60 L/min  
and 16 cm H2O at 120 L/min.  
4
5
6
7
Connect one end of the air tubing firmly onto the air outlet of the H4i.  
Connect the mask system to the free end of the air tubing.  
Select the mask type (select Setup menu, then Clinical Settings, then Advanced Settings).  
Perform Learn Circuit (see “Setup menu: Options” on page 16).  
Attaching the H4i heated humidifier for noninvasive use  
Use of the H4i heated humidifier may be recommended by your clinician. For information  
on using the H4i, see the H4i user guide.  
WARNING  
Always place the H4i on a level surface below the level of the patient to prevent  
the mask and tubing from filling with water.  
Make sure that the water chamber is empty and thoroughly dried before  
transporting the humidifier.  
The H4i heated humidifier is not intended for mobile use.  
Do not overfill the water chamber, as during use this will cause water to spill into  
the air circuit.  
For optimal accuracy and synchrony, perform Learn Circuit with a change of the  
circuit configuration, in particular when adding or removing high impedance  
components (eg, antibacterial filter, external humidifier, water trap, nasal pillow  
type mask or air tubing). See “Setup menu: Options” on page 16.  
CAUTION  
Check the air circuit for water condensation. Use a water trap or a tubing wrap if  
humidification is causing water condensation within the tube.  
Notes:  
A humidifier increases resistance in the air circuit and may affect triggering and cycling, and  
accuracy of display and delivered pressures. Therefore perform the Learn Circuit function  
(see “Setup menu: Options” on page 16). The device adjusts the airflow resistance.  
The heating feature of the H4i is disabled when the device is not mains powered.  
Setting up for invasive use  
The Stellar can be used invasively only with the ResMed Leak Valve.  
WARNING  
Make sure that all the air inlets at the rear of the device and under the device and  
vents at the mask or at the ResMed Leak Valve are unobstructed. If you put the  
device on the floor, make sure the area is free from dust and clear of bedding,  
clothes or other objects that could block the air inlets.  
When using a Heated Moisture Exchange Filter (HMEF), replace the HMEF  
regularly as specified in the instructions provided with the HMEF.  
The H4i is contraindicated for invasive use. An external humidifier approved for  
invasive use is recommended according to EN ISO 8185 with an absolute  
humidity of > 33 mg/L.  
For optimal accuracy and synchrony, perform Learn Circuit with a change of the  
circuit configuration, in particular when adding or removing high impedance  
components (eg, antibacterial filter, external humidifier, water trap, nasal pillow  
type mask or air tubing). See “Setup menu: Options” on page 16.  
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5
   
CAUTION  
When using a humidifier check the breathing system regularly for accumulated water.  
Note: When the mask type is set to Trach, the Non-Vented Mask alarm will be  
automatically enabled to alert you when the ResMed Leak Valve has no vent holes or when  
the vent holes are blocked.  
Catheter mount**  
ResMed Leak Valve  
Learn Circuit  
configuration  
HMEF*  
2
Antibacterial filter  
10  
5
1
3
6
4
Air tubing  
External humidifier*  
AC power cord  
AC locking clip  
1
2
3
4
Connect the power cord.  
Plug the free end of the power cord into a power outlet.  
Connect the antibacterial filter firmly onto the air outlet of the device.  
Connect the external humidifier to the other side of the antibacterial filter.  
*If not using an external humidifier, the HMEF can be connected to the ResMed Leak Valve  
(at step 9).  
5
6
Connect the air tubing to the external humidifier.  
Connect the ResMed Leak Valve to the air tubing. Position the ResMed Leak Valve so that  
air from the vent holes does not blow directly onto the patient's chest.  
WARNING  
Always set up the ResMed Leak Valve in the breathing circuit with the arrows and the  
symbol  
pointing in the direction of air flow from the Stellar to the patient.  
7
Select the mask type Trach (select Setup menu, then Clinical Settings, then Advanced  
Settings).  
8
9
Perform Learn Circuit (see “Setup menu: Options” on page 16).  
If an external humidifier is not being used, you can connect the HMEF to the patient side  
of the ResMed Leak Valve.  
10 Connect the catheter mount.  
** The ResMed Leak Valve or the HMEF can be connected to standardised tracheostomy  
interfaces including connector pieces like catheter mounts.  
The catheter mount and the external humidifier are not part of the ResMed component.  
6
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Working with other optional accessories  
Attaching the pulse oximeter  
1
2
Use of a pulse oximeter may be recommended by your clinician.  
Contraindication  
The pulse oximeter does not meet defibrillation-proof requirement per IEC 60601-1: 1990,  
clause 17.h.  
1
2
Connect the plug of the finger pulse sensor to the plug of the pulse oximeter.  
Connect the plug of the pulse oximeter at the rear of the device.  
To view the oximetry values, from the Monitoring menu, select Monitoring.  
Adding supplemental oxygen  
Oxygen may be prescribed by your clinician.  
Note: Up to 30 L/min at maximum oxygen pressure of 50 mbar (0.73 psi) can be added.  
WARNING  
Oxygen flow must be turned off when the device is not operating, so that unused  
oxygen does not accumulate within the device and create a risk of fire.  
Use only certified, clean oxygen sources.  
ResMed strongly recommends adding oxygen into Stellars oxygen inlet at the  
rear of the device. Entraining oxygen elsewhere, ie into the breathing system via  
a side port or at the mask, has potential to impair triggering and accuracy of  
therapy/monitoring and alarms (eg, High Leak alarm, Non-vented mask alarm). If  
used in this way, therapy and alarm operation must be verified each time oxygen  
flow is adjusted.  
Oxygen supports combustion. Oxygen must not be used while smoking or in the  
presence of an open flame. Only use oxygen supply in well-ventilated rooms.  
The breathing system and the oxygen source must be kept at a minimum  
distance of 2 m away from any sources of ignition (eg, electrical devices).  
Oxygen must not be used while the device is being operated within the mobility bag.  
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2
Oxygen  
supply  
1
2
Press spring to release  
connection after use  
Starting therapy using oxygen  
1
2
3
4
Fit the oxygen connector to the oxygen inlet of the device.  
Attach the other end of the oxygen supply tubing to the oxygen supply.  
Press to start treatment.  
Turn on oxygen.  
Stopping therapy using oxygen  
1
Turn off oxygen.  
2
Press to stop treatment.  
Using the FiO2 monitoring sensor  
Use of the FiO2 monitoring sensor may be recommended by your clinician.  
CAUTION  
Do not use the FiO2 monitoring sensor with the H4i humidifier.  
Preparing to use a new sensor  
1
2
3
Before use, leave the FiO2 monitoring sensor open to the air for 15 minutes.  
Attach a new FiO2 monitoring sensor (as shown below).  
Perform the sensor calibration (see “Setup menu” on page 16).  
Note: The FiO2 monitoring sensor must be replaced every 12 months.  
3
5
1
2
4
8
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Connecting a sensor  
1
2
3
4
5
6
Connect the air tubing to the T-piece adapter.  
Connect the FiO2 monitoring sensor to the T-piece adapter.  
Connect the adapter to the air outlet of the device.  
Connect one end of the cable to the FiO2 monitoring sensor.  
Connect the other end of the cable to the rear of the device.  
Start calibration (see “Setup menu: Options” on page 16). This should be repeated  
periodically at the recommendation of your clinician.  
Attaching an antibacterial filter  
The use of an antibacterial filter may be recommended by your clinician. One antibacterial  
filter—product code 24966—can be purchased separately from ResMed.  
Regularly check the filter for entry of moisture or other contaminants. The filter must be  
replaced according to the manufacturer‘s specifications.  
Note: ResMed recommends using a filter with a low impedance (less than 2 cm H2O at  
60 L/min, eg, PALL BB 50 filter).  
WARNING  
Do not use the antibacterial filter (product code 24966) with the H4i.  
1
2
1
2
3
4
Fit the antibacterial filter to the air outlet of the device.  
Attach the air tubing to the other side of the filter.  
Attach the mask system to the free end of the air tubing.  
Perform the Learn Circuit function (see “Setup menu: Options” on page 16). From the  
Setup menu, select Options. This enables the device to compensate for the impedance  
introduced by the filters.  
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Stellar basics  
About the control panel  
l
Mains Power LED  
LCD Screen  
On when operating on  
mains power.  
External power supply  
LED  
On when external battery is  
connected.  
Internal battery LED  
On when internal battery is in  
use. Flashes when device is  
turned off and battery is  
charging.  
Monitoring menu  
Setup menu  
Info menu  
Alarm LED  
Red or yellow during an  
alarm or during alarm  
testing.  
Push dial (rotate/  
click)  
Alarm mute button LED  
On when  
is pressed.  
Therapy LED  
On during treatment.  
Flashes during mask-  
fitting operation.  
Start/stop button  
Key  
Function  
Start/Stop  
Starts or stops treatment.  
Extended hold for at least three seconds starts the  
mask-fitting feature.  
Alarm mute  
During therapy: Press once to mute an alarm. Press a  
second time to un-mute an alarm. If the problem is still  
present, the alarm will sound again after two minutes.  
See “Working with alarms” on page 13.  
In stand-by mode: Extended hold for at least three  
seconds starts the alarm LED and alarm buzzer test.  
Menu keys  
Push dial  
Press the appropriate menu button (Monitoring, Setup, Info)  
to enter and scroll through the relevant menu.  
Turning the dial allows you to scroll through the menu and  
change settings. Pushing the dial allows you to enter into a  
menu or confirm your choice.  
10  
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LCD screen  
The LCD screen displays the menus, monitoring screens and alarm status.  
Values on this LCD screen and other screens throughout the User Guide are examples  
only.  
Warm-up feature H4i  
Ramp time  
Program  
ResMed USB stick  
Mains power  
Therapy mode  
External power supply  
Patient mode or  
Clinical mode  
Current screen/number of  
screens within the menu  
Internal battery  
Title bar  
Settings  
Scroll bar  
Therapy status bar  
Starting therapy  
Performing a functional test  
Make sure your device is functioning properly each time before starting therapy.  
If any problems occur, see “Troubleshooting” on page 22. Please also check other  
provided User Instructions for troubleshooting information.  
1
2
Turn off the device by pressing the power switch  
Check condition of device and accessories.  
at the back of the device.  
Inspect the device and all the provided accessories. If there are any visible defects, the  
system should not be used.  
3
4
Check the circuit configuration.  
Check the integrity of the circuit configuration (device and provided accessories) according  
to the setup descriptions in this User Guide and that all connections are secure.  
Turn on the device and check alarms.  
Press the power switch  
at the back of the device once to turn on the device.  
Check that the alarm sounds a test beep and the LEDs (visual indicator) for the alarm signal  
and the Alarm mute button flash. The device is ready for use when the Treatment screen  
is displayed. If the display shows the Reminder page, follow the instructions, then press  
to display the Treatment screen.  
5
Check batteries.  
Disconnect the device from the mains and external battery (if in use) so that the device is  
powered by the internal battery. Check that the Battery use alarm is displayed and the  
battery LED is on.  
Note: If the charge state of the internal battery is too low, or if the battery is empty, an  
alarm occurs. See the Alarm troubleshooting section on page 22 for further information.  
Reconnect the external battery (if in use) and check that the LED for the external power  
supply is lit. The External DC power use alarm will be displayed and the Alarm LED will light.  
Reconnect the device to the mains.  
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11  
     
6
Check H4i heated humidifier (if in use).  
Check that the warm-up feature is displayed in the Treatment screen. Start the warm-up  
feature. Check that the humidifier warm-up symbol is displayed on top of the screen.  
You can use the warm-up feature to pre-heat  
the water in the humidifier prior to starting  
treatment. The humidifier will be automatically  
detected when the device is turned on. The  
Treatment screen provides the option to start  
warming the humidifier. If the humidifier is  
heating, the related symbol is displayed at the  
top of the LCD screen.  
Warm-up humidifier  
Note: The H4i in heating mode can only be used  
when the device is connected to mains supply.  
7
8
Check the FiO2 monitoring sensor (if in use).  
Start the FiO2 sensor calibration. Select Setup menu, then Options (see “Setup menu:  
Options” on page 16). Follow the instructions on the display.  
Check pulse oximeter (if in use).  
Attach the accessories according to the setup descriptions (see “Attaching the pulse  
oximeter” on page 7). From the Monitoring menu, go to the Monitoring screen. Check that  
the values for SpO2 and Heart rate are displayed.  
9
Check oxygen connection (if in use).  
Attach the accessories according to the setup descriptions (see “Adding supplemental  
oxygen” on page 7).  
Starting therapy  
CAUTION  
The Clinical mode is only for clinicians. If the device is operating in clinical mode  
press the power switch at the back to re-start the device in patient mode  
Fit your patient interface (mask or catheter mount) as described in the user instructions.  
.
1
2
Lie down and arrange the air tubing so that it is free to move if you turn in your sleep or  
arrange the tubing so it is comfortable in your wheelchair.  
3
To start treatment, press  
into your patient interface and treatment will begin.  
or if the SmartStart/Stop function is enabled, simply breathe  
Stopping therapy  
You can stop therapy at any time, simply remove the patient interface and press  
to stop  
airflow or if SmartStart/Stop is enabled, simply remove the patient interface, and treatment  
will stop automatically.  
Notes:  
SmartStop may not work if Full face or Trach is selected as mask type; the High Leak  
alarm or the Low Min Vent alarm is enabled; “Confirm Therapy Stop“ is enabled; or the  
mask-fitting feature is running.  
When the device is stopped and operating in standby mode with an integrated  
humidifier connected, it will continue to blow air gently to assist cooling of the  
humidifier’s heater plate.  
Masks with high resistance (eg, paediatric masks) may cause the operation of the  
SmartStop feature to be restricted.  
When using with oxygen, turn off oxygen flow before stopping therapy.  
12  
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Turning off the power  
1
Stop the therapy.  
2
Press the power switch  
the display.  
at the back of the device once and follow the instructions on  
Note: To disconnect the device from the mains power pull out the power cord from the  
power socket.  
Working with alarms  
WARNING  
This device is not intended to be used for vital signs monitoring. If vital signs  
monitoring is required, a dedicated device should be used for this purpose.  
This device is fitted with alarms to alert you to changes that will affect your treatment.  
Alarm message  
Alarm LED  
Alarm mute key  
Alarm messages are displayed along the top of the screen. High priority alarms are  
displayed in red, medium priority alarms in yellow and low priority alarms in light blue. The  
Alarm LED lights red during high priority alarms and yellow during medium and low priority  
alarms.  
The alarm volume can be set Low, Medium or High. From the Setup menu, select Alarm  
Settings. After the set value has been confirmed, the alarm will sound and the alarm LED  
lights.  
Alarm settings, see “Setup menu: Alarm Settings (Alarm Volume)” on page 16.  
You can mute an alarm by pressing  
once. By pressing the Alarm mute key again, the  
alarm sounds again. When an alarm is muted, the Alarm mute key LED will light constantly.  
For a high or medium priority alarm, if after two minutes the problem is still present, the  
alarm will sound again. Any active low priority alarm will be permanently muted and the  
Internal Battery Use alarm will be cleared until the alarm condition is fulfilled again.  
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13  
   
Tailoring treatment setup options  
Setting Ramp  
Ramp time is a feature that can be enabled  
by your clinician by setting a maximum ramp  
time. Designed to make the beginning of  
treatment more comfortable, ramp time is  
the period during which the pressure  
increases from a low start pressure to the  
treatment pressure. See “Setup menu:  
Options” on page 16.  
Ramp time  
Programs  
Program  
If the Clinician has selected both, ie, dual,  
you can choose the program to use on the  
Treatment screen. If only a single program is  
selected, the option does not display.  
Using mask-fit  
You can use mask-fit to help you fit your mask properly. This feature delivers constant  
treatment pressure for a three-minute period, prior to starting treatment, during which you  
can check and adjust your mask-fit to minimise leaks. The mask-fit pressure is the set  
CPAP or EPAP pressure or 10 cm H2O, whichever is greater.  
1
2
3
Put the mask on according to the mask user guide.  
Hold down  
for at least three seconds until pressure delivery starts.  
If necessary adjust the mask, mask cushion and headgear until you have a good mask fit.  
After three minutes treatment will begin. Mask-fit can be stopped at any time by pressing  
.
Notes:  
Press  
for at least three seconds during mask-fit to start the treatment immediately.  
The mask-fitting feature is disabled when the mask type Trach is selected.  
14  
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Using the menus  
The device has three menus (Monitoring, Setup, Info) accessed by the equivalent buttons  
on the right of the LCD screen. In each menu there are screens that display settings, device  
or therapy information.  
SETUP  
MONITORING  
INFO  
Treatment  
Clinical Settings  
Event Summary  
Monitoring  
Leak  
Pressure / Flow  
Alarm Settings  
Minute Ventilation  
Tidal Volume  
Min Vent/Resp Rate  
or MV/Va (iVAPS  
Mode)  
Respiratory Rate  
Options  
Leak  
I:E Ratio  
Tidal Volume  
Pressure Support  
Synchronisation  
AHI  
Oximetry  
SpO  
2
Used Hours  
Device Information  
Reminder  
Note: iVAPS mode is only available in Stellar 150.  
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15  
 
Setup menu  
Setup menu: Clinical Settings (Mask Type)  
1
Press  
to display the Clinical Settings screen.  
2
Use the push dial to scroll through the menu and change the Mask Type in the Advanced  
Settings screen.  
Mask type options: Nasal, Ultra, Pillow, Full Face, Trach, Pediatric.  
Note: When Mask Type is set to Trach or Full Face the Non-Vented Mask alarm  
automatically turns on.  
For a full list of compatible masks for this device, see the Mask/Device Compatibility List  
on www.resmed.com on the Products page under Service & Support. If you do not have  
internet access, please contact your ResMed representative.  
Setup menu: Alarm Settings (Alarm Volume)  
1
Press  
to display the Alarm Settings screen.  
2
Use the push dial  
medium or high.  
to scroll through the menu and change the Alarm Volume to low,  
Setup menu: Options  
1
Press  
to display the Options screen.  
2
Use the push dial  
in the table below).  
to scroll through the menu and change parameters (see descriptions  
16  
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Parameter  
Description  
Learn Circuit  
The device is calibrated according to your air tubing system.  
1. If in use, turn off the oxygen flow.  
2. Select the mask type.  
3. Set up the air circuit including accessories and patient interface.  
Note: For invasive use, do not connect a catheter mount,  
tracheostomy tube or HMEF, see “Setting up for invasive use”  
on page 5).  
4. Leave the air circuit unobstructed and open to the air.  
5. Press  
to start the Learn Circuit.  
6. Wait for the device to complete its automated tests (<30 sec).  
The results are displayed when complete. If the circuit  
configuration has been successfully learnt,  
displays. If  
unsuccessful, displays (see “Troubleshooting” on page 22).  
FiO2 Sensor  
Calibration  
The device starts the calibration of the FiO2 monitoring sensor to  
measure the oxygen concentration of the breathable air.  
1. Press  
to start the FiO2 sensor calibration.  
2. Wait for the device to complete its calibration.  
The results are displayed when complete.  
Note: Turn off the oxygen flow.  
Ramp Time  
If Max Ramp Time has been set by the clinician, you may select any  
value up to this time.  
Options: 0 min-Max Ramp Time (max 45 minutes, 5 minutes  
increments)  
Setup menu: Configuration Menu  
Parameter  
Description  
Language  
Sets the display language.  
Options: Depending on regional configuration  
Brightness  
Backlight  
Sets the LCD backlight brightness.  
Options: 20-100%, 10% increments  
Enables the LCD and keypad backlight.  
If the AUTO setting is selected the backlight turns dark after five  
minutes without any actions and turns on again if any button is  
pressed again or an alarm occurs.  
Options: On, Auto  
Time format  
Date format  
Sets the time format.  
Options: 24 hrs,12 hrs  
Sets the date format.  
Options: dd/mm/yyyy, mm/dd/yyyy  
To return to the Options screen press the Return button  
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17  
 
Info menu  
Event Summary  
Event summary displays the summary of three  
types of events: changes in settings, alarms and  
system events (eg, connection of ResMed USB  
stick). There are up to 200 events of each type,  
displayed in chronological order, with the most  
recent event displayed at the top by default.  
Used Hours  
Used Hours during the last seven days of  
treatment are displayed in a bar graph and can be  
compared to the data of the last 365 days.  
Device Information  
This screen shows the serial number (displayed  
as Device SN), software version and other  
component versions. Data on this screen may be  
requested for servicing or as part of problem-  
solving by a technician.  
Reminders  
The Clinician uses the Reminders menu to alert  
you to specific events; for example, when to  
replace the mask, when to replace the filter and  
so on. The reminder appears in yellow as the date  
approaches (within 10% of the reminder period).  
The reminder also displays when the device is  
powered on. You can clear a reminder message  
by selecting ‘Reset’, which clears the current  
reminder date to OFF, or displays the next pre-  
set Reminder date.  
18  
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Data management  
There are two data ports at the rear of the device for connecting a USB stick (see “Stellar  
at a glance” on page 2). Therapy and device data can be stored on it or read from it to be  
used with ResMed software applications.  
WARNING  
Do not connect any device to the data ports other than specially designed devices  
recommended by ResMed. Connection of other devices could result in injury, or  
damage to the Stellar (see “General warnings and cautions” on page 32).  
CAUTION  
Do not disconnect the ResMed USB stick while data transfer is in progress. Otherwise  
loss of data or incorrect data may result. The download time depends on the data  
volume.  
Notes:  
You cannot connect two ResMed USB sticks simultaneously for data communication.  
If data transfer is not possible or failed please read the troubleshooting section.  
Do not store files on the USB stick other than those created by the device or  
application. Unknown files may be lost during data transfer.  
1
2
Plug the ResMed USB stick to one of the two USB connections on the rear side of the  
device.  
The first dialogue for the USB data transfer is displayed automatically on the LCD. The device  
checks if there is enough memory capacity on the USB stick and if readable data is available.  
Select one of the available options  
Read settings  
The settings will be transfered from the connected ResMed USB stick to the Stellar.  
Write settings  
Settings of the device will be stored on the ResMed USB stick.  
Write settings and loggings  
Settings and loggings of the device will be stored on the ResMed USB stick.  
Cancel  
3
Confirm the data transfer.  
Cleaning and maintenance  
The cleaning and maintenance described in this section should be carried out regularly.  
This also helps to prevent the risk of cross contamination. Refer to the mask, humidifier  
and other accessories user guide for detailed instructions for care and maintenance.  
WARNING  
Beware of electric shock. Do not immerse the device, pulse oximeter or power  
cord in water. Turn off the device, unplug the power cord from the power socket  
and the device before cleaning and be sure that it is dry before reconnecting.  
The mask system and air tubing are subject to normal wear and tear. Inspect  
them regularly for damage.  
CAUTION  
The device cannot be sterilised.  
Daily  
Disconnect the air tubing from the device (and humidifier, if used) and hang it in a clean,  
dry place until next use. If the device is visibly soiled, wipe the exterior surfaces of the  
device and the pulse oximeter (if used) with a damp cloth and mild detergent.  
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19  
     
CAUTION  
Do not hang the air tubing in direct sunlight as the tubing may harden over time  
and eventually crack.  
Do not use bleach, chlorine, alcohol or aromatic-based solutions (including all  
scented oils), moisturising or antibacterial soaps to clean the air tubing or the  
device on a daily basis (other than the approved cleaning agents Mikrozid® AF or  
CaviCide®). These solutions may cause hardening and reduce the life of the  
product. The use of cleaners and disinfecting solutions containing alcohol (other  
than the approved cleaning agents) is acceptable for periodic cleaning of the  
device, such as for cleaning between patients or especially for service periods,  
but not recommended for daily use.  
Weekly  
1
2
3
4
5
Remove the air tubing from the device and the patient interface.  
Wash the air tubing in warm water using mild detergent.  
Rinse thoroughly, hang and allow to dry.  
Reconnect the air tubing to the air outlet and patient interface.  
If the device is visibly soiled, wipe the exterior surfaces of the device and the pulse  
oximeter (if used) with a damp cloth and mild detergent.  
Monthly  
1
Wipe the exterior of the device and the pulse oximeter (if used) with a damp cloth and mild  
detergent.  
2
Visually inspect the air filter to check if it is blocked by dirt or contains holes.  
Replacing the air filter  
Replace the air filter every six months (or more often if necessary).  
WARNING  
Do not wash the air filter. The air filter is not washable or reusable.  
1
2
3
4
Remove the air filter cover from the back of the device.  
Remove and discard the old air filter.  
Insert a new air filter.  
Refit the air filter cover.  
20  
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.
Air filter  
Air filter cover  
Disinfection  
Disinfection of your device helps to prevent the risk of cross contamination.  
Disinfect the exterior of the device, and especially the air outlet, with a damp cloth and a  
disinfection solution (eg, Microzid).  
Multipatient use  
WARNING  
An antibacterial filter is mandatory if the device is used on multiple patients.  
In a mulitpatient use environment, you must perform the following before the  
device is provided to a new patient:  
Air filter and the  
antibacterial filter  
Replace.  
Mask  
Reprocess; Cleaning, disinfection and sterilisation  
instructions are available from the ResMed website,  
Internet access, please contact your ResMed representative.  
Air tubing  
Device  
Replace the air tubing. Alternatively, consult the air tubing  
instructions for cleaning and disinfection information.  
Disinfect the Stellar as follows:  
Use an anti-bacterial cleaning/disinfectant solution such as  
Mikrozid® AF or CaviCide® with a clean non-dyed  
disposable cloth to clean and disinfect the exterior surfaces  
of the device. Wipe all accessible surfaces of the device,  
including the air outlet (avoid liquid entering any openings in  
the device). Follow the manufacturers recommended  
cleaning instructions.  
Humidifier  
As instructions for humidifiers vary, see the user guide for  
the humidifier in use. For multipatient use environment, use  
the H4i water chamber (disposable) in place of the H4i  
reusable water chamber.  
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21  
   
Servicing  
CAUTION  
Inspection and repair should only be performed by an authorised agent. Under no  
circumstances should you attempt to open, service or repair the device yourself.  
This product should be inspected by an authorised ResMed service centre five years from  
the date of manufacture, except for the internal battery which ResMed recommends be  
tested after two years to assess the battery life. Prior to this, the device is intended to  
provide safe and reliable operation provided that it is operated and maintained in  
accordance with the instructions provided by ResMed. Applicable ResMed warranty  
details are provided with the device at the time of original supply. Of course, as with all  
electrical devices, if any irregularity becomes apparent, you should exercise caution and  
have the device inspected by an authorised ResMed service centre.  
Troubleshooting  
If there is a problem, try the following suggestions. If a problem cannot be solved, contact  
ResMed.  
Alarm troubleshooting  
The most common reason for an alarm to sound is because the system has not been  
properly assembled. Check that the air tubing has been properly attached to the device and  
patient interface (and humidifier if used).  
Notes:  
The alarm log and alarm settings are maintained when the device is powered down and  
in the event of a power loss.  
If multiple alarms are active simultaneously, the alarm with the highest priority will be  
displayed first.  
If an alarm activates repeatedly, discontinue use and return the device for servicing.  
Problem / possible cause  
Action  
LCD: Internal Battery Empty!  
The remaining battery charge is below  
15%. The device can be powered by the  
internal battery for maximum 2 minutes.  
Connect the device to mains power.  
Note: In case of a total power failure, the  
therapy settings will be stored and therapy  
will resume when the device is powered  
again.  
LCD: System Failure!  
Component failure.  
1. Power-off the device.  
The device stops delivering air pressure  
(system failure 6, 7, 9, 22, 38). Therapy  
cannot be started (system failure 21).  
2. Power-on the device again.  
Component failure (system failure 8, 25).  
1. Power-off the device.  
2. Power-on the device again.  
LCD: Over Pressure!  
The device generates a pressure that is  
greater than 59 cm H2O. Treatment will  
be stopped.  
1. Power-off the device.  
2. Check that the air tubing is connected  
properly.  
3. Power-on the device again.  
4. Start Learn Circuit function.  
Note: If the alarm activates repeatedly  
internal components may be defective.  
Discontinue use and return the device for  
servicing.  
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Problem / possible cause  
Action  
LCD: Blocked Tube!  
Air path is blocked.  
1. Check the air path for any blockages.  
2. Remove the blockages.  
3. If the alarm is not cleared, stop  
treatment.  
4. Re-start treatment.  
LCD: High Temperature [10, 11, 12, 23]!  
The temperature inside the device is too  
high. Treatment may lead to stop.  
Ensure the ambient temperature is within  
the specified operating range. If the  
problem persists within the specified  
operating conditions please return the  
device for servicing.  
Contact your clinician.  
LCD: High Pressure!  
Therapy pressure exceeds pre-set alarm  
level.  
1. Stop treatment.  
2. Re-start treatment.  
If the problem persists contact your  
clinician.  
LCD: Low Pressure!  
The air tubing is not connected properly.  
1. Check the air circuit integrity and  
reconnect.  
2. If the alarm doesn‘t get cleared, stop  
treatment.  
3. Re-start treatment.  
LCD: Circuit disconnected!  
The air circuit is not connected properly.  
1. Check the air circuit integrity and  
reconnect.  
2. If the alarm is not cleared, stop  
treatment.  
3. Re-start treatment.  
LCD: Low Minute Ventilation!  
Minute ventilation level has dropped  
below the alarm setting level.  
Contact your clinician.  
LCD: Low Respiratory Rate!, High Respiratory Rate!  
The respiratory rate level has dropped  
below or has exceeded the alarm setting  
level.  
Contact your clinician.  
LCD: High Leak!  
High mask leak for more than 20  
seconds.  
Adjust the mask to minimise leak (see  
“Using mask-fit” on page 14).  
Check the air circuit integrity and  
reconnect.  
If the problem persists contact your  
clinician.  
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23  
Problem / possible cause  
LCD: Non-Vented Mask!  
Action  
Connection of a non-vented mask.  
Mask vents may be blocked.  
ResMed Leak Valve is missing or vent  
is blocked.  
Ensure the mask has vents.  
Ensure the mask vents are not  
blocked.  
Ensure the ResMed Leak Valve is  
installed and that the vent is not  
blocked.  
Ensure oxygen (if in use) has only been  
connected at the rear of the device.  
If the problem persists contact your  
clinician.  
LCD: Apnoea!  
The device detects an apnoea that has  
exceeded the pre-set alarm level.  
Breathe normally to disable the alarm.  
If the problem persists contact your  
clinician.  
LCD: Internal Battery Low!  
The internal battery capacity is below 30%.  
LCD: Low SpO2!  
Connect the device to mains power.  
SpO2 has dropped below pre-set alarm  
level.  
Check the attachment of the sensor.  
If the problem persists contact your  
clinician.  
LCD: SpO2 finger sensor failure!  
The finger sensor is not connected  
properly or delivers faulty values.  
Check if the finger sensor is attached  
properly to the finger and connection to  
the pulse oximeter.  
LCD: Xpod oximeter disconnected!  
The pulse oximeter is disconnected.  
Check if the pulse oximeter is connected  
properly to the device.  
LCD: Low FiO2 Level!  
FiO2 has dropped below the pre-set  
alarm level.  
Perform FiO2 sensor calibration.  
If the problem persists contact your  
clinician.  
LCD: High FiO2 Level!  
FiO2 has exceeded the pre-set alarm  
level.  
Perform FiO2 sensor calibration.  
If the problem persists contact your  
clinician.  
LCD: Keypad Failure!  
One of the keys was held down for more  
than 10 seconds or got stuck.  
Remove any blockages from the keypad.  
LCD: Attention High Temp [42, 43, 44, 45]!  
The temperature inside the device is  
high.  
Ensure the ambient temperature  
conditions are within the specified  
operating range.  
LCD: Internal Battery Use!  
The device is using the internal battery.  
Check if the power cord is properly  
connected to the device if you want to  
run from mains power.  
Press the Alarm mute button  
the alarm.  
to cancel  
24  
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Problem / possible cause  
Action  
LCD: External DC Power Use!  
The device is powered by an external  
battery.  
Check if the AC power cord is properly  
connected to the device if you want to  
run from mains power.  
Note: The alarm will be cleared  
automatically after one minute.  
Other troubleshooting  
Problem / possible cause  
Solution  
No display  
Power failure. The device stops delivering  
air pressure.  
Remove the mask or the catheter mount  
from the tracheostomy tube until power  
is restored.  
Power not connected or device is not  
switched on.  
Ensure the power cord is connected and  
press the switch at the back of the device  
once.  
Treatment pressure seems low  
Ramp time is in use.  
Wait for air pressure to build up.  
Replace air filter.  
Air filter is dirty.  
Air tubing is kinked or punctured.  
Air tubing is not connected properly.  
Straighten or replace tubing.  
Connect the air tubing firmly at both  
ends.  
Mask and headgear not positioned  
correctly.  
Adjust position of mask and headgear.  
Plug(s) missing from access port(s) on  
mask.  
Replace plug(s).  
Pressure required for treatment may  
have changed.  
See your clinician to adjust the pressure.  
Perfom the Learn Circuit function.  
There is a large impedance (eg,  
antibacterial filter) in the air circuit.  
Humidifier control dial set too high,  
resulting in accumulation of water in the  
air tubing.  
Turn humidifier control down and empty  
the water from the air tubing.  
Treatment pressure seems high  
Pressure required for treatment may  
have changed.  
Consult your clinician.  
There is a change in the impedance in the  
circuit configuration.  
Perform the Learn Circuit function.  
The device does not start when you breathe into the mask  
SmartStart/Stop not on.  
Consult your clinician.  
Breath is not deep enough to trigger  
SmartStart.  
Take a deep breath in and out through the  
mask.  
There is excessive leak.  
Adjust position of mask and headgear.  
Replace plug(s).  
Plug(s) missing from port(s) on mask.  
Air tubing is not connected properly.  
Air tubing is kinked or punctured.  
Connect firmly at both ends.  
Straighten or replace tubing.  
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25  
 
Problem / possible cause  
Solution  
There is a large impedance (eg,  
antibacterial filter) in the air circuit.  
Perform the Learn Circuit function.  
The device does not stop when you remove your mask  
SmartStart/Stop is disabled.  
Consult your clinician.  
Use of a full face mask or tracheostomy  
tube.  
SmartStart is disabled if Full face mask or  
Trach is selected as interface.  
Incompatible accessories (eg, humidifier  
or mask system) with high resistance  
being used.  
Use only equipment as recommended  
and supplied by ResMed.  
High Leak Alarm or Low Min Vent alarms  
are set to ON.  
Consult your clinician.  
Consult your clinician.  
Confirm Stopis enabled.  
High Leak Alarm is enabled, but alarm does not activate when the mask  
is removed during treatment  
Incompatible air delivery system being  
used.  
Use only equipment as recommended  
and supplied by ResMed.  
Pressure settings are too low for the air  
delivery components being used.  
Perform the Learn Circuit function to  
adjust the therapy pressure according to  
your air tubing system.  
Learn Circuit failed  
The circuit configuration is  
inappropriate as the impedance  
detected is too high.  
Too many components have been  
included or the impedance of  
accessories in use is above ResMed’s  
recommendation, eg, type of filter,  
external humidifier, air tubing.  
Review the components included in the  
circuit configuration and adjust as  
appropriate, then rerun Learn Circuit (see  
“Setup menu” on page 16).  
The delivered airflow is not humid/heated although the H4i humidifier is  
in use  
The humidifier is not properly attached.  
The humidifier does not heat.  
Correctly attach the humidifier.  
The device is currently powered by  
battery use or not connected to the  
mains.  
The humidifier does not work.  
Return the device and the humidifier for  
servicing.  
The water chamber is empty.  
Fill the water chamber of the humidifier.  
USB stick is not readable or writeable  
The USB stick contains unreadable data,  
does not have enough space available, is  
not compatible with the device.  
Consult your clinician.  
USB stick is defective.  
Replace the USB stick after consulting  
your clinician.  
FiO2 sensor calibration failure  
FiO2 sensor is not attached properly.  
For the correct attachment of the FiO2  
sensor, see “Using the FiO2 monitoring  
sensor” on page 8.  
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Problem / possible cause  
Solution  
FiO2 sensor is used or defective.  
If the lifetime of the FiO2 sensor has  
exceeded one year please replace the  
FiO2 sensor and start calibration again.  
LCD:  
is displayed in the header.  
Battery is not charging.  
Ensure the ambient temperature  
conditions are within the specified  
operating range. If the problem persists  
within the specified operating conditions  
please return the device for servicing.  
Power off the device. Power son the  
device again.  
Technical specifications  
Operating pressure  
range  
IPAP: 2 cm H2O to 40 cm H2O (in S, ST, T, PAC mode)  
PS: 0 cm H2O to 38 cm H2O (in S, ST, T, PAC mode)  
EPAP: 2 cm H2O to 25 cm H2O (in S, ST, T, iVAPS, PAC  
mode)  
CPAP: 4 cm H2O to 20 cm H2O (in CPAP mode only)  
Min PS: 0 cm H2O to 20 cm H2O (in iVAPS mode)  
Max PS: 0 cm H2O to 30 cm H2O (in iVAPS mode)  
Note: iVAPS mode is only available in Stellar 150.  
Maximum single fault  
pressure  
60 cm H2O (in all modes)  
Maximum breathing  
resistance under single  
fault  
2 cm H2O at 30 L/min;  
7. 2 c m H2O at 60 L/min  
Maximum flow  
Flow accuracy  
> 200 L/min at 20 cm H2O  
5 L/min or 20% measured value, whichever is greater  
Test condition: T mode, IPAP: 40 cm H2O, EPAP: 2 cm  
H2O, Rise Time: MIN, Fall Time: MIN, Ti: 4.0 sec,  
Respiratory Rate: 10 bpm, with ResMed calibration cap.  
Therapy pressure  
tolerance  
IPAP: 0.5 cm H2O 10% of set pressure (end of  
inspiration)  
EPAP/PEEP: 0.5 cm H2O 4% of set pressure  
CPAP: 0.5 cm H2O 10% of set pressure  
Test condition: T mode, IPAP: 40 cm H2O, EPAP: 2 cm  
H2O, Rise Time: MIN, Fall Time: MIN, Ti: 4.0 sec,  
Respiratory Rate: 10 bpm, with ResMed calibration cap.  
Sound pressure level  
29 dBA as measured according to ISO 17510 – 1; 2002.  
32 dBA with uncertainty of 3 dBA as measured according  
to ISO 17510 – 1:2007.  
Alarm Volume Range  
Dimensions (L x W x H)  
Weight  
> 45 dBA - <85 dBA at 1 meter (3 steps: low, medium, high)  
230 mm x 170 mm x 120 mm  
2.1 kg  
Air outlet  
22 mm taper, compatible with ISO 5356-1:2004  
Anaesthetic & Respiratory Equipment - Conical  
Connectors  
Pressure measurement  
Flow measurement  
Internally mounted pressure transducer  
Internally mounted flow transducer  
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27  
 
Power supply  
AC 100–240V, 50–60Hz, 2.2 A, max. 65 W  
24 V, 3 A  
External DC Power  
Supply (isolated)  
Internal Battery  
Lithium-Ion battery, 14.4 V, 1.6 Ah, 23 Wh  
Operating hours: 2 h with a new battery under normal  
conditions (see below).  
Patient type: home chronic; pressure: IPAP/EPAP 15/5  
cm H2O; mask type: Ultra Mirage; air tubing: 2 m; leak:  
0; respiratory rate: 20 bpm; battery capacity: 100%  
Patient type: hospital acute; pressure: IPAP/EPAP 20/5  
cm H2O; mask type: Ultra Mirage; air tubing: 2 m; leak:  
0; respiratory rate: 45 bpm; battery capacity: 100%  
Housing construction  
Flame retardant engineering thermoplastic  
Environmental  
conditions  
Operating temperature: 0°C to 35°C  
Operating humidity: 10%–95% non-condensing  
Storage and transport temperature: -20°C to 60°C  
(+50°C*)  
Storage and transport humidity: 10%–95% non-  
condensing  
Air pressure: 680hPa to 1,100hPa; Altitude: 3,000 m  
*NONIN XPOD  
Electromagnetic  
compatibility  
Product complies with all applicable electromagnetic  
compatibility requirements (EMC) according to  
IEC60601-1-2, for residential, commercial, and light  
industry environments. For further details see “Guidance  
and manufacturers declaration – electromagnetic  
emissions and immunity” on page 29.  
Air filter  
Electro static fibre mesh with TPE frame structure. Bacterial  
filtration efficiency of 99.540% on area weight 100g/m².  
Air tubing  
Flexible plastic, 2 m or 3 m length (22 mm diameter)  
Flexible plastic, 1.83 m length (15 mm diameter)  
SlimLine air tubing  
IEC 60601-1  
classifications  
Class II (Clause 3.14—double insulation). This  
adherence means the need for an protective earthing  
(ie, an earthed plug) is not necessary.  
Type BF  
Continuous operation  
Air travel requirements  
Medical-Portable Electronic Devices (M-PED) that meet  
the Federal Aviation Administration (FAA) requirements  
of RTCA/DO-160 can be used during all phases of air  
travel without further testing or approval by the airline  
operator. ResMed confirms that the Stellar meets RTCA/  
DO-160 requirements.  
This device is not suitable for use in the presence of a flammable anesthetic mixture.  
Notes:  
The manufacturer reserves the right to change these specifications without notice.  
Pressure may be displayed in cm H2O or hPa.  
28  
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Guidance and manufacturer’s declaration – electromagnetic  
emissions and immunity  
Medical Electrical Equipment needs special precautions regarding EMC and needs to be  
installed and put into service according to EMC information provided in this document.  
Guidance and manufacturer’s declaration – electromagnetic emissions  
The device is intended for use in the electromagnetic environment specified below. The customer or the user of the  
device should assure that it is used in such an environment.  
Emissions test  
Compliance  
Electromagnetic environment - guidance  
RF emissions CISPR11  
Group 1  
The device uses RF energy only for its internal function.  
Therefore, its RF emissions are very low and are not  
likely to cause any interference in nearby electronic  
equipment.  
RF emissions CISPR 11  
Class B  
Class A  
The device is suitable for use in all establishments,  
including domestic establishments and those directly  
connected to the public low-voltage network that  
supplies buildings used for domestic purposes.  
Harmonic Emissions  
IEC 61000-3-2  
Voltage Fluctuations/Flicker  
Emissions IEC 61000-3-3  
Complies  
Warnings: 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 (eg, humidifiers) other than those specified in this manual is not recommended. They may  
result in increased emissions or decreased immunity of the device.  
Guidance and manufacturer’s declaration – electromagnetic immunity  
The device is intended for use in the electromagnetic environment specified below. The customer or the user of the  
device should assure that it is used in such an environment.  
IEC60601-1-2 test  
level  
Immunity test  
Compliance level  
Electromagnetic environment –guidance  
Electrostatic  
discharge (ESD)  
IEC 61000-4-2  
6 kV contact  
8 kV air  
6 kV contact  
8 kV air  
Floors should be wood, concrete or ceramic tile.  
If floors are covered with synthetic material, the  
relative humidity should be at least 30%.  
Electrical fast  
transient/burst  
IEC 61000-4-4  
2 kV for power  
supply lines  
2 kV  
1 kV  
Mains power quality should be that of a typical  
commercial or hospital environment.  
1 kV for input/output  
lines  
Surge IEC  
61000-4-5  
1 kV differential  
mode  
1 kV differential  
mode  
Mains power quality should be that of a typical  
commercial or hospital environment.  
2 kV common mode  
2 kV common  
mode  
Voltage dips,  
short  
interruptions  
and voltage  
variations on  
power supply  
input lines  
<5% Ut (>95% dip in  
Ut) for 0.5 cycle  
< 12 V (>95% dip in  
240V) for 0.5 cycle  
Mains power quality should be that of a typical  
commercial or hospital environment.  
If the user of the device requires continued  
operation during power mains interruptions, it is  
recommended that the device be powered from  
an uninterruptible power source.  
40% Ut (60% dip in  
Ut) for 5 cycles  
96 V (60% dip in  
240 V) for 5 cycles  
70% Ut (30% dip in  
Ut) for 25 cycles  
168 V (30% dip in  
240 V) for 25 cycles  
IEC 61000-4-11  
<5% Ut (>95% dip in  
Ut) for 5 sec  
<12 V (>95% dip in  
240 V) for 5 sec  
Power  
3 A/m  
3 A/m  
Power frequency magnetic fields should be at  
levels characteristic of a typical location in a  
typical commercial or hospital environment.  
frequency  
(50/60 Hz)  
magnetic field  
IEC 61000-4-8  
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29  
 
Portable and mobile RF communications  
equipment should be used no closer to any part  
of the device, including cables, than the  
recommended separation distance calculated  
from the equation applicable to the frequency of  
the transmitter.  
Recommended separation distance:  
Conducted RF  
IEC 61000-4-6  
3 Vrms  
150 kHz to 80 MHz  
d = 1.17 P  
3 Vrms  
3 V/m  
Radiated RF  
IEC 61000-4-3  
3 V/m  
80 MHz to 2.5 GHz  
d = 1.17 P 80 MHz to 800 MHz  
d = 2.33 P 800 MHz to 2.5 GHz  
where  
P
is the maximum output power rating of  
the transmitter in watts (W) according to the  
transmitter manufacturer and is the  
d
recommended separation distance in metres (m).  
Field strengths from fixed RF transmitters, as  
a
determined by an electromagnetic site survey,  
should be less than the compliance level in each  
b
frequency range.  
Interference may occur in the vicinity of  
equipment marked with the following symbol:  
NOTE 1: Ut is the AC mains voltage prior to application of the test level.  
NOTE 2: At 80 MHz and 800 MHz, the higher frequency range applies.  
NOTE 3: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection  
from structures, objects and people.  
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios,  
amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the  
electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the  
measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, the device  
should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary,  
such as reorienting or relocating the device.  
b
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.  
Recommended separation distances between portable and mobile RF communications equipment and the  
device  
The device is intended for use in an environment in which radiated RF disturbances are controlled. The customer or  
the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between  
portable and mobile RF communications equipment (transmitters) and the device as recommended below, according  
to the maximum output power of the communications equipment.  
Separation distance according to frequency of transmitter (m)  
Rated maximum output  
power of transmitter (W)  
150 kHz to 80 MHz  
d = 1.17 P  
80 MHz to 800 MHz  
d = 1.17 P  
800 MHz to 2.5 GHz  
d = 2.33 P  
0.01  
0.1  
1
0.12  
0.37  
1.17  
0.12  
0.37  
1.17  
0.23  
0.74  
2.33  
7. 3 7  
10  
3.70  
11.70  
3.70  
11.70  
100  
23.30  
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in  
metres (m) can be determined using the equation applicable to the frequency of the transmitter, where P is the  
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.  
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.  
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and  
reflection from structures, objects and people.  
30  
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Symbols  
Follow instructions for use;  
Class II equipment;  
Type BF applied part;  
Bell (Remote Alarm); IP31 Device is protected against solid foreign objects of 2.5 mm  
diameter and greater and vertically falling water drops;  
sign (see H4i connector plug and AC connection on the device);  
state for a part of equipment;  
Caution;  
General warning  
Standby or preparatory  
Connection for oxygen supply; max 30 l/min (max 30 L/  
CE labeling in accordance with EC directive 93/42/EEC, class II b;  
min);  
Data port;  
+
+
60 °C  
140 °F  
-
-
20 °C  
°F  
4
Temperature limitation for storage and transport;  
Handle with care;  
Maximum  
humidity;  
Serial number;  
away from sunlight;  
Keep dry;  
Manufacturer;  
Batch code;  
Upside;  
Do not re-use;  
Catalogue number;  
Use by date;  
Latex-free  
Keep  
LATEX  
Do not use if package is damaged;  
Environmental information This device must be disposed of in accordance with the laws  
and regulations of the country in which disposal occurs.  
The crossed-out wheeled bin symbol  
indicates that the product bearing this symbol  
may not be disposed of together with general household waste, but instead requires  
separate disposal. This requirement for separate disposal is based on the European  
Directive 2002/96/EC for electrical and electronic equipment, and the European Directive  
2006/66/EC for batteries. You can hand in the product at a municipal collection point, for  
example. This reduces the impact on natural resources and prevents contamination of the  
environment through the release of hazardous substances.  
Batteries containing more than 0.0005 percent of mercury by mass, more than 0.002  
percent of cadmium by mass or more than 0.004 percent of lead by mass are marked  
below the crossed-bin symbol with the chemical symbols (Hg, Cd, Pb) of the metals for  
which the limit is exceeded.  
For further information regarding product disposal, please contact your local ResMed office  
Dispose of used air filters and air tubings according to the directives in your country.  
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31  
 
General warnings and cautions  
WARNINGS  
A warning alerts you to possible injury.  
Read the entire manual before using the device.  
This device should only be used with air tubing and accessories recommended by  
ResMed or the prescribing clinician. Use of incorrect air tubing and accessories may  
affect the functioning of this device.  
The device and the accessories are to be used for the specified intended use only.  
The device must only be used with masks (and connectors1) recommended by  
ResMed, or by a clinician or respiratory therapist. A mask should not be used unless  
the device is turned on and operating properly. The vent hole or holes associated with  
the mask should never be blocked.  
Explanation: The Stellar is intended to be used with special masks (or connectors1)  
which have vent holes to allow continuous flow of air out of the mask. When the device  
is turned on and functioning properly, new air from the device flushes the exhaled air out  
through the mask vent holes. However, when the device is not operating, insufficient  
fresh air will be provided through the mask, and the exhaled air may be rebreathed.  
Rebreathing of exhaled air for longer than several minutes can, in some circumstances,  
lead to suffocation. This applies to most Positive Airway Pressure devices.  
In the event of power failure2 or machine malfunction, remove the mask or the  
catheter mount from the tracheostomy tube.  
Explosion hazard – do not use in the vicinity of flammable anesthetics.  
Do not use the device if there are obvious external defects, unexplained changes in  
performance.  
Only use orignal and approved ResMed accessories and parts.  
Use only accessories from the original package. If the packaging is damaged, the  
respective product must not be used, and should be disposed along with the packaging.  
Before using the device and the accessories for the first time, ensure that all  
components are in a proper condition and that their operational safety is guaranteed. If  
there are any defects, the system should not be used.  
Additional equipment connected to medical electrical equipment must comply with the  
respective IEC or ISO standards (eg, IEC 60950 for data processing equipment).  
Furthermore all configurations shall comply with the requirements for medical electrical  
systems (see IEC 60601-1-1 or clause 16 of the 3Ed. of IEC 60601-1, respectively).  
Anybody connecting additional equipment to medical electrical equipment configures a  
medical system and is therefore responsible that the system complies with the  
requirements for medical electrical systems. Attention is drawn to the fact that local  
laws take priority over the above mentioned requirements. If in doubt, consult your local  
representative or the technical service department.  
No modification of this equipment is allowed.  
CAUTIONS  
A caution explains special measures for the safe and effective use of the device.  
When using accessories, read the manufacturers User Manual. For consumables  
important information can be provided on the packaging, see also symbols on page 31.  
At low pressures, the flow through the mask vent holes may be inadequate to clear all  
exhaled gas, and some rebreathing may occur.  
The device may not be exposed to excessive force.  
If the device should fall accidentally on the ground, please contact your authorised  
service agent.  
Pay attention to leaks and other unusual sounds. If there is a problem, contact an  
authorised service agent.  
1 Ports may be incorporated into the mask or in connectors that are near the mask.  
2 During partial (below rated minimum voltage) or total power failure, therapy pressures will not be  
delivered. When power is restored, operation can be proceeded with no change to settings.  
32  
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Notes:  
A note advises to special product features.  
The above are general warnings and cautions. Further specific warnings, cautions and  
notes appear next to the relevant instructions in the user guide.  
Only trained and authorised personnel are allowed to make clinical setting changes.  
Position the device ensuring the power cord can be easily removed from the power  
outlet.  
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33  
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  
90 days  
and tubing)—excluding single-use devices  
Accessories—excluding single-use devices  
Flex-type finger pulse sensors  
Humidifier water tubs  
Batteries for use in ResMed internal and external battery  
systems  
6 months  
1 year  
Clip-type finger pulse sensors  
CPAP and bilevel device data modules  
Oximeters and CPAP and bilevel device oximeter adapters  
Humidifiers and humidifier cleanable water tubs  
Titration control devices  
CPAP, bilevel and ventilation devices (including external  
power supply units)  
2 years  
Battery accessories  
Portable diagnostic/screening devices  
This warranty is only available to the initial consumer. It is not transferable.  
If the product fails under conditions of normal use, ResMed will repair or replace, at its  
option, the defective product or any of its components.  
This limited warranty does not cover: a) any damage caused as a result of improper use,  
abuse, modification or alteration of the product; b) repairs carried out by any service  
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 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.  
R001-325/2 09 09  
34  
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Respiratory Care Solutions  
Making quality of care easy  
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248578-Eng/1 2012-06  
Stellar 100  
Stellar 150  
USER  
EUR1  
Manufacturer: ResMed Germany Inc. Fraunhoferstr. 16, 82152 Martinsried Germany.  
Distributed by: ResMed Ltd 1 Elizabeth Macarthur Drive Bella Vista NSW 2153 Australia.  
ResMed Corp 9001 Spectrum Center Blvd. San Diego, CA 92123 USA.  
ResMed (UK) Ltd 96 Milton Park Abingdon Oxfordshire OX14 4RY UK.  
ResMed, SlimLine, SmartStart, Stellar, and TiCONTROL are trademarks of ResMed Ltd. ResMed, SlimLine, SmartStart and Stellar are registered in U.S. Patent and  
Trademark Office. © 2012 ResMed Ltd  
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Global leaders in sleep and respiratory medicine www.resmed.com  

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