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The AirMini system combines ResMed's AirMini self-adjusting pressure machine, masks and the AirMini app.
Read this entire guide before using the machine.
Built-in AirMini and AirMini app security features, steps patients take to protect their smart devices against malware, and software and firmware updates will help safeguard patient privacy, protect patients' smart devices and ensure optimal performance.
The AirMini and the AirMini app use security features to help protect patient privacy and prevent unauthorized access to patient data. These include:
Protecting patients' smart devices against malware helps keep their personal information and sleep data safe and secure. ResMed recommends the following:
To ensure optimal performance, ResMed recommends that software and firmware versions be kept up to date.
Once a firmware update becomes available for AirMini, a message will appear on the user's smart device when the AirMini app is accessed.
Advise patients to follow the on-screen prompts to install software and firmware updates.
AirMini
The AirMini self-adjusting system is indicated for the treatment of obstructive sleep apnea (OSA) in patients (female patients with mild to moderate OSA when using AutoSet for Her treatment mode) weighing more than 66 lb (30 kg).
It is intended for home and hospital use.
AirMini app
The AirMini app is a mobile application for patients to remotely operate a prescribed compatible ResMed machine and transfer, analyze and display usage and therapeutic information. The AirMini app also allows healthcare professionals to remotely configure compatible OSA therapy devices.
Positive airway pressure therapy may be contraindicated in some patients with the following preexisting conditions:
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:
The AirMini system includes the AirMini machine, a power supply unit, a drawstring bag, and one of the following:
The AirMini system is comprised of the AirMini machine and one mask pack.
The AirMini machine is compatible with ResMed's F20 and N20 series masks and with the AirFit P10 for AirMini. Ensure that all parts and accessories used with the machine are compatible. For compatibility information, refer to www.resmed.com for more information.
The AirMini machine is also designed to work with ResMed's AirMini app. While the AirMini app is not required to operate the machine, it is essential to clinicians for accessing, viewing and configuring therapy settings.
Refer to ResMed.com/AirMini app for a list of smart devices compatible with the AirMini app.
In addition, Android operating system version 4.4 (minimum) is required.
See Using clinical mode, Using the device settings menu and AirMini app Dashboard for information about the AirMini app.
The treatment pressure required by the patient may vary due to changes in sleep state, body position and airway resistance. In AutoSet mode, the machine provides only that amount of pressure required to maintain upper airway patency.
The machine analyzes the state of the patient's upper airway on a breath-by-breath basis and delivers pressure within the allowed range according to the degree of obstruction. The AutoSet algorithm adjusts treatment pressure as a function of three parameters: inspiratory flow limitation, snore, and apnea.
When the patient is breathing normally, the inspiratory flow measured by the machine as a function of time shows a typically rounded curve for each breath.
As the upper airway begins to collapse, the shape of the inspiratory flow-time curve changes. The AirMini recognizes and treats traditional as well as less common flow-limited breath wave forms.
Snoring is sound generated by vibrations of the walls of the upper airway. It is often preceded by flow limitation or a partial obstruction of the airway.
The enhanced AutoSet algorithm detects both obstructive and central apneas. If an apnea occurs, the machine responds appropriately.
Obstructive apnea
An obstructive apnea is when the upper airway becomes severely limited or completely obstructed. AutoSet generally prevents obstructive apneas from occurring by responding to flow limitation and snoring. If an obstructive apnea occurs, the machine will respond by increasing pressure.
Central apnea
During a central apnea, the airway will remain open, but there is no flow. When a central apnea is detected, the machine responds appropriately by not increasing pressure.
AutoSet for Her mode is based on key aspects of ResMed's AutoSet algorithm and delivers therapeutic responses tailored to the characteristics of female OSA patients.
The AutoSet for Her is similar to ResMed's AutoSet algorithm with the following modifications:
If two apneas occur within a minute, the pressure reached in response to the second apnea will become the new minimum treatment pressure until the next treatment session.
Patients who use AutoSet for Her will still get the benefits of ResMed's AutoSet technology including improved sensitivity to flow-limitation and Central Sleep Apnea Detection with Forced Oscillation Technique.
In CPAP mode, a fixed pressure is delivered—with optional Expiratory Pressure Relief (EPR).
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 prescribed treatment pressure. Ramp Time is available in all modes.
In AutoSet and AutoSet for Her mode, ramp time defines the period during which the pressure gradually increases from a lower more comfortable start pressure to the minimum treatment pressure before the auto-adjusting algorithm commences.
In CPAP mode, the pressure increases from a low pressure (Start Pressure) to the prescribed treatment pressure.
Ramp Time can be set to Off, 5 to 45 minutes or Auto. When Ramp Time is set to Auto, the machine will detect sleep onset and then gradually increase from the start pressure to the minimum treatment pressure at a rate of 1 cm H2O (1 hPa) per minute. However, if sleep onset is not detected, the machine will reach the target pressure within 30 minutes.
Designed to make therapy more comfortable, Expiratory Pressure Relief (EPR) maintains optimal treatment for the patient during inhalation and reduces the delivered mask pressure during exhalation.
EPR | On—EPR is enabled. Off—EPR is disabled and not visible in Patient Mode. |
The following settings are only available if EPR is On:
EPR Type | Full Time—If set to Full Time, EPR is enabled for the whole therapy session. Ramp Only—If set to Ramp Only, EPR is only enabled during ramp time. |
EPR Level | 1, 2, 3 cm H2O (1, 2, 3 hPa) |
When EPR is enabled, the delivered pressure will not drop below a minimum pressure of 4 cm H2O (4 hPa), regardless of the settings.
For patients who are sensitive to faster changes in pressure during therapy, AutoSet Response can be set to either Standard or Soft. If set to soft, patients will receive gentler pressure rises during therapy.
Patients who use the AutoSet Response feature will still get the benefits of ResMed's AutoSet technology including improved sensitivity to flow-limitation and CSA Detection with Forced Oscillation Technique.
When SmartStart is turned on, therapy starts automatically when the patient breathes into their mask.
When SmartStop is turned on, once the patient removes their mask, therapy stops automatically after a few seconds.
The HumidX and HumidX Plus are waterless humidifiers. They are designed to provide more comfort by improving the moisture level in the air the patient breathes and offering relief from possible dryness.
The HumidX is a good starting point for finding the right level of humidification. The HumidX Plus will improve the humidity level further. It is useful when the ambient humidity level is very low. For example, at high altitudes or on an aircraft.
The HumidX and HumidX Plus can be used with the N20 connector for AirMini and AirFit P10 for AirMini only.
Note: The HumidX and HumidX Plus must be replaced within 30 days of opening the HumidX/HumidX Plus pack.
Before setting up the machine, ensure that the selected mask is compatible and that it is correctly positioned on the patient's face. The machine is compatible with ResMed's F20 and N20 series masks and with the P10 for AirMini. Refer to the mask device compatibility list on www.resmed.com for more information. Refer to the mask user guide for fitting information.
See Using clinical mode for information on preparing to use the AirMini app with a smart device.
For N20 or AirFit P10 for AirMini only:
To insert the HumidX or HumidX Plus:
Attach the connector to the mask.
Before connecting the AirMini machine to a smart device, ensure that the latest version of the AirMini app is installed on the smart device. If not, the app can be downloaded on Google Play.
Notes:
Bluetooth status indicators | ||
![]() | Bluetooth indicator light is flashing blue | The AirMini machine is in discoverable mode and ready for pairing. |
![]() | Bluetooth indicator light is constantly blue | The AirMini machine is connected to a smart device. |
![]() | Bluetooth indicator light is constantly white (airplane mode) | Bluetooth is disabled on your AirMini machine. |
Bluetooth indicator light is off | The AirMini machine is not connected to a smart device. |
Note: Once therapy starts, the indicator light will start to fade.
Using the AirMini machine:
Press the start/stop button on the machine. Or, if SmartStart is enabled, the machine will start automatically when the patient breathes into their mask normally.
Using the AirMini app:
Stop therapy using one of the following methods:
Using the AirMini machine:
Press the start/stop button on the machine. Or, if SmartStop is enabled, the machine will stop automatically when the patient removes their mask.
Using the AirMini app:
Tap STOP on the Sleep screen.
In clinical mode, ResMed's AirMini app acts as the clinical menu and as the patient's user interface. You can access, view and change therapy and machine settings using the AirMini app.
Note: Data sent through Bluetooth is encrypted.
To access clinical mode from the Welcome screen:
On the Welcome screen, hold one finger on the ResMed logo and one finger on the AirMini logo simultaneously for 3 seconds.
Note: This option is only visible until the terms and conditions have been accepted. Once they are accepted, it is no longer possible to access clinical mode from the Welcome screen.
Clinical mode opens.
To access clinical mode from the Bluetooth screen:
On the Bluetooth screen, hold one finger on the ResMed logo and one finger on the AirMini logo simultaneously for 3 seconds.
Note: Tap the Bluetooth icon in top, right corner of the Dashboard to open the Bluetooth screen.
Note: When setting up a patient for the first time, you must pair and connect a smart device through Bluetooth to the AirMini machine. See Connecting machine and smart device for information on pairing.
To exit clinical mode, open the Navigation drawer and tap Exit.
In clinical mode (machine settings) you can scroll through clinical settings and change them as required.
Adjusting the clinical settings
The following clinical settings must be configured for each patient individually and should be periodically reassessed to ensure optimal therapy:
Therapy | |||||
Parameter | Description | Mode | Range | ||
AutoSet | AutoSet for Her | CPAP | |||
Mode | Sets the therapy mode available on the machine. | ![]() | ![]() | ![]() | |
Max Pressure | Sets the upper limit of treatment pressure. | ![]() | ![]() | Min–20 cm H2O (Min–20 hPa), 0.2 cm H2O (0.2 hPa) increments | |
Min Pressure | Sets the lower limit of treatment pressure. | ![]() | ![]() | 4–Max cm H 2 O (hPa), 0.2 cm H2O (hPa) increments | |
Set Pressure | Sets the fixed treatment pressure. | ![]() | 4–20 cm H 2 O (4–20 hPa), 0.2 cm H2O (0.2 hPa) increments | ||
Comfort | |||||
Parameter | Description | Mode | Range | ||
AutoSet | AutoSet for Her | CPAP | |||
Response | Sets the rate of pressure rises during therapy. | ![]() | Standard / Soft | ||
Ramp Time | If Auto is selected, the machine will detect sleep onset and automatically rise to the prescribed treatment pressure. | ![]() | ![]() | ![]() | Off / 5–45 mins / Auto |
Start Pressure | Sets the pressure at the start of ramp time, up to treatment pressure. | ![]() | ![]() | ![]() | 4–Set pressure (CPAP), 0.2 cm H2O (0.2 hPa) increments 4–Min pressure (AutoSet and AutoSet for Her), 0.2 cm H2O (0.2 hPa) increments |
EPR | Enable / disable EPR. | ![]() | ![]() | ![]() | On / Off |
EPR Type | Available when EPR is enabled. | ![]() | ![]() | ![]() | Full Time / Ramp Only |
EPR Level | Sets the EPR value. | ![]() | ![]() | ![]() | 1 / 2 / 3 cm H2O (1 / 2 / 3 hPa) |
Options | |||||
Parameter | Description | Selection | |||
SmartStart | If you switch the feature on, the machine will start automatically when the patient breathes into their mask. | Off / On | |||
SmartStop | If you switch the feature on, the machine will stop automatically when the patient removes their mask. | Off / On | |||
Configuration | |||||
Parameter | Description | Selection | |||
Pressure Units | Sets the unit in which pressure is displayed | cm H2O / hPa | |||
Other options | |||||
Button | Description | ||||
Therapy/Mask Fit | Launches the Sleep screen, which provides access to mask fit and therapy functions. | ||||
Restore default settings | Tapping the Restore default settings button opens a confirmation dialog. Once you confirm that you want to restore default settings, factory default clinical settings will be restored. Note: Default language, date and time settings will not be restored. | ||||
Erase data | Tapping the Erase data button opens a confirmation dialog. Once you confirm that you want to erase data, information stored on the AirMini machine will be erased. Note: Settings, date, time and machine run hours will not be erased. |
To change a setting:
To enable or disable EPR or to switch SmartStart or SmartStop on or off:
Functions in the Sleep screen are arranged in two sections, Mask Fit and Therapy.
Mask Fit provides access to mask fit and Therapy provides patient access to therapy functions and comfort settings.
Running mask fit
The Dashboard provides a snapshot of the patient's therapy data including sleep score, usage hours, mask seal, events per hour, mask on/off events and air pressure delivered during the majority of the previous night of sleep.
Note: The displayed air pressure is equal to or less than the highest pressure level of the air delivered to the patient by the AirMini during 95 percent of the patient's therapy the previous night.
To access the Dashboard, tap the Dashboard icon in the Navigation drawer.
The About AirMini machine screen provides the following information about the AirMini:
To access the About AirMini machine screen, select About AirMini machine from the More menu.
It is important that the AirMini machine is cleaned regularly to ensure optimal therapy. The following sections will help with disassembling, cleaning and replacing parts.
If any visible deterioration of a system component is apparent (cracking, discoloration, tears etc.), the component should be discarded and replaced.
The following sections provide instructions for disassembling components before cleaning.
For F20 and N20 only:
Remove the connector from the mask by pressing the side buttons and pulling the connector away.
For F20 only
Disconnect the F20 connector from the AirMini tubing by gently twisting it and pulling it apart.
For N20 and AirFit P10 for AirMini only
Disconnect the vent module from the AirMini tubing by gently twisting it and pulling it apart.
For N20 and AirFit P10 for AirMini only:
Note: The HumidX and HumidX Plus cannot be washed.
Disconnecting the AirMini tubing
Disconnect the AirMini tubing from the machine by pressing the side buttons on the cuff and pulling it away.
Unplug the power supply unit from the power outlet and the machine.
Note: For mask disassembly instructions, refer to the mask user guide.
After detaching all components according to the disassembly instructions, ensure that the HumidX or HumidX Plus is removed and stored in a clean, dry location.
Note: The HumidX and HumidX Plus cannot be washed.
Note: Do not wash the AirMini tubing in a dish washer or washing machine.
Note: Do not wash the F20 connector in a dish washer or washing machine.
Note: Do not wash the N20 connector in a dish washer or washing machine.
Refer to your mask guide for cleaning instructions.
Replace the air filter at least every 6 months. It cannot be washed. Check and replace it more often if there are any holes or blockages caused by dirt or dust.
To change the air filter:
Notes:
Wipe the exterior of the AirMini machine with a dry cloth each week.
If the AirMini machine is used by multiple patients, the AirMini air tubing as well as the HumidX must be discarded and replaced because they cannot be disinfected.
For mask cleaning instructions, refer to the mask user guide.
Patients can take their AirMini machine wherever they go.
Advise patients to take an appropriate power adapter for the region of travel. For information on purchasing an adapter, contact a ResMed representative.
Traveling by airplane
Some airlines do not classify medical equipment as carry-on luggage and therefore, the AirMini might not count toward carry-on luggage limits. Advise patients to check with their airline to determine their policies.
The AirMini machine can be used on an airplane because it meets Federal Aviation Administration (FAA) requirements.
Air travel compliance letters can be downloaded and printed from www.resmed.com.
To use the AirMini machine on an airplane:
If you experience problems, try the following suggestions. If you are not able to fix the problem, contact your local ResMed dealer or ResMed office. If you experience problems with the AirMini machine, do not open it.
Problem/possible cause | Solution |
A Bluetooth connection cannot be established. | |
Bluetooth may be disabled. | Ensure that Bluetooth is enabled on the patient's smart device ![]() Check the AirMini machine to determine whether Bluetooth is enabled. When the Bluetooth indicator light on the machine flashes blue ![]() Reconnect and pair the AirMini machine with the patient's smart device. Refer to Connecting machine and smart device for more information. If these solutions do not resolve the issue, try restarting the patient's smart device. If a Bluetooth connection between the patient's AirMini machine and the AirMini app cannot be established, advise the patient that therapy can be started manually by pressing the Start/Stop button ![]() |
The Bluetooth connection may be poor. | Ensure that the AirMini machine is placed away from potential sources of interference such as microwaves, wireless local area network (WLAN) routers or cordless phones. If a Bluetooth connection between the patient's AirMini machine and the AirMini app cannot be established, advise the patient that therapy can be started manually by pressing the Start/Stop button ![]() |
The AirMini machine may be in airplane mode. | If a white light ![]() To disable airplane mode, press the Bluetooth button ![]() Once airplane mode has been disabled and the light on the machine begins to flash blue ![]() |
The patient's smart device may be in airplane mode. | Turn off airplane mode on the patient's smart device. If airplane mode cannot be disabled, advise the patient that therapy can be started manually by pressing the Start/Stop button ![]() |
The Bluetooth indicator light on the AirMini machine is constantly white. It is not possible to pair to the machine. | |
Bluetooth is disabled. Turn off airplane mode on the patient's smart device. | Press the Bluetooth button ![]() ![]() |
The patient's therapy data has not been transmitted. | |
Bluetooth may be disabled. | Ensure that Bluetooth is enabled on the patient's smart device ![]() Ensure that Bluetooth is enabled on the AirMini machine by pressing the Bluetooth button ![]() ![]() Reconnect and pair the AirMini machine with the patient's smart device. Refer to Connecting machine and smart device for more information. If these solutions do not resolve the issue, try restarting the patient's smart device. |
The patient's smart device may be in airplane mode. | Turn off airplane mode on the patient's smart device. |
Air is leaking from around the patient's mask or the mask is too noisy. | |
The patient's mask may be fitted incorrectly. | Ensure that the patient's mask is fitted correctly. Refer to the mask user guide for fitting instructions or perform the mask fit function using the AirMini app to check the patient's mask fit and seal. |
The AirMini system may be assembled incorrectly. | Ensure that the AirMini system is assembled correctly. Refer to Setup for more information. |
The patient feels that the air pressure in their mask is too low or that they are not getting enough air. | |
Ramp may be in progress. | Use the AirMini app to confirm that the Ramp Time comfort feature has been enabled. If so, advise the patient to wait for air pressure to build up or to turn off the Ramp Time feature using the AirMini app. |
The HumidX or vent might be blocked. | Inspect the HumidX and vent for blockages or damage. |
The HumidX may be wet. | The HumidX should be dry when starting therapy. Determine whether the HumidX is wet and replace it if necessary. |
Ramp start pressure may be too low. | Increase ramp start pressure using the AirMini app. |
The patient feels that too much air is being delivered from the AirMini machine. | |
The Ramp Time feature may be turned off. | Turn on the Ramp Time feature using the AirMini app. |
Therapy will not start. | |
Power may not be connected. | Connect the power supply unit and ensure that the plug is fully inserted. The green indicator light on the power supply unit should be illuminated. Ensure that the green indicator light above the Start/Stop button ![]() |
Therapy has stopped. | |
The air tubing may be disconnected. | Ensure that the air tubing is properly connected. Press the Start/Stop button on the AirMini machine to continue therapy. |
The patient may be experiencing high mask leak while the SmartStop feature is enabled. | Ensure that the patient's mask is fitted correctly. Perform the mask fit function using the AirMini app to check the patient's mask fit and seal. Alternatively, disable the SmartStop feature using the AirMini app. |
It isn't possible to scan the QR code to pair with the AirMini machine. | |
The camera is not focused or broken, or the QR code label is damaged. | Pair the AirMini machine manually by entering into the patient's smart device the four-digit key found on the back of the machine. |
The light above the Start/Stop button on the AirMini is flashing green. | |
An error has occurred on the AirMini machine. | Unplug the AirMini machine, wait a few seconds, and then plug it back in. |
The patient is experiencing dryness or has a dry or blocked nose. | |
The patient's mask may be fitted incorrectly. | Adjust and refit the patient's mask to improve the seal. Ensure that no air is leaking from it. Refer to the mask user guide for fitting instructions or perform the mask fit function using the AirMini app to check the patient's mask fit and seal. If the patient's mask fit is good, advise the patient to try the HumidX Plus. |
Humidification may be required. | Advise the patient to try therapy with the HumidX. |
The patient is using the HumidX or HumidX Plus and is getting uncomfortable droplets of water on their nose, mask or air tubing. | |
The humidity level is too high. | If the patient is using the HumidX, advise them to remove it and try therapy without humidification. If the patient is using the HumidX Plus, advise them to try the HumidX instead. This will help to reduce the water droplets. |
Note: The patient may need to use the HumidX or HumidX Plus when ambient humidity conditions change. | |
The AirMini machine appears in the machine selection list, but it is not possible to establish a connection. | |
The AirMini machine name was not selected in the machine selection list. | Tap the device name in the machine selection list to confirm that you want to connect to that machine. |
Power supply unit | |||
AC input range: | 100–240V, 50–60Hz 115V, 400Hz (nominal for aircraft use) | ||
DC output: | 24V ![]() | ||
Typical power consumption: | 6.3W | ||
Peak power consumption: | 27W | ||
If power is interrupted during therapy, the machine will automatically restart therapy when power is restored. | |||
AirMini power | |||
Standby power consumption: | 1 W | ||
Environmental conditions | |||
Operating temperature: | +41°F to +95°F (+5°C to +35°C) Note: Under extreme ambient temperature conditions (104°F/40°C) the air and parts of the tubing near the mask may reach temperatures up to 109°F/43°C. These parts of the tubing are not in contact with the user and the machine remains safe under these extreme conditions. | ||
Operating humidity: | 10 to 95% relative humidity, non-condensing | ||
Operating altitude: | Sea level to 8,500' (2,591 m); air pressure range 1013 hPa to 738 hPa | ||
Storage and transport temperature: | -13°F to + 158°F (-25°C to + 70°C) | ||
Storage and transport humidity: | 5 to 95% relative humidity, non-condensing | ||
Sensors | |||
Pressure sensor: | Internally located at device outlet, analog gauge pressure type, -5 to +45 cm H2O (hPa) | ||
Flow sensor: | Internally located at device inlet, digital mass flow type, -70 to +110 L/min | ||
Maximum single fault steady pressure Machine will shut down in the presence of a single fault if the steady state pressure exceeds 30 cm H2O (30 hPa) for more than 6 sec or 40 cm H2O (40 hPa) for more than 1 sec. | |||
Sound | |||
Declared dual-number noise emission values in accordance with ISO 4871:1996 | |||
Pressure level measured according to ISO 80601-2-70:2015 (CPAP mode) | 30 dBA with uncertainty of 2 dBA | ||
Power level measured according to ISO 80601-2-70:2015 (CPAP mode) | 38 dBA with uncertainty of 2 dBA | ||
The A-weighted sound pressure level measured according to ISO 17510:2015: | |||
Air tubing connected to AirMini F20 connector with mask | 19 dBA with uncertainty of 3 dBA | ||
Air tubing connected to AirMini N20 or P10 connectors with mask | 17 dBA with uncertainty of 3 dBA | ||
The A-weighted sound power level measured according to ISO 17510:2015: | |||
Air tubing connected to AirMini F20 connector with mask | 27 dBA with uncertainty of 3 dBA | ||
Air tubing connected to the AirMini N20 or P10 connectors with mask | 25 dBA with uncertainty of 3 dBA | ||
AirMini machine | |||
Dimensions: | 5.4" (W) x 3.3" (D) x 2.1"(H) 136 mm (W) x 84 mm (D) x 52 mm (H) | ||
Weight: | 300g (10.6 oz) | ||
Housing construction: | Flame retardant engineering thermoplastic | ||
Air outlet: | Proprietry connector, 16mm inner diameter. Not compatible with EN ISO 5356-1 connectors. | ||
Air filter | |||
Standard: | Material: Polyester non woven fiber Average arrestance: >75% for ~7 micron dust | ||
Hypoallergenic: | Material: Acrylic and polypropylene fibers in a polypropylene carrier Efficiency: >98% for ~7-8 micron dust; >80% for ~0.5 micron dust | ||
AirMini air tubing | |||
Material: | Flexible plastic | ||
Length: | 6'2" (1.9 m) | ||
Inner diameter: | 0.6" (15 mm) | ||
Aircraft use ResMed confirms that machine meets the Federal Aviation Administration (FAA) requirements (RTCA/DO-160, section 21, category M) for all phases of air travel. | |||
Wireless technology | |||
Technology used: | Bluetooth | ||
Connection types: | SPP, iAP2, GATT | ||
Frequency: | 2402 to 2480 MHz | ||
Max RF power output: | +4 dBm | ||
Operating range: | 10 m (Class 2) | ||
It is recommended that the machine is at a minimum distance of 0.43" (1.1 cm) from the body during operation. Not applicable to masks, air tubing or accessories. | |||
Operating pressure range | |||
AutoSet, AutoSet For Her, CPAP: | 4 to 20 cm H2O (4 to 20 hPa) | ||
Design life | |||
Machine, power supply unit: | 5 years | ||
Air tubing, connectors: | 6 months | ||
HumidX: | 30 days | ||
Pneumatic flow path | |||
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General The patient is an intended operator. | |||
Pressure flow curve (ISO17510:2015) | |||
![]() | Pressure [cm H2O (hPa)] | Flow [L/min] | |
4 | 21 | ||
8 | 26 | ||
12 | 29 | ||
16 | 31 | ||
20 | 33 | ||
Displayed values | |||
Value | Range | Display resolution | |
Pressure sensor at air outlet: Mask pressure | 4-20 cm H2O (4-20 hPa) | 0.1 cm H2O (0.1 hPa) | |
Inspiratory and expiratory resistance with AAV open to atmosphere (ISO 17510:2015) | F20 connector | ||
Inspiration at 50L/min | 0.7 cm H2O (hPa) | ||
Expiration at 50L/min | 0.5 cm H2O (hPa) | ||
AAV Pressures (ISO17510:2015) | F20 connector | ||
Open-to-atmosphere pressure | 0.9 cm H2O (hPa) | ||
Closed-to-atmosphere pressure | 1.0 cm H2 O (hPa) | ||
Measurement system uncertainties In accordance with ISO 80601-2-70:2015 the measurement uncertainty of the manufacturer's test equipment is: | |||
For measures of flow | ± 1.5 L/min or ± 2.7% of reading (whichever is greater) | ||
For measures of static pressure | ± 0.15 cm H2O (0.15 hPa) | ||
For measures of dynamic pressure | ± 0.27 cm H2O (0.15 hPa) | ||
For measures of volume (< 100 mL) | ± 5 mL or 6% of reading (whichever is greater) | ||
For measures of volume (≥ 100 mL) | ± 20 mL or 3% of reading (whichever is greater) | ||
For measures of time | ± 10 ms | ||
Note: ISO 80601-2-70:2015 stated accuracies and test results provided in this manual for these items already include the relevant measurement uncertainty from the table above. | |||
Pressure accuracy | |||
Maximum static pressure variation at 10 cm H2O (10 hPa) according to ISO 80601-2-70:2015: | |||
Tested with full face mask: ±0.5 cm H20 (0.5 hPa) | |||
Maximum dynamic pressure variation according to ISO 80601-2-70:2015 | |||
Machine with full face mask | |||
Pressure [cm H2O (hPa)] | 10 BPM | 15 BPM | 20 BPM |
4 | 0.5 | 0.7 | 1.0 |
8 | 0.5 | 0.7 | 1.0 |
12 | 0.5 | 0.7 | 1.0 |
16 | 0.5 | 0.7 | 1.0 |
20 | 0.5 | 0.7 | 1.0 |
Flow (maximum) at set pressures The following are measured accordingly to ISO 80601-2-70:2015 at the end of the specified air tubing: | |||
Pressure cm H2O (hPa) | AirMini machine and AirMini air tubing L/min (including uncertainty) | ||
4 | 119 | ||
8 | 116 | ||
12 | 112 | ||
16 | 108 | ||
20 | 105 | ||
Electromagnetic emissions The following are measured accordingly to ISO 80601-2-70:2015 at the end of the specified air tubing: | |||
Emissions test | Compliance | ||
RF emissions CISPR 11 | Class B | ||
Harmonic Emissions IEC 61000-3-2 | Class A | ||
Voltage Fluctuations/Flicker Emissions IEC 61000-3-3 | Complies | ||
Electromagnetic immunity | |||
Immunity test | Compliance level | ||
Electrostatic discharge (ESD) IEC 61000-4-2 | ±8 kV contact ±15 kV air | ||
Electrical fast transient/burst IEC 61000-4-4 | ±2 kV ±1 kV for input/output lines | ||
Surge | ±1 kV differential mode | ||
IEC 61000-4-5 | ±2 kV common mode | ||
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 | 100V 240V | ||
Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 | 30 A/m | ||
Conducted RF IEC 61000-4-6 | 3 Vrms 150 kHz to 80 MHz | ||
Radiated RF IEC 61000-4-3 | |||
Frequency (MHz) | Immunity test level (V/m) | Frequency (MHz) | Immunity test level (V/m) |
80 MHz – 2.5 GHz | 10 | 930 | 28 |
385 | 27 | 1720 | 28 |
450 | 28 | 1845 | 28 |
710 | 9 | 1970 | 28 |
745 | 9 | 2450 | 28 |
780 | 9 | 5240 | 9 |
810 | 28 | 5500 | 9 |
870 | 28 | 5785 | 9 |
Note: Portable and mobile RF communications equipment should be used no closer to any part of the machine, including cables, than the recommended 30 cm separation distance. |
Notes:
The following symbols may appear on the product or packaging.
Indicates a warning or caution.
Manufacturer.
European Authorized Representative.
Batch code.
Catalog number.
Serial number.
Device number.
On / Off.
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.
Bluetooth.
Prescription only (In the US, Federal law restricts these devices to sale by or on the order of a physician).
Operating altitude.
Atmospheric pressure limitation.
MR unsafe (do not use in the vicinity of an MRI device).
Do not use if package is damaged.
The AirMini machine is intended to provide safe and reliable operation when operated in accordance with the instructions provided by ResMed. ResMed recommends that the AirMini machine be inspected and serviced by an authorized ResMed Service Centre if there is any sign of wear or concern with device function. Otherwise, service and inspection of the products generally should not be required during their design life.
ResMed 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
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
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