settings and device congurations including accessories, according to your health care professional’s prescription.

products are not approved or recommended, and may adversely affect your device safety and performance.

• The device should only be used with compatible patient interfaces (e.g., masks, circuits and exhalation ports). Proper operation of the

• An exhalation port is required. Do not block the exhalation port. This can reduce airow and result in rebreathing of exhaled air.

• At low expiratory pressures, the ow through the exhalation port may be inadequate to clear all exhaled gas from the tubing –

• When using oxygen with this system, the oxygen supply must comply with local regulations for medical oxygen.

• Oxygen supports combustion. Oxygen should not be used while smoking or in the presence of an open ame.

• When using oxygen with this system, turn the device on before turning on the oxygen. Turn the oxygen off before turning the

• When using oxygen with this system, a Philips Respironics Pressure Valve must be placed in-line with the patient circuit between

• Do not connect the device to an unregulated or high pressure oxygen source.

• If you notice any unexplained changes in the performance of this device, if it is making unusual or harsh sounds, if it has been

• Repairs and adjustments must be performed by Philips Respironics-authorized service personnel only. Unauthorized service could

• Do not use any accessories, detachable parts, and materials not recommended by Philips Respironics. Incompatible parts or

• Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment. See the EMC section of this manual

• Do not use this device near active high frequency surgical equipment and the Radio Frequency shielded room of a Medical

• MR Unsafe - Projectile hazard. Keep outside of MRI scan room (Zone IV).

• Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper

• Do not cover the tubing with a blanket or heat it in an incubator or with an overhead heater. This can affect the quality of the

• If the device is used by multiple persons (such as rental devices), a low-resistance, main ow bacteria lter should be installed in-

• If using a humidier, do not use the humidier at an altitude above 2286 m (7500 ft) or outside a temperature of 5° C to 40° C

• To prevent disconnection of the tubing or tubing system during use, only tubes in compliance with ISO 5367 or ISO 80601-2-74

• Humidication can increase the resistance of the bacteria lter and the operator must monitor the bacteria lter frequently for

• Use only Philips Respironics recommended pulse oximeter and sensors. Use of incompatible sensors can result in inaccurate pulse

• Do not use a damaged pulse oximeter or sensor.

• Before use, carefully read these instructions and the instructions for use provided with the pulse oximeter and sensor.

• Medical electrical equipment needs special precautions regarding EMC and needs to be installed according to EMC information.

The following symbols may appear on the device, power supply and accessories. For a full list and description of the symbols used on

the device and its packaging, see www.symbols.philips.com.

Country of Manufacture - Indicates the country of manufacture of the product. Note: When applied to

the label, “CC” is replaced by the country code.

Indicates the manufacturer’s catalogue number so the medical device can be identied.

Identies the manufacturer’s serial number for the medical device.

Should you experience trouble with this equipment or require assistance setting up, using, or maintaining the device

or accessories, please contact your home care provider. If you need to contact Philips Respironics directly, call

the Philips Respironics Customer Service department at 1-800-345-6443 or 1-724-387-4000. You can also use the

following address:

Respironics, Inc.

Murrysville, PA 15668

increase until your prescription pressure is reached. Also, the Flex comfort feature provides you with pressure relief

when you exhale during therapy.

If the Therapy On/Off button LED is ashing, you may have a pending

4 Door, SD card & Filter Access This door lifts open for access to the SD card and lter area.

7 Door, Accessory Access This door lifts open for access to the (optional) accessories.

8 Humidier Connector

Humidier connects to the back of the therapy device. The humidier

The reusable blue lter is supplied with the device. A disposable light-blue ultra-ne lter may also be included. If your

lter is not already installed when you receive your device, you must at least install the reusable lter before using the

This device has an automatic air lter reminder. Every 30 days, the device will display a message reminding you to

check your lters and replace them as directed.

an upload a second time, or contact your home care provider if the issue persists.

Flex This allows you to adjust the level of air pressure relief that you feel when you

exhale during therapy. Your home care provider can enable or disable this

feature. When your provider enables Flex, a level will already be set for you on

“1” provides a small amount of pressure relief, with higher numbers providing

you cannot nd this resistance setting for your mask.

mm tubing, (15) for the Philips Respironics 15 mm tubing, or (12) for the optional

Philips Respironics 12 mm tubing. When using Heated Tubing, the device will

automatically change this setting to the appropriate tubing type (HT15) and you

is turned off, it will automatically turn on again after 3 days. Only displays when

you may adjust the time in 30 minute increments to match your local time zone.

1. With your therapy device powered up and the blower off, initiate Bluetooth Setup from the DreamMapper mobile

The following icon will appear on your therapy device screen with “Pair?”:

Rotate the therapy device’s Control Dial to select “yes,” and press the Control Dial. Your therapy device will display

a red bar indicates improvement is needed. After the test, normal therapy will start and the screen will either display

a green checkmark or a red “X”. The green checkmark indicates that the leak found allows for optimal performance

of the device. The red “X” indicates that the leak may affect device performance, however, the device will remain

Your device provides summary information about your therapy use each time the therapy is turned off. The rst

screen displays your “Three Night Summary.” It shows your nightly usage for the last 3 sleep sessions (measured in

24 hour periods, ending at noon each day). The most recent session is displayed in the right hand bar, labeled with the

This device automatically compensates for altitude up to 7,500 feet. No manual adjustment is necessary.

setting for the next

be identied by the

accept pairing (Yes),

or decline (No), then

conrm selection.

Reinsert SD card, or

achieved at least 4

oximetry use. Appears

problem may exist

it was ejected during

continues to occur,

Heated tube may

from humidier,

Conrm a compatible

the user interface. Press the Therapy button on top of the device to start airow.

If the airow does not turn on, there may be a problem with your device. Contact

mishandled, or

Unplug the device. Reapply power to the device. If the problem continues, relocate

the device to an area with lower EMI emissions (away from electronic equipment

such as cellular phones, cordless phones, computers, TVs, electronic games, hair

dryers, etc.). If the problem still occurs, contact your home care provider for

If your provider has enabled Ramp, but the feature still does not work, check the

minimum setting (4.0 cm H

O), or the Ramp starting pressure is the same as the

therapy pressure, the Ramp feature will not work. Make sure that the ramp time

The air lters may

Rinse or replace the reusable air lter or replace the disposable ultra-ne lter.

is away from direct sunlight and heating equipment.

If using the humidier with the device, check the humidier settings. Refer to the

humidier instructions to make sure the humidier is working properly.

If the problem continues, contact your home care provider.

Make sure the Tubing type setting (22, 15, or 12) matches the tubing that you are

using (Philips Respironics 22, 15, or 12 mm tubing).

If you are using the Heated Tubing, this setting will be 15H and you cannot change it.

Make sure the 80W power supply is being used or a compatible battery or DC cable

and/or heated tube, and reconnect the device’s power supply. Turn the blower on; if

the settings are still not visible, contact your provider for assistance.

Water chamber

leak is excessively

Under most conditions, a full water chamber should last for a typical sleep

session. However, many factors impact water consumption, including: the ambient

temperature and humidity in your bedroom, your humidier or heated tube settings,

the level of mask leak, and the duration of your sleep session.

First, make sure that the water chamber is lled to the maximum ll line at the start

humidier or tube is

The humidier seals

Check therapy device air inlet is not obstructed, and lters are free of debris and

properly inserted. Conrm that the device, humidier, and tube are connected

properly and not leaking. Conrm that the humidier lid seal and dry box seal are

present and properly seated; if needed, gently press around the perimeter of the

A small amount of water spilled in the basin of the humidier will not harm your

spilled water. Once the heater plate has cooled, wipe the inside of the humidier

with a paper towel or soft cloth. If needed, dry the underside of the humidier and

conrm that your table top is dry. Reconnect the humidier and power supply, and

Static pressure accuracy has a measurement uncertainty of 3.7%

Maximum dynamic pressure variation, according to ISO 80601-2-70:2015:

85 124 131 132 128

86 127 134 133 117

85 95 94 100 102

1845, 1970, and 2450 MHz

at 28 V/m

385 MHz at 27 V/m

710, 745, 780, 5240, 5500,

and 5785 MHz at 9 V/m

1845, 1970, and 2450 MHz

at 28 V/m

385 MHz at 27 V/m

710, 745, 780, 5240, 5500,

and 5785 MHz at 9 V/m

RFID Reader frequencies

as specied in AIM

7351731:

433 MHz at 3 V/m

860 MHz to 960 MHz at

RFID Reader frequencies

as specied in AIM

7351731:

433 MHz at 3 V/m

860 MHz to 960 MHz at