S8 Escape

™

System

USER’S MANUAL

English

338215-Eng/3 05 08

1

338215r3 Illustrations.qxd 25/08/2005 1:50 PM Page 1

B INTEGRATED HUMIDIFIER / HUMIDIFICATEUR INTÉGRÉ/

HUMIDIFICADOR INTEGRADO / HUMIDIFICADOR INTEGRADO

Component of 338215/3

Composant du 338215/3

Componente de 338215/3

Componente de 338215/3

S8 Escape ™

ILLUSTRATIONS

ILLUSTRATIONS

FIGURAS

ILUSTRAÇÕES

A

SYSTEM COMPONENTS / COMPOSANTS DU SYSTÈME / COMPONENTES DEL

SISTEMA / COMPONENTES DO SISTEMA

Carry handle

Poignée de transport

Asa para el transporte

Pega de transporte

Keypad

Clavier

Teclado

Teclado

LCD screen

Écran LCD

Visor

Mostrador LCD

Air outlet

Sortie d'air

Salida de aire

Saída de ar

Connector plug

Cache du connecteur

Enchufe conector

Tampa do conector

1

HumidAire 3i ™

C OTHER ACCESSORIES / AUTRES ACCESSOIRES / OTROS ACCESORIOS /

OUTROS ACESSÓRIOS

Module

Module

Módulo

Módulo

DC input

Entrée CC

Entrada de CC

Entrada CC

2

Air filter cover

Couvercle du logement du filtre à air

Cubierta del filtro de aire

Tampa do filtro de ar

Air inlet

Entrée d'air

Entrada de aire

Entrada de ar

AC input

Entrée CA

Entrada de CA

Entrada CA

1

9’ 10”/3 m

2

21”/52 cm

3

4 5

3 4

6’ 6”/2 m

5

D

SETTING UP THE S8™ / INSTALLATION DE LA S8 / INSTALACIÓN DEL S8

/ MONTAGEM DO S8

1

3

4

2

338215r3 Illustrations.qxd 25/08/2005 1:50 PM Page 2

E HUMIDAIRE 3i and S8 ESCAPE / HUMIDAIRE 3i et S8 ESCAPE /

HUMIDAIRE 3i y S8 ESCAPE / HUMIDAIRE 3i e S8 ESCAPE

H USING THE DATA CARD / UTILISATION DE LA CARTE DE DONNÉES / USO DE LA TARJETA DE DATOS /

COMO USAR O CARTÃO DE DADOS

F

1

BLANK MODULE / MODULE VIERGE / MÓDULO EN BLANCO /

MÓDULO EM BRANCO

Data communications port

Port de communication des données

Puerto de comunicación de datos

Porta de comunicação de dados

2

G

DATA CARD MODULE / MODULE DE CARTE DE DONNÉES /

MÓDULO TARJETA DE DATOS / COMO USAR O CARTÃO DE DADOS

I

1 2 3

USING A HUMIDAIRE™ / UTILISATION D'UN HUMIDAIRE / USO DE UN HUMIDAIRE / UTILIZAÇÃO DE UM HUMIDAIRE

2

3

1

4

5

0

6

7

8

3

2

1

4

5

0

6

7

8

2

1

0

5

6

7

8

J

1 2 3 4

USING A RESMED PASSOVER / UTILISATION D'UN PASSOVER RESMED / USO DE UN PASSOVER DE RESMED / UTILIZAÇÃO DE UM RESMED PASSOVER

1 2

Note: Some products not available in all regions. / Remarque : certains produits ne sont pas disponibles dans tous les pays. / Nota: algunos productos no están disponibles en todas las regiones. / Nota:Alguns produtos não se encontram disponíveis em todas as regiões.

1 2 3 4

C ONTENTS

I

NTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

Y OUR R ESPONSIBILITY 5

M EDICAL I NFORMATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5

A BOUT THE S8 E SCAPE ™

C ONTRAINDICATIONS 6

W ARNINGS

C AUTIONS

A DVERSE E FFECTS

6

7

8

T

HE

S8 E

SCAPE

S

YSTEM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9

S8 E SCAPE 9

M ASKS 9

H UMIDIFIERS 10

R ES S CAN D ATA C ARD M ODULE 10

A CCESSORIES 10

H OW TO U SE THE S8 E SCAPE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

S ET U P THE S8 E SCAPE 11

A SSEMBLE THE M ASK 11

S TART T REATMENT 11

S TOP T REATMENT 12

H OW TO A TTACH A H UMIDIFIER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

A TTACH A H UMID A IRE 3

I

H UMIDIFIER 13

A TTACH A H UMID A IRE H UMIDIFIER 13

A TTACH A R ES M ED P ASSOVER H UMIDIFIER 14

H

OW TO USE THE

K

EYPAD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15

H OW TO C HANGE THE S ETTINGS ON YOUR S8 E SCAPE 16

S8 M ODULES . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19

U SING A B LANK M ODULE 19

U SING A R ES S CAN D ATA C ARD M ODULE 19

C LEANING AND M AINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

D AILY C LEANING 22

W EEKLY C LEANING 22

P ERIODIC C LEANING 22

R EPLACING THE A IR F ILTER 23

S ERVICING 23

F

REQUENTLY

A

SKED

Q

UESTIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

T ROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

C ONTENTS 3

4

S

YSTEM

S

PECIFICATIONS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29

S8 E SCAPE 29

A CCESSORIES 29

L

IMITED

W

ARRANTY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35

I NDEX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37

I

NTRODUCTION

Thank you for choosing the S8 E SCAPE ™ flow generator. The S8 E SCAPE is a compact, all-in-one package with an inbuilt power supply and the option of integrated data management and humidification.

This user manual contains the information you need for the correct use of your

S8 E SCAPE

.

Y OUR R ESPONSIBILITY

•

•

The owner or user of this system shall have sole responsibility and liability for any injury to persons or damage to property resulting from: operation which is not in accordance with the operating instructions supplied maintenance or modifications carried out unless in accordance with authorized instructions and by authorized persons.

•

•

•

Please read this manual carefully before use.

This manual contains special terms and icons that appear in the margins to draw your attention to specific and important information.

Warning alerts you to possible injury.

Caution explains special measures for the safe and effective use of the device.

Note is an informative or helpful note.

M

EDICAL

I

NFORMATION

A BOUT THE S8 E SCAPE ™

The S8 E SCAPE continuous positive airway pressure (CPAP) system is indicated for the treatment of obstructive sleep apnea (OSA) in adult patients.

The S8 E SCAPE CPAP system is intended for home and hospital use.

!

CAUTION

In the US, Federal law restricts this device to sale by or on the order of a physician.

I NTRODUCTION 5

6

C ONTRAINDICATIONS

•

•

•

•

•

The S8 E SCAPE is not a life support device and may stop operating during power failure or certain fault conditions. It should not be used by patients who are dependent on continuous therapy.

Positive airway pressure therapy may be contraindicated in some patients with the following pre-existing conditions: severe bullous lung disease pneumothorax pathologically low blood pressure dehydration cerebrospinal fluid leak, recent cranial surgery, or trauma.

W ARNINGS

•

•

•

•

Read the entire manual before using the S8 E SCAPE .

Advice contained in this manual should not supersede instructions given by the prescribing physician.

A patient should not connect a device to the data communication port unless instructed to do so by their health care provider or physician. Only ResMed products are designed to be connected to the data communication port.

Connecting other devices could result in injury, or damage to the S8 E SCAPE device.

The S8 E SCAPE should only be used with masks (and connectors) * recommended by ResMed, or by a physician or respiratory therapist. A mask should not be used unless the S8 E SCAPE device is turned on and operating properly. The vent hole or holes associated with the mask should never be blocked.

Explanation: The S8 E SCAPE is intended to be used with special masks (or connectors)

*

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 models of CPAP devices.

•

•

In the event of power failure or machine malfunction, remove the mask.

The S8 E SCAPE

can be set to deliver pressures up to 20 cm H

2 event of certain fault conditions, pressures up to 30 cm H

2

O. In the unlikely

O are possible.

* Ports may be incorporated into the mask or in connectors that are near the mask.

•

•

•

•

If oxygen is used with this device, the oxygen flow must be turned off when the device is not operating.

If oxygen has been left on, turn off the flow generator, then wait 30 minutes before turning on the flow generatory again.

Explanation: When the CPAP device is not in operation and the oxygen flow is left on, oxygen delivered into the air delivery tubing may accumulate within the

CPAP machine enclosure and create a risk of fire. This applies to most types of

CPAP machines.

•

•

•

Oxygen supports combustion. Oxygen should not be used while you are smoking or in the presence of an open flame.

Always ensure airflow is being generated by the device before the oxygen supply is turned on.

Always turn the oxygen supply off before stopping the airflow from the device.

Note: At a fixed rate of supplemental oxygen flow, the inhaled oxygen concentration will vary, depending on where the oxygen is introduced, the pressure settings, patient breathing pattern, mask selection, and leak rate.

Do not use the S8 E SCAPE if there are obvious external defects or unexplained changes in performance.

Do not open the S8 E SCAPE case. There are no user serviceable parts inside.

Repairs and internal servicing should only be performed by an authorized service agent.

Explosion hazard—do not use in the vicinity of flammable anesthetics.

C AUTIONS

•

•

•

•

•

At low pressures, the flow through the exhalation ports of your mask may not clear all exhaled gas from the tubing. Some rebreathing may occur.

The airflow for breathing produced by this device can be as much as 11 o

F (6 o

C) higher than the temperature of the room. Caution should be exercised if the room temperature is warmer than 90 o

F (32 o

C).

When AC mains power (100–240V AC) is not available, always use a ResMed

DC-12 converter. (The DC-12 converter is available as an optional accessory. It is not supplied with all models.)

If supplied, the Data Card module is designed for use with specific ResMed devices.

Only use the Data Card module (if supplied) as specified in this manual.

Note: The above are general warnings and cautions. Specific warnings, cautions, and notes appear with the relevant instructions in the manual.

M EDICAL I NFORMATION 7

8

A DVERSE E FFECTS

•

•

•

•

•

•

•

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 CPAP device: drying of the nose, mouth, or throat nosebleed bloating ear or sinus discomfort eye irritation skin rashes chest discomfort.

T

HE

S8 E

SCAPE

S

YSTEM

•

•

•

•

•

The S8 E SCAPE

device is part of a system that consists of five elements:

S8 E SCAPE flow generator

Mask

Humidifier

Data management products

Accessories.

S8 E SCAPE

Please refer to the illustrations in section A of the illustration sheet.

F RONT VIEW (A-1)

Shows the keypad and LCD screen, and the air outlet.

R EAR VIEW (A-2)

Shows where the module attaches, and the location of the air filter and power sockets.

P OWER CORD (A-3)

Power cord to attach the S8 E SCAPE to the AC (mains) power.

C ARRY BAG (A-4)

The S8 E SCAPE carry bag contains two pouches: one for storing the S8 device, the other for storing the H UMID A IRE 3i™ . When storing the H UMID A IRE 3i , always put it in the larger, mesh pouch.

A IR TUBING

The 6’6” (2 m) air tubing ( A-5) connects the S8 E SCAPE to your mask . You will need medium 21” (52 cm) air tubing (see C-3) to connect the S8 E SCAPE

to the

H UMID A IRE ™ and ResMed P ASSOVER humidifiers.

M ASKS

You will also need a ResMed mask system (supplied separately).

The ResMed mask systems that are recommended for use with the S8 E SCAPE are:

•

•

•

•

•

•

•

N ASAL M ASKS

M ODULAR N ASAL M ASK

M IRAGE V ISTA ™ N ASAL M ASK

U LTRA M IRAGE ™ N ASAL M ASK

M IRAGE ™ N ASAL M ASK

P ROTEGE ™ N ASAL M ASK

M IRAGE A CTIVA ™ N ASAL M ASK

P APILLON ™.

•

N ASAL P ILLOWS S YSTEMS

M IRAGE S WIFT ™ N ASAL P ILLOWS S YSTEM .

T HE S8 E SCAPE S YSTEM 9

10

!

•

•

•

F ULL F ACE M ASKS

M IRAGE ™ F ULL F ACE M ASK

M IRAGE ™ F ULL F ACE M ASK S ERIES 2

U LTRA M IRAGE ™ F ULL F ACE M ASK .

WARNING

Only ResMed mask systems are compatible for use with the S8 Escape. Please refer to “Warnings” on page 6.

H UMIDIFIERS

•

•

•

A humidifier may be required if you are experiencing dryness of the nose, throat, or mouth. The S8 E SCAPE is compatible for use with:

H UMID A IRE 3i integrated heated humidifier ( Figure B on the illustrations sheet )

H UMID A IRE heated humidifier ( Figure I on the illustrations sheet )

ResMed P ASSOVER humidifier ( Figure J on the illustrations sheet ).

R ES S CAN D ATA C ARD M ODULE

The R ES S CAN ™ Data Card module and R ES S CAN Data Card ( C-1) may be used with the S8 E SCAPE either to help your clinician to monitor your treatment or to provide you with updates to your device settings. See “Using a ResScan Data Card Module” on page 19 for information about how to use the Data Card module and Data Card.

A CCESSORIES

Please refer to the illustrations in section C of the illustration sheet.

•

•

•

•

Other accessories for use with the S8 E SCAPE :

Air tubing 9‘10” (3 m) ( C-2)

Medium air tubing 21” (52 cm) for H UMID A IRE and ResMed P ASSOVER connection

( C-3)

DC-12 converter ( C-4)

Blank module ( C-5).

Note: ResMed regularly releases new products. Please check our website at

<www.myresmed.com>.

H

OW TO

U

SE THE

S8 E

SCAPE

Please refer to the illustrations in section D of the illustration sheet.

S ET U P THE S8 E SCAPE

1 Place the S8 E SCAPE

on a table near the head of your bed.

!

CAUTION

Be careful not to place the device where it can be bumped or where someone is likely to trip over the power cord.

Note: You can also place your S8 Escape on the floor beside or underneath your bed.

Ensure that the area is free from dust and clear of bedding, clothes, or any other objects that could block the air inlet.

2 Connect the power cord to the socket at the rear of the flow generator ( D-1). Plug the other end of the power cord into the power outlet.

!

WARNING

Make sure the power cord and plug are in good condition and the equipment is not damaged.

3 Connect one end of the air tubing firmly onto the air outlet ( D-2).

!

•

•

•

WARNING

Only ResMed air tubing should be used with your flow generator. A different type of air tubing may alter the pressure you actually receive, reducing the effectiveness of your treatment.

Blocking the hose while in operation could lead to overheating of the device.

In the clinical environment any personal computer that is used with your CPAP system must be at least 5’ (1.5 m) away from, or at least 8’ (2.5 m) above, the patient. It must also comply with the relevant test standard. For personal computers the international standard is IEC 60950 or equivalent.

A SSEMBLE THE M ASK

1 Assemble your mask system according to the mask user instructions.

2 Connect your mask system to the free end of the air tubing ( D-3).

The S8 E SCAPE

is now ready for use ( D-4).

S TART T REATMENT

1 Make sure the power is on.

The product name is displayed briefly on the LCD screen, then the standby (Ramp) screen appears. The key and LCD backlights also turn on.

H OW TO U SE THE S8 E SCAPE 11

12

2 Lie down and arrange the air tubing so that it is free to move if you turn in your sleep.

!

•

•

CAUTION

Do not leave long lengths of air tubing around the top of your bed. They could twist around your head or neck while you are sleeping.

Make sure the area around the flow generator is dry and clean. It should also be clear of bedding, clothes, and other potential blockages.

3 Alter the ramp time if required (see “How to Change the Ramp Time” on page 17).

4 To start treatment, press the Start/Stop key.

5 Fit your mask as described in the mask user instructions.

!

WARNING

A mask should not be used unless the S8 Escape device is turned on and operating properly.

6 When ramping begins the LCD will display the word "RAMPING", with the current pressure indicated as dashes. Each dash is approximately equivalent to 2 cm H

2 example, 6 dashes represents approximately 12 cm H

2

O pressure.

O. For

S TOP T REATMENT

To stop treatment at any time, remove your mask and press the Start/Stop key.

H

OW TO

A

TTACH A

H

UMIDIFIER

A TTACH A H UMID A IRE 3 i H UMIDIFIER

Please refer to the illustration in section E of the illustration sheet, and your HumidAire 3i manual.

The H UMID A IRE 3i attaches to the front of the S8 E SCAPE

to provide heated humidification. No other accessories are required for its use.

Notes: a. Make sure the water chamber of the HumidAire 3i is empty before you attach or detach the humidifier.

b. Remove the connector plug on the S8 Escape (see section A of the illustration sheet) before you attach the HumidAire 3i. Reattach the connector plug firmly after you detach the HumidAire 3i.

S TORING THE H UMID A IRE 3 i

Store the H UMID A IRE 3i in the larger, mesh-top pouch of the S8 E SCAPE carry bag when not in use.

A

TTACH A

H

UMID

A

IRE

H

UMIDIFIER

Please refer to the illustrations in section I of the illustration sheet.

To connect your S8 E SCAPE

to a H UMID A IRE

humidifier you need medium sized

21” (52 cm) air tubing.

1 Fill the H UMID A IRE water chamber and place inside the H UMID A IRE . Connect the medium 21” (52 cm) and long 6’6” (2 m) air tubing ( I-1), and close the humidifier lid.

2 Place the S8 E SCAPE

on top of the H UMID A IRE

( I-2) and connect the free end of the medium air tubing to the air outlet ( I-3).

Note: To avoid water spilling into the S8 E SCAPE , do not put it underneath the humidifier.

3 Assemble your mask system and connect it to the free end of the long air tubing ( I-4).

4 Plug the H UMID A IRE power cord into a power outlet. Connect the S8 E SCAPE power cord to the socket at the rear of the S8 E SCAPE

and plug the other end into a power outlet.

!

Please refer to the HumidAire User’s Manual for further details.

WARNING

Make sure that the power cord and plug are in good condition and the equipment is not damaged.

The S8 E SCAPE

is now ready for use with the H UMID A IRE

.

H OW TO A TTACH A H UMIDIFIER 13

14

A TTACH A R ES M ED P ASSOVER H UMIDIFIER

Please refer to the illustrations in section J of the illustration sheet.

To connect your S8 E SCAPE to a ResMed P ASSOVER humidifier you need medium sized

21” (52 cm) air tubing.

1 Fill the P ASSOVER with water and connect the medium 21” (52 cm) and long

6’6” (2 m) air tubing ( J-1).

2 Place the S8 E SCAPE on top of the P ASSOVER ( J-2) and connect the free end of the medium air tubing to the air outlet ( J-3).

Note: To avoid water spilling into the S8 E SCAPE , do not place it underneath the humidifier.

3 Assemble your mask system and connect it to the free end of the long air tubing ( J-4).

4 Connect the power cord to the socket at the rear of the S8 E SCAPE and plug the other end into a power outlet.

Please refer to the ResMed Passover User’s Manual for further details.

!

WARNING

Make sure that the power cord and plug are in good condition and the equipment is not damaged.

The S8 E SCAPE is now ready for use with the P ASSOVER .

H

OW TO USE THE

K

EYPAD

The control panel of the S8 E SCAPE

includes an LCD screen and keypad for navigating through the menus and delivering treatment.

LCD screen

Up key

Left key

Down key

LCD S CREEN

The LCD screen displays the menus and treatment screens.

Right key

Start/Stop key

K EYPAD K EYS

The S8 E SCAPE

keypad has the following keys:

Key

Start/Stop

Function

• Starts or stops treatment.

Up

Down

• Allows you to increase settings options and scroll through the S8 E SCAPE menu.

• Allows you to decrease settings options and scroll through the S8 E SCAPE menu.

Left

Right

• Performs the function indicated by the guiding text displayed above it on the LCD screen. Guiding text includes menu,

change, and apply.

• Performs the function indicated by the guiding text displayed above it on the LCD screen. Guiding text includes exit and cancel .

B ACKLIGHTS

The keypad and LCD are equipped with backlights that come on when the device is powered. The LCD backlight turns off after two minutes of inactivity, and comes back

H OW TO USE THE K EYPAD 15

16 on when you press a key. Once the Start/Stop key has been pressed to start treatment, the LCD backlight stays on for two minutes. The keypad backlight is always on while the S8 E SCAPE

is on.

H OW TO C HANGE THE S ETTINGS ON YOUR S8 E SCAPE

You can change settings (such as Ramp Time, Altitude) on the S8 E SCAPE

by using the keypad and LCD. When the S8 E SCAPE is in standby mode you can display a series of screens (a menu) on the LCD screen in order to view and change the settings for a particular function.

S8 ESCAPE

Menu

ALT: 0-2000ft

Change Exit

USED HRS: 960

Exit

USAGE: 120/180

Exit

LANG: ENGLISH US

Change Exit

SW: SX123456789

Exit

Use the menu screens to change the ramp time, altitude compensation, and language.

You can also view details about the usage and software version of your S8 E SCAPE

.

H OW TO ENTER THE MENU SCREENS

When the S8 E SCAPE standby screen is displayed you will see the word ‘Menu’ in the left-hand corner. To select the S8 E SCAPE menu, press the Left key.

H OW TO SCROLL THROUGH THE MENU

When you are in the menu, scroll through items by pressing the Up or Down keys.

H OW TO CHANGE A SETTING OPTION

When you have scrolled to the item you require:

1. Press the Left key (Change).

2. Press the Up or Down keys until you see the setting option that you require.

3. Press the Left key (Apply) to select the setting option.

If you wish to exit without changing the option, press the Right key (Cancel).

H OW TO EXIT OUT OF A MENU

Press the Right key (Exit). This will take you back to the Patient Menu screen.

H OW TO EXIT OUT OF AN ITEM WITHIN THE MENU

Press the Right key (Exit).

H OW TO C HANGE THE R AMP T IME

During ramp time, the pressure increases from a low pressure to the prescribed treatment pressure. You can set the ramp time in 5-minute intervals, from 0 minutes

(OFF) up to a maximum ramp time set by your clinician.

The standby screen displays the current ramp time in the right-hand corner. To change the ramp time, press the Up or Down key until the desired ramp time appears.

Once a ramp time is selected, begin therapy by pressing the Start/Stop key.

When ramping begins the LCD will display the word "RAMPING", with the current pressure indicated as dashes. Each dash is approximately equivalent to 2 cm H

2 example, six dashes represents approximately 12 cm H

2

O pressure.

O. For

H OW TO CHANGE THE A LTITUDE SETTING

If you move or travel with your S8 E SCAPE

to areas of different altitude, you will need to adjust the altitude compensation setting. Changes in altitude will affect the pressure delivered by the S8 E SCAPE .

You can use the Altitude setting (ALT) to specify the altitude range at which you are using your S8 E SCAPE . Select the S8 E SCAPE

menu by pressing the Left key in the standby (RAMP) screen. Scroll to ALT and select Change ( Left key). Press the Up or

Down keys until you see the setting option that you require.

There are four altitude settings to choose from:

•

•

0–2000ft (0–609 m)

2001–4000ft (610–1219 m)

•

4001–6000ft (1220–1828 m)

•

6001–8500ft (1829–2591 m).

For example, if you are at an altitude of 3107’ (947 m), your altitude compensation setting would be 2001–4000ft (610–1219 m), as 3107’ (947 m) falls within that range.

Press the Left key (Apply) to select the correct setting.

H OW TO CHANGE THE LANGUAGE SETTING

To display menus and messages in a different language, select the S8 E SCAPE menu by pressing the Left key in the standby (Ramp) screen. Scroll to LANG and select Change

( Left key). Press the Up or Down keys until you see the language that you require.

O THER VIEWABLE INFORMATION

You can also view the total number of hours of treatment (USED HRS); the number of sessions that the S8 E SCAPE was used in a usage period (USAGE); and the current software version installed on your unit (SW). Access to all of these screens is provided via the menu. See “How to enter the menu screens” on page 16.

H OW TO USE THE K EYPAD 17

18

M ESSAGES ON THE S8 E SCAPE LCD

Your clinician may have set your S8 E SCAPE

to remind you about important events, such as when to replace your mask, when to insert your Data Card (if your device is

Data Card enabled) and so on.

The reminder message is displayed on the LCD and is visible if the device is not delivering therapy. The backlight on the LCD flashes when a message is displayed.

Your clinician can set any of the following reminders on your LCD:

Message

INSERT CARD

REPLACE

MASK

CALL

PROVIDER

Description

May appear if your device is

Data Card enabled.

Action

Insert your Data Card and follow any instructions that your clinician has given you. When you have done this, the message will disappear from the LCD.

Pressing the Left (Ok) key will also remove the message.

Press the Left (Ok) key to remove the message from your LCD, and replace your mask with a new one.

Press the Left (Ok) key to remove the message from your LCD, and contact your clinician.

REPLACE

FILTER

SERVICE DUE

May appear when your mask is due for replacement.

May appear as a reminder to contact your clinician; for example to discuss how your therapy is going.

May appear as a reminder to replace the air filter on your device.

May appear as a reminder to return your device for service.

Press the Left (Ok) key to remove the message from your LCD, and replace the air filter.

Press the Left (Ok) key to remove the message from your LCD, and contact your clinician.

S8 M

ODULES

Note: Do not remove modules while power is connected to the S8 Escape.

Your S8 E SCAPE

will have one of two modules fitted to the back: a blank module or a

R ES S CAN ™ Data Card module.

U SING A B LANK M ODULE

Please refer to the illustrations in section F of the illustration sheet.

The blank module is a protective cover on the S8 E SCAPE . At times, you may wish to remove or attach this module, for example to use the serial adapter.

To remove the blank module, pull it off the back of the S8 E SCAPE

to show the data communications port ( F-1).

To attach the blank module, push the blank module onto the data communications port, until the module clicks into place ( F-2).

Note: To protect the data communications port, always ensure there is a module attached to the device.

U SING A R ES S CAN D ATA C ARD M ODULE

Please refer to the illustrations in section G of the illustration sheet.

The R ES S CAN

Data Card module is an accessory to the S8 E SCAPE

. Use a R ES S CAN

Data

Card with the Data Card module to collect data and update settings in the S8 E SCAPE

.

The module and card give your clinician convenient access to data about your treatment, and can provide you with new device settings from your clinician without you having to leave home.

A TTACHING THE M ODULE

To attach the Data Card module, push it onto the data communications port at the back of your S8 E SCAPE until it clicks into place ( G-1).

R EMOVING THE M ODULE

To remove the Data Card module, pull it off the back of the S8 E SCAPE ( G-2).

Note: To protect the data communications port, always ensure there is a module attached to the device.

U SING THE D ATA C ARD TO C OLLECT DATA

Please refer to the illustrations in section H of the illustration sheet.

If your clinician needs to review your treatment, they will ask you to use the Data Card to copy data from your S8 E SCAPE , and to return the card to them. The Data Card will be provided in a convenient mailback envelope.

Data that is copied to a Data Card is still stored and available on the S8 E SCAPE

.

It takes approximately five seconds to copy data onto the Data Card.

S8 M ODULES 19

20

•

•

•

1 I NSERT THE D ATA C ARD

Switch on the S8 E SCAPE and wait until you see the standby (Ramp) screen.

Hold the Data Card with the arrow facing up and insert it into the slot in the Data

Card module ( H-1).

Push the card in smoothly until it stops moving ( H-2) and messages start appearing on the LCD.

•

•

•

•

2 C OPY D ATA ONTO THE D ATA C ARD

Data copying starts automatically when the Data Card is inserted into the Data

Card module.

The “Card Inserted Please Wait” message is displayed on the S8 E SCAPE

LCD while data is being copied. Copying takes approximately five seconds.

The “Copy Complete Remove Card” message is displayed on the LCD when copying has finished.

Remove the Data Card from the Data Card module.

3 R EMOVE THE D ATA C ARD

Grip the end of the Data Card and pull it out of the Data Card module ( H-3).

4 S TORE THE D ATA C ARD

Your Data Card should be stored in its mailback envelope when not in use.

5 M AIL THE D ATA C ARD TO YOUR C LINICIAN

A bubble mailer envelope is provided to ensure safe transportation of the Data Card.

When mailing the Data Card to your clinician:

1. Insert the Data Card into the pocket provided on the mailback envelope. Fold up the mailback envelope.

2. Place the mailback envelope containing the Data Card in the bubble mailer envelope and seal it.

3. Make sure that your clinician’s name and address details are on the bubble mailer envelope, and mail it back immediately.

U SING THE D ATA C ARD TO U PDATE S ETTINGS

If your clinician has provided a Data Card with new device settings:

•

•

•

With the device in standby (Ramp) mode, insert the Data Card into the slot on the Data Card module. Updating will start automatically.

The “Card Inserted Please Wait” message is displayed on the LCD while updating is in progress. Updating takes approximately five seconds.

The “Settings Success Remove Card” message is displayed on the LCD if the settings were updated successfully.

•

•

Note: This message only appears once. If you re-insert the Data Card after you have updated your settings, this message is not displayed.

Remove the Data Card from the Data Card module.

Store the Data Card in its mailback envelope when not in use.

!

WARNING

If your clinician has told you to use this Data Card to update the settings on your device and the “Settings Success” message does not appear, contact your clinician immediately.

S8 M ODULES 21

22

C

LEANING AND

M

AINTENANCE

You should regularly carry out the cleaning and maintenance described in this section.

Refer to your mask manual for detailed instructions.

D AILY C LEANING

Mask

Clean the mask according to the instructions supplied with the mask.

Air tubing

Disconnect the air tubing from the S8 E SCAPE (and humidifier, if used) and hang the tubing and mask in a clean, dry place until next use.

Humidifier

If you are using a humidifier, clean it according to the instructions in the humidifier user’s manual.

W EEKLY C LEANING

1. Remove the air tubing from the S8 E SCAPE and the mask.

2. Wash the air tubing in warm water using mild detergent. Rinse thoroughly, hang, and allow to dry.

3. Before next use, assemble the mask and headgear according to the user instructions.

4. Reconnect the air tubing to the air outlet and mask.

P ERIODIC C LEANING

!

1. Clean the exterior of the S8 E SCAPE with a damp cloth and mild detergent.

2. Check the air filter for blockage or holes (see “Replacing the Air Filter” on page 23).

•

•

WARNING

Beware of electric shock. Do not immerse the unit or power cord in water.

Always unplug the unit before cleaning and be sure it is dry before plugging back in.

The mask system and air tubing are subject to normal wear and tear. Inspect them regularly for damage.

R EPLACING THE A IR F ILTER

To replace the air filter:

1. Remove the air filter cover at the back of the S8 E SCAPE

.

Air filter cover

!

2. Remove and discard the old air filter.

3. Insert a new filter with the blue tinted side facing out from the device.

4. Replace the air filter cover.

Inspect the air filter every month to check if it is blocked by dirt or contains holes. With normal use of an S8 E SCAPE , the air filter needs to be replaced every six months (or more often if your device is in a dusty environment).

•

•

WARNING

Do not wash the air filter. The air filter is not washable or reusable.

The air filter cover protects the device in the event of accidental liquid spillage onto the device. Ensure the air filter and air filter cover are fitted at all times.

S ERVICING

!

•

•

CAUTION

Do not attempt to open the S8 Escape case. There are no user serviceable parts inside.

Inspection and repair should only be performed by an authorized agent. Under no circumstances should you attempt to service or repair the flow generator yourself.

This product ( S8 E SCAPE

) should be inspected by an authorized ResMed Service

Center five years from the date of manufacture. 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 Authorized ResMed Service Center.

If you feel that your flow generator is not performing properly, see “Troubleshooting” on page 26.

C LEANING AND M AINTENANCE 23

24

F

REQUENTLY

A

SKED

Q

UESTIONS

H OW WILL IT FEEL WHEN I AM BREATHING WITH THE S8 E SCAPE ?

When you first use your S8 E SCAPE , you may feel uncomfortable breathing against the airflow. This is normal. You will continue to breathe normally while you sleep. Take time to adjust to this new sensation.

W HAT DO I DO WHEN I WANT TO GET UP IN THE NIGHT ?

If you need to get up during the night, remove your mask and stop therapy. Always remember to restart therapy and put your mask on when you return to bed.

W HAT DO I DO IF I FEEL AIR LEAKING OUT OF THE MASK ?

The flow generator delivers the most effective treatment when the mask is well fitted and comfortable. Treatment can be affected by leaks, so it is important to eliminate any leaks that may arise. For example, try repositioning the mask and adjusting the straps.

If you are using a nasal mask, try to keep your mouth closed during treatment. Air leaks from your mouth can decrease the effectiveness of your treatment. If mouth leaks are a problem, a full face mask or chin strap may help. Contact your clinician or equipment supplier for further details.

If you are using a full face mask and you have problems trying to get a comfortable mask fit, contact your sleep clinic or equipment supplier. You may benefit from a different size or style of mask.

A NYTHING SPECIAL I SHOULD DO BEFORE PUTTING THE MASK ON ?

Before wearing your mask, wash your face to remove excess facial oils. This will allow a better fit and prolong the life of the mask cushion.

Do not use moisturizer when wearing a mask.

M Y MOUTH FEELS DRY DURING TREATMENT — WHAT CAN I DO ?

You may experience dryness of the nose, mouth, and/or throat during the course of treatment, especially during winter. In many cases, a humidifier may resolve this discomfort. Contact your clinician for advice.

M Y NOSE IS IRRITATED DURING TREATMENT — WHAT CAN I DO ?

You may experience sneezing and/or a runny or blocked nose during the first few weeks of treatment. In many cases, nasal irritation can be resolved with a humidifier.

Consult your clinician or equipment supplier for advice.

C AN I TRAVEL WITH THE S8 E SCAPE ?

International use

Your S8 E SCAPE

flow generator has an internal power supply that enables it to operate in other countries. It will operate on power supplies of 100–240 V and 50/60 Hz. No special adjustment is necessary, but you may need a plug adapter for the power outlet.

!

Altitude changes

If you are moving or traveling to a higher or lower altitude, see “How to change the

Altitude setting” on page 17.

On an aircraft

Please consult the medical services department of your carrier if you intend to use your

S8 E SCAPE on an aircraft. The S8 E SCAPE complies with US FCC Part 15, Class B requirements.

Note: Do not use your S8 Escape while the aircraft is taking off or landing.

C AN I USE MY S8 E SCAPE IF MAINS (AC) POWER IS NOT AVAILABLE ?

A DC-12 converter is available to connect the S8 E SCAPE to a 12V or 24V DC power source. Contact your clinician for details.

CAUTION

The device should not be connected to both AC and DC power sources simultaneously.

F REQUENTLY A SKED Q UESTIONS 25

26

T

ROUBLESHOOTING

If there is a problem, try the following suggestions. If the problem cannot be solved, contact your equipment supplier or ResMed. Do not attempt to open the device.

Problem

No display.

Possible Cause

Power not connected.

Solution

Ensure the appropriate power cord is connected to your

S8 Escape and the power switch

(if available) is on.

Wait for air pressure to build up or change ramp time.

Insufficient air delivered from

S8 Escape.

Ramp Time is in use.

Excessive air delivered from the S8 Escape.

Air filter is dirty.

Air tubing is kinked or punctured.

Air tubing not connected properly.

Mask and headgear not positioned correctly.

Cap(s) missing from access port(s) on mask.

Altitude compensation setting is incorrect.

Pressure required for treatment may have changed.

Altitude compensation setting is incorrect.

Replace air filter.

Straighten or replace tubing.

Check air tubing.

Adjust position of mask and headgear.

Replace cap(s).

Adjust altitude compensation setting to the correct altitude range.

See your clinician to adjust the pressure.

Adjust altitude compensation setting to the correct altitude range.

Problem

Display error message:

Exxxx

Call Service

(where xxxx defines an error) or

MOTOR FAULT

Call Service or

UPLOAD LANGUAGES

Call Service or

DATA LOST

Call Service

The following message is displayed on the

LCD after you try to update settings using the Data Card:

Card Error

Remove Card

Possible Cause

Component failure.

The Data Card is not inserted correctly.

Solution

Call Service.

Ensure that the Data Card is inserted with the arrow facing up and pointing towards the device.

Ensure that the device is switched on and in standby mode before you insert the Data Card.

The following message is displayed on the

LCD after you try to copy data to a Data

Card:

Card Error

Remove Card

The following message is displayed on the

LCD after you try to update the settings using the Data Card:

Settings Invalid

Remove Card

The Data Card is only partly inserted.

You may have removed the Data

Card before settings were copied to the S8 Escape.

The card is not a ResScan Data

Card.

The Data Card is not inserted correctly.

The card is not a ResScan Data

Card.

The identification details on the

Data Card do not match the details on your device.

Ensure that the Data Card is inserted into the slot on the Data

Card module as far as it will go.

Reinsert the Data Card and wait for the

Settings Success

Remove Card message to appear on the LCD.

Only use a ResScan Data Card.

Ensure that the Data Card is inserted with the arrow facing up and pointing toward the device.

Use a ResScan Data Card, as specified in this manual.

Contact your clinician immediately.

T ROUBLESHOOTING 27

28

Problem

The following message is displayed on the

LCD after you try to update the settings using the Data Card:

Settings Error

Remove Card

The following message is NOT displayed on the LCD after you try to update the settings using the Data Card:

Settings Success

Remove Card

Possible Cause

There is a data error on the Data

Card.

The settings were not updated.

Solution

Contact your clinician immediately.

Contact your clinician immediately.

S

YSTEM

S

PECIFICATIONS

S8 E SCAPE

Performance: Operating pressure range: 4 to 20 cm H

2

O

Dimensions (H x W x D): 4.6” x 6.5” x 5.7” (112 mm x 164 mm x 145 mm)

Weight: 2.9lb (1.3 kg)

•

•

Power Supply

Input range for S8 E SCAPE

with H UMID A IRE 3i :100–240V, 50/60Hz; 110V, 400Hz;

2.5A < 140VA (110W) (maximum power consumption). Instantaneous peak power consumption <340 VA.

Refer to the DC-12 converter instructions for DC ratings. Only use the ResMed

DC-12 converter for DC input.

Actual power consumption will vary, depending on factors such as the use of accessories, height above sea level, and ambient temperature. Power consumption values for typical treatment conditions (using a breathing machine set to 0.5 L and

15 breaths/min with 2 m (6’6”) air tubing and an U LTRA M IRAGE mask) are given in the following table.

Device

S8 E SCAPE

Pressure

(cm H

2

O)

5

10

15

20

Power

(VA)

17

23

29

34

Power

(W)

8

12

16

20

Power outlet for HumidAire 3i

Outlet range: 100–240V, 50/60Hz; 110V, 400Hz; 2.0A

Air Filter: Two-layered, powder-bonded, polyester non-woven fiber

Air Tubing: Flexible plastic, 6’6” (2 m)

Air Outlet: The 22 mm conical outlet complies with EN 1281-1

IEC 60601-1 Classifications: Class II (double insulation), Type CF

Noise Level: Radiated sound pressure is measured at <30dBA at 10 cm H

2

3’3.36” (1 m) according to ISO17510-1.

O and

A CCESSORIES

D ATA C ARD

Dimensions (L x W x D): 2.56” x 0.87” x 0.03” (65.04 mm x 22.15 mm x 0.85 mm)

S YSTEM S PECIFICATIONS 29

30

D ATA C ARD M ODULE

Dimensions (H x W x D): 1.95” x 1.66” x 0.47” (49.7 mm x 42.2 mm x 12 mm)

A LL D EVICES ( WHERE APPLICABLE )

Housing Construction: Flame retardant engineering thermoplastic

Environmental Conditions

Operating Temperature: +41°F to +104°F (+5°C to +40°C)

Operating Humidity: 10%–95% non-condensing

Storage and Transport Temperature: -4°F to +140°F (-20°C to +60°C)

Storage and Transport Humidity: 10%–95% non-condensing

Operating Altitude: sea level to 8500’ (2591 m)

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 Manufacturer’s Declaration -

Electromagnetic Emissions and Immunity” on page 31.

Note: The manufacturer reserves the right to change these specifications without notice.

S YMBOLS WHICH APPEAR ON THE DEVICE

Attention, consult accompanying documents

Type CF equipment

Class II equipment

Drip proof

Dangerous voltage

Start/Stop

G UIDANCE AND M ANUFACTURER ’ S D ECLARATION - E LECTROMAGNETIC

E MISSIONS AND I MMUNITY

Guidance and manufacturer’s declaration—electromagnetic emissions

The S8 series of devices is intended for use in the electromagnetic environment specified below. The customer or the user of the S8 device should assure that the device is used in such an environment.

Emissions test Compliance

Electromagnetic environment— guidance

RF emissions CISPR11 Group 1 The S8 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

Harmonic Emissions

IEC 61000-3-2

Class B*

Class A

The S8 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.

Voltage Fluctuations/Flicker

Emissions IEC 61000-3-3

Complies

* Class B for all system configurations except when a PC is attached to the S8 device via a serial adapter, in which case the system is Class A compliant. Class A is suitable for use in all establishments other than domestic and those directly connected to a low voltage power supply network which supplies buildings used for domestic purposes.

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.

Warnings: The S8 device should not be used adjacent to or stacked with other equipment.

If adjacent or stacked use is necessary, the S8 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 S8 device.

S YSTEM S PECIFICATIONS 31

32

Guidance and manufacturer’s declaration—electromagnetic immunity

The S8 series of devices is intended for use in the electromagnetic environment specified below. The customer or the user of the S8 device should assure that the device is used in such an environment.

Immunity test

IEC60601-1-2 test level

Compliance level

Electromagnetic environment—guidance

Electrostatic discharge (ESD)

IEC 61000-4-2

Electrical fast transient/burst

IEC 61000-4-4

±6 kV contact

±8 kV air

±6 kV contact

±8 kV air

±2 kV

Not Applicable

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Mains power quality should be that of a typical commercial or hospital environment.

Surge

IEC 61000-4-5

Voltage dips, short interruptions and voltage variations on power supply input lines.

IEC 61000-4-11

Power frequency

(50/60 Hz) magnetic field

IEC 61000-4-8

±2 kV for power supply lines

±1 kV for input/ output lines

±1 kV differential mode

±2 kV common mode

<5% Ut

(>95% dip in Ut) for 0.5 cycle

40% Ut

(60% dip in Ut) for 5 cycles

70% Ut

(30% dip in Ut) for 25 cycles

<5% Ut

(>95%dip in Ut) for 5 sec

3 A/m

±1 kV differential mode

±2 kV common mode

< 12V

(>95% dip in 240V) for 0.5 cycle

96V

(60% dip in 240V) for 5 cycles

168V

(30% dip in 240V) for 25 cycles

<12V

(>95%dip in 240V) for 5 sec

3 A/m

Mains power quality should be that of a typical commercial or hospital environment.

Mains power quality should be that of a typical commercial or hospital environment.

If the user of the S8 device requires continued operation during power mains interruptions, it is recommended that the S8 device be powered from an uninterruptible power source.

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

NOTE: Ut is the AC mains voltage prior to application of the test level.

Guidance and manufacturer’s declaration—electromagnetic immunity

The S8 series of devices is intended for use in the electromagnetic environment specified below. The customer or the user of the S8 device should assure that the device is used in such an environment.

Immunity test

IEC60601-1-2 test level

Compliance level

Electromagnetic environment—guidance

3 Vrms

Portable and mobile RF communications equipment should be used no closer to any part of the S8 device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance d = 1.17 √P Conducted RF

IEC 61000-4-6

Radiated RF

IEC 61000-4-3

3 Vrms

150 kHz to 80 MHz

10 V/m

80 MHz to 2.5 GHz

10 V/m d = 0.35 √P 80 MHz to 800 MHz d = 0.70 √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 d is the recommended separation distance in meters (m).

Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, a should be less than the compliance level in each frequency range.

b

Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE 1: At 80 MHz and 800 MHz, 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.

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 S8 device is used exceeds the applicable RF compliance level above, the S8 device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the

S8 device.

b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.

S YSTEM S PECIFICATIONS 33

34

Recommended separation distances between portable and mobile RF communications equipment and the S8 series of devices

The S8 series of devices is intended for use in an environment in which radiated RF disturbances are controlled.

The customer or the user of the S8 device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the S8 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

0.01

0.1

150 kHz to 80 MHz d = 1.17 √P

0.17

0.37

80 MHz to 800 MHz d = 0.35 √P

0.04

0.11

800MHz to 2.5 GHz d = 0.7 √P

0.07

0.22

1

10

1.17

3.69

0.35

1.11

0.7

2.21

100 11.70

3.50

7.0

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.

L

IMITED

W

ARRANTY

ResMed warrants that your ResMed product shall be free from defects in material and workmanship for the period specified below from the date of purchase by the initial consumer. This warranty is not transferable.

Product Warranty Period

ResMed humidifiers, ResControl™, ResLink™

ResMed flow generators

1 Year

2 Years

Accessories, mask systems (including mask frame, cushion, headgear and tubing). Excludes single-use devices.

90 Days

Note: Some models are not available in all regions.

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; d) any damage caused by water being spilled on or into a flow generator.

To make a warranty claim, the initial consumer must return the defective product to the point of purchase, freight prepaid.

This warranty is in lieu of all other express 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 occurred as a result of 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.

L IMITED W ARRANTY 35

36

I NDEX

A accessories 10 air filter 9 , 26 replacing 23 air pressure 26 air tubing 9 cleaning 22 connect to air outlet 11 kinked 26 positioning 12 aircraft 25 airflow breathing with 24 altitude setting 17 , 25 , 26

B backlight

LCD and keypad 15

C carry bag 9 cleaning periodic 22 contraindications 6

CPAP 5

D daily cleaning 22

Data Card 19 copying data 20 inserting 20 mailback envelope 20 removing 20 data card 27

Data Card module 19

DC-12 converter 25 down key 15 dryness mouth, nose or throat 24

E error message 27

F frequently asked questions 24

H headgear 26

HumidAire attaching 13

HumidAire 3i attaching 13 storage 9 humidifier 24 cleaning 22 humidifiers 10

I international use 24

K keypad 9 , 15 keypad keys functions 15

L language setting 17

LCD 9 , 11 , 15 error messages 27 messages 18 left key 15

M mailback envelope 20 mask 24 , 26 air leak 24 attaching 11 cleaning 22 removing 24 mask leak 24 mask port 26 masks 9 medical information 5 menu screens 16 access 16 change 16 exit 17 scrolling 16 module attaching 9 blank 19

Data Card 19 modules 19 blank 19

I NDEX 37

38

N nasal irritation 24

P

Passover attaching 14 power cord 9 , 26 connecting 11 power sockets 9 power sources 25 power supply 29

R ramp time 12 , 17 , 26 reminder replace mask 18 reminders 18

ResScan Data Card module 10 right key 15

S

S8 Escape dimensions 29 , 30 servicing 23 settings 16 set-up 11 start treatment 12 stop treatment 12 travelling with 24 setting up 11 software version number 17 standby screen 11 start/stop key 15

SW 17 system specifications 29

T troubleshooting 26

U up key 15

Usage 17 use on aircraft 25

Used hours 17

W weekly cleaning 22