Drive Medical DV64D-HHPD Le manuel du propriétaire

EN

DeVilbiss IntelliPAP

®

2 Positive

Airway Pressure Device Instruction

Guide

RX ONLY

Made in USA of US and Imported Parts. Not manufactured with natural rubber latex.

ES

Guía de instrucciones del

Dispositivo de presión positiva en

las vías respiratorias DeVilbiss

IntelliPAP

®

2

SOLO CON PRESCRIPCIÓN

Hecho en EE. UU. con piezas nacionales e importadas. No está hecho de látex de

caucho natural.

FR

Guide d’instructions pour l’appareil

à pression positive DeVilbiss

IntelliPAP

®

2

UNIQUEMENT SUR PRESCRIPTION

Fabriqué aux États-Unis avec des pièces des États-Unis et des pièces importées. Non

fabriqué avec du latex de caoutchouc naturel.

for air travel!

Approved

DV63 DeVilbiss

®

Standard Plus &

DV64 DeVilbiss AutoAdjust

®

CPAP Series

EN - 2 A-DV64

QUICK START – OPERATING YOUR CPAP

OPTION A

Press ON/OFF button OR

THERAPY

OPTION B

Breathe into mask**

Display

OPTION A

Press ON/OFF button OR

Stopping Therapy

To turn blower off:

OPTION B

Remove mask**

Display

**if Auto-START/STOP feature is activated

Press RAMP button

To start ramp:

Display

Press RAMP button again

To stop ramp: (begin

prescription pressure)

Display

Humidification (optional)

Clean, ll and install humidier

chamber daily. NOTE: Use distilled

water to avoid mineral deposit build

up inside the chamber.

To Set Humidication Controls:

1. Select Humidity.

2. Choose humidity setting

of OFF or 1 through 5 bars.

(NOTE- 5 bars is the

highest humidity)

Starting Therapy

To turn blower on:

PRESSURE RAMP HUMIDIFICATION

When activated, this feature gradually ramps up the device to

prescription pressure to help you fall asleep easier. Ramp time

can be set from 0-45 minutes; refer to Features & Settings for

details on adjusting length of time.

Ramp On

(Time

Remaining)

Ramp Off

NOTE – For models with heated

humidication option, please refer

to humidier guide for device set

up.

EN - 3A-DV64

ENGLISH.................................................................... EN - 2

ESPAÑOL ................................................................... ES - 31

FRANÇAIS ................................................................. FR - 62

TABLE OF CONTENTS

Quick Start - Operating Your CPAP ................................................................ EN - 2

Symbol Definitions .......................................................................................... EN - 4

Important Safeguards ..................................................................................... EN - 4

Introduction ..................................................................................................... EN - 6

Intended Use .............................................................................................. EN - 6

Contraindications ....................................................................................... EN - 6

Set Up ............................................................................................................ EN - 6

Important Parts .............................................................................................. EN - 7

Understanding your Display ....................................................................... EN - 7

Understanding your Controls ..................................................................... EN - 8

Understanding your Device ........................................................................ EN - 8

System Assembly ........................................................................................... EN - 9

Features and Settings .................................................................................... EN - 10

Main Menu Items ....................................................................................... EN - 10

Quick View Menus ..................................................................................... EN - 10

SmartCode

®

Data Menus ........................................................................... EN - 11

SmartCode Rx Submenu ....................................................................... EN - 11

CPAP Settings Menus ................................................................................ EN - 12

Rx Pressure ........................................................................................... EN - 12

Auto Mode ............................................................................................. EN - 12

CPAP Mode ........................................................................................... EN - 12

SmartFlex™ Exhalation Relief Comfort Technology ............................. EN - 12

Ramp Options ........................................................................................ EN - 13

Humidity Settings ................................................................................... EN - 13

Tubing Settings ...................................................................................... EN - 13

Master Volume Settings ......................................................................... EN - 14

Brightness Settings ................................................................................ EN - 14

Enable Menu .................................................................................................. EN - 14

Clock Settings Menus ..................................................................................... EN - 15

Clock - Current Time .................................................................................. EN - 15

Format ........................................................................................................ EN - 15

Wake-Up Alert ............................................................................................ EN - 15

Add-Ons ......................................................................................................... EN - 16

Bluetooth ................................................................................................... EN - 16

Oximeter ..................................................................................................... EN - 16

Info ............................................................................................................. EN - 16

Patient Messages ........................................................................................... EN - 17

Notifications ................................................................................................ EN - 17

Messages ................................................................................................... EN - 17

Add-On Device Messages ......................................................................... EN - 17

Service Codes ............................................................................................ EN - 17

SmartLink

®

Patient Therapy Management System ........................................ EN - 18

Using an SD Card ...................................................................................... EN - 18

Travel Information ........................................................................................... EN - 19

Supplemental Oxygen .................................................................................... EN - 20

Replacement Items/Spare Parts .................................................................... EN - 21

Cleaning ......................................................................................................... EN - 22

Maintenance ................................................................................................... EN - 24

Expected Service Life ..................................................................................... EN - 24

Product Disposal ............................................................................................ EN - 24

Network/Data Coupling .................................................................................. EN - 24

Troubleshooting .............................................................................................. EN - 25

Specifications ................................................................................................. EN - 27

Guidance and Manufacturer’s Declaration ..................................................... EN - 29

EN - 4 A-DV64

SYMBOL DEFINITIONS

It is mandatory to read Operating

Instructions prior to use.

Heat

Consult instructions for use

RTCA / DO-160 Section 21

Category M for battery use only

Rx Only = Prescription required Manufacturer

Class II electrical protection-

double insulated

Date of Manufacture

DC input Radio Transmitter

DC Jack

C US

TUV Rheinland C-US approval mark

Type BF equipment-applied part

EC REP

European Representative

Catalog Number European Rep CE mark

Serial Number

MR Unsafe – Unsafe for Magnetic

Resonance Environment

IP21

Ingress Protection - Protected against nger access to hazardous parts;

protected against vertically falling water drops

This device contains electrical and/or electronic equipment that must be

recycled per EU Directive 2012/19/EU-Waste Electrical & Electronic Equipment

IMPORTANT SAFEGUARDS

READ ALL INSTRUCTIONS BEFORE USING THIS DEVICE.

SAVE THESE INSTRUCTIONS.

The device is to be used only on the instruction of a licensed physician. The system can

deliver CPAP therapy or Auto-CPAP therapy. For enhanced pressure relief, the device can

also deliver SmartFlex pressure relief. Your home care provider will make the correct

pressure settings according to your health care professional’s prescription.

When set in the Auto-CPAP therapy, the system will monitor your breathing as you sleep

and automatically adjust the pressure to meet your needs. When in CPAP therapy, the

system will deliver a continuous, set pressure during the night.

WARNING

A warning indicates the possibility of injury to the user or the operator.

• Electric Shock Hazard – Do not use while bathing.

• Electric Shock Hazard – Do not immerse this device into water or any other liquid.

• Electric Shock Hazard – Do not attempt to open or remove the cabinet; there are no

user-serviceable internal components. If service is required, contact your equipment

provider for instructions on obtaining service. Opening or attempting to service your

device will void the warranty.

• Refer to International Standard IEC 60601-1 Ed 3.0 Amendment 1 for safety

requirements applicable to Medical Electrical Systems

• Oxygen supports combustion. To avoid possible physical injury, do not smoke while

using this device with supplemental oxygen. Do not use this device near hot objects,

volatile substances or sources of open ames.

• Always turn on the CPAP device before turning on the oxygen source. Turn off the

oxygen source before turning off the device. Never allow the oxygen source to run

continuously while connected to the device if the device is not in use. If the device is

not being used, turn off the oxygen ow.

• CPAP pressure must be set higher than 8 cmH2O for supplemental oxygen use to

prevent patient breathing pattern from forcing oxygen back into the CPAP.

• At a xed ow rate of supplemental oxygen, the inhaled oxygen concentration will vary

depending on the pressure setting, patient breathing pattern, mask selection, and leak

rate. This warning applies to most types of CPAP devices.

• The device should be used only with vented CPAP masks recommended by DeVilbiss,

your physician or respiratory therapist. These include nasal, full face, nasal pillow and

nasal cannula masks designed for CPAP use. Do Not use a non-vented mask with this

CPAP device.

• To avoid rebreathing of exhaled air, do not use a CPAP mask unless the device is

turned on and providing a supply of air. Venting in the mask should never be blocked.

When the device is turned on and providing a fresh supply of air, exhaled air is

ushed out of the mask vent. However, when the device is not operating, exhaled air

may be rebreathed. Rebreathing of exhaled air for longer than several minutes can in

some circumstances lead to suffocation. This warning applies to most CPAP devices.

• The device is not a life support device and may stop operating with certain device

faults or with a power failure. It is intended to be used on spontaneously breathing

individuals weighing 66 lbs/30 kg or greater.

• To avoid electric shock, always unplug power cord from wall outlet power source when

cleaning or servicing.

EN - 5A-DV64

• The following surface temperatures may exceed 41 ˚C under certain conditions:

• External surface of CPAP ........................................ 43˚C

• Patient tubing connector .......................................... 45˚C

• Encoder shaft (with control knob removed) ............. 42˚C

• Humidier heater plate ............................................ 65˚C

• External power supply ............................................. 42˚C

• Equipment not suitable for use in the presence of a ammable anesthetic mixture with

air or with oxygen or nitrous oxide.

• Medical Electrical Equipment needs special precautions regarding EMC and needs to

be installed and put into service according to the Electromagnetic Compatibility [EMC]

information provided in the accompanying documents.

• Portable and Mobile RF Communications Equipment can affect Medical Electrical

Equipment.

• The equipment or system should not be used adjacent to or stacked with other

equipment and that if adjacent or stacked use is necessary, the equipment or system

should be observed to verify normal operation in the conguration in which it will be

used.

• If you are using a full face mask (a mask covering both your mouth and your nose),

the mask must be equipped with a safety (entrainment) valve.

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

• Do not use the device near a source of toxic or harmful vapors.

• Do not use this device if the room temperature is warmer than 40° C (104° F). If the

device is used at room temperatures warmer than 40° C (104° F), the temperature of

the airow may exceed 43° C (109° F). This could cause irritation or injury to your

airway.

• Do not operate the device in direct sunlight or near a heating appliance because

these conditions can increase the temperature of the air coming out of the device.

• Contact your health care professional if symptoms of sleep apnea recur.

• If you notice any unexplained changes in the performance of this device, if it is

making unusual or harsh sounds, if it has been dropped or mishandled, if water is

spilled into the enclosure, or if the enclosure is broken, disconnect the power cord

and discontinue use. Contact your home care provider.

• Periodically inspect electrical cords and cables for damage or signs of wear.

Discontinue use and replace if damaged.

CAUTION

A Caution indicates the possibility of damage to the device.

• For proper operation, place system on a at, sturdy, level surface. Do not place the

device where it can be knocked onto the oor or where the power cord may create a

trip hazard.

• Never block air openings of the device. Do not insert objects into any openings or

tubes.

• Use only accessories recommended by DeVilbiss.

• The USB port located on the back of the device is for provider use only. The port

must only be used with accessories approved for use by DeVilbiss. Do not attempt to

attach any other device to this port as it may damage the CPAP or the accessory

device.

• Only the DeVilbiss DV6 series Heated Humidier system is recommended for use

with this device. Other humidier systems may prevent the device from detecting

respiratory events and may cause inappropriate pressure levels in the mask.

• The height of the device must be lower than the mask when using a humidier to

prevent water from getting into the mask

• Never rinse or place the device in water. Never allow liquids to get into or around any

of the ports, switches or air lter; doing so will result in product damage. If this

occurs, do not use the device. Disconnect the power cord and contact your

equipment provider for service.

• Condensation may damage the device. If this device has been exposed to either very

hot or very cold temperatures, allow it to adjust to room temperature (operating

temperature) before starting therapy. Do not operate the device outside of the

operating temperature range shown in the Specications.

• Do not place the device directly onto carpet, fabric, or other ammable materials.

• Tobacco smoke may cause tar build-up within the device, which may result in the

device malfunctioning.

• Dirty inlet lters may cause high operating temperatures that may affect device

performance. Regularly examine the inlet lters as needed for integrity and

cleanliness.

• Never install a wet lter into the device. You must ensure sufcient drying time for the

cleaned lter.

• Only use a DeVilbiss DC Power Cord and Battery Adapter Cable. Use of any other

system may cause damage to the device.

• Oxygen is a prescribed gas and should only be administered under the supervision of

a physician.

EN - 6 A-DV64

SET UP

First, unpack your CPAP and identify all items.

1. Carrying Case

2. Tubing

3. Filter Cover

4. Extra Air Inlet Filters

5. Optional Fine Particle Filter

6. SD Card (optional)

7. Power Supply

8. Power Cord

9. CPAP Device

Instruction Guide (not shown)

NOTE - Contents vary by model. Please refer to the contents list on the

device carton for items specic to your model.

NOTE - For models with heated humidication option, please refer to

humidier guide for device set up.

Contents

6

1

2

3

4

7

9

8

5

• The ow setting of the oxygen source must be specied by a physician.

• Maximum oxygen pressure is 50 psi. Maximum oxygen ow rate is 10 lpm.

• Always turn on CPAP before turning on oxygen ow.

• Always turn off oxygen ow before turning off CPAP.

• Proper lter function is important for the operation of the device and to protect the device from

damage.

INTRODUCTION

Intended Use

The DeVilbiss Intellipap2/DeVilbiss BLUE Series is intended for use in treating OSA in spontaneously

breathing patients 30 Kg (66 lbs) and above by means of application of positive air pressure. The

Device is to be used in Home and Healthcare Environments.

Contraindications

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 uid leak, recent cranial surgery or trauma

• a bypassed upper airway

• hypoventilation

The use of positive airway pressure therapy may be temporarily contraindicated if you exhibit signs of a

sinus or middle ear infection. Contact your physician if you have any questions concerning your therapy.

MR Unsafe

Do not bring the device or accessories into a Magnetic Resonance (MR) environment as it may cause

unacceptable risk to the patient or damage to the CPAP or MR medical devices. The device and

accessories have not been evaluated for safety in an MR environment.

Do not use the device or accessories in an environment with electromagnetic equipment such as CT

scanners, Diathermy, RFID and electromagnetic security systems (metal detectors) as it may cause

unacceptable risk to the patient or damage to the CPAP. Some electromagnetic sources may not be

apparent, if you notice any unexplained changes in the performance of this device, if it is making

unusual or harsh sounds, disconnect the power cord and discontinue use. Contact your home care

provider.

This device is for single patient reuse only.

EN - 7A-DV64

IMPORTANT PARTS

Understanding Your Display

Therapy Screen: Blower On

Clock (if active)

Status Icons (see inset)

Current delivered

pressure

Ramp On and Time

Remaining Indicator

SmartFlex On Indicator

Mode Indicator

Blower On Indicator

Humidifier On and Setting

Indicator (only illuminated if

optional humidifier is attached)

Idle Screen: Blower Off

Inset: Status Icons

Bluetooth Signal Indicator

Wake-Up Alert Indicator

Oximeter Connected Indicator

USB Connected Indicator

Submenu Title

Screen Overview

Back Indicator

Setting Locked Indicator

Idle Screen: Blower On

Ramp Indicator

Therapy

Pressure

Blower On Indicator

Idle Screen: Blower On (Without Clock)

Page Indicator

Idle Screen: Blower Off (Without Clock)

EN - 8 A-DV64

IMPORTANT PARTS

Understanding Your Controls

Heater On / Hot Surface LED Indicator

(only active with optional heated humidification)

Blower ON / OFF

Button - starts and

stops Therapy

Ramp Button - starts

and stops Ramp

Rotary Knob - Simple

Press & Turn opera

-

tion

Display

- returns to Idle Screen after 10 seconds

without user action when in Main Menu.

- returns to Main Menu after 2 minutes

without user action when in any sub

-

menu.

Understanding Your Device

Display

Rotary Knob

Ramp Button

Filter Cover

Blower On/Off Button

Speaker

Tubing

Connector

Power

Connector

SD Card

Slot

USB Port (for

provider use only)

Air Supply Port Cover

Air Filter

EN - 9A-DV64

SYSTEM ASSEMBLY

1. Place system components on a stable surface.

NOTE – For models with heated humidication option,

please refer to humidier guide for device set up.

5. Prepare mask and connect to tubing.

4. Attach tubing to device.

2. Insert power cord into back of device and wall outlet.

6. Insert SD card into slot (if applicable).

3. Verify air supply port cover is inserted into port on

bottom of device.

EN - 10 A-DV64

FEATURES AND SETTINGS

Navigating

Screens: Simply

turn rotary knob to

desired item and

press knob to

select item.

Your device has many features and settings to

personalize and improve your therapy experience. Many

of these are fully adjustable, while others may have

limited or no adjustability. The following legend is used

throughout this section:



Informational Only - Indicates a non-adjustable

setting



Enabled/Disabled – Allows you to turn selected

options on or off



Locked - Indicates a setting that can be locked by

your provider. Locked or unlocked  icon will

be shown in the upper right side of the Display.

Locked settings are only adjustable by your

provider.



Shown/Hidden - Indicates a feature that can be

hidden by your provider. If a feature is hidden, you

will not see it in your device.

Within menu, select Back to return to previous

screen. NOTE: Pressing On/Off button while in

any menu will exit to therapy screen.

Main Menu Items

Without humidier option:

Quick View Menus 



Quick View shows an overview of your therapy, as well

as more-detailed information for a preset number of

days. There is no user adjustability in Quick View. Your

provider will contact you for this information if required by

your insurer.

1. Press to select Quick View.

2. Overview screen appears.

3. Turn knob to choose

number of days to view.

SmartCode Adherence

Score™

With optional humidier:

Navigating

Screens: Simply

turn rotary knob to

desired item and

press knob to

select item.

EN - 11A-DV64

FEATURES AND SETTINGS

SmartCode

®

Data Menus 

SmartCode data sets offer a detailed look at your therapy through an encrypted code.

The decrypted data includes info required by many insurers to continue coverage of your

equipment. Data sets can be decrypted by visiting the www.intellipap.com website and

entering the code. Your provider will contact you for this data set if required by your

insurer.

1. Select SmartCode option

2. 1-Day data set appears

3. Continue to turn knob to view screens:

• 7 Days

• 30 Days

• 90 Days

• Compliance

• Date

• Serial number

• SmartCode Rx (see

following section)

SmartCode Rx Submenu

This submenu allows your provider to adjust your prescription through input of an

encrypted code. Code may contain letters or numbers and knob may be turned

either way to roll through 0-9 and A-Z.

1. Select SmartCode Rx to input

code supplied by your provider

2. Highlight, then turn knob

to select rst digit and press.

3. Continue through all digits

4. Write down Verify Code and

give to provider

Generating Compliance Reports for Employer/Insurer/Physician

SmartCode reports satisfy most requirements for ongoing compliance/adherence informa-

tion, and the software retains 2,046 days (5.6 years) of data. We recommend you work with

your provider to establish a routine for clearing SmartCode data to ensure current usage

information is available. Compliance meter should be cleared only after the required report

is generated, submitted, and approved by the requestor. Once cleared, a new cycle of 5.6

years begins and the only source for the previous data will be the hard-copy reports.

NOTE-Only the provider has access to clear the meter.

EN - 12 A-DV64

FEATURES AND SETTINGS

CPAP Settings Menus

RX Pressure 

Select Rx Pressure

View your prescription

pressure setting

SmartFlex™ Pressure Relief Comfort Technology 

1. Select SmartFlex

2. Select Setting

3. Choose 1-3 or OFF

NOTE – 1 is the least relief

and 3 is the most.

4. Press to choose

Always On or Ramp Only

5. Select Flow Rounding

6. Choose 0-5 for Inhalation

7. Choose 0-5 for Exhalation

NOTE – 0 is the least rounding and 5 is the most.

When activated, the SmartFlex pressure relief feature helps make it easier for you to exhale against your prescribed pressure by slightly

lowering the pressure during exhalation. If you experience a respiratory event when using the pressure relief function, the device will

automatically deactivate this function until normal breathing resumes.

Auto Mode

View your prescription

pressure setting

CPAP Mode

Always On = SmartFlex

pressure relief is active

throughout the night.

Ramp Only = SmartFlex

pressure relief is on

during ramp only.

FLX

(Flow Rounding determines the speed at which the

SmartFlex pressure relief changes.)

EN - 13A-DV64

Ramp Options  

1. Select Ramp

2. Choose Ramp Time.

(if unlocked).

3. Set Ramp Time

(From 0-45 minutes in 5

min increments)

4. View Ramp Pressure 

(set by the provider)

Humidity Settings

1. Select Humidity

2. Choose humidity

setting of OFF or 1

through 5 bars. NOTE: 5

bars is the highest

humidity.

Tubing Settings 

1. Select Tubing

2. Select Diameter: 15mm or 22mm

3. Select Length if 22 mm

Diameter. NOTE: These

settings must match the tubing

you are using for pressure at

the mask to be correct.

FEATURES AND SETTINGS

CPAP Settings Menus

Diameter 15mm 22 mm

Length 1.8 m (6’) 1.8 m (6’), 2.4 m (8’), 3.0 m (10’), 3.7 m (12’)

When activated, this feature gradually ramps up

the device to prescription pressure to help you fall

asleep easier.

Allows adjustment for optimal therapy based on your

tubing dimensions.

(Setting only applicable if you

have the optional heated

humidication.)

NOTE: Refer to Replacement Items/Spare Parts section to verify

tubing diameter.

NOTE: Bacteria lter option is set by the provider.

EN - 14 A-DV64

CPAP Settings Menus

FEATURES AND SETTINGS

Brightness Settings

1. Select Brightness

2. Select Display

(brightness of display

area) or Controls

(brightness of top buttons,

heater-on indicator, and

rotary knob)

3. Select Active or

Standby

4. Select Brightness Level

Enable Menu

= Enabled (ACTIVATED)

1. Select Enable and then

select desired options

2. Auto-STOP  NOTE-

If Auto-STOP is enabled,

Auto-START is

automatically enabled.

3. Auto-START

4. Notications

 (Refer to

Patient Messages for details.)

Active = Brightness during user activity (when using

buttons or menus). Settings from 10% to 100% (must be

equal to or higher than Standby brightness)

Standby = Brightness when no user activity (idle).

Settings from 0% to Active (must be equal to or lower than

Active brightness)

Display and controls change to Standby brightness after 2

minutes of no activity.

NOTE – If Standby controls brightness is set to 0, the

heater on indicator remains on at a low level.

Allows adjustment of display and controls brightness.

Allows Auto-Start/Stop feature and Notications to be

activated or deactivated. Activating Auto-Start/Stop allows you

to start therapy by breathing into your mask and to stop

therapy by removing your mask. Activating Notications will

ensure they are displayed on your screen when generated.

Master Volume Settings

1. Select Volume

2. Set Master Volume

(sound level) from 0-100%

0 = Off (mute)

Allows adjustment of alert volume for

patient messages.

EN - 15A-DV64

FEATURES AND SETTINGS

Clock Settings Menu



Clock - Current Time

1. Select Current Time

2. Set hour, minutes, and

AM/PM (if applicable)

Format

1. Select 12 or 24 hour

Clock Format

Wake-Up Alert



1. Select Wake-Up Alert

2. Select Wake-Up Alert

On

3. Select & Set Alert Time

4. Select Volume

5. Set Wake-UP Alert

Volume (sound level)

0=Off (mute)

NOTE – Wake-Up Alert Volume is separate from Master Volume.

If provider hides clock, wake up alert is hidden. If clock is shown, wake up alert can be shown or hidden.

NOTE – If Standby display brightness of 0% (Off) is chosen, the Clock will not be visible when idle.

Wake-Up Alert is available and changes the screen to Active upon activation.

12

24

Wake up alert allows your CPAP to also function as an alarm clock.

EN - 16 A-DV64

This menu allows the connection of the

Nonin

®

WristOx2

®

wireless oximeter.

FEATURES AND SETTINGS

Add-Ons

1. Select Bluetooth and press to

select On.

1. Select Oximeter

2. Select search.

3. Searching for Bluetooth

devices. Shows list of oximeters

in range. Click the item serial

number to pair with the CPAP.

1. Connect wireless

oximeter to CPAP and place

probe on nger.

2. Wait until your CPAP

display shows the pop-up

message “Oximeter Logging

Started” which means your

CPAP is recording data from

the oximeter.

NOTE – If more than one

person in the house is using

a wireless oximeter, each

person must do this check

at a different time.

NIGHTLY

Bluetooth

®

Oximeter

Bluetooth allows connection of the

Bluetooth enabled oximeter.

Information on optional Nonin WristOx2 wireless oximeter.

2. Oximeter information

screen. NOTE – Refer to

Oximeter Instruction Guide

for details.

Info



Allows you to see basic device information.

2. Turn knob to scroll through

Compliance Meter, Serial Number,

Firmware, and BIOS screens.

1. Select Info.

For Airline Use – Select Bluetooth

and press to select Off.

3. After recording is

nished, remove nger

probe and disconnect the

sensor cable from the

oximeter. The CPAP will

display a message ‘Oximeter

Logging Stopped’ and beep

once.

EN - 17A-DV64

PATIENT MESSAGES

Various messages may be displayed during your therapy; some include an audible alert

that is controlled by Master Volume Setting.

1. Notifications



These are friendly reminders to clean or replace components and, if enabled, are

generated as follows. Dismiss from Display by Button Press or Knob Movement.

Displayed Notification Recurrence interval

Air Intake Filter Due for Cleaning 50 hours of use (while breathing)

Mask, Tubing, and Chamber Due for Cleaning 35 hours of use (while breathing)

2. Messages

These identify conditions that may require action by you/your provider or are

informational only. Dismiss from Display by Button Press or Knob Movement.

Displayed Message Condition for Occurrence

Mask Off Please Check Mask Fit 10 seconds after mask off condition detected.

Auto-STOP Detected When Auto-STOP occurs.

Auto-START Detected When Auto-START occurs.

Wake-Up Alert <current time> When Wake-Up Alert activates (alarm clock).

Error with Code, Prescription Not

Updated

When SmartCode Rx is entered but incorrect.

Card Detected Please Wait … When SD card is detected. Do not remove SD

card while this message is displayed.

Card Removed Send to Provider When SD card is removed after data transfer.

Card Error Contact Provider If SD card error condition detected.

Settings Not Updated Contact

Provider

When prescription change via SD Card fails.

Card Transfer Successful When valid SD Card inserted and data transfer

complete.

Card Detected Ready for use When valid SD Card is inserted.

Firmware Update Please Wait … When SD Card containing firmware update is

inserted.

3. Add-On Device Messages

These messages may be displayed when Add-On items are in use, Dismiss from Display

by Button Press or Knob Movement.

Displayed Message Condition for Occurrence

Oximeter Logging Started

SpO2 _____

Pulse Rate _____

When Oximeter first detected and logging

starts

Oximeter Logging Stopped When Oximeter signal is lost and logging

stops

Oximeter Finger Probe Off When Oximeter finger probe off condition

detected

Oximeter Finger Probe On

SpO2 _____

Pulse Rate _____

When Oximeter finger probe off condition cor-

rected

4. Service Codes

These are divided into Critical or Non-Critical. Critical service codes put the unit in a fail-

safe (blower off) state.

Displayed Message Action

Critical Service Code E0X - Where (X) is a

number or letter

NOTE – Code E01 is always shown in

English since language setting is unknown

Contact your equipment provider to

return unit for service. Message remains

on Display and cannot be dismissed.

Service Code E8X (non-critical - Where (X)

is a number or letter

Contact your equipment provider.

Dismiss from Display by Button Press or

Knob Movement.

NOTE- Service Code alerts are unaffected by notication enable/disable setting.

EN - 18 A-DV64

DEVILBISS SMARTLINK

®

PATIENT THERAPY MANAGEMENT SYSTEM

DeVilbiss SmartLink technology is included in every device. It is used by your provider in conjunction with our exclusive software to monitor the effectiveness of your therapy and how

consistently you use the device. Information can be obtained through the use of an SD card or by direct download to a computer with SmartLink software installed.

Using an SD Card

Your provider may give you an SD card to collect data. It should be installed during device set up and kept in device. Your provider will instruct you on when to return the card.

1. Insert card face up.

Press until it clicks into

place.

2. Message will display

and tone will sound.

Card Detected

Ready For Use

1. Device is copying

card. Card should remain

in device until copying is

complete

1. Press and release card;

remove from CPAP.

Card Detected

Please Wait...

2. Message will display

and tone will sound.

To install the card Data transfer To remove the card

NOTE – DO NOT remove

SD card while showing

“Card Detected Please

Wait.” SD card may be

corrupted if removed

during this message.

Card Removed

Send to Provider

EN - 19A-DV64

TRAVEL INFORMATION

NOTE – For details on part numbers for alternate power sources, refer to Replacement Items/Spare Parts.

Air Travel

Your device is RTCA/D0-160 Section 21 Category M approved for use on commercial airlines when using battery power. You must turn off the Bluetooth. Refer to Features & Settings -

Add-Ons in this guide for details on Bluetooth.

International Travel

Your device is capable of accepting line voltages of 100-240V~, 50/60Hz. For travel to another country, simply order the correct power cord for that region from your provider or use

proper adapter.

Altitude

This device automatically compensates for altitude between 1060 hPa and 700 hPa (~ 1,400 ft below sea level to 9,800 ft). At higher altitudes, breathing patterns change and you may

lose some benet of your CPAP therapy.

Battery/DC Operation

Several DC power source options are available:

1. Your device can be operated from a 12 V DC power source by using the optional DC Cable.

2. Lastly, instead of connecting12V DC power directly to the CPAP device, you can pass the DC power through an AC Inverter that will deliver AC power to the system. The power

rating of the inverter must be at least 200 watts @ 110V~ / 400 watts @ 220V~.

Approximate Battery Operation Run Time

Example Battery Size = 100 W/Hr

CPAP Only

CPAP with Heated Humidier CPAP with Heated Humidier and PulseDose Module

Heater Setting = 3 Heater Setting = 5 Heater Setting = 3 Heater Setting = 5

CPAP Setting (cmH20) Minimum Run Time (Hrs) Minimum Run Time (Hrs) Minimum Run Time (Hrs) Minimum Run Time (Hrs) Minimum Run Time (Hrs)

5 16.9 8.7 5.6 9.5 5.9

10 11.9 7.5 4.7 7.8 5.4

15 8.7 6.4 4.4 7.1 4.7

20 6.8 5.8 4.0 6.1 4.4

NOTE – Run times are at a breath rate of 20 breaths per minute and standard mask leak.

EN - 20 A-DV64

1. Place optional oxygen

adapter into air supply port.

3. Attach oxygen

tubing to the adapter.

2. Insert CPAP tubing

into adapter.

1. Attach oxygen tubing directly to the oxygen port on

the mask.

OR

Always turn on CPAP before

turning on oxygen ow.

Always turn off oxygen ow

before turning off CPAP.

SUPPLEMENTAL OXYGEN

WARNING-OXYGEN USE

• Oxygen supports combustion. To avoid possible physical injury, do not smoke while using this device with supplemental oxygen. Do not use this device near hot objects,

volatile substances or sources of open ames.

• Always turn on the CPAP device before turning on the oxygen source. Turn off the oxygen source before turning off the device. Never allow the oxygen source to run

continuously while connected to the device if the device is not in use. If the device is not being used, turn off the oxygen ow.

• CPAP pressure must be set higher than 8 cmH2O for supplemental oxygen use to prevent patient breathing pattern from forcing oxygen back into the CPAP.

• At a xed ow rate of supplemental oxygen, the inhaled oxygen concentration will vary depending on the pressure setting, patient breathing pattern, mask selection, and leak rate.

This warning applies to most types of CPAP devices.

CAUTION

• Oxygen is a prescribed gas and should only be administered under the supervision of a physician.

• The ow setting of the oxygen source must be specied by a physician.

• Maximum oxygen pressure is 50 psi. Maximum oxygen ow rate is 10 lpm.

If your physician prescribed supplemental oxygen it can be added one of two ways:

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