Everflo User Manual

1053621
EN, DE
DSF 4/16/08
EverFlo
EverFlo Q
English
EverFlo / EverFlo Q User Manual

Table of Contents
Symbol Key ....................................................................................................... 2
Abbreviations ................................................................................................... 2
Chapter 1: Introduction ................................................................ 3

Intended Use .................................................................................................... 3
About Your EverFlo / EverFlo Q .................................................................3
Parts of Your Concentrator .......................................................................... 3
Accessory Equipment and Replacement Parts .................................... 3
Warnings and Cautions ................................................................................ 4
Chapter 2: Operating Instructions.............................................. 5

Chapter 3: Cleaning & Maintenance .......................................... 7
Cleaning ............................................................................................................. 7
Service ................................................................................................................ 7
How to Contact Respironics........................................................................ 7
Chapter 4: Alarms and Troubleshooting ................................... 8

Troubleshooting Guide ................................................................................ 9
Chapter 5: Specifications............................................................10
Appendix A: EMC Information ..................................................12
Limited Warranty .........................................................................14
Symbol Key
Follow Instructions for Use
AC Power
Type BF Applied Part
REF
Model Number
Class II equipment
SN
Serial Number
No smoking
On (Power)
No oil or grease
Off (Power)
Do not disassemble
IPX1
Drip proof equipment
General Alarm
Action Required, Check System Notification
European Declaration of
Conformity
Compliant with the Waste Electrical and Electronic

Equipment/Restriction of the Use of Certain
Hazardous Substances in Electrical and Electronic
Equipment (WEEE/RoHS) recycling directives
Canadian/US
Certification
Abbreviations
LED
Light Emitting Diode
LPM
Liters per Minute
OPI
Oxygen Percentage Indicator
EverFlo is a trademark of Respironics, Inc. and its aliates.

2008 Respironics, Inc. and its aliates. All rights reserved.
English
Chapter 1: Introduction
Your health care professional has determined that supplemental oxygen is of benet to you and has prescribed
an oxygen concentrator set at a specic ow setting to meet your needs. DO NOT change the ow settings
unless your health care professional tells you to do so. Please read and understand this entire manual before
using the device.
Intended Use
The EverFlo / EverFlo Q Oxygen Concentrator is intended to provide supplemental oxygen to persons
requiring oxygen therapy. The device is not intended to be life supporting or life sustaining.
About Your EverFlo / EverFlo Q

The device produces concentrated oxygen from room air for delivery to a patient requiring low ow oxygen
therapy. The oxygen from the air is concentrated using a molecular sieve and a pressure swing adsorption
process. Your home care provider will show you how to operate the concentrator and will be available to answer
any questions. If you have additional questions or problems, contact your home care provider.
Parts of Your Concentrator

Humidifier Bottle
Mounting Strap
Air Inlet Filter
Oxygen Outlet
Port
Humidifier
Connector
Tube
Control Panel
On/Off Switch
Flow Meter
Filter Door
Accessory Equipment and Replacement Parts

Contact your home care provider if you have questions about this equipment. Use only the following
Respironics accessories and replacement parts with this device:
- Air Inlet Filter
- Humidier Connector Tube
3
Warnings and Cautions

Warnings
A warning represents the possibility of harm to the operator or patient.
For proper operation, your concentrator requires unobstructed ventilation. The ventilation ports are located at the rear
base of the device and at the side air inlet filter. Keep the device at least 15 to 30 cm away from walls, furniture, and
especially curtains that could impede adequate airflow to the device. Do not place the concentrator in a small closed
space (such as a closet).
Do not remove the covers of this device. Servicing must be referred to an authorized and trained Respironics home
care provider.
In the event of an equipment alarm or if you are experiencing any signs of discomfort consult your home care provider
and/or your health care professional immediately.
Oxygen generated by this concentrator is supplemental and should not be considered life supporting or life sustaining.
In certain circumstances oxygen therapy can be hazardous; any user should seek medical advice prior to using this
device.
Where the prescribing health care professional has determined that an interruption in the supply of oxygen, for any
reason, may have serious consequences to the user, an alternate source of oxygen should be available for immediate use.
Oxygen vigorously accelerates combustion and should be kept away from heat or open flame. Not suitable for use in
the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.
Do not smoke, allow others to smoke or have open flames near the concentrator when it is in use.
Do not use oil or grease on the concentrator or its components as these substances, when combined with oxygen, can
greatly increase the potential for a fire hazard and personal injury.
Do not use the oxygen concentrator if either the plug or power cord is damaged. Do not use extension cords or
electrical adapters.
Do not attempt to clean the concentrator while it is plugged into an electrical outlet.
Device operation above or outside of the voltage, LPM, temperature, humidity and/or altitude values specified may
decrease oxygen concentration levels.
Your home care provider is responsible for performing appropriate preventive maintenance at the intervals
recommended by the device manufacturer.
Cautions
A caution represents the possibility of damage to the equipment.
Do not place liquids on or near the device.
If liquid is spilled on the device, turn the power off and unplug from electrical outlet before attempting to clean up
spill. Call your home care provider if device does not continue to work properly.
Chapter 2: Operating Instructions
English
Oxygen Outlet Port
Warning: Do not use extension cords or electrical adapters.

1.
Select a location that allows the concentrator to draw in room air

without being restricted. Make sure that the device is at least 15 to
30 cm away from walls, furniture, and especially curtains that could
impede adequate airflow to the device. Do not place the device near
any heat source.
2. After reading this entire manual, plug the power cord into an electrical
outlet.
3. Do either Step A or Step B below.
A. If you are not using a humidifier, connect your nasal cannula to the
Oxygen Outlet Port, as shown in the top illustration on the right.
B. If you are using a humidifier, follow the steps below:
1. Open the filter door on the back of the device as shown.
2. Remove the humidifier connector tube from the back of the filter
door and replace the filter door, as shown.
3. Fill your humidifier bottle according to the manufacturer's
instructions.
4. Mount the filled humidifier on the top of the EverFlo / EverFlo Q
device inside the velcro strap, as shown in the illustration on the
right.
5. Tighten the velcro strap around the bottle and secure it so it is
held firmly in place.
6. Connect the humidifier connector tube (that you retrieved from
the filter door) to the Oxygen Outlet Port (as shown in Step 3-A
above).
7. Connect the other end of the humidifier connector tube
to the top of the humidifier with the elbow in the tubing
facing the front, as shown here.
8. Connect your cannula to the humidifier bottle according
to the humidifier bottle manufacturer's specifications.
Step 3-A
Step 3-B1
Step 3-B4
Step 3-B7

4.
Press the power switch to the On [I] position. Initially, all the LEDs will illuminate and the audible
alert will beep for a few seconds. After that time, only the green LED should remain lit. You can begin
breathing from the device immediately even though it typically takes 10 minutes to reach oxygen purity
specifications.
5.
Adjust the flow to the prescribed setting by turning the knob on the top of the flow meter until the ball is
centered on the line marking the specific flow rate.
Flow Meter Knob
6.
7.
8.
Be sure oxygen is flowing through the cannula. If it is not, refer to the Troubleshooting Guide in this
manual.
Put on the cannula as directed by your home care provider.
When you are not using the oxygen concentrator, press the power switch to the Off [O] position.
English
Chapter 3: Cleaning & Maintenance

Warning: It is important to unplug the device before you perform any cleaning.
Caution: Excess moisture may impair the proper operation of the device.
Cleaning
Periodically, use a damp cloth to wipe down the exterior case of the EverFlo / EverFlo Q device. If you use
medical disinfectants, be sure to follow the manufacturer's instructions.
If you are using a humidier, clean your device according to your home care provider's or manufacturer's
instructions.
Service
The EverFlo / EverFlo Q Oxygen Concentrator contains no user-servicable parts.
Warning: Do not remove the covers of this device. Servicing must be referred to an authorized and
trained Respironics home care provider.
How to Contact Respironics

To have your device serviced, contact your home care provider. If you need to contact Respironics directly,
call the Respironics Customer Service department at 1-724-387-4000 or Respironics Deutschland at
+49 8152 93060. You can also use the following addresses:
Respironics
1001 Murry Ridge Lane
Murrysville, PA 15668
USA
Respironics Deutschland
Gewerbestrasse 17
82211 Herrsching
Germany
Visit the EverFlo web site at: www.evero.respironics.com
Chapter 4: Alarms and Troubleshooting

Alarm and Indicators
The device has an audible alarm and three LED indicators, as shown below.
NORMAL
Green Power On Indicator

Yellow Check System Indicator
Red Alarm Indicator
Audible Alarm / Colored LED
Possible Cause
Your Action
All 3 LEDs illuminate continuously and the

Audible Alarm is sounding continuously.
The device has detected a

system malfunction.
Immediately turn off the device, connect to a

back up oxygen source, and call your home care
provider.
The Audible Alarm is sounding continuously.

None of the LEDs are illuminated.
The device is turned on but

is not operating. Often this
indicates that the device is not
plugged in or there is a power
failure.
Check the power outlet and verify that the device

is plugged in. If the problem continues, connect
to a back up oxygen source and call your home
care provider.
Red LED illuminates continuously and the

Audible Alarm is sounding continuously.
The device has detected a

system malfunction.
Immediately turn off the device and wait

5 minutes. Restart the device. If the condition
persists turn the unit off, connect to a back up
oxygen source, and call your home care provider.
Yellow LED illuminates continuously. The

Red LED is blinking and the Audible Alarm is
beeping periodically.
The device has detected

an impeded oxygen flow
condition.
Follow the troubleshooting guide on the next

page. Connect to a back up oxygen source
and call your home care provider if your
troubleshooting actions fail to end this alert
condition.
Yellow LED illuminates continuously. The Red

LED is off and the Audible Alarm is silent.
The device has detected a low

oxygen condition (OPI units
only).
Continue using the unit but call your home care

provider about this condition.
Problem
Why it Happened
What to Do
Yellow LED is blinking. The Red LED is off and the

Audible Alarm is beeping periodically.
The device has detected a high oxygen

flow condition.
Turn the flow rate down to your

prescribed level. Wait at least 2 minutes.
If the condition persists turn the unit off,
connect to a back up oxygen source, and
call your home care provider.
Green LED illuminates continuously. The other

LEDs are off and the Audible Alarm is silent.
The device is turned on and working

properly.
Take no action.
The power cord plug is not properly

inserted into the electrical outlet.
Make sure the device is properly plugged

in to the electrical outlet.
The unit is not receiving power from

the electrical outlet.
Check your household outlet fuse or

circuit.
Internal part failure.
Connect to a back up oxygen source and

contact your home care provider.
Internal part failure.
Connect to a back up oxygen source and

contact your home care provider.
The airflow to the device is impeded

or blocked.
Remove any items that appear to be

blocking the airflow into the device.
The flow meter knob is completely

closed.
Turn the flow meter knob

counterclockwise to center the ball on the
prescribed LPM flow.
The oxygen tubing is kinked and

blocking the delivery of oxygen.
Check to see that the tubing is not kinked

or blocked. Replace if necessary.
The oxygen tubing or cannula is faulty.
Inspect and replace the items if

necessary.
There is a poor connection to a device

accessory.
Ensure that all connections are free from

leaks.
The device is not working when it is turned on.

(The Audible Alarm is sounding continuously.
All LEDs are off.)
English
Troubleshooting Guide
The device is not working when it is turned on.

(The Audible Alarm is sounding continuously
and all 3 LEDs are illuminated.)
Impeded oxygen flow indication is activated.

(The Yellow LED illuminates continuously,
the Red LED is blinking and the Audible Alarm is
beeping periodically.)
Limited oxygen flow to the user without any

fault indication.
(All LEDs are off and the Audible Alarm is silent.)
Chapter 5: Specifications
Environmental
Operating
Transport & Storage
13 to 32C
-34 to 71C
15 to 95%, noncondensing
15 to 95%, noncondensing
0 to 2286 m
N/A
Temperature
Relative Humidity
Altitude
Physical
Dimensions 58 cm x 38 cm x 24 cm
Weight 14 to 15 kg
Standards Compliance
This device is designed to conform to the following standards:
- IEC 60601-1 Medical Electrical Equipment, Part 1: General Requirement for Safety
- IEC 60601-1-2 2nd edition, Medical Electrical Equipment, Part 1-2: General Requirement for Safety Collateral Standard:
Electromagnetic Compatibility Requirements and Tests.
- ISO 8359 Oxygen Concentrators for Medical Use Safety Requirements
Electrical, AC Power Consumption

Models 1020000, 1020001
1020002, 1020003 120 VAC 10%, 350 W, 60 Hz
1020014, 1020015
1020004, 1020005 230 VAC 10%, 320 W, 60 Hz
1020006,1020007, 1020008
1020009, 1020010
230 VAC 10%, <300 W, 50 Hz
1020011, 1020012
1020016, 1020017
1020013 230 VAC 10%, <300 W, 60 Hz
10
English
Oxygen
Oxygen Concentration*
(All Models except 90-96% from 0.5 to 5 LPM
1020007, 1020008)
Models 1020007, 1020008 87-96% from 0.5 to 5 LPM
*
Device operation above or outside of the voltage, LPM, temperature, humidity and/or altitude values
specified may decrease oxygen concentration levels.
Sound Level
Models 1020000, 1020001
1020002, 1020003 45 dBA typical
1020013
1020004, 1020005
1020006, 1020008
1020009, 1020010 43 dBA typical
1020011, 1020012
1020016, 1020017
1020007, 1020014
<40 dBA typical
1020015
Classification
The EverFlo / EverFlo Q Oxygen Concentrator is classied as:
IEC Class II Equipment
Type BF Applied Part
IPX1 Drip Proof
Not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous
oxide.
Continuous Operation
Disposal
Dispose of the device in accordance with local regulations.
WEEE/RoHS Recycling Directives

If you are subject to the WEEE/RoHS recycling directives, refer to www.respironics.com for the passport for
recycling this product.
11
Appendix A: EMC Information

GUIDANCE AND MANUFACTURERS DECLARATION ELECTROMAGNETIC EMISSIONS: This device is intended for use in the
electromagnetic environment specied below. The user of this device should make sure it is used in such an environment.
EMISSIONS TEST
COMPLIANCE
ELECTROMAGNETIC ENVIRONMENT GUIDANCE
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its internal function. Therefore, its
RF emissions are very low and are not likely to cause any interference
in nearby electronic equipment.
RF emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000-3-2
Class A
The device is suitable for use in all establishments, including

domestic establishments and those directly connected to the public
low-voltage power supply network.
Voltage fluctuations/Flicker emissions

IEC 61000-3-3
Complies
GUIDANCE AND MANUFACTURERS DECLARATION ELECTROMAGNETIC IMMUNITY: This device is intended for use in the
IMMUNITY TEST
IEC 60601 TEST

LEVEL
COMPLIANCE LEVEL
ELECTROMAGNETIC ENVIRONMENT
GUIDANCE
Electrostatic Discharge (ESD)

IEC 61000-4-2
6 kV contact
8 kV air
6 kV contact
8 kV air
Floors should be wood, concrete or ceramic

tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical Fast Transient/Burst

IEC 61000-4-4
2 kV for power supply lines

1 kV for input-output lines
2 kV for supply mains

1 kV for input/output lines
Mains power quality should be that of a

typical home or hospital environment.
Surge
IEC 61000-4-5
1 kV differential mode
2 kV common mode
1 kV differential mode
2 kV for common mode

typical home or hospital environment.
Voltage dips, short

interruptions and voltage
variations on power supply
input lines
IEC 61000-4-11
<5% UT
(>95% dip in UT) for 0.5 cycle
40% UT
(60% dip in UT) for 5 cycles
70% UT
<5% UT
(>95% dip in UT) for 5 sec
<5% UT
(>95% dip in UT) for 0.5 cycle
40% UT
70% UT
<5% UT
(>95% dip in UT) for 5 sec

typical home or hospital environment. If
the user of the device requires continued
operation during power mains interruptions,
it is recommended that the device be
powered from an uninterruptible power
supply or a battery.
Power frequency (50/60 Hz)

magnetic field
IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields should be

at levels characteristic of a typical location in
a typical hospital or home environment.
Note: UT is the a.c. mains voltage prior to application of the test level.
12

GUIDANCE AND MANUFACTURERS DECLARATION ELECTROMAGNETIC IMMUNITY: This device is intended for use in the
IMMUNITY TEST
IEC 60601 TEST LEVEL
COMPLIANCE LEVEL
English
ELECTROMAGNETIC ENVIRONMENT GUIDANCE
Portable and mobile RF communications equipment should be
used no closer to any part of the device, including cables, than
the recommended separation distance calculated from the
equation applicable to the frequency of the transmitter.
Conducted RF
IEC 61000-4-6
3 Vrms
150 kHz to 80!MHz
3 Vrms
Recommended separation distance:

d = 1.2
150 kHz to 80!MHz
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d = 1.2
d = 2.3
80 MHz to 800 MHz

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 device is
used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the device.
b: Over the frequency range 150 kHz to 80 MHz, the field strengths should be less than 3 V/m.
RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THIS
DEVICE: The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer
or the user of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile
RF communications equipment (transmitters) and this device as recommended below, according to the maximum output power of the
communications equipment.
RATED MAXIMUM POWER
OUTPUT OF TRANSMITTER
(W)
SEPARATION DISTANCE ACCORDING TO FREQUENCY OF TRANSMITTER

(m)
150 KHZ TO 80 MHZ
d = 1.2
80 MHZ TO 800 MHZ

d = 1.2
800 MHZ TO 2.5 GHZ

d = 2.3
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance (d) in meters (m) can be
estimated 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.
13
Limited Warranty
Respironics, Inc. warrants that the system shall be free from defects of workmanship and materials and will
perform in accordance with the product specications for a period of three (3) years from the date of sale by
Respironics, Inc. to the dealer. Respironics warrants that the EverFlo / EverFlo Q units serviced by Respironics,
or an authorized service center, will be free from defects in serviced materials for a period of 90 days and free
from defects in workmanship for a period of 90 days from the time of service. Respironics accessories are
warranted to be free of defects in materials and workmanship for a period of 90 days from the time of purchase.
If the product fails to perform in accordance with the product specications, Respironics, Inc. will repair or
replace at its option the defective material or part. Respironics, Inc. will pay customary freight charges from
Respironics, Inc. to the dealer location only. This warranty does not cover damage caused by accident, misuse,
abuse, alteration, and other defects not related to material or workmanship.
Respironics, Inc. disclaims all liability for economic loss, loss of prots, overhead, or consequential damages
which may be claimed to arise from any sale or use of this product. Some states do not allow the exclusion or
limitation of incidental or consequential damages, so the above limitation or exclusion may not apply to you.
This warranty is given in lieu of all other express or implied warranties, including the implied warranties of
merchantability and tness for a particular purpose. In addition, in no event shall Respironics be liable for lost
prots, loss of good will, or incidental or consequential damages, even if Respironics has been advised of the
possibility of the same. Some states or provinces do not allow the exclusion of limitation of implied warranties
or the disclaimer of incidental and consequential damages. Accordingly, the laws of your state or province may
give you additional protections.
To exercise your rights under this warranty, contact your local authorized Respironics, Inc. dealer or contact
Respironics, Inc. at:
14
Respironics
1001 Murry Ridge Lane
Murrysville, PA 15668
USA
Respironics Deutschland
Gewerbestrasse 17
82211 Herrsching
Germany
1-724-387-4000
+49 8152 93060

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1053621

EverFlo / EverFlo Q User Manual

EverFlo / EverFlo Q User Manual

Chapter 1: Introduction ................................................................ 3

Chapter 2: Operating Instructions.............................................. 5

Chapter 4: Alarms and Troubleshooting ................................... 8

EverFlo / EverFlo Q User Manual

Type BF Applied Part

Drip proof equipment

Action Required, Check System Notification

Compliant with the Waste Electrical and Electronic

Light Emitting Diode

Liters per Minute

Oxygen Percentage Indicator

EverFlo is a trademark of Respironics, Inc. and its aliates.

EverFlo / EverFlo Q User Manual

About Your EverFlo / EverFlo Q

Parts of Your Concentrator

Accessory Equipment and Replacement Parts

EverFlo / EverFlo Q User Manual

Warnings and Cautions

Do not place liquids on or near the device.

EverFlo / EverFlo Q User Manual

Chapter 2: Operating Instructions

Oxygen Outlet Port

Warning: Do not use extension cords or electrical adapters.

Select a location that allows the concentrator to draw in room air

EverFlo / EverFlo Q User Manual

Flow Meter Knob

EverFlo / EverFlo Q User Manual

Chapter 3: Cleaning & Maintenance

How to Contact Respironics

Visit the EverFlo web site at: www.evero.respironics.com

EverFlo / EverFlo Q User Manual

Chapter 4: Alarms and Troubleshooting

Green Power On Indicator

Audible Alarm / Colored LED

All 3 LEDs illuminate continuously and the

The device has detected a

Immediately turn off the device, connect to a

The Audible Alarm is sounding continuously.

The device is turned on but

Check the power outlet and verify that the device

Red LED illuminates continuously and the

The device has detected a

Immediately turn off the device and wait

Yellow LED illuminates continuously. The

The device has detected

Follow the troubleshooting guide on the next

Yellow LED illuminates continuously. The Red

The device has detected a low

Continue using the unit but call your home care

EverFlo / EverFlo Q User Manual

Yellow LED is blinking. The Red LED is off and the

The device has detected a high oxygen

Turn the flow rate down to your

Green LED illuminates continuously. The other

The device is turned on and working

The power cord plug is not properly

Make sure the device is properly plugged