Aeroneb | Go | Instruction manual | Aeroneb Go Instruction manual

Aeroneb Go Instruction manual
Instruction Manual
Table of Contents
Introduction........................................................ 1
Important Safeguards........................................ 2
Warranty............................................................ 5
Classifications and Markings............................. 6
Aeroneb® Go System Parts............................... 7
Unit Assembly and Usage................................. 7
Prior to Assembly.............................................. 7
Assembly/Functional Test.................................. 8
How to Operate the Aeroneb® Go Nebulizer..... 9
Cleaning and Storing Your Aeroneb® Go......... 11
Troubleshooting Guide.................................... 14
Electromagnetic Susceptibility......................... 15
Specifications.................................................. 17
Performance.................................................... 18
Replacement Parts and Accessories............... 20
Appendix 1: EMC tables.................................. 21
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INTRODUCTION
Be sure to read these instructions fully before use.
Thank you for purchasing the Aeroneb® Go Nebulizer. Certain
conditions such as asthma, COPD (chronic obstructive
pulmonary disease) and cystic fibrosis require that prescribed
liquid medication be turned into a fine mist, called an aerosol,
and then inhaled into the lungs. The Aeroneb® Go turns liquid
medication into an aerosol, which you can then inhale through
a mouthpiece or an aerosol mask into your lungs.
The Aeroneb® Go uses the unique OnQ™ Aerosol Generator,
which is unlike any other nebulizer technology available.
When you turn on your nebulizer, OnQ pumps liquid through
tiny holes in a wafer-thin metal plate to create a soft mist
aerosol.
The Aeroneb® Go, for use by paediatric and adult patients,
is intended to aerosolize physician-prescribed solutions for
inhalation that are approved for use with a general-purpose
nebulizer.
Designed with your needs in mind, the Aeroneb® Go is
portable, lightweight, compact and silent. The control module
operates with three (3) “AA” disposable or rechargeable
batteries (not included), or can alternatively be powered by
the AC/DC adapter.
1
IMPORTANT SAFEGUARDS
When you use electrical products, always follow basic safety
precautions. As with any electrical device take particular care
around children.
READ ALL WARNINGS AND INSTRUCTIONS BEFORE
YOU USE YOUR NEBULIZER
WARNING:
If this product is being used to treat a life threatening
condition, a backup device is necessary.
2
•
As with any electronic device, this product may become
unusable due to an electrical outage, battery depletion,
or mechanical failure. We recommend that you have
spare batteries and have a backup device available to
you.
•
The AC/DC adapter does not charge batteries.
•
If you are using batteries and the green light is flashing,
your batteries are low. You may finish your treatment and
then change (or replace and recharge) the three “AA”
batteries immediately.
•
Do not share your Aeroneb® Go Nebulizer with others.
It is intended for use by a single user. If more than one
person uses it, there is a risk of spreading infectious
illness.
•
As with all electronic devices, it is recommended that the
product is unplugged when not in use.
•
Adult supervision is required when this product is used by
children and individuals who require special assistance.
•
Use this product only for physician-prescribed solutions
for inhalation as described in this manual.
WARNINGS CONTINUED:
•
Do not use components or attachments that are not
recommended by Aerogen. Refer to the Replacement
Parts and Accessories section in this manual (page 20).
•
Never operate this product if any of the parts are not
working properly or have been damaged.
•
Do not use the Aeroneb® Go Nebulizer in the presence
of a flammable anaesthetic mixture with air, oxygen or
nitrous oxide. As with any electrical equipment, take care
when using the device in a potentially oxygen enriched
environment.
•
Do not use the Aeroneb® Go Nebulizer with anaesthetic
breathing systems or lung ventilator breathing systems.
•
Do not place or drop this product into water or any liquid
when it is plugged into a power source.
•
Keep this product and cords away from heated surfaces.
•
Be sure the device has been properly cleaned before
use to avoid possible contamination.
•
If after proper cleaning it takes longer than 12 minutes to
deliver 3 mL of normal saline (0.9%), the Nebulizer Unit
should be replaced.
•
The user should ensure that exhaled medication is
directed away from bystanders.
•
Do not microwave any parts.
•
By connecting the AC/DC adapter to the Aeroneb® Go
Control Module, the Aeroneb® Go Control Module and
batteries are not being charged.
•
As with any cables keep all cables tidy to avoid tripping
or strangulation hazards and take particular care around
children.
3
WARNINGS CONTINUED:
4
•
Do not nebulize alcohol-based drugs in an oxygen-rich/
high pressure environment.
•
In event of loss of mains power, remove the AC/DC cable
from the control module and operate with batteries (refer
to page 9).
•
Never clean your Nebulizer Unit with solvents, chemicals,
alcohol or abrasive cleaners.
•
Do not use brushes, sharp tools or abrasive cloths that
could scratch or damage the surfaces.
•
Do not clean parts in a dishwasher.
•
Store your Aeroneb® Go in the carrying case.
•
Do not store the Aeroneb® Go in a location where it is
exposed to direct sunlight, extreme heat or cold, dust or
water. Store out of reach of children.
•
Follow local laws and recycling plans regarding disposal
or recycling of components, batteries and packaging.
•
Before storing your Aeroneb® Go for an extended period,
remove the batteries from the Aeroneb® Go Control
Module and store them separately. If you do not take the
batteries out, they may leak and cause your nebulizer to
stop working.
WARRANTY
The Aeroneb® Go Control Module and AC/DC Adapter are
warranted for a period of two years from the date of purchase
against defects in manufacturing. The Aeroneb® Go nebulizer
unit is warranted for one year from date of purchase against
defects in manufacturing. All warranties are based on typical
usage.
The life of the Aeroneb® Go nebulizer unit has been validated
for use for 100 disinfecting treatments (boiling or baby
bottle steam steriliser). This is based on a minimum of one
year typical usage profile of 2 treatments per day and two
disinfecting treatments per week. The user should note that
any use in excess if this may result in reduced life of the
product.
5
CLASSIFICATIONS AND MARKINGS
The symbols that appear on the Aeroneb® Go Nebulizer and
its accessories are described in the table below:
Symbol
Meaning
Attention, consult accompanying documents
Class II equipment per IEC/EN 60601-1
Type BF equipment per IEC/EN 60601-1. This label
applies to Aeroneb® Go nebulizer unit only
US
Classified by TUV with respect to electric shock, fire
and mechanical hazards
SN
Serial number
REF
Model number
Manufacturer
Input
Output
DC Voltage
AC Voltage
Power On/Off
Fragile – Handle with care
Keep Dry
+60 oC
–20 C
o
0050
Transient storage temperature limits: -20°C to 60°C
This device complies with the requirements of the
Medical Devices Directive (93/42/EEC)
Consult Instructions for Use
6
AERONEB® GO SYSTEM PARTS:
Medication Cup Cap
Mouthpiece
Cable
Nebulizer body
Base
Control Module
AC/DC Adapter*
Mask Adapters
*Available with complete
Aeroneb® Go System
UNIT ASSEMBLY AND USAGE
NOTE: Clean all parts of your Aeroneb® Go Nebulizer
(described on page 11) before first use, after each use, or after
extended storage.
PRIOR TO ASSEMBLY:
Check all parts for visible damage. Replace any damaged
parts before you use the Aeroneb® Go. In the case of missing
parts, malfunction or damage, contact your local Aeroneb® Go
representative or equipment supplier.
7
ASSEMBLY/FUNCTIONAL TEST
1. Connect the Medication Cup to the
Nebulizer Body by lining up the notches
on the medication cup and nebulizer
body.
NOTE: Ensure the Aeroneb Go
handset is not connected to the
controller when adding medication to
the medication cup.
2. Insert the nebulizer cable into the back of
the nebulizer unit.
3. Add Aeroneb® Go base to the bottom of
the handset.
4. Fill the Medication Cup with the
prescribed nebulizer medication. Never
pour more than 6 mL into the cup. The
continuous line on the inside surface of
the cup indicates the maximum filling
level. CAUTION: To avoid damage
to the nebulizer unit, do not use a
syringe with needle.
5. Place the Cap on Medication Cup.
6. Attach Mouthpiece or Mask Connector
and mask to Nebulizer Body.
8
HOW TO OPERATE THE AERONEB® GO NEBULIZER
3 x AA LR6
1. Turn the Aeroneb® Go Control Module
upside down. Slide the battery cover
in the direction of the arrow to remove
the lid. Put in three (3) “AA” batteries
(not included). Replace the cover on
the Control Module and slide the cover
until it locks in place. You can expect at
least three (3) hours of operation from
a new set of disposable batteries, (up
to five (5) hours from high performance
batteries).
2. Connect the nebulizer cable to the
Aeroneb® Go Control Module, indicated
by the Output symbol (
).
3. Turn on the unit by pressing the “On/Off”
button on the Control Module. You will
see a green light on the Control Module
light up.
3 x AA LR6
4. Visually verify that aerosol is coming out
of the mouthpiece or mask to indicate
that the device is functioning properly.
NOTE: Do not cover the ventilation
holes during use.
9
5. Alternatively, you can power the device
by using the AC/DC Adapter if provided
(refer page 7). Plug the AC/DC adapter
into a standard AC electrical outlet, a
green light on the adapter indicates that
the AC/DC adapter is turned on.
6. Plug the AC/DC cable into the Control
Module, indicated by the DC Voltage
Symbol (
).
NOTE: The AC/DC adapter does not
charge batteries.
7. Press the “On/Off” button and visually
verify that aerosol is coming out of the
mouthpiece or mask to indicate that the
device is functioning properly.
8. Place the mouthpiece between your
teeth, with your lips firmly sealed
around the mouthpiece. If you use an
aerosol mask, place the mask over your
mouth and nose. Breathe in and out
slowly through your mouth until aerosol
formation stops.
NOTE: Aerosol mask is not provided.
Do not cover ventilation holes.
9. To turn off nebulizer, press the “On/Off”
button on the Control Module.
PAGE 10
10
CLEANING AND STORING YOUR AERONEB® GO
AFTER EVERY USE:
Disconnect the control module before you take the nebulizer
apart to rinse it.
1. Rinse the Nebulizer Unit (Medication Cup, Nebulizer
Body, Base and Mouthpiece or Mask Adapter) under
running hot tap water after every use.
2. Shake off excess water, and allow parts to fully air dry on
a clean, dry towel, out of the reach of children.
3. Make certain that all cleaned parts are completely dry
before you store or use them.
DAILY:
Disconnect the power source before you take the nebulizer
apart to clean it.
1. Wash the Nebulizer Unit (Medication Cup and Cap,
Nebulizer Body, Base and Mouthpiece or Mask Adapter)
by hand in a solution of warm water and mild liquid
dishwashing soap. Use soap intended only for washing
dishes by hand. Do not use dishwasher detergent. Do not
leave parts soaking.
2. Rinse all pieces thoroughly under running hot tap water.
Make sure that no soap is left on any of the parts.
3. Shake off excess water, and allow parts to fully air dry on
a clean, dry towel, out of the reach of children.
4. Make certain that all cleaned parts are completely dry
before you store or use them.
11
OPTIONAL DISINFECTION:
If you would like to disinfect your Aeroneb® Go Nebulizer,
you may choose one of the following two options; Boiling or
Vinegar Solution.
1.
BOILING:
i.
ii.
iii.
iv.
v.
vi.
Rinse the Nebulizer Unit (Medication Cup,
Nebulizer Body, Base and Mouthpiece or
Mask Adapter) under running hot tap water
after every use.
Shake off excess water, and allow parts to fully
air dry on a clean, dry towel, out of the reach
of children.
Bring a saucepan of DISTILLED water to the
boil and allow it to continue to boil.
NOTE: Using regular tap water to boil the
nebulizer unit will greatly reduce the life of the
nebulizer unit.
Carefully immerse the Nebulizer Unit in the
boiling water. Leave the nebulizer immersed
in the boiling water for a maximum of
twenty (20) minutes.
Carefully remove the nebulizer from the boiling
water and shake off the excess water. Allow
parts to fully air dry on a clean, dry towel, out
of the reach of children.
Make certain that all parts are completely dry
before you store or use them.
Similarly, the Nebulizer Unit may be steam disinfected in a
standard baby bottle steam sterilizer for fifteen (15) minutes.
Refer to manufacturers instructions.
12
OPTIONAL DISINFECTION
2.
VINEGAR SOLUTION:
i.
ii.
iii.
iv.
v.
vi.
vii.
Rinse the Nebulizer Unit (Medication Cup,
Nebulizer Body, Base and Mouthpiece or
Mask Adapter) under running hot tap water
after every use.
Shake off excess water, and allow parts to fully
air dry on a clean, dry towel, out of the reach
of children.
Fill a container with a mixture of three (3) parts
hot water to one (1) part white distilled vinegar.
Soak the Nebulizer Unit Parts (Medication Cup
and Cap, Nebulizer Body, and Mouthpiece
or Mask Adapter) in the solution for thirty
(30) minutes.
Rinse all pieces thoroughly under running hot
tap water.
Shake off excess water, and allow parts to air
dry on a clean, dry towel, out of the reach of
children.
Make certain that all disinfected parts are
completely dry before you store or use them.
Cleaning of Control Module, Cable, AC/DC Adapter:
Wipe with a clean cloth dampened with warm water and mild
liquid detergent.
•
Do not immerse in liquid.
•
Do not use abrasive or sharp tools.
•
Do not spray liquid directly onto the control
module.
•
Do not immerse control module in liquid.
13
TROUBLESHOOTING GUIDE
If you have difficulty operating your Aeroneb® Go, check the
following points:
Problem
Check
Remedy
No visible
aerosol
when using
batteries
Check that the
batteries are
inserted correctly.
Using the markings
under each battery
location, place
each battery in the
Control Module
housing. Match (+)
and (-).
Check to see if the
low battery power
light is flashing.
Replace the
batteries or use the
AC/DC Adapter.
Check that the
Control Module
cable is connected
properly to the
nebulizer and to the
Control Module.
Connect the cable
properly to the
nebulizer and the
Control Module
(Refer to page 8).
Check that the
AC/DC Adapter is
plugged correctly
into a working AC
outlet and the green
light is on the AC/DC
Adapter.
Insert the plug into
a working outlet
and verify that the
green light on the
controller is lit (Refer
to page 10).
Check that the
AC/DC Adapter
cable is connected
properly to the
Control Module.
Connect the
AC/DC Adapter
cable properly to
the Control Module
(Refer to page 10).
No visible
aerosol when
using AC/DC
adapter
14
Problem
No visible
aerosol
when power
source is
functioning
Check
Remedy
Check that the
AC/DC Adapter is
not faulty.
Try to operate the
Control Module
by using batteries
instead of the
AC/DC Adapter. If
the Control Module
functions properly
with batteries but
not with the AC/DC
adapter, replace the
AC/DC Adapter.
Check that there is
medication in the
Medication Cup.
Fill the Medication
Cup with prescribed
medication.
Check that the
nebulizer has been
properly cleaned.
Clean the
Aeroneb® Go. Refer
to page 11.
If above remedies do not work, call your local supplier.
ELECTROMAGNETIC SUSCEPTIBILITY
This device meets the requirements of IEC/EN60601‑1‑2
which
describes
requirements
for
electromagnetic
compatibility (EMC) of medical devices. This includes
immunity to radio frequency electric fields and electrostatic
discharge, in addition to the other applicable requirements
of the standard. Compliance with EMC standards does not
mean a device has total immunity; certain devices (cellular
phones, pagers, etc.) can interrupt operation if they are used
near medical equipment.
15
WARNINGS:
•
Only use the Aeroneb® Go nebulizer with components
specified in the Instructions for Use. Use of the Aeroneb®
Go nebulizer with components other than those specified
in the Instructions for Use may result in increased
emissions or decreased immunity of the Aeroneb® Go
nebulizer system.
•
Do not use the Aeroneb® Go adjacent to or stacked with
other equipment. If adjacent or stacked use is necessary,
the device should be observed to verify normal operation
in this configuration.
•
The Aeroneb® Go needs special precautions regarding
electromagnetic compatibility (“EMC”) and must be
installed and put into service according to the EMC
information provided in the Instructions for Use.
•
Portable and mobile radio frequency (“RF”)
communication devices can disrupt medical electrical
equipment.
Refer to Appendix 1 for EMC Tables as per IEC/EN 60601-1-2
16
SPECIFICATIONS
Physical
Aeroneb Go nebulizer unit (assembled): 40 x 105 x 95 mm
Aeroneb Go Control Module: 70 x 110 x 32 mm
AC/DC adapter: 74 (H) x 72 (D) x 49 (L) mm
Aeroneb Go Nebulizer Unit: 65 g
Aeroneb Go Control Module with batteries: 260 g
AC/DC Adapter: 100 g
Medication Cup capacity: Maximum of 6 mL
Environmental
Recommended Operating Environment:
Temperature range: 5°C to +45°C (+41°F to +113°F)
Atmospheric pressure: 450 to 1100 mBars
Humidity: up to 95% relative humidity
Noise Level: <35 dB at 0.3 m distance
Recommended Storage & Transport Environment:
Transient temperature range: -20°C to +60°C (-4°F to +140°F)
Atmospheric pressure: 450 to 1100 mBars
Humidity: up to 95% relative humidity
17
PERFORMANCE:
Aerosol flow rate: > 0.3 mL/min
Average tested flow rate: 0.4 mL/min
Particle Size:
As measured with the Andersen Cascade Impactor:
-
-
Specification Range: 1-5 μm.
Average Tested: 3.1 μm.
As measured with the Marple 298 Cascade Impactor:
-
-
Specification Range: 1.5-6.2 μm.
Average Tested: 3.9 μm.
As per EN 13544-1:
-
Aerosol output rate: 0.25 mL/min
-
Aerosol Output: 0.86 mL emitted of 2.0 mL dose
-
Residual Volume: <0.1 mL for a 3 mL dose
Performance may vary depending on the type of drug and
nebulizer unit used. For additional information contact
Aerogen or your drug supplier.
The temperature of the medication will not rise more than
10°C (18°F) above ambient temperature during normal use.
For additional information contact Aerogen or your drug
supplier.
18
Representative particle size distribution graph for Albuterol
as per EN13544-1 is shown below:
Cumulative Mass (%)
100.0
50.0
0.0
0.1 1 10100
Aerodynamic Size (µm)
Power
Power Source:
Aeroneb Go Control Module - 4.5 VDC (3 “AA” disposable or
rechargeable batteries), 350 mA.
AC/DC Adapter: 100-240 VAC, 5 VDC, 315 mA, 50-60 Hz.
Power Consumption: Less than 2 watts (nebulizing)
Patient Isolation: Control module circuitry provides 4 kilovolt
(kV) patient isolation and complies with IEC/EN 60601-1
19
REPLACEMENT PARTS AND ACCESSORIES:
PART
Aeroneb® Go System
Medication Cup Cap
Aeroneb® Go Handset
Mouthpiece
Handset Base (pack of 10)
AC/DC Adapter*
Control Module
Control Module Cable
Mask Adapter (22 mm M)
Mask Adapter (22 mm F)
Carrying Case
Instruction Manual*
REORDER NUMBER
AG-AG4200-XX*
AG-AG3010
AG-AG4300
AG-AG3040
AG-AG4030
AG-AG3410-XX*
AG-AG3060
AG-AG4070
AG-AG3080
AG-AG3090
AG-AG3110
AG-AG4120-XX*
*Contact your local supplier for reorder number specific for
your geographical region.
To order replacement parts or accessories, contact your local
supplier.
If you have any questions or problems regarding your
Aeroneb® Go nebulizer unit, call your local supplier.
20
Appendix 1
EMC tables:
The following Tables are provided in accordance with IEC/ EN 60601-1-2:
Guidance and manufacturer’s declaration – electromagnetic emissions
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment specified below. The customer or the user of the Aeroneb Go
nebulizer system should assure that it is used in such an environment.
Emissions test
Compliance
RF Emissions
CISPR 11
Group 1
RF Emissions
CISPR 11
Class B
Harmonic emissions
IEC 61000‑3‑2
Not Applicable
Voltage fluctuations/
flicker emissions
IEC 61000‑3‑3
Not Applicable
Electromagnetic
environment – guidance
The Aeroneb Go nebulizer
system 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.
The Aeroneb Go nebulizer
system is suitable for
use in all establishments,
including domestic
establishments and those
directly connected to the
public low voltage power
supply network that
supplies buildings used for
domestic purposes.
21
Recommended separation distances between portable and mobile RF
communication equipment and the Aeroneb Go
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment in which radiated RF disturbances are controlled. The customer
or the user of the Aeroneb Go can help prevent electromagnetic interference
by maintaining a minimum distance between port and mobile RF
communications equipment (transmitters) and the Aeroneb Go nebulizer
system as recommended below, according to the maximum output power
of the communications equipment.
Rated maximum
output power of
transmitter
W
Separation distance according to frequency of
transmitter
m
150 kHz to
80 MHz
80 MHz to
800 MHz
800 MHz to
2.5 GHz
d = [1.17] √P
d = [1.17] √P
d = [2.33] √P
0.01
0.12
0.12
0.23
0.1
0.37
0.37
0.75
1
1.17
1.17
2.33
10
3.70
3.70
7.36
100
11.70
11.70
23.30
For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in metres (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.
Guidance and manufacturer’s declaration – electromagnetic immunity
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment specified below. The customer or the user of the Aeroneb Go
should assure that it is used in such an environment.
Immunity test
IEC/EN 60601
Test level
Compliance
level
Electrostatic
discharge (ESD)
±6 kV contact
±6 kV contact
IEC 61000‑4‑2
±8 kV air
±8 kV air
Electrical fast
Transient/burst
±2 kV for power
supply lines
±2 kV for power
supply lines
IEC 61000‑4‑4
±1 kV for input/
output lines
±1 kV for input/
output lines
Surge
±1 kV differential
mode
±1 kV differential
mode
IEC 61000‑4‑5
±2 kV common
mode
±2 kV common
mode
Voltage
dips, short
interruptions and
voltage variations
on power supply
input lines
<5% Ut
(>95% dip in Ut)
for 0.5 cycle
<5% Ut
(>95% dip in Ut)
for 0.5 cycle
40% Ut
(60% dip in Ut)
for 5 cycles
40% Ut
(60% dip in Ut)
for 5 cycles
70% Ut
(30% dip in Ut)
for 25 cycles
70% Ut
(30% dip in Ut)
for 25 cycles
<5% Ut
(>95% dip in Ut)
for 5 sec
<5% Ut
(>95% dip in Ut)
for 5 sec
IEC 61000‑4‑11
Electromagnetic
environment –
guidance
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.
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 Aeroneb Go
requires continued
operation during
power mains
interruption, it is
recommended that
the Aeroneb Go
be powered from
an uninterruptible
power supply or
battery.
Immunity test
Power
frequency
(50/60 Hz)
Magnetic field
IEC/EN 60601
Test level
3 A/m
Compliance level
3 A/m
IEC 61000‑4‑8
Electromagnetic
environment –
guidance
Power frequency
magnetic fields
should be at levels
characteristic of
a typical location
in a typical
commercial
or hospital
environment.
Note: Ut is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration – electromagnetic immunity
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment specified below. The customer or the user of the Aeroneb Go
should assure that it is used in such an environment.
Immunity
test
IEC/EN 60601 Compliance
Test level
level
Conducted
RF
3 Vrms
IEC
61000‑4‑6
150 kHz to
80 MHz
[3]V
Electromagnetic environment –
guidance
Portable and mobile RF
communications equipment
should be used no closer to any
part of the Aeroneb Go, 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
d = [1.17] √P... 80 MHz to 800 MHz
Radiated RF 3 Vrms
IEC
61000‑4‑3
80 MHz to
2.5 GHz
[3]V
d = [2.33] √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 metres (m).
Guidance and manufacturer’s declaration – electromagnetic immunity
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment specified below. The customer or the user of the Aeroneb Go
should assure that it is used in such an environment.
Immunity
test
IEC/EN 60601 Compliance
Test level
level
Electromagnetic environment –
guidance
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 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.
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 Aeroneb Go is used
exceeds the applicable RF compliance level above, the Aeroneb Go should
be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as re-orientating or relocating
the Aeroneb Go nebulizer system.
Over the frequency range 150 kHz to 80 MHz, field strengths should be less
than [3]V/m
b
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Aerogen Limited,
Galway Business Park,
Dangan,
Galway,
Ireland.
www.aerogen.com
Ph: +353 91 540400
©2013 Aerogen Limited
AG-AG4120-EN Rev D 2013
Manufacturing no.: 30-553 Rev D
0050
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