Areoneb Nebulizer PDF

Instruction Manual
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Aeroneb Professional
Nebulizer System
Instruction Manual
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Table of contents
Introduction ............................................................................. 1
System description............................................................. 2
Warnings ............................................................................ 4
Warnings ............................................................................ 5
Electromagnetic susceptibility ............................................ 6
Warnings ............................................................................ 7
Symbols ............................................................................. 8
Warranty........................................................................... 12
Life of Product .................................................................. 12
Assembly and Installation ..................................................... 13
Recharging the Battery .................................................... 15
Installation for use with a ventilator.................................. 16
Installation for use with a mask ........................................ 20
Installation for use with a mouthpiece.............................. 22
Adding medication ........................................................... 23
Nebulization .......................................................................... 25
Functional test ....................................................................... 27
Cleaning, disinfection and sterilization .................................. 28
Troubleshooting .................................................................... 33
Order numbers ...................................................................... 36
Specifications ........................................................................ 38
Physical ............................................................................ 38
Environmental .................................................................. 38
Performance .................................................................... 39
Appendix 1 EMC Tables ....................................................... 41
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Aeroneb Professional Nebulizer System Instruction Manual i
List of Figures
Figure 1: Aeroneb Pro ............................................................. 2
Figure 2: Aeroneb Pro controls and indicators...................... 10
Figure 3: Connecting nebulizer unit to T-piece ..................... 13
Figure 4: Connecting control module and nebulizer unit ...... 14
Figure 5: Connecting the AC/DC adapter ............................. 15
Figure 6: Connecting to an adult breathing circuit ................ 17
Figure 7: Connecting to a pediatric breathing circuit ............ 17
Figure 8: Connecting to a neonatal breathing circuit ............ 17
Figure 9: Alternative neonatal breathing circuit
using neonate T-piece.......................................... 18
Figure 10: Control module and universal mounting bracket
(vertical)................................................................ 18
Figure 11: Control module and universal mounting bracket
(horizontal) ........................................................... 19
Figure 12: Equipment mount adapter ................................... 19
Figure 13: Connecting to a mask .......................................... 21
Figure 14: Connecting to a mouthpiece ................................ 22
Figure 15: Filling the nebulizer unit with
a pre-filled ampoule .............................................. 23
Figure 16: Maximum fill indication point ................................ 24
Figure 17: Starting and stopping nebulization....................... 26
List of Tables
Table 1: Aeroneb Pro symbols ................................................ 8
Table 2: Aeroneb Pro controls and indicators ....................... 11
Table 3: Aeroneb Pro troubleshooting .................................. 33
Table 4: Aeroneb Pro parts list ............................................. 36
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ii Aeroneb Professional Nebulizer System Instruction Manual
Introduction
The Aeroneb® Professional Nebulizer System is a portable

medical device for multiple patient use that is intended to
aerosolize physician-prescribed medications for inhalation that
are approved for use with a general purpose nebulizer. This
device can be used by patients on and off mechanical
ventilation or other positive pressure breathing assistance.
Aeroneb® Pro is suitable for use by neonate, pediatric to adult
patients as described in this manual. It incorporates the
Aerogen® OnQTM Aerosol Generator.
Aeroneb® Pro is designed to operate in-line with standard
ventilator circuits and mechanical ventilators. It operates
without changing patient ventilator parameters and can be
refilled without interrupting ventilation.
The control module operates from the AC/DC adapter and can
be operated on its internal rechargeable battery for up to
45 minutes when fully charged. The product operates without
compressed gas, making it suitable for portable applications.
Indications for Use:

The Aeroneb® Professional Nebulizer System is a portable
medical device for multiple patient use that is intended to
aerosolize physician-prescribed solutions for inhalation
to patients on and off ventilation or other positive pressure
breathing assistance. The Aeroneb® Professional Nebulizer
System is suitable for use in adult, pediatric and neonate
patients.
®
Aeroneb Professional Nebulizer System Instruction Manual 1
System description
The Aeroneb Professional Nebulizer System (Figure 1)
includes the following components: nebulizer unit (Aerosol
Generator and filler cap), T-piece (adult) with plug, control
module, control module cable, AC/DC adapter, and mounting
brackets.
Filler Cap T-piece plug
1. Nebulizer unit with filler cap 2. T-piece (adult) with plug
3. Control module 4. Control Module Cable
5. AC/DC adapter 6. Universal mounting bracket
7. Equipment mount adapter
Figure 1: Aeroneb Pro
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2 Aeroneb Professional Nebulizer System Instruction Manual
1. The nebulizer unit holds up to 10 mL of liquid
medication. The nebulizer unit is translucent to allow
visual monitoring of medication levels and
aerosolization. When the nebulizer unit is connected
into the breathing circuit, the filler cap can be opened
or removed from the nebulizer unit without causing
loss of circuit pressure.
Within the nebulizer unit is an OnQTM Aerosol
Generator, which consists of a domed aperture plate
with precision-formed holes that control the size of the
aerosol droplets and a vibrational element that creates
micro-pumping action to aerosolize medication.
Gravity brings the medication in contact with the
aerosol generator; the liquid is then drawn through the
aperture plate and converted into an aerosol.
2. The T-piece securely connects the nebulizer unit into
the breathing circuit and can be easily removed for
cleaning. The T-piece connections are standard male
and female 22 mm ISO conical ports and connect to
standard patient breathing circuits.
3,4,5. The control module can operate from the AC/DC
adapter or the internal rechargeable battery. The
control module includes an On/Off power button and
sockets for the control module cable and the AC/DC
adapter. The control module also includes indicators
for nebulization cycle selection (15 or 30 minutes),
battery charge status and fault conditions.
6. A universal mounting bracket clamps the control
module to standard IV poles and medical rail systems.
7. An equipment mount adapter mounts the control
module on standard equipment mounts.
Pediatric T-piece, neonate adapters, mask adapter kits, elbow
connectors and mouthpiece are sold separately.
®
Warnings
Read and study all instructions before using Aeroneb Pro.
Only medical personnel should operate the device.
During use observe for correct functioning of the nebulizer by
regularly verifying aerosol is visible and no flashing indicator
lights.
Do not use a filter or heat-moisture exchanger (HME) between
the nebulizer and patient airway.
Do not attach a continuous supply of medication to the
nebulizer; the device operates in 15 or 30 minute cycles.
Clean, sterilize, assemble and perform a functional test
(page 27) according to the instructions in this manual before
first use and between patients.
Do not place the control module in an incubator during use.
To avoid exhaled medication affecting the ventilator, follow
ventilator manufacturer’s recommendations for use of a
bacterial filter in the expiratory limb of a breathing circuit.
To ensure optimum drug administration, consult the drug
manufacturer’s instructions regarding suitability for
nebulization.
Do not use in the presence of a flammable anesthetic mixture
combined with air or with oxygen or nitrous oxide.
Do not use to aerosolize alcohol-based medications, which
can ignite in oxygen-enriched air under high pressure.
To avoid the risk of fire, do not use in the presence of
flammable substances.
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Warnings
To avoid damage to the nebulizer:

 Prior to use, autoclave according to specified
directions and temperature given in the Cleaning,
disinfection and sterilization section of this
Instruction Manual only. Any deviation from
directions given in this Instruction Manual may
cause damage to the nebulizer unit and render
it inoperable.
 Do not apply undue pressure to the domed aperture
plate in the center of the nebulizer.
 Do not push out the OnQTM Aerosol Generator.
 Do not use a syringe with a needle to add
medication.
 Do not use abrasive or sharp tools to clean the
nebulizer unit.
Inspect all parts before use, and do not use if any parts are
missing, cracked or damaged. In case of missing parts,
malfunction or damage, contact your Aeroneb Pro nebulizer
system sales representative.
Disconnect nebulizer unit from control module before cleaning.
Do not immerse or autoclave the control module or AC/DC
adapter.
Disassemble all parts before autoclaving.
Use only with components specified by Aerogen.
Do not use or store outside of specified environmental
conditions.
To avoid mechanical or electrical damage, do not drop the
nebulizer unit or the control module.
®
Do not use in the presence of devices generating high
electromagnetic fields such as magnetic resonance imaging
(MRI) equipment.
The Aeroneb Pro control module contains a nickel metal
hydride (NiMH) rechargeable battery, which should be
disposed of in accordance with local governing restrictions at
the end of its useful life.
Electromagnetic susceptibility
This device meets the requirements of the Electromagnetic
Compatibility (EMC), pursuant to the Collateral Standard,
IEC/EN 60601-1-2 which addresses EMC in North America,
Europe and other global communities. 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. Follow institutional protocol regarding the use and
location of devices that could interfere with medical equipment
operation.
Note: This device is classified as Class II Type BF medical

electrical equipment and the device complies with specified
safety levels for electrical isolation and leakage current. The
Aeroneb Pro AC/DC adapter has no connection to earth
ground because the necessary level of protection is achieved
through the use of double insulation.
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Warnings
 Only use the Aeroneb Pro nebulizer with components

specified in the Instructions for Use. Use of the
Aeroneb Pro nebulizer with components other than
those specified in the Instructions for Use may result in
increased emissions or decreased immunity of the
Aeroneb Pro nebulizer system.
 Do not use the Aeroneb Pro 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 Pro 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
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Symbols
The following symbols apply to Aeroneb Pro and appear on
the back of the control module and on the packaging:
Table 1: Aeroneb Pro symbols
Symbol Meaning
Serial number, where YY is the year of

AP-YYXXXX
manufacture and XXXX is the serial number.
Attention, consult accompanying documents.
Degree of protection against dripping water.
Class II equipment per IEC/EN 60601-1.
Type BF equipment per IEC/EN 60601-1.
On/Off power button (standby).
Timer selection (to select the 15 minute or

30 minute nebulization cycles)
Control Module Input – DC voltage.
~ Control Module Output – AC voltage.
Output
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Table 1: Aeroneb Pro symbols
Symbol Meaning
Does not contain natural rubber latex.
Battery status indicator.
Fragile, handle with care.
+60C
Transient storage temperature limitations
-20C –20 C to +60 C.
Keep dry.
This device complies with the requirements

of the Medical Devices Directive
(93/42/EEC).
Consult Instructions for Use
Manufacturer
®
Controls and indicators
On/Off Power
Fault Indicator
Timer Selection
30 Min. Indicator
Battery Status
Indicator
15 Min. Indicator
9V D.C. Input
Control Module
Cable Input
Figure 2: Aeroneb Pro controls and indicators
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Table 2: Aeroneb Pro controls and indicators
Control/indicator Function
15 Min. indicator  Green (steadily lit) = 15 minute
nebulization cycle on
 Green (flashing) = Low battery power
 Nebulizer unit automatically powers
off after 15 minutes have elapsed
30 Min. indicator  Green (steadily lit) = 30 minute
nebulization cycle on
 Green (flashing) = Low battery power
 Nebulizer unit automatically powers
off after 30 minutes have elapsed
Fault indicator  Amber = Faulty electrical connection
On/Off power  Pressing and immediately releasing
button selects the 15 minute nebulization
cycle
 Pressing and holding for at least three
seconds selects the 30 minute
nebulization cycle
 Pressing during nebulization turns off
power to the nebulizer
Battery status  Green = Battery fully charged
indicator  Amber = Battery charging
 No light = Battery in operation
®
Warranty
The Aeroneb Pro nebulizer unit is warranted for one year from
date of purchase against defects in manufacturing. The
Aeroneb Pro Control Module and AC/DC Adapter are
warranted for a period of two years from the date of purchase
against defects in manufacturing. All warranties are based on
typical usage.
Life of Product
As with all active electronic components, the Aeroneb Pro

nebulizer unit has a defined life. In the case of the Aeroneb
Pro Controller, the life of the controller unit has been validated
for use for 1460 doses. This is based on a typical product
usage profile over a two year period, including four treatments
per day, 50% of the time.
The life of the Aeroneb Pro nebulizer and components have

been validated for use for 730 doses and 26 autoclave
treatments based on a typical one year usage profile of four
treatments per day and one sterilization per week, where the
device is assumed to be in service for 50% of the time.
The user should note that any use in excess of this may
result in reduced life of the product.
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Assembly and Installation
1. Clean and sterilize the nebulizer unit and T-piece(s) as
described in the Cleaning, disinfection and sterilization
section of this manual.
Note: The nebulizer unit and T-piece, as packaged, are not
sterile.
2. Perform a functional test of Aeroneb Pro before use and

between patients as described in the functional test
section of this manual.
3. Insert the filler cap into the opening on the nebulizer unit.
4. Connect the nebulizer unit to the T-piece by pushing the
nebulizer unit firmly onto the T-piece (Figure 3).
Figure 3: Connecting nebulizer unit to T-piece
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5. Connect the control module and the nebulizer unit
together using the control module cable (Figure 4).
Figure 4: Connecting control module and nebulizer unit
6. To operate on AC power (the primary mode of operation),

insert the AC/DC adapter connector into the control
module and plug the adapter into an AC power source
(Figure 5).
7. Aeroneb Pro can be battery-operated for portable
applications. The rechargeable battery can power the
System for up to 45 minutes when fully charged. In the
case of AC power failure the control module will
automatically switch to battery operation.
Note: Allow a minimum of four hours for the internal battery to
fully recharge.
Note: To ensure uninterrupted operation of Aeroneb Pro,
secure both the AC/DC adapter cable and the control module
cable so they cannot become disconnected during treatment.
If clips are available on patient circuits, run the cables through
the eyes of the clips. If clips are not available, ensure that all
cables are routed safely.
®
Figure 5: Connecting the AC/DC adapter
Recharging the Battery

To recharge the battery, connect the AC/DC adapter to the
control module and AC power (Figure 5). The battery status
indicator is amber while charging and green when fully
charged. Allow a minimum of four hours for the internal
battery to fully recharge.
Note: If the control module is placed in long-term storage, it is
recommended that the battery be recharged every 3 months.
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Installation for use with a ventilator
1. For adult breathing circuits, connect the nebulizer unit
with adult T-piece into the inspiratory limb of the breathing
circuit before the patient Y (Figure 6).
For pediatric breathing circuits, connect the nebulizer
unit with pediatric T-piece into the inspiratory limb of the
breathing circuit before the patient Y (Figure 7).
For neonatal breathing circuits, connect the nebulizer
unit with the pediatric T-piece and the neonate adapters
approximately 30cm (12 in.) back from the patient Y
(Figure 8). Alternatively connect the nebulizer with the
Neonate T-piece 30cm (12 in.) back from the patient Y
(Figure 9).
WARNING:
 Always maintain the nebulizer in a vertical orientation
(with the filler cap uppermost) while in the patient circuit
(Figures 6, 7, 8 and 9). This orientation prevents
condensate from blocking the nebulizer and ensures
proper nebulization. Always visually inspect the nebulizer
prior to placing in the ventilator circuit to assure that no
secretions are blocking the OnQTM Aerosol Generator.
 When removing the nebulizer unit from the patient circuit
always replace the T-piece plug to maintain circuit
pressure.
 Condensate can collect and occlude ventilator circuits.
Always position ventilator circuits so that fluid condensate
drains away from the patient.
 Always connect a bacteria filter to the expiratory inlet of
the ventilator. Otherwise the function of the expiratory
channel may be degraded.
®
Y
ADULT
From ventilator
Adult T-piece
Figure 6: Connecting to an adult breathing circuit
Y PEDIATRIC
From ventilator
Pediatric T-piece
Figure 7: Connecting to a pediatric breathing circuit
Neonate
adapters
Y
NEONATE
From ventilator
Pediatric T-piece
Figure 8: Connecting to a neonatal breathing circuit
®
From ventilator
Neonate T-Piece
Figure 9: Alternative neonatal breathing circuit

using neonate T-piece
2. Always perform a leak test of the breathing circuit after

inserting or removing the nebulizer unit. Follow ventilator
manufacturer instructions for performing a leak test.
3. Use the universal mounting bracket to attach the control
module to an IV pole or bed rail in either a vertical or
horizontal orientation (Figure 10 and Figure 11). Do not
over-tighten knob.
Where a standard equipment mount is available, use the
equipment mount adapter to support the control module
(Figure 12).
Figure 10: Control module and universal mounting

bracket (vertical)
®
Figure 11: Control module and universal mounting
bracket (horizontal)
Standard
equipment
mount
Figure 12: Equipment mount adapter
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Installation for use with a mask
Mask kits, which include a vented elbow and mask elbow, are
available separately (see Order numbers section). Contact
your Aeroneb Pro nebulizer system sales representative for
ordering information.
1. When using a mask, connect the vented elbow, mask
elbow and mask to the nebulizer unit by firmly pushing
the parts together.
2. Rotate the vented elbow to suit the position of the patient
(Figure 13).
CAUTION: To ensure proper nebulization, maintain the
nebulizer in a vertical orientation (Figure 13).
®
Facemask
Elbow
Vented Elbow
Patient Upright
Patient Reclined
Figure 13: Connecting to a mask
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Installation for use with a mouthpiece
Aeroneb Pro works with any standard ISO 22 mm nebulizer
mouthpiece inserted into the adult T-piece.
When using a mouthpiece, connect the nebulizer unit to the
T-piece as shown in Figure 3 in this manual, and then
connect the T-piece to the mouthpiece by pushing the parts
firmly together (Figure 14).
Figure 14: Connecting to a mouthpiece
CAUTION: To ensure proper nebulization, maintain the

nebulizer in a vertical orientation (Figure 14).
®
Adding medication
1. Open the filler cap tab on the nebulizer unit.
2. Use a pre-filled ampoule or syringe to add medication into
the filler port of the nebulizer (Figure 15).
3. Close the filler cap tab.
CAUTION: To avoid damage to the nebulizer unit, do not use
a syringe with needle.
The maximum capacity of the nebulizer unit is 10 mL. Do not
fill the nebulizer unit beyond the maximum fill indication point
(Figure 16). The underside of the filler cap represents
maximum fill indication point.
Figure 15: Filling the nebulizer unit with a pre-filled

ampoule
Note: Medication can also be added in this manner during

nebulization. This does not interrupt nebulization or
ventilation.
®
Max. fill
indication
point
Figure 16: Maximum fill indication point
®
Nebulization
For doses less than or equal to 3 mL.
1. To start a 15 minute nebulization cycle, add the
medication and press and release the blue On/Off power
button (Figure 17). The green 15 Min. indicator lights to
indicate that the 15 minute nebulization cycle is in
progress.
For doses greater than 3 mL.
2. To start a 30 minute nebulization cycle, add the
medication and press and hold the blue On/Off power
button for at least three seconds. The green 30 Min.
indicator lights to indicate that the 30 minute nebulization
cycle is in progress.
3. To stop the nebulizer at any time, press the On/Off power
button. The indicator turns off to indicate that nebulization
has stopped.
Note: When delivering a dose greater than 3 mL, select the

30 minute cycle.
®
On/Off Power Button
Press and release to
select 15 min
Press and hold for three
seconds to select 30 min.
30 Min. Indicator
15 Min. Indicator
Figure 17: Starting and stopping nebulization
®
Functional test
Perform a functional test of Aeroneb Pro prior to first use,
after each sterilization before each patient use or at any time
to verify proper operation. Follow these steps:
1. Visually inspect each part of the System for cracks or

damage and replace if any defects are visible.
2. Pour 1-5 mL of normal saline (0.9%) into the nebulizer
unit.
3. Connect the nebulizer unit to the control module using the
control module cable. Connect the control module to the
AC/DC adapter and plug the AC/DC adapter into an AC
power source.
4. Press and release the blue On/Off power button and
verify that the green 15 Min. indicator lights and that
aerosol is visible.
5. Press the On/Off power button again to turn the System
off. Press and hold the button for at least three seconds.
Verify that the green 30 Min. indicator lights and that
aerosol is visible.
6. Disconnect the control module from the AC/DC adapter
and verify that nebulization continues and that the battery
status indicator turns off.
7. Turn the System off and verify that the 15 Min. and
30 Min. indicators are off.
8. Discard any remaining liquid before patient use.
®
Cleaning, disinfection and
sterilization
This section describes how to clean, disinfect, sterilize and
inspect Aeroneb Pro system components. It is important that
Aeroneb Pro device components are cleaned and sterilized
prior to first patient use. The components are:
 Nebulizer unit (including filler cap)

 T-piece (including T-piece plug) for adult and
pediatric
 Neonate adapters
 Control module†, control module cable†, and
AC/DC adapter†
 Mounting bracket†
† Components not to be autoclaved.
CAUTION: Always clean, sterilize and disinfect in accordance

with current hospital protocols.
To avoid damage to the nebulizer:

 Autoclave according to specified directions and
temperature given in the “Cleaning, disinfection and
sterilization” section of this Instruction Manual only.
Any deviation from directions given in this Instruction
Manual may cause damage to the nebulizer unit and
render it inoperable.
 Do not apply undue pressure to the domed aperture
plate in the center of the nebulizer.
 Do not push out the OnQTM Aerosol Generator
®
Cleaning nebulizer unit, T-pieces and neonate adapters
1. Ensure there is no medication remaining in the device.
2. Remove nebulizer unit from T-piece. Remove filler cap
from nebulizer unit.
3. Clean all parts with warm water and mild liquid detergent
in accordance with current hospital protocols.
4. Rinse parts with sterile water.
5. Shake excess water from parts and allow parts to fully
air dry.
CAUTION: Do not use abrasive or sharp tools to clean the
nebulizer unit.
Disinfection of nebulizer unit, T-pieces and neonate
adapters
1. Follow steps 1 through 3 above.
2. Completely immerse parts in appropriate disinfecting
agent in accordance with current hospital protocols
and disinfectant agent manufacturer guidelines.
NOTE: Aerogen approves the following disinfection solutions

for use with its Aeroneb Pro Nebulization System regarding
material compatibility. With respect to microbiological
effectiveness, please ask the manufacturer. Refer to the
product labeling for specific instructions regarding activation,
safe use and disposal of these solutions.
 Isopropyl (70%)
 CIDEX®
 NU-CIDEX®
 CIDEX® OPA
 Hexanios G+R
®
Sterilization of nebulizer unit, T-pieces and neonate
adapters
1. Disconnect the nebulizer unit from the control module,
and then remove the nebulizer unit and adapters from the
ventilator circuit, mask or mouthpiece.
2. Disassemble the nebulizer unit and adapters into
individual components.
3. Remove the filler cap from the nebulizer unit
4. Clean all parts with warm water and mild liquid detergent
in accordance with current hospital protocols. Rinse
thoroughly and air dry.
5. Check for cracks or damage and replace if any defects
are visible.
6. Place the disassembled components into appropriate
sterilization wrapping.
CAUTION: Do not reassemble parts prior to autoclaving.
Sterilize components:
a. Steam sterilization can be performed using the
following three methods:
(i) autoclave wrapped parts using steam
sterilization pre-vacuum cycle, a minimum of
134C (270°F - 275°F) for 3.5 minutes with
drying cycle (134C wrapped cycle).
(ii) autoclave wrapped parts using steam
121C (250°F) for 20 minutes with drying cycle
(121C wrapped cycle).
(iii) autoclave wrapped parts using steam
134C (270°F - 275°F) for 20 minutes with
drying cycle (sometimes referred to as a
“Prion cycle”).
®
NOTE: Sterilization using the long autoclave cycle ((iii)
above) may cause some areas of the nebulizer to become
discolored. This is not indicative of the performance of the
nebulizer unit.
b. To sterilize with hydrogen peroxide gas plasma,

place wrapped parts in a STERRAD® System, and
use the long cycle.
CAUTION: Users should refer to the product labelling for the

STERRAD® 100S Sterilization System for specific instructions
regarding its proper operation.
Prior to next use:
(i) Check for cracks or damage and replace if any

defects are visible.
(ii) Perform a functional test as described in this
manual.
Cleaning of mounting brackets

Wipe clean with a damp cloth and mild liquid detergent. Do
not use abrasive or sharp tools.
®
Cleaning of control module, control module cable and
AC/DC adapter
1. Wipe clean with a soft cloth dampened with mild
detergent and water.
2. Check for exposed wiring, damaged connectors, or other
defects and replace if any are visible.
3. Visually inspect for damage and replace the control
module if any damage is observed.
CAUTIONS:
Do not autoclave.
Do not use abrasive or sharp tools
Do not spray liquid directly onto the control module.
Do not immerse control module in liquid
Caution: The Aeroneb Pro nebulizer unit contains active

electronic components. Aerogen has validated the
methods of cleaning, disinfection and sterilization above.
The use of any other means of cleaning, disinfection or
sterilization has not been validated and is likely to reduce
the life of your nebulizer and will invalidate your warranty.
®
Troubleshooting
If these suggestions do not correct the problem, discontinue
use of any device that appears to be damaged or is not
operating properly and contact your local Aeroneb Pro
nebulizer system sales representative.
Table 3: Aeroneb Pro troubleshooting
If this happens: It could mean: Try this:

The 15 Min. or Battery power Recharge battery
30 Min. indicator is low. (see Recharging
flashes during the battery).
nebulization.
Battery will not It may be time to Contact your local
recharge. replace the Aeroneb Pro
Constant green battery. nebulizer system
light showing on sales
the battery status representative.
indicator and
flashing green
light on either the
15 Min. or
30 Min. indicator
light, when the
control module is
connected to the
AC/DC adapter.
Battery will not Rechargeable Contact your local
retain initial battery may need Aeroneb Pro sales
charge. to be replaced. representative.
®

The 15 Min. or No medication in Refill medication
30 Min. indicator nebulizer unit. through filler cap in
lights, but the nebulizer unit
aerosol is not (see Adding
visible. medication during
nebulization).
Nebulizer unit has Clean nebulizer unit
not been properly (see Cleaning and
cleaned. sterilization).
It may be time to See Warranty and
replace the End of Life.
nebulizer unit. Refer to Aeroneb
Pro parts list.
15 Min. or There is no power Verify that AC/DC
30 Min. indicator to the System. adapter is securely
does not light attached to control
when On/Off module.
power button is Rechargeable Recharge battery
pressed. battery is (see Recharging
depleted. the battery).
The fault The control Verify that control
indicator lights. module cable is module cable is
incorrectly correctly connected
connected, or to both the
electronics are nebulizer unit and
malfunctioning. the control module.
®

Longer than Rechargeable Recharge battery
expected battery is depleted. (see Recharging the
treatment time. battery).
e.g. 3ml of Normal Nebulizer unit has Clean nebulizer
Saline (0.9%) not been properly (see Cleaning and
should take no cleaned. sterilization).
longer than
15 minutes to It may be time to See Warranty and
nebulize replace the Life of product.
nebulizer unit. Refer to Aeroneb Pro
parts list.
Medication is left Nebulizer was not Ensure that nebulizer
in the nebulizer turned on or is connected to
unit after connected to power. power and turned on.
nebulization cycle. Rechargeable Recharge battery
battery is depleted. (see Recharging the
battery).
Nebulizer unit has Clean nebulizer
not been properly (see Cleaning and
cleaned. sterilization).
A 15 minute cycle Run an additional
was selected and a 15 minute cycle.
volume greater When delivering a
than 3mL was dose greater than 3
added to the mL select the
nebulizer unit. 30 minute cycle.
It may be time to See Warranty and
replace the Life of Product.
nebulizer unit. Refer to Aeroneb Pro
parts list.
Note: The rechargeable battery in the control module should

only be replaced by Aerogen authorized personnel: contact
your Aeroneb Pro nebulizer system sales representative.
®
Order numbers
Table 4 lists the Aeroneb Pro nebulizer system order
numbers (see Figure 1 for pictures)
Table 4: Aeroneb Pro parts list
Description Order number
Aeroneb Professional Nebulizer System AG-AP6000-XX*

Nebulizer unit with filler cap AG-AP1000
Silicone Plug (Pack of 5) AG-AP1005
Adult T-piece with silicone plug (Pack of 5)
AG-AP1010
22mm Female - 22mm Female Elbow - 22mm Male
Pediatric T-piece with silicone plug (Pack of 5)
AG-AP1020
15mm Male - 22mm Female Elbow -15mm Female
Neonate T-Piece with silicone plug (Pack of 5)
12mm Male - 22mm Female Elbow - 12mm Female AG-AP1035
Fits Fisher & Paykel Neonate breathing circuit
Neonate T-Piece with silicone plug (Pack of 5)
AG-AP1036
10mm Female – 22mm Female Elbow - 10mm Male
Pediatric T-Piece & Neonate Adapter Kit (Pack of 5)
 15mm Male - 22mm Female Elbow -15mm Female
 Silicone Plug AG-AP1015
 Adapters: 15mm Male, 10mm OD to 7.5mm OD
15mm Female, 10mm OD and 7.5mm ID
Neonate Adapter Kit (Pack of 5)
 15mm Male, 10mm OD to 7.5mm OD AG-AP1025
 15mm Female, 10mm OD and 7.5mm ID
Vented Elbow (Pack of 5) AG-AP1055
Mask Kit, US (Pack of 5 Kits)
AG-AP1065
 17mm Male - 22mm Male Elbow
®
 22mm Female - 22mm Female Vented Elbow
Mask Kit, International (Pack of 5 Kits)
 22mm female-22mm Male Elbow AG-AP1075
 22mm female-22mm Female Vented Elbow
Nebulizer Filler Cap (Pack of 5) AG-AP1030
AC/DC Adapter AG-AP1040-XX*
Control Module AG-AP1050-XX*
Control Module Cable AG-AP1085
Universal Mounting Bracket AG-AP1060
Equipment Mount Adapter AG-AP1070
Instruction Manual AG-AP1080-XX*
* consult your local representative for the order code extension
specific to your country and for pricing information
®
Specifications
Physical
Nebulizer unit dimensions: 45 mm H x 50 mm W x 50 mm D
(1.8 in. H x 2.0 in. W x 2.0 in. D)
Control module dimensions: 33 mm H x 75 mm W x 131 mm D
(1.3 in. H x 2.9 in. W x 5.2 in. D)
Control module cable: 1.8 m (5.9 ft.) long
AC/DC adapter cable: 2.1 m (6.7 ft.) long
Nebulizer unit weight: 25 g (0.9 oz.) nebulizer unit and filler cap
Control module weight: 230 g (8.1 oz.), including battery and cable
Nebulizer unit capacity: maximum 10 mL
Environmental
Operating:
Maintains specified performance at circuit pressures up to 90 cmH2O
and temperatures from 5°C (41°F) up to 45°C (113°F).
Atmospheric pressure: 450 to 1100 hPa.
Humidity: 15 to 95% relative humidity.
Noise level: < 35 dB measured at 0.3 m distance.
Storage and transport:

Transient temperature range: -20 to +60°C (-4 to +140°F).
Atmospheric pressure: 450 to 1100 hPa.
Humidity: 15 to 95% relative humidity.
®
Performance
Flow rate
>0.2 mL/min (Average:  0.4 mL/min).
Particle size:
Mass Median Aerodynamic Diameter (MMAD):
<3.0µm with a geometric Standard Deviation (≤2.2)
As per EN 13544-1, with a starting dose of 2mL:

Aerosol output rate: 0.24mL/min
Aerosol output: 1.08 mL emitted of 2.0 mL dose
Residual volume: < 0.1 mL for 3 mL dose
Performance may vary depending upon the type of drug and nebulizer
unit used. For additional information contact Aerogen or drug supplier.
The temperature of the medication will not rise more than 10°C (18°F)
above ambient temperature during normal use.
Representative particle size distribution for Albuterol as per EN 13544-1

is shown below:
100%
Cumulative undersize %
80%
60%
40%
20%
0%
0.1 1 10
Particle size (microns)
®
Power
Power source: can operate from AC/DC adapter (input 100 to 240 VAC
50 – 60 Hz, output 9 V) or internal rechargeable battery (4.8 V nominal
output).
Power consumption: < 6.5 Watts (charging),  2.0 Watts (nebulizing).
Patient isolation: control module circuitry provides 4 kilovolt (kV)

patient isolation and complies with IEC/ EN 60601-1.
®
Appendix 1
EMC Tables
®
Aeroneb Professional Nebulizer System Instruction Manual
The following Tables are provided in accordance with IEC/ EN
60601-1-2:
Guidance and manufacturer’s declaration –

electromagnetic emissions
The Aeroneb Pro nebulizer system is intended for use in the

electromagnetic environment specified below. The customer or the
user of the Aeroneb Pro nebulizer system should assure that it is used
in such an environment.
Emissions test Compliance Electromagnetic environment –

guidance
The Aeroneb Pro nebulizer

system uses RF energy only for
RF Emissions its internal function. Therefore,
Group 1 its RF emissions are very low
CISPR 11 and are not likely to cause any
interference in nearby
electronic equipment.
RF Emissions
Class B
CISPR 11
The Aeroneb Pro nebulizer
Harmonic system is suitable for use in all
emissions establishments, including
EN 61000-3-2 Not Applicable domestic establishments and
those directly connected to the
Voltage
public low voltage power supply
fluctuations /
network that supplies buildings
flicker
used for domestic purposes.
emissions
EN 61000-3-3 Not Applicable
®
Recommended separation distances between portable and
mobile RF communication equipment and the Aeroneb Pro

electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the Aeroneb Pro nebulizer
system can help prevent electromagnetic interference by maintaining a
minimum distance between port and mobile RF communications
equipment (transmitters) and the Aeroneb Pro nebulizer system as
recommended below, according to the maximum output power of the
communications equipment.
Rated maximum Separation distance according to frequency
output power of of transmitter
transmitter m
W 150 kHz to 80 MHz to 800 MHz to
80 MHz 800 MHz 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.
®
electromagnetic immunity

Immunity test IEC/EN Compliance Electromagnetic
60601 Test level environment –
level guidance
Electrostatic ±6 kV contact ±6 kV contact Floors should be

discharge wood, concrete or
(ESD) ceramic tile.
If floors are
EN 61000-4-2 ±8 kV air ±8 kV air covered with
synthetic material,
the relative
humidity should
be at least 30%.
Electrical fast ±2 kV for ±2 kV for Mains power

Transient/burst power supply power supply quality should be
lines lines that of a typical
commercial or
EN 61000-4-4 hospital
±1 kV for ±1 kV for
input/output input/output environment.
lines lines
Surge ±1 kV ±1 kV Mains power

differential differential quality should be
mode mode that of a typical
commercial or
EN 61000-4-5 ±2 kV ±2 kV hospital
common common environment.
mode mode
®
Voltage dips, <5 % Ut <5 % Ut Mains power
short (>95 % dip (>95 % dip quality should be
interruptions in Ut) in Ut) that of a typical
and voltage for 0.5 cycle for 0.5 cycle commercial or
variations on hospital
power supply environment.
input lines 40 % Ut 40 % Ut If the user of
(60 % dip (60 % dip the Aeroneb Pro
EN 61000-4-11 in Ut) in Ut) requires continued
for 5 cycles for 5 cycles operation during
power mains
interruption, it is
70 % Ut 70 % Ut
recommended
(30 % dip (30 % dip that the Aeroneb
in Ut) in Ut) Pro be powered
for 25 cycles for 25 cycles from an
uninterruptible
<5 % Ut <5 % Ut power supply
or battery.
(>95 % dip (>95 % dip
in Ut) in Ut)
for 5 sec for 5 sec
Power Power frequency

frequency magnetic fields
(50/60 Hz) should be at
Magnetic field levels
characteristic of
3 A/m 3 A/m
a typical location
EN 61000-4-8 in a typical
commercial or
hospital
environment.
Note: Ut is the a.c. mains voltage prior to application of the test level.
®
electromagnetic immunity

Immunity IEC/EN Compliance Electromagnetic

test 60601 level environment –
Test level guidance
Portable and mobile

RF communications
equipment should be
used no closer to any
part of the Aeroneb
Pro, including cables,
than the
recommended
separation distance
calculated from the
equation applicable
to the frequency of
the transmitter.
Recommended
Conducted RF 3 Vrms [3]V separation distance
EN 61000-4-6 150 kHz to d = [1.17] √P

80 MHz
d = [1.17] √P...
80MHz to 800MHz
Radiated RF 3 Vrms [3]V
EN 61000-4-3 80 MHz to d = [2.33] √P...

2.5 GHz 800MHz to 2.5GHz
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).
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 Pro nebulizer system is used exceeds
the applicable RF compliance level above, the Aeroneb Pro nebulizer
system 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 Pro nebulizer system.
b
Over the frequency range 150 kHz to 80 MHz, field strengths
should be less than [3]V/m
®
Manufacturer:
Aerogen Limited
Galway Business Park
Dangan
Galway
Ireland
Customer Service:
International:
Telephone: +353 91 540400
US:
Telephone: 1-866-4AEROGEN (1-866-423-7643)
www.aerogen.com
Part No. AG-AP1080-UK

Rev J © 2011 Aerogen Ltd
Manufacturing no.: 30-012 Rev J

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Instruction Manual

The Aeroneb® Professional Nebulizer System is a portable

Indications for Use:

Filler Cap T-piece plug

1. Nebulizer unit with filler cap 2. T-piece (adult) with plug

3. Control module 4. Control Module Cable

5. AC/DC adapter 6. Universal mounting bracket

7. Equipment mount adapter

Figure 1: Aeroneb Pro

To avoid damage to the nebulizer:

Note: This device is classified as Class II Type BF medical

 Only use the Aeroneb Pro nebulizer with components

Refer to appendix 1 for EMC tables as per IEC / EN 60601-1-2

Serial number, where YY is the year of

Attention, consult accompanying documents.

Degree of protection against dripping water.

Class II equipment per IEC/EN 60601-1.

Type BF equipment per IEC/EN 60601-1.

On/Off power button (standby).

Timer selection (to select the 15 minute or

Control Module Input – DC voltage.

~ Control Module Output – AC voltage.

Does not contain natural rubber latex.

Battery status indicator.

Fragile, handle with care.

This device complies with the requirements

Consult Instructions for Use

Figure 2: Aeroneb Pro controls and indicators

As with all active electronic components, the Aeroneb Pro

The life of the Aeroneb Pro nebulizer and components have

2. Perform a functional test of Aeroneb Pro before use and

Figure 3: Connecting nebulizer unit to T-piece

Figure 4: Connecting control module and nebulizer unit

6. To operate on AC power (the primary mode of operation),

Recharging the Battery

Figure 6: Connecting to an adult breathing circuit

Figure 7: Connecting to a pediatric breathing circuit

Figure 8: Connecting to a neonatal breathing circuit

Figure 9: Alternative neonatal breathing circuit

2. Always perform a leak test of the breathing circuit after

Figure 10: Control module and universal mounting

Figure 12: Equipment mount adapter

Figure 13: Connecting to a mask

Figure 14: Connecting to a mouthpiece

CAUTION: To ensure proper nebulization, maintain the

Figure 15: Filling the nebulizer unit with a pre-filled

Note: Medication can also be added in this manner during

Figure 16: Maximum fill indication point

Note: When delivering a dose greater than 3 mL, select the

Figure 17: Starting and stopping nebulization

1. Visually inspect each part of the System for cracks or

 Nebulizer unit (including filler cap)

CAUTION: Always clean, sterilize and disinfect in accordance

To avoid damage to the nebulizer:

NOTE: Aerogen approves the following disinfection solutions

CAUTION: Do not reassemble parts prior to autoclaving.

b. To sterilize with hydrogen peroxide gas plasma,

CAUTION: Users should refer to the product labelling for the

Prior to next use: