Nanosonics Trophon EPR User manual

trophon®EPR User Manual –N00020 L00034 1.0 03/2014 1
trophon®EPR
User Manual
ENGLISH

trophon®EPR User Manual –N00020 L00034 1.0 03/2014 2
This manual must be read prior to operating the trophon®EPR to ensure correct
procedures are followed and the specified disinfection results are achieved.
All technical specifications and system approvals are found in Appendix I of this
manual.
©2014 Nanosonics Limited. All rights reserved.
The written and graphic product descriptions in this manual are correct at the time
of printing.
trophon®and NanoNebulant®are registered trademarks of Nanosonics Limited.
Nanosonics’ technologies are protected by a combination of patents, trademarks,
and exclusive proprietary rights.
Your sales representative is:
Visit the Nanosonics website to obtain this user manual in other languages.
Conforming to MDD 93/42/EEC
FSZ 2009/05867 25/12/2009
Email:
Nanosonics Limited
Unit 24, 566 Gardeners Rd
Alexandria NSW 2015
Australia
Tel: [phone]
Fax: [phone]
[email protected].au
www.nanosonics.com.au
Nanosonics Europe GmbH
Falkenried 88,
House A, D-20251
Hamburg –Germany
Tel: [phone]
Fax: [phone]
www.nanosonics.eu
Russian Distributor: AVA Medica
Kondratyevskiy prospect
15/3 Office 344,
St Petersburg Russia
Tel: [phone]
Attach Business Card or information sticker/stamp here

trophon®EPR User Manual –N00020 L00034 1.0 03/2014 3
Table of Contents
PART A –INTRODUCTION AND INITIAL SETUP.......................................................... 4
SECTION A1: INTRODUCTION TO THE TROPHON EPR ...................................................4
SECTION A2: IMPORTANT WARNINGS, LABELS and SYMBOLS ....................................5
SECTION A3: OVERVIEW OF DEVICE FEATURES ............................................................8
SECTION A4: INSTALLATION GUIDE...............................................................................10
PART B –ROUTINE USE AND MAINTENANCE ......................................................... 14
SECTION B1: LOADING THE DISINFECTANT ..................................................................14
SECTION B2: ROUTINE HIGH LEVEL DISINFECTION CYCLE..........................................15
SECTION B3: PURGE CYCLE...........................................................................................19
SECTION B4: REMOVING and DISPOSING OF USED DISINFECTANT CARTRIDGES ..20
SECTION B5: INCOMPLETE OR FAILED CYCLES ...........................................................21
SECTION B6: ROUTINE CARE AND MAINTENANCE .....................................................23
SECTION B7: DISPOSAL OF DEVICE ..............................................................................23
PART C –TROUBLESHOOTING................................................................................. 24
PART D –TROPHON PRINTER (Accessory)............................................................. 26
SECTION D1: INTRODUCTION AND SETUP....................................................................26
SECTION D2: ROUTINE CARE AND MAINTENANCE.....................................................29
SECTION D3: TROPHON PRINTER TROUBLESHOOTING ...............................................30
SECTION D4: TROPHON PRINTER DISPOSAL.................................................................32
SECTION D5: REORDER INFORMATION ........................................................................32
SECTION D6: TROPHON PRINTER TECHNICAL SPECIFICATIONS ................................32
PART E –SERVICE AND WARRANTY........................................................................ 33
APPENDIX 1: TROPHON EPR TECHNICAL SPECIFICATIONS................................... 33
APPENDIX 2: PRODUCT WARRANTY AND REGISTRATION FORM.......................... 34

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PART A –INTRODUCTION AND INITIAL SETUP
SECTION A1: INTRODUCTION TO THE TROPHON EPR
For any operating, fault or maintenance queries, please contact your customer service
representative.
A1.1 Validated Probes
NOTE: Do NOT use the trophon EPR to disinfect non-approved devices or instruments.
Refer to www.nanosonics.eu/trophon-EPR/Brochures for a list of Validated Probes for use with
trophon EPR.
Refer to the original equipment manufacturers of the ultrasound equipment for their
recommendations and the most up-to-date list of validated disinfectants for use with their
probes.
A1.2 Training
It is the owner’s responsibility to ensure that all users:
Are trained as per the instructions contained in this manual to ensure safe operation.
Are aware of the potential hazards in dealing with the disinfectant and safety
procedures associated with the device.
Visit the Nanosonics website to complete the online training module and receive your
trophon EPR certification, before setting up or using your trophon EPR,
www.nanosonics.eu
A1.3 User and Environment Profile
NOTE: The following description is intended for general information only. For specific
operating instructions, please refer to the relevant sections of this manual.
The trophon EPR will be used in typical health care environments, under the control of health
professionals such as:
Sonographers
General Practitioners
Nurses
Radiographers
Specialist Doctors (e.g. cardiologists, obstetricians, gynaecologists, sonologists)
In locations such as:
Hospitals with centralised cleaning rooms
Hospitals without specific cleaning rooms
Radiology/Ultrasound sites with centralised cleaning rooms
General practices and specialised doctors rooms without cleaning rooms

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Intended Use:
The sole purpose of the trophon EPR is to high level disinfect validated ultrasound
probes (see section B2.1) according to the specified processes outlined in this manual.
It is not intended for any other use. Do NOT use this device for any application other
than its expressed purpose.
The trophon EPR together with the NanoNebulant is a high-level instrument grade
disinfectant system.
The trophon EPR is NOT intended to reprocess single use devices
The trophon EPR is NOT intended to pre-clean ultrasound probes
The cable management system is an accessory designed for use with the trophon EPR
(see section A4.2)
Chemical Indicator use is required with every disinfection cycle. More information can
be found in the Chemical Indicator Instructions for use, provided with the Chemical
Indicator.
The trophon Printer, trophon Connect, trophon Wall Mount and the trophon Cart are
accessories designed for use with the trophon EPR; contact your customer service
representative or visit the Nanosonics website for additional information. Refer to Part D
for information on the trophon Printer.
Disinfection Process:
At the beginning of the cycle, the trophon EPR creates an aerosol of concentrated
hydrogen peroxide. This is quickly and evenly distributed over the surface of the probe,
including very small crevices. This process provides thorough, high level disinfection of the
shaft and the handle of the probe. The device breaks down the hydrogen peroxide into
small amounts of water and oxygen and safely vents them into the external environment.
Notes:
1) NanoNebulant is the product name of the trophon Disinfectant.
2) The contact conditions are fixed cycle parameters that are not able to be modified by the
end user.
SECTION A2: IMPORTANT WARNINGS, LABELS and SYMBOLS
Failure to read the following sections may result in damage to the trophon EPR, disinfectant
cartridges or other equipment, or cause serious injury to the operator or other persons. If the
device is used in a manner not specified by the manufacturer, the protection provided by
the device may be impaired.
A2.1 Warnings
Hot Temperatures
Risk of burns from the hot surfaces in the internal chamber. Do NOT touch these
surfaces. A hot surface symbol is located inside the trophon EPR chamber as a
reminder.
Failure to correctly load the probe into the chamber may result in damage to the
probe. Probe must NOT come into contact with the chamber wall. Refer to section
B2.3 for correct positioning of probe.

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Malfunctions
Do NOT attempt to open the chamber door during a cycle or in the event of a power
failure or system malfunction (see section B5.1).
All repairs must be carried out by trained personnel ONLY. Do NOT attempt to repair or
modify any part of the device. The trophon EPR contains no end user serviceable parts.
Transporting the Device
The device weighs approximately 17kg (38lb). Use safe lifting techniques as per your
Occupational Health and Safety Lifting Guidelines for your institution.
Do not move, relocate or transport the device if hydrogen peroxide is present; purge
the device before moving or relocation (See section B3).
Electrical Device
Equipment must be connected to an earthed power outlet. Ensure power cable
supplied with the device is used.
Spilled fluid can result in electrical shock. Do not allow any fluid to spill onto or around
the device or immerse any parts of the trophon EPR in liquid.
Connect the device only to an electrical source with the proper voltage and
frequency as specified in Appendix 1. If incorrect voltage is used, the device may be
damaged when it is switched on.
Attempting to open any component of the device to gain access to the internal
mechanics may result in electrical shock.
trophon Chemical Indicator
ONLY to be used with the trophon EPR. Do NOT use with non-approved devices.
Use one Chemical Indicator with every trophon EPR cycle.
Do NOT use damaged and/or out-of-date indicators.
Ensure indicator is red and not exposed before use.
More information can be found in the Chemical Indicator Instructions for Use, provided
with the Chemical Indicator.
trophon NanoNebulant
Read the Instructions for Use (IFU) leaflet enclosed with the trophon NanoNebulant and
the Material Safety Data Sheet (MSDS) enclosed with the device.
Always wear disposable gloves when handling disinfectant cartridges and running the
trophon EPR device.
Ensure appropriate personal protective equipment (PPE) is worn during spills
(according to the Occupational Health and Safety Guidelines for your institution and
NanoNebulant MSDS).

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A2.2 Labels and Symbols
Caution
Corrosive
Consult instructions for use
Warning
Start (of action)
Single Use Only
Fragile / Handle With Care
Warning: Hot
Surface
Do not disassemble
Dangerous
Voltage
Separate collection for
electrical and electronic
equipment
Keep Dry
Keep Out of Direct Sunlight
Expires
(year and month)
Batch Number
Product Number
Cannot be transported by air
freight
This Way Up
UN 2014
Wear Gloves
when handling
cartridges
Probe Guide

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SECTION A3: OVERVIEW OF DEVICE FEATURES
A3.1 Front Panel and Back Panel
Figure 1
Front Closed
(Figure 1)
1. User screen: displays
messages and menu
2. Start button
3. Soft key buttons
4. Chamber door handle
Figure 2
Back
(Figure 2)
5. Adjustable Feet (for
levelling the device)
Note: Serial Number (SN)
can be located on the
back label

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A3.2 Chamber (Figure 3)
Figure 3
Chamber
(Figure 3)
6. Chamber door
(opened)
7. Probe in correct
position
8. Cable clamp
9. Gland seal
A3.3 Side Panels (Figure 4 & 5)
Figure 4
Left Side
(Figure 4)
10.Power switch
11.Power socket
12. Serial port (for
authorised personnel
only)
Note: Serial Number can
be located on the label
above the power socket

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Figure 5
Right Side
(Figure 5)
Do NOT force open the
cartridge door. Cartridge
door will automatically
open when required.
13. Cartridge door
14. Waste container
SECTION A4: INSTALLATION GUIDE
A4.1 Positioning the device
NOTE: Ensure the device is placed on a surface that can support the weight of the device
(see Appendix 1).
1. Ensure the area around the device is free from other equipment and clutter. Positioning
the trophon EPR as shown in Figure 6 will ensure access to all features including the
cartridge system and for disconnecting the device.
Figure 6
Distance on each side
of device:
A = 250mm (10 in)
B = 250mm (10 in)
(Figure 6 –not to scale)
2. Level the device by adjusting the back feet –turning feet clockwise or anti-clockwise
(see Figure 2). Ensure feet are present at all times, and are not loose.
NOTE: If the device needs to be relocated, see section B3.3 –Transportation

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A4.2 Cable Management System Installation
The Cable Management System is designed to facilitate ease of use of the trophon EPR by
holding the ultrasound cable away from the chamber door, and providing a convenient
location to store the cable during High Level Disinfection. Refer to section B2.3 for using the
Cable Management System.
To install the Cable Management System:
1. Open the chamber door before mounting the Cable Management System to the
device.
2. Peel back the protective strip from the double sided tape on the bottom of the Cable
Management System (see Figure 7)
3. Align and slide the two hooks on the front of the Cable Management System into the
slots in the device chamber (see Figure 8-1) until it cannot slide any further.
4. Push Cable Management System down on top of the device to secure it in place (see
Figure 8-2).
A4.3 Powering On
1. Attach the power cable supplied with the device to the device power socket.
Equipment must be connected to an earthed outlet.
2. Switch on at the mains power
3. Turn on the power switch, located on the side of the device to ‘ON’
Figure 7
Figure 8

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A4.4 Basic Settings
Date and Time
1. Press the soft key button underneath MENU on the screen
2. Using the soft key buttons under the LCD:
Scroll to SETUP using the buttons under the arrows and press OK
Scroll to SET DATE AND TIME using the buttons under the arrows
Set the date and time by using the button under NEXT to move through each set
point and the arrows to scroll to the desired date and time
Once each set point is set press OK
The screen will now revert back to the menu screen
To change date and time format select SETUP using the buttons under the arrows
and press OK
Scroll to CHANGE DATE FORMAT or CHANGE TIME FORMAT using the buttons under
the arrows
Press OK once complete
The screen will now revert back to the menu screen.
Language
1. Press the soft key button underneath MENU on the screen
2. Using the soft key buttons under the LCD:
Scroll to SETUP using the buttons under the arrows and press OK
Scroll to LANGUAGE using the buttons under the arrows and press OK
Scroll to the desired language using the buttons under the arrows and press OK
The screen will now revert back to the menu screen
Alarm Settings
1. Press the soft key button underneath MENU on the screen
2. Using the soft key buttons under the LCD:
Scroll to SETUP using the buttons under the arrows and press OK
Scroll to ALARM SETTINGS using the buttons under the arrows and press OK
Set the alarm volume by pressing the up & down buttons to set the volume on high
or low. Press Ok to confirm selection.
Scroll to ALARM REPEAT using the buttons under the arrows and press OK
Set the alarm to repeat by pressing the up & down buttons to turn on or off the
alarm repeat. Press OK to confirm selection
If alarm repeat is enabled, the alarm will repeat every minute for the following
situations:
a. The probe is left in the device
b. Error message is displayed and requires a response

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A4.5 Warm-up Cycle
1. This cycle prepares the device for operation
2. The warm up will begin automatically
Screen Message
Approximate Warm Up Time
(minutes)
Quick Warm Up
< 2 minutes
Warming Up
2 –30 minutes
Extended Warm Up
> 30 minutes
3. During the warm up cycle some instructions may appear on the screen. Please follow
these instructions, which may include:
Close Chamber Door
Cartridge Empty. Replace Cartridge Now (Refer to section B1)
Remove Probe From Chamber
4. When completed, the screen message will read: LOAD PROBE AND INDICATOR
5. The machine is now ready for use
NOTE: It is recommended that the device remains switched on at all times to maximise the
life of the disinfectant cartridge, unless the machine needs to be moved.

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PART B –ROUTINE USE AND MAINTENANCE
SECTION B1: LOADING THE DISINFECTANT
B1.1 Disinfectant Specifications and Handling
Read the Instructions for Use (IFU) leaflet enclosed with the trophon NanoNebulant and the
Material Safety Data Sheet (MSDS) enclosed with the device.
Always wear disposable gloves when handling disinfectant cartridges.
WARNING: Failure to follow specifications and handling instructions may compromise the
effectiveness of the disinfection process and/or cause injury to the operator.
B1.2 Inserting the Disinfectant Cartridge
1. Cartridge door will automatically open when cartridge needs replacing. Do NOT
force the Cartridge Door open as this may damage and render the device non
functional.
2. Screen message: CARTRIDGE EMPTY. REPLACE CARTRIDGE NOW is displayed.
3. Press the button under OK to open the cartridge door.
4. Do NOT insert empty cartridges into the device.
NOTE: Always check the expiration date on the cartridge before use. If the cartridge has
expired, dispose of as per local environment and government regulatory requirements. Do
not attempt to open or load a damaged or distorted cartridge. Do not manually pierce the
cartridge.
Refer to IFU enclosed with the trophon NanoNebulant for detailed instructions on how to install
and/or replace trophon NanoNebulant cartridges
NOTE: Cartridges will last for approximately one month from date of installing, depending on
usage and whether the device has been switched off.
B1.3 Spillage of Disinfectant
Wear PPE appropriate for the spill (according to the Occupational Health and
Safety Guidelines for your institution and NanoNebulant MSDS).
Never return spills to original cartridges for re-use.
Contain and clean-up the spill by placing spill control materials over the entire spill
area.
B1.4 Customised Disinfectant Cartridges
Use ONLY the trophon NanoNebulant cartridges which are validated for use with
the trophon EPR
Each cartridge is to be used ONCE. Do NOT refill or reuse cartridges

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SECTION B2: ROUTINE HIGH LEVEL DISINFECTION CYCLE
The effectiveness of the device cannot be guaranteed if non-approved accessories are
used. Do NOT use the trophon EPR to disinfect non-approved devices or instruments.
B2.1 Validated Probes for use with trophon EPR
For details of probes that are able to be used in the trophon EPR refer to the following:
Nanosonics website www.nanosonics.eu
The manufacturer of ultrasound equipment for their recommendations and the most
up-to-date list of validated disinfectants for use with their probes
NOTE: Only validated probes should be placed in the trophon EPR. All probes referred to on
the Validated Probe List have been tested and validated according to the manufacturer’s
specifications.
B2.2 Preparing the Probe
The probe must be pre-cleaned and dried BEFORE the High-Level Disinfection process can
commence in the trophon EPR.
NOTE: Failure to clean and dry the probe may result in:
high-level disinfection will not be achieved during the trophon EPR disinfection cycle
residual disinfectant remaining on the probe
potential exposure to residual disinfectant, which may cause injury, when removing
probe; this may lead to temporary bleaching and/or irritation of the skin if no gloves
are worn
Refer to probe manufacturer’s instructions for correct cleaning process.
B2.3 Positioning the Probe
NOTE: Probe must be correctly inserted in the device for a high-level disinfection cycle to
occur.
1. When the device is ready, screen message: LOAD PROBE AND INDICATOR
2. Open chamber door
3. The probe is held securely in the chamber by the use of two clamps; refer to Figure
9(a).
The probe has a short sleeve at the back of the handle, covering the electrical cable.
This is referred to as the PROBE GLAND - Figure 9(a)
Wearing gloves, insert the Probe correctly as follows:
Press the probe’s electrical cable into the cable clamp (at the top of the chamber)
Hold the probe by its handle, press the top of the PROBE GLAND into the gland seal -
Figure 9(a), ensuring the top of the probe cable gland is above the gland seal -
Figure 9(b)
Ensure the probe is straight and not touching the walls or the bottom of the
chamber

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Figure 9
Figure 10
Figure 11

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4. Additionally the probe shall be suspended with the tip located no lower than the line
across the chamber (see Figures 10 & 11)
5. If a cable management system has been installed on your device, (see section A4.2),
secure the external portion of the cable and connector by:
Placing the connector carefully inside the tray
Coiling the cable neatly and safely around the cable holder on the side of the tray
assembly.
NOTE: Incorrect positioning of the probe may result in:
High-level disinfection will not be achieved during the trophon EPR disinfection cycle
Residual disinfectant remaining on the probe surface. This may lead to temporary
bleaching and/ or irritation of the skin if no gloves are worn.
Damage to the probe may occur if in contact with the chamber wall
NOTE: Curved Probes must be correctly inserted in the device. Refer to Figure 12 for incorrect
and correct positioning of probe.
Figure 12

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B2.4 Inserting the Chemical Indicator
A Chemical Indicator must be used for each disinfection cycle and can only be used once.
After correctly loading the probe into the chamber, a chemical indicator shall be placed
into the holder. Refer to the Chemical Indicator Instructions For Use (IFU).
B2.5 Closing the Chamber Door
The door will automatically lock at the start of a high-level disinfection cycle.
If the door is not properly closed, screen message: CLOSE CHAMBER DOOR
B2.6 Disinfecting the Probe
Screen message: IS THE PROBE CLEAN AND DRY?
YES
1. If the probe has been pre-cleaned and dried according to section B2.2 above, press
YES using the soft key button. The device will then check device readiness to perform a
disinfection cycle. Once ready screen message: PRESS START TO BEGIN
2. Press the START button to initiate the cycle or CANCEL using the soft key buttons to
unlock the machine and remove the probe
3. The progress of the disinfection cycle is indicated on the screen
4. Screen message: DISINFECTING
5. High Level Disinfection cycle will take 7 minutes to complete.
NO
1. If the probe has NOT been pre-cleaned and dried according to section B2.2, select NO
using the soft key button
2. Screen message: REMOVE AND CLEAN THE PROBE
3. Remove the probe and complete pre-clean as directed in section B2.2. Then follow
instructions from section B2.3.
NOTE: If mist is visibly escaping from the chamber, remain at a distance from the device until
completion of the operating cycle, and until the mist stops. Do not come into direct contact
with the mist. Contact your customer service representative (see Part C - Troubleshooting).
B2.7 Removing the Probe
It is important to wear clean gloves when handling probes before and after a disinfection
cycle.
1. When the cycle has been successfully completed, the device will sound an audible
alarm. Screen message: CYCLE COMPLETE REMOVE AND WIPE PROBE
NOTE: If the probe is not removed within 1 minute of the cycle being complete, the warm-up
time will increase for the subsequent cycle.
2. Wear new gloves. Remove the used Chemical Indicator from the device and compare
colour change against the chart on the Chemical Indicator carton (refer to the
Chemical Indicator IFU for further instructions).
3. Discard used Chemical Indicator
4. Remove the probe carefully using minimal contact after the cycle is complete. Avoid
touching the probe against the chamber’s hot surface

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5. Wipe the probe with an absorbent, single-use, dry, low lint cloth. Visually inspect the
probe and ensure any disinfectant residue is removed
6. Discard gloves
7. Close the chamber door
8. The probe is now ready for use or storage.
NOTE: After correct use, at the completion of a successful disinfection cycle, the Ultrasound
probe may have surface temperatures up to 450C. The probe will feel warm to touch and is
safe for handling and use.
B2.8 Sleep Mode and Shut Down Procedures
If the device is not used for 120 minutes or a probe has been left inside the device
for an extended amount of time, it will automatically enter sleep mode. To restart
the device from sleep mode press RESTART. The device will begin to warm up.
To obtain maximum use of disinfectant from each NanoNebulant cartridge, it is
advised the trophon EPR is left connected to power and switched ON at all times.
The device will automatically switch into sleep mode if it is not used for extended
periods in order to save power. Switching the system off for more than 24 hours will
result in reduced usage from each NanoNebulant cartridge.
SECTION B3: PURGE CYCLE
The purge cycle removes any remaining disinfectant from the cartridge and the inside of the
device and converts the NanoNebulant into oxygen and water. Oxygen is vented into the
atmosphere. Water is collected in the waste container inside the device (maximum capacity
150ml).
B3.1 Reasons for Running a Purge Cycle
1. A purge cycle is required when the device detects that the disinfectant has expired or
if an error has been detected by the device that cannot be rectified without a service
call.
2. An onscreen message will be displayed when your device requires purging.
To purge the liquid, press PURGE to initiate cycle using the soft key button and
proceed to section B3.2.
3. A purge cycle must be manually initiated before lifting or moving the device. To do
this:
Select MENU using the soft key button
Select PURGE.
Screen message: REMOVE ALL DISINFECTANT FROM SYSTEM
Select YES using the soft key button
Then proceed to section B3.2.
NOTE: Once the purge cycle has been commenced it may be paused for a period of time
but it cannot be cancelled. Do not switch the device off during purging as this will restart the
purge cycle.
B3.2 Running the Purge Cycle
NOTE: Always wear disposable gloves when handling the waste container.

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1. Ensure the empty waste container is fully inserted into the device
2. Purge cycle will commence automatically
NOTE: The device will not purge if the waste container is not present
3. The purge cycle will typically take 35 minutes (maximum of 100 minutes). Screen
message: PURGING
NOTE: Do NOT attempt to open the cartridge door during the purge cycle.
4. Purge cycle can be paused by pressing the soft key button under PAUSE. Screen
message: PURGE PAUSED
5. To continue the cycle, press the soft key button underneath RESUME
6. When purging is complete screen message: REMOVE AND EMPTY WASTE CONTAINER
7. Remove the waste container from the device and ensure it is empty
8. Screen message: LOAD WASTE CONTAINER
9. Screen message: CARTRIDGE EMPTY. REPLACE CARTRIDGE NOW
10.The empty cartridge can now be removed –proceed to section B4.
B3.3 Transporting the Device
Before transporting the trophon EPR, you must purge the disinfectant and switch off
the device at the power switch.
Do not move excessively or drag the device across the mounting surface.
Keep device upright at ALL times even during transportation. The device should only
be moved in an upright position.
SECTION B4: REMOVING and DISPOSING OF USED DISINFECTANT CARTRIDGES
IMPORTANT: Cartridges are punctured at the top and on the side near the bottom when the
cartridge door is closed and locked. A small amount of disinfectant may remain in the
cartridge, even when it has been fully used. Follow the instructions carefully to avoid injury.
B4.1 Removing the Cartridge
1. Wear gloves
2. Screen message: REPLACE THE CARTRIDGE AND CLOSE CARTRIDGE DOOR
NOTE: Cartridge door opens automatically. Do NOT force the cartridge door open.
3. Lift the cartridge out by touching the areas exposed while the bottle is in the holder
and avoid touching pierced area
4. Do NOT shake or change the orientation of the cartridge
5. Refer to IFU enclosed with the trophon NanoNebulant for detailed instructions on how
to install a new cartridge.
B4.2 Disposing of Empty Cartridge
Empty used cartridges should be disposed of in the nearest waste receptacle or according
to the disposal guidelines of your Institution.
NOTE: Do NOT insert empty cartridges into the device.