Defibtech DDU-2300 User manual

DAC-A2530EN-BK
Defibtech Automated External Defibrillator
• Lifeline/ReviveR VIEW DDU-2300
• Lifeline/ReviveR ECG DDU-2450
Operating Guide
For concise guidance on
set-up, use, maintenance
and technical specifications
ELECTRONIC
DISTRIBUTION

DAC-A2530EN-BK
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DAC-A2530EN-BK (Issued: 2018- 06-08)
This Operating Guide is to be used for concise guidance on set-up, use,
maintenance and technical specifications on DDU-2000 Series AEDs.
For comprehensive training on set-up, use and maintenance as well as complete
technical specifications, refer to the User Manual at www.defibtech.com
Contents
Quick Use Instructions...................................................................... 4
When to Use (Indications, Contraindications, Summary of Primary
Clinical Studies, Potential Adverse Effects of the Device on Health,
Operator Training Requirements) .......................................................... 5
Diagram of Components................................................................... 6
Setting Up the AED ........................................................................... 8
Using the AED...................................................................................10
Using the AED - ECG Display (DDU-2450 only)............................................ 14
The Defibrillation Pads.....................................................................15
The Battery Pack...............................................................................16
The Defibtech Data Card (optional) ....................................................17
Checking AED Status .......................................................................18
Maintenance......................................................................................19
Troubleshooting............................................................................... 22
Warnings and Cautions....................................................................24
Technical Specifications ................................................................. 26
Glossary of Symbols ....................................................................... 28
Warranty Information.......................................................................31
Contacts............................................................................................ 32
This manual applies to the following models and trade names
Trade Names Model Number
Lifeline/ReviveR VIEW DDU-2300
Lifeline/ReviveR ECG DDU-2450
The Lifeline/ReviveR VIEW is referred to as the DDU-2300 from this point forward in this manual.
The Lifeline/ReviveR ECG is referred to as the DDU-2450 from this point forward in this manual.
Statements that apply to all trade names/model numbers listed above are referred to in this manual
as “DDU-2000 Series.”
Notices
Defibtech, L.L.C. shall not be liable for errors contained herein or for incidental or consequential
damages in connection with the furnishing, performance, or use of this material. Information in
this document is subject to change without notice. Names and data used in any examples are
fictitious unless otherwise noted.
For more detailed information regarding the Defibtech DDU-2000 Series AED, please refer to the
User Manual at www.defibtech.com.
Limited Warranty
The “Limited Warranty” shipped with Defibtech AED products serves as the sole and exclusive
warranty provided by Defibtech, L.L.C. , with respect to the products contained herein.
Copyright
Copyright © 2018 Defibtech, L.L.C.
All rights reserved. Copyright questions should be directed to Defibtech. For contact information,
refer to the “Contacts” section of this guide.
Tracking
U.S.A. federal regulations require Defibtech to maintain records for each AED it distributes
(reference 21 CFR 821, Medical Device Tracking). These requirements also apply anytime there is
a change in the AED’s location, including if you move, sell, donate, give away, export or even throw
it away. We depend on AED owners/users to contact us when these things happen to ensure the
tracking information remains accurate in the event we need to share important product notices.
If your location is outside the U.S.A., we ask you share your information for exactly the same
reasons. To keep your information up to date, please visit www.defibtech.com/register.
Federal Law (USA) restricts this
device to sale by or on the order
of a physician.
!
CAUTION

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For more detailed information, refer to the User Manual (at www.defibtech.com).
QUICK USE INSTRUCTIONS WHEN TO USE
1
2
3
PRESS “ON”
BUTTON
APPLY PADS
FOLLOW AED
INSTRUCTIONS
INDICATIONS
Lifeline/ReviveR VIEW DDU-2300 and Lifeline/ReviveR ECG DDU-2450 Automated
External Defibrillators (AEDs) are indicated for use on victims of sudden cardiac
arrest (SCA) who are:
• Unconscious and unresponsive
• Not breathing or not breathing normally
Lifeline/ReviveR VIEW DDU-2300 and Lifeline/ReviveR ECG DDU-2450 AEDs
may be used with Defibtech adult defibrillation pads (model number DDP-2001).
For patients under 8 years old, or weighing less than 55 lbs (25 kg), use Defibtech
child/infant defibrillation pads (model number DDP-2002), if available.
CONTRAINDICATIONS
Lifeline/ReviveR VIEW DDU-2300 and Lifeline/ReviveR ECG DDU-2450 Automated
External Defibrillators (AEDs) should not be used if the victim is responsive
or conscious.
IMPORTANT
Do not delay therapy to determine exact age or weight. If pediatric pads are
not available, apply adult pads in the position as shown for a child/infant and
use the AED.
OPERATOR TRAINING REQUIREMENTS
In order to safely and effectively operate the DDU-2000 Series AED, a person
shall have met the following requirements:
• Defibtech DDU-2000 Series AED and/or defibrillation training as required
by local, state, provincial, or national regulations.
• Any additional training as required by the authorizing physician.
• Thorough knowledge and understanding of the material presented in the
User Manual (available for viewing/download at www.defibtech.com).
Refer to User Manual Section 9.1.7 for Summary of Primary Clinical Studies and
User Manual Section 9.1.8 for Potential Adverse Effects of the Device on Health.

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DIAGRAM OF COMPONENTS
OPERATING GUIDE
(For more detailed information,
refer to the User Manual
at www.defibtech.com)
Active Status Indicator (ASI) –
Indicates the current status of the AED
Softkey Buttons
(Top, Center, Bottom) –
Buttons used to navigate
menus or select options
Pads Connector Socket –
Socket for pads connector
USB and Defibtech
Data Card (DDC Card)
Access Door –Access to the
USB connector port and
Defibtech Data Card slot
Display Screen –
Displays video,
text prompts
and information
Speaker
Defibtech
Data Card
(DDC Card)
(Optional)
USB Port
FRONT OF AED
ON/OFF Button –
Turns AED on and off
SHOCK Button –
Flashes when a
shock is advised.
Pressing this button
will deliver a shock
when the button is
flashing.
DEFIBRILLATION
PADS PACKAGE
BATTERY PACK
BACK OF AED
Pads
Connector
Defibrillation Pads
Expiration Date
(on back of package)
Defibrillation Pads
(inside of package)
Battery Pack Opening Battery Pack
Eject Release
Latch
Pad Storage Area
Operating Guide
Defibtech Automated
External Defibrillator

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For more detailed information, refer to the User Manual (at www.defibtech.com).
SETTING UP THE AED
The DDU-2000 Series AED is designed to be stored in a “ready”
state so that few steps are required to begin using the AED.
1
2
CONNECT
THE PADS TO
THE AED
INSTALL THE
BATTERY PACK
Ensure that the pads package has not
expired. Expired pads must not be used.
For more information, refer to page 15.
Ensure that the battery pack has not expired.
Expired battery packs must not be used.
When the battery pack is installed, the AED will turn
on and run a battery pack test. Wait for the test to
complete and for the unit to turn off.
For more information, refer to page 16.
3
4
CHECK THE
STATUS
READ THE
USER MANUAL
(at www.defibtech.com)
For more information, refer to page 18.
With the AED off,
press and release the
CENTER softkey button.
Ensure that the AED
Status screen appears
and that the “AED
Status” is “OK”.
AND
When the AED is off, the
Active Status Indicator (ASI)
should flash green. If the ASI
flashes red, is solid red, or if
there is no flashing light, the
unit requires service.
Comprehensive information about the
DDU-2000 Series AED can be found in the
User Manual (at www.defibtech.com).
AED Status screen
AED status OK
Battery status
Expires 01/20xx
Pads status Adult
Expires 06/20xx
AED S/N 099999999
Battery S/N 099999999
Software version Vx.x

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For more detailed information, refer to the User Manual (at www.defibtech.com).
USING THE AED
1
2
TURN
AED ON
PREPARE
THE PATIENT
Press “ON/OFF” button to turn AED on.
Follow the voice and onscreen instructions.
(NOTE: To power off the AED at any time, press and
hold the ON/OFF button for approximately 2 seconds.)
Remove clothing from patient’s chest.
If necessary, dry chest and remove excess chest hair.
3
4
PREPARE
PADS
PLACE
PADS
Peel adhesive pads
from blue liner.
Tear open
pads package.
Apply pads to patient’s bare chest.
For more information, refer to page 15.
ADULT
PATIENT
CHILD/INFANT
PATIENT
OR
Note : When this Information Softkey Icon is present on the screen,
the user may press the corresponding softkey button for additional
information with video instruction. To exit, press the softkey button again.
If the patient is unconscious or unresponsive, and is
not breathing or not breathing normally, ensure emergency
medical assistance has been called and start using the AED.

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For more detailed information, refer to the User Manual (at www.defibtech.com).
USING THE AED (continued)
5
6
STAND CLEAR
IF INSTRUCTED,
PRESS SHOCK
BUTTON
When instructed, do not touch the patient.
If instructed, press “SHOCK” button.
7
8
PERFORM CPR
CONTINUE
TO FOLLOW
INSTRUCTIONS
Follow instructions to perform CPR, if needed.
Continue to follow the voice
and onscreen instructions.
Note : When this Information Softkey Icon is present on the screen,
the user may press the corresponding softkey button for additional
information with video instruction. To exit, press the softkey button again.

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For more detailed information, refer to the User Manual (at www.defibtech.com).
USING THE AED - ECG DISPLAY
( D D U - 2 4 5 0 O N LY )
THE DEFIBRILLATION PADS
HOW TO CONNECT THE PADS
Insert the connector end of the defibrillation pad cable into the pads
connector socket on the top-left corner of the DDU-2000 Series AED as
shown. Insert pads connector firmly until it is fully seated in the unit. The
connector will only fit in one way – if the connector does not fit, rotate the
connector before trying again.
The connected pads package should be stored in the pad storage area
on the back of the DDU-2000 Series AED (see diagram on page 7).
After connecting the pads connector to the unit, push the pads pack-
age, rounded end first, with the pictures on the package facing out, into the pad storage area.
When the pads package is fully inserted, press the pad cable into the groove in the back of the
unit to hold the cable in place and tuck any excess cable behind the pads package.
WHICH PADS TO USE
WHEN TO REPLACE THE PADS
The Defibtech defibrillation pads are intended for one time use only. The pads must be
replaced after each use or if the package has been damaged.
It is important to check the expiration date of the pads. Do not use pads past their expiration
date. Discard expired pads. Use only Defibtech defibrillation pads.
You may check the status of the pads when the unit is off by pressing the center softkey
button to display the AED Status screen.
The expiration date is also printed on the outside of the sealed package.
For adults and children
8 years or older or over
55 pounds (25 kg),
use adult pads
For infants and children under 8 years
or less than 55 pounds (25 kg), use child/
infant pads (Note: child/infant pads can be
identified by their blue connector
and blue pads package)
ADULT PADS CHILD/INFANT PADS
SELECTING ECG DISPLAY
The DDU-2450 allows the user to display
the patient ECG when the unit is being
used as an AED.
To select ECG display, press the
bottom softkey button next to
the Mode Select Icon (shown
at left) to bring up the Mode of
Operation screen (shown at right).
Press the corresponding softkey (bottom
button) to select AED / ECG Mode.
Mode of Operation screen
(with corresponding softkey buttons)
Mode of Operation
AED / Video Mode
AED / ECG Mode
ECG Display screen
Analyzing
!
WARNING
Possible misinterpretation of ECG data. The frequency
response of the LCD display is intended for basic ECG
rhythm identification; it does not provide the resolution
required for pacemaker pulse identification or accurate
measurements, such as QRS duration and ST segment
interpretation. For such purposes an ECG Monitor with
an appropriate frequency response should be used.

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For more detailed information, refer to the User Manual (at www.defibtech.com).
THE BATTERY PACK THE DEFIBTECH DATA CARD (OPTIONAL)
HOW TO INSERT AND REMOVE THE DEFIBTECH DATA CARD
The optional Defibtech Data Card (DDC card) is used to store event and audio information
collected by the AED. All DDU-2000 Series AEDs will operate without DDC cards and will still
store select event information internally. Information stored on the DDC card is retrievable
with a separate Defibtech PC-based software package. (Refer to the “DefibView” section of
the DDU-2000 Series User Manual available at www.defibtech.com.)
Before installing the DDC card, ensure the AED
is turned OFF. Locate the data card/USB port
access door on the right-hand side of the unit.
Open the data card/USB port access door by
slightly pushing and then sliding the door down
to release the latch. The door will spring open.
Insert the DDC card into the thin slot in the
side of the AED centered above the USB port
opening, notched end first, label side up, until it
clicks into place. The card should be flush with
the surface of the slot. If the card does not push
in all the way, it may have been inserted upside
down. In that case, remove the card, flip it over,
and try inserting it again.
To remove the DDC card, press the card as far as it will go and then release. Upon release,
the DDC card will be partially ejected and can be removed by pulling the DDC card the rest
of the way out.
Close the data card/USB port access door by closing and then pushing the door up until the
door latch engages.
!
CAUTION
Using non-Defibtech Data Cards (DDC cards) may damage
the unit and will void the warranty.
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HOW TO INSERT AND
REMOVE THE BATTERY PACK
Before inserting the battery pack into the DDU-
2000 Series AED, ensure that the battery pack
opening in the back of the AED is clean and clear
of any foreign objects. Insert the battery pack
into the opening in the back of the AED.
Push the pack all the way in until the latch clicks.
The battery pack will only fit in one way. If the
battery pack does not fit, rotate the battery pack
before trying again. Once fully inserted, the
battery pack surface should be flush with the
back of the AED. Within moments of insertion,
the DDU-2000 Series AED will turn on and run
a battery pack insertion test. When the test is
completed, the unit will report the status of the
battery pack and shut down. (Note: The battery
pack must have been removed from the unit for
at least 10 seconds for the battery pack self-test
to be performed automatically.)
To remove the battery pack, push the battery
pack eject release latch. After the battery pack
is partially ejected, pull the battery pack out.
WHEN TO REPLACE THE BATTERY PACK
It is important to check the expiration date of the
battery pack. The battery pack should be used
before the expiration date. When the battery
pack is low, the unit will indicate “battery low”
or “replace battery now” and the Active Status
Indicator will flash red. The battery pack should
be replaced immediately. Use only Defibtech
battery packs.
You may check the status of the battery pack
when the unit is off by pressing the center
softkey button to display the AED Status Screen.
The expiration date is also printed on the label on
the battery pack as shown at right.
Battery Pack Label
Located Here

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For more detailed information, refer to the User Manual (at www.defibtech.com).
MAINTENANCE
ROUTINE MAINTENANCE
The DDU-2000 Series AED is designed to be very low maintenance. Simple maintenance tasks
are recommended to be performed regularly to ensure its readiness (see sample maintenance
table below). Different maintenance intervals may be appropriate depending on the environ-
ment where the AED is deployed, and ultimately the maintenance program is at the discretion
of the emergency response program’s medical director.
Daily Monthly After Each Use Action
• • •
Check that the Active Status Indicator is flashing green
• • Check the condition of the unit and accessories
•Run manually-initiated self-test
•Replace pads
•Check pad and battery pack expiration dates
•Check the DDC card, if one was installed
Note: If the unit has been dropped, mishandled, or abused, a manually-initiated self-test
should be performed.
If the unit still requires attention after a manually-initiated self-test has been performed, refer
to “Troubleshooting” on page 22 or call Defibtech for service. For contact information, refer
to the “Contacts” section on page 32.
SAMPLE
SAMPLE
SAMPLE
SAMPLE
Check that the Active Status Indicator is flashing green
SAMPLE
Check that the Active Status Indicator is flashing green
Check the condition of the unit and accessories
SAMPLE
Check the condition of the unit and accessories
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
SAMPLE
Run manually-initiated self-test
SAMPLE
Run manually-initiated self-test
Replace pads
SAMPLE
Replace pads
Check pad and battery pack expiration dates
SAMPLE
Check pad and battery pack expiration dates
MAINTENANCE MODE (AED Main Menu)
Maintenance Mode permits the user to perform
maintenance-related actions, such as viewing
unit information, initiating unit self-tests, changing
unit parameters, downloading rescue data, and
upgrading software.
To enter Maintenance Mode, press
the bottom softkey button to the right
of the Tool Icon (shown at left) on the
AED Status screen (for instructions on
how to access the AED Status screen, see previous
page). The AED Main Menu will now be displayed,
as shown at right. If the AED is needed to perform a
rescue while in Maintenance Mode, navigate to and
select the “Rescue now” menu option.
AED Main Menu screen
(Maintenance Mode)
Rescue now
AED status
AED maintenance
AED options
Rescue options
Help topics
Turn AED off
AED Main Menu
CHECKING AED STATUS
• Flashing Green: The DDU-2000 Series AED is OFF and
ready for use.
• Solid Green: The DDU-2000 Series AED is ON and ready
for use.
• Flashing or Solid Red: The DDU-2000 Series AED needs
immediate service. Refer to“Troubleshooting” on page 22 or
call Defibtech for service.
• No Flashing Light: The DDU-2000 Series AED needs
immediate service. Refer to“Troubleshooting” on page 22 or
call Defibtech for service.
Active
Status
Indicator
ACTIVE STATUS INDICATOR (ASI)
The Active Status Indicator (ASI) should be visually checked on a regular basis to ensure that
the AED is ready for use. The ASI should flash green. If the ASI flashes red, is solid red, or if
there is no flashing light, the unit requires service. The unit will also “beep” periodically to
call attention to itself when the ASI is flashing red.
AED STATUS SCREEN
The AED Status screen is used to provide
a quick overview of the DDU-2000 Series
AED’s status and to display select informa-
tion without turning the unit on for a rescue.
With the AED off, press and release the
CENTER softkey button to display the AED
Status screen. The AED Status screen will
briefly be displayed.
If the unit does not turn on at all, check to
make sure a good battery pack is installed
(refer to “Troubleshooting” on page 22).
AED Status screen
AED status OK
Battery status
Expires 01/20xx
Pads status Adult
Expires 06/20xx
AED S/N 099999999
Battery S/N 099999999
Software version Vx.x

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For more detailed information, refer to the User Manual (at www.defibtech.com).
MAINTENANCE MODE (AED Maintenance)
The AED Maintenance screen allows the user to select
such options as AED tests, software upgrades, data
backups, and data card functions.
For detailed information about each of the functions
that can be accessed from this screen,
refer to the DDU-
2000 Series User Manual, which can be viewed at or
downloaded from www.defibtech.com.
MAINTENANCE MODE (Help Topics)
The Help Topics screen provides a list of available videos
that detail various aspects of using and maintaining the
DDU-2000 Series AED.
To exit Maintenance Mode, turn the unit off by pressing
the ON/OFF button or navigate to the AED Status Screen
by selecting the “Go to main menu” option and then
navigate to and select the “Turn AED off” option.
MAINTENANCE MODE (AED Options)
The AED Options screen allows the user to manually
configure AED options such as time, date, volume, and
audio recording.
For detailed information about each of the functions
that can be accessed from this screen,
refer to the
DDU-2000 Series User Manual, which can be viewed at
or downloaded from www.defibtech.com.
MAINTENANCE MODE (Rescue Options)
The Rescue Options screen allows the user to manually
configure rescue options such as rescue protocol and
CPR breathing. (Note: The “Default view” option is
only available on DDU-2450 units.)
For detailed information about the functions that can
be accessed from this screen,
refer to the DDU-2000
Series User Manual at www.defibtech.com.
Rescue now
Perform AED test
Upgrade AED
Transfer data to card
Format data card
Run application from card
Go to main menu
AED Maintenence
Rescue now
Preparing the patient
Analyzing and shocking
Performing CPR
Replacing the battery
Replacing the pads
Checking the AED status
Replacing the data card
Go to main menu
Help Topics
Rescue now
System time hh:mm:ss
System date yyyy mm dd
Volume level High
Audio recording Disabled
Status broadcast Disabled
Go to main menu
AED Options
Rescue now
CPR breathing Disabled
Rescue protocol AHA
Settings
1 / 2 / 30 / 50 / 100
Default view Video
Go to main menu
Rescue Options
CLEANING
After each use, clean the DDU-2000 Series AED of any dirt or contaminants on the case and
connector socket. The following are important guidelines to be adhered to when cleaning the
device:
• The battery pack should be installed when cleaning the DDU-2000 Series AED.
• Do not immerse the DDU-2000 Series AED in fluids or allow fluids to enter the unit.
• Do not spray cleaning solutions directly on the unit or its connectors.
• Do not use abrasive materials or strong solvents such as acetone or acetone based
cleaning agents.
• To wipe the DDU-2000 Series AED’s case clean, use a soft cloth dampened with one of
the following recommended cleaning agents:
– Soapy water
– Ammonia based cleaners
– Hydrogen peroxide
– Isopropyl alcohol (70 percent solution)
– Chlorine bleach (30 ml/liter water)
• Ensure that the connector socket is completely dry before reinstalling the pads cable.
After cleaning, allow the unit to completely dry. Before returning it to service, always
check the AED operational status (refer to “AED Status Screen” on page 18).
Please note that none of the items provided with the DDU-2000 Series AED (including the AED
itself) are sterile or require sterilization.
!
WARNING
Do not sterilize the DDU-2000 Series AED or its accessories.
MAINTENANCE (continued)

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For more detailed information, refer to the User Manual (at www.defibtech.com).
The following table lists the symptoms, the possible causes, and the possible corrective actions
for common problems. Refer to the User Manual (available at www.defibtech.com) for detailed
explanations on how to implement the corrective actions. If the unit continues to be non-
functional,
call Defibtech for service (refer to the “Contacts” section on page 32).
Symptom Possible Cause Corrective Action
Unit will not turn on
Battery pack not inserted Insert battery pack
Battery pack depleted or
needs servicing
Replace battery pack
or call for service
Unit needs servicing Call for service
Unit immediately turns off
Battery pack depleted Replace battery pack
Unit needs servicing Call for service
ASI flashes red and/or unit
makes periodic ”beep” sound
Unit needs servicing
Go to AED Status Screen by
pressing the CENTER softkey
button or call for service
Battery pack non-functional Replace battery pack
Defibrillation pads are not
pre-connected to unit
Connect defibrillation pads to
unit
Defibrillation pads or battery pack
expired Replace expired component
ASI does not flash at all
while the unit is in standby
(powered off)
Battery pack not inserted Insert battery pack
Battery pack is low or needs
servicing
Replace battery pack or call for
service
Unit needs servicing Call for service
“Power on test failed, service
code ‘xxxx’” prompt Unit needs servicing Record code number and call for service
“Battery test failed, service
code ‘xxxx’” prompt Battery pack needs servicing Record code number and call for service
“Service required” prompt Unit needs servicing Call for service
“Replace battery now” prompt Battery pack capacity is
critically low
Unit may not deliver a shock,
replace battery pack immediately
“Battery low” prompt Battery pack capacity is
getting low
Replace battery pack as soon as
possible
Display screen does not work
Battery pack depleted Replace battery pack
Battery pack not inserted properly
Make sure battery pack is
oriented correctly and fully
inserted
Unit needs servicing Call for service
TROUBLESHOOTING
Symptom Possible Cause Corrective Action
“Pads missing” prompt Pads not connected to unit
Make sure pads connector
is oriented correctly and fully
inserted into unit
“Plug in pads connector”
prompt
Pads connector not plugged in Plug in pads connector
Pads connector broken Replace pads
Unit’s connector broken Call for service
“Pads expired” prompt Pads are beyond expiration date
shown on pads package Replace pads
“Apply pads to patient’s bare
chest as shown” prompt
Pads not connected to patient Place pads on patient
Pads not making good connection
to patient Check pad connection to patient
Pads or pad cable damaged Replace pads
“Poor pad contact to patient”,
“Press pads firmly”, “Replace
pads”, “Non-rescue pads” or
“Warning” prompt
Dry pads Replace pads
Partial pad connection Check that pads are placed
securely on patient
Pads touching Separate pads and place
correctly on patient
Non-rescue pads (e.g. trainer
pads) connected while in AED
(rescue) mode
Replace non-rescue pads with
rescue pads
“Check pads” prompt Pads touching Separate pads and place
correctly on patient
“Stop motion” prompt Patient motion has been detected Stop patient motion
“Stop interference” prompt External interference
has been detected Stop external interference
“Analyzing interrupted” prompt Motion or interference detected Stop motion or interference
“Shock cancelled” prompt
Patient’s ECG rhythm changed No action necessary
Shock button not pressed
within 30 seconds
Press shock button
within 30 seconds
Low battery – insufficient to charge Replace battery pack
Bad pad to patient connection Check that pads are placed
securely on patient
Dry pads Replace pads
“Replace data card” prompt
DDC card is full Replace DDC card with a card
that is not full
DDC card has failed Replace DDC card

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For more detailed information, refer to the User Manual (at www.defibtech.com).
WARNINGS AND CAUTIONS
!
WARNINGS:
Immediate hazards that will result in
serious personal injury or death.
• Hazardous electrical output. This equipment is for use only by
qualified personnel.
• Possible fire or explosion. Do not use in the presence of
flammable gases or anesthetics. Use care when operating this
device close to oxygen sources (such as bag-valve-mask devices
or ventilator tubing). Turn off gas source or move source away
from patient during defibrillation, if necessary.
• The DDU-2000 Series AED has not been evaluated or approved
for use in hazardous locations as defined in the National Electric
Code standard. In compliance with IEC classification, the DDU-
2000 Series AED is not to be used in the presence of flammable
substance/air mixtures.
Conditions, hazards, or unsafe practices that
may result in serious personal injury or death.
• Not intended to be used in an environment with high-frequency
electrosurgical equipment.
• Improper use can cause injury. Use the DDU-2000 Series AED only
as instructed in the User Manual and Operating Guide. The DDU-
2000 Series AED delivers electrical energy that can potentially
cause death or injury if it is used or discharged improperly.
• Improper maintenance can cause the DDU-2000 Series AED
not to function. Maintain the DDU-2000 Series AED only as
described in the User Manual and Operating Guide. The AED
contains no user serviceable parts – do not take the unit apart.
• No modification of this equipment is allowed.
• Electrical Shock Hazard. Dangerous high voltages and currents
are present. Do not open unit, remove cover (or back), or attempt
repair. There are no user serviceable components in the DDU-
2000 Series AED. Refer servicing to qualified service personnel.
• Lithium metal battery packs are not rechargeable. Any attempt
to recharge a lithium metal battery pack may result in fire or
explosion. Do not attempt to recharge the primary battery pack.
• Do not immerse battery pack in water or other liquids. Immersion
in fluids may result in fire or explosion.
• Do not attempt to recharge, short-circuit, puncture, or deform
battery. Do not expose battery to temperatures above 50°C
(122°F). Remove battery when depleted.
• Do not let fluids get into the DDU-2000 Series AED. Avoid spilling
fluids on the AED or its accessories. Spilling fluids into the DDU-
2000 Series AED may damage it or cause a fire or shock hazard.
WARNINGS (continued)
• Do not sterilize the DDU-2000 Series AED or its accessories.
• Use only Defibtech disposable self-adhesive defibrillation pads,
battery packs, and other accessories supplied by Defibtech or its
authorized distributors. Substitution of non-Defibtech approved
accessories may cause the device to perform improperly.
• Do not open sealed pads package until pads are to be used.
The packaging should be opened only immediately prior to use,
otherwise the pads may dry out and become non-functional.
• Do not touch the patient during defibrillation. Defibrillation current
can cause operator or bystander injury.
• Do not allow pads to touch metal objects or equipment in
contact with the patient. Do not touch equipment connected to
the patient during defibrillation. Disconnect all non-defibrillator
proof equipment from the patient before defibrillation to prevent
electrical shock hazard and potential damage to that equipment.
• Do not shock with defibrillation pads touching each other. Do not
shock with gel surface exposed.
• Do not allow defibrillation pads to touch each other, or to touch
other ECG electrodes, lead wires, dressings, transdermal
patches, etc. Such contact can cause electrical arcing and patient
skin burns during defibrillation and may divert defibrillating energy
away from the heart.
• The defibrillation pads are intended for one time use only and
must be discarded after use. Reuse can lead to potential cross
infection, improper performance of the device, inadequate
delivery of therapy and/or injury to the patient or operator.
• Avoid contact between parts of the patient’s body and conductive
fluids such as water, gel, blood or saline, and metal objects,
which may provide unwanted pathways for defibrillating current.
• Do not connect the DDU-2000 Series AED to a PC or other
device (using the USB port) while the unit’s electrodes are still
connected to the patient.
• Aggressive or prolonged CPR to a patient with defibrillation pads
attached can cause damage to the pads. Replace the defibrillation
pads if they become damaged during use.
• Possible Radio Frequency (RF) interference from RF devices
such as cellular phones and two-way radios can cause improper
AED operation. Normally using a cell phone near the AED
should not cause a problem; however, a distance of 2 meters
(6 feet) between RF devices and the DDU-2000 Series AED is
recommended.
• CPR during analysis can cause incorrect or delayed diagnosis by
the patient analysis system.
• Do not place adult defibrillation pads in the anterior-posterior
(front-back) position. A shock or no shock decision may be
inappropriately advised. The DDU-2000 Series AED requires
that the adult defibrillation pads be placed in the anterior-anterior
(front-front) position.
WARNINGS (continued)
• Some very low amplitude or low frequency VF rhythms may not
be interpreted as shockable. Some very low amplitude or low
frequency VT rhythms may not be interpreted as shockable.
• Handling or transporting the patient in any way during ECG analysis
can cause incorrect or delayed diagnosis, especially if very low
amplitude or low frequency rhythms are present. If the patient is
being transported, stop vehicle before beginning ECG analysis.
• In patients with cardiac pacemakers, the DDU-2000 Series
AED may have reduced sensitivity and not detect all shockable
rhythms. If you know the patient has an implanted pacemaker, do
not place electrodes directly over an implanted device.
• During defibrillation, air pockets between the skin and
defibrillation pads can cause patient skin burns. To help
prevent air pockets, make sure self-adhesive defibrillation pads
completely adhere to the skin. Do not use dried out or expired
defibrillation pads.
• Defibrillation may cause skin burns around the defibrillation pads
area.
• User-initiated and automatic self-tests are designed to assess the
DDU-2000 Series AED’s readiness for use. However, no degree
of testing can assure performance or detect abuse, damage, or a
defect that occurred after the most recent test is completed.
• Use of damaged equipment or accessories may cause the device to
perform improperly and/or result in injury to the patient or operator.
• Possible misinterpretation of ECG data. The frequency response
of the LCD display is intended for basic ECG rhythm identification;
it does not provide the resolution required for pacemaker pulse
identification or accurate measurements, such as QRS duration
and ST segment interpretation. For such purposes an ECG
Monitor with an appropriate frequency response should be used.
• Follow voice prompts if the LCD screen becomes blank or
unreadable.
• It may be possible for the AED to not detect a shockable rhythm,
not deliver a shock to a shockable rhythm or not deliver the
intended energy during defibrillation.
• It may be possible that the AED recommends a shock for a
non-shockable rhythm, and if a shock is delivered, VF or cardiac
arrest may occur.
• Even if defibrillation occurs, the sudden cardiac arrest event may
not result in survival.
• Defibrillation may cause myocardial damage or post-shock
dysfunction.
• Therapy cannot be delivered while an AED software update is in
process.
• Do not turn off the AED or remove the battery pack or the update
data card until an AED software update process is complete
as these actions may render the AED incapable of delivering
therapy. If any of these interruptions occur, restart the update
procedure from the beginning.
WARNINGS (continued)
• While in demonstration mode, the AED cannot perform a rescue.
If at any time during the demonstration there is a need to perform
a rescue, press and hold the green on/off button for two seconds
to power off the AED. Then press the green on/off button to power
on the unit and begin a rescue protocol. The demonstration card
does not need to be removed in order to perform a rescue.
!
CAUTIONS:
Conditions, hazards, or unsafe practices that
may result in minor personal injury, damage to
the DDU-2000 Series AED, or loss of data.
• Follow all battery pack labeling instructions. Do not install battery
packs after the expiration date.
• Follow all defibrillation pad label instructions. Use defibrillation
pads prior to their expiration date.
• The defibrillation pads should not be in continuous contact with
the patient’s skin for more than 24 hours.
• Allergic dermatitis or a minor skin rash may result in patients that are
sensitive to the materials used for the defibrillation pads. Remove
the defibrillation pads from the patient as soon as practical.
• Recycle or dispose of lithium battery packs in accordance with
local, state, provincial, and/or national regulations.
To avoid fire and explosion hazard, do not burn or incinerate the
battery pack. Do not crush.
• Use and store the DDU-2000 Series AED only within the range of
environmental conditions specified in the technical specifications.
• If possible, disconnect the DDU-2000 Series AED from the patient
prior to use of other defibrillators.
• Using non-Defibtech Data Cards (DDC cards) may damage the
unit and will void the warranty.
• DefibView software is not intended for clinical use. Information
presented by DefibView should not be used for making clinical
decisions.
• Although the DDU-2000 Series AED is designed for a wide variety
of field use conditions, rough handling beyond specifications may
result in damage to the unit.
• Federal Law (USA) restricts this device to sale by or on the order
of a physician.

DAC-A2530EN-BK DAC-A2530EN-BK
26 27
For more detailed information, refer to the User Manual (at www.defibtech.com).
PATIENT ANALYSIS
Automatically evaluates patient impedance for proper
pad contact. Monitors signal quality and analyzes
patient ECG for shockable/non-shockable rhythms.
SENSITIVITY/SPECIFICITY
Meets IEC 60601-2-4 and AAMI DF80 specifications
and AHA recommendations.
PATIENT ANALYSIS SYSTEM
TYPE
Automated external defibrillator
MODEL
DDU-2000 Series
WAVEFORM
Impedance Compensated Biphasic
Truncated Exponential
RESCUE PROTOCOL
AHA/ERC (default);
Supports protocol updates by the
user (password protected)
ENERGY*
Adult: 150 Joules
Child/Infant: 50 Joules
CHARGE TIME
4 seconds or less
(from shock advised)**
CONTROLS
Lighted ON/OFF button
3 softkey buttons
Lighted Shock button
DISPLAY
High-resolution color LCD
VIDEO PROMPTS
Full motion video
On-screen text prompts
CPR COACHING
Video and voice coaching
On-demand video help
VOICE PROMPTS
Extensive voice prompts guide
user through operation of the unit.
DEFIBRILLATOR
*Nominal into 50 ohm load
**Typical, new battery, at 25°C
MODEL
DBP-2003 (standard),
DBP-2013
(aviation; TSO C-142a)
POWER
12VDC, 2800 mAh
TYPE
Lithium/Manganese
Dioxide Disposable,
recyclable,
non-rechargeable
CAPACITY*
125 shocks or 8 hours
continuous operation
STANDBY LIFE*
4 years
LOW BATTERY
INDICATIONS
Visible
Audible
BATTERY PACKS
*Typical, new battery, at 25°C
AED MODE (ALL MODELS)
High resolution video display
(animated instructions and CPR coaching)
ECG DISPLAY (DDU-2450 ONLY)
Displays ECG data and event information
OPERATING MODES
AUTOMATIC
Automatic daily, weekly, monthly
and quarterly circuitry tests
BATTERY INSERTION
System integrity test on battery
insertion
PAD PRESENCE
Pads preconnected tested daily
USER-INITIATED
Unit and battery pack system test
initiated by the user
STATUS INDICATION
Visual and audible indication
of unit status
STATUS SCREEN
Unit self-tests results
Pads and battery information
(status and expiration)
SELF-TESTS
TECHNICAL SPECIFICATIONS
(see User Manual for complete specifications)
Specifications subject to change without notice.
MODEL
Adult: DDP-2001
Child/Infant: DDP-2002
SURFACE AREA
Adult: 12 inches2(77cm2)
(nominal, each pad)
Child/Infant: 7.75 inches2(50cm2)
(nominal, each pad)
TYPE
Pre-connected, single-use,
non-polarized, disposable,
self-adhesive electrodes
with cable and connector
DEFIBRILLATION / MONITORING PADS
INTERNAL EVENT RECORD
Select ECG segments and rescue
event parameters are recorded
and can be downloaded to a
removable data card.
PC-BASED EVENT REVIEW
ECG with event tag display, and
audio playback when available.
REMOVABLE STORAGE
(optional)
Up to 30 hours of ECG and event
data storage (no audio option)
or up to 3 hours of audio (audio
option). ECG and event storage
on a removable data card. Actual
length of storage is dependent
on card capacity. Data card must
already be installed at the time
of event.
USB PORT
Event download and maintenance
operations.
EVENT DOCUMENTATION
TEMPERATURE
Operating: 0 to 50°C (32 to 122°F)
One Hour Operating Temperature
Limit (extreme cold)*: -20°C (-4°F)
Standby: 0 to 50°C (32 to 122°F)
RELATIVE HUMIDITY
Operating/Standby: 5%-95%
(non-condensing)
ALTITUDE
-500 to 15,000ft (-150 to 4500m)
per MIL-STD-810F 500.4
Procedure ll
VIBRATION
Ground (MIL-STD-810F 514.5
Category 20)
Helicopter (RTCA/DO-160D,
Section 8.8.2, Cat R. Zone 2,
Curve G)
Jet Aircraft (RTCA/DO-160D
Section 8. Cat H, Zone 2,
Curves B & R)
SHOCK/DROP ABUSE
TOLERANCE
MIL-STD-810F 516.5 Procedure IV
48 inches (1.2 meters), any edge,
corner, or surface, in standby
mode
SEALING/WATER
RESISTANCE
IEC 60529 class IP55;
Dust protected, Protected against
water jets (battery pack installed)
ESD
IEC 61000-4-2: (Open air up to
15kV or direct contact up to 8kV)
EMC (Emission)
CISPR 11 Group 1 Level B and
FCC Part 15
EMC (Immunity)
IEC 61000-4-3 and IEC 61000-4-8
EMC (Separation Distances)
DDU-2000 Series AEDs
are intended for use in an
electromagnetic environment in
which radiated RF disturbances
are controlled. The AED user can
help prevent electromagnetic
interference by maintaining a
minimum distance between
portable and mobile RF
communications equipment
(transmitters) and the AED.
Recommended separation
distances can be found in the
DDU-2000 Series User Manual
at www.defibtech.com.
AIRCRAFT
Meets RTCA /DO-160G,
Section 21, RF Radiated
Emissions, Category M
ENVIRONMENTAL
SIZE
7.3 x 9.5 x 2.3 inches
(18.5 x 24 x 5.8 cm)
WEIGHT
Less than 3 lbs (1.4kg)
(with battery)
PHYSICAL
0197
*From room temperature to
temperature extreme, one hour
duration, updated specification for
DDU-2000 Series AEDs running
software revision 2.4 or above.

DAC-A2530EN-BK DAC-A2530EN-BK
28 29
GLOSSARY OF SYMBOLS
Symbol Meaning
High voltage present.
SHOCK Button – Delivers defibrillation shock to the patient when the device is ready to
shock.
!
Caution, consult accompanying documents.
ON/OFF/DISARM Button –
• Turns the device ON when it is OFF.
• Turns the device OFF when it is ON.
XXXX
YYYY
Do not expose to high heat or open flame. Do not incinerate.
XXXX
YYYY
Recyclable.
XXXX
YYYY
Consult operating instructions.
Refer to instruction manual / booklet.
XXXX
YYYY
Do not damage or crush.
XXXX
YYYY
Follow proper disposal procedures.
Meets the requirements of the European Medical Device Directive.
Meets the requirements of the Radio Equipment and Telecommunications Directive,
1999/5/EC.
Symbol Meaning
Classified by TUV Rheinland of NA with respect to electric shock, fire, and mechanical
hazard only in accordance with UL 60601-1, CAN/CSA C22.2 No.601.1-M90, IEC 60601-1,
and IEC 60601-2-4. Conforms to UL Standard UL 60601-1. Certified to CAN/CSA Standard
C22.2 No. 601.1-M90.
EC REP
Authorized European Representative:
EMERGO EUROPE
Prinsessegracht 20
2514 AP The Hague
The Netherlands
XXXX
YYYY
Operational temperature limitation.
XXXX
YYYY
Use by yyyy-mm-dd.
XXXX
YYYY
Defibrillation proof - Can withstand the effects of an externally applied defibrillation
shock. Internally powered with defibrillator-proof BF-type patient applied parts
(per EN 60601-1).
XXXX
YYYY-MM-DD YYYY-MM-DD
Manufacturer.
XXXX
YYYY-MM-DD
YYYY-MM-DD
Date of manufacture.
XXXX
YYYY-MM-DD
YYYY-MM-DD
Manufacturer and date of manufacture.
XXXX
YYYY
Do not reuse.
XXXX
YYYY
For USA users only.
Federal Law (USA) restricts this device to sale by or on the order of a physician.
XXXX
YYYY
Catalogue number.

DAC-A2530EN-BK DAC-A2530EN-BK
30 31
GLOSSARY OF SYMBOLS (continued)
ORIGINAL END USER’S LIMITED WARRANTY*
COVERAGE
Defibtech, LLC provides a limited warranty that the defibrillator
and its associated accessories (e.g., batteries and pads),
whether purchased concurrently with the defibrillator as part
of a configuration or separately, shall be substantially free
from defects in material and workmanship. Defibtech’s limited
warranty shall only extend to the original end user, where
the original end user purchased the items from an authorized
Defibtech, LLC retailer. This limited warranty may not be assigned
or transferred. The terms of the limited warranty in effect as of
the date of original purchase shall apply to any warranty claims.
LENGTH OF WARRANTY
The defibrillator’s limited warranty is for a period of eight (8)
years from the date of purchase. The battery’s limited warranty
is for a period of four (4) years from the date of purchase, but
in no event shall the limited warranty period extend past the
date printed on the battery. Single use accessories (e.g., the
pads) shall have a limited warranty up to use or for a period
up to the expiration date, whichever is earlier. The limited
warranty for all other accessories is for a period of one (1) year
from the date of purchase, or to the expiration date, whichever
is earlier.
LIMITED WARRANTY LIMITATIONS
This limited warranty does not cover damage of any sort
resulting from, but not limited to, accidents, improper
storage, improper operation, alterations, unauthorized service,
tampering, abuse, neglect, fire, flood, war, or acts of God.
Additionally, this limited warranty does not cover damage of any
sort to the defibrillator or its associated accessories resulting
from the use of the defibrillator with unapproved accessories or
use of the accessories with unapproved medical devices. The
defibrillator and its associated accessories are not warranted
to be compatible with any other medical device.
LIMITED WARRANTY VOIDED
The limited warranty is immediately voided if: the defibrillator
or its associated accessories are serviced or repaired by any
entity, including persons, not authorized by Defibtech, LLC;
specified maintenance is not performed; the defibrillator is used
with one, or more, unauthorized accessories; the associated
accessories are used with an unauthorized defibrillator; or
the defibrillator or associated accessories are not used in
accordance with Defibtech, LLC approved instructions.
EXCLUSIVE REMEDY
At Defibtech, LLC’s sole discretion, Defibtech shall have the
option to repair, replace, or provide a credit. In the event
of replacement, Defibtech shall have the right at its sole
discretion to replace the item with a new, or refurbished, same
or similar item. Determination of a similar item shall be at
the sole discretion of Defibtech. In the case of replacement,
the replacement at a minimum shall reflect the prorated
time remaining for the item based on the remaining limited
warranty period. In the case of a credit, the credit shall be the
prorated value of the item based on the lower of the original
item cost of the same or similar item and the remaining limited
warranty period. In no event, shall the limited warranty period
of a replacement item extend past the limited warranty period
of the item it is replacing.
WARRANTY SERVICE
In order to obtain warranty service, contact the retailer from
whom the item was purchased, or Defibtech, LLC customer
service. In the event an item must be returned, a Return
Material Authorization (RMA) number is required. Items
returned without an RMA number will not be accepted. The
item shall be shipped at the original end user’s expense to a
destination specified by the retailer or Defibtech, LLC.
OBLIGATIONS AND WARRANTY LIMITS
THE FOREGOING LIMITED WARRANTY IS IN LIEU OF AND
SPECIFICALLY EXCLUDES AND REPLACES, TO THE DEGREE
PERMITTED BY APPLICABLE STATE LAW, ALL OTHER EXPRESS
OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED
TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND
FITNESS FOR A PARTICULAR PURPOSE.
NO PERSON (INCLUDING ANY AGENT, DEALER, OR
REPRESENTATIVE OF DEFIBTECH, LLC) IS AUTHORIZED TO
MAKE ANY REPRESENTATION OR WARRANTY CONCERNING
THE DEFIBRILLATOR OR ITS ASSOCIATED ACCESSORIES,
EXCEPT TO REFER TO THIS LIMITED WARRANTY.
THE EXCLUSIVE REMEDY WITH RESPECT TO ANY AND
ALL LOSSES OR DAMAGES RESULTING FROM ANY
CAUSE WHATSOEVER SHALL BE AS SPECIFIED ABOVE.
DEFIBTECH, LLC SHALL IN NO EVENT BE LIABLE FOR ANY
CONSEQUENTIAL OR INCIDENTAL DAMAGES OF ANY KIND,
INCLUDING, BUT NOT LIMITED TO, EXEMPLARY DAMAGES,
SPECIAL, PUNITIVE, COMMERCIAL LOSS FROM ANY
CAUSE, BUSINESS INTERRUPTION OF ANY NATURE, LOSS
OF PROFITS OR PERSONAL INJURY, EVEN IF DEFIBTECH,
LLC HAS BEEN ADVISED OF THE POSSIBILITIES OF SUCH
DAMAGES, HOWEVER OCCASIONED, WHETHER BY
NEGLIGENCE OR OTHERWISE, UNLESS APPLICABLE STATE
LAW DOES NOT ALLOW SUCH EXCLUSION OR LIMITATION.
WARRANTY INFORMATION
*Applicable to defibrillators and associated accessories
having a date of manufacture on or after January 1, 2013. For
all others, refer to warranty information in effect at the time
of manufacture.
Symbol Meaning
Keep dry.
Handle with care.
Transportation and storage requirements.
See environmental requirements on packaging.
LATEX Does not contain latex.
Lot number.
IP55 Dust protected; Protected against water jets.
Serial number.
Lithium manganese dioxide battery.
Lithium-ion battery.
Product is not sterile.
Defibrillation proof - Can withstand the effects of an externally applied defibrillation
shock. Internally powered with defibrillator-proof CF-type patient applied parts
(per EN 60601-1).

DAC-A2530EN-BK
32
CONTACTS
Manufacturer
Defibtech, L.L.C.
741 Boston Post Road, Suite 201
Guilford, CT 06437 USA
XXXX
YYYY YYYY
Tel.: [phone] (Toll-free within North America)
1-[phone]
Fax: [phone]
Email:
sales@defibtech.com (Sales)
reporting@defibtech.com (Medical Device Reporting)
service@defibtech.com (Service and Repair)
This product and its accessories are manufactured and sold under license to at least one or
more of the following United States patents: 5,591,213; 5,593,427; 5,601,612; 5,607,454;
5,611,815; 5,617,853; 5,620,470; 5,662,690; 5,735,879; 5,749,904; 5,749,905; 5,776,166;
5,800,460; 5,803,927; 5,836,978; 5,836,993; 5,879,374; 6,016,059; 6,047,212; 6,075,369;
6,438,415; 6,441,582.
For additional patent information, please see:
www.defibtech.com/patents