Defibtech DDU-2000 Series, DDU-2400, DDU-2300, DDU-2450 Operating Manual

Defibtech DDU-2000 Series
Automated External Defibrillator

• DDU-2300

• DDU-2400

• DDU-2450

AHA/ERC 2010

Operating Guide

ELECTRONIC

DISTRIBUTION

DAC-E25 30EN- BB

Notices

Defibtech, LLC 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 the examples are fictitious unless otherwise noted.

For more detailed information regarding the Defibtech DDU-2000 Series AED, please
refer to the User Manual on the Defibtech User CD.

Limited Warranty

The “Limited Warranty” shipped with Defibtech AED products serves as the sole
and exclusive warranty provided by Defibtech, LLC, with respect to the products
contained herein.

Copyright

Copyright © 2013 Defibtech, LLC

All rights reserved. Copyright questions should be directed to Defibtech. For contact
information, refer to the “Contacts” section of this guide.

Contents

Quick Use Instructions ....................................................................... 4

When To Use ....................................................................................... 5

Diagram Of Components ................................................................... 6

Setting Up The AED ............................................................................ 8

Using The AED ...................................................................................10

Using The AED - ECG Display Monitor (DDU-2400 & DDU-2450 only) .... 14

Using The AED - Manual Mode (DDU-2400 only) ................................ 15

Checking AED Status ....................................................................... 16

Routine Maintenance ........................................................................17

The Defibrillation Pads ......................................................................18

The Battery Pack ................................................................................19

Dangers, Warnings, And Cautions ................................................... 20

Technical Specifications ................................................................... 22

Warranty Information ....................................................................... 24

Contacts ............................................................................................ 25

This DDU-2000 Series Operating Guide

is to be used for quick reference.

For comprehensive information go to the

User Manual on the Defibtech User CD.

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QUICK USE INSTRUCTIONS WHEN TO USE

PRESS “ON”

BUTTON

1

APPLY PADS

FOLLOW AED

INSTRUCTIONS

2

IF INSTRUCTED,

PRESS “SHOCK”

BUTTON

3

WHEN TO USE THE AED (INDICATIONS)

The DDU-2000 Series Semi-Automatic External Defibrillator (AED) is indicated for
use on victims of sudden cardiac arrest (SCA) who are:

• Unconscious and unresponsive

• Not breathing

For patients under 8 years old or less than 55 pounds (25kg), use child/infant
electrode pads. Do not delay therapy to determine exact age or weight.

WHEN NOT TO USE THE AED

The AED should not be used if the patient shows any of the following signs:

• Conscious and/or responsive

• Breathing

• Has a detectable pulse

OPERATOR TRAINING REQUIREMENTS

In order to safely and effectively operate the AED, a person shall have met the
following requirements:

• AED and/or debrillation 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 this

User Manual.

Manual Mode (DDU-2400) is intended for use only by qualified medical personnel
trained in advanced life support skills and ECG recognition who want to deliver a
shock independent of AED Mode.

ECG Monitor Mode (DDU-2400 and DDU-2450 only) is intended to be used by
personnel trained in basic life and/or advanced life support, or other physician-

authorized emergency medical training. Users should be trained in ECG

recognition to allow for rhythm and heart rate monitoring using standard ECG
monitoring electrodes.

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For more detailed information, refer to the User Manual (on Defibtech User CD).

DIAGRAM OF COMPONENTS

LL LA

RA

LA

LL

Unit Serial Number

Display Screen –

Displays video,
text prompts
and information

SHOCK Button –
Enabled/disabled by
software to allow the
user to discharge a
shock to the patient

Speaker

ON/OFF Button –

Turns AED on and off

FRONT OF AED

Active Status Indicator (ASI) –

Indicates the current status of the AED

Pads Connector Socket –
Socket for pads connector

Softkey Buttons

(Top, Center, Bottom) –

Buttons used to navigate

menus or select options

USB Port

Defibtech

Data Card

(DDC Card)

(Optional)

USB and Defibtech

Data Card (DDC Card)

Access Door – Access to the

USB connector port and

Defibtech Data Card slot

Battery Pack Opening

Battery Pack

Eject Release Latch

Pad Storage Area

Pads Connector

ECG Monitoring Adapter

(Optional; DDU-2400/2450 only)

BACK OF AED

LL

LA

XX

RA

XX

XX

Defibtech DDU-2000 Series
Automated External Defibrillator

•DDU-2300

•DDU-2400

•DDU-2450

Defibrillation Pads

Expiration Date

(on back of package)

Battery Pack

Serial Number

Battery Pack

Expiration Date

BATTERY PACK

Operating Guide

OPERATING GUIDE

BOOKLET

Quick Reference

Defibrillation

Pads

DEFIBTECH USER CD

Comprehensive User Manual

can be found on the CD

DEFIBRILLATION

PADS PACKAGE

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For more detailed information, refer to the User Manual (on Defibtech User CD).

7

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.

CONNECT

THE PADS TO

THE AED

1

Ensure that the pads package has not expired.

Expired pads must not be used.

For more information refer to page 18 of this guide.

INSTALL THE

BATTERY PACK

CHECK THE

STAT U S

3

READ THE

USER MANUAL

(CD)

AED status OK

Battery status
Expires 01/2017
Pads status Adult
Expires 06/2017
AED S/N 099999999
Battery S/N 099999999
Software version V2.1

AED Status screen

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.

For more information refer to page 16 of this guide.

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”.

2

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 19 of this guide.

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4

Comprehensive information about the

DDU-2000 Series AED is found in the
User Manual (on Defibtech User CD).

For more detailed information, refer to the User Manual (on Defibtech User CD).

USING THE AED

Turn the unit ON and then follow

the voice and display 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.

TURN

AED ON

1

PREPARE

THE PATIENT

2

Press “ON” button

PREPARE

ELECTRODE

PADS

3

PLACE PADS

4

Tear open

pads package

ADULT

PATIENT

Peel pads

from blue liner

CHILD/INFANT

PATIENT

OR

Remove clothing from patient’s chest.

If necessary, dry chest and remove excess chest hair.

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For more detailed information, refer to the User Manual (on Defibtech User CD).

Apply pads to patient’s

bare chest as shown

USING THE AED (continued)

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.

STAND CLEAR

5

IF INSTRUCTED,

PRESS SHOCK

BUTTON

When instructed, do not touch the patient

PERFORM CPR

7

Follow instructions to perform CPR

CONTINUE

TO FOLLOW

INSTRUCTIONS

6

If instructed, press “SHOCK” button

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8

Continue to follow the voice

and display instructions

For more detailed information, refer to the User Manual (on Defibtech User CD).

USING THE AED - ECG DISPLAY MONITOR

(DDU-2400 AND DDU-2450 ONLY)

USING THE AED - MANUAL MODE

(DDU-2400 ONLY)

SELECTING ECG DISPLAY

The DDU-2400 and DDU-2450 allow 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.

USING THE 3-LEAD ECG MONITORING ADAPTER

The DDU-2400 and DDU-2450 allow
the user to perform 3-lead monitoring
using the optional ECG Monitoring
Adapter (DAC-2020/2021).

To enable ECG Monitor Mode, unplug
the defibrillation pads and plug the ECG
Monitoring Adapter into the pads connector
socket. The AED will automatically switch
to ECG Monitor Mode.

To perform a rescue, unplug the ECG
Monitoring Adapter and plug in the
defibrillation pads.

The ECG Display provides non-diagnostic ECG of the patient’s

!

WARNING

heart rhythm. It is not intended to provide diagnostic or ST
segment interpretation.

AED / Video Mode

Manual Mode

AED / ECG Mode

(with corresponding softkey buttons)

Mode of Operation

Mode of Operation screen

Monitoring

ECG Monitor Mode screen

The DDU-2400 AED provides a Manual Mode to override the AED features of the defibrillator.
Manual Mode provides operator-initiated analysis, charge, shock, and disarm functions and is
intended for use by qualified medical personnel trained in advanced life support skills and ECG
recognition who want to deliver a shock independent of AED Mode.

The DDU-2400 Manual Mode Charge feature is intended for use

!

WARNING

SELECTING MANUAL MODE

To select Manual Mode, 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 (middle button)
to select Manual Mode.

only by authorized operators who have been specically trained in

cardiac rhythm recognition and in manual defibrillation therapy.

Mode of Operation

AED / Video mode

Manual Mode

AED / ECG Mode

Mode of Operation screen

USING MANUAL MODE

While in Manual Mode, pressing the softkey as­sociated with the icons below allows the user to:

Energy Select: Select the desired
energy level (top button).

CHARGE: Initiates a charge
(middle button).

DISARM: Cancels a charge
(middle button after a charge
is initiated).

When charging is complete, press the ashing SHOCK button.

Manual Mode

Manual Override

Manual Mode screen

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For more detailed information, refer to the User Manual (on Defibtech User CD).

CHECKING AED STATUS ROUTINE MAINTENANCE

ACTIVE STATUS INDICATOR (ASI)

Visually check the Active Status Indicator (ASI) on a daily basis. The ASI should flash green.
If the ASI flashes red, is solid red, or if there is no flashing light, the unit requires service.
Anytime the ASI flashes red, the unit will also “beep” periodically to call attention to itself.

• 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 the“Troubleshooting” section of the

Active
Status

Indicator

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 informa­tion 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
be displayed for a short period of time.

If the unit does not turn on at all, check to
make sure a good battery pack is installed.
(Refer to the “Troubleshooting” section of
the User Manual (on Defibtech User CD).

User Manual (on Defibtech User CD) or call Defibtech for service.

• No Flashing Light: The DDU-2000 Series AED needs immediate

service. Refer to the “Troubleshooting” section of the User
Manual (on Defibtech User CD) or call Defibtech for service.

AED status OK

Battery status
Expires 01/2017
Pads status Adult
Expires 06/2017
AED S/N 099999999
Battery S/N 099999999
Software version V2.1

AED Status screen

Although the DDU-2000 Series AED is designed to be very low maintenance, simple maintenance
tasks must be performed by the owner/operator on a regular basis to ensure the unit’s dependability.

Daily Monthly After Each Use Action

• • •

• •

•

•

•

•

If the unit needs attention, refer to the “Troubleshooting” section of the User Manual
(on Defibtech User CD) or call Defibtech for service. For contact information, refer to the
“Contacts” section of this guide.

MAINTENANCE MODE

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).
To exit Maintenance Mode, simply turn the unit off
by pressing the ON/OFF button. For comprehensive
information about Maintenance Mode, refer to
Chapter 8 of the User Manual (on Defibtech User CD).

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

AED Main Menu

Rescue now

AED status

AED maintenance

AED options

Rescue options

Help topics

Turn AED off

The display screen during

Maintenance Mode

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For more detailed information, refer to the User Manual (on Defibtech User CD).

THE DEFIBRILLATION PADS

THE BATTERY PACK

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 can then 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 pack­age, 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

ADULT PADS CHILD/INFANT PADS

HOW TO INSERT AND
REMOVE THE BATTERY PACK

Before inserting the battery pack into the DDU­2000 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. (The battery pack
must be removed from the unit for more than
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.

For adults and children 8

years or older or over

55 pounds (25kgs), use

adult pads

For infants and children under 8 years

or less than 55 pounds (25kgs), use child/

infant pads (Note: child/infant pads can be

identified by their blue connector

and blue pads package)

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. The expiration date is printed on
the outside of the sealed package. Do not use pads past their expiration date. Discard
expired pads. Use only Defibtech defibrillation pads.

You may also check the status of the pads when the unit is off by pressing the center softkey
button to display the AED Status screen and enter Maintenance Mode.

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WHEN TO REPLACE THE BATTERY PACK

It is important to check the expiration date of the
battery pack. The expiration date is printed on
the label on 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 also check the status of the battery
pack when the unit is off by pressing the center
softkey button to display the AED Status Screen
and enter Maintenance Mode.

For more detailed information, refer to the User Manual (on Defibtech User CD).

Battery Pack

Expiration Date

DANGERS, WARNINGS, AND CAUTIONS

!

!

!

DANGERS:

Immediate hazards that will result in
serious personal injury or death.

• Hazardous electrical output. This equipment is for use

only by qualified personnel.

• Potential for explosion

not suitable for use in an oxygen-enriched atmosphere
or in the presence of a flammable anesthetic mixture
with air or nitrous oxide.

• The DDU-2000 Series AED has not been evaluated or

approved for use in hazardous locations as dened 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.

WARNINGS:

Conditions, hazards, or unsafe practices
that may result in serious personal injury
or death.

. The DDU-2000 Series AED is

• Improper use can cause injury. Use the DDU-2000

Series AED only as instructed in the User Manual. 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. The
AED contains no user serviceable parts – do not take
the unit apart.

• No modication 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 battery packs are not rechargeable. Any

attempt to recharge a lithium battery pack may result in
fire or explosion.

WARNINGS (continued)

• Do not immerse battery pack in water or other liquids.

Immersion in fluids may result in fire or explosion.

• Do not let uids 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 re or shock hazard.

• Do not sterilize the DDU-2000 Series AED or its

accessories.

• Use only Debtech disposable self-adhesive

defibrillation pads, battery packs, and other accessories

supplied by Debtech 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.

• Do not touch the patient during debrillation.

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 other electrical equipment from the patient
before defibrillation.

• Do not shock with debrillation pads touching each

other. Do not shock with gel surface exposed.

• Do not allow debrillation 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 debrillation 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.

• Disconnect all non-debrillator proof equipment from the

patient before defibrillation to prevent electrical shock

hazard and potential damage to that equipment.

WARNINGS (continued)

• 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.

• 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 debrillation, 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.

•

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.

•

The DDU-2400 Manual Mode Charge feature
can deliver dangerous energy when used
inappropriately; Manual Mode is intended for use

by authorized operators who have been specically

trained in cardiac rhythm recognition and in manual
defibrillation therapy.

WARNINGS (continued)

•

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.

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 debrillation pad label instructions. Use

defibrillation pads prior to their expiration date. Do not
re-use defibrillation pads. Discard defibrillation pads
after use (in the event of suspected pad malfunction,
return pads to Defibtech for testing).

• Recycle or dispose of lithium battery packs in

accordance with federal, state, and/or local laws.

To avoid re 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.

• Do not connect the DDU-2000 Series to a PC or other

device (using the USB port) while the unit’s electrodes
are still connected to the patient.

• Using non Debtech Data Cards (DDC cards) may

damage the unit and will void the warranty.

• 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.

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For more detailed information, refer to the User Manual (on Defibtech User CD).

TECHNICAL SPECIFICATIONS

OPERATING MODES

AED MODE (ALL MODELS)

High resolution video display

(animated instructions and CPR
coaching)

ECG MONITOR MODE
(DDU-2400&2450ONLY)

Displays ECG data and event
information (with 3-lead
electrodes)

DEFIBRILLATOR

TYPE
Semi-Automatic external
defibrillator

MODEL
DDU-2000 Series

WAVEFORM
Impedance Compensated
Biphasic Truncated
Exponential

RESCUE PROTOCOL
AHA/ERC 2010
Supports protocol
updates by the user
(password protected)

ENERGY*
AED Mode:

Adult: 150 Joules
Child/Infant: 50 Joules

Manual Mode:

Adult: User selectable
from 25-200 Joules
Child/Infant: User
selectable from
25-100 Joules
(50 Joules only when
using DDP-2002
attenuating pediatric
defibrillation pads)

PATIENT ANALYSIS SYSTEM

PATIENT ANALYSIS
Automatically evaluates patient impedance for proper

pad contact. Monitors signal quality and analyzes

patent ECG for shockable/non-shockable rhythms.

BATTERY PACKS

MODEL
DBP-2003 (standard),
DBP-2013
(aviation; TSO C-142a)

POWER
12VDC, 2800 mAh

TYPE
Lithium/Manganese
Dioxide Disposable,
recyclable, non­rechargeable

MANUAL MODE

(DDU-2400ONLY)
Displays ECG data and event infor­mation and defibrillation energy
selection from 25-200 Joules with
charge, shock and disarm control

CHARGE TIME
AED Mode:

4 seconds or less
(from shock advised)**

Manual Mode:

9 seconds or less
(150 Joules)***
12 seconds or less
(200 Joules)***

CONTROLS
Lighted ON/OFF button
Lighted Shock button

DISPLAY
High-resolution
color LCD

SENSITIVITY/SPECIFICITY

Meets AAMI-DF-80 specications and AHA

recommendations.

CAPACITY*
125 shocks or 8 hours
continuous operation

STANDBY LIFE*
4 years

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.

*Nominal into 50 ohm load
**Typical, new battery, at 25°C
***Typical, new battery depleted
by 6 shocks, at 25°C

LOW BATTERY
INDICATIONS

Visible
Audible

*Typical, new battery, at 25°C

DEFIBRILLATION / MONITORING PADS

MODEL
Adult – DDP-2001
Child/Infant –
DDP-2002 and DDP-2003

SURFACE AREA
Adult – 77cm2 (nominal, each pad)
Child/Infant –
50cm2 (nominal, each pad)

EVENT DOCUMENTATION

INTERNAL EVENT RECORD
Critical ECG segments and rescue
event parameters are recorded
(greater than 60 minutes) 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).

ENVIRONMENTAL

TEMPERATURE
Operating: 0 to 50°C
(32 to 122°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

CRUSH TEST
1,000 pounds (450kg)

SEALING/WATER
RESISTANCE

IEC 60529 class IP55;
Dust protected, Protected against
water jets (battery pack installed)

TYPE
Pre-connected, single-use,
non-polarized, disposable,
self-adhesive electrodes
with cable and connector

ECG and event storage on a
removable data card. Actual length
of storage is dependent on card
capacity.

USB PORT
Event download and maintenance
operations.

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

AIRCRAFT
Meets RTCA/DO-160G,
Section 21, RF Radiated
Emissions, Category M

SELF-TESTS

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)

PHYSICAL

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)

0197

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Specifications subject to change without notice

WARRANTY INFORMATION CONTACTS

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 LI MITATIONS

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 Debtech, LLC;

specified maintenance is not performed; the defibrillator is used

with one, or more, unauthorized accessories; the associated
accessories are used with an unauthorized debrillator; or

the defibrillator or associated accessories are not used in
accordance with Defibtech, LLC approved instructions.

*Applicable to defibrillators and associ ated accessories

having a date of manufacture on or after January 1, 2013. For
all others, refer to warranty informatio n in effect at the time
of manufacture.

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DAC-E25 30EN- BB DAC-E25 30EN- BB

EXC LUS IVE RE ME DY

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.

Manufacturer

Defibtech, L.L.C.
741 Boston Post Road
Guilford, CT 06437 USA

Patents pending.

This product and its accessories are manufactured and sold under one or more of the
following United States patents: D523,393, D548,346, D551,628.

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.

NOTES

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DAC-E25 30EN- BB