User Manual

DM7000
DEFIBRILLATOR MONITOR

M&B Electronic Instruments

M&B PART NUMBER DM7000PLUS-101-REVISION V3.4
 Contents
CONTENTS .......................................................................................................................................... I

1 PREFACE ................................................................................................................................... 1

1.1 MANUFACTURER............................................................................................................................. 1

1.2 USER'S RESPONSIBILITY .................................................................................................................... 1

1.3 MANUFACTURER'S RESPONSIBILITY..................................................................................................... 2

1.4 CONTACT AND TECHNICAL SUPPORT ................................................................................................... 2

1.5 DECLARATION OF CONFORMITY ......................................................................................................... 2

1.5.1 Declares that the CE-marketed product ........................................................................... 3

1.5.2 Applicable standards ........................................................................................................ 3

1.6 SYMBOLS ....................................................................................................................................... 4

1.7 ICONS ........................................................................................................................................... 7

2 SAFETY ...................................................................................................................................... 8

2.1 CONVENTIONS USED IN THE MANUAL ................................................................................................. 8

2.1.1 Warnings .......................................................................................................................... 8

2.1.2 Cautions ............................................................................................................................ 8

2.1.3 Notices .............................................................................................................................. 9

2.1.4 Voice prompts ................................................................................................................... 9

2.1.5 Safety information is organized in six groups: .................................................................. 9

2.2 GENERAL CAUTIONS AND NOTICES ................................................................................................... 10

2.2.1 Dropped or Damaged ..................................................................................................... 10

2.2.2 Ferromagnetic Equipment .............................................................................................. 10

2.2.3 Labels .............................................................................................................................. 10

2.2.4 Perormance..................................................................................................................... 10

2.2.5 Notices ............................................................................................................................ 10

2.2.6 Attention ......................................................................................................................... 11

2.3 PATIENT SAFETY ............................................................................................................................ 12

2.3.1 General ........................................................................................................................... 12

I
 2.3.2 Shock Hazard .................................................................................................................. 12

2.3.3 Burn ................................................................................................................................ 13

2.3.4 Electrical Energy ............................................................................................................. 13

2.3.5 ECG Miss Interpretation .................................................................................................. 14

2.4 DEFIBRILLATOR AND ELECTRODE PADS .............................................................................................. 15

2.4.1 Explosion ......................................................................................................................... 15

2.4.2 Electrical Shock or Fire Hazard........................................................................................ 15

2.4.3 Improper Device Performance ........................................................................................ 16

2.5 BATTERY...................................................................................................................................... 16

2.5.1 Battery Care .................................................................................................................... 16

2.5.2 Battery indication ........................................................................................................... 17

2.6 CARE AND STORAGE ...................................................................................................................... 18

2.6.1 Cleaning and Sterilization ............................................................................................... 18

2.6.2 Electrodes ....................................................................................................................... 18

2.6.3 Warning pacing pulse suppression ................................................................................. 19

2.6.4 Handles ........................................................................................................................... 19

2.6.5 Periodic self-test ............................................................................................................. 20

2.6.6 Disposal........................................................................................................................... 21

3 INTRODUCING THE DM7000 DEFIBRILLATOR MONITOR ......................................................... 21

3.1 INTENDED USE .............................................................................................................................. 21

3.1.1 Defibrillator Function ...................................................................................................... 21

3.1.2 Monitor function ............................................................................................................. 22

3.1.3 Indication ........................................................................................................................ 22

3.1.4 Qualified Operators ........................................................................................................ 23

3.1.5 Contraindications ............................................................................................................ 23

3.1.6 Duration of use or contact with the body ....................................................................... 23

3.1.7 Side effects/complications .............................................................................................. 23

3.2 OVERVIEW OF THE DM7000 DEFIBRILLATOR MONITOR....................................................................... 24

3.2.1 Overview ......................................................................................................................... 24

II
4 DEFIBRILLATION MODE ........................................................................................................... 32

4.1 AUTOMATIC DEFIBRILLATION (AED WITHOUT SPO2 MODULE) ............................................................. 32

4.1.1 System Settings ............................................................................................................... 32

4.1.2 Switching Gain ................................................................................................................ 33

5 MONITOR MODE .................................................................................................................... 44

5.1 MONITOR MODE 1 (WITHOUT SPO2/BP/CO2)................................................................................. 45

5.1.1 System Setup................................................................................................................... 45

6 PACER OPERATION ................................................................................................................. 87

6.1 PACER DETECTION......................................................................................................................... 88

6.2 PACER SETTINGS ........................................................................................................................... 88

7 MAINTAINING THE DM7000 ................................................................................................... 92

7.1 MAINTENANCE ............................................................................................................................. 92

7.1.1 The frequency of inspection ............................................................................................ 93

8 SPECIFICATION ...................................................................................................................... 100

8.1 GENERAL ................................................................................................................................... 100

9 GLOSSARY ............................................................................................................................. 117

III
1 Preface

This manual is intended to provide information for the proper operation of the
M&B DM7000.

Do not attempt to use this equipment without thoroughly reading and

understanding these instructions.

1.1 Manufacturer

Manufacturer Room 6319, Building 1, No.27, Yongwang Road, Daxing

Bioengineering and Medicine Industry Base, Zhongguancun
Science Park, Daxing District 102629 Beijing PEOPLE'S
REPUBLIC OF CHINA
Product Defibrillator Monitor
Name
Device Type DM7000

1.2 User's Responsibility

The user is required to be trained in basic monitoring, vital signs assessment

and emergency cardiac care. The user should be completely knowledgeable of
the information in the User Instruction Manual. As with all other electronic
patient care monitors，good clinical judgment should be used when operating
the M&B DM7000. User must save all shipping containers and packaging
materials. When shipping the DM7000 System and accessories for calibration,
service, or upgrades, the original shipping containers and packaging materials
must be used.

1
1.3 Manufacturer's Responsibility

M&B (Beijing M&B Electronic Instruments, Co., Ltd) is responsible for the
safety, reliability, and performance of the DM7000 Defibrillator Monitor, only
if the following conditions are met:
• Assembly operations, extensions, readjustments, modifications or
repairs are carried out by persons authorized by M&B.
• The electrical installation of the relevant room complies with the
appropriate requirements.
• The DM7000 equipment is used in accordance with the instructions for
use.
To ensure patient safety and proper operation, use only M&B authorized
parts and accessories.

1.4 Contact and Technical Support

Please contact M&B if you have any questions regarding this notice.
Telephone +86 10 6125 3803
Fax +86 10 6125 3794
Internet www.mbelec.com

E-mail market@mbelec.com

1.5 Declaration of Conformity

Manufacturer Beijing M&B Electronic Instruments, Co., Ltd

No. 27, Yongwang Road, Beijing Bioengineering and
Medicine, Industry Base, Huangcun Town, Daxing
District, 102600 Beijing, PEOPLE’S REPUBLIC OF CHINA

2
1.5.1 Declares that the CE-marketed product

Product Name: Defibrillator Monitor

Device Type: BF(Defibrillator) and CF(Monitor)

Model Number: DM7000
Accessories: See list in manual
Complies with Council Directive 93/42/EEC (Medical Device Directive) of June 14
1993 class IIb Annex II

1.5.2 Applicable standards

Num. serial numbers of the The names of the standards

standards
1 EN ISO13485:2016
2 EN ISO14971:2012
3 EN ISO 15223-1:2016
Medical devices — Quality management
systems — Requirements for regulatory
purposes
Medical devices - Application of risk
management to medical devices
Symbols for use in the labelling of medical
devices

4 EN1041:2008 +A1 2013 Medical devices - Information supplied by

5 EN
60601-1:2006/A1:2013
6 EN 60601-1-2:2015
manufacturer
Medical electrical equipment -- Part 1: General
requirements for basic safety and essential
performance
Medical electrical equipment - Part 1-2: General
requirements for basic safety and essential
performance - Collateral Standard:
Electromagnetic compatibility-requirements and
tests

3
 7 EN 60601-1-6:2010
8 EN 60601-2-4:2010
9 EN ISO 10993-1：
2009/AC2010
Medical electrical equipment - Part 1-6: General
requirements for basic safety and essential
performance- Collateral Standard: Usability
Medical electrical equipment -- Part 2-4:
Particular requirements for the safety of cardiac
defibrillators
Biological evaluation of medical devices - Part 1:
Evaluation and testing within a risk
management process

10 EN62304：2006/A1：2008 Medical device software - Software life-cycle

processes
11 EN Medical electrical equipment -- Part 1-8:
60601-1-8:2007/A11:2017 General requirements for basic safety and
essential performance - Collateral Standard:
General requirements, tests and guidance for
alarm systems in medical electrical equipment
and medical electrical systems
12 IEC 60601-2-27:2011 Medical electrical equipment -- Part 2-27:
Particular requirements for the safety, including
essential performance, of electrocardiographic
monitoring equipment

1.6 Symbols

Graphical symbols, letter symbols and signs listed below may be found on the
DM7000 System and accessories distributed by M&B. Please note the use of these
symbols for safe and proper use of the equipment.

4
 Machine symbols

Registered trademarks

BF and Defibrillation-proof applied

parts
CF and Defibrillation-proof applied
parts

Caution

Alternating current

Protective earth
(ground)

Equipotentiality

Earth (ground)

Defibrillator
discharge button
On=Power on
OFF=Power off

APEX APEX

STERNUM STERNUM

Nameplate symbols

Serial number

Date of manufacture

5
 Manufacturer

Do not throw it away

European Representative: Shanghai

International Holding Corp.
GmbH(Europe) Eiffestrasses 80,
20537 Hanburg, Germany

Outer signs of packing box

Temperature limitation

Keep dry

Keep up

Fragile

STACKING LIMIT BY NUMBER

Pads symbols

CONFORMITE EUROPEENNE

Do not reuse

Keep away from sunlight

LETEX Do not contains or presence of

FREE natural rubber latex

High voltage

6
 Temperature limitation

Do not use if package is damaged

Use by

Batch code

Consult instructions for use

Weighing less than 25 kg can not be

used

Do not open the seal unless the Pad

is to be used at once
The continuous working time can
not exceed 24 hours

1.7 Icons

Graphical and text icons listed below may be found on the display of the DM7000
System during operation.

Alarm off

Alarm on

Auto heart rate set

at 60 BPM

Mute

7
2 Safety

2.1 Conventions Used in the Manual

This section includes a list of conventions used in this manual.

2.1.1 Warnings

Warnings alert the user to a special condition that could result in serious personal
injury or death. In this manual, warnings are displayed as shown in the following
example:

WARNING!

Includes conditions, hazards, or unsafe that can result in

serious personal death.

2.1.2 Cautions

Cautions alert the user to a special condition that could result in minor personal
injury or damage to the equipment. In this manual, cautions are displayed as shown
in the following example:

Caution

Conditions, hazards, or unsafe practices that can result in

minor personal injury, damage to the DM7000 Defibrillator
Monitor, or loss of data.

8
2.1.3 Notices

Note contain information that augments or clarifies an operating step. Note do not
normally contain actions. They follow the procedural steps to which they refer. In
this manual, note are displayed as shown in the following example:

Note

If the DM7000 Defibrillator Monitor is used more than once

per month, it is recommended that authorized service
personnel perform a periodic inspection servicing at least
once per year.

2.1.4 Voice prompts

The DM7000 Defibrillator Monitor provides audio instructions through the built-in
speaker to provide operating instruction and assist the user during defibrillation. In
this manual, voice prompts are displayed as shown in the following example:

Check the electrodes.

2.1.5 Safety information is organized in six groups:

 General Cautions and Notices

 Patient Safety
 Defibrillator and Electrode Pads
 Battery
 Care and Storage
 Safety Symbols

9
2.2 General Cautions and Notices

2.2.1 Dropped or Damaged

If the device has been dropped or damaged in any way, refer the device to qualified
service personnel for servicing.

2.2.2 Ferromagnetic Equipment

ECG electrodes and cables contain ferromagnetic materials. They must not be used
in the presence of large magnetic fields created by magnetic resonance imaging (MRI)
equipment. The large magnetic fields generated by an MRI device could move
ferromagnetic equipment with an extremely violent force that could cause serious
personal injury or death to persons between the equipment and the MRI device.

2.2.3 Labels

Observe all CAUTION and WARNING labels on the equipment and accessories.

2.2.4 Perormance

The DM7000 Defibrillator Monitor may not meet performance specifications if

stored, transported or used outside the specified storage or operating
environmental range limits.

2.2.5 Notices

1. Any operator using the DM7000 Defibrillator Monitor should be completely

knowledgeable of the information in the User Instruction Manual.

10
2. Each chapter describes the function of the equipment, and how to make rational
use of equipment.
3. Comply with all instructions recommended repair. If there is fault, should
immediately stop using, repair. The device is detected by the appropriate personnel,
can not continue to use the equipment.
4. DM7000 defibrillation/monitor can output up to 360 Joule energy. To make the
equipment totally disabled, must power off and remove the battery pack.
5. Please don’t use mobile phone near DM7000 Defibrillator Monitor, radiation field
produced by mobile phone will interfere DM7000 Defibrillator Monitor’s function.
6. If the battery pack is removed for any reason, the user must label the DM7000
Defibrillator Monitor as "Out of service due to battery operation."
7. In CPR, patients will be placed on a solid surface.
8. A warning that DM7000 Defibrillator Monitor should not be used adjacent to or
stacked with other equipment and that if adjacent or stacked use in necessary,
DM7000 Defibrillator Monitor should be observed to verify normal operation in the
configuration in which in will be used.
9. To avoid the risk of electric shock, this equipment must only be connected
to a supply mains with protective earth
10. Do not to position the DM7000 so that itis difficult to operate the disconnection
device

2.2.6 Attention

Electric and magnetic fields can interfere equipment regular work. Therefore, please
ensure all the external device complied with EMC demands near the equipment. Due
to X-ray or MRI equipment emits premier electromagnetic radial, they would be
aggressor.

11
2.3 Patient Safety

2.3.1 General

For over 8 years of age and weight is greater than

Warning
25kg
The DM7000 Defibrillator Monitor AED mode is not
to be used on patients less than 8 years old or
weight is less than 25kg.
Patient Physical Harm
Caution

Place the DM7000 Defibrillator Monitor in a position

where it cannot harm the patient should it fall. Do
not use adjacent to or stacked with other
equipment. Keep all cables and connectors away
from the patient's neck.

2.3.2 Shock Hazard

Defibrillation current can cause injury

Warning
Do not touch the patient during defibrillation.

Do not touch equipment connected to or metal objects in

contact with the patient during defibrillation.
Disconnect other electrical equipment which has no
DEFIBRILLATION-PROOF applied parts from the patient
before defibrillating.
Avoid contact between parts of the Patient’s body such as
exposed skin of head or limbs, conductive fluids such as
gel, blood or saline and metal objects such as a bed frame
or a stretcher which may provide unwanted pathways for

12
 the defibrillating current.

2.3.3 Burn

Properly place defibrillation pads

Warning
Do not allow defibrillation pads to touch each other, or to
touch other electrodes, lead wires, dressings, transdermal
patches, etc. Such contact can cause patient skin burns
during defibrillation and may divert defibrillating current
away from the heart. Remove excessive body hair, which
may cause skin burns or ineffective energy transfer. Do
not use alcohol, iodine or other skin preparations. These
can dry the skin and may cause the DM7000 to function
improperly or may cause skin bums
DEFIBRILLATOR ELECTRODES shall be kept well clear of
other electrodes or metal parts in contact with the
PATIENT.

2.3.4 Electrical Energy

DM7000 can deliver 360 joules of electrical energy

Warning
Disconnect any medical electronic device that is not
labeled "defibrillation protected" from the patient. If this
electrical energy is not discharged properly, it could
cause personal injury or death to the operator or
bystander. During defibrillation, the operator and all
other people must stand clear of the patient, bed and all
conductive surfaces in contact with the patient.

13
 Properly place defibrillation pads
Warning
Do not place electrodes near the generator of an
internal pacemaker. Always apply electrodes to flat
areas of skin. Avoid application over folds of skin such as
those underneath the breast or on obese patients.
Excessive hair, poor adhesion, or air under electrode
may produce bums.

2.3.5 ECG Miss Interpretation

Properly place defibrillation pads

Warning
Improperly placed pads may produce incorrect analysis
and an inappropriate shock or no shock decision advisory.

Do not move patient

Warning
Handling or transporting the patient during ECG analysis
can cause incorrect or delayed diagnosis. Follow all
instructions in the Users Manual.
Cardiac pacemakers may affect rhythm analysis
Warning
Patient pacemakers may reduce the sensitivity of the
DM7000 Defibrillator Monitor analysis and errors in
detecting shockable rhythms.
Radio frequency (RF) interference
Warning
Do not operate the DM7000 Defibrillator Monitor in
conjunction with electrocautery or diathermy equipment.
Any equipment that emits strong radio frequency signals
can cause electrical interference and distort the ECG signal
to cause inaccurate interpretation of rhythm.

14
2.4 Defibrillator and Electrode Pads

2.4.1 Explosion

Explosion hazard
Warning
Possible explosion and fire hazard if used in the presence
of flammable agents or in an oxygen enriched
atmosphere.

2.4.2 Electrical Shock or Fire Hazard

Do not short handles or pads to deliver shock.

Warning
If do that, it may destroyed the machine.
No internal, operator-serviceable parts
Warning
Do not open unit, remove covers or attempt to repair the
DM7000 Defibrillator Monitor. All servicing must be
performed by qualified personnel.

Improper use can cause injury

Warning
The DM7000 Defibrillator Monitor contains an automatic
disarm of the stored energy. If the operator has not
delivered the energy to a patient or a test load, an internal
timer will disarm the stored energy. This stored electrical
energy can potentially cause death or injury if discharged
improperly. Follow all instructions in this Users Manual.
Do not immerse or expose the DM7000 Defibrillator
Caution
Monitor to water or other liquids
Do not use the defibrillator if unit has been immersed in
liquid or if excessive condensation is visible on the device.
Conductive parts should not contact other conductive
Caution
parts including the earth

15
2.4.3 Improper Device Performance

Properly use electrode pads

Warning
Do not attempt to warm the electrodes with a heat source
greater than 35°C (95°F). Do not immerse or clean
electrodes with alcohol or solvents. Do not perform chest
compressions (CPR) through electrodes. These actions
may damage the electrode pads cause the Jump Start to
function improperly.
Use only M&B approved accessories
Warning
Do not use defibrillation pads, batteries, and other
accessories not approved by M&B. Use of unauthorized
accessories may cause the device to operate improperly
and provide false measurements. Follow all labeling
instructions on the defibrillation pads and the battery.
Do not repeatedly charge and discharge defibrillator in
Caution
rapid succession
If a need for repetitive testing arises, wait at least 1
minute for every third discharge to avoid damaging
equipment.
Improper maintenance can cause improper performance
Caution
Follow instructions in the Users Manual.

2.5 Battery

2.5.1 Battery Care

Use only M&B batteries

Caution
Use only M&B Part No. Ni-MH 12V rechargeable batteries.

16
 Use of any other battery can damage the DM7000
Defibrillator Monitor.
Always verify remaining capacity of a non-rechargeable
Caution
battery after use
Check capacity and change if battery is low.

Replace battery at 3 years

Caution
Battery replacement at 3 years is recommended due to
degradation of the battery chemistry. Periodic
maintenance and testing is highly recommended to
ensure proper battery performance.
Changing the battery is carried out by persons authorized
Caution
by M&B.

2.5.2 Battery indication

Battery status Display single Front penal LED Description

Battery full Green Battery full

Battery low Orange Still can work

normally, but the
battery is no enough,
suggest plug into
main power for
charging.
Battery very low Flash red Machine has not run
properly，have to
immediately plug into
17
 main power for
charging.
The machine already
The battery is Flash green 1.Please plug into
main power for
charging charging
2.Charging
completely，the LED
will off.

2.6 Care and Storage

2.6.1 Cleaning and Sterilization

Clean and maintain the DM7000 Defibrillator Monitor

Caution
according to instructions. See Chapter 4, Maintaining the
DM7000 Defibrillator Monitor.
Do not clean the DM7000 Defibrillator Monitor. With
alcohol, ketone, or any flammable agent. Do not autoclave
the DM7000 Defibrillator Monitor or attempt to sterilize
the DM7000 Defibrillator Monitor or any of its
accessories.

2.6.2 Electrodes

Follow manufacturer's instructions for use of

Warning
defibrillation electrodes
Improper use of defibrillation electrodes may cause the
DM7000 Defibrillator Monitor to function improperly or

18
 may cause skin bums. Do not use expired, dry electrodes.
Do not reuse disposable electrodes. Only use M&B
approved electrodes.
Properly store and use defibrillation pads
Caution
Store electrodes in a cool, dry location (between 60° and
95°F or 15°C and 35°C). Do not sterilize the pads, immerse,
or clean the electrodes with alcohol or solvents.

Packaging and validity

Caution
Disposable electrode is valid for two years.
Suggested check the date once every month,
And check packaging intact.

2.6.3 Warning pacing pulse suppression

May be due to detect heart rate not accurate.

When possible arrhythmias or cardiac arrest included the
Warning
pacing pulse
Do not rely solely on rate meter alarms. Should be closely
monitoring patients with pacemakers.

2.6.4 Handles

Follow manufacturer's instructions for use of handles

Warning
Improper use of handles may cause the DM7000
Defibrillator Monitor to function improperly or may cause
skin bums. Only use M&B approved handles.

Properly store and use handles

Caution
Store handles in a cool, dry location. Sterilize the
handles, immerse, or clean the handles with alcohol or
solvents.

19
 Follow manufacturer's instructions for use of handles
Warning
Improper use of handles may cause the DM7000
Defibrillator Monitor to function improperly or may cause
skin bums. Only use M&B approved handles.
Properly store and use handles
Caution
Store handles in a cool, dry location. Sterilize the
handles, immerse, or clean the handles with alcohol or
solvents.
Integrity handle cable
Caution
1, each use, check the handle cables, connectors, handles
and defibrillation adapter cable for damage.
2, every one a month, check the handle cables,
connectors, handles and defibrillation adapter cable for
damage.
Clear
Caution
After each use, use distilled water and wipe them clean.
If the long-term is not used for three months to determine
clean the dirt surface at least every handle.

2.6.5 Periodic self-test

Periodic self-test
Caution
Every other month on a self-test machine to ensure its
basic functions intact. Self-test methods are:
The handle is connected to the host, the two handles were
placed above a fixed slot machine. Switch to manual mode
and proceed through the handle of the charging and
discharging 50J. If you can complete normally, indicating
self-qualified.

20
2.6.6 Disposal

Disposal device and its accessories

Warning
Please dispose device and its accessories which have
exceeded their operating time according to relevant
regulations. Or recycling by manufacturer .If you have
any question on device disposal or need more detailed
information, please contact us or our service centers.

3 Introducing the DM7000 Defibrillator Monitor

This chapter provides an introduction to the DM7000 system and presents an

overview of the DM7000 controls, indicators, displays, and prompts. It also provides
instructions for getting the DM7000 ready for use and preparing the unit for storage
and operating the unit to normal work.

Caution

Before preceding this chapter, you should first read the safety section.

3.1 Intended use

The DM7000 is intended for use in hospital settings by qualified medical

personnel trained in the operation of the device and qualified by training in basic life
support, advanced cardiac life support or defibrillation.

Note: The Dm7000 do not intended for use in the emergency medical
services environment

3.1.1 Defibrillator Function

•Unconsciousness

•Absence of breathing, and

21
 •Absence of pulse.
DM7000 contain a DC defibrillator capable of delivering up to 360 joules of
energy. It may be used in synchronized mode to perform synchronized cardioversion
by using the R-wave of the patient’s ECG as a timing reference. The unit uses paddles
or disposable, pre-gelled, MFE Pads for defibrillation. DM7000 must be prescribed
for use by a physician or medical advisor of an emergency response team.
Note: The defibrillator function can't be used as long-time ECG monitor.
Note: The DM7000 do not use as pacer.

3.1.2 Monitor function

•averaged heart rate, derived from measuring R to R intervals

•lead selections — I, II, III, aVR, aVL, aVF, V (with ECG cable),

•ECG size — 0.25,0.5, 1, 2, 4, cm/mV

•other operational prompts, messages, and diagnostic codes The patient’s ECG is
monitored by connecting the patient to the unit via the 3 lead or 5 lead wire
patient cable,.
Monitoring or diagnostic ECG bandwidth is selectable.

3.1.3 Indication

Prior to using the DM7000 defibrillator function, the patient should be assessed
by a trained person. If defibrillation with the DM7000 is indicated, all of the following
signs should be present during patient assessment:
• Unconsciousness
• Absence of breathing
• Unresponsiveness (no signs of circulation)

22
3.1.4 Qualified Operators

When operating as a semi-automatic external defibrillator in AED Mode, the

DM7000 is suitable for use by medical personnel trained in basic life support that
includes the use of an AED.

When operating in Monitor or Manual Defib, the DM7000 is suitable for use by
healthcare professionals trained in advanced cardiac life support

3.1.5 Contraindications

The DM7000 defibrillator function should NOT be used if the patient exhibits
any of the following
signs:
• Patient is conscious
• Patient is breathing
• Patient is responsive (has signs of circulation)

3.1.6 Duration of use or contact with the body

The unit uses the paddles or MFE Pads to contact the patient chest when need
defibrillation.
The unit uses the ECG electrodes to contact the patient chest when need
monitor.

3.1.7 Side effects/complications

After defibrillation, the skin will have a slight burn, and the skin will appear
erythema, but it will usually disappear within 1 day.
If defibrillation is not timely, it may be accompanied by other physical damage,
but the damage is not from defibrillation.
23
3.2 Overview of the DM7000 Defibrillator Monitor

3.2.1 Overview

The DM7000 Defibrillator Monitor is a safe, easy to use defibrillation and

monitor device. The System is an extremely flexible device that incorporates a
MANUAL defibrillation mode, MONITOR mode and AED mode.

MANUAL mode
When the DM7000 works in MANUAL mode, it analyzes the patient’s ECG waveform,
to show the Heart Rate. The operator doctor must judge when to defibrillation. The
machine delivers the defibrillation shock through the handles or the defibrillator
pads.
When in MANUAL mode press SYNC button, the DM7000 can recognize atria
fibrillation and indicate R peak at ECG waveform. The DM7000 transfers ENERGY at
the first R peak when the operator press SHOCK button.

AED mode
When the DM7000 works in AED mode, it can recognize ventricular fibrillation and
other ventricular tachycardia and guides operators through the defibrillation process.
When properly connected to a patient who is unconscious, not breathing, and
without a pulse, the DM7000 analyzes the patient's heart rhythm, provides text and
audio instruction prompts, determines if a shockable situation exists and if
appropriate, press the Shock button.
The DM7000 delivers the defibrillation shock through two self-adhesive, pre-gelled,
low-impedance electrode defibrillator pads. The pads are sold as disposable kits.

MONITOR mode
The MONITOR mode function of the DM7000 is used to monitor ECG waveform and
show the heart rate, and to alarm when heart rate is above or below limits set by the
24
operator. In the MONITOR mode it can display ECG waveform by the 3 lines cable or
5 lines cable.

The DM7000 is designed for COMMON USE，and the term used to describe a
DEFIBRILLATOR designed to endure less than 2500 discharges.

3.2.2 Features
DM7000 features include:
Three modes process
extensive voice and visual prompts for the operator
biphasic energy output
lock-out protection to prevent inadvertent defibrillation

3.2.3 Qualified Operators

Manual mode should be used only by qualified medical personnel for converting
ventricular fibrillation and rapid ventricular tachycardia to sinus rhythm or other
cardiac rhythms capable of producing hemodynamically significant heart beats.
AED mode is designed for use by emergency care personnel who have completed
training and certification requirements applicable to the use of a defibrillator where
the device operator controls delivery of shocks to the patient..

3.2.4 Indication for Use

Prior to using the DM7000 defibrillator function, the patient should be
assessed by a trained person. If defibrillation with the DM7000 is indicated, all of the
following signs should be present during patient assessment:
• Unconsciousness
• Absence of breathing
• Unresponsiveness (no signs of circulation)

25
3.2.5 Contraindications

The DM7000 defibrillator function should NOT be used if the patient exhibits any of
the following signs:
• Patient is conscious
• Patient is breathing
• Patient is responsive (has signs of circulation)

3.3 Getting the DM7000 Ready

Carefully unpack and inspect all the DM7000 system components and
accessories. Install the battery. Verify that the self-test passes before putting the unit
into service. The operator must perform a test mode before turned on.

3.3.1 Unpacking and Inspecting

Visually inspect the carton for any signs of damage or mishandling (carton
perforations, cuts, or dents; bent or collapsed corners; or broken carton seal).
Remove the DM7000 from the carton and inspect it carefully.

Before proceeding:
1. Open and carefully unpack each carton.
2. Examine the instruments and accessories for signs of damage.
3. Check the packing list to determine that all accessories have been received.
4. Contact M&B, Service Department at (+86)10-61253747 if anything looks
damaged or is missing.

Installing the Battery

DM7000 uses an extended-life, Ni-MH rechargeable battery.

26
To install the battery:

1. Open the battery compartment (located near the bottom of the backside of the
DM7000) by removing the thumbscrews and then sliding the battery cover up and
off.
2. Locate the battery contact pins in the bottom-right comer of the battery
compartment
3. Push the 2-pin battery connector onto the contact pins.
4. Place the battery into the battery compartment and replace the battery cover.
Slide the cover back so that the screw holes are aligned.
5. Replace the thumbscrews
6. When only the battery power supply, it can be started and the LCD can display
power symbol.
Test the DM7000
After installing the battery, the DM7000 power up and performs a test.

27
Test steps:
1. Place the handles as the above figure
2. Press the ENERGY SELECT button, select 50J
3. Press the CHARGE button, then the energy will charge to admired
4. Press the SHOCK button, deliver the energy
Above steps can be finished, then the Test is passed.

3.4 Getting to Know the DM7000

The DM7000 is a multi-function device includes MANUAL mode, AED mode and
MONITOR mode.
MANUAL mode
It features the ECG waveform show, 2-360J can be selected, extensive voice and
visual prompts assist the operator.
This mode can support the defibrillator pads and the handles.
When the patient atria fibrillation, the operator can press SYNC button, then the
DM7000 will indicates R peak at ECG waveform. The machine must use the
defibrillator pads so that ensure accurate analyzing.
AED mode
It features a straightforward, three-step operating design that uses extensive voice,
ECG waveform show and visual prompts to assist the operator. It must use the
defibrillator pads so that ensure accurate analyzing.
MONITOR mode
It only monitors the patient real-time condition that shows the real-time ECG
waveform and the Heart Rate. The 3-line cable and 5-line cable can be setup by
setting the menu.
Functions
This section describes the following DM7000 features:
Summary of Operations
LCD Prompts

28
Voice Prompts
Battery Level Indicator

3.5 User Interface

3.5.1 Summary of Operations

The DM7000 is designed for multi-function, so the operator must decide to turn the
knob from OFF to MANUAL, AED or MONITOR.

MANUAL mode
After putting the defibrillator pads or handles on the patient and connecting them to
DM7000, the operator performs the following process:
Turn the knob from OFF to MANUAL
The operator press the ENERGY UP(▲)or the ENERGY DOWN (▼)to select which
energy levels.
When use the defibrillator pads, the operator presses the CHARGE button on the
panel. When use the handles, the operator presses the yellow button on the right
handle of APEX.The DM7000 will charge to the energy that has been selected.
When use the defibrillator pads, press SHOCK button to deliver the energy.When use
the handles, press the red button at the same time until deliver the energy to the
patient.
AED mode
After putting the defibrillator pads on the patient and connecting them to DM7000,
the operator performs this simple three-step process:
Turn the knob from OFF to AED.
Follow LCD prompts on the panel and voice prompts from the speaker.
If prompted, deliver shock by pressing the red SHOCK button.
MONITOR mode
After putting the 3-lines cable or the 5-lines cable on the patient and connecting
them to DM7000, then set LEAD mode as 3 lines or 5 lines.
Turn the knob OFF to MONITOR.

29
set the menu.

LCD prompts and Voice Prompts

The DM7000 prompt feature provides LCD prompts to guide the user through the
defibrillation process.
The DM7000 provides audio instructions through the built-in speaker to provide
operating instruction and assist the user during defibrillation.

The voice prompts listed in the following table.

1 Check the electrodes.

Analyzing
2
Do not touch the patient.
3 Shock advised.

4 No shock advised.
5 Charging to –J(150J/200J).
Stand clear
6
Press SHOCK.
7 Shock delivered.
8 Start CPR
9 Continue for 90s

10 Continue for 60s.

11 Continue for 30s.
Stop CPR
12
Start analysis 10s later.
Time out
13
Analysis restart.
14 Shock cancelled.
15 System failure.

Battery Level Indicator:

30
 Indicates the charge left in the battery is full.

Indicates the charge left in the battery is partially

depleted.

3.6 DM7000 Accessories Part List

ERP
No Type Remark
number

1 Three Channel ECG cable EC3029AO 205006

2 Five Channel ECG cable EC3059AO 205161

3 Grounding line Dixian(TY)-0 206211

4 Power supply cable XD-004-D 0.75×2M 205163

5 AED Pads connector DM7000-07-0 104028

6 Certificate of Quality 205040

7 Warranty card 205041

8 User manual 201161

9 Adult pads YH-1 205356

10 Children pads YH-2 205358

Defibrillator Pads for

11 EDC-1035-1 206098
Adult
Defibrillator Pads for
12 EDC-1035-2 206093
Children

13 Defibrillator paddles DM7000-DJSB-0 104029

31
14 Thermal paper 50mm, with graph 205141

Note: All accessories are available only with M&B Company, if not,

the Company shall not be responsible for any problems.

4 Defibrillation mode

There are two modes of defibrillation: automatic defibrillation (AED) and manual
defibrillation. In defibrillation mode, only the blood oxygen module is optional.

4.1 Automatic Defibrillation (AED without SPO2 Module)

4.1.1 System Settings

You can enter the setup menu to set the basic functions of defibrillation. To enter
the setting menu, there are three ways to use: shortcut buttons, digital knob and
touch click.
Shortcut Buttons

Press shortcut button to enter the settings menu.

Digital Knob

32
Rotate the digital knob to move the blue cursor to the setting icon , and press the

digital knob again to enter the setting menu.

Touch Screen

Press directly to enter the settings menu.

4.1.2 Switching Gain

The gain can be switched in three ways: shortcut button, digital knob and touch
screen
Shortcut Button

Press Shortcut button to switch gain

Digital Knob

Rotate the digital knob to move the blue cursor to the icon , and press the digital

knob again to switch gain.

Touch Screen

Press button to switch gain.

4.1.3 Date and Time

For the setting of date and time, please refer to the section Date and Time of
Monitoring Mode

4.1.4 Filter Status

4.1.5 ECG display gain

4.1.6 ECG display rate

4.1.7 ECG file storage status

4.1.8 Alarm sound status

4.1.9 Battery status

33
4.1.10 Heart rate

4.1.11 Heart rate alarm limit

4.1.12 Body impedance

4.1.13 Defibrillation energy value

4.1.14 Defibrillator working time

4.1.15 Defibrillation times

4.1.16 Printer Status

Printer Rate The printing rate of the printer is the same as that of
the ECG display
Print Gain The printer print gain is consistent with the ECG display
gain
Printer Normal The printer works normally, and data printing can be
performed at this time

No Paper The printing paper in the printer paper compartment is

exhausted, and the printing paper should be replaced
at this time.
No Roller The printer paper compartment cover is not closed
High The temperature of the print head of the printer is too
Temperature high, the printer will stop printing at this time

4.1.17 Automatic defibrillation (AED) working status

4.1.18 ECG diagnosis results

In automatic defibrillation mode, the device analyzes ECG data in real time and
displays the diagnosis results on the main interface

4.1.19 Defibrillation Pads Status

34
In automatic defibrillation mode, only electrode pads are supported. If the current
device is equipped with a defibrillation handle, the device will prompt "Please
replace the handle with electrode pads".
The device is equipped with electrode pads, the device will measure the impedance
of the human body and display the impedance value of the human body on the main
interface.
Normal impedance The defibrillation pads status will disappear and
the device will enter the automatic defibrillation
process
low impedance Prompt "Pads shortcut“
high independence Prompt "Pads off".

4.2 Automatic defibrillation (AED with SPO2 Module)

4.2.1 SPO2 alarm limit

When the SPO2 exceeds the upper or lower limit of the alarm threshold, the device
will start the SPO2 alarm, the blood oxygen value and the alarm indicator will flash,
and an alarm sound will be output.
The SPO2 alarm is a physiological alarm.

4.2.2 SPO2 value

4.2.3 SpO2 probe status

SpO2 Probe off The SPO2 probe is not clamped to the finger or is not
35
 clamped as specified
SpO2 Probe The SpO2 probe has detected the finger, and the
detecting SpO2 data analysis is in progress
SpO2 Probe normal The SpO2 probe status will disappear, and the SpO2
value will be displayed on the main interface

4.3 Manual defibrillation mode one (without SPO2 installed)

4.3.1 Synchronized defibrillation status

Indicates whether the synchronized defibrillation function is currently enabled. The
synchronized defibrillation function can be toggled on or off using the synchronized
defibrillation button on the front panel.
When the synchronized defibrillation function is turned off, the device performs
defibrillation discharges immediately after pressing the defibrillation button on the
front panel.
After the synchronous defibrillation function is turned on, the device will
automatically detect and mark the position of the R wave of the ECG waveform.
Press the defibrillation button on the front panel and hold it down. When the device
detects the next R wave, the device will automatically perform defibrillation
discharge.

4.3.2 Handle or pad status

In manual defibrillation mode, either the handle or the pads can be installed. No
matter the handle or electrode pads are installed, the device will measure and

36
calculate the impedance and display the impedance value of the human body on the
main interface.
After the pads are installed, the status of the defibrillation pads is displayed. After
the handle is installed, the handle state is displayed.
Install electrode pads Install the handle
Normal body The state of the defibrillation The handle state disappears,
impedance pads disappears, and the and the device can perform
device can perform manual manual charging and
charging and discharging discharging operations
operations
Low Prompt "Pads shortcut" Prompt "handle shortcut"
impedance

High Prompt "Pads off". Prompt "handle

impedance disconnected"

4.4 Manual defibrillation mode two (with SPO2 installed)

4.5 System Settings

37
4.5.1 Language

This option is used to set the display language for defibrillation mode. The automatic
defibrillation mode and the manual defibrillation mode share the same language
setting item, that is, if the display language is modified in the automatic defibrillation
mode, the display language in the manual mode will also be changed, and vice versa.
For language setting, please refer to the section of language in monitoring mode.

4.5.2 Print time

This option is used to set the time to print ECG or SPO2 waveform in the main
interface
To set the printing time, please refer to the section of printing time in monitoring.

4.5.3 Print mode

without SPO2 module installed
38
With SPO2 module installed

This option controls the type of waveform printed after pressing the print key on the
main interface.
To set the print mode, please refer to the section of print mode in monitor mode

4.5.4 Volume

This option controls the heartbeat volume, alarm volume and voice volume in
defibrillation mode.
To set the volume, please refer to the volume in monitoring mode section

4.5.5 Heartbeat sound

This option controls whether the heartbeat sound is output.

To set the heartbeat sound, please refer to the section on heartbeat sound in
monitoring mode

4.5.6 Alarm sound inhibit time

This option controls the time when the alarm sound is temporarily disabled.

39
To set the alarm sound inhibit time, please refer to the section Alarm sound inhibit
time in monitoring mode.

4.5.7 Automatically print after defibrillation

This option sets no printing, immediate printing or delayed printing after

defibrillation. The currently used option is displayed in green.
Operation via shortcut buttons, digital knob and touch screen.
Shortcut Button

Use the shortcut button to move the blue cursor to the option to be selected,

then press the shortcut button to set a new option. Press the shortcut button

to discard the setting and return to the setting menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the option to be selected, and
then press the digital knob to set a new option. Move the blue cursor to (Exit )and
press the digital knob to return to the setup menu.
Touch Screen
Click on the option you want to select to set a new option. Click the (Exit) option to
return to the settings menu.

4.5.8 Return to default settings

This option restores all system parameters to their default settings.

For the operation of restoring default settings, please refer to the section Restoring
Default Settings in Monitoring Mode.

40
4.5.9 Event records

Event records are used to record some key or special moments.

For the operation of event recording, please refer to the section on event recording
in monitoring mode

4.5.10 Digital knob

This option sets the function of the rotation direction of the Digital knob.
For the operation of digital knob setting, please refer to the section of digital knob in
monitoring mode

4.5.11 About

The About menu displays the version information of the current device.

4.6 ECG Menu

41
4.6.1 ECG display rate

This option controls the display speed of the ECG waveform on the main interface.
For the operation of setting the ECG display rate, please refer to the section on ECG
display rate in monitoring mode.

4.6.2 ECG gain

This option is used to control the display amplitude of ECG waveform on the main
interface.
For the operation of setting ECG gain, please refer to the section on ECG gain in
monitoring mode

4.6.3 Heart rate alarm limit

42
This option sets the upper and lower limits of the heart rate alarm.
For the function and operation of the heart rate alarm threshold, please refer to the
heart rate alarm threshold section in monitoring mode.

4.6.4 AC filter

This option sets the filter frequency of the AC filter.

For the function and operation of the AC filter, please refer to the section AC Filter in
Monitoring Mode

4.6.5 EMG filter

This option controls whether to use an EMG filter.

For the function and operation of the EMG filter, please refer to the section EMG
filter in monitoring mode.

4.6.6 Low pass filter

This option controls whether a low pass filter is used.

For the function and operation of the low-pass filter, please refer to the section on
the low-pass filter in monitoring mode.
43
4.7 SPO2 menu

4.7.1 SPO2 alarm limit

This option sets the upper and lower limits of the limit alarm.
For the function and operation of the SPO2 alarm limit, please refer to the section on
SPO2 alarm limit in monitoring mode.

5 Monitor Mode

Under Monitor mode, physiological parameters include four modes: ECG, SpO2, BP
and CO2. ECG is standard mode. SpO2, BP and CO2 are optional modes. About
optional modes, equipment will set related monitor main interface and function
according to factory installation.

44
5.1 Monitor Mode 1 (without SpO2/BP/CO2)

*Note: The numbers in the figure correspond to the third-level title numbers of the
following chapters. Similar content pictures appear in the following paragraphs,
and the same rules must be followed

5.1.1 System Setup.

Monitor mode basic function can be set under system setup menu. User can use the
shortcut button, digital knob and touch screen to operate.
Shortcut Button

Press shortcut button to enter system setup menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the setting icon, and press the
digital knob again to enter the system setting menu.
Touch Screen

Click the settings icon directly to enter the system settings menu.

5.1.2 Freeze
Use Freeze function to replay previous period ECG waveform.

45
Open Freeze Function
User can use the shortcut button, digital knob and touch screen to open freeze
function.
Shortcut Button

Press shortcut button to open freeze function.

Digital Knob

Switch Digital Knob to move cursor on blue icon and then press the knob to

open freeze function.

Touch Screen

Click setup icon directly to open freeze function.

Waveform Browsing
After entering the freeze function, browse the waveforms through the page turning
function. The waveform can be browsed through three ways: shortcut buttons,
digital knob and touch screen
Shortcut Button

Press shortcut button to turn page.

Digital Knob
Switch digital knob to flip waveform page.
Touch Screen

Click icon to flip page.

Exit Freeze Function.

Shortcut Button

Press shortcut button to exit Freeze function.

Digital Knob
Under freeze mode, pressing digital knob also can exit freeze function.
Touch Screen

Click the restore icon to exit the freeze function.

46
5.1.3 Switch Leads
Under 3-lead model, switchover leads according to the cyclic order IIIIII. Under
5-lead model, switchover leads according to the cyclic order
IIIIIIAVRAVLAVFV. User can use the shortcut button, digital knob and
touch screen to switchover leads.
Shortcut Button

Press the shortcut button corresponding to the switch lead icon on the panel to

switch the lead.

Digital Knob

Rotate the digital knob to move the blue cursor to the switch lead icon , and then

press the digital knob to switch leads.

Touch Screen

Click the switch lead icon to switch leads

5.1.4 Switch Gain

Switch gain can be finished according to the cyclic order x1/4x1/2x1x2x4.
User can use the shortcut button, digital knob and touch screen to switch gain.
Shortcut Button

Press the shortcut button corresponding to the switch gain icon on the panel to

switch the gain.

Digital Knob

Rotate the digital knob to move the blue cursor to the switch gain icon , then press

the digital knob to switch the gain

Touch Screen

Click the switch gain icon to switch the gain

47
5.1.5 Moving Cursor.
The function of moving the cursor is the same as that of the digital knob. Press the

shortcut button on the panel to move the blue cursor in the interface.

5.1.6 Date and Time

Enter into Date and Time Menu

The date and time menu can be accessed using both the digital knob and the touch
screen
Digital Knob
Rotate digital knob to move blue cursor on Date and Time, and then press the digital
knob to enter Date and Time Menu.
Touch Screen
Click Date & Time to enter the date and time settings menu
Setting Date and Time.
User can set Date and Time in three ways: shortcut button, digital knob and touch
screen.
Shortcut Button

Press shortcut button to move blue cursor on date and time, and then press

shortcut button to change date and time. After changing, press button to

set new date and time. Press button to abandon the setting and return to the

main interface.
Digital Knob
Rotate the digital knob to move the blue cursor to the date or time to be modified,
press the digital knob, the date or time to be modified will turn blue, then rotate the
48
digital knob to change the date or time value, press the digital knob after finishing to
restore the blue cursor, after the date and time have been modified, move the blue
cursor to confirm the option (OK), and press the digital knob to set the new date and
time. Move the blue cursor to the cancel option (Cancel), press the digital knob to
abandon the setting and return to the main interface
Touch Screen
Click on the date or time to cyclically modify its value. After the modification is
completed, click the OK option to set a new date and time. Click the Cancel option to
abandon the settings and return to the main interface

5.1.7 ECG Lead

ECG has 3 leads or 5 leads.

5.1.8 Filter State

The settings of the AC, EMG and low-pass filter options in the ECG menu will
determine the display content of the filter status on the main interface
Filter State AC Filter Myoelectric Lowpass
Filter Filter
Filter OFF OFF OFF OFF
LP OFF OFF ON

MV OFF ON OFF
MV LP OFF ON ON
AC50 50HZ OFF OFF
AC50 LP 50HZ OFF ON
AC50 MV 50HZ ON OFF
AC50 MV LP 50HZ ON ON

AC60 60HZ OFF OFF

AC60 LP 60HZ OFF ON
AC60 MV 60HZ ON OFF
AC60 MV LP 60HZ ON ON

49
5.1.9 ECG Gain
X1/4 X1/2 X1 X2 X4

5.1.10 ECG Rate

10mm/S 12.5mm/S 25mm/S 50mm/S

5.1.11 ECG Width Mode

It includes monitor, operation and diagnostic three modes.

5.1.12 ECG Data Storage.

5.1.13 Alarm Sound State.

5.1.14 Battery State.

5.1.15 Heart Rate Alarm Limitation

The option of Heart Rate Alarm Limitation in ECG menu will determine Heart Rate
Alarm Limitation in main interface.

5.1.16 Heart Rate

5.1.17 ECG Diagnostic Result

5.1.18 Printer State

Pint Speed Print speed is same with ECG rate.
Print Gain The printer print gain is consistent with the ECG
display gain
Printer Printer works normally and can print data.
Normal
No paper The printing paper in the printer compartment is
exhausted, and the printing paper should be
replaced now
No Roller The printer paper compartment cover is not
closed
High Printer will stop printing because of printer head

50
 Temperature with a high temperature.

5.1.19 ECG Lead State

NORMAL The state of the ECG leads disappears and
the ECG waveform starts to be output

ABNORMAL The abnormal lead is displayed, and the

ECG waveform is forced to the baseline.

5.2 Monitor Mode 2(with SpO2 only)

5.2.1 SPO2 Data Storage

5.2.2 SPO2 Value

5.2.3 SPO2 Alarm Limitation.

The option of SPO2 alarm limitation in SPO2 menu will determine SPO2 alarm
limitation of main interface.

5.3 Monitor Mode 3 (with BP only)

5.3.1 BP Measurement

Press shortcut button BP measuring icon to start BP measurement.

5.3.2 Mean Blood Pressure Value and Alarm Limitation.

51
The option of BP alarm limitation in BP menu will determine BP alarm limitation of
main interface.

5.3.3 DBP Value and Alarm Limitation.

The option of DBP alarm limitation in BP menu will determine DBP alarm limitation
of main interface.

5.3.4 SBP Value and Alarm Limitation.

The option of SBP alarm limitation in BP menu will determine SBP alarm limitation of
main interface.

5.3.5 BP Measurement State.

End of BP BP Measuring BP Mode Self-test
Measurement Failure
Cuff OFF Cuff Air Leak Cuff twist
Weak Signal. Over Measurement Body move when
Range measuring

Pressure overrun Signal Saturation Low Pressure

BP Measurement BP Measurement BP Measurement Stop
Abnormal Overtime
Measuring Static Press BP button to
pressure start.

5.4 Monitor Mode 4 (with SPO2 and BP)

52
 5.5 Monitor Mode 5 (with CO2 only)

5.5.1 CO2 Value

5.5.2 CO2 Alarm Limitation

The option of CO2 alarm limitation in CO2 menu will determine CO2 alarm limitation
of main interface.

5.6 Monitor Mode 6 (with SPO2 and CO2)

5.7 Monitor Mode 7 (with BP and CO2)

53
5.8 Monitor Mode 8(with SPO2,BP and CO2)

5.9 System Setting.

54
After entering the system setting menu, there are three ways to operate: shortcut
button, digital knob and touch screen
Shortcut Button

Press the shortcut button corresponding to the icon to move the blue cursor,

move the blue cursor to the option to enter, and then press the shortcut button

corresponding to the icon to enter the corresponding option. Press the shortcut

button corresponding to the icon to return to the main interface

Digital Knob
Rotate digital knob to move blue cursor on the option to choose, and then press the
knob to enter the option. Move the blue cursor on Exit and press the knob to return
to the main interface.
Touch Screen
Click the option to choose directly will enter it. Click the Exit to return to the main
interface.

5.9.1 Language

The currently used language option is shown in green.

The language menu can be operated in three ways: shortcut buttons, digital knob
and touch screen
Shortcut Button

Press shortcut button to move blue cursor on language to choose, and then

press shortcut button to confirm language. Press button to exit the setting

and return to the main interface.

55
Digital Knob
Rotate digital knob to move blue cursor on the language to choose, and then press
the knob will confirm the language. Move the blue cursor on Exit and press the knob
to exit the setting and return to the main interface.
Touch Screen
Click the language to need directly to select it. Click the Exit and exit the option and
return to the setting menu.

5.9.2 Print Time.

The option is to control the print time after pressing Print button in the main
interface.
The currently used print time option is shown in green
The print time menu can be operated in three ways: shortcut buttons, digital knob
and touch screen.
Shortcut Button

Press shortcut button to move blue cursor on the option of print time to

select, and then press shortcut button to confirm print time. Press button to

exist the setting and return to the main interface.

Digital Knob
Rotate digital knob to move blue cursor on the option of print time to select, and
then press the knob will confirm the time. Move the blue cursor on Exit and press
the knob to exit the setting and return to the main interface.

Touch Screen

56
Click the option of print time to need to select the print time. Click the Exit and exit
the option and return to the setting menu.

5.9.3 Print Mode

Print Menu of Monitor Mode 1 and 3

Print Menu of Monitor Mode 2 and 4

Print Menu of Monitor Mode 5 and 7

Print Menu of Monitor Mode 6 and 8

The option is to control the printing waveform type after pressing Print button in the
main interface.
The currently used print mode option is displayed in green.
The print mode menu can be operated in three ways: shortcut buttons, digital knob
and touch screen
Shortcut Button

Press shortcut button to move blue cursor on the option of print mode to

select, and then press shortcut button to confirm the print mode. Press button

to exit the setting and return to the main interface.

57
Digital Knob
Rotate digital knob to move blue cursor on the option of print mode to select, and
then press the knob will set the mode. Move the blue cursor on Exit and press the
knob to exit the setting and return to main interface.

Touch Screen
Click the option of print mode to need to select the print mode. Click the Exit and
exit the option and return to setting menu.

5.9.4 Volume

The option is to control the alarm volume and voice prompt volume. Volume value
will be 0~4. 0 is MUTE. 4 is maximum. When it is 0, the alarm volume will be

permanent forbid. Alarm volume state will show .

Volume Setting Menu can be operated with Shortcut button, Digital Knob and Touch
Screen these 3 methods.

Shortcut Button

Press shortcut button to change volume, and then press shortcut button

to confirm volume. Press button to exit setting and return to the main interface.

Digital Knob

Rotate the digital knob to move the blue cursor to the volume icon , then press the

digital knob, the volume value turns blue, at this time, rotate the digital knob to
modify the volume value, after the volume value is modified, press the digital knob
again, the volume value returns to white, and finally, move the blue cursor to
confirm the option (OK), and press the digital knob to set the volume. Move the blue

58
cursor to the cancel option, press the digital knob not to modify the volume value,
and return to the setting menu.
Touch Screen
Click the left of volume bar will reduce volume value. Click the right of volume bar
will increase the value. Then click the OK option to confirm the volume value. Click
the Cancel option and not change value to return to main interface.

5.9.5 Hear Beat Sound

The option is to control whether there is heart bear sound to output.

The currently used heartbeat sound option is displayed in green. The volume of the
heartbeat sound is controlled by the volume menu
Hear Beat Sound Menu can be operated with Shortcut button, Digital Knob and
Touch Screen these 3 methods.

Shortcut Button

Press shortcut button to move blue cursor on the option of heart beat sound

to select, and then press shortcut button to set whether output the heart beat

sound. Press button to exit setting and return to the main interface.

Digital Knob
Rotate digital knob to move blue cursor on the option of heart beat sound to select,
and then press the knob will set whether to output heart beat sound. Move the blue
cursor on Exit and press the knob to exit the setting and return to main interface.

Touch Screen
Click the option of heart beat sound to select to confirm whether to output heart
beat sound. Click the Exit and exit the option and return to setting menu.
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5.9.6 Prohibition Time of Alarm Time

This option controls the time when the alarm sound is temporarily disabled. This
option works only if the volume value is not 0
When the alarm sound pause button is pressed, the alarm sound will be temporarily
disabled, and the disable time is set by this option

The alarm sound status is displayed as , when the disable time expires, the alarm

sound will be re-enabled.

Alarm sound prohibition time menu can be operated in three ways: shortcut button,
digital knob and touch screen

Shortcut Button

Use the shortcut button to move the blue cursor to the prohibition time option

to be selected, and then press the shortcut button to set the prohibition time.

Press the shortcut button to abandon the setting and return to the setting menu

Digital Knob
Rotate the digital knob to move the blue cursor to the prohibited time option to be
selected Press the digital knob again to set the prohibition time. Move the blue
cursor to the exit option, press the digital knob to abandon the setting and return to
the setting menu
Touch Screen
Press OK to restore the default settings, press Cancel not to restore the default
settings, and return to the main interface.

5.9.7 Event Record

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Event records are used to record some key or special moments. The time and name
of the event will be displayed in the event log
Event record can use shortcut button, digital knob and touch screen to operate.
Shortcut button

When there are multiple pages of recorded events, use the shortcut button to

page up or down, and press the shortcut button to print the event record. Press

the shortcut button to return to the settings menu

Digital knob
Rotating the digital knob can browse up page or down page directly.
Touch Screen

Press to browse up page or down page, press to return setting menu.

5.9.8 Digital Knob

This option is to set the function of the digital knob direction of rotation. The current
use of setting is in Green.
Digital Knob setting menu can use shortcut button, digital knob and touch screen to
operate.
Shortcut button

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Press shortcut button to move the blue cursor to the select options, then

press shortcut button to set the rotation function of digital knob. Press

shortcut button to quite settings and return to setting menu.

Digital Knob
Rotate the digital knob to move the blue cursor to select options, and then press
digital knob to set up the rotation function of digital knob. Move the blue cursor to
Exit, and press digital knob to quit setting and return to the setting menu.
Touch Screen
Click to selected option to set the rotation function of digital knob. Click the Exit
option to quit the setting and return to the setting menu.

5.9.9 About

About menu display the version information of current device.

5.10 ECG Menu

5.10.1 ECG Display Rate

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This option controls the display speed of ECG wave on the main interface. Currently
used rate display in green.
This menu can use shortcut button, digital knob and touch screen to operate.
Shortcut Button

Press shortcut button to move the blue cursor to the select rate options, then

press shortcut button to set display rate. Press shortcut button to quit the

settings and return to the ECG menu.

Digital Knob
Rotate the digital knob and move the blue cursor to select Rate options, and then
press digital knob to set up the display rate. Move the blue cursor to Exit, press
digital knob to quit the setting and return to the ECG menu.
Touch Screen
Click the selected Rate option to set the display rate . Click the Exit option, then quit
the setting and return to the ECG menu.

5.10.2 ECG display gain

This option is used to control the display width of ECG waveform in the main
interface. The current use of gain display in green.
This menu can use shortcut button, digital knob and touch screen to operate.
Shortcut Button

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Press shortcut button to move the blue cursor to the select gain options, then

press shortcut button to set ECG Gain. Press shortcut button to quit the

settings and return to the ECG menu.

Digital knob
Rotate the digital knob and move the blue cursor to select Gain options, and then
press digital knob, to set up the ECG Gain. Move the blue cursor to Exit, press digital
knob to quit the setting and return to the ECG menu.
Touch screen: Click the selected Gain option to set the ECG Gain. Click the Exit option,
then quit the setting and return to the ECG menu.

5.10.3 HR Alarm Limitation

This option sets the upper and lower limits of the heart rate alarm. When heart rate
beyond the upper and lower range, the device will start HR alarm. After modify the
HR alarm upper and lower limits, the upper and lower limits of HR on the main
interface will be also changed.
The heart rate alarm is a physiological alarm.
This menu can be operated in three ways: shortcut buttons, digital knob and touch
screen
Shortcut button

Press shortcut button to move the blue cursor to the modified value, then

press shortcut button to modify the value. After finish the modification, press

shortcut button to set the value. Press shortcut button to quit the settings and

return to the ECG menu.

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Digital Knob
Rotate the digital knob, move the blue cursor to the value need to modify, and then
press digital knob, the value turn blue , at this time, modify the value by rotating the
digital knob, after modified, re-press the digital knob, recover the blue cursor. After
modification, move the blue cursor to the OK , press digital knob to set value. Move
the blue cursor to Exit, and press digital knob to quit the setting and return to the
ECG menu.
Touch Screen
Click the value to modify, after modification, press OK to set value. Click the Exit
option, then quit the setting and return to the ECG menu.

5.10.4 HR Trend

This option is used to count changes in heart rate values over a period of time. If no
statistical data, no data will be displayed in the heart rate trend graph, otherwise,
the statistical bar chart will be output
The interval of heart rate statistics is 1 minute.
The date and period of the current statistics are at the bottom of the chart. The
statistics bar chart is displayed for 6 hours at a time. You can change the time range
to view the statistics chart of a day.
You can also view the heart rate at a certain time in the statistical chart. By moving
the observation box, you can view the heart rate at every moment within 30 minutes
and display it in the form of a table at the bottom of the statistical chart.
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This menu can use shortcut button, digital knob and touch screen to operate.
Shortcut button

Press shortcut button to move the blue cursor to the date selection, then press

shortcut button to modify the date to check the statistics for different dates.

Move the blue cursor to time range and use shortcut button to modify time

range to view statistics of different time ranges. Move the blue cursor to View

options and press shortcut button to move observe frame to the right or left to

view the heart rate at a certain moment in the table below the chart. Press button

to print the statistics of the current time range. Press shortcut button to return

to the ECG menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the date option, press the digital
knob to switch to view the statistics of different dates. Move the blue cursor to time
range option and press digital knob to switch and view statistics of different time
periods. Move the blue cursor to Checking and press digital knob to move the
viewing frame circularly, The heart rate at a certain time can be viewed in the table
below the chart. Move the blue cursor to Exit and press digital knob to return to the
ECG menu.
Touch Screen
Click DATE option to switch to view the statistical figure of different date. Click time
period option to switch to check the statistical chart during the different time
periods. Click to view the location in the statistical chart, observation box will move
to the location to view, and in the table below shows the heart rate value within
every moment in observation frame. Click Exit and return to the ECG menu.

5.10.5 ECG Width Module

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This option sets the working bandwidth of the ECG filter to adapt the working
bandwidth of the filter to the current application environment
The current working bandwidth is in green.
After modify the working bandwidth, the working bandwidth status on the main
screen also changes.
This menu can be operated using shortcut buttons, digital knob and touch screen.
Shortcut buttons

Press shortcut button to move the blue cursor to the selected working

bandwidth, then press shortcut button to set working bandwidth. Press shortcut

button to quit the settings and return to the ECG menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select working bandwidth, and then
press digital knob to set up the new working bandwidth. Move the blue cursor to Exit,
press digital knob to quit the setting and return to the ECG menu.
Touch Screen
Click the selected working bandwidth to set the new working bandwidth . Click the
Exit option, then quit the setting and return to the ECG menu.

5.10.6 Alternating Current Filter

This option sets the filter frequency for the AC filter. The current filter options in use
is shown in green.
After the filter option of AC filter is modified, the filter state on the main screen will
also change.
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This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Button

Press shortcut button to move the blue cursor to the select Filter options, then

press shortcut button to set the new Filter. Press shortcut button to quit the

settings and return to the ECG menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select Filter options, and then press
digital knob to set up the new Filter. Move the blue cursor to Exit, press digital knob
to quit the setting and return to the ECG menu.
Touch Screen
Click to selected Filter option to set the new Filter . Click the Exit option, then quit
the setting and return to the ECG menu

5.10.7 Muscle Filter

This option controls whether to use muscle filter. The filter options currently in use
are shown in green.
After the filter option of Muscle filter is modified, the filter state on the main screen
will also change.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Button

Press shortcut button to move the blue cursor to the select Filter options, then

press shortcut button to set the new Filter. Press shortcut button to quit the

settings and return to the ECG menu.

Digital Knob

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Rotate the digital knob, move the blue cursor to select Filter options, and then press
digital knob to set up the new Filter. Move the blue cursor to Exit, press digital knob
to quit the setting and return to the ECG menu.
Touch Screen
Click to selected Filter option to set the new Filter . Click the Exit option, then quit
the setting and return to the ECG menu

5.10.8 Low-Pass Filter

This option controls whether a low pass filter is used. The filter options currently in
use are shown in green.
After the filter option of Low-Pass filter is modified, the filter state on the main
screen will also change.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Buttons

Press shortcut button to move the blue cursor to the select Filter options, then

press shortcut button to set the new Filter. Press shortcut button to quit the

settings and return to the ECG menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select Filter options, and then press
digital knob to set up the new Filter. Move the blue cursor to Exit, press digital knob
to quit the setting and return to the ECG menu.
Touch Screen
Click the selected Filter option to set the new Filter . Click the Exit option, then quit
the setting and return to the ECG menu

5.10.9 Lead Mode

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This option controls the ECG Lead mode is three-lines or five-lines mode. The current
line system is shown in green.
After the lead line mode is modified, the ECG waveform display on the main
interface is also changed. Choose three-lines system to display one waveform, and
choose five-lines system to display two waveforms.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut buttons

Press shortcut button to move the blue cursor to the select Lead Mode, then

press shortcut button to set the new Lead Mode. Press shortcut button to quit

the settings and return to the ECG menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select Lead Mode, and then press
digital knob to set up the new lead mode. Move the blue cursor to Exit, press digital
knob to quit the setting and return to the ECG menu.
Touch Screen
Click the selected Lead Mode option to set the new lead mode . Click the Exit option,
then quit the setting and return to the ECG menu

5.11 SpO2 Menu

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5.11.1 SpO2 Alarm Limitation

This option sets the upper and lower limits of blood oxygen alarms. When the blood
oxygen value exceeds the upper and lower limits, the equipment will start the blood
oxygen alarm. After changing the upper and lower limits of blood oxygen alarm, the
upper and lower limits of blood oxygen on the main screen will also be changed.
Blood oxygen alarm is a physiological alarm.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Buttons

Press shortcut button to move the blue cursor to the value need to be modified,

then press shortcut button to change value. After modified value, press

shortcut button to set the new value. Press shortcut button to quit the settings

and return to the SpO2 menu.

Digital Knob
Rotate the digital knob, move the blue cursor to the value need to modify, press
digital knob, the value will turn blue, at this time modify the value by rotating the
digital knob, after modified, re-press the digital knob, recover the blue cursor. After

71
modification, move the blue cursor to the OK , press digital knob to set value. Move
the blue cursor to Exit, press digital knob to quit the setting and return to the SpO2
menu.
Touch Screen
Click the value to modify, after modification, press OK to set value. Click the Exit
option, then quit the setting and return to the SpO2 menu.

5.11 2 SpO2 Trend

This option is used for statistics of SpO2 value changes within a period of time.
Without statistics value, SpO2 trend chart will display no data. Otherwise, output the
blood oxygen bar chart.
The interval of SpO2 statistics is 1 minute.
The date and period of the current statistics are at the bottom of the chart. The
statistics bar chart is displayed for 6 hours at a time. You can change the time range
to view the statistics chart of a day.
You can also view the SpO2 value at a certain time in the statistical chart. By moving
the observation box, you can view the SpO2 Value at every moment within 30
minutes and display it in the form of a table at the bottom of the statistical chart.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut buttons

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Press shortcut button to move the blue cursor to the date selection, then press

shortcut button to modify the date to check the statistics for different dates.

Move the blue cursor to time range and use shortcut button to modify time

range to view statistics of different time ranges. Moving the blue cursor to View

options, press shortcut button to move observe frame to the right or left to

view the SpO2 value at a certain time in the table below the chart. Press button to

print the statistics of the current time range. Press shortcut button to return to

the SpO2 menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the date option, press the digital
knob to switch and view the statistical graph of different dates. Move the blue cursor
to the time period option and press the digital knob to switch and view the statistical
graphs of different time periods. Move the blue cursor to Checking, press digital
knob to move the viewing frame circularly, The SpO2 value at a certain time can be
viewed in the table below the chart. Move the blue cursor to Exit, press digital knob
to return to the SpO2 menu.
Touch Screen
Click DATE option to switch to view the statistical figure of different date. Click time
period option to switch to check the statistical chart during the different time
periods. Click to view the location in the statistical chart, observation box will move
to the location to view, and in the table below shows the SpO2 value within every
moment in observation frame Click Exit , return to the SpO2 menu.

5.12 BP menu

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5.12.1 BP Measure Mode

This option controls blood pressure using adult mode or child mode. The current
blood pressure measurement model in use is shown in green.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut buttons

Press shortcut button to move the blue cursor to the select the measure mode,

then press shortcut button to set the new measure mode. Press shortcut button

to quit the settings and return to the BP menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select the measure mode, and then
press digital knob to set up the new measure mode. Move the blue cursor to Exit,
press digital knob to quit setting and return to the BP menu.
Touch Screen
Click to selected measure mode to set the new measure mode . Click the Exit option,
then quit the setting and return to the BP menu.

5.12.2 BP Measure Period

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This option controls the cycle time of blood pressure measurements. The blood
pressure measurement cycle currently in use is shown in green.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut buttons

Press shortcut button to move the blue cursor to the select measure period,

then press shortcut button to set the new measure period. Press shortcut button

to quit the settings and return to the BP menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select measure period, and then
press digital knob to set up the new measure period. Move the blue cursor to Exit,
press digital knob to quit the setting and return to the BP menu.
Touch Screen
Click the selected measure period to set the new measure period . Click the Exit
option, then quit the setting and return to the BP menu.

5.12.3 BP Measure Type

This option sets single or continuous blood pressure measurements. The type of
blood pressure measurement currently in use is shown in green.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Buttons

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Press shortcut button to move the blue cursor to the select measure type, then

press shortcut button to set the new measure type. Press shortcut button to

quit the settings and return to the BP menu.

Digital Knob
Rotate the digital knob, move the blue cursor to select measure type, and then press
digital knob to set up the new measure type. Move the blue cursor to Exit, press
digital knob to quit the setting and return to the BP menu.
Touch Screen
Click to selected measure type to set the new measure type . Click the Exit option,
then quit the setting and return to the BP menu.

5.12.4 Systolic Pressure Alarm Limits

This option is to set the systolic pressure alarm upper and lower limits. When the
systolic blood pressure beyond the upper and lower range, the systolic blood
pressure alarm will start. After modified the systolic blood pressure alarm of upper
and lower limits, systolic blood pressure on the main interface of upper and lower
limit value will be also changed.
Systolic pressure alarm is a physiological alarm.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Buttons

Press shortcut button to move the blue cursor to the modified value, then press

shortcut button to modify the value. After finish the modification, press

shortcut button to set the value. Press shortcut button to quit the settings and

return to the BP menu.

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Digital Knob
Rotate the digital knob, move the blue cursor to the value need to modify, and then
press digital knob, the value will turn blue, at this time, modify the value by rotating
the digital knob, after modified, re-press the digital knob, recover the blue cursor.
After modification, move the blue cursor to the OK , press digital knob to set new
value. Move the blue cursor to Exit, press digital knob to quit the setting and return
to the BP menu.
Touch Screen
Click the value to modify, after modification, press OK to set value. Click the Exit
option, then quit the setting and return to the BP menu.

5.12.5 Diastolic Pressure Alarm Limits

This option is to set diastolic pressure alarm upper and lower limits. When the
diastolic pressure is beyond the scope of upper and lower, the diastolic pressure
alarm will start. After modified the diastolic pressure alarm of the upper and lower
limits , the diastolic blood pressure on the main interface of upper limit and lower
limit value will be also changed.
Diastolic pressure alarm is a physiological alarm.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut buttons

Press shortcut button to move the blue cursor to the modified value, then press

shortcut button to modify the value. After finish the modification, press

shortcut button to set the new value. Press shortcut button to quit the

settings and return to the BP menu.

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Digital Knob
Rotate the digital knob, move the blue cursor to the value need to modify, and then
press digital knob, the value will turn blue, at this time, modify the value by rotating
the digital knob, after modified, re-press the digital knob, recover the blue cursor.
After modification, move the blue cursor to the OK , press digital knob to set value.
Move the blue cursor to Exit, press digital knob to quit the setting and return to the
BP menu.
Touch Screen
Click the value to modify, after modification, press OK to set new value. Click the Exit
option, then quit the setting and return to the BP menu.

5.12.6 MEAN Alarm Limits

This option is to set MEAN alarm upper and lower limits. When the MEAN is beyond
the scope of upper and lower, the MEAN alarm will start. After modified the MEAN
alarm of the upper and lower limits , the MEAN on the main interface of upper limit
and lower limit value will be also changed.
The average pressure alarm is a physiological alarm.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Button

Press shortcut button to move the blue cursor to the modified value, then press

shortcut button to modify the value. After finishing the modification, press

shortcut button to set the new value. Press shortcut button to quit the

settings and return to the BP menu.

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Digital Knob
Rotate the digital knob, move the blue cursor to the value need to modify, and then
press digital knob, the value will turn blue, at this time, modify the value by rotating
the digital knob, after modified, re-press the digital knob, recover the blue cursor.
After modification, move the blue cursor to the OK , press digital knob to set new
value. Move the blue cursor to Exit, press digital knob to quit the setting and return
to the BP menu.
Touch Screen
Click the value to modify, after modification, press OK to set new value. Click the Exit
option, then quit the setting and return to the BP menu.

5.12.7 Systolic Blood Pressure Trend

This option is used for statistics of Systolic Blood Pressure value changes within a
period of time. Without statistics value, Systolic Blood Pressure trend chart will
display no data. Otherwise, output systolic blood pressure bar chart.
The time interval for systolic blood pressure statistics is 1 minute.
The date and period of the current statistics are at the bottom of the chart. The
statistics bar chart is displayed for 6 hours at a time. You can change the time range
to view the statistics chart of a day.
You can also view the Systolic blood pressure values at a certain time in the
statistical chart. By moving the observation box, you can view the Systolic blood

79
pressure values at every moment within 30 minutes and display it in the form of a
table at the bottom of the statistical chart.
This menu can be operated by shortcut buttons, digital knob and touch screen.
Shortcut Buttons

Press shortcut button to move the blue cursor to the date selection, then press

shortcut button to modify the date to check the statistics for different dates.

Move the blue cursor to time range and use shortcut button to modify time

range to view statistics of different time ranges. Moving the blue cursor to View

options, press shortcut button to move observe frame to the right or left to

view the Systolic blood pressure values at a certain time in the table below the chart.

Press button to print the statistics of the current time range. Press shortcut

button to return to the BP menu.

Digital Knob
Rotate the digital knob, move the blue cursor to the date, and then press digital
knob to switch and view statistics on different dates. Move the blue cursor to time
range option, press digital knob to switch and view statistics of different time
periods. Move the blue cursor to Checking and press digital knob to move the
viewing frame circularly, The Systolic blood pressure values at a certain time can be
viewed in the table below the chart. Move the blue cursor to Exit and press digital
knob to return to the BP menu.
Touch Screen
Click on the date option to toggle between viewing charts for different dates. Click
the time period option to switch to view the statistical graphs of different time
periods. Click the position to be viewed in the statistical graph, the observation box
will move to the position to be viewed, and the systolic blood pressure value at each
moment within the scope of the observation frame will be displayed in the table
below. Click the Exit option to return to the blood pressure menu.

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5.12.8 Diastolic blood pressure trends

This option is used to count changes in diastolic blood pressure values over a period
of time. If no statistical data, no data will be displayed in the diastolic blood pressure
trend graph, otherwise, the diastolic blood pressure bar chart will be output.
The time interval for diastolic blood pressure statistics is 1 minute.
At the bottom of the chart is the date and time period of the current statistical data.
The statistical graph can display a 6-hour statistical histogram at a time, and you can
view a one-day statistical graph by switching the time period.
You can also view the diastolic blood pressure value at a certain time in the
statistical graph. By moving the observation frame, you can view the diastolic blood
pressure value at each moment within 30 minutes, and display it in the form of a
number table below the statistical graph.
This menu can be operated using shortcut buttons, digital knob and touch screen.
Shortcut Button

Use the shortcut button to move the blue cursor to the date option, use the

shortcut button to modify the date, and you can view the statistical graph of

different dates. Move the blue cursor to the time period option, and use the

shortcut button to modify the time period to view the statistical graphs of

different time periods. Move the blue cursor to the viewing option, and use the

81
shortcut button to move the observation frame to the left or right to view the

diastolic blood pressure at a certain moment in the number table below the

statistical graph. Press the shortcut button to print a statistical graph for the

current time period. Press the shortcut button to return to the blood pressure

menu.
Digital Knob
Rotate the digital knob to move the blue cursor to the date option, press the digital
knob to switch to view the statistical graph of different dates. Move the blue cursor
to the time period option, and press the digital knob to switch to view the statistical
graphs of different time periods. Move the blue cursor to the viewing option, press
the digital knob to move the observation frame circularly, The diastolic blood
pressure value at a certain time can be viewed in the number table below the
statistical graph. Move the blue cursor to Exit and press the digital knob to return to
the blood pressure menu.

Touch Screen
Click on the date option to toggle between viewing charts for different dates. Click
the time period option to switch to view the statistical graphs of different time
periods. Click the position to be viewed in the statistical graph, the observation
frame will move to the position to be viewed, and the diastolic blood pressure value
at each moment within the scope of the observation frame will be displayed in the
table below. Click the Exit option to return to the blood pressure menu.

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5.12.9 Mean pressure trend

This option is used to count the changes of the average pressure value over a period
of time. If there is no statistical data, no data will be displayed in the mean pressure
trend graph, otherwise, the mean pressure bar chart will be output.
The time interval for mean pressure statistics is 1 minute.
At the bottom of the chart is the date and time period of the current statistical data.
The statistical graph can display a 6-hour statistical histogram at a time, and you can
view a one-day statistical graph by switching the time period.
The mean pressure value at a certain moment can also be viewed in the statistical
graph. By moving the observation frame, the mean pressure value at each moment
within 30 minutes can be viewed, and displayed in the form of a number table below
the statistical graph.
This menu can be operated using shortcut buttons, digital knob and touch screen.
Shortcut Button

Use the shortcut button to move the blue cursor to the date option, use the

shortcut button to modify the date, and you can view the statistical graph of

different dates. Move the blue cursor to the time period option, and use the

shortcut button to modify the time period to view the statistical graphs of

different time periods. Move the blue cursor to the viewing option, and use the

83
shortcut button to move the observation frame to the left or right to view the

mean pressure at a certain moment in the number table below the statistical graph.

Press the shortcut button to print a statistical graph for the current time period.

Press the shortcut button to return to the blood pressure menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the date option, press the digital
knob to switch to view the statistical graph of different dates. Move the blue cursor
to the time period option, and press the digital knob to switch to view the statistical
graphs of different time periods. Move the blue cursor to the viewing option, press
the digital knob to move the observation frame circularly, and view the mean
pressure value at a certain moment in the number table below the statistical graph.
Move the blue cursor to Exit and press the digital knob to return to the blood
pressure menu.
Touch Screen
Click on the date option to toggle between viewing charts for different dates. Click
the time period option to switch to view the statistical graphs of different time
periods. Click on the position to be viewed in the statistical graph, the observation
frame will move to the position to be viewed, and the mean pressure value at each
moment within the range of the observation frame will be displayed in the table
below. Click the Exit option to return to the blood pressure menu.

5.13 CO2 menu

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5.13.1 CO2 Alarm Limits

This option sets the upper and lower limits of the CO2 alarm. When the CO2 exceeds
the upper and lower limits, the device will start the CO2 alarm. After modifying the
upper and lower limits of CO2 alarm, the upper and lower limits of CO2 on the main
interface will also change accordingly.
The CO2 alarm is a physiological alarm.
This menu can be operated using shortcut buttons, digital knob and touch screen.
Shortcut Buttons

Use the shortcut button to move the blue cursor to the value to be modified,

and then use the shortcut button to change the value. After the value is

modified, press the shortcut button to set a new value, press the shortcut button

to abandon the setting and return to the CO2 menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the value to be modified, and
then press the digital knob, the value turns blue, then rotate the digital knob to
change the value, after the modification is completed, press the digital knob again to
restore the blue cursor. After all the values are modified, move the blue cursor to
the OK option, and press the digital knob to set the new value. Move the blue cursor
to Exit, press the digital knob to abandon the setting and return to the CO2 menu.
Touch Screen.

Click the value to modify it. After modification, click （OK） to set the value. Click the

Exit option to discard the settings and return to the CO2 menu.

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5.13.2 CO2 trend

This option is used to count changes in CO2 values over a period of time. If there is
no statistical data, no data will be displayed in the CO2 trend graph, otherwise, a
CO2 bar chart will be output.
The time interval for CO2 statistics is 1 minute.
At the bottom of the chart is the date and time period of the current statistical data.
The statistical graph can display a 6-hour statistical histogram at a time, and you can
view a one-day statistical graph by switching the time period.
The CO2 value at a certain moment can also be viewed in the statistical graph. By
moving the observation frame, the CO2 value at each moment within 30 minutes can
be viewed, and displayed in the form of a number table below the statistical graph.
This menu can be operated using shortcut buttons, digital knob and touch screen.
Shortcut Button

Use the shortcut button to move the blue cursor to the date option, use the

shortcut button to modify the date, and you can view the statistical graph of

different dates. Move the blue cursor to the time period option, and use the

shortcut button to modify the time period to view the statistical graphs of

different time periods. Move the blue cursor to the viewing option, and use the

shortcut button to move the observation frame to the left or right to view the

86
CO2 value at a certain moment in the number table below the statistical graph. Press

the shortcut button to print a statistical graph for the current time period. Press

the shortcut button to return to the CO2 menu.

Digital Knob
Rotate the digital knob to move the blue cursor to the date option, press the digital
knob to switch to view the statistical graph of different dates. Move the blue cursor
to the time period option, and press the digital knob to switch to view the statistical
graphs of different time periods. Move the blue cursor to the viewing option, press
the digital knob to move the observation frame circularly, and view the CO2 value at
a certain moment in the number table below the statistical graph. Move the blue

cursor to （Exit） and press the digital knob to return to the CO2 menu.

Touch Screen
Click on the date option to toggle between viewing charts for different dates. Click
the time period option to switch to view the statistical graphs of different time
periods. Click on the position to be viewed in the statistical graph, the observation
frame will move to the position to be viewed, and the CO2 value at each moment
within the range of the observation frame will be displayed in the table below. Click

（Exit） to return to the CO2 menu.

6 Pacer Operation

PACER module installed in DM7000 is used for pacing the patient.

 Must be in manual mode to activate pacing.

87
 6.1 Pacer Detection

The pacing function of DM7000 can only be used after the PACER module is
installed. If no PACER module is installed, DM7000 will prompt "No PACER module"

6.2 Pacer Settings

Press the PACER button on the left side of the panel to enter the PACER mode

Modifiable options are pacer current, pacer frequency, and pacer mode

88
Pacer Current

Pacer current setting range is 10 mA ~ 180mA, each step is 10mA

Pacer current can be modified by the current modify button on the PACER panel
Pacer Frequency

Pacer frequency controls the pacing interval. Its unit is heart rate / minute, which is
the number of pacing performed per minute.
Pacer frequency setting range is 30 ~ 180, each step is 2
The pacer frequency can be modified by the frequency modification button on the
PACER panel
 How pacer works is affected by both pacer frequency and pacer mode
89
Pacer Mode

On-demand pacer

Independent pacer
Pacer mode includes on-demand pacer and independent pacer
On-demand pacer
If no ECG R wave is detected during the pacing cycle, pacer is performed, otherwise
pacer is not performed
Independent pacer
Pacing only according to the pacing cycle
Pacer mode can be switched by the frequency mode button on the PACER panel
90
Pacer Initiation
Select the manual mode by the knob on the from panel,
Press the start button on the PACER panel to start pacing. At the same time, the
pacing status changes from PACER OFF to PACER ON and starts blinking

After pacing starts, pacer pulses will be output according to the set pacer current,
pacer frequency and pacer mode. And automatically mark at pacing time
 During pacing, you can also modify the pacer current, pacer frequency,
and pacer mode. The modified settings will take effect at the next pacing
pulse.
 Must be in manual mode to activate pacing.
Pacer Stop and Withdrawal
Pressing the start button during pacing will stop pacing

91
After pacing is stopped, pressing the pacer button will exit the pacer mode
 Cannot exit pacer mode during pacing

7 Maintaining the DM7000

The maintaining, cleaning and Troubleshooting of the DM7000

will be described in this section:
 Maintaining
 Cleaning and disinfecting
 Troubleshooting

7.1 Maintenance

The maintenances are needed for the optimized operation of the

DM7000. The maintaining should be performed periodically, usually
weekly or monthly inspections are recommended, but the actual
checking period depends on the using frequency of the DM7000.

92
7.1.1 The frequency of inspection

Usually, we recommend inspecting the DM7000 once a week or

twice a month, but if the using of the DM7000 is so frequent, more
inspections should be performed.
The table below describes a general rule to perform the inspection:
Frequency of use (n/month) inspection

1/month Once a week

2~3/month Twice a week
Infrequent using(1~2 a year) Once a month

Caution

If the DM7000 should be used more than 4 times a month, we

recommend that the DM7000 should be inspected by authorized
service personnel at least once in half a year.

Inspection schedule
The general inspection schedules are described below, the operator should follow
the rules to perform the inspection, and improper inspection may cause damage to
the DM7000.
Check the status of indicator and the voice prompt.
If the DM7000 starts without electrode pads connection, the indicator of “Check pad”
will be flickering and a voice prompt of “Check the electrode” will be broadcast. If
either the two information does not appear, contact the authorized service
personnel or the DM7000 customer service to make a professional repair for the
DM7000.

WARNING!

If the conditions above are observed during the inspection of the

DM7000, the DM7000 must not used to any patient.

93
Check the DEFIBRILLATOR ELECTRODES
Inspect the packaging of any disposable DEFIBRILLATOR ELECTRODES to ensure
integrity of any seals and validity of any expiry date.
Charge the ENERGY STORAGE DEVICE once a year. Please contact our service centers
or agencies to do this.

Cleaning and disinfecting

The cleaning and disinfecting of the DM7000 should be done frequently.
The followings are the guidelines of cleaning and disinfecting of the DM7000:
Cleaning
Before cleaning the DM7000, making sure that the DM7000 has been power off,
because any cleaning with the machine powered on may cause a shock hazard to the
cleaners.

Note

We recommend that the cleaners use warm water to clean the

DM7000.Other cleansers without strong solvents could also be used.

Caution

Don’t let the water or other cleansers get into the DM7000 when
clean the machine, because these liquid may cause some damage to
the DM7000 or a shock hazard to the cleaners.

Use the soft cloth to wipe up the DM7000, but a cleaning with a brush should never
be done.

94
 Caution

When cleaning the electrode pads socket of the DM7000, don’t use
too much water or cleanser.

Disinfecting
We recommend making disinfection to the DM7000 with the alcohol (it is easy to get
in the hospitals or the clinics) or other cleansers without strong solvents.

Caution

Never use the following cleansers to the DM7000:

Acetone, Ammonia cleanser, Glutaraldehyde.

Troubleshooting
Some Problem may occur during the operation of the DM7000. The indicators and
the voice prompts will be given to the operator to indicate the problem by the
DM7000.
The general trouble shootings are described below, which help the operator to solve
some problem.

Note

The operator could try to solve the problem which occurring prior to or
during the operation according to these trouble shootings below.

The troubleshooting of attaching electrode pads

Problem description:

95
The voice prompt of “Check the electrode” is still broadcast when the electrode pads
have been placed on the patient and the pads connector has been connect to the
socket of the DM7000.

Check the electrodes.

Solution:

If the electrode pads are dry, damaged or out-of-date, replace

the current pads with a new one and try again.
Ensure that the electrode pads have been properly adhered
to the patient. If doesn’t, wipe off the water or moisture from
the chest and shave the hair from the chest, then press the
pads firmly on the chest of the patient.
Make sure that the two pads don’t touch each other.

If the pads connector is inadequately connected to the socket

of the DM7000, push the connector firmly into the socket.
Troubleshooting of analyzing

Problem description:

The analyzing is interrupted during the analyzing period, and the voice prompt of
“Check the electrode” is broadcast.

Solution:

Shut down the DM7000 and check the pads placed on the
patient, if they are not properly connected, press the pads
firmly on the chest of the patient, then start the DM7000
again.
If the patient has moved during the analyzing period, shut
down the DM7000 and stop the patient motion if possible.

96
 Troubleshooting of charging

Problem description:

The charging is stopped during the charging period, and the voice prompt of
“Charging cancel, check the electrode” is broadcast.

Charging cancelled, check the electrodes.

Solution:

Shut down the DM7000 and check pads connector. If the

connector inadequately connects to the socket of the
DM7000, push the connector firmly into the socket.

Shut down the DM7000 and check the pads contacting with
patient’s bare chest. If the pads are poorly contacted, wipe off
the moisture and press the pads firmly on the chest of the
patient.
Troubleshooting of defibrillation

Problem description:

The DM7000 automatically has an internal discharging after the charging is finished
and broadcast a voice prompts of “Time out, analysis restart”.

Time out, analysis restart.

Solution:

If the operator doesn’t press the shock button in 30 seconds

after the charging is finished, the DM7000 will automatically
make an internal discharging.

97
 Press the shock button in 30 seconds after the voice prompts
of “press flashing shock button”.

Press flashing shock button.

Troubleshooting of Monitor
ECG and HR Measuring
phenome Additional Cause Resolving Methods
na sorts phenomenas

1）You haven’t cleaned

After cleaned the skin of the
the patient skin when
patient, stick the new electrode
connecting the electrode
pieces.
pieces.

2）The time of opening

Change the electrode pieces
the electrode pieces is
1.The which have good electricity
too long and the
results of transmitting capablities and in
electricity transmitting
HR a) ECG wave is the insurance period.
capablity is not well.
Measure foul-up.
Add the grounding line to the
and PR
3)prevent disturbance of device, ensure that not to impact
Measure
high frequency electric the ECG measure of the patient
have great
knife when the electric knife is not
difference
cutting the skin.
s
Please set the device far from
4) Other electric
the high-power device or
disturbance.
instrument.

The lead of present Switch the monitor Lead and

b) ECG signal is too
monitoring for the enhance the ECG GAIN to make
small to distinguish.
patient is not clear. the wave more clearly.

98
 Switch the monitor Lead to make
c) ECG signals are
The present monitoring the “R”wave more clearly, if the
steady, while the
Lead of the patient “P”, effect is not obvious, we can
discrepancy of HR
“R”, “T” wave highness check the electrode situation and
data and PR data is 2
difference is too small. make it conform to the measure
or 3 times.
requirement.
Turn on the AC Filter in the ECG
d) ECG signals are settings, when monitoring, we
AC disturbance is too
dense and we can’t should set the “monitor
grave
see clearly. mode”according to the using
requirement.
“Multi Mode” and V Make the V Lead of the Multi
There is no wave of V
Lead” measuring settings Lead conform to the V Lead
Lead.
are different measure settings.

Pull out the ECG

2．ECG
lines, there are mixed
wave is a ECG Lead is broken Change the ECG Lead line.
waves when touching
straight
by hand.
line
Pull out the ECG
lines, there are no There is something wrong
Inform the repair department.
mixed waves when with the inner device.
touching by hand.

99
8 Specification

The Specification of physical, electronic isolation, defibrillator,

battery, electromagnetic compatibility, and rhythm recognition
performance will be described in this section:
 General . . . . . . . . . . . . . . . . . . . . . . . . . . .
 Defibrillator. . . . . . . . . . . . . . . . . . . . . . . . .
 Monitor/Display . . . . . . . . . . . . . . . . . . . . .
 Recorder . . . . . . . . . . . . . . . . . . . . . . . . . .
 Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . .
 Safety Effectiveness Summary . . . . . . . . .
 AED Rhythm Recognition Performance .

8.1 General

Weight: 11 pounds (5kg) (basic configuration).

Size: 13 x 9.6 x 7.2 inches (33 x 24 x 18 cm).
Operating:
Temperature*: 0 to 40° C
Humidity* (NC): 15 to 95% RH
Altitude: Up to 4572 M (15,000 feet)
Transport and Storage:
Temperature: -20 to 55°C
Humidity: 15 to 95% RH (non-condensing)
Atmospheric pressure: 860 to 1060 hPa
Shock/vibration: ISTA 1A
Water: IEC 529, IPxx.
Operating Power: Ni-MH 12 volt - M&B
Defibrillator
Category Parameter
Waveform: Truncated Exponential Biphasic

100
Energy Select: 2, 5, 7, 10, 20, 30, 50, 70, 100, 150, 200, 300, 360 J.
Output Energy +/- 15% or 1J (whichever is greater) at 25 to 175
Accuracy: ohms
+/- 5% or 1J at 50 ohms
AED Energy Sequence 150, 200J（twice）
150, 150, 200J（three times）
150,150, 150, 200J（Four times）
manual mode
no battery, 100% AC <9 seconds
mains voltage,charge
to max energy(360J)
New battery, ,charge <14 seconds
to max energy(360J)
no battery, 90% AC <9 seconds
mains voltage,charge
to max energy(360J)
with a Ni-MH 12 volt - <15 seconds
M&B battery after 15
discharges, charge to
max energy(360J)
no battery, 90% AC <20 seconds
mains voltage,from
system on to charge
max energy complete

with a Ni-MH 12 volt - <25 seconds

M&B battery after 15
discharges, from
system on to charge
max energy complete

101
AED mode
no battery, 100% AC <7 seconds
mains voltage,charge
to max energy(200J)
New battery, ,charge <9 seconds
to max energy(200J)

no battery, 90% AC <7 seconds

mains voltage,charge
to max energy(200J)
with a Ni-MH 12 volt - <10 seconds
M&B battery after 15
discharges, charge to
max energy(200J)
no battery, 90% AC <25 seconds
mains voltage,from
system on to charge
max energy complete
with a Ni-MH 12 volt - <28 seconds
M&B battery after 15
discharges, from
system on to charge
max energy complete
Analyzing time 9 seconds

The Maximum Voltage 1340±50V

Defibrilator AED 20Ω to 200Ω

Resistor mode
range Manual 20Ω to 1500Ω
mode

102
 Synchronous delay <60ms
time

De-select synchronized press "syn" key again

mode condition switch to AED mode
switch to monitor mode

Waveform Details:
The tables below provide details of the waveforms delivered by the DM7000 when
connected to resistive loads of 25, 50, and 100 Ohms and set to its maximum output.
The waveforms are characterized by DM7000 values for peak current (Ip), for
biphasic: duration of the first output phase (tphase1), and duration of the second
output phase (tphase2). The values shown are within 15%.
Waveform: Truncated Exponential Biphasic

103
 Energy(J) Load（Ω） Ip1 Ip2 Phase1 Phase2 interval
(Amps) (Amps) (ms) (ms) (ms)
200 25 46 34.0 5.5 3.3 0.7
50 23 17.0 10.9 6.6 0.7

75 15.3 11.3 16.3 8.9 0.7

100 11.5 8.5 19.7 9.6 0.7
125 9.2 6.8 20.5 10.2 0.7
150 7.6 5.8 19.8 10 0.7
175 6.5 5.2 19.8 10 0.7
360 25 53.6 39.2 5.6 3.8 0.7

50 26.8 19.6 11.3 7.6 0.7

75 17.9 13.1 16.9 9.9 0.7
100 13.4 9.8 19.7 9.5 0.7
125 10.7 7.8 19.5 9.9 0.7
150 8.9 6.8 19.9 10.1 0.7
175 7.7 6.1 20.1 9.8 0.7

Waveforms of the delivered pulses when the DEFIBRILLATOR is connected in turn to

resistive loads of 25 Ω, 50Ω,75Ω,100Ω,125Ω,150Ω and 175Ω set to 360J output

104
Waveforms of the delivered pulses when the DEFIBRILLATOR is connected in turn to
resistive loads of 25 Ω, 50Ω,75Ω,100Ω,125Ω,150Ω and 175Ω set to 200J output

105
Under different load discharge energy data

Load 25 50 75 100 125 150 175

(Ω)

Energy(J)
2 1.5 1.6 1.5 1.5 1.6 1.7 1.6

5 4.4 4.3 4.1 4.2 4.1 3.9 3.8

7 6.3 6.4 6.5 6.4 6.7 6.2 5.8
10 9.2 9.3 9.4 9.4 9.6 8.7 7.9

106
 20 17.8 18.2 17.7 17.6 16.8 16.8 15.2
30 27.6 27.3 28.3 27.5 26.6 26 23.5
50 45.8 45.4 45.5 45 42.5 43.1 39

70 64.6 63.8 64.3 64.6 59.7 61.2 55.1

100 90.7 92.4 90.4 92.2 82.9 72.3 63.9
150 163.9 136.6 139.7 139.3 123.4 109.2 108
200 235.9 183.2 186.4 186.2 168.2 160.5 144.4
300 340.5 269.9 269.6 262.7 229.8 197.2 198.4
360 342.4 322.8 305.3 279 262.7 234.7 213.1

Monitor

Heart Rate meter range and Accuracy: 27 to 300 BPM. ±3 per/min

Electrosurgery protection:
The HF SURGICAL EQUIPMENT which is used comply with IEC 60601-2-2 and shall
have a minimum power cut mode capability of 300 W, a minimum coagulation mode
of 100 W and working frequency of 400 kHz ±10 %.
input circuit loop leak current: <0.1μA;
Tall T-wave rejection capability:<0.8mV
Heart rate averaging:3 times. Heart rate shows refresh speed of 500ms.
Heart rate meter accuracy and response to irregular rhythm.:
indicated heart rate: 80bpm、60bpm、90bpm，, after a 20 s EQUIPMENT stabilization
period, for the four types of alternating ECG complexes A1 to A4 described in Figure
101.
Response time of heart rate meter to change in heart rate: <10s
Time to ALARM for tachycardia:<6s
Pacemaker pulse rejection warning label.

Warning: for patients with pacemakers! The pacemaker pulse may be included
in the heart rate meter in the event of cardiac arrest or tachycardia. Do not rely

107
entirely on heart rate meter alarm, should closely monitor patients with pacemakers.
See this manual for the ability of equipment to suppress pacemaker impulses.
Visual and auditory ALARM SIGNAL disclosure.
auditory alarm:
High alarm frequency : 0.125Hz
Low alarm frequency : 0.042Hz
Visual alarm:
High alarm: red LED flashing, and the flashing frequency is 2Hz
Low alarm : yellow LED always light on.
INTERNALLY POWERED ME EQUIPMENT.
It takes 8 hours for the battery to charge 90% of the electricity in the exhausted state.
The machine is connected to the AC power supply, the switch is turned on, and the
battery begins to enter the charging state. The battery should stop using in the
exhausted state and change to AC power supply. When using battery power supply,
the performance of each parameter of the equipment is not affected.
Auxiliary output.
The signal input and output interface "communication port" provided by this
equipment is a special signal input and output interface, which can only be
connected to devices that conform to safety standards, and the connected
equipment must support the company's networking protocol.
Pacer pulse detection disabling
Pace Detect switch:On/Off.
Sweep Speeds
The available time displays of the equipment: always.
The input impedance：>5Mohm(within a d.c. offset voltage range of ±300 mV)
Recovery time from electrode polarization after defibrillation: <10s.
Battery
High Capacity Type: Ni-MH 12V volt - M&B Up to 4 hours ECG monitoring or 90
full-energy dis-charges or 3 hours combined ECG,and monitoring Proper battery care
is required to maintain maximum avail-able capacity.
108
Low Battery Indicator: Flashing low battery icon on display and flashing LED on front
panel.
Recharge Rate: 80% in 7.5 hours. 100% in 9 hours.

defibrillation pads
Category Parameter
reusable No, just Single use.
Store condition between 60° and 95°F or 15°C and 35°C

Shelf life 2 years

Note

Do not use defibrillation pads not approved by M&B. Use of

unauthorized defibrillation pads may cause the device to operate
improperly and provide false measurements. Follow all labeling
instructions on the defibrillation pads.
Guidance and manufacturer's declaration
Electromagnetic emissions (IEC 60601-1-2 Table 201)
The DM7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DM7000 should assure that it is used in such an
environment.
Emissions test Compliance Electromagnetic environment – guidance
RF emissions Group 1 The DM7000 uses RF energy only for its
CISPR 11 internal function. Therefore, its RF
emissions are very low and are not likely to
cause any interference in nearby electronic
equipment.

RF emissions
Class B
CISPR 11

109
 Harmonic Not
emissions IEC applicable
61000-3-2
Voltage Not
fluctuations/ applicable
flicker emissions
IEC 61000-3-3
Medical Electrical Equipment needs special precautions regarding EMC and
needs to be installed and put into service according to EMC information
provided in this document.

Electromagnetic immunity (IEC 60601-1-2 Table 202)

The DM7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DM7000 should assure that it is used in such an
environment.
Compliance Electromagnetic
Immunity test IEC 60601 test level level environment–guidance
Electrostatic ±6kV contact ±6kV contact Floors should be wood,
discharge (ESD) concrete or ceramic tile. If
IEC 61000-4-2 ±8kV air ±8kV air floors are covered with
synthetic material, the
relative humidity should be
at least 30 %.
Electrical fast ±2 kV for power ±2 kV for Mains power quality should
transient/burst supply lines power supply be that of
IEC 61000-4-4 ±1 kV for lines a typical commercial or
input/output lines ±1 kV for hospital
input/output environment.
lines

110
Surge ±1kV differential ±1kV Mains power quality should
IEC 61000-4-5 mode differential be that of
±2kV common mode mode a typical commercial or
±2kV hospital
common environment.
mode
Voltage dips, <5% UT (>95% dip in <5% UT (>95% Mains power quality should
short UT) for 0.5 cycle dip in UT) for be that of
interruptions 40% UT (60% dip in 0.5 cycle a typical commercial or
and voltage UT) for 5 cycles 40% UT (60% hospital
variations on 70% UT (30% dip in dip in UT) for environment. If the user of
power supply UT) for 25 cycles 5 cycles the DM7000
input lines <5% UT (>95 % dip in 70% UT (30% requires continued
IEC 61000-4-11 UT) for 5 sec dip in UT) for operation during
25 cycles power mains interruptions,
<5% UT it is
(>95 % dip in recommended that the
UT) for 5 sec DM7000 be powered
from an uninterruptible
power supply
or a battery.
Power 3 A/m 3 A/m Power frequency magnetic
frequency fields should be at levels
(50/60 Hz) characteristic of a
magnetic field tyDM7000al location in a
IEC 61000-4-8 tyDM7000al commercial or
hospital environment.

NOTE. UT is the AC mains voltage prior to application of the test level.

Electromagnetic immunity (IEC 60601-1-2 Table 203)

111
 The DM7000 is intended for use in the electromagnetic environment specified below.
The customer or the user of the DM7000 should assure that it is used in such an
environment.

Immunity IEC 60601 Complianc

Electromagnetic environment – guidance
test test level e level
Portable and mobile RF communications
equipment should be used no closer to any
part of the DM7000, including cables, than
the recommended separation distance
calculated from the equation applicable to
3Vrms
Conducted RF the frequency of the transmitter.
150kHz to 3V/m
IEC 61000-4-6
80MHz

Recommended separation distance

d  1.2 P 150kHz ~ 80MHz

d  0.6 P 80MHz ~ 800 MHz

d  1.15 P 800 MHz ~ 2.5 GHz

Where P is the maximum output power

10V/m 80
Radiated RF rating of the transmitter in watts (W) and d is
MHz to 2.5 20V/m
IEC 61000-4-3 the recommended separation distance in
GHz
meters (m). b
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site
survey c, should be less than the compliance
level in each frequency range d. Interference
may occur in the vicinity of equipment

112
 marked with the following symbol:

NOTE 1. At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2. These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
a. The ISM (industrial, scientific, and medical) bands between 150KHz and 80MHz are
6.765MHz to
6.795MHz; 13.553MHz to 13.567MHz; 26.957MHz to 27.283MHz; and 40.66MHz to
40.70MHz.
b. The compliance levels in the ISM frequency bands between 150kHz and 80MHz and in
the frequency
range 80MHz to 2.5GHz are intended to decrease the likelihood that mobile/portable
communications
equipment could cause interference if it is inadvertently brought into patient areas. For this
reason, an
additional factor of 10/3 is used in calculating the recommended separation distance for
transmitters in
these frequency ranges.
c. Field strengths from fixed transmitters, such as base stations for radio (cellular /
cordless) telephones
and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast
cannot be
predicted theoretically with accuracy. To assess the electromagnetic environment due to
fixed RF
transmitters, an electromagnetic site survey should be considered. If the measured field
strength in the
location in which the M&B DM7000 is used exceeds the applicable RF compliance level
above, the DM7000
should be observed to verify normal operation. If abnormal performance is observed,

113
additional measures
may be necessary, such as reorienting or relocating the DM7000.
d. Over the frequency range 150kHz to 80MHz, field strengths should be less than 3V/m.
Recommended separation distances between portable and mobile RF
communications equipment and the DM7000 (IEC 60601-1-2 Table 205)
The DM7000 is intended for use in an environment in which radiated RF
disturbances are controlled. The customer or the user of the DM7000 can help
prevent electromagnetic interference by maintaining a minimum distance between
portable and mobile RF communications equipment (transmitters) mad the DM7000
as recommended below, according to the maximum output power of the
communications equipment.
Rated Separation distance according to frequency of transmitter
maximum m
output power 150kHz ~ 80MHz 800 MHz to 2.5 GHz
of transmitter 80 MHz to 800 MHz
d  1.2  P d  1.15  P
W
d  0.6  P

0.01 0.12 0.06 0.115

0.1 0.379 0.19 0.364
1 1.2 0.6 1.15
10 3.79 1.90 3.637
100 12 6 11.5

For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in meters (m) can be estimated using the
equation applicable to the frequency of the transmitter, where P is the maximum
output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.
NOTE 1. At 80 MHz and 800 MHz, the separation distance for the higher frequency
range applies.
NOTE 2. The ISM (industrial, scientific and medical) bands between 150 kHz and 80

114
 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283
MHz; and 40.66 MHz to 40.70 MHz.
NOTE 3. An additional factor of 10/3 is used in calculating the recommended
separation distance for transmitters in the ISM frequency bands between 150 kHz
and 80 MHz and in the frequency range 80 MHz to 2.5 GHz to decrease the likelihood
that mobile/portable communications equipment could cause interference if it is
inadvertently brought into patient areas.
NOTE 4. These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects and
people.

NOTE 1. DM7000 needs special precautions regarding EMC and needs to be

installed and put into service according to the EMC information provided in this
document;
NOTE 2. Portable and mobile RF communications equipment can affect the
behavior of DM7000.
NOTE3: pulse oximeter function module do not intended for use during patient
transport outside the healthcare facility。

warning 1：the use of ACCESSORIES, transducers and cables other than those
specified, with the exception of transducers and cables sold by the M&B of the
DM7000 as replacement parts for internal components, may result in increased
EMISSIONS or decreased IMMUNITY of the DM7000.
warning 2： DM7000 should not be used adjacent to or stacked with other
equipment and that if adjacent or stacked use is necessary, DM7000 should be
observed to verify normal operation in the configuration in which it will be used.

AED Rhythm Recognition Performance

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The DM7000 AED algorithm exceeds the requirements of ANSI/AAMI DF39-1993
section 3.3.18 and the sensitivity and specificity levels recommended by the AHA
(Automatic External Defibrillators for Public Access Use: Recommendations for
Specifying and Reporting Arrhythmia Analysis Algorithm Performance). The test
database includes shockable rhythms consisting of ventricular fibrillation rhythms
(>99uV) and wide-complex ventricular tachycardia at a rate greater than 160 BPM.
Non-shockable rhythms include various sinus rhythms including supraventricular
tachycardia, atrial fibrillation, atrial flutter, sinus rhythm with PVC’s, asystole,
pacemaker rhythms, and ventricular tachycardia with a rate less than 160 BPM
and/or narrow complexes. Each Analysis time is 9s±1s。the data come from ECG
simulator, and they are the Ⅱ ECG.

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9 Glossary

AED automatic external defibrillator

AHA American Heart Association

ALS advanced life support
arrhythmia irregular rhythm of the heart muscle
cardiac arrest cessation of the heart muscle
CPR cardiopulmonary resuscitation
defibrillation high-energy pulse of electricity (shock) delivered to
the heart muscle to restore normal cardiac activity
ECG electrocardiogram
electrocardiogram curve traced by an electrocardiograph
electrocardiograph instrument used to record electrical currents
associated with heart muscle activity
fibrillation rapid twitching movements that replace the
normal rhythmic contraction of the heart and may
cause a lack of circulation and pulse
joule The amount of energy delivered during
defibrillation, related to the intensity of the shock
delivered.
log list of ECG samples and time-stamped system
events

non-shockable rhythm patient heart rhythms that are not a candidate for
defibrillation pulse
NSR normal sinus rhythm
RF radio frequency
SCA sudden cardiac arrest
self-test automatic test performed at system power-up to

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 check readiness of battery, internal circuitry, main
processor, and defibrillator
shock defibrillation electrical pulse
shockable rhythm abnormal heart rhythm which is a candidate for
defibrillation pulse

tachycardia an abnormally fast heart rate

time-stamped event any change in heart rhythm or any shock delivered
by the defibrillator

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