Premium, Prism, QUIK CONNECT V, QUICK CONNECT, QT Guard, SMART-PAC, SMARTLOOK, Spiral
Lok, Sweetheart, UNITY, Universal, Waterfall, and Walkmom are trademarks of GE Medical Systems
Information Technologies.
Each page of this manual has the document part number and revision
letter at the bottom of the page. The revision letter identifies the
document’s update level. The re vision history of this document is
summarized below.
Revision History
RevisionDateComment
A19 December 2002Initial release of this manual.
B28 February 2002Corrections were made.
This manual supplies technical information for service representatives
and technical personnel so they can maintain the equipment to the
assembly level. Use it as a guide for maintenance and electrical repairs
considered field repairable. Where necessary the manual identifies
additional sources of relevant information and technical assistance.
See the operator’s manual for the in structions necessary to operate the
equipment safely in accordance with its function and intended use.
This manual is intended for service representatives and technical
personnel who maintain, troubleshoot, or repair this equipment.
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Safety Information
INTRODUCTION: Safety Information
Responsibility of the
Manufacturer
General
GE Medical Systems Information Technologies is responsible for the
effects of safety , reliability, and performance only if:
•Assembly operations, extensions, readjustments, modifications, or
repairs are carried out by persons authorized by GE.
•The electrical installation of the relevant room complies with the
requirements of the appropriate regulations.
•The equipment is used in accordance with the instructions for use.
This device is intended for use under the direct supervision of a licensed
health care practitioner.
This device is not intended for home use.
Federal law restricts this device to be sold by or on the order of a
physician.
Contact GE for information before connecting any devices to the
equipment that are not recommended in this manual.
Parts and accessories used must meet the requirements of the applicable
IEC 601 series safety standards, and/or the system configurati on must
meet the requirements of the IEC 60601-1-1 medical electrical systems
standard.
Periodically, and whenever the integrity of the device is in doubt, test all
functions.
The use of ACCESSORY equipment not complying with the equivalent
safety requirements of this equipment may lead to a reduced level of
safety of the resulting system. Consideration relating to the choice shall
include:
•use of the accessory in the PATIENT VICINITY; and
•evidence that the safety certification of the ACCESSORY has been
performed in accordance to the appropriate IEC 60601-1 and/or IEC
60601-1-1 harmonized national standard.
If the installation of the equipment, in the USA, will use 240V rather
than 120V, the source must be a center-tapped, 240V, single-phase
circuit.
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INTRODUCTION: Safety Information
Warnings, Cautions,
and Notes
The terms danger, warning, and caution are used throughout this
manual to point out hazards and to designate a degree or level or
seriousness. Familiarize yourself with their definitions and significance.
Hazard is defined as a source of potential injury to a person.
DANGER indicates an imminent hazard which, if not avoided, will
result in death or serious injury.
WARNING indicates a potential hazard or unsafe practice which, if not
avoided, could result in death or serious injury.
CAUTION indicates a potential hazard or unsafe practice which, if not
avoided, could result in minor personal injury or product/property
damage.
NOTE provides application tips or other useful information to assure
that you get the most from your equipment.
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INTRODUCTION: Safety Information
Equipment Symbols
Some of the following symbols appear on the equipment.
ATTENTION: Consult accompanying documents before using the
equipment.
In Europe, this symbol means dangerous or high voltage. In the Unite d
States, this symbol represents the caution notice below:
To reduce the risk of electric shock, do NOT remove cover (or back).
Refer servicing to qualified personnel.
Defibrillator-proof type CF equipment; type CF equipment is
specifically designed for applications where a conductive connection
directly to the heart is established. The paddles indicate the equipment
is defibrillator proof.
Defibrillator-proof type BF equipment; type BF equipment is suitable
for intentional external and internal application to the patient,
excluding direct cardiac application. Type BF equipment is type B
equipment with an F-type isolated (floa ting ) part. The paddles indica te
the equipment is defibrillator proof.
Type B equipment; type B equipment is suitable for intentional
external and internal application to the patient, excluding direct
cardiac application.
Equipotentiality
Alternating current (AC)
Power;
Fuse
Battery
Indicates the Ethernet connection for the monitor.
I = ON; O= OFF
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INTRODUCTION: Safety Information
PRESS
814A
815A
816A
817A
818A
4P41
Press to open.
POWER
GRAPH GO/STOP
NBP GO/STOP
ZERO ALL
SILENCE ALARM/ADMIT
Medical Equipment
With respect to electric shock, fire and mechanical hazards only in
accordance with UL 2601-1, and CAN/CSA C22.2 NO. 601.1.
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INTRODUCTION: Service Information
Service Information
Service
Requirements
Equipment
Identification
Follow the service requirements listed below.
•Refer equipment servicing to GE authorized service personnel only.
•Any unauthorized attempt to repair equipment under warranty voids
that warranty.
•It is the user’s responsibility to report the need for service to GE or to
one of their authorized agents.
•Failure on the part of the responsible individual, hospital, or
institution using this equipment to implement a satisfactory
maintenance schedule may cause undue equipment failure and
possible health hazards.
•Regular maintenance, irrespective of usage, is essential to ensure
that the equipment will always be functional when required.
Every GE device has a unique serial number for identification. A sample
of the information found on a serial number label is shown below.
D 0 XX 0005 G XX
Month
Manufactured
A = January
B = February
C = March
D = April
E = May
F = June
G = July
H = August
J = September
K = October
L = November
M = December
Year
Manufactured
0 = 2000
1 = 2001
2 = 2002
(and so on)
Product Code
Two-character
product
descriptor
Product
Sequence
Number
Manufacturing
number (of total
units
manufactured)
Division
F = Cardiology
G = Monitoring
Device Characterist ics
One or two letters that
further describe the unit,
for example:
P = prototype not
conforming to marketing
specification
R = refurbished equipment
S = special product
documented under Specials
part numbers
U = upgraded unit
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2EQUIPMENT OVERVIEW
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For your notes
EQUIPMENT OVERVI EW:
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Components
Trim Knob
NBP Go/Stop
Zero All
Silence Alarm/
Admit
Graph
Power
Charging Status
A
B
AC Battery
EQUIPMENT OVERVIEW: Components
The Monitoring
System
The Patient Monitor
The Dash 3000/4000 patient monitor can function by itself with a built-in
writer, or it can be cabled in with the optional Unity Network via
Ethernet. Optional components are, if using Wireless LAN or cabled to
Ethernet, a Centralscope central station and the Clinical Information
Center.
This device is designed to monitor a fixed set of parameters including
ECG, noninvasive blood pressure, impedance respiration, SpO2, and
temperature. Invasive pressure and EtCO2 are optional features.
Additional specialized features include cardiac output, cardiac
calculations, pulmonary calculations, dose calculations, PA wedge (PA
wedge is only available with the invasive pressure option), ICG module
interface, and SAM module interface.
Silence Alarm/
Zero AllNBP Go/StopGraph Go/StopPowerCharging Status
Admit
051C
Dash 3000 Monitor
AB
Dash 4000
001C
Dash 4000 Monitor
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EQUIPMENT OVERVIEW: Components
Right Side View
Left Side View
All of the patient cable connectors are located on the right side of the
monitor. A Trim Knob control provides single control operation of
virtually all monitor functions.
Patient Cable
Connectors
002A
On the left of the monitor, you can find the built-in writer and the
battery compartment.
Optional Built-in Writer—
The built-in, 4 channel
writer is located in the
center of the left side of the
monitor .
Battery Compartment—
The battery packs are
located in this
compartment.
003A
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EQUIPMENT OVERVIEW: Components
Back View
Network Connector—A cable
can be connected to this port
for monitors used in patient
monitoring network
configurations.
Equipotential Terminal—For
measurements in or ne ar the heart
we recommend connecting the
monitor to the potential
equalization system. U se the
green and yellow potential
equalization cable and connect it
to this pin.
AC Power Connector
On the back of the monitor you will find all connectors for equipment and
network.
Line V oltage Selector—This s elector
is factory set to match the line
voltage rating for your country.
Audible Alarm Enunciator—The
internal speaker provides sound
for audible alarms. For better
sound quality do not block
speaker.
Aux Port—Used for
RAC 2A, other
compatible auxiliary
devices, and software
updates.
Defib Sync Connector—Provides
ECG analog output signals to
user-supplied equipment. A 5-
004A
volt, 2-millisecond artificial pacer
spike is added to the analog
output when PACE is on and
detection occurs.
Peripheral Expansion Port
Optional Alarm Light
Indicator
An optional alarm light indicator can be built into the handle of the Dash
3000 monitor or into the display bezel of the Dash 4000 monitor. When
activated, the LED indicator fl ashes red for CRISIS patient status
alarms and yellow for WARNING patient status and system alarms.
alarm light indicator
Dash 3000 Monitor
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Dash 4000 Monitor
052B
EQUIPMENT OVERVIEW: Components
User Interface
Flat Panel Display
Tri m Knob Control
Power Key
Function Keys
The User Interface consists of a flat panel display and the keypad
assembly which consists of a Trim Knob, five function keys, and four
LED indicators.
The active-matrix color liquid crystal display (LCD) is assembled into a
shock absorbing isolator that fits within the monitor’s front bezel to
protect the display from mechanical shock during use.
The acrylic optical filter protects the display panel from impact and
enhances visibility with its non-glare surface coating on the viewing side
of the filter. It also has a scratch-resistance surface coating.
The Trim Knob control is a 24-position rotary control with a push
selection switch.
The monitor is powered at all times when it is plugged into AC power.
When the monitor is not plugged in to AC power, this key turns the
monitor On and Off.
When AC power is present, this key toggles the operational mode of the
monitor between normal operation and stand-by mode. In standby mode
patient monitoring discontinues. Only the charging function continues
and the charging status indicators operate as described below.
Fixed Keys
Four fixed function keys are provided for GRAPH GO/STOP, NBP GO/
STOP, ZERO ALL, and SILENCE ALARM/ADMIT.
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EQUIPMENT OVERVIEW: Components
Indicators
While the monitor powers up or changes between normal mode and
standby mode, all four front panel indicators illuminate.
AC Power Indicator
The indicator illuminates green when AC mains power is applied to the
monitor (including when the monitor is in the standby mode). The
indicator does not illuminate when the monitor is not powered by AC
mains power.
Battery Power Indicator
The indicator illuminates yellow when the monitor is operating on
battery power. The indicator does not illuminate when the monitor is not
battery powered.
Charging Status Indicators
The following table explains what the Charging Status indicators mean.
LED ColorExplanation:
YellowTwo battery icons, labeled Charging Status A and B,
illuminate yellow when the respective battery is being
charged. If both batteries are present and require
charging, then both icons illuminate yellow even
though they charge sequentially.
GreenThe icon illuminates green when the respective
battery is fully charged.
No LightThe icon does not illuminate under the following
conditions:
•The respective battery is not installed.
•The monitor is operating on battery power.
•A failure condition has been detected for the
respective battery.
“Battery In Use” Indicators
The “Battery In Use” indicator (inside the battery door) illuminates
green when the monitor is receiving power solely from the respective
battery. The indicators do not illuminate when the monitor is not battery
powered.
Neither indicator illuminates when the monitor is operating from both
batteries simultaneously (i.e., in a very low battery charge condition
when both batteries are joined together in order to sustain operation of
the monitor).
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EQUIPMENT OVERVIEW: Components
Optional RAC 2A
Module Housing
Optional Dash Port
Docking Station
The RAC 2A module housing currently supports the SAM and ICG
modules.
797B
An integral power supply is used to run the RAC 2A and support the
needed voltages.
The docking station is a quick mount/dismount base for a Dash patient
monitor. It gives the monitor easy connect/disconnect access to AC
power, the Unity Network, and to auxiliary devices.
NOTE: When a Dash monitor is connected to the docking station, only
the docking station’s Ethernet connector is active. The Dash
monitor’s network connector remains inactive until the monitor
is disconnected from the docking station.
823A
Optional ICG Module
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The ICG module (impedance cardiography) measures and processes
patient hemodynamic data.
825A
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EQUIPMENT OVERVIEW: Components
Optional Wireless
LAN System
Access Points
The flexibility of the optional GE Unity Network is increased by using
the Wireless LAN system. The Wireless LAN system allows the user to
roam from one access point to another, maintaining a strong, seamless
connection to the Unity network.
The monitor, with its optional built-in Wireless LAN, functionally
performs the same as a monitor connected directly to the optional Unity
network. It can be viewed at the central station and by other GE
monitors on the network (i.e. Dash 3000/4000, Eagle 4000, and Solar
patient monitors). Monitors with Wireless LAN sends and receives
patient data via the access points of the Unity network.
NOTE: Wireless patient monitors that are moved from room to room
must have the monitor type configured as Rover or Rover/Combo
monitoring.
To integrate the wireless network with the wired network, one or more
access points are necessary. An access point connects the wireless
monitor to the wired network infrastructure within the building, and
acts as a bridge between the wired and wireless networks. The areas
covered by each access point overlap to insure continuous coverage.
NOTE: The monitor will only work with a Symbol Access Point. The
monitor will not communicate directly with a Wireless LAN
device from Aironet.
050A
Optional Remote
Control
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The optional remote control provides all patient monitor controls on a
portable component with a Trim Knob control, and allows the user to
operate the patient monitor from across the room. Eighteen hard keys
are configured for adult, neonatal, or operating room applications.
821A
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EQUIPMENT OVER VIE W : Softwar e Pa ck age s and Sof twar e Op tion s
Software Packages and Software Options
Software Packages
The Dash monitor comes configured with the Basic software package.
This package consists of standard-of-care parameters, lethal arrhythmia
detection, dose calculations, and features required by clinicians caring
for acutely ill patients.
Two additional software packages can be purchased separately or in any
combination. These packages provide a variety of features which allow
the monitor to be configured to best meet the needs of its intended
environment.
The Cardiac software package focuses on cardiac conductivity. Its
features include full arrhythmia analysis and storage, as well as ST
segment trending, storage, and templates. The ability to adjust the ST
measurement point is also included in this package.
The Cardiopulmonary software package centers upon cardiac and
pulmonary hemodynamics. Features include the PA insert and wedge
algorithms, the intra-aortic balloon pump algorithm, and the
thermodilution cardiac output algorithm, including predefined
computation constants for the catheters of major manufacturers. Also
included are cardiac and pulmonary calculations.
Software Options
Three software options can be purchased separately or in any
combination with the software packages and software options.
The High Resolution CRG Trends option provides storage of up to 100
CRG events, and up to 24 hours of CRG trend data, in addition to the
CRG feature set found in the Basic software package.
The 12SL ECG analysis program with Gender Specific Criteria and the
Acute Cardiac Ischemia–Time Insensitive Predictive Instrument (ACITIPI) analysis option uses recorded ECG data to produce a numerical
score which is the predicted probability of acute cardiac ischemia. In
addition, the gender specific criteria improves the detection of acute
myocardial infarctions (AMI) in women.
The Unity Network option enables you to view other patients on the
network, interface with a central station and other network devices, and
perform Combo or Rover Combo monitoring.
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EQUIPMENT OVERVIEW: Technical Specifications
Technical Specifications
Due to continual product innovation, specifications are subject to change
without notice. The follo win g sp ecifi cat ions are accurate as of t he date of
this publication, and pertain to the Dash 3000/4000 Patient Monitor.
Performance
Specifications
Display
Size:
Type:
Color:Active-Matrix Liquid Crystal Display (LCD)
Resolution:640 by 480 pixels
Dash 3000:
Dash 4000:
8.4-inch diagonal
10.4-inch diagonal
Controls
Number of traces:6 (maximum)
Number of seconds/trace:
Dash 3000:
Dash 4000:
Sweep speed:
All waveforms6.25, 12.5 or 25 mm/sec (with erase bar)
Information window:Displays non-real-time information without obstructing
Display organization:Prioritized by parameter
Standard:Trim Knob control plus 5 hard keys: POWER, NBP
Optional remote control Trim Knob control and 18 active hard keys.
4.9 at 25 mm/sec
5.9 at 25 mm/sec
and full grid modes
the display of real-time information
GO/STOP, ZERO ALL, SILENCE ALARM/ADMIT, and
GRAPH GO/STOP.
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Alarms
ECG
EQUIPMENT OVERVIEW: Technical Specifications
Categories:Patient Status and System Status
Priorities:4 levels — Crisis, Warning, Advisory, and Message
Notification:Audible and visual
Setting:Default and individual
Silencing:1 minute, current alarm only
Pause:5 minutes (adult); 3 minutes (neonatal); 5, 15 minutes,
permanent (OR mode)
Volume:Default 70 dB measured at 1 meter
5 Leadwire cable:I, II, III, V, aVR, aVL, and aVF
10 Leadwire cable (12SL option): V2, V3, V4, V5 and V6
Leads analyzed simultaneously:I, II, III, and V (multi-lead mode)
Lead fail:Identifies failed lead
Alarms:User-selectable upper and lower heart rate limits
Input specifications:
Voltage range:
Signal width:
Heart rate range:
Accuracy:
Input impedance:
Common mode:
Differential:
Common mode rejection:
Output specifications:
Heart rate averaging:
Frequency response:
Display:
Diagnostic Mode:
Monitoring Mode:
Moderate Mode:
Maximum Mode:
Impulse Response:
±0.5 mV to ±5 mV
40 ms to 120 ms (Q to S)
30 to 300 BPM
±1% or ±1 BPM, whichever is greater
>10 MΩ at 50/60 Hz
>2.5 MΩ from dc to 60 Hz
90dB minimum at 50 Hz or 60 Hz
8 beats with a 2-second update rate of display
Response of non-permanent displays is limited by
resolution to 40 Hz (-3dB) @ 25 mm/s. Specified upper
frequency limits may vary by ± 2 Hz.
0.67(+0.4 dB) to 100 Hz (-3 dB)
For compliance with China National Standard: 1.0 Hz
(+0.4 dB) to 75 Hz (-3 dB)
0.67 (+0.4 dB) to 40 Hz (-3 dB)
0.67 (+0.4 dB) to 25 Hz (-3 dB)
5.0 Hz (-3 dB) to 25 Hz (-3 dB)
For an impulse of 3 mV applied for 100 ms:
Displacement following impulse: < 0.1 mV
Slope following impulse: < 0.3 mV/s
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