NOTE: The information in this manual only applies to Dash 3000/4000 patient monitors with software
versions 5.4 and Dash 3000/4000/5000 patient monitors with software versions 6 or later. It does not apply to
earlier software versions. Due to continuing product innovation, specifications in this manual are subject to
change without notice.
NOTE: For technical documentation purposes, the abbreviation GE is used for the legal entity name, GE
Medical Systems Information Technologies.
Listed below are GE Medical Systems Information Technologies trademarks. All other trademarks contained
herein are the property of their respective owners.
DASH, DINAMAP, EAGLE, MULTI-LINK, MUSE, SAM, SOLAR, TRIM KNOB, and UNITY NETWORK are
trademarks of GE Medical Systems Information Technologies registered in the United States Patent and
Trademark Office.
12SL, CENTRALSCOPE, INTELLIRATE, MENTOR, and SUPERSTAT are trademarks of GE Medical Systems
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 revision history of this document is
summarized below.
RevisionComment
Manual Purpose
Introduction: Manual Information
AInitial release of this manual.
BAdded information for 802.11b wireless and BISx. Updated Technical
Specifications and Checkout.
CAdded software version 5.4 information where applicable.
Intended Audience
Ordering Manuals
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 instructions 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.
A paper copy of this manual will be provided upon request. Contact your
local GE representative and request the part number on the first page of
the manual.
GE 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.
General
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/EN 60601 series safety standards, and/or the system configuration
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.
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.
NOTE: Some symbols may not appear on all equipment.
ATTENTION: Consult accompanying documents before using the equipment.
In Europe, this symbol means dangerous or high voltage. In the United 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 (floating) part. The paddles indicate
the equipment is defibrillator proof.
Introduction: Equipment Symbols
Type B equipment; type B equipment is suitable for intentional external and internal
application to the patient, excluding direct cardiac application.
Equipotential Stud: A ground wire from another device can be tied here to ensure the
devices share a common reference.
Alternating current (AC)
I = ON; O= OFF
Power;
Fuse
Battery
Indicates the Ethernet connection for the patient monitor.
Medical Equipment
With respect to electric shock, fire and mechanical hazards only in accordance with UL
60601-1, CAN/CSA C22.2 NO. 601.1, IEC 60601-1, IEC 60601-2-27, IEC 60601-2-30. IEC
60601-2-34, and IEC 60601-2-49.
This symbol indicates that the waste of electrical and electronic equipment must not be
disposed as unsorted municipal waste and must be collected separately. Please contact an
authorized representative of the manufacturer for information concerning the
decommissioning of your equipment.
This symbol indicates the date of manufacture of this device. The first four digits identify the
year and the last two digits identify the month.
2005-08
Non-ionizing electromagnetic radiation: To indicate elevated, potentially dangerous, levels
of non-ionizing radiation. Note - In case of application in a warning sign the rules according
to ISO 3864-1 shall be adhered to.
IEC 60878 note: See safety sign ISO 7010 - W005 "Warning, non-ionizing radiation".
Dash 3000/4000 patient monitors with DJ product code as shown on the
sample label below, were shipped from the factory with MPC821
processor board. These patient monitors cannot support software
versions later than 5.x.
D 1 DJ 0005 G XX
Product Code
NOTE
If the MPC821 processor board was replaced with an MPC823
processor board, then the patient monitor can run software version 6
or later. The hardware version can be identified in the Boot Loader
program. See “Boot Loader Service Menu” on page 4-4 for steps to
access Boot Loader.
The Dash patient monitor can function as a portable monitoring device
with a built-in writer, or as a flexible care monitoring device connected to
the optional Unity Network™ via Ethernet. If using the wireless card or
Ethernet connection, optional components are a Clinical Information
Center (CIC Pro™) and a Centralscope™ central station.
This device is designed to monitor a fixed set of parameters including
ECG, noninvasive blood pressure, impedance respiration, SpO2, and
temperature. Invasive pressure, BISx, 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.
AC Battery
Power
Charging Status
A
B
Graph
NBP Go/Stop
Zero All
Trim Knob
Silence Alarm/
Admit
001C051D003A
Dash 4000 MonitorDash 3000 Monitor
Dash 5000 Monitor
NOTE
For compatibility information, contact Technical Support.
All of the patient cable connectors are located on the right side of the
patient monitor. A Trim Knob™ control provides single control
operation of virtually all patient monitor functions.
Patient Cable
Connectors
Left Side View
002A
On the left of the patient 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.
The battery compartment
may be a single plastic
door or two silicone doors.
An optional alarm light indicator may be built into the handle of the
Dash 3000 patient monitor or into the display bezel of the Dash 4000/
5000 patient monitor. When activated, the LED indicator flashes red for
Crisis patient status alarms and yellow for Warning patient status and
system alarms.
Controls and Indicators
Equipment Overview: Components
Alarm Light Indicator
052B536A
Dash 3000 MonitorDash 4000 and 5000 Monitors
Flat Panel Display
Trim Knob Control
Function/Power Keys
The user interface consists of a flat panel display and the keypad
assembly that includes a Trim Knob control, function keys, and LED
indicators.
The active-matrix color liquid crystal display (LCD) is assembled into a
shock absorbing isolator that fits within the patient 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.
Dash 3000/4000 Patient Monitors
Power, Print, NBP Go/Stop, Zero All, Silence Alarm/Admit.
Dash 5000 Patient Monitor
Power, Standby, Admit/Discharge, NBP Go/Stop, NBP Auto,
Print, Silence Alarm, Zero All, Trend, Main Display.
The patient monitor is powered at all times when it is plugged into AC
power. When the patient monitor is not plugged in to AC power, this key
turns the patient monitor On and Off.
When AC power is present, this key toggles the operational mode of the
patient 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.
While the patient monitor powers up or changes between normal mode
and standby mode, all four front panel indicators illuminate.
AC Power Indicator
The indicator lights green when AC mains power is applied to the patient
monitor (including when the patient monitor is in the standby mode).
The indicator does not illuminate when the patient monitor has no AC
mains power.
Battery Power Indicator
The indicator lights yellow when the patient monitor is operating on
battery power. The indicator does not illuminate when the patient
monitor has no battery power. Battery indicators are located on the front
panel of the patient monitor. They indicate when battery power is used
and the battery charging status.
An icon for each battery indicates its charging status. The battery icon
lights yellow when the respective battery is being charged. If both
batteries are present and require charging, then both icons illuminate
even though they will be charged sequentially. The battery icon lights
green when the respective battery is fully charged.
When the patient monitor is operating under battery power the battery
icons are not illuminated. The icons are also not illuminated when the
respective battery is either not being charged, not installed, or has failed.
The following table explains what the charging status indicators mean.
NOTE
No specific indicator distinguishes a failed battery pack condition
from a condition where the battery is not installed or is not being
charged. Go to the Service Menu for Battery Status. Refer to “Battery
Alarms and Messages” on page 6-7 for further information.
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 lights 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 patient monitor is operating on battery power.
A failure condition has been detected for the respective battery.
Battery Status Indicators
The battery status indicators are located inside the battery
compartment. One green LED indicator is located above each of the two
battery slots and lights green when the patient monitor is receiving
power solely from the respective battery. The indicators do not
illuminate when the patient monitor is not battery powered.
Neither indicator lights when the patient 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 patient monitor).
On-screen capacity gauges indicate the battery's current state of health
and charge status. A battery capacity gauge for each battery present
displays below the parameter blocks in the lower right corner of the
display. The capacity gauge indicates the remaining charge capacity
(usable energy left) for each battery.
The capacity gauges fill in from left to right proportional to the battery
charge level. The solid portion represents the full charge capacity of the
battery as a percentage of its design capacity.
Exchangeable/Compatible Battery Packs
809A
Battery Capacity Gauges
WARNING
EXPLOSION OR FIRE - Using non-recommended
batteries could result in injury/burns to patients and
users. Only use batteries recommended or manufactured
by GE. The warranty can be voided if non-recommended
batteries are used.
Dash patient monitors running versions 5.4 or later only recognize and
charge GE recommended batteries. Non-recommended batteries will run,
but not charge, the Dash patient monitor. If battery is labeled GE
Approved, the battery is compatible.
NOTE
Incompatible batteries display an “ERROR” message in the Battery
Capacity Guage on the bottom right corner of the patien monitor
screen.
Verify compatibility of an unmarked battery as follows.
1. Install a battery pack in the patient monitor.
2. Using the Trim Knob control, access the Service Mode menu
starting from the Main Menu. Select MORE MENUS > MONITOR
SETUP > SERVICE MODE.
3. Enter password using the Trim Knob control to select the day and
month from patient monitor screen with leading zeros. (e.g. July 4 =
0407).
4. Select BATTERY SERVICE.
5. Verify that the MANUFACTURER NAME does not display
INCOMPAT, NME, or UNKNOWN for the battery corresponding to
BATTERY A or BATTERY B slot.
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.
Dash Port 2 Docking Station
The docking station is a quick mount/dismount base for a Dash patient
monitor. It gives the patient monitor easy connect/disconnect access to
AC power, Unity Network
See the Dash Port 2 Docking Station Operating Instructions and the
Dash Port 2 Docking Station Service Manual for additional information.
NOTE
™
, a remote display, and auxiliary devices.
When a Dash patient monitor is connected to the docking station,
only the docking station’s Ethernet port is active. The Dash patient
monitor’s network port remains inactive until the patient monitor is
disconnected from the docking station.
823B
An optional remote display can be connected to the system for viewing on
a larger monitor, or in a separate room. The remote display requires:
Dash Port 2 docking station,
Dash 3000/4000 patient monitor software version 5 or later, or
Dash patient monitor software version 6 with Dash Port 2 software
version 2.0, and
Must be within 150 feet of the Dash patient monitor.
The flexibility of the optional GE Unity Network is increased by using
the wireless network. The wireless connection allows the user to roam
from one access point to another, maintaining a strong seamless
connection to the Unity Network. GE offers 802.11 and 802.11b wireless
options.
The patient monitor, with its optional built-in wireless card, functionally
performs the same as a patient 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 3000/4000/5000, Eagle
™
Solar
patient monitors). Patient monitors with a wireless connection
™
4000, and
can send and receive patient data via the access points to the Unity
Network.
NOTE
It is recommended that wireless patient monitors that are moved
from room to room have their patient monitor type configured as
Rover or Rover/Combo monitoring.
To extend the Unity Network to a hospital’s 802.11b wireless network, a
proper installation and configuration needs to be performed. To maintain
continuous wireless patient monitoring, refer to the Wireless LAN
Configuration Guide and contact GE for consultation in integrating the
Unity Network to a 802.11b wireless network.
To identify a patient monitor with the wireless option, look for the
wireless LAN label.
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.