127(Due to continuing product innovation, specifications in this manual are subject to change without
notice.
Listed below are the GE Medical Systems Informatio n Technologies trademarks used in this document. All
other trademarks contained herein are the property of their respective owners.
APEX, CD TELEMETRY, CRG PLUS, DASH, MUSE, RAC, RAMS, RSVP, SAM, SOLAR, TRAM,
TRAM-NET, TRAM-RAC, TRIM KNOB, and UNITY NETWORK are trademarks of GE Medical Systems
Information Technologies registered in the United States Patent and Trademark Office.
Each page of the document has the document part number and revision
letter at the bottom of the page. The revision letter changes whenever
the document is updated.
RevisionDateComment
A14 October 2002Initial release of this manual, corresponding
B4 December 2002Document revised to correct certain technical
C17 February 2003Document revised to reflect changes to field
Introduction: Manual Information
to software version 4.
specifications.
replaceable units.
Manual Purpose
Intended Audience
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 repaira ble. 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.
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Introduction: Safety Information
Safety Information
Responsibility of the Manuf acturer
GE Medical Systems Information Technologies is responsible for the
effects of safety, reliability, and performance only if:
Assembly operations, extensions, readju stments, modifications, or
repairs are carrie d out by persons aut horized b y GE Medica l Systems
Information Technologies.
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 Medical Systems Information Technologies for information
before connecting any devices to the equipment that are not
recommended in this manual.
Parts and accessories used must meet t he requireme nts of t he appli cable
IEC 601 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.
1-4Solar 8000M Patient MonitorRevision C
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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.
Revision CSolar 8000M Patient Monitor1-5
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Equipment Symbols
Introduction: Safety Information
127(
Some symbols may not appear on all equipment.
ATTENTION: Consult accompanying documents.
CAUTION: To reduce the risk of electric shock, do NOT remove cover. Refer servicing to
qualified service personnel.
127(
The rating of
protection against
electric shock
(indicated by
symbol for CF or
BF) is achieved only
when used with
patient applied
parts recommended
by GE Medical
Systems
Information
Technologies.
TYPE CF APPLIED PART: Isolated (floating) applied part suitable for intentional external and
internal application to the patient including direct cardiac application. “Paddles” outside the
box indicate the applied part is defibrillator proof.
[Medical Standard Definition:] F-type applied part (floating/isolated) complying with the
specified requirements of IEC 60601-1/UL 2601-1/CSA 601.1 Medical Standards to provide a
higher degree of protection against electric shock than that provided by type BF applied parts.
TYPE BF APPLIED PART: Isolated (floating) applied part suitable for intentional external and
internal application to the patient excluding direct cardiac application. “Paddles” outside the
box indicate the applied part is defibrillator proof.
[Medical Standard Definition:] F-type applied part (floating/isolated) complying with the
specified requirements of IEC 60601-1/UL 2601-1/CSA 601.1 Medical Standards to provide a
higher degree of protection against electric shock than that provided by type B applied parts.
TYPE B APPLIED PART: Non-isolated applied part suitable for intentional external and
internal application to the patient excluding direct cardiac application.
[Medical Standard Definition:] Applied part complying with the specified requirements of IEC
60601-1/UL 2601-1/CSA 601.1 Medical Standards to provide protection against electric
shock, particularly regarding allowable leakage current.
Fuse
Equipotential
Alternating current (AC)
Power; I = ON; O = OFF
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Service Information
Service Requirements
Follow the service requirements listed below.
Introduction: Service Information
Refer equipment servicing to GE Medical Systems Information
Technologies’ authorized service personnel only.
Any unauthorized attempt to repair equipment under warr anty voids
that warranty.
It is the user’s responsibility to report the need for service to GE
Medical Systems Information Technologies 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.
Equipment Identification
Every GE Medical Systems Information Technologies 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 GXX
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 Characteristics
One or 2 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
Revision CSolar 8000M Patient Monitor1-7
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For your notes
Introduction: Service Information
1-8Solar 8000M Patient MonitorRevision C
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2Equipment Overview
Revision CSolar 8000M Patient Monitor2-1
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For your notes
2-2Solar 8000M Patient MonitorRevision C
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Equipment Overview: System Components
System Components
Solar 8000M Patient Monitoring System
The Solar 8000M patient monitoring system consists of the following
standard components:
Solar 8000M processing unit
Display
Keypad and/or remote control
Tram-rac® housing with acquisition module(s)
Additional, option al components include:
Tram-net interface adapter (TIA)
Clinical Information Center (central station)
Remote display, VGA and DFP
Printer PRN 50/PRN 50-M
Octanet® or Unity Networ k® ID connectivity device
Solar 8000M Patient Monitor
The patient monitor consists of a Solar 8000M processing unit with
compatible display purchased from GE Medical Systems Information Technologies or another vendor.
The processing unit is the center of the Solar 8000M patient monitoring
system. It provides the user controls, the process ors to communicate with
various patient monitoring modules, and it analyzes patient data. It can
display up to eight different waveforms at one time . System software
may be updated using a laptop computer connected to the Solar 8000M
processing unit or the Unity Network or from a Clinical Information
Center (CIC) on the Unity Network.
Revision CSolar 8000M Patient Monitor2-3
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Equipment Overview: System Components
UnityView Remote Display Controller
The UnityView remote display controller consists of a remote display
controller with a compatible display purchased from GE Medical
Systems Information Technologies or another vendor. The controller
connects to the Unity Network and may be configured to display any
patient waveforms broadcasted on the network for better visibility as a
remote full-view display, or as an in-room telemetry display. System
software may be updated using a laptop computer connected to the
UnityView remote display controller or the Unity Network or from a
Clinical Information Center (CIC) on the Unity Network.
Tram-rac Housing
The Tram-rac housing (remote acquisition case) acquires patient data for
the patient monitor. Th ere are two Tram-rac housings available for the
monitor:
Tram-rac 2 housing — h olds a single Tram module.
Tram-rac 4A housing — holds a Tram module and two additional
single-high modules.
See the Tram-rac Housing Service Manual for additional information.
Shown below is a Tram-rac 4A housing with a Tram module and two
single parameter modules inserte d .
2-4Solar 8000M Patient MonitorRevision C
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Connectivity Devices
Equipment Overview: System Components
The Octanet or the Unity Network ID connectivity device ac quires digita l
data from eight individually isolated serial ports. The data is collected
from up to eight peripheral devices (not necessarily manufactured by GE
Medical Systems Information Technologies), then the device transmi ts
the formatted da ta to the Solar 8000M patient monitor. See the
appropriate connectivity device service manual for additional
information.
PRN 50/PRN 50-M Digital Writer
The PRN 50/PRN 50-M digital writer thermally records patient data on a
paper strip. Any parameter or trace that can be monitored on a monitor
can be graphed by the writer. Graphs initiate automatically when an
alarm is activated, or they can be initiated manually from the monitor.
127(
The PRN 50-M digital writer is an M-Port device. To make an
AutoPort device (such as PRN 50) M-Port compatible, use the
AutoPort to M-Port adapter, pn 2001973-001. The adapter is not
required if connecting to an Octanet.
Revision CSolar 8000M Patient Monitor2-5
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Laser Printer
Equipment Overview: System Components
An optional laser printer can be connected directly to the monitor via one
of the M-Ports. The laser printer must have a serial port, and an
interface adapter is required for the cable between the laser printer and
the monitor. Refer to the Interface to a Laser Printer from a Solar 8000M
Patient Monitor Installation Instructions, pn 2013626-001, for details on
the interface adapter and installing a serial card in a laser printer.
:$51,1*
SHOCK HAZARD. Laser printers are UL 60950/IEC
60950 certified equipment, which may not meet the
leakage current requirements of patient care equipment.
This equipment must not be located in the patient
vicinity unless the medical system standard IEC
60601-1-1 is followed.
Do not connect a laser printer to a multiple portable
socket outlet (MPSO) supplying patient care equipment.
The use of an MPSO for a system will result in an
enclosure leakage current equal to the sum of all the
individual earth leak age currents of the s ystem if th ere is
an interruption of the MP SO protective earth conductor.
Remote Control/Keypad
The remote control/keypad 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 a room. Eighteen hard keys are
configured for adult, neonatal, or operating room applications. The
keypad is ‘fixed mounted’ on the front of the Solar 8000M patient monitor
or on a separate holster that has various mounting configurations.
2-6Solar 8000M Patient MonitorRevision C
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Equipment Overview: System Components
Remote Displays
Depending on your Solar 8000M configuration, there are up to two VGA
(CRT/analog flat panel) ports and two DFP (digital flat panel) ports for
remote viewing.
Tram-net Interface Adapter
The Tram-net interface adapter connects a specific device to the Solar
8000M patient monitor using Tram-net communication. Each adapter is
preprogrammed at the factory to interface with a specific device
manufactured by a company other than GE Medical Systems
Information Technologies. For more details about the Tram-net interface
adapter, refer to the Modular Patient Monitor Accessories Service
Manual.
Revision CSolar 8000M Patient Monitor2-7
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Equipment Overview: Device Compatibility
Device Compatibility
The tables in this section are current as of the publication date of this
manual and are subject to change. For current information, contact your
Service or Sales Representative.
Acquisition Devices
The Solar 8000M patient monitor is compatible with the following
acquisition modules.
The Solar 8000M patient monitor is compatible with the following
peripheral devices.
ProductSoftwareInterface
Solar 8000M RMT1AM-Port or M-Port compatible Octanet
Solar 8000M Keypad1AM-Port or M-Port compatible Octanet
PRN 501A, 2AOctanet or M-Port with M-Port compatible
RM ModuleO3Octanet or M-Port with M-Port compatible RM
module
Polled Data Services1ASerial Port #1
Serial download N/ASerial Port #1
Elo TouchscreenN/ASerial Port #2
RAMS1C, 1DOctonet or TIA
Remote AlarmN/AM-Port
Laser printerN/AM-Port
The Solar 8000M patient monitor is compatible with the following Unity
Network devices.
ProductSoftware
ADU/Pager LAN3G, 3H
ApexPro1.1 and later
CDT-LAN5H, 6A, 6C, 6D
Centralscope: CS 1210A, 10B, 10C, 10D
CIC1.5, 2.2 and later
Dash 20002A
Dash 3000/40002B and later
Eagle 30003A, 3B, 4A
Eagle 40005B, 6A, 6B, 6C, 6D, 6F, 6G
2-10Solar 8000M Patient MonitorRevision C
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Equipment Overview: Device Compatibility
ProductSoftware
HL73.0, 4.0
ICMMS/Service Web3.0, 4.0
Impact Pager2.53, 3.10
Managed Care1C
MARS-CRS4.0a, 4.1
MUSE / MUSE NT4B, 5A, 5B, 5C
Octacomm2B, 2C, 2D, 2E
Octanet2B
QS5.03.0, 5.05.0, 5.06.0
RSVP2.0, 3.0, 4.0
Solar 7000/80003C, 4B, 4C (Special), 5B, 5D, 5E, 6A, 7A, 7B, 7C
Solar 9000/9500S9500-1A, 2A and later
ST Guard4B
Tramscope 127D, 17F, 17G, 17H (Special)
Auto View2.0, 3.0, 4.0
TRAM XX09B, 10A, 10B, 11A
CO2 ModuleCap Combo: 1.2 & 1.4, Cap MS: 1.2 & 1.4
Pryon SS: 3.0 & 3.1
ECG/RESP Module1A
Resp Mech ModuleNovametrix Release 1A
SAM Module3B, 4D
SpO2 Module1A
SvO2 ModuleSYS-08.01/ANLG-05.02
Masimo Sp02 Module1A and later
Transcutaneous Module1B
Revision CSolar 8000M Patient Monitor2-11
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Interfaces
Equipment Overview: Device Compatibility
The Solar 8000M patient monitor supports the following interfaces
through an Octanet connectivity device, Unity Netwo r k ID connectivity
device, or TIA.
127(
Although this list was accurate at the time of publishing, it may no
longer be comprehensive. Contact your sales repres entative to obtain
current information.
Product MfgModelTIAOctanet
Nellcor PB7200E/SPE/AEXXXTIAPB7200AE=X420915-001
SiemensSV 900C/D/EXXXTIASS900CD=X420915-002
EngstromEAS 9000/9010/9020XXTIAE9010=X420915-003
DatexCapnomac UltimaXXXTIADU=X420915-004
Allied Health
Care
HamiltonVeolar/AmadeusXXXTIAHV= X420915-007
Nellcor PBInfant Star 500/950XXXTIAIS=X420915-008
Nellcor PBAdult Star 1500/2000XXXTIAAS=X420915-009
SiemensSV 300XXXTIASS300=X420915-011
GEMS ITRAMSXXTIARAMS=X420915-012
GEMS ITTauras/Xpar/CommX420915-013
OhmedaRascal II Anes GasXXXTIAOHRASII=X420915-014
Ohmeda5250 RGM: Resp GasXXXTIAOH5250=X420915-015
N Amer Drager Narkomed 2B/2C/3/4/GSXXXTIANARKO=X420915-016
X(internal)
Solar 8000M Remote Control
(Adult)
Solar 8000M Remote Control
(OR)
Solar 8000M Remote Control
(Neo)
Solar 8000M Keypad (Adult)
Solar 8000M Keypad (OR)
Solar 8000M Keypad (Neo)
2-14Solar 8000M Patient MonitorRevision C
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