Service Manual
192 Pages
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GE Healthcare
Solar™ 8000M/i patient monitor Service Manual Software Version 5
Solar™ 8000M/i patient monitor English 2026266-004 (CD) 2026264-042D (paper) © 2007, 2008 General Electric Company All rights reserved.
NOTE: The information in this manual applies to Solar 8000i and Solar 8000M Patient Monitors. 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. APEX, DASH, MUSE, RSVP, SOLAR, TRAM, TRIM KNOB, and UNITY NETWORK are trademarks of GE Medical Systems Information Technologies registered in the United States Patent and Trademark Office. CARESCAPE is a trademark of GE Medical Systems Information Technologies.
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Contents
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Introduction... 1-1 Manual information... 1-2 Revision history... 1-2 Intended use... 1-2 Intended audience... 1-2 Ordering manuals... 1-2 Safety information... 1-3 Responsibility of the manufacturer... 1-3 General... 1-3 Warnings, cautions, and notes... 1-4 Equipment symbols... 1-5 Service information... 1-7 Service requirements... 1-7 Equipment identification... 1-7
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Equipment overview... 2-1 System components... 2-2 Solar 8000M/i patient monitoring system... 2-2 Solar 8000M/i patient monitor... 2-3 iPanel computer... 2-4 UnityView remote display controller... 2-4 Tram-rac housing... 2-5 Patient Data Module (PDM)... 2-6 Connectivity devices... 2-6 PRN 50/PRN 50-M digital writer... 2-7 Laser printer... 2-7 Remote control or keypad... 2-8 Remote displays... 2-8 Device compatibility... 2-9 Acquisition modules... 2-9 Peripheral devices... 2-10 Unity Network devices... 2-11 Interfacing with other peripheral devices... 2-12 Theory of operation... 2-13 Block diagram of internal connections... 2-14 Processor board... 2-15 Power supply... 2-22 Speaker... 2-22
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Installation... 3-1 Back panel connections... 3-2 TRAM-NET... 3-4 ETHERNET... 3-6 VGA VID 1 and 2... 3-7 DFP VID 1 and 2... 3-7 RS-232 1... 3-8 RS-232 2... 3-8 Front panel connectors and indicators... 3-9 M-Ports... 3-9 Indicators... 3-12 Power up... 3-12 TRAM-NET communication... 3-13 Overview... 3-13 Internal hub... 3-13 Ethernet communication... 3-14 About ethernet... 3-14 Twisted pair... 3-14 Network terms... 3-15
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Maintenance and checkout... 4-1 Maintenance schedule... 4-2 Manufacturer recommendations... 4-2 Manufacturer responsibility... 4-2 Preventive maintenance... 4-2 Visual inspection... 4-3 Cleaning... 4-4 Cleaning precautions... 4-4 Exterior cleaning... 4-4 Cleaning, disinfecting and storing GE ECG cables and leadwires... 4-5 Electrical safety tests... 4-8 Recommendations... 4-8 Set up... 4-9 Power outlet test... 4-9 Ground (earth) integrity... 4-9 Ground (earth) wire leakage current tests... 4-11 Enclosure leakage current test... 4-12 Patient (source) leakage current test... 4-13 Patient (sink) leakage current test... 4-14 Test completion... 4-15
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Checkout procedure... 4-16 General... 4-16 Required tools and equipment... 4-16 Set up... 4-17 Procedures... 4-18 Completion... 4-36 Maintenance Checklist... 4-37 “Visual inspection” on page 4-3... 4-37 “Cleaning” on page 4-4... 4-37 “Electrical safety tests” on page 4-8... 4-37 “Checkout procedure” on page 4-16... 4-37 Repair Log... 4-39
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Troubleshooting... 5-1 Terms used... 5-2 Abort (main code)... 5-2 Boot loader or boot code... 5-2 Cold start... 5-2 Continue (main code)... 5-2 Monitor memory... 5-3 Protected memory... 5-3 Power cycle or reboot... 5-3 Service mode (main code)... 5-3 Service menu (boot code)... 5-3 Warm start (boot code)... 5-3 Country selection... 5-3 Set language... 5-3 Service menus... 5-4 Boot code Service Menu... 5-4 Main code SERVICE MODE menu... 5-6 Fault analysis... 5-10 Overview... 5-10 Calibration... 5-10 AC line voltage test... 5-11 120 VAC, 50/60 Hz... 5-11 240 VAC, 50/60 Hz... 5-11 Troubleshooting procedure... 5-12 Problems and solutions... 5-13 LED troubleshooting... 5-16 Troubleshooting software updates... 5-19 Error messages... 5-20
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Reviewing error/event logs... 5-22 Accessing error/event logs... 5-22 Useful error data... 5-23 Get error logs... 5-27 Get logs via PC using netUpdate... 5-27
6
Configuration... 6-1 Configuring a patient monitor... 6-2 General... 6-2 Set unit name... 6-3 Set bed number... 6-3 Patient monitor type... 6-4 Set graph locations... 6-5 Admit Menu... 6-6 Set line frequency... 6-7 Set defib sync voltage and pulse width... 6-7 Set country selection... 6-8 Set language... 6-8 Calibrate touchscreen... 6-8 Completion... 6-8 Advanced user procedures... 6-9 Procedures... 6-9 Set time and date... 6-9 Change software level... 6-10 Enable options... 6-10 Transfer monitor defaults... 6-10 Change Ethernet address... 6-14 Set internet address... 6-15 Power cycle... 6-16
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Field replaceable units... 7-1 Ordering parts... 7-2 Field replaceable units... 7-3 Hardware kit... 7-4 Keypads and remote controls... 7-6 Cables... 7-6 Disassembly... 7-7 Guidelines... 7-7
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Disassembly procedures... 7-8
Appendix A – Technical specifications... A-1 Solar 8000M/i patient monitor... A-2 Tram-rac 2 and 4A module housings... A-5 Tram modules and Solar parameter functionality... A-7 Dual temperature module (400 and 700 series)... A-14 Capnostat mainstream CO2 module... A-15 ICG module... A-17 BIS/EEG module... A-18 Patient Data Module... A-19 Solar SpO2 Masimo SET module... A-19 SvO2 module... A-19 Solar 8000M/i display... A-20 Purchaser’s responsibility...A-20 Medical-grade displays...A-20 Non-medical grade displays...A-21 Required specifications for non-medical grade CRT displays...A-22 Recommended specifications for non-medical grade CRT displays...A-23 Required specifications for non-medical grade digital flat panel displays...A-24 Recommended specifications for non-medical grade digital flat panel displays .A-25
Appendix B – Electromagnetic compatibility... B-1 Electromagnetic compatibility (EMC)... B-2 Guidance and manufacturer’s declaration - electromagnetic emissions...B-2 Guidance and manufacturer’s declaration - electromagnetic immunity...B-3 Recommended separation distances...B-5 Compliant cables and accessories...B-6
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Introduction
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Introduction: Manual information
Manual information Revision history 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. Revision
Comment
A
Initial release
B
Updated document with editorial changes.
C
Updated document with cpu and related hardware changes.
D
Updated document with information about connecting the power cord.
Intended use 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.
Intended audience This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment.
Ordering manuals 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.
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Introduction: Safety information
Safety information Responsibility of the manufacturer 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 EN 60601 series safety standards, and/or the system configuration must meet the requirements of the EN 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 EN 60601-1 and/or EN 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 NOTE: 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. NOTE: 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. 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/EN/UL 60601-1 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/EN/UL 60601-1 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/ EN/UL 60601-1 Medical Standards to provide protection against electric shock, particularly regarding allowable leakage current.
Fuse Equipotential Stud: A ground wire from another device can be tied here to ensure the devices share a common reference. Alternating current (AC) Power; I = ON; O = OFF Medical Equipment
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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.
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Introduction: Safety information
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. 2006-04 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”. Manufacturer name and address.
European authorized representative. NOTE The following symbols (required by China law only) are representative of what you may see on your equipment. The number in the symbol indicates the EFUP period in years, as explained below. Check the symbol on your equipment for its EFUP period. This symbol indicates the product contains hazardous materials in excess of the limits established by the Chinese standard SJ/T11363-2006 Requirements for Concentration Limits for Certain Hazardous Substances in Electronic Information Products. The number in the symbol is the Environment-friendly User Period (EFUP), which indicates the period during which the toxic or hazardous substances or elements contained in electronic information products will not leak or mutate under normal operating conditions so that the use of such electronic information products will not result in any severe environmental pollution, any bodily injury or damage to any assets. The unit of the period is “Year”. In order to maintain the declared EFUP, the product shall be operated normally according to the instructions and environmental conditions as defined in the product manual, and periodic maintenance schedules specified in Product Maintenance Procedures shall be followed strictly. Consumables or certain parts may have their own label with an EFUP value less than the product. Periodic replacement of those consumables or parts to maintain the declared EFUP shall be done in accordance with the Product Maintenance Procedures. This product must not be disposed of as unsorted municipal waste, and must be collected separately and handled properly after decommissioning. This symbol indicates that this electronic information product does not contain any toxic or hazardous substance or elements above the maximum concentration value established by the Chinese standard SJ/T11363-2006, and can be recycled after being discarded, and should not be casually discarded.
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Introduction: Service information
Service information Service requirements 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.
Equipment identification Every GE device has a unique serial number for identification. A sample of the information found on a serial number label is shown below.
### ## ## #### # #
A
B
C
D
E
F
Description
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product code
B
year manufactured
C
fiscal week manufactured
D
production sequence number
E
manufacturing site
F
miscellaneous characteristic
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Equipment overview
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Equipment overview: System components
System components Solar 8000M/i patient monitoring system The Solar 8000M/i patient monitoring system consists of the following standard components:
Solar 8000M/i processing unit
Display
Keypad and/or remote control
Two possible acquisition devices:
Tram-rac housing with acquisition module(s)
Patient Data Module (also referred to as PDM)
Optional components include:
iPanel™ computer
Clinical Information Center (central station)
Remote display, VGA and DFP NOTE Available on Solar 8000M and Solar 8000i patient monitors with dual display capability.
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Printer PRN 50/PRN 50-M
Unity Network™ ID connectivity device
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Equipment overview: System components
Solar 8000M/i patient monitor The patient monitor consists of a Solar 8000M/i processing unit with compatible display purchased from GE or another vendor. The processing unit is the center of the Solar 8000M/i patient monitoring system. It provides the user controls, the processors 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/i processing unit or the Unity Network or from a Clinical Information Center (CIC) on the Unity Network.
001C
042B
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Equipment overview: System components
iPanel computer The iPanel computer is a self contained medical grade computer with flat panel display for use in the patient area. The iPanel contains the iPanel software that provides one touch access to patient data on the enterprise network. The iPanel application is compatible with the following patient data web portals:
Centricity CIV
Centricity CV Cardiology Web
MUSE CV Web
Centricity Enterprise Web
037A
UnityView remote display controller The UnityView remote display controller consists of a remote display controller with a compatible display purchased from GE 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.
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Equipment overview: System components
Tram-rac housing The Tram-rac housing (remote acquisition case) acquires patient data for the patient monitor. There are two Tram-rac housings available for the monitor:
Tram-rac 2 housing - holds one Tram module.
Tram-rac 4A housing - holds one 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 inserted.
005B
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