Agilent M1165/66/67/75/76/77A
Component Monitoring System
and
Agilent M1205A V24 & V26
User’s Reference Manual
Volume 1
System Information
s1
Part Number M1046-900 1L
Printed 06/2000
First Edition
Notice
This document contains proprietary information which is protected by copyright. All Rights
Reserved. Reproduction, adaptation, or translation without prior w rit ten permission is
prohibited, except as a llowed under the copyright laws.
Agilent Technologies
3000 Minuteman Road
Andover, MA 01810-1085
(978) 687-1501
Publication number
M1046-9001L
Warranty
The information contained in this document is subject to change without n otice.
Agilent Technologies ma kes no warranty of any kind with regard to this material, including,
but not limited to, the implied warranties or merchantability and fitness for a particular
purpose.
Agilent Technologies shall no t be liable for errors contained herein or for incidental or
consequential damages in connection with the furnishing, performance, or use of this
material.
New editions of this document will incorporate all material updated since the previous edition.
Update packages may be issued bet ween editions and contain replac ement and additional
pages to be merged by a re vision date at the bottom of the pa ge. Note that pages which are
rearranged due to ch anges on a previous page are not considered revised.
The documentation printing date and part number indicate its current edition. The printing
date changes when a new edition is printed. (Minor corrections and updates which are
incorporated at reprint do not cause the date to change.) The document part number changes
when extensive technical ch anges are incorporated.
United States federal law restricts these devices to sale by or on the order of a physician.
The M1165/66/75/76A Systems comply with UL544, CSA 22.2-125, IEC 601-1, EN 60601-1, and
EN 60601-1-2 and car r ies Marking to Counci l Dir ec ti ve 93/ 4 2/ EEC, E ur opean Medical
Device Directive (MDD).
The M1167/77A Systems comply with UL2601-1, CSA 22.2 No. 601.1-M90, IEC 601-1,
EN 60601-1, and EN 60601-1-2 and carries Marking to Council Directive 93/42/EEC,
0366
European Medical Device Directive (MDD).
The M1205A Systems comply with UL2601, IEC 601-1, CSA C22.2 no. 601-1, EN60601-1, and
EN60601-1-2 and carries Marking to Council Directive 93/42/EEC, European Medical
Device Directive (MDD).
iii
Electromagnetic Interference
Anomalies due to electromagnetic interference are not unique to the M1165/66/67/75/76/77A
or the M1205A but are chara cteristic of patient monitors in use today. This performance is
due to the very sensitive high gain front end amplifiers used to display the physiological
signals. Among the many similarly performing monitors already in use by customers,
interference from electromagnetic sources is rarely a problem in actual use.
Avoiding Electromagnetic Interference
When electromagnetic interference (EMI) is encountered there are a number of actions that
can be taken to mitigate the problem.
•Eliminate the source. Possible sources of EMI can be turned off or moved away to
reduce their strength.
•Attenuate the coupling. If the coupling path is through the patient leads, the
interference may be reduced by moving and/or rearranging the leads. If the coupling is
through the power cord, plugging the monitor into a dif ferent circuit may help.
•Reduce the sensitivity of th e syst em . In all o f th e EM C t esti n g the m oni to r wa s adju ste d
to maximum sensitivity. For the ECG amplifier the gain was four times what is
normally required. By reducing the gain of the system receiving the EMI, the
interference can often be eliminated.
•Add external attenuat ors. I f E MI becomes an unusually difficult problem external
devices such as an isolation transf ormer or a transient suppressor ma y be of help. An
Agilent Customer Engineer can be of help in determining the need for external devices.
iv
Intended Use
Intended Use
Description
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 Monitors are ne tw ork connectable bedside patient monitoring devices.
The Agilent M1205A Models V24CT and V26 CT may powered by either AC line power or by
battery power.
Purpose
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 monitors measure and display multiple ph ysiological parameters and w aves, and
generate alarms and recordings. They exchange information with compatible devices. The
Agilent M1165/66/67 /75/76/77A Component Monitoring System and the Agile nt M1205A V24
and V26 monitors are not therapeutic devices.
Patient Population
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 monitors are intended to be used on adult, pediatric, an d neonatal patients.
Environment
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 monitors are intended to be used in a clinical environment by trained healthcare
professionals. They are not intended for home use.
They communicate with de vices such as a central station through network interface ports and
a serial I/O port.
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 Monitors are pres cription devices and will carry the following label, “United
States Federal law restricts this device to sale by or on the order of a physic ian.”
v
Indications for Use
Indications for Use
Condition
The Agilent M1165/66/6 7/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 Monitors are generally indicated when the clinician decides there is a need to
measure and display multiple physiological parameters and waves, to generate alarms and
recordings of adult, pediatric, or neonatal patie nts.
Part of Body or Type of Tissue with Which the Device Interacts
The Agilent M1165/66/6 7/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 monitors do no t c ontact the body or tissue of the patient. Signals are obtain ed
from accessory electrode, transducer, and sensor devices.
Frequency of Use
The Agilent M1165/66/6 7/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 monitors ar e indicated for use when presc ribed by a clinician.
Physiological Purpose
The Agilent M1165/66/6 7/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 Monitors are indicated when the purpose is to gain information for treatment, to
assess adequacy of treatment, or to rule out causes of symptoms. The Agilent M1165/66/67/
75/76/77A Compon e nt Mo n it or i n g Syste m an d the Agi le n t M120 5A V24 an d V26 mo n itors are
well suited for patient m onitoring.
Patient Population
Adult, pediatric, and neonatal non-ambulatory patients.
vi
Indications for Use
Prescription Versus Over-the-Counter
The Agilent M1165/66/67/75/76/77A Component Monitoring System and the Agilent M1205A
V24 and V26 Monitors are prescription devices.
vii
Indications for Use
Warnings, Cautions, and Notes
Warnings, cautions, and notes are us ed throughout this User’s Manual to give you additional
information about the Agilent M1165/66/67/75/76/77A Component Monitoring System and the
Agilent M1205A V24 and V26 monitors. The warnings and cautions included in this safety
section refer to the equipment in general.
WarningWarning
A “warning” calls attention to the user of imminent hazard to people if proper
procedures are not followed.
•For continued safe use of this equipment, it is necessary that the listed instructions are
followed. Instructions in this manual in no way supersede established medical
procedures.
•Explosion Hazard- Do n ot u se th i s equipment in the pre s en ce o f fl am ma bl e an esth etics.
•Alarms - Do not rely exclusively on the audible alarm system for patient monitoring.
Adjustment of alarm volume to a low level or off during patient monit oring may result
in patient jeopardy. Remember that the most relia ble method of patient monitoring
combines close persona l surveillance with correct operation of m onitoring equipment.
•This equipment is only intende d fo r use in healthcare facilities by trained healthcare
professionals.
•The product is not intended for outside hospital use such as a helicopt ers or
ambulances.
•This product is not intended for home use.
•To reduce the risk of elect ric al shock, do NOT remove any cover. Refer servicing to
qualified personnel.
•This equipment may interfere with ultrasound imaging equipment by causi ng
interference on the ultrasound display. Try to keep the instruments as far apart as
possible.
viii
Indications for Use
•Exposure of electrical contacts or connections to saline or other liquids and gels is
dangerous. Electrical contacts and connections such as cable connectors, power
supplies, parameter module plu g-in connections and rack connec tions must be kept
clean and dry. Thoroughly dry any electrical connections that become contaminated
with liquids. If additional decontamination is required please contact your biomedical
department or Agilent Tech nologies Response Center.
•Although this equipment is shielded against Electromagnetic Interference (EMI), it is
recommended to avoid the use of electrically radiating devices in close proximity to this
equipment.
•Connecting the Agilent monitoring network (SDN) cable when the product is powered
on is not supported. Error c odes and Agilent monitoring network (SDN) interface lockup may occur. Power cycling the product will recover the product. No permanent
damage will result. To prevent unintentional disruption in monitoring, be sure th e SDN
interface cable is properly secured at both ends when c onnecting to the Agilent
monitoring network (SDN).
•Do not connect a second rack by a cable when using a module rack docked to the back
of the Agilent V24CT or V26CT. Using a second rack connected by a cable may disrupt
module communication.
Caution
A “caution” calls attention to a c ondition or possible situation that co uld cause injury to the
user.
•Ventilation Requirements - Failure to meet ventilation requirements may cause
equipment failure an d, in turn, jeopardize the functions of automated monitoring. Do not
locate equipment in an enclosed ar ea which could restrict heat dissipation.
•Maintenance - Failure on the part of the responsible individual, hospital, or institution
employing the use of this equipment to implement a satisfactory maintenance schedule
may cause undue equipment failure and possible healt h hazards.
•Do not spray cleaning solut ions directly onto the monitor. Moisture droplets may enter
the internal components and cause equipment mal function or failure. Cleaning solutions
should be applied to a cloth and the cloth used to wipe the monitor clea n. The monitor
should be turned off during cleaning.
ix
Indications for Use
•Replacement Parts - It is highly recommended that only Agilent Technologies
recommended parts and a ccessories be used with this equipment. Failure to do so may
result in the degradation of performance. Accessorie s and parts for individual modules
and components are listed at the back of the appropriate section in th is manual.
Note—
A note gives special instructions to highlight an operating procedure or practice. Notes
may precede or follow the applicable text.
At this time, Agilent Technologies will ma ke available on request, and in E nglish only, such
circuit diagrams, component part lists, descriptions, calibration instructions, or other
information which wil l assist the user’s appropriate qualified technical pers onnel to repair
those parts of the equipment which are classified by Agilent Technologies to be repairable. A
list of Agilent Sales and Support Of fices is provided at the end of this manual.
x
Indications for Use
Using This Manual
To enable you to find information easily, there is a contents list at the front of the guide and a
comprehensive index at the back.
The User’s Reference Manual is separated into two parts; the core document and the
parameter module guides.
The Core Document
This section of the guide contains al l the general information about the sy stem. It is a good
place for new users to start because it gives an introd uction to the system and the way it
works, and shows you how to get start ed. Here is a list of the major sections:
•Introducing the Agilent M1165/66/67/75/76/77A Component Monitoring System and the
Agilent M1205A V24 and V2 6 monitors
•Getting Started
•Configuring the System
•Other Patients
•Alarm Functions
•Recording Functions
•Trends and Data Management
•Installation and Patient Safety
•Care and Cleaning
xi
Indications for Use
Monitor Setup
Parameter Module Sections
These sections each contain information for one parameter module. This covers setting-up,
monitoring, and problem solving if you encounter difficulty. Each section is separ at ed with a
white tab which has the title of the section.
Note—
The User’s Reference Manual contains information for all the parameter modules
available for the system. This means, of course, that depending on the model and number of
modules you have ordered, the screens w ill not always apply to your system. However, the
information for the param eters and functions is valid for all the system s.
Note—
The screenshots displayed in this manual were generated in demo mode and may
therefore differ from what actually appears on your screen during patient monitoring.
Notice to the User
Although there may be products in your area that look similar to the Agilent M1165/66/67/75/
76/77A Component Monitoring System and the Agilent M1205A V24 and V26 monitors, their
functionality may not be the same. This User’s Reference Manual is intende d t o be used with
the Agilent M1165 / 66/67/75/76/77A Component Monitoring System, the M1026A Anest hetic
Gas Module and the Agilent M1205A V24 and V26 monitors only.
This Manual is only applicable for Release C.0 versions of the monitors listed above. A
Release C.0 monitor can be identified by:
xii
a. the Release C.0 label on the monitor, or
b. the suffix of the EPROMpack part number. To view this number, press
→ → .
Monitor RevisionShow SW Rev
The suffix of the EPROMpack part number on a Release C.0 Agilent CMS is A.
The Software R evision of a Releas e C.0 Agilent V24 or V26 monitor is L.xx.xx
Responsibility of the Manufacturer
Responsibility of the Manufacturer
Agilent Technologies only considers itself responsible for any effects on safety, reliability and
performance of the equipment if:
assembly operations, extensions, re-adjustments, modifications or repairs are carried out
by persons authorized by Agilent , and
the electrical installation of t he relevant room complies with nationa l standards, and
the instrument is used in accordance with the instructions for use.
To ensure optimum usage, we recommend that Agilent parts and accessories are used in
conjunction with the Agilent M1165/66/67/75/76/77A Co mponent Monitoring System, the
Agilent M1026A Anesthetic Gas Module and the Agilent M120 5A V24 and V26 Monitors,
wherever available. If non-Agilent parts are used, Agilent Technologies is not liable for any
damage that these parts may cause to the Agilent equipment.
Manufacturer´s Address
For South America, North America and Canada:
Agilent Technologies, Inc.
3000 Minuteman Road
Andover
MA 01810-1099
The Agilent M1165/66/67/75/76/77 CMS and the Agilent M1205A V24 and
V26 Monitors, hereafter referred to as the “monitor”, are modular patient
monitors with networking and data management capabilities. All the
systems can have modules added or removed at a later time as need ed,
or you can interchange the modules between systems in your unit.
Note—
Some features expla ined in this manual are not availa ble for both
the Agilent CMS, V24 and V26 Monitors. The respective sections are
marked throughout the manual with either “Agilent CMS only” or
“Agilent V24 and V26 only”.
The following system types are available:
CMSThe Agilent CMS is available as a choice of three system types. Each
system consists of three individual parts; a display module, a computer
module and param et er modules:
1. M1167/77A Color Flatscreen Display and Computer Module with
Satellite Module Rack
Note—
This system is also available with an External Alarm Device and
an XGA compatible display controller to drive commercially available
ITE (Information Technology Equipment) displays (XGA Type).
2. M1165/75A Monochr ome CRT Display and Computer Module w ith
Integral Module Rack
3. M1166/76A color CRT Display and Computer Module with Integral
Module Rack
All system types are also av ailable as a choice of three diff erent model
types:
Full TitleAbbreviation
The Agilent Component Monitoring SystemAgilent CMS
The Agilent Component Monitoring System for
Agilent ACMS
Anesthesia Care
The Agilent Component Monitoring System for
Agilent NCMS
Neonatal Care
Note—
In this manual, the system will be referred to as the Agilent CMS,
the Agilent ACMS and the Agilent NCMS.
The Agilent CMS, V24 and V26 Monitors
1-5
Introduction
The Agilent CMS, V24
Display
Modules
and V26 Monitors
Below are labeled diagrams of the display modules provided by Agilent
Technologies. The control panel is described in more detail in the
following sections
.
M1095A Flatscreen Display Module
M1092A / M1094B CRT Display Module
1-6 The Agilent CMS, V24 and V26 Monitors
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