HP M1165, M1166, M1167, M1175, M1176 User manual

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HP M1165/66/67/75/76/77A

Viridia Component Monitorinc

System and

HP M1205A Viridia 26/24 Ser

User’s Reference Manual

Volume 1

System Information

	Ca	HEWLETT®
		PACKARD
ΠΠ	Part Number M1046-9001K
ΠΠ	Printed	02/99

First Edition

M1046-9001K

Notice

This document contains proprietary information which is protected by copyrigt Reserved. Reproduction, adaptation, or translation without prior written permis prohibited, except as allowed under the copyright laws.

Hewlett-Packard

3000 Minuteman Road

Andover, MA 01810-1085

(978) 687-1501

Publication number

M1046-9001K

Warranty

The information contained in this document is subject to change without notice

Hewlett-Packard makes no warranty	of	any kind with regard	to this	material, in
not limited to, the implied warranties	or	merchantability and	fitness	for a partic

Hewlett-Packard shall not be liable for errors contained herein or for incidental consequential damages in connection with the furnishing, performance, or use « material.

Printing		History
New	editions	of this	document will incorporate all			material updated since the p
Update packages may be issued between					editions and contain replacement and
pages to be merged by a revision date at					the bottom	of the	page. Note that page
rearranged due to changes				on a previous	page are not considered revised.
The	documentation		printing	date and part number		indicate	its current edition. *
date changes when a new edition is printed. (Minor corrections and updates wi
incorporated at reprint do not cause the					date to change.) The document part ni
when extensive technical changes are incorporated.
PFistEditon................................					February		1999

Important

United States federal law restricts these devices to sale by or on the order of a

The	M1165/66/75/76A Systems comply with				UL544, CSA		22.2-125, TEC 601-1,		ЕК
EN	60601-1-2 and	carries	C€o363	Marking	to Council		Directive	93/42/EEC,	Eu
Device Directive		(MDD).
The	M1167/77A Systems comply with UL2601-1, CSA					22.2 No. 601.1-M90, TEC			6
EN	60601-1, and EN 60601-1-2 and carries				CE&o3s66	Marking to		Council Directi
European Medical		Device	Directive	(MDD).

The M1205A option 020 and 022 complies with UL2601, IEC 601-1, CSA C22.2 n EN60601-1, and EN60601-1-2 and carries C€o123 Marking to Council Directiv European Medical Device Directive (MDD).

The M1205A option	021	complies with UL2601, IEC 601-1, CSA C22.2 no. 601-1,
_ ; through 5, and VDE	0871	level A.

Electromagnetic Compatibility (M1205A Viridia 26/24

The electromagnetic compatibility (EMC) validation of the M1205A included tes performed according to international standards for EMC with medical devices. | Manufacturer’s Declaration for details.

EMC Testing

During the		test program the M1205A was subjected to		many	EMC	tests, both	int
standard	and		HP proprietary tests. During most of the	testing no		anomalies	wer
For two	of	the	tests, IEC 801-3 Radiated Immunity and IEC		801-4	Fast Transient

Immunity, some reduced performance was observed. IEC 801-3 specifies that th

subjected

to a

field

3 V/m

over

frequency

range

26 to 1000 MHz

with no

performance.

At many

the

test

frequencies

over the

specified

range

anom:

| observed.

However

a number

test points,

increased width

of the

ECG

and

observed.

For

these

test points the radiated field was reduced to the

level

at wh

returned

to normal.

These

reduced

levels are

shown

the table

below.

From

to 200

MHz

From

200

Immunity

Levels (V/m)

ECG

„175

worst

case

.220

worst

case

Pleth

no problems

.391

worst

case

IEC 801-4 specifies

that the product

subjected

to high

speed pulses

100

the

power

cord and

all I/O cables greater than 3 m. During and after most

the

anomalies

were

observed.

However

pulse levels greater

than

680

appliec

power cord, anomalies were sometimes observed in the form

display

transier

numerics and RS-232 disruption. At

voltages greater than

300

applied

the R

disruption in RS-232

communication

was

observed.

compliance

with

IEC 801-4, the M1205A performs its intended function

withc

satefy hazard,

at the

reduced

levels

specified above.

	System	Characteristics
	The phenomena		discussed above are not unique	to	the M1205A but are charact
%	patient monitors		in use today. This performance	is	due to the very sensitive hig
\|	amplifiers	used	to display the physiological signals.		Among the many similarly \|
	monitors already in use by customers, interference from electromagnetic sourc
	problem in	actual use.

Avoiding

Electromagnetic

Interference

When electromagnetic interference

(EMD

is encountered there are

a number

can be taken to mitigate the problem.

Eliminate the source. Possible sources of EMI can be

turned off

mover

reduce

their

strength.

Attenuate

the

coupling.

If the

coupling path is through

the patient

leads, t

may be reduced by moving and/or rearranging the leads. If the

coupling

power cord, plugging the M1205A

into a different circuit may

help.

Reduce

the sensitivity of the

system.

In all of the EMC

testing

the

M1205/

to maximum

sensitivity.

For

the ECG

amplifier the gain was four times

required. By reducing the gain of the system receiving

the EMI,

the interf

often be

eliminated.

Add external attenuators. If EMI becomes an unusually difficult

problem

devices such as an isolation transformer or a transient suppressor may be

Customer

Engineer can

be of

help

determining the

need for

external

Intended Use

Description

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the E

Viridia	26/24 Series Monitors are network connectable bedside patient monitori
The HP	M1205A Viridia Models 24CT and 26 CT may powered by either AC line
battery	power.

Purpose

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the E Viridia 26/24 Series measures and displays multiple physiological parameters an generates alarms and recordings. It exchanges information with compatible dev M1165/66/67/75/76/77A Viridia Component Monitoring System and the HP M120: 24 Series Monitors are not therapeutic devices.

Patient Population

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the E Viridia 26/24 Series is intended to be used on adult, pediatric, and neonatal patie

Environment

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the H

Viridia		26/24 Series is intended to be used in a clinical environment by licensed \|
is	not	intended for home use.
It	communicates with devices such as a central station through network interfac
serial		1/0 port.

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the E Viridia 26/24 Series Monitors are prescription devices and will carry the followi “United States Federal jaw restricts this device to sale by or on the order of a pl

Indications for Use

Condition

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the] Viridia 26/24 Series Monitors are generally indicated when the clinician decides to measure and display multiple physiological parameters and waves, to gener: recordings of adult, pediatric, or neonatal patients.

Part of Body or Type of Tissue with Which the Device Interac

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the|

Viridia 26/24 Series does	not contact	the body or	tissue of the patient. Signals a
from accessory electrode,	transducer,	and sensor	devices.

Frequency		of	Use
The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the \|
Viridia 26/24	Series		Monitors are	indicated for	use when prescribed by a clinici
Physiological			Purpose
The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the \|
Viridia 26/24 Series Monitors are				indicated when the purpose is to gain informe
treatment, to	assess adequacy of			treatment, or	to rule out causes of symptoms.
- 66/67/75/76/77A		Viridia Component Monitoring			System and the HP M1205A Vir
are well suited		for	patient monitoring.

Patient Population

Adult, pediatric, and neonatal non-ambulatory patients.

Indications for Use

Prescription Versus Over-the-Counter

The HP M1165/66/67/75/76/77A Viridia Component Monitoring System and the H Viridia 26/24 Series Monitors are prescription devices.

viii

Warnings, Cautions, and Notes

Warnings, cautions, and notes are used throughout this User’s Manual to give y

information		about			the The HP M1165/66/67/75/76/77A Viridia Component Monit
and the	HP	M1205A			Viridia 26/24 Series. The warnings and cautions included ix
section	refer		to	the	equipment in general.
Warning
A “warning”			calls		attention to the user of imminent hazard to people it
procedures			are	not followed.

*For continued safe use of this equipment, it is necessary that the listed in followed. Instructions in this manual in no way supersede established me procedures.

«Explosion HazardDo not use this equipment in the presence of flammab

eAlarms - Do not rely exclusively on the audible alarm system for patient 1 Adjustment of alarm volume to a low level or off during patient monitorů patient jeopardy. Remember that the most reliable method of patient mo:

combines close personal surveillance with correct operation of monitorů

+This equipment is only intended for use in healthcare facilities by trained professionals.

The product is not intended for outside hospital use such as a helicopter: ambulances.

+	This product is not intended for home	use.
®	To reduce the risk of electrical shock,	do NOT remove any cover. Refer:
	qualified personnel.

This equipment may interfere with ultrasound imaging equipment by cau interference on the ultrasound display. Try to keep the instruments as fa possible.

Indications for Use

+Exposure of electrical contacts or connections to saline or other liquids a:

dangerous. Electrical contacts and connections such as cable					connectors,
supplies, parameter module plug-in connections and rack connections						mu
clean	and dry.		Thoroughly dry any electrical connections that		become	cor
with	liquids.	If	additional decontamination	is required please	contact	yow
department		or	Hewlett-Packard Response	Center.

*Although this equipment is shielded against Electromagnetic Interference

recommended

to avoid

the use

electrically

radiating

devices

close pr

this

equipment.

Connecting

the

HP Viridia monitoring network (SDN)

cable when

the

pro:

powered

not supported. Error codes and HP Viridia monitoring

neti

interface lock-up may occur. Power cycling the product will recover

the p

permanent

damage will result.

To prevent unintentional disruption in

mor

sure

the

SDN interface

cable is

properly secured at both ends when conne

Viridia monitoring

network

(SDN).

not connect

a second

rack

by a

cable when

using a

module

rack docke

of the Viridia Model 24CT

or 26CT.

Using a second rack connected

a cz

disrupt

Viridia

module

communication.

Caution

A “caution” calls attention to a condition or possible situation that could cause. user.

®Ventilation Requirements - Failure to meet ventilation requirements may «

equipment	failure and,	in turn, jeopardize	the functions	of automated mor
not locate	equipment	in an enclosed area	which could	restrict heat dissip:

*Maintenance - Failure on the part of the responsible individual, hospital, c

	employing		the use	of this equipment to implement a satisfactory		maintene
	may	cause	undue	equipment	failure and possible health hazards.
+	Do	not spray cleaning solutions directly onto the monitor. Moisture drop]
	the	internal components and cause equipment malfunction or failure. Cle:
	solutions		should be applied to a cloth and the cloth used to wipe			the mon
	The	monitor should be turned			off during cleaning.

Replacement Parts - It is highly recommended that only Hewlett-Packard parts and accessories be used with this equipment. Failure to do so may 1 degradation of performance. Accessories and parts for individual module components are listed at the back of the appropriate section in this manu


Note—A note		gives special			instructions	to highlight an operating procedure		or	{
may precede		or	follow the		applicable text.
At this time, Hewlett-Packard will make							available on request, and in English on
diagrams,	component			part	lists, descriptions, calibration instructions, or other
which will assist			the	user's	appropriate	qualified technical personnel to repair{
the equipment which are classified by						Hewlett-Packard to be repairable. A		list	«
Support	Offices		is provided		at the end	of	this manual.

Indications for Use

Using	This		Manual
To enable	you	to	find	information easily, there is a contents list at the front of th
comprehensive		index		at the back.

The User's Reference Manual is separated into two parts; the core document an parameter module guides.

The	Core	Document
This	section	of the guide contains all the general			information	about	the system.	\|
place	for new	users to	start	because it gives an introduction		to the	system and	tl
works, and shows you			how	to get started. Here	is a list of the	major	sections:
*	* Introducing the HP M1165/66/67/75/76/77A				Viridia Component		Monitoring
	the HP M1205A Viridia 26/24 Series
+	Getting	Started

« Configuring the System

* Other Patients

* Alarm Functions

Recording Functions

* Trends and Data Management

+ Installation and Patient Safety

Care and Cleaning

xii

Parameter Module Sections

These sections each contain information for one parameter module. This cover


monitoring,	and	problem		solving if you		encounter difficulty. Each	section is	sey
white tab which		has the title			of the section.
Note— The	User’s		Reference		Manual contains information for all the parameter
available for the			system.	This	means, of	course, that depending on	the model	ar

modules you have ordered, the screens will not always apply to your system. H information for the parameters and functions is valid for ail the systems.

Note—The screenshots displayed in this manual were generated in demo mode therefore differ from what actually appears on your screen during patient moni

Notice

the

User

Although

there

may be products in your

area

that look

similar to the HP M1165

77A Viridia Component Monitoring System and the

M1205A Viridia

26/24

functionality

may not be the

same. This

User’s

Reference

Manual is

intended

the HP M1165/66/67/75/76/77A Viridia Component Monitoring

System,

the M102

Gas

Module

and the

HP M1205A Viridia

26/24

Series

only.

This

Manual

only applicable for Release B.0

versions

the

monitors

listed

B.0

monitor

can be identified by:

the

Release B.0 label on the monitor, or

the

suffix

of the

EPROMpack

part

number.

To view

this

number, pre

— © Monitor Revision”:

—

‘Show SW

Rev.

The

suffix

of the

EPROMpack

part

number

a Release

B.0

Monito

Responsibility of the Manufacturer

Hewlett-Packard only considers itself responsible for any effects on safety, reli: performance of the equipment if:

assembly operations, extensions,	re-adjustments, modifications or repairs
out by persons authorized by HP,	and

the electrical installation of the relevant room complies with national star

the instrument is used in accordance with the instructions for use.

To ensure optimum usage, we recommend that HP parts and accessories are us

conjunction with the	HP M1165/66/67/75/76/77A		Viridia	Component Monitoring
HP M1026A Anesthetic Gas Module		and the HP	M1205A	Viridia 26/24	Series	Mo
wherever available. If non-HP parts		are used, Hewlett Packard is not			liable	for z
that these parts may	cause to the HP	equipment.

Manufacturer’s Address

For South America, North America and Canada:

Hewlett-Packard Company

3000 Minuteman Road

Andover

MA 01810-1099

For all other countries:

Hewlett-Packard GmbH

Herrenberger Str. 130

71034 Béblingen

Germany

xiv

Condition							erkreeer
Part of	Body		or	Type	of Tissue with	Which the Device	Interacts
FreguencyofUse.....................							ea
Physiological			Purpose
Paient	Population						eee	en
Prescription Versus Over-the-Counter
Responsibility		of	the	Manufacturer.
Manufacturers				Address.			ekkn kk	knne
Declaration	of	Conformity			(according to	ISO/IEC Guide 22	and EN 45014) ....
Declaration	of	Conformity

The HP Viridia CMS and

26/24 Series Monitors


The Handheld			Keypad
External		Alarm	Device.
Hardkey		Eunctions.		κ κκ νε	εκ	κ κ εν
HP Viridia Model 26CT/24CT Power Supply
Battery		Power	Supply
Parameter	Modules
Operating	Levels
Main	Screen			enken	serene,
Selection Window
Task WindoW				rr
Getting into the Operating Levels
The Viridia		CMS Computer		Modules
M1046A		Computer Module

M1046B		Computer Modulk.........................................
ECG	Output		and Defibrillator	Marker	Input ............................
The Viridia 26/24 Series Parameter Module Rack ...........................
Operating	Rules		to Remember ......................		,...................
Performance Specifications of the HP Displays .............................
M1095AFlatscreenDisplay .......................................
M1094A/B			and M1092A CRT	Display.	. 2. 22 2
Using an	ÎTE	Display ..................................			,......,......
Safety

Getting Started
Setting up	theMonitor(Viridia26/24only)		................................
Setting up the Parameter Modules
Atlaching	the	Patient.	n eens
Adjusting		Screen Contrast ..........................................
Starting Monitoring
Screen	Messages ..................		, ..............................
Reserving		a Channel ...........................................	,,.
Power	Failure

Setting	up	your	Monitor
Changing		Display Screens .......................................				,....,
Selecting		a Screen			sk kk skr	rerrker
	Procedure ....
Freezing		Waves	(Viridia CMS	only)
What	you	Can	Configure,
Changes		to the	Configuration .......	,...................................
MakingChangestotheMainDisplay...............................
Assigning		WavestoScreenChannels.....................................
	Procedure iie
Selecting		a Screen
	Procedure				laa	ira

Selecting Screen Labels for Realtime Display Screens

Procedure

Contents-2

Selecting

the

Number

Waves

Procedure

..................

aaa

. Changing

the

Wave

Overlap

Procedure .

esse nesker

krkkee

Selecting

Realtime

Wave

Speeds

Procedure

Numerics

On/Off ...

Additional Information

Selecting

an Application

Window

Procedure

.....................

cece

een

tees

Displaying Split Screen

Trends ........................................

OxyCRG

Display

aaa

NotesonoxyCRG.....................

eee

CSA Display (Viridia CMS only)

Notes

CSA

Wave

Replace

Procedure

Trace

Mode

eee

eens

Procedure ...............

eee

Configuring a Second Independent Display (Viridia

CMS

only)

..............

Other Functions You Can Configure

Adjusting

the

Volume

Control

Procedure .....................................................

Adjusting the Date and Time

Procedure ......................

Selecting Waves for Central Recorders . .................................

Configuring Module, Bedside and Central Recordings. .....................

Other Patients	Controls ..............................................
The Status LogFuncüon..................			5	1
The Monitor	Revision Function.	. . .
Changing Default Settings and Patient Category
Changing the	Patient Category
ECG................		eee

Changing	the Configuration		Set
Procedure			rr	e rara
Changing	Operating	Modes	.......................,.........,..........
Procedure ............
The Test	Signals Function. .
Procedure ................
Analog Output		(CMS only)..
Parameter	Settings	Transfer	..........
Parameter	Settings	Transfer	Messages

Other Patients
OvervieW	deu	eee	eee
HP Viridia Patient Care System ..............
The Other Patients Selection Window
Automatic AlarmOtherPatients..................................
Configuring the Other Patients Controls ...............................
Using HP Viridia Patient Care System with an Arrhythmia Computer
Extended	Overview (Viridia CMS only) ...............................		,..
To View an Extended Other Patients Bed
Alert	Notification

Alarm Functions

Alarm Display		....................			,.......
Alarm	Functions		on the	Control	Panel. ...........	,....................
Suspending Alarms ...............
Silencing		and Resetting		Alarms. .
Alarm	Priorities		..............
Individual		Parameter Alarms......
When	an	Alarm	Occurs	..........
Alarm Setup.						n
Getting	into the		Alarms	Selection	Window

Changing the Alarm Limits

Setting the Volume Control

The Nurse Call Relay

Recording Functions

General Recorder Information

Recorders

Contents-4

Changing		the	Recorder.		............................................
Continuing		a	Timed	Recording ......................................
Inserting	a	Calibration			Signal .............................			,........
Recording		Layouts		...........
Recording Status			Messages.
Loading Paper...........
Cemntral	Recorders.					ccc	ence	eee	eee
Loading	Paper into			the	Plug-In Recorder ..............................
To Replace Paper in the Plug-In Recorder. .............................
Cleaning the Printhead in the Plug-In						Recorder .........................
Loading	Paper into			the	Four Channel	(M1117A) Recorder	(Viridia	CMS	only)
Cleaning	the		Roller	on	the Four Channel (M1117A) Recorder. .............

Admit/Discharge/End				Case
Admitting a Patient ................						PPP				PPP
Changing		Patient Information .......................................
DischargingaPatient/EndingaCase..................................
Trends and	Calculations
Introduction to Trends & Calculations ....................................
ViewingPatientData.......................								öle
Trending		Priority
Viewing Blood Measure-ments .
Viewing		Vital Signs.......................
Selecting Parameters for Graph Trends...
ViewingGraphTrends................
Performing	and		Reviewing		Calculations......
Performing			Calculations ...........................................
Changing-or			Eniering		an Input Value		..............................			,..
ReviewingCalculations.........................................
Printing Reports.						еее		некие	ene	ees
Printing		Task Window			Reports ......................................
Printing		ScheduledReports.................................
What	to	Do	If Your	Report		Does Not	Print. .

Drug Calculator..........................0 a

Neonatal Event	Review
Introduction to	Neonatal Byent Review	νο «ενω εν ωνων εν εν ν ων ων ων ων ως
Contents-6


Viewing Neonatal			Events.	............................................
Manual	Event		Storage. ...........................................
Graphical		Details ...............................................
Operating		Controls		νο νεο	νεο εννοω	ων ων ών εν ων ων ως
Viewing oxyCRG			Episodes ...........................................
Operating		Controls ............			,.................................
Adjusting Neonatal			Event	Review	Settings .
Event	Criteria

Data Transfer			-
DataTransferModule...................................					8
What	is Transferred	.............................................
Types of	Transfer. «νο	νε ενω	ρω ω ρω ρω ρε νε ων	ωρών ων εν κ ρω ων	κ ων νώ ων ως
ToModule...............................				0...	iie
ToMonitor..............................						eee
TransferringBlood		Analysis	Data...................................
Combining Data esserearara
Time	Conversion.					νο
Vital Signs, Blood Review and			Graphs .	0
TimeStamp...................
Reports ....
Troubleshooting.........

Performance Specifications .........................

Data Transfer Module. ..........................................

Monitor Installation and Patient Safety

Viridia CMS.............................			,..
Power Source Require-ments .
Grounding	the System ..........................................
Combining	Equipment .		eee never
Environ-ment ...................		1	ilan
Conden-sation iie				ννο
xplanation	of Symbofs used	νε ων	νεο εν εωωο εννοωωνών ων ον
Maintenance Checks ...............................................

Performing the Invasive ..........................................

Pressure Module Self-Test . .

Performing the NBP Module Self-Test

Performing the SpO2/Pleth Module Self-Test

Performing the Cardiac Output Module Self-Test......................

Performing the tepO2/AcpCO2 Module Self-Test

Performing the CO2 Module Self-Test. ..............................

Performing the TemperatureModuleself-Tesı........................

Performing the Blood AnalysisModuleSelf-Test......................

Performing the Recorder Module Self-Test ...........................

Performing the Data Management Database Self-Test...................

Tests for Vuelink Module and Anesthetic Gas Module ..................

Contents-10

The HP Viridia CN

26/24 Series Mc

This chapter provides an overview of the HP Viri 24 Series Monitors. It includes the following sectic

Parameter Modules.....................

HP Viridia Model 26CT/24CT Power Supply

Operatinglevels.......................

The Viridia CMS Computer Modules ......

The Viridia 26/24 Series Parameter Module

Operating Rules to Remember............

The HP Viridia CMS and 26/24 Ser

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	E

Introduction

The HP

M1165/66/67/75/76/77 Viridia CMS and

the

M120

24 Series Monitors, hereafter referred to as the

“monitor”,

patient

monitors with networking

and

data

management

the systems can have modules added or removed at a

later

needed,

you

can interchange

the modules

between

syste

unit.

Note—Some

features

explained

this

manual

are

not

avail:

the HP

Viridia

CMS

and the HP

Viridia

26/24

Series

Monitor

respective sections are marked throughout the manual witl

“Viridia CMS

only”

or “Viridia

26/24

Series

only’.

The following system types are available:

Viridia CMS

The HP

Viridia

CMS

is available

a choice

three system

system consists of three individual parts; a display module,

module

and

parameter modules:

1.M1167/77A Color Flatscreen Display and Computer Satellite Module Rack

Note—This system		is also available with an External		Alarm
an	XGA compatible	display controller to	drive commerciali
ITE	(information Technology Equipment)		displays	(XGA T

2.M1165/75/A Monochrome CRT Display and Computer

Integral Module Rack

3.M1166/76A color CRT Display and Computer Module Module Rack

1-2 The HP Viridia CMS and 26/24 Series Monitors

M1167/77A System

		Display
		Module
	OO	Computer
RU	eae	Module parameter
	a	Modules

Display Module		M1095A	10.4” Flatscreen Display
Computer	Module	M1046B	Computer Module
Parameter	Modules	Satellite	Rack

The HP Viridia CMS and 26/24 Serie

£a

ο ὢ |

q 5

Ts oc cu FP

Introduction

M1167/77A System with External Alarm Device

XGA Display

External Alarm Device

Computer		©
Module	o	+

Display Module		ITE Display (XGA		Type)
Computer	Module	M1046B	Computer	Module
Parameter	Modules	Satellite	Rack

1-4 The HP Viridia CMS and 26/24 Series Monitors

M1165/75A and M1166/76A System

Display

Module

Parameter

Modules

Display Module		M1094A/B/92A		14"	CRT	Display
Computer	Module	M1046A	Computer		Module
Parameter	Modules	Integral	and/or	Satellite		Rack

Medel Types	All system types are also available as a choice of three dif
	types:

Full	Title			-		Abb
The	HP	Viridia	Component	Monitoring	System	НРУ
The	HP	Viridia	Component	Monitoring	System	HP \
for	Anesthesia		Care
The	HP	Viridia	Component	Monitoring	System	HPA
for	Neonatal Care

Note—In this manual, the system will be referred to as the CMS, the HP Viridia ACMS and the HP Viridia NCMS.

The HP Viridia CMS and 26/24 Serie

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Introduction

Display	Below are	labeled	diagrams	of	the display	modules. The co
Modules	described	in more	detail in	the	following	sections

mama

Power indicator light

Screen brightness

control è

Power on/off switch (also remote on/oft for power supply)

Control

Panel

	Connector for rer
indicator light	keypad cable
	Screen
Power On/Off	Brightness control
switch	Screen'
	Screen'
	Contrast contro!

M1092A/ M1094B CRT Display Module

1-6 The HP Viridia CMS and 26/24 Series Monitors

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