Mindray Rosebud Accutorr V User Manual

Vital Signs Monitor
USER MANUAL
Accutorr® is a registered trademark of Mindray DS USA, Inc.
f
®
Mindray
®
Nellcor
is a U.S. registered trademark of Tyco International Ltd.
SmarTemp
®
is a U.S. registered trademark of Masimo Corp.
is a trademark or a registered trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
is a trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Copyright © Mindray DS USA, Inc., 2009. All rights reserved. Contents of this publication may not be reproduced in any
orm without permission of Mindray DS USA, Inc.
Accutorr V Service Manual 0070-10-0702
Table of Contents
Preface ....................................................................................................................................... v
Warnings, Cautions, and Notes..................................................................................................... vii
Warnings.................................................................................................................................... vii
Cautions ..................................................................................................................................... viii
Notes ......................................................................................................................................... x
Safety Designations ...................................................................................................................... xi
Product Limitations........................................................................................................................ xii
Unpacking................................................................................................................................... xiii
Symbols and Descriptions.............................................................................................................. xiii
Theory of Operation ......................................................................................................... 1 - 1
Introduction ................................................................................................................................. 1 - 2
Controls and Indicators ................................................................................................................. 1 - 2
System Overview .........................................................................................................................1 - 2
Hardware Structure ......................................................................................................................1 - 4
Main Board ..........................................................................................................................1 - 5
Power Board ......................................................................................................................... 1 - 6
Key and Displays Board .........................................................................................................1-7
Parameter Boards .................................................................................................................. 1 - 8
SpO
Module ................................................................................................................1 - 8
2
NIBP Module ................................................................................................................. 1 - 9
Optional Temperature Module .........................................................................................1 - 9
Recorder...............................................................................................................................1 - 10
Bar Code Scanner .................................................................................................................1 - 10
Specifications.................................................................................................................... 2 - 1
Introduction ................................................................................................................................. 2 - 2
NIBP Measurement.......................................................................................................................2 - 2
Blood Pressure.......................................................................................................................2 - 2
Static Accuracy .....................................................................................................................2 - 2
Maximum Cuff Pressure ..........................................................................................................2-2
Cuff Inflation ......................................................................................................................... 2 - 3
Maximum Leakage.................................................................................................................2 - 3
Deflation Rate........................................................................................................................ 2 - 3
Update Period .......................................................................................................................2 - 3
Initial NIBP Pressure Setup and Range ...................................................................................... 2 - 3
NIBP Measurement Cycle ..............................................................................................................2 - 4
Cuff Inflation Time..................................................................................................................2 - 4
Cuff Pressure Automatic Check Algorithm ..........................................................................2 - 4
Automatically Adjusted Inflation Value after First Measurement ....................................................2 - 5
Pulse Rate .............................................................................................................................2 - 5
SpO2 Measurement......................................................................................................................2 - 6
DPM SpO2 Module Performance............................................................................................. 2 - 6
SpO2 ...........................................................................................................................2 - 6
Pulse Rate ...................................................................................................................... 2 - 6
Alarm setting range ........................................................................................................ 2 - 6
Masimo MS-2013 SpO
Performance ...................................................................................... 2 - 7
2
Accutorr V Service Manual 0070-10-0702 i
Table of Contents
SpO2 ............................................................................................................................ 2 - 7
Pulse Rate ...................................................................................................................... 2 - 8
Alarm Setting Range ....................................................................................................... 2 - 8
Nellcor NELL-3 SpO
SpO
............................................................................................................................ 2 - 9
2
Performance...........................................................................................2 - 9
2
Pulse Rate ...................................................................................................................... 2 - 9
Alarm Setting Range ....................................................................................................... 2 - 9
Temperature ................................................................................................................................ 2 - 10
Display Area, Indicator, and Controller........................................................................................... 2 - 10
Display Area.........................................................................................................................2 - 10
LCD .............................................................................................................................. 2 - 10
7-Segment Digit Display .................................................................................................. 2 - 11
Monochrome LED Indicator .............................................................................................. 2 - 11
Power Indicator ..............................................................................................................2 -11
Overlay and labeling ............................................................................................................. 2 - 11
Alarm Lamp .......................................................................................................................... 2 - 12
Keys.....................................................................................................................................2 - 12
Patient Cable Connectors........................................................................................................2 - 13
Audio Indicator............................................................................................................................2 - 14
Pulse Tone Function................................................................................................................ 2 - 14
Multiple-Level Volume ............................................................................................................. 2 - 14
Real-time Clock ............................................................................................................................2 - 14
Standby Mode.............................................................................................................................2 - 15
Alarm Information ........................................................................................................................ 2 - 16
Basics................................................................................................................................... 2 - 16
Alarm Notification ................................................................................................................. 2 - 16
Audio Alarm Pause, Audio Alarm Off, and Audio Alarm Silencing .............................................. 2 - 16
Configuration management ...........................................................................................................2 - 16
Barcode scanner .......................................................................................................................... 2 - 16
Troubleshooting................................................................................................................ 3-1
Introduction ................................................................................................................................. 3 - 2
Part Replacement.......................................................................................................................... 3 - 2
Monitor Status Check.................................................................................................................... 3 - 2
Technical Alarm Check .................................................................................................................3 - 3
Troubleshooting Guide..................................................................................................................3 - 4
Power On/Off Failures ..........................................................................................................3 - 4
Display Failure ...................................................................................................................... 3 - 4
LED Digital Display and Indication Lamp Failure ........................................................................3 - 4
Alarm Problems ....................................................................................................................3 - 5
Key Failure .......................................................................................................................... 3 - 5
Recorder Failures...................................................................................................................3 - 6
Interface Failures ..................................................................................................................3 - 6
Power Supply Failures ............................................................................................................3 - 6
Network Related Problems ..................................................................................................... 3 -7
Software Upgrade Problems ................................................................................................... 3 - 8
Bar Code Scanner Failures...................................................................................................... 3-8
ii 0070-10-0702 Accutorr V Service Manual
Table of Contents
NIBP Measurement Failures..................................................................................................... 3 -9
SpO
Measurement Failure ....................................................................................................3 - 9
2
Temperature Measurement Failures ......................................................................................... 3 - 9
Repair and Disassembly ................................................................................................... 4 - 1
Tools........................................................................................................................................... 4 - 2
Preparation for Disassembly ..........................................................................................................4 - 2
Disassembly................................................................................................................................ 4 - 3
Separating the Front and Rear Halves of the Monitor ................................................................ 4 - 3
Disassembling the Front Housing Assembly ..............................................................................4 - 6
Removing the Main Rack Assembly .......................................................................................... 4 - 9
Removing NIBP Module .........................................................................................................4 -11
Removing the Main (CPU) Board ............................................................................................4 - 12
Removing the Power Board .....................................................................................................4 - 13
Removing the Battery Connector Assembly ................................................................................ 4 - 13
Removing the Fan and Speaker ...............................................................................................4 - 14
Removing the Power Socket ...................................................................................................4 - 15
Disassembling the Temperature Module.................................................................................... 4 - 16
Disassembling SpO
Disassembling a DPM SpO Disassembling a Masimo SpO Disassembling a Nellcor SpO
Modules ................................................................................................. 4 - 17
2
module ................................................................................. 4 - 17
2
module ............................................................................ 4 - 18
2
module ............................................................................. 4 - 19
2
Disassembling the NIBP Module .............................................................................................. 4 - 20
Removing the NIBP Pump ................................................................................................4 - 20
Removing the NIBP Dump Valve .......................................................................................4 - 20
Removing the NIBP Bleed Valve .......................................................................................4 - 21
Parts ................................................................................................................................5 - 1
Main Assembly ............................................................................................................................5 - 2
Front Assembly (Color LCD) ........................................................................................................... 5 - 3
Front Assembly (Black-and-White LCD) ............................................................................................5 - 7
Rear Housing Assembly.................................................................................................................5 - 11
Main Bracket Assembly.................................................................................................................5 - 12
NIBP Assembly (Pump M6Q-100003- - -)......................................................................................... 5 - 14
NIBP Assembly (Pump 082-000056-00)..........................................................................................5 - 17
Temperature Module Subassembly .................................................................................................5-20
Temperature Power Module Subassembly........................................................................................5 - 22
Test and Calibration.......................................................................................................... 6 -1
Introduction ................................................................................................................................. 6 - 2
Test Report ............................................................................................................................6 - 2
Recommended Frequency ....................................................................................................... 6 - 2
Visual Test ................................................................................................................................... 6 - 4
Power-on Test............................................................................................................................... 6 - 4
NIBP Calibration .......................................................................................................................... 6 - 5
NIBP Accuracy Test ...................................................................................................................... 6 - 9
NIBP Leakage Test .................................................................................................................6 - 10
Test ...................................................................................................................................6 - 13
SpO
2
Accutorr V Service Manual 0070-10-0702 iii
SpO2 Test Under Normal Conditions .................................................................................6 - 13
SpO
Test in Motion Mode...............................................................................................6 - 13
2
Summary of Test Methods.................................................................................................6 - 14
DPM SpO Nellcor SpO Masimo SpO
..............................................................................................................6 - 14
2
..........................................................................................................6 - 14
2
.........................................................................................................6 - 14
2
Testing the Optional Temperature Module .................................................................................6 - 15
Nurse Call Performance Test....................................................................................................6-17
Bar Code Scanner Test ...........................................................................................................6 - 19
Electrical Safety Tests..............................................................................................................6 - 21
Enclosure Leakage Current Test .........................................................................................6 - 21
Earth Leakage Current Test ...............................................................................................6 - 21
Patient Leakage Current Test .............................................................................................6 - 22
Patient Auxiliary Leakage Current Test................................................................................6 - 22
Recorder Check .....................................................................................................................6 - 23
Software upgrade ..................................................................................................................6 - 24
1 - iv 0070-10-0702 Accutorr V Service Manual
Preface Introduction

Preface

This manual provides detailed information about the assembling, disassembling, testing, and troubleshooting of the equipment to support effective troubleshooting and repair. It is not intended to be a comprehensive, in-depth explanation of the product architecture or technical implementation. Observance of the manual is a prerequisite for proper equipment maintenance and prevents equipment damage and personnel injury.
Refer to the Accutorr V Operating Instructions: P/N 0070-00-0699-XX for information for operating this instrument.
This manual is based on the maximum configuration. Therefore, some contents may not be applicable. For questions, contact Service.
This manual is for biomedical engineers, authorized technicians, or service representatives responsible for troubleshooting, repairing, and maintaining the monitors.
Contents of this manual are subject to change without prior notice.
A password is required to access the service mode. The service password is 321.
The Accutorr V configurations are:
Accutorr V with Nellcor® Pulse Oximetry—
includes NIBP, Nellcor SpO
Accutorr V with Nellcor
includes NIBP, Nellcor SpO
a Trend Display, and Recorder
2,
®
Pulse Oximetry and SmarTemp™
SmarTemp, a Trend Display, and Recorder
2,
Accutorr V with Masimo SET® Pulse Oximetry—
includes NIBP, Masimo SpO2, a Trend Display, and Recorder
Accutorr V with Masimo SET® Pulse Oximetry and SmarTemp™—
includes NIBP, Masimo SpO2, SmarTemp, a LCD, and Recorder
Accutorr V with DPM Pulse Oximetry
includes NIBP, DPM SpO2, a Liquid Crystal Display (LCD), and Recorder
Accutorr V with DPM Pulse Oximetry and SmarTemp™
includes NIBP, DPM SpO
SmarTemp, a Liquid Crystal Display (LCD), and Recorder
2,
• Accutorr V with DPM NIBP and SmarTemp™
includes NIBP, SmarTemp, a Trend Display, and Recorder
• Accutorr V with DPM NIBP only
includes NIBP, a LCD, and Recorder
All Accutorr V configurations can be upgraded with a barcode scanner.
Masimo Patents: This device (MASIMO SpO2 Module) is covered under one or more of the following U.S. Patents 5,758,644, 5,823,950, 6,011,986, 6,157,850, 6,263,222, 6,501,975, and other applicable patents listed at: www.masimo.com/patents.htm. Possession or purchase of this device does not convey any express or implied license to use the device with replacement parts which would, alone, or in combination with this device, fall within the scope of one or more of the patents relating to this device.
Accutorr V Service Manual 0070-10-0702 v
Introduction Preface
Nellcor Patents: This device (Nellcor SpO2 Module) is covered under one or more of the following U.S. Patents Patent No. 5,485,847, 5,676,141, 5,743,263, 6,035,223, 6,226,539, 6,411,833, 6,463,310, 6,591,123, 6,708,049, 7,016,715, 7,039,538, 7,120,479, 7,120,480, 7,142,142, 7,162,288, 7,190,985, 7,194,293, 7,209,774, 7,400,919, and 7,212,847. Possession or purchase of this device does not convey any express or implied license to use the device with replacement parts which would, alone, or in combination with this device, fall within the scope of one or more of the patents relating to this device.
vi 0070-10-0702 Accutorr V Service Manual
Warnings, Cautions, and Notes Introduction

Warnings, Cautions, and Notes

Read and adhere to all of the warnings and cautions listed throughout this manual.
A WARNING is provided to alert the user to potentially serious outcomes (death, injury or serious adverse events) to the patient or the user.
A CAUTION is provided to alert the user that special care should be taken for the safe and effective use of the device. They will include actions to be taken to avoid effects on patients or users that will not be potentially life threatening or result in serious injury, but about which the user should be aware.
A NOTE is provided when additional general information is available.

Warnings

WARNING: Internal Electrical Shock Hazard - This unit does not contain
any user-serviceable parts. Do not remove instrument covers. Refer servicing to qualified personnel. When the integrity of the protective earth conductor, in the installation or its arrangement, is in doubt, the equipment should be operated from its internal battery. Observe all CAUTION and WARNING labels on the unit.
WARNING: Possible explosion hazard. Do not operate machine near
flammable anesthetic agents or other flammable substances. Do not use flammable anesthetic agents (i.e., ether or cyclopropane.)
WARNING: Always place the unit on a flat, rigid surface or onto a
WARNING: To ensure proper performance and safety and to prevent
WARNING: Use only cuffs with approved quick connect type connectors.
WARNING: The Accutorr V is not intended for use in a magnetic
WARNING: Danger of explosion if battery is incorrectly replaced.
WARNING: Do not use a damaged or broken unit or accessory.
Mindray approved stable mounting bracket.
the voiding of the warranty, only use authorized parts and accessories with the Accutorr V. Use of unauthorized accessories may result in erroneous readings.
resonance imaging (MRI) environment and may interfere with MRI procedures.
Replace only with the same or equivalent type recommended by the manufacturer. Dispose of used batteries according to the manufacturers instructions and local regulations. Batteries used in this device may present a risk of fire or chemical burn if mistreated. Do not incinerate battery, possible explosion may occur.
WARNING: Operation of the Accutorr V below the minimum amplitude
or value of patient physiological signal may cause inaccurate results.
Accutorr V Service Manual 0070-10-0702 vii
Introduction Cautions
WARNING: Use of accessories, transducers, and cables other than those
WARNING: Perform the decontamination or cleaning process with the
WARNING: Electrical safety tests are a proven means of verifying the
WARNING: Commercially available test equipment such as a safety
WARNING: Electrical safety tests should meet the requirements of the
WARNING: These electrical safety tests do not supersede local
WARNING: All devices using the AC mains and connected to medical
specified in the manual may result in increased Electromagnetic Emissions or decreased Electromagnetic Immunity of the Accutorr V. It can also cause delayed recovery after the discharge of a cardiac defibrillator.
unit powered down and power cord removed.
electrical safety of the monitor. They are intended for determining potential electrical hazards. Failure to identify these hazards in a timely manner may cause personnel injury.
analyzer can be used for electrical safety tests. Verify that the test equipment can be safely and reliably used with the monitor before use. The service personnel should acquaint themselves with the use of the test equipment.
latest editions of EN 60601-1 and UL 60601.
requirements.
equipment within patient environments must meet the requirements of the IEC 60601-1-1 medical electrical systems standard and should be put under electrical safety tests at the frequency recommended for the monitor.

Cautions

CAUTION: Observe extreme caution when a defibrillator is in use. Do
not touch any part of the patient, table, or monitor when a defibrillator is in use. The Accutorr V should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the Accutorr V should be observed to verify normal operation in the configuration in which it will be used.
CAUTION: The unit should be checked periodically for obstructed vents.
CAUTION: At the end of their life, dispose of the Accutorr V,
CAUTION: When equipped with Nellcor
CAUTION: When equipped with MASIMO
If an obstruction is found, refer the unit to qualified service personnel.
accessories, and single use supplies in accordance with local regulations. Dispose of packaging waste in accordance with local regulations.
®
oxygen transducers including Nellcor dedicated adhesive sensors. Use of other oxygen transducers may cause improper oximeter performance.
oxygen transducers including MASIMO LNOP
®
LNCS
patient dedicated adhesive sensors and MASIMO PC Series Patient Cable. Use of other oxygen transducers may cause improper Oximetry performance.
SpO2, use only Nellcor®
®
Oxisensor® patient
®
SpO2, use only MASIMO®
®
and MASIMO
viii 0070-10-0702 Accutorr V Service Manual
Cautions Introduction
CAUTION: Inaccurate readings may be caused by incorrect sensor
CAUTION: Route cables neatly. Ensure cables, hoses, and wires are
CAUTION: When cleaning sensors, do not use excessive amounts of
CAUTION: Recharge the Lithium ion battery while in the unit at room
application or use; significant levels of dysfunctional hemoglobins (i.e. carbohemoglobins or methemoglobin); or intra-vascular dyes such as indocyanine green or methylene blue; exposure to excessive illumination, such as surgical lamps (especially ones with a Xenon light source), bilirubin lamps, fluorescent lights, infrared heating lamps, or direct sunlight; excessive patient movement; venous pulsations; electro-surgical interference; and placement of a sensor on an extremity that has a blood pressure cuff, arterial catheter, or intra-vascular line.
kept away from patient’s neck to avoid strangulation. Keep floors and walkways free of cables to reduce risk to hospital personnel, patients, and visitors. If the sensor or patient cable is damaged in any way, discontinue use immediately.
liquid. Wipe the sensor surface with a soft cloth, dampened with the cleaning solution. To prevent damage, do not soak or immerse the sensor in any liquid solution. DO NOT ATTEMPT TO STERILIZE.
temperature. If using the Accutorr V in a hot environment, the Lithium ion battery may not charge when the unit is connected to the AC mains.
CAUTION: Remove the battery if the Accutorr V is not used for an
extended period of time.
CAUTION: The Communications Connectors on the Accutorr V are only
for use with IEC 60601-1-1 compliant equipment.
CAUTION: Never place fluids on top of this monitor. If fluid spills on the
unit, wipe clean immediately and refer the unit to qualified service personnel.
CAUTION: Before disassembling the monitor, eliminate static charges.
CAUTION: Properly connect the cables or wires when reassembling the
CAUTION: All tests should be performed by qualified personnel only.
CAUTION: Disconnect the monitor from the patient and make sure that
When disassembling the parts labeled with static-sensitive symbols, wear electrostatic discharge protection such as antistatic wristband or gloves. Follow the correct sequence to disassemble the monitor. Otherwise, the monitor may be damaged permanently. Disconnect all the cables before disassembling any parts. Take care not to damage any cables or connectors.
monitor to avoid short circuit. When assembling the monitor, select proper screws. If the wrong size screw is tightened by force, the monitor may be damaged and the screw or the part may not function as expected.
important data is saved before upgrading the monitor.
CAUTION: Do not shut down or power off the equipment when
upgrading the bootstrap program. Otherwise, it may cause the equipment to break down.
Accutorr V Service Manual 0070-10-0702 ix
Introduction Notes
CAUTION: Program upgrades should be performed by qualified
service personnel only.

Notes

NOTE: The Accutorr V should be operated only by trained and
qualified personnel.
NOTE: Use disposable and single use accessories only once.
NOTE: Place the equipment in a location where the screen can
easily be seen and the operating controls can easily be accessed.
NOTE: The instructions in this manual are based on the maximum
configuration.
NOTE: The optional Temperature module kit must be installed only
by trained personnel, and proper ESD prevention methods must be followed.
NOTE: Only devices specified by Mindray DS USA, Inc.
Bio-Medical Electronics Co. , Ltd shall be connecte
NOTE: When
NOTE: Disconnect the Accutorr V from the mains to isolate it from
the RS-232 connector is used for DIAP, barcode power must be set to OFF.
the mains power during an emergency.
/Shenzhen Mindray
d the RS-232 port.
x 0070-10-0702 Accutorr V Service Manual
Safety Designations Introduction

Safety Designations

Safety designations per IEC 60601-1 Standard:
Type of protection against electric shock Class 1 with internal electric power source.
Where the integrity of the external protective earth (ground) in the installation or its conductors is in doubt, the equipment shall be operated from its internal electric power source.
Degree of protection against electric shock Monitor - Type B applied part.
NIBP - Type BF defibrillation protected applied part. SpO
- Type BF protected applied part.
2
Temp - Type BF protected applied part.
Supply Connection 100 – 240 V
50/60 Hz
0.85 – 0.5 A
Mode of Operation Continuous
Protection Against Hazard of Explosion Not Protected (Ordinary)
Protection Against Ingress of Liquids IPX1
Degree of Electrical Connection Between Equipment and Patient
Degree of Mobility Portable
Equipment designed for direct electrical and non-electrical connection to the patient.
AC
Accutorr V Service Manual 0070-10-0702 xi
Introduction Product Limitations

Product Limitations

Non-invasive blood pressure (NIBP) accuracy depends on the application of the proper cuff size. See Chapter 3.0 of the Operating Instructions for detailed information.
The Accutorr V will not operate effectively on patients who are experiencing convulsions or tremors.
The Accutorr V is a portable device intended for intra-hospital use.
If the pressure cuff is not placed at the patient’s heart level, the NIBP measurement may be subject to error, due to the hydrostatic effect.
The pulse rate data displayed on the Accutorr V is computed from the measurement of peripheral pulses (peripheral pulses taken only during a measurement cycle). The rate measured by the Accutorr V may differ from the rate of an ECG monitor. This is because the ECG is an electrical signal that may not always result in a peripheral pulse.
Administration of certain vasoconstrictor drugs (for example, norepinephrine), may reduce peripheral perfusion to a level that prevents the Accutorr V from taking pulse rate measurements.
Arterial compression, tricuspid regurgitation, or other conditions may reduce perfusion to a level that prevents the Accutorr V from taking pulse rate measurements.
The presence of arrhythmias may increase the time required to complete a measurement and may extend this time so that a measurement cannot complete.
The Accutorr V is not intended for use during CPR. The monitor uses an oscillometric technique based on normal peripheral circulation to compute blood pressure.
xii 0070-10-0702 Accutorr V Service Manual
Unpacking Introduction
T1

Unpacking

Remove the instrument from the shipping carton and examine it for signs of shipping damage. Save all packing materials, invoice, and bill of lading. These may be required to process a claim with the carrier. Check all materials against the packing list. Contact the Customer Service Department (800) 288-2121 or (201) 265-8800 for prompt assistance in resolving shipping problems.
NOTE: The Accutorr V should only be shipped in its original
packing materials to avoid shipping damage.

Symbols and Descriptions

SYMBOL DESCRIPTION SYMBOL DESCRIPTION
Attention, Consult Accompanying Documents / Refer to Manual
Equipotentiality Equipotential grounding
Alternating Current (AC) Adult
Predictive Thermometer Connector
Type BF Equipment
Defibrillator-proof Type BF Equipment
Pediatric/Child
SpO
SpO
2
Accutorr V Service Manual 0070-10-0702 xiii
Connector Neonate
2
Electrical connectors Operating on battery power
Battery Manufacturer
Connected to AC mains
NIBP Connector
Power On/Off – Standby Recycle
Serial number Up key
Introduction Symbols and Descriptions
SYMBOL DESCRIPTION SYMBOL DESCRIPTION
REF
Part Number Confirm key
Patient Information key Down key
Main menu key Deflate Cuff key
Set alarms key Patient Size key
Start NIBP key Alarm Silence key
Display Tabular Trends/Pleth Wav e
NIBP interval key SP1
NC1 Nurse Call connector
RS-232 connector (Serial Port 1)
Print key (front panel) CS1 Network connector
Print key (recorder)
Alarm Silenced indicator on LCD display
Alarm Disabled indicator on LCD display
Audio Alarm Off indicator on LCD display
Classified by Underwriters Laboratories Inc. with respect to electric shock, fire and mechanical hazards, only in accordance with UL 60601-1, CAN/CSA C22.2 NO.601-1, IEC 60601-1-1, IEC 60601-2-30, IEC 60601-2-49.
xiv 0070-10-0702 Accutorr V Service Manual
1.0

Theory of Operation

Introduction.................................................................................................... 1 - 2
Controls and Indicators ................................................................................... 1 - 2
System Overview............................................................................................ 1 - 2
Hardware Structure......................................................................................... 1 - 4
Accutorr V Service Manual 0070-10-0702 1 - 1
Introduction Theory of Operation

1.1 Introduction

The Accutorr V monitors the following patient vital signs: non-invasive blood pressure (NIBP), pulse oxygen saturation (SpO2), pulse rate (PR), and temperature (Temp) for a single adult, pediatric, or neonatal patient. Temperature is measured using the optional Temperature Module.

1.2 Controls and Indicators

For information on controls, connectors, and indicators, refer to the Accutorr V Operating Instructions, Part Number 0070-10-0699-02.

1.3 System Overview

FIGURE 1-1 shows the relationship of the Accutorr V monitoring system’s mechanical, hardware, and software components.
FIGURE 1-2 shows the Accutorr V monitoring system’s PC board connections.
SYSTEM
MECHANICAL
MAIN UNIT
RECORDER
BATTERY
CHAMBER
TEMP
MODULE
CHAMBER
BARCODE SCANNER
SUPPORT
HARDWARE
MAIN BOARD
POWER BOARD
KEY &
DISPLAY
PAR AM ETER
BOARDS
RECORDER
BOARD
BARCODE SCANNER
SOFTWARE
FIGURE 1-1 System Mechanical, Hardware, and Software Overview
SYSTEM
SOFTWARE
PARAMETER
SOFTWARE
UPGRADE
SOFTWARE
PRINT
SOFTWARE
GATEWAY
SOFTWARE
1 - 2 0070-10-0702 Accutorr V Service Manual
Theory of Operation System Overview
PARAMETER RECEPTACLE
J6
RECORDER
J2
J3
AC
INLET
J2
POWER
J4 J5
FAN
J1
J6
BATTERY
J2 J3 J4 J5
J1
J8 J9
J7
P3 P4
P5
KEY & DISPLAY
BOARD
P2
LCD
FIGURE 1-2 The System PCBA Connections
J1
SpO
2
J2
P2
ISOLATION
POWER BOARD
P1
MAIN BOARD
BDM
PORT
TEMP
ISOLATION
POWER BOARD
J10
SPEAKER
J2
NIBP
J4
J4
J3
J11 J12 J13
NETWORK CONNECTOR
NURSE CALL
J2
RS232
Accutorr V Service Manual 0070-10-0702 1 - 3
Hardware Structure Theory of Operation

1.4 Hardware Structure

FIGURE 1-3 shows the Accutorr V’s Hardware Structure. The core of the system is the main board, which supplies power for all parameter modules. The parameter modules directly communicate with the main board. The the main board processes measurements and the status of all modules, and displays them through the key and display board.
SpO
NIBP MODULE
MODULE
2
TEMP MODULE
ISOLATION
POWER BOARD
POWER BOARD
COMMUNICATIONS
/POWER SUPPLY
BATTERY
KEY &
DISPLAY
BOARD
LED &
KEY
LCD
POWER SUPPLY
SPEAKER
COMMUNICATIONS
/POWER SUPPLY
RECORDER
ISOLATION
POWER BOARD
MAIN BOARD
FAN
ACCUTORR V
FIGURE 1-3 The Accutorr V’s Hardware Structure
NOTE: The SpO2 isolation power board does not apply to models
with DPM Pulse Oximetry.
ETHERNET
RS232
NURSE CALL
AC
1 - 4 0070-10-0702 Accutorr V Service Manual
Theory of Operation Hardware Structure

1.4.1 Main Board

FIGURE 1-4 shows the main board, which provides resources and support for the overall system. It controls the LCD, LED, keyboard, speaker, and recorder. It also communicates with parameter modules and connectors. The main board also controls communication with the speaker, the recorder, and all external connectors.
WATCH DOG
RTC E2 PROM
ETHERNET
NURSE CALL
SPEAKER
PHY RTL8201
CPU
AUDIO PROCESS
CIRCUIT
FLASHSDRAM
1.5V
LINEAR POWER
3.3V LCD
5.0V 12V LED KEY
SERIAL PORT 0
FPGA
RS232 IC
RS232
SERIAL PORT 1:
NIBP
SERIAL PORT 2:
SpO
2
SERIAL PORT 3:
TEMP
SERIAL PORT 4:
RECORDER
FIGURE 1-4 Main Board Principle Diagram
The main board communicates with all parameter modules and the recorder through an FPGA extended serial port.
The main board supplies information using FPGA to the key and display board. It drives the display, detects the keys, and implements the user interface.
The main board controls the alarm indicator using FPGA.
The main board controls the speaker to give audible alarms, key tones, and Pitch Tone.
The main board provides the nurse call connection, network connection, and R232 connection.
The real-time clock is implemented by the RTC chip. The RT clock is powered by the AC mains, battery, or button cell on the main board. The button cell ensures the continuous working of the clock in the event that the AC mains and batteries are not available.
SDRAM stores running program instructions and data temporarily. The system memory and trend data memory is flashed. The device configuration memory is EEPROM.
Accutorr V Service Manual 0070-10-0702 1 - 5
Hardware Structure Theory of Operation

1.4.2 Power Board

The power board, shown in FIGURE 1-5, converts the input power (AC mains or battery) to different working voltages for other boards. It also charges the battery.
AC
INPUT
EMI
FILTER
RECTIFIER
& FILTER
PMW
CONTROLLER
FLYBACK
CONVERTER
CURRENT
DETECTION
COUPLER
FEEDBACK &
ISOLATION
CIRCUIT
FIGURE 1-5 Power Board Principle Diagram
RECTIFIER
& FILTER
0VP&0PP
16.8V DC/DC
CONVERTER
DC/DC
CONVERTER
CHARGING
CIRCUIT
DC/DC
CONVERTER
SWITCH CIRCUIT
PCON
0VP&0CP
BATTERY
0VP&0CP
12V
OUTPUT
5V
OUTPUT
3.3V
OUTPUT
The AC flows through the EMI filter and the rectifier and filter. The rectifier and filter converts the AC to 16.8V DC voltage by the Flyback converter. The 16.8V DC voltage is the main input to the DC/DC converters and charging circuit. The DC/DC converters convert 16.8V DC to 12V, 5V, and 3.3V DC. The charging circuit charges the lithium battery. When the Accutorr V is not connected to the AC mains, the battery supplies power to the DC/DC converters.
The 16.8V DC output is protected against over-voltage and over-power. The 12V, 5V, and
3.3V DC outputs are protected against over-voltage, short-circuit, and over–current.
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Theory of Operation Hardware Structure

1.4.3 Key and Displays Board

The key and displays board, shown in FIGURE 1-6, provides the user interface. The board contains the LCD module, 7-segment digital display, LED indication lamp, and keys.
LCD
SIGNAL
ADV
3.3V
VSB
FSTN LCD
MODULE
KEY MATRIX
3.3V
DISABLE
LED
CPLD
Switch
START-UP
CIRCUIT
LED&KEY
DETECTION
FIGURE 1-6 Key and displays Board Principle Diagram
The LCD module adjusts brightness and contrast (only for black-and-white LCD display).
NOTE: The monitor with color LCD does not have “Contrast ”
setting item in the common setup menu.
The 7-segment digit units display parameter data.
The AC indicator is driven by the ADV output from the power board, and the working status indicator (built in the Power On/Off key) is driven by 3.3V voltage. The battery indicator is jointly controlled by the flash control signal, ADV signal, and VBC signal.
The keypad contains the power ON/OFF key and the other 13 function keys.
Accutorr V Service Manual 0070-10-0702 1 - 7
Hardware Structure Theory of Operation

1.4.4 Parameter Boards

1.4.4.1 SpO
FIGURE 1-7 shows the SpO2 module parameter board diagram.
WATC HDOG
DRIVE DAC
Module
2
LED DRIVE
CIRCUITRY
SENSOR
/RST
WDI
GAIN CONTROL
CIRCUITRY
PROGRAMMABLE
GAIN CIRCUITRY
CPU
OFFSET DAC
OFFSET
AMPLIFIER
DRAM
FLASH
ISOLATED SERIAL
IN/OUTPUT PORT
4KV ISOLATED
POWER SUPPLY
+3.3V +5V
-5V
A/D
CONVERTER
HOST
+12V
FIGURE 1-7 SpO
The SpO
sensor collects the pulsing red and infrared light signals transmitting through the
2
Module Principle Diagram
2
finger or toe, and processes the collected signals to create the measured result. The SpO2 module controls the LED drive circuit and the amplifying circuit gain corresponding to the finger or toe perfusions and transmittances.
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Theory of Operation Hardware Structure
1.4.4.2 NIBP Module
FIGURE 1-8 shows the NIBP module parameter board diagram.
CUFF
MANIFOLD
VALVES
AND PUMP
PRESSURE
SENSOR
FOR
PROTECT
PRESSURE
SENSOR
PRESSURE
SIGNAL
AMPLIFIER
CIRCUITS
FOR
PROTECT
VALV E
CIRCUIT
PRESSURE
SIGNAL
PRESSURE
SIGNAL
AMPLIFIER
CIRCUITS
MOTOR CONTROL FEEDBACK SIGNAL
PUMP AND
CONTROL
OVER
PRESSURE
PROTECT
CIRCUIT
WATC HDOG
A/D
CONVERTER
FLASH DRAM
CPU
ASYCHRONOUS
SERIAL
COMMUNICATION
FIGURE 1-8 NIBP Module Principle Diagram
The Accutorr V calculates NIBP values using the oscillometric method of noninvasive blood pressure measurement. These measurements correspond to comparisons with auscultatory values, measured using the fifth Korotkoff sound within ANSI/AAMI SP10 standards for accuracy.
1.4.4.3 Optional Temperature Module
FIGURE 1-9 shows the Temperature module parameter board diagram.
PROBE
RECOGNIZE
CIRCUIT
TEMPERATURE
DETECT
CIRCUIT
A/D
CIRCUIT
PROBE
HEAT
CIRCUIT
CPU SYSTEM
(ROM & RAM
WATCH DOG )
FIGURE 1-9 Optional Temperature Module Principle Diagram
The Temperature Module uses a thermistor as a sensor for measuring temperature. The resistance of a given thermistor is nonlinearly relative to the temperature. The Temperature Module measures the resistance of the thermistor and converts it into temperature.
Accutorr V Service Manual 0070-10-0702 1 - 9
POWER
& SIGNAL ISOLATE CIRCUIT
MAIN
BOARD
Hardware Structure Theory of Operation

1.4.5 Recorder

The recorder receives data from the main board and sends it to the thermal printhead for printing. It has a button to start or stop printing and a green LED to indicate the presence or absence of paper.

1.4.6 Bar Code Scanner

The bar code scanner reads one-dimensional and two-dimensional bar codes to simplify admitting a patient. The bar code scanner communicates with the monitor. The serial port supplies it with power. The scanner’s serial port is defined in the following table:
PIN DEFINITION
2Barcode_RX
3Barcode_TX
5GND
9VCC5VDC
The monitor’s serial port is defined in the following table:
PIN DEFINITION
2 Monitor_TX
3 Monitor_RX
5GND
9VCC5VDC
Basic settings of the bar code scanner are listed in the following table:
HOST PARAMETERS BAR CODE SCANNER FACTORY DEFAULT
Baud Rate 9600 9600
Data Bits 8 8
Stop Bits 1 1
Calibration bit 0 0
Handshaking None None
USER PARAMETERS BAR CODE SCANNER FACTORY DEFAULT
Beeper Tone Medium Medium
Beeper Volume Medium High
Trigger Mode Level Auto Aim
Parameter Scanning Disable Enable
DATA FORMAT BAR CODE SCANNER FACTORY DEFAULT
Prefix Value 7013 <CR><LF> 7013 <CR><LF>
Suffix 1 Value Suffix 2 Value
Scan Data Transmission Format <PREFIX><DATA><SUFFIX 1><SUFFIX 2> Data only
7013 <CR><LF> 7013 <CR><LF>
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Theory of Operation Hardware Structure
To change parameter settings, scan the following bar codes in sequence.
1. Set parameter defaults:
2. Set beeper volume:
3. Set trigger mode:
4. Set scan data transmission format:
Accutorr V Service Manual 0070-10-0702 1 - 11
Hardware Structure Theory of Operation
5. Disable parameter scanning:
1 - 12 0070-10-0702 Accutorr V Service Manual
2.0

Specifications

Introduction..............................................................................................2 - 2
NIBP Measurement ...................................................................................2 - 2
NIBP Measurement Cycle ..........................................................................2 - 4
SpO2 Measurement..................................................................................2 - 6
Temperature .............................................................................................2 - 10
Display Area, Indicator, and Controller .......................................................2 - 10
Audio Indicator ........................................................................................2 - 14
Real-time Clock ........................................................................................2 - 14
Standby Mode .........................................................................................2 - 15
Alarm Information.....................................................................................2 - 16
Configuration management .......................................................................2 - 16
Barcode scanner ......................................................................................2 - 16
Accutorr V Service Manual 0070-10-0702 2 - 1
Introduction Specifications

2.1 Introduction

The Accutorr V monitors patient vital signs (including non-invasive blood pressure (NIBP), pulse oxygen saturation (SpO2), and pulse rate (PR)) for a single adult, pediatric, or neonatal patient. It also monitors oral or rectal mode temperature (Temp) for a single adult or pediatric patient; or axillary mode temperature for a single neonate, adult, or pediatric patient using the optional Temperature Module.

2.2 NIBP Measurement

The NIBP module is used to measure the systolic pressure, diastolic pressure, and mean pressure in the neonatal, pediatric, and adult modes. The Accutorr V calculates NIBP values using the oscillometric method of noninvasive blood pressure measurement. These measurements correspond to comparisons with auscultatory values, measured using the fifth Korotkoff sound within ANSI/AAMI SP10 standards for accuracy.

2.2.1 Blood Pressure

PARAMETER PATIENT SIZE RANGE
Systolic pressure measurement Adult
Pediatric Neonate
Diastolic pressure measurement Adult
Pediatric Neonate
Mean pressure measurement Adult
Pediatric Neonate
Measurement accuracy Mean error: <±5 mmHg
Standard deviation: <±8 mmHg
Measurements outside of the stated ranges are not guaranteed to be accurate.
55 – 235 mmHg 55 – 160 mmHg 45 – 120 mmHg
30 – 200 mmHg 30 – 150 mmHg 20 – 100 mmHg
30 – 235 mmHg 30 – 160 mmHg 20 – 120 mmHg

2.2.2 Static Accuracy

Measurement range: 0 – 300 mmHg Static pressure measurement accuracy: ±3 mmHg

2.2.3 Maximum Cuff Pressure

Normal Use Over Pressure Protection
In normal use, the over-pressure detection is controlled by software. Once the cuff pressure exceeds the threshold, the software enables the system to deflate the cuff.
Adult 300 mmHg
Pediatric 200 mmHg
Neonate 150 mmHg
Single Fault Over-pressure protection
2 - 2 0070-10-0702 Accutorr V Service Manual
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