S e r v i c e M a n u a l
Accutorr® is a registered trademark of Mindray DS USA, Inc.
Masimo SET® is a U.S. registered trademark of Masimo Corp.
Mindray® is a trademark or a registered trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Nellcor® is a U.S. registered trademark of Tyco International Ltd.
SmarTemp™ is a trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Copyright © Mindray DS USA, Inc., 2009. Printed in U.S.A. All rights reserved. Contents of this publication may not be reproduced in any form 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......................................................................................................................................... |
x |
|
|
Product Limitations .......................................................................................................................................... |
xi |
|
|
Unpacking ..................................................................................................................................................... |
xi |
|
|
Symbols and Descriptions ................................................................................................................................ |
xii |
|
|
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 |
SpO2 Module ................................................................................................................................. |
1 |
- |
8 |
NIBP Module .................................................................................................................................. |
1 |
- |
9 |
Optional Temperature Module .......................................................................................................... |
1 |
- |
9 |
Recorder ................................................................................................................................................ |
1 |
- |
10 |
Bar Code Scanner ................................................................................................................................... |
1 |
- |
11 |
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 SpO2 Performance........................................................................................................ |
2 - 7 |
||
SpO2 ............................................................................................................................................. |
2 |
- 7 |
|
Pulse Rate ....................................................................................................................................... |
2 |
- 8 |
|
Alarm Setting Range ........................................................................................................................ |
2 |
- 8 |
|
Nellcor NELL-3 SpO2 Performance............................................................................................................. |
2 |
- 9 |
|
SpO2 ............................................................................................................................................ |
2 |
- 9 |
|
Pulse Rate ....................................................................................................................................... |
2 |
- 9 |
|
Alarm Setting Range ........................................................................................................................ |
2 |
- 9 |
Accutorr V Service Manual |
0070-10-0702 |
i |
Table of Contents
Temperature................................................................................................................................................... |
2 |
- 10 |
Display Area, Indicator, and Controller ............................................................................................................. |
2 |
- 10 |
Display Area........................................................................................................................................... |
2 |
- 10 |
LCD ............................................................................................................................................... |
2 |
- 10 |
7-Segment Digit Display ................................................................................................................... |
2 |
- 10 |
Monochrome LED Indicator ............................................................................................................... |
2 |
- 10 |
Power Indicator ............................................................................................................................... |
2 |
- 11 |
Overlay and labeling............................................................................................................................... |
2 |
- 11 |
Alarm Lamp ............................................................................................................................................ |
2 |
- 11 |
Keys ...................................................................................................................................................... |
2 |
- 12 |
Patient Cable Connectors ......................................................................................................................... |
2 |
- 13 |
Audio Indicator .............................................................................................................................................. |
2 |
- 13 |
Pulse Tone Function.................................................................................................................................. |
2 |
- 13 |
Multiple-Level Volume............................................................................................................................... |
2 |
- 13 |
Real-time Clock............................................................................................................................................... |
2 |
- 13 |
Standby Mode ............................................................................................................................................... |
2 |
- 14 |
Alarm Information ........................................................................................................................................... |
2 |
- 15 |
Basics .................................................................................................................................................... |
2 |
- 15 |
Alarm Notification ................................................................................................................................... |
2 |
- 15 |
Audio Alarm Pause, Audio Alarm Off, and Audio Alarm Silencing ................................................................ |
2 |
- 15 |
Configuration management.............................................................................................................................. |
2 |
- 15 |
Barcode scanner............................................................................................................................................. |
2 |
- 15 |
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 |
NIBP Measurement Failures ...................................................................................................................... |
3 |
- 9 |
SpO2 Measurement Failure ...................................................................................................................... |
3 |
- 9 |
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 |
- 8 |
Removing NIBP Module ........................................................................................................................... |
4 |
- 11 |
Removing the Main (CPU) Board .............................................................................................................. |
4 |
- 12 |
Removing the Power Board....................................................................................................................... |
4 |
- 13 |
ii |
0070-10-0702 |
Accutorr V Service Manual |
Table of Contents
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 SpO2 Modules................................................................................................................... |
4 |
- 17 |
Disassembling a DPM SpO2 module .................................................................................................. |
4 - 17 |
|
Disassembling a Masimo SpO2 module ............................................................................................. |
4 |
- 17 |
Disassembling a Nellcor SpO2 module .............................................................................................. |
4 - 18 |
|
Disassembling the NIBP Module ................................................................................................................ |
4 - 19 |
|
Removing the NIBP Pump ................................................................................................................. |
4 |
- 19 |
Removing the NIBP Dump Valve ........................................................................................................ |
4 |
- 19 |
Removing the NIBP Bleed Valve ........................................................................................................ |
4 |
- 20 |
Parts ................................................................................................................................ |
5 - 1 |
|
Main Assembly............................................................................................................................................... |
5 |
- 2 |
Front Assembly ............................................................................................................................................... |
5 |
- 3 |
Rear Housing Assembly ................................................................................................................................... |
5 |
- 7 |
Main Bracket Assembly ................................................................................................................................... |
5 |
- 8 |
NIBP Assembly (Pump M6Q-100003- - -) ........................................................................................................... |
5 |
- 10 |
NIBP Assembly (Pump 082-000056-00) ............................................................................................................ |
5 |
- 13 |
Temperature Module Subassembly .................................................................................................................... |
5 |
- 16 |
Temperature Power Module Subassembly .......................................................................................................... |
5 |
- 18 |
Test and Calibration.......................................................................................................... |
6 - 1 |
|
Introduction.................................................................................................................................................... |
6 |
- 2 |
Test Report.............................................................................................................................................. |
6 |
- 3 |
Recommended Frequency ......................................................................................................................... |
6 |
- 3 |
Visual Test...................................................................................................................................................... |
6 |
- 4 |
Power-on Test ................................................................................................................................................. |
6 |
- 4 |
NIBP Calibration............................................................................................................................................. |
6 |
- 4 |
NIBP Accuracy Test......................................................................................................................................... |
6 |
- 8 |
NIBP Leakage Test ................................................................................................................................... |
6 |
- 9 |
SpO2 Test...................................................................................................................................................... |
6 |
- 12 |
SpO2 Test Under Normal Conditions ......................................................................................................... |
6 |
- 12 |
SpO2 Test in Motion Mode....................................................................................................................... |
6 |
- 12 |
Summary of Test Methods......................................................................................................................... |
6 |
- 13 |
DPM SpO2 ..................................................................................................................................... |
6 |
- 13 |
Nellcor SpO2 ................................................................................................................................. |
6 |
- 13 |
Masimo SpO2 ................................................................................................................................. |
6 |
- 13 |
Testing the Optional Temperature Module.......................................................................................................... |
6 |
- 14 |
Nurse Call Performance Test ............................................................................................................................ |
6 |
- 16 |
Bar Code Scanner Test .................................................................................................................................... |
6 |
- 18 |
Electrical Safety Tests ...................................................................................................................................... |
6 |
- 20 |
Enclosure Leakage Current Test ................................................................................................................. |
6 |
- 20 |
Earth Leakage Current Test ....................................................................................................................... |
6 |
- 20 |
Patient Leakage Current Test ..................................................................................................................... |
6 |
- 21 |
Patient Auxiliary Leakage Current Test........................................................................................................ |
6 |
- 21 |
Recorder Check .............................................................................................................................................. |
6 |
- 22 |
Software upgrade........................................................................................................................................... |
6 |
- 23 |
Accutorr V Service Manual |
0070-10-0702 |
iii |
Table of Contents
This page intentionally left blank.
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 OximetryÑ
includes NIBP, Nellcor SpO2, a Trend Display, and Recorder
¥Accutorr V with Nellcor® Pulse Oximetry and SmarTemp™Ñ includes NIBP, Nellcor SpO2, SmarTemp, a Trend Display, and Recorder
¥Accutorr V with Masimo SET® Pulse OximetryÑ includes NIBP, Masimo SpO2, a Trend Display, and Recorder
¥Accutorr V with Masimo SET® Pulse Oximetry and SmarTemp™Ñ includes NIBP, Masimo SpO2, SmarTemp, a Trend Display, and Recorder
¥Accutorr V with DPM Pulse OximetryÑ
includes NIBP, DPM SpO2, a Liquid Crystal Display (LCD), and Recorder
¥Accutorr V with DPM Pulse Oximetry and SmarTemp™Ñ
includes NIBP, DPM SpO2, SmarTemp, a Liquid Crystal Display (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.
AWARNING is provided to alert the user to potentially serious outcomes (death, injury or serious adverse events) to the patient or the user.
ACAUTION 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.
ANOTE is provided when additional general information is available.
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
Mindray approved stable mounting bracket.
WARNING: To ensure proper performance and safety and to prevent the voiding of the warranty, only use authorized parts and accessories with the Accutorr V. Use of unauthorized accessories may result in erroneous readings.
WARNING: Use only cuffs with approved quick connect type connectors.
WARNING: The Accutorr V is not intended for use in a magnetic resonance imaging (MRI) environment and may interfere with MRI procedures.
WARNING: Danger of explosion if battery is incorrectly replaced. 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: Do not use a damaged or broken unit or accessory.
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 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.
WARNING: Perform the decontamination or cleaning process with the unit powered down and power cord removed.
WARNING: Electrical safety tests are a proven means of verifying the 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.
WARNING: Commercially available test equipment such as a safety 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.
WARNING: Electrical safety tests should meet the requirements of the latest editions of EN 60601-1 and UL 60601.
WARNING: These electrical safety tests do not supersede local requirements.
WARNING: All devices using the AC mains and connected to medical 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. If an obstruction is found, refer the unit to qualified service personnel.
CAUTION: At the end of their life, dispose of the Accutorr V, accessories, and single use supplies in accordance with local regulations. Dispose of packaging waste in accordance with local regulations.
CAUTION: When equipped with Nellcor® SpO2, use only Nellcor® oxygen transducers including Nellcor® Oxisensor® patient dedicated adhesive sensors. Use of other oxygen transducers may cause improper oximeter performance.
CAUTION: When equipped with MASIMO® SpO2, use only MASIMO® oxygen transducers including MASIMO LNOP® and MASIMO LNCS® patient dedicated adhesive sensors and MASIMO PC Series Patient Cable. Use of other oxygen transducers may cause improper Oximetry performance.
viii |
0070-10-0702 |
Accutorr V Service Manual |
Cautions |
Introduction |
|
|
CAUTION: Inaccurate readings may be caused by incorrect sensor 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.
CAUTION: Route cables neatly. Ensure cables, hoses, and wires are 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.
CAUTION: When cleaning sensors, do not use excessive amounts of 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.
CAUTION: Recharge the Lithium ion battery while in the unit at room 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. 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.
CAUTION: Properly connect the cables or wires when reassembling the 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.
CAUTION: All tests should be performed by qualified personnel only.
CAUTION: Disconnect the monitor from the patient and make sure that 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. shall be |
|
connected the RS-232 port |
NOTE: |
When the RS-232 connector is used for DIAP, barcode power |
|
must be set to OFF. |
NOTE: |
Disconnect the Accutorr V from the mains to isolate it from |
|
the mains power during an emergency. |
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. |
|
SpO2 - Type BF protected applied part. |
|
Temp - Type BF protected applied part. |
Supply Connection |
100 Ð 240 VAC |
|
50/60 Hz |
|
0.85 Ð 0.5 A |
Mode of Operation |
Continuous |
x |
0070-10-0702 |
Accutorr V Service Manual |
Product Limitations |
Introduction |
|
|
Protection Against Hazard of Explosion |
Not Protected (Ordinary) |
Protection Against Ingress of Liquids |
IPX1 |
Degree of Electrical Connection Between |
Equipment designed for direct electrical and |
Equipment and Patient |
non-electrical connection to the patient. |
Degree of Mobility |
Portable |
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 patientÕs 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.
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. |
Accutorr V Service Manual |
0070-10-0702 |
xi |
Introduction |
Symbols and Descriptions |
|
|
Symbols and Descriptions
SYMBOL
T1
SpO2
REF
DESCRIPTION |
SYMBOL |
DESCRIPTION |
Attention, Consult |
|
|
Accompanying Documents / |
|
Type BF Equipment |
Refer to Manual |
|
|
Equipotentiality |
|
Defibrillator-proof Type BF |
Equipotential grounding |
|
Equipment |
Alternating Current (AC) |
|
Adult |
Predictive Thermometer |
|
Pediatric/Child |
Connector |
|
|
|
|
|
SpO2 Connector |
|
Neonate |
Electrical connectors |
|
Operating on battery power |
Battery |
|
Manufacturer |
Connected to AC mains |
|
NIBP Connector |
|
|
|
Power On/Off Ð Standby |
|
Recycle |
Serial number |
|
Up key |
Part Number |
|
Confirm key |
Patient Information key |
|
Down key |
Main menu key |
|
Deflate Cuff key |
xii |
0070-10-0702 |
Accutorr V Service Manual |
Symbols and Descriptions |
Introduction |
|
|
SYMBOL |
DESCRIPTION |
SYMBOL |
DESCRIPTION |
Set alarms key |
|
|
Start NIBP key |
|
|
Display Tabular Trends/Pleth |
NC1 |
|
Wave |
||
|
||
NIBP interval key |
SP1 |
|
Print key (front panel) |
CS1 |
|
Print key (recorder) |
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Alarm Silenced indicator on |
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LCD display |
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Patient Size key
Alarm Silence key
Nurse Call connector
RS-232 connector (Serial Port 1)
Network connector
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.
Accutorr V Service Manual |
0070-10-0702 |
xiii |
Introduction |
Symbols and Descriptions |
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This page intentionally left blank.
xiv |
0070-10-0702 |
Accutorr V Service Manual |
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 |
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1.1Introduction
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.
For information on controls, connectors, and indicators, refer to the Accutorr V Operating
Instructions, Part Number 0070-10-0699-02.
FIGURE 1-1 shows the relationship of the Accutorr V monitoring systemÕs mechanical, hardware, and software components.
FIGURE 1-2 shows the Accutorr V monitoring systemÕs PC board connections.
SYSTEM
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RECORDER |
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DISPLAY |
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TEMP |
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PARAMETER |
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BARCODE |
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RECORDER |
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BARCODE
SCANNER
FIGURE 1-1 System Mechanical, Hardware, and Software Overview
1 - 2 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
System Overview |
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J6
RECORDER
J2
PARAMETER RECEPTACLE
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ISOLATION |
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ISOLATION |
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P5 |
KEY & DISPLAY |
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FIGURE 1-2 The System PCBA Connections
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J3 |
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SPEAKER |
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CONNECTORNETWORK |
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RS232 |
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BDM |
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Accutorr V Service Manual |
0070-10-0702 |
1 - 3 |
Hardware Structure |
Theory of Operation |
|
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1.4Hardware Structure
FIGURE 1-3 shows the Accutorr VÕs 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.
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NIBP MODULE |
SpO2 MODULE |
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TEMP MODULE |
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ISOLATION |
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ISOLATION |
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POWER BOARD |
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POWER BOARD |
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COMMUNICATIONS |
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COMMUNICATIONS |
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/POWER SUPPLY |
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/POWER SUPPLY |
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LED & |
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KEY |
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ETHERNET |
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DISPLAY |
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RS232 |
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BOARD |
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POWER |
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NURSE CALL |
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SUPPLY |
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RECORDER |
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AC |
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ACCUTORR V |
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FIGURE 1-3 The Accutorr VÕs Hardware Structure |
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NOTE: |
The SpO2 isolation power board does not apply to models |
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with DPM Pulse Oximetry. |
1 - 4 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
Hardware Structure |
|
|
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.
WATCHDOG
RTC |
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E2 PROM |
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ETHERNET |
PHY RTL8201 |
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NURSE CALL |
SERIAL PORT 0 |
RS232 |
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RS232 IC |
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SPEAKER |
AUDIO PROCESS |
SERIAL PORT 1: |
CIRCUIT |
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NIBP |
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SDRAM |
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FLASH |
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1.5V
LINEAR POWER
FPGA
SERIAL PORT 2: SpO2
SERIAL PORT 3: TEMP
SERIAL PORT 4:
RECORDER
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3.3V |
5.0V |
12V |
LCD |
LED KEY |
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 |
|
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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.
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16.8V |
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12V |
AC |
EMI |
RECTIFIER |
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RECTIFIER |
DC/DC |
0VP&0CP |
OUTPUT |
INPUT |
FILTER |
& FILTER |
FLYBACK |
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CONVERTER |
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CONVERTER |
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5V |
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DC/DC |
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OUTPUT |
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CONVERTER |
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CURRENT |
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DETECTION |
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PMW |
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CHARGING |
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CIRCUIT |
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COUPLER |
0VP&0PP |
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ISOLATION |
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3.3V |
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DC/DC |
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CONVERTER |
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SWITCH |
0VP&0CP |
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CIRCUIT |
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PCON |
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FIGURE 1-5 Power Board Principle Diagram
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 overÐcurrent.
1 - 6 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
Hardware Structure |
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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 |
FSTN LCD |
LED |
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MODULE |
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CPLD |
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START-UP |
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Switch |
DETECTION |
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KEY MATRIX |
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ADV |
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3.3V |
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VSB |
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FIGURE 1-6 Key and displays Board Principle Diagram |
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The LCD module adjusts contrast and brightness.
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 |
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1.4.4.1SpO2 Module
FIGURE 1-7 shows the SpO2 module parameter board diagram.
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FIGURE 1-7 SpO2 Module Principle Diagram
The SpO2 sensor collects the pulsing red and infrared light signals transmitting through the 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.
1 - 8 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
Hardware Structure |
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FIGURE 1-8 shows the NIBP module parameter board diagram.
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PRESSURE |
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CUFF |
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PRESSURE |
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PROTECT |
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SENSOR |
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AMPLIFIER |
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CONVERTER |
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PUMP AND |
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VALVES |
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VALVE |
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FLASH |
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DRAM |
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CONTROL |
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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.
FIGURE 1-9 shows the Temperature module parameter board diagram.
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PROBE |
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RECOGNIZE |
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TEMPERATURE |
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A/D |
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& |
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MAIN |
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DETECT |
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(ROM & RAM |
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SIGNAL |
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CIRCUIT |
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CIRCUIT |
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WATCHDOG) |
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ISOLATE |
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BOARD |
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PROBE
HEAT
CIRCUIT
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 |
Hardware Structure |
Theory of Operation |
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|
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 - 10 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
Hardware Structure |
|
|
1.4.6Bar 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 scannerÕs serial port is defined in the following table:
PIN |
DEFINITION |
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2 |
Barcode_RX |
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3 |
Barcode_TX |
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5 |
GND |
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9 |
VCC5VDC |
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The monitorÕs serial port is defined in the following table:
PIN |
DEFINITION |
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2 |
Monitor_TX |
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3 |
Monitor_RX |
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5 |
GND |
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9 |
VCC5VDC |
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Basic settings of the bar code scanner are listed in the following table:
HOST PARAMETERS |
BAR CODE SCANNER |
FACTORY DEFAULT |
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Baud Rate |
9600 |
9600 |
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Data Bits |
8 |
8 |
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Stop Bits |
1 |
1 |
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Calibration bit |
0 |
0 |
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Handshaking |
None |
None |
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USER PARAMETERS |
BAR CODE SCANNER |
FACTORY DEFAULT |
Beeper Tone |
Medium |
Medium |
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Beeper Volume |
Medium |
High |
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Trigger Mode |
Level |
Auto Aim |
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Parameter Scanning |
Disable |
Enable |
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DATA FORMAT |
BAR CODE SCANNER |
FACTORY DEFAULT |
Prefix Value |
7013 <CR><LF> |
7013 <CR><LF> |
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Suffix 1 Value |
7013 <CR><LF> |
7013 <CR><LF> |
Suffix 2 Value |
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Scan Data Transmission Format |
<PREFIX><DATA><SUFFIX 1><SUFFIX 2> |
Data only |
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Accutorr V Service Manual |
0070-10-0702 |
1 - 11 |
Hardware Structure |
Theory of Operation |
|
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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:
1 - 12 |
0070-10-0702 |
Accutorr V Service Manual |
Theory of Operation |
Hardware Structure |
|
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5. Disable parameter scanning:
Accutorr V Service Manual |
0070-10-0702 |
1 - 13 |
Hardware Structure |
Theory of Operation |
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1 - 14 |
0070-10-0702 |
Accutorr V Service Manual |