Mindray dpm 3 User manual

DPM 3 Vital Signs Monitor
Operator’s Manual

I
Revision History
This manual has a revision number. This revision number changes whenever the manual is
updated due to software or technical specification change. Contents of this manual are subject
to change without prior notice.
 Revision number: 6.0
 Release time: 20 2-12
© Copyright 2008-20 2 Mindray DS USA, Inc. All rights reserved.
WARNING
 Federal Law (USA) restricts this device to sale by or on the order of a physician.

II
Intellectual Property State ent
Mindray DS USA, Inc. (hereinafter called Mindray DS) owns the intellectual property rights
to this product and this manual. This manual may refer to information protected by
copyrights or patents and does not convey any license under the copyright and the patent
rights of Mindray DS, nor the rights of others.
Mindray DS intends to maintain the contents of this manual as confidential information.
Disclosure of the information in this manual in any manner whatsoever without the written
permission of Mindray DS is strictly forbidden. Release, amendment, reproduction,
distribution, rental, adaption and translation of this manual in any manner whatsoever without
the written permission of Mindray DS is strictly forbidden.
is a trademark or a registered trademark of Shenzhen Mindray Bio-Medical
Electronics Co., Ltd. All third-party trademarks that appear in this manual are used solely for
editorial purposes and are the property of their respective owners.
Contents of this manual are subject to changes without prior notice.
© 2008-20 2 Mindray DS USA, Inc. All rights reserved.

III
Manufacturer’s Responsibility
All information contained in this manual is believed to be correct. Mindray DS shall not be
liable for errors contained herein nor for incidental or consequential damages in connection
with the furnishing or use of this manual.
Mindray will not be liable for the effects on safety, reliability and performance of this product
if:
 all installation operations, expansions, changes, modifications and repairs of this product
are not conducted by Mindray DS authorized personnel; and
 the electrical installation of the relevant room does not comply with the applicable
national and local requirements; and
 the product is not used in accordance with the instructions for use.
Warranty
This warranty is exclusive and is in lieu of all other warranties, expressed or implied,
including warranties of merchantability or fitness for any particular purpose.
Exe ptions
Mindray DS's obligation or liability under this warranty does not include any transportation
or other charges or liability for direct, indirect or consequential damages or delay resulting
from the improper use or application of the product or the use of parts or accessories not
approved by Mindray DS or repairs by people other than Mindray DS authorized personnel.
This warranty shall not extend to
 Any Mindray DS product which has been subjected to misuse, negligence or accident;
or
 Any Mindray DS product from which Mindray DS's original serial number tag or
product identification markings have been altered or removed; or
 Any product of any other manufacturer.

IV
Return Policy
In the event that it becomes necessary to return a unit to Mindray DS, follow the instructions
below.
. Return authorization.
Contact the Customer Service Department and obtain a Customer Service Authorization
number. This number must appear on the outside of the shipping container. Returned
shipments will not be accepted if the number is not clearly visible. Please provide the model
number, serial number, and a brief description of the reason for return.
2. Freight policy
The customer is responsible for freight charges when this product is shipped to Mindray DS
for service (this includes customs charges).
3. Return address
Please send the part(s) or equipment to the address offered by the Customer Service
Department.
Contact Infor ation
Manufacturer: Mindray DS USA, Inc.
Address: 800 MacArthur Blvd.Mahwah, New Jersey 07430 USA
Tel: .[phone] , .20 .995.8000
Website: www.mindray.com

Preface
Manual Purpose
This manual contains the instructions necessary to operate the product safely and in
accordance with its function and intended use. Observance of this manual is a prerequisite for
proper product performance and correct operation and ensures patient and operator safety.
This manual is based on the maximum configuration and therefore some contents may not
apply to your product. If you have any question, please contact us.
This manual is an integral part of the product. It should always be kept close to the equipment
so that it can be obtained conveniently when needed.
Intended Audience
This manual is geared for clinical professionals who are expected to have a working
knowledge of medical procedures, practices and terminology as required for monitoring of
critically ill patients.
Illustrations
All illustrations in this manual serve as examples only. They may not necessarily reflect the
setup or data displayed on your patient monitor.
Conventions
 Italic text is used in this manual to quote the referenced chapters or sections.
 The terms warning, and caution are used throughout this manual to point out hazards
and to designate a degree or level of severity.
 → is used to indicate operational procedures.

2
FOR YOUR NOTES

Contents
1 Safety................................................................................................................................. 1-1
. Safety Information .......................................................................................................... -
. . Warnings............................................................................................................. -2
. .2 Cautions ............................................................................................................. -3
. .3 Notes .................................................................................................................. -4
.2 Equipment Symbols ........................................................................................................ -4
2 The asics ......................................................................................................................... 2-1
2. Monitor Description........................................................................................................ 2-
2. . Intended Use....................................................................................................... 2-
2. .2 Contraindications ............................................................................................... 2-
2. .3 Components........................................................................................................ 2-2
2. .4 Functions............................................................................................................ 2-2
2.2 Appearance...................................................................................................................... 2-3
2.2. Front Panel ......................................................................................................... 2-3
2.2.2 Rear Panel .......................................................................................................... 2-7
2.2.3 Recorder............................................................................................................. 2-8
2.3 Display ............................................................................................................................ 2-9
2.3. Cursor................................................................................................................. 2-9
2.4 Battery........................................................................................................................... 2- 0
2.4. Battery Maintenance .........................................................................................2-
2.4.2 Battery Recycling............................................................................................. 2- 2
3 Installation and Maintenance.......................................................................................... 3-1
3. Installation....................................................................................................................... 3-
3. . Unpacking and Checking ................................................................................... 3-
3. .2 Environmental Requirements............................................................................. 3-2
3. .3 Power Supply Requirements .............................................................................. 3-2
3. .4 Bracket Mounting............................................................................................... 3-2
3. .5 Installation Method ............................................................................................ 3-3
3. .6 Powering on the Monitor.................................................................................... 3-7
3. .7 Powering off the Monitor................................................................................... 3-7
3.2 Maintenance .................................................................................................................... 3-7
3.2. Inspection ........................................................................................................... 3-8
3.2.2 Cleaning ............................................................................................................. 3-8
3.2.3 Disinfection...................................................................................................... 3- 0
4 Menus and Screens........................................................................................................... 4-1
4. Patient Information.......................................................................................................... 4-
4.2 System Setup................................................................................................................... 4-2

2
4.2. Common Setup................................................................................................... 4-2
4.2.2 Network Setup.................................................................................................... 4-3
4.2.3 Time Setup ......................................................................................................... 4-4
4.2.4 User Maintenance............................................................................................... 4-4
4.2.5 Nurse Call Setup ................................................................................................ 4-5
4.2.6 Version................................................................................................................ 4-6
4.2.7 Configuration ..................................................................................................... 4-6
4.2.8 Exporting Data ................................................................................................... 4-7
4.3 Normal Screen................................................................................................................. 4-7
4.4 Trend Screen ................................................................................................................... 4-8
4.5 Standby State................................................................................................................... 4-9
4.5. Entering the Standby State ................................................................................. 4-9
4.5.2 Exiting the Standby State ................................................................................... 4-9
4.6 Patient Review System Software .................................................................................. 4- 0
5 Alarms ............................................................................................................................... 5-1
5. Overview......................................................................................................................... 5-
5. . Alarm Categories................................................................................................ 5-
5. .2 Alarm Levels ...................................................................................................... 5-2
5.2 Alarm Indications ............................................................................................................ 5-2
5.2. Alarm Lamp ....................................................................................................... 5-3
5.2.2 Audible Alarms................................................................................................... 5-3
5.2.3 Alarm Messages ................................................................................................. 5-3
5.3 Alarm Status .................................................................................................................... 5-4
5.3. Audio Off ........................................................................................................... 5-4
5.3.2 Physiological Alarm Off..................................................................................... 5-5
5.3.3 Alarms Paused.................................................................................................... 5-5
5.3.4 Alarm Silenced................................................................................................... 5-6
5.3.5 Status Switchover............................................................................................... 5-6
5.4 Clearing Alarm Indications ............................................................................................. 5-7
5.5 Setting Alarms................................................................................................................. 5-7
5.6 SpO2 Sensor Off Alarm ................................................................................................... 5-8
5.7 When an Alarm Occurs ................................................................................................... 5-8
6 Recording.......................................................................................................................... 6-1
6. Overview......................................................................................................................... 6-
6.2 Using the Recorder.......................................................................................................... 6-
6.2. Printing Real-time PLETH waveform................................................................ 6-
6.2.2 Printing Currently Displayed Trend Data........................................................... 6-
6.2.3 Printing All Trend Data of the Current Patient................................................... 6-
6.3 Loading Paper ................................................................................................................. 6-2
6.4 Removing Paper Jam....................................................................................................... 6-3
7 SpO2 Monitoring .............................................................................................................. 7-1

3
7. Introduction..................................................................................................................... 7-
7.2 Safety .............................................................................................................................. 7-2
7.3 Monitoring Procedure ..................................................................................................... 7-3
7.4 Measurement Limitations................................................................................................ 7-3
7.5 Masimo Information........................................................................................................ 7-4
7.6 Nellcor Information......................................................................................................... 7-4
8 NI P Monitoring.............................................................................................................. 8-1
8. Overview......................................................................................................................... 8-
8.2 Monitoring Procedure ..................................................................................................... 8-2
8.2. Cuff Selection and Placement ............................................................................ 8-2
8.2.2 Operation Guides ............................................................................................... 8-3
8.3 Measurement Limitations................................................................................................ 8-4
8.4 Setting Initial Cuff Inflation Pressure, NIBP Reset, Calibration and Test for Air Leakage
............................................................................................................................................... 8-5
8.4. Setting Initial Cuff Inflation Pressure ................................................................ 8-5
8.4.2 Resetting NIBP................................................................................................... 8-5
8.4.3 Calibrating NIBP................................................................................................ 8-6
8.4.4 NIBP Leakage Test............................................................................................. 8-7
9 TEMP Monitoring............................................................................................................ 9-1
9. Overview......................................................................................................................... 9-
9.2 Temperature Setup........................................................................................................... 9-2
9.3 Monitoring Procedure ..................................................................................................... 9-2
9.3. TEMP position ................................................................................................... 9-2
9.3.2 Oral Temperature Measurement......................................................................... 9-3
9.3.3 Axillary Temperature Measurement................................................................... 9-3
9.3.4 Measuring Rectal Temperature .......................................................................... 9-4
9.3.5 Temperature Measurement in MONITOR Mode ............................................... 9-5
9.4 Decontamination of the SmarTemp™ TEMP Probe....................................................... 9-5
9.5 Precautions ...................................................................................................................... 9-6
10 Accessories .................................................................................................................... 10-1
0. SpO2 Accessories ........................................................................................................ 0-
0.2 NIBP Accessories........................................................................................................ 0-3
0.3 TEMP Accessories ...................................................................................................... 0-4
0.4 Others.......................................................................................................................... 0-4
A Product Specifications.................................................................................................... A-1
A. Safety Specifications..................................................................................................... A-
A.2 Environmental Specifications........................................................................................ A-
A.3 Power Requirements ..................................................................................................... A-2
A.4 Hardware Specification................................................................................................. A-3
A.5 Signal Output ................................................................................................................ A-4

4
A.6 SpO2 Specification ........................................................................................................ A-4
A.6. Mindray DS SpO2 Specification....................................................................... A-4
A.6.2 Masimo SpO2 Specification ............................................................................. A-5
A.6.3 Nellcor SpO2 Specification .............................................................................. A-6
A.7 NIBP Specification........................................................................................................ A-6
A.8 TEMP Specification ...................................................................................................... A-7
EMC.................................................................................................................................. -1
C Alarm Messages and Prompt Information................................................................... C-1
C. Physiological Alarm Messages.......................................................................................C-
C.2 Technical Alarm Messages .............................................................................................C-
C.2. General Alarm Messages of Parameter Modules...............................................C-2
C.2.2 NIBP Module Alarm Messages .........................................................................C-2
C.2.3 Mindray DS SpO2 Module Alarm Messages.....................................................C-4
C.2.4 Masimo SpO2 Module Alarm Messages............................................................C-5
C.2.5 Nellcor SpO2 Module Alarm Messages.............................................................C-7
C.2.6 SmarTemp™ TEMP Module Alarm Messages..................................................C-8
C.2.7 Recorder Module Alarm Messages....................................................................C-9
C.2.8 System Alarm Messages..................................................................................C-
C.3 Prompt Messages..........................................................................................................C- 2
D Factory Defaults ............................................................................................................. D-1
D. Patient Information........................................................................................................ D-
D.2 System Setup................................................................................................................. D-2
D.3 Alarm Limit................................................................................................................... D-3
E Symbols and Abbreviation..............................................................................................E-1
E. Units ............................................................................................................................... E-
E.2 Symbols .......................................................................................................................... E-2
E.3 Abbreviations..................................................................................................................E-3

-
1 Safety
1.1 Safety Infor ation
The safety statements presented in this chapter refer to the basic safety information that the
operator shall pay attention to and abide by. There are additional safety statements in other
chapters or sections, which may be the same as or similar to the followings, or specific to
the operations.
WARNING
 Indicates a potential hazard or unsafe practice that, if not avoided, could result in
death or serious injury.
CAUTION
 Indicates a potential hazard or unsafe practice that, if not avoided, could result in
minor personal injury or product/property damage.
NOTE
 Provides application tips or other useful information to ensure that you get the
most from your product.

-2
1.1.1 Warnings
WARNING
 This monitor is not applicable for prolonged and continuous SpO2 monitoring,
which may increase the risks of irritation and burns at the site of the sensor.
 This monitor is not applicable for prolonged and continuous temperature
monitoring for more than 5 minutes.
 This monitor is intended for use by qualified clinical physicians or well-trained
nurses in the specified places.
 It is your responsibility to verify the device and accessories can function safely
and normally before use
 The disposable accessories should be disposed of in accordance with the hospital
regulations.
 A possible fire or explosion hazard exists when used in the presence of
flammable anesthetics or other flammable or explosive substances in
combination with air, oxygen-enriched environments, or nitrous oxide.
 Do not rely exclusively on the audible alarm system for patient monitoring.
Adjustment of alarm volume to a low level or off may result in a hazard to the
patient. Remember that alarm settings should be customized according to
different patient situations and always keeping the patient under close
surveillance is the most reliable way for safe patient monitoring.
 Opening the monitor housing presents a risk of hazard due to electrical shock.
All servicing and future upgrades to this equipment must be carried out by
personnel trained and authorized by Mindray DS only.
 Do not touch the patient or equipment connected to the patient during
defibrillation. A risk of serious injury or death is present.
 When using the equipment with electrosurgical units (ESU), make sure the
patient is safe.
 Dispose of the package material according to the applicable waste control
regulations and keep it out of children’s reach.
 The device must be connected to a properly installed power outlet with
protective earth contacts only. If the installation does not provide for a
protective earth conductor, disconnect the monitor from the power line and
operate it on battery power, if possible.

-3
1.1.2 Cautions
CAUTION
 To ensure patient safety, use only parts and accessories specified in this manual.
 Remove the battery from the monitor if it will not be used or not be connected to
the power line for a long period.
 Carefully route patient cabling to reduce the possibility of patient entanglement
or strangulation.
 Disposable devices are intended for single use only. They should not be reused as
performance could degrade or contamination could occur.
 At the end of its service life, the product described in this manual, as well as its
accessories, must be disposed of in compliance with the guidelines regulating the
disposal of such products. If you have any questions concerning disposal of the
products, please contact with us.
 Magnetic and electrical fields are capable of interfering with the proper
performance of the device. For this reason make sure that all external devices
operated in the vicinity of the monitor comply with the relevant EMC
requirements. Mobile phone, X-ray equipment or MRI devices are a possible
source of interference as they may emit higher levels of electromagnetic
radiation.
 efore connecting this monitor to the power line, check that the voltage and
frequency ratings of the power line are the same as those indicated on the label
or in this manual.
 Install or carry the monitor properly to avoid damages caused by drop, impact,
strong vibration or other mechanical force.
 If you spill liquid on the equipment or accessories, contact us or your service
personnel.

-4
1.1.3 Notes
NOTES
 Put the equipment in a location where you can easily see the screen and access
the operating controls.
 This monitor complies with the requirements of CISPR11 (EN55011) class A.
 The software was developed per IEC60601-1-4. The possibility of hazards
arising from program errors is minimized.
 Put the monitor in a location where you can easily see the screen and access the
operating controls.
 The instructions of this manual are based on the maximum configuration. Some
of them may not apply to your monitor.
 Devices connected the RS232 port shall be Mindray DS -specified only.
1.2 Equip ent Sy bols
Caution: Consult
accompanying documents
(this manual).
Up
Power ON/OFF Selection
Alternating current (AC) Down
Battery indicator Pulse Rate (PR)
Defibrillation-proof type CF
applied part Neonate
NIBP Pediatric/Child
PATIENT INFO. Adult
MENU
Equipotential grounding

-5
SET ALARMS NurseCall output
DISPLAY RS-232 connector
INTERVAL
Date of manufacture
European community
representative
Manufacturer
RECORD Serial number
Alarm Silenced Network connector
The following definition of the WEEE label applies to EU member states only.
This symbol indicates that this product should not be treated as household
waste. By ensuring that this product is disposed of correctly, you will help
prevent bringing potential negative consequences to the environment and
human health. For more detailed information with regard to returning and
recycling this product, please consult the distributor from whom you purchased
it.
* For system products, this label may be attached to the main unit only.

1-6
The machine has only one of the certification labels below.
Please refer to the label attached to the machine to determine the applicable certification label.
The presence of this label indicates the machine was certified by ETL with
the statement:
CONFORMS TO UL STD 60601-1, IEC 60601-2-30, IEC 60601-2-49,
IEC60601-1-1.
CERTIFIED TO CSA STD C22.2 NO 601.1, NO 60601-2-30, NO
60601-2-49, CSA STD C22.2 NO 601-1-1
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.

2-
2 The Basics
2.1 Monitor Description
2.1.1 Intended Use
This device is to monitor physiologic parameters, including SpO2, PR, NIBP and TEMP, on
adult, pediatric, and neonatal patients in healthcare facilities by clinical physicians or
appropriate medical staff under the direction of physicians. It is not intended for transport.
WARNING
 This device is to be operated by clinical physicians or appropriate medical staffs
under the direction of physicians. The operator of the monitor must be well
tranined. Any operation by unauthorized or non-tranined personnel is forbidden.
 The physiological parameters and the alarm information displayed by the monitor
are only for the reference of physicians, but cannot be used directly to determine
the clinical treatment.
CAUTION
 The environment and power supply of this monitor must meet the requirements
specified in A Product Specifications.
2.1.2 Contraindications
None

2-2
2.1.3 Co ponents
This monitor is composed of a main unit, NIBP cuff, SpO2 sensor and TEMP probe. Note
that some of the mentioned parts are optional and may not be found in your monitor.
2.1.4 Functions
This monitor has the following functions and features:
 SpO2 measurement: pulse oxygen saturation (SpO2), pulse rate (PR), and SpO2
plethysmogram.
 NIBP measurement: systolic pressure (S), diastolic pressure (D), mean pressure (M),
and pulse rate (PR).
 TEMP measurement: temperature (TEMP).
 Alarm: support visual/audible alarms and prompt messages.
 Record: support the function of recording NIBP trend data and PLETH waveform.
 Patient ID input by bar code scanning.
 Nurse call.
 Storage of trend data: support the function of storing up to 200 groups of measured
results.
 Powerful system menu.
 Large LED digit display.
 Adjustable LCD brightness and contrast.
 Network communication: support the function of being connected to the CMS or PC
for data output or upgrade.
 Rechargeable lead-acid battery or lithium battery.