Mindray dpm 3 Operator's Manual

updated due to software or technical specification change. Contents of this manual are subject to change without prior notice. � Revision number: 3.0 � Release time: 2010-04 © Copyright 2008-2010 Mindray DS USA, Inc. All rights reserved. WARNING � Federal Law (USA) restricts this device to sale by or on the order of a physician. ...

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 ...

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: � any 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 produc ...

below. 1. 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 sen ...

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 professio ...

1.1 Safety Information .......................................................................................................... 1-1 1.1.1 Warnings............................................................................. ...

4.2 System Setup................................................................................................................... 4-2 4.2.1 Common Setup................................................................................................... 4-2 4.2.2 Network Setup.................................................................................................... 4-3 4.2.3 Time Setup ......................................................................................................... 4-4 4.2.4 User Main ...

7.1 Introduction..................................................................................................................... 7-1 7.2 Safety .............................................................................................................................. 7-2 7.3 Monitoring Procedure ..................................................................................................... 7-3 7.4 Measurement Limitations....................................................................................... ...

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 B EMC................................................... ...

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 inf ...

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 ...

� 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 ...

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 Equipment Symbols Caution: Consu ...

European community representative Manufacturer RECORD Serial number Alarm Silenced Network connector 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. 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 nega ...

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 or home use. 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 dis ...

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. � Patie ...