Gima CMS8000 User manual

NEW CMS 8000 MULTIPARAMETER
PATIENT MONITOR
User Manual
PROFESSIONAL MEDICAL PRODUCTS
0123
M35152-GB-Rev.0-06.20
35152 / CMS8000
CONTEC MEDICAL SYSTEMS CO., LTD
No.112 Qinhuang West Street,
Economic & Technical Development Zone,
Qinhuangdao, Hebei Province, PEOPLE’S REPUBLIC OF CHINA
Made in China
Shanghai International Holding Corp. GmbH (Europe)
Eiffestrasse 80, 20537 Hamburg, Germany

I
Copyright
Statement
Our company owns all rights to this unpublished work and intends to maintain this work as confidential. We may also
seek to maintain this work as an unpublished copyright. This publication is to be used solely for the purposes of
reference, operation, maintenance, or repair of our equipment. No part of this can be disseminated for other purposes.
In the event of inadvertent or deliberate publication, our company intends to enforce its rights to this work under
copyright laws as a published work. Those having access to this work may not copy, use, or disclose the information in
this work unless expressly authorized by us to do so.
All information contained in this publication is believed to be correct. Our company shall not be liable for errors
contained herein nor for incidental or consequential damages in connection with the furnishing, performance, or use of
this material. This publication may refer to information and protected by copyrights or patents and does not convey any
license under the patent rights of our company, nor the rights of others. Our company does not assume any liability
arising out of any infringements of patents or other rights of third parties.
Content of this manual is subject to change without prior notice.
Responsibility on the manufacturer party
Our company is responsible for safety, reliability and performance of this equipment only in the conditions that:
n All installation, expansion, change, modification and repair of this equipment are conducted by our qualified
personnel;
n Applied electrical appliance is in compliance with relevant National Standards;
n The monitor is operated under strict observance of this manual.
WARNING
l This monitor is not a device for treatment purpose.
NOTE:
l This equipment is not intended for family usage.
It is important for the hospital or organization that employs this equipment to carry out a reasonable maintenance
schedule. Neglect of this may result in machine breakdown or injury of human health.
Upon request, our company may provide, with compensation, necessary circuit diagrams, calibration illustration list and
other information to help qualified technician to maintain and repair some parts, which our company may define as user
serviceable.

II
Warranty
Workmanship & Materials
Our company guarantees new equipment other than accessories to be free from defects in workmanship and materials
for a period of 18 months (six months for multi-site probes and SpO2sensor) from date of shipment under normal use
and service. Our company's obligation under this warranty is limited to repairing only.
Exemptions
Our company'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 parts or
accessories of the product or the substitution upon it not approved by us or repaired by anyone other than a our
company authorized personal. This warranty shall not extend to any instrument which has been subjected to abnormal
use, maintenance negligence or damaged; any instrument from which our company's original serial number tag or
product identification markings have been altered or removed, or any product of any other manufacturer.
Safety, Reliability and Performance
Our company is not responsible for the effects on safety, reliability and performance of the Monitor if:
n The components are disassembled, stretched or re-adjusted.
n The Monitor is not used in accordance with the instructions for use, or the electrical installation of the relevant
room does not comply with NFPA 70: National Electrical Code or NFPA 99: Standard for Health Care Facilities
(Outside the United States, the relevant room must comply with all electrical installation regulations mandated by
the local and regional bodies of government).

III
Return Policy
Return Procedure
In the event that it becomes necessary to return a unit to our company, the following procedure should be followed:
n Obtain return authorization. Contact our Service Department and tell us the product serial number. The number is
marked on the outside of the shipping package. Return shipments would 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.
n Freight policy. The customer is responsible for freight charges when equipment is shipped to our company for
service (this includes customs charges).
Preface
This manual gives detailed description to the Monitor concerning its performance, operation, and other safety
information. Please read the user manual carefully before use in order to operate this product correctly and guarantee
the safety of patient and operator.
Keep the user manual near the product for convenient and timely accessed when needed.
Following symbols represent some important facts that you have to pay special attention to:
Safety warnings indicate the severity of potential hazards.
Warning: prompting potential dangerous or unsafe operations, if not avoided, it may result in death or severe
personal injury or property damage.
Caution: prompting potential dangerous or unsafe operations, if not avoided, it may result in slight personal
injury, product failure or damage, or property damage.
Note: emphasizing important attentions, providing explanations or interpretations for better use.
NOTE:
l The user manual contains descriptions concerning all configurations, so part of the content may not suitable
for the product your purchased. If you have any doubts, please contact with us.
l Refer to the device for its date of manufacture and service life.
This manual is intended for persons who are familiar with the functioning measurements and have experience in
operating the monitoring equipment.

IV
Contents
Chapter 1 Safety ......................................................................................................................................................1
1.1 Safety information.....................................................................................................................................1
1.2 Precautionary measures.............................................................................................................................2
Chapter 2 General....................................................................................................................................................3
2.1 Introduction ...............................................................................................................................................3
2.2 Contraindications.......................................................................................................................................3
2.3 Main unit ...................................................................................................................................................3
2.4 Display.......................................................................................................................................................9
Chapter 3 Installation ............................................................................................................................................11
3.1 Open the Package and Check ..................................................................................................................11
3.2 Environmental requirement .....................................................................................................................12
3.3 Install the Monitor ...................................................................................................................................12
3.4 Connect the Power Cables.......................................................................................................................12
3.5 Power on..................................................................................................................................................13
3.6 Power off .................................................................................................................................................14
Chapter 4 System Menu ........................................................................................................................................15
4.1 Patient Information Setup........................................................................................................................15
4.2 Default setup............................................................................................................................................16
4.3 Trend Review, Measurement Review and Alarm Event Review.............................................................16
4.4 System setup............................................................................................................................................17
4.5 Machine version ......................................................................................................................................23
4.6 Drug calculation ......................................................................................................................................23
4.7 Maintain...................................................................................................................................................23
4.8 Demo .......................................................................................................................................................26
Chapter 5 Alarm ....................................................................................................................................................27
5.1 Alarm classification.................................................................................................................................27
5.2 Alarm level..............................................................................................................................................27
5.3 Alarm mode.............................................................................................................................................28
5.4 Alarm setup .............................................................................................................................................28
5.5 Alarm status.............................................................................................................................................30
5.6 Measures for Alarm occurs......................................................................................................................31
5.7 Probe-off alarm........................................................................................................................................31
Chapter 6 Freeze....................................................................................................................................................32
6.1 Enter/Exit Freeze Status ..........................................................................................................................32
6.2 FREEZE Menu ........................................................................................................................................32
6.3 Reviewing Frozen Waveform..................................................................................................................32
6.4 Recording Frozen Waveform...................................................................................................................33