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CMS50D
P u l s e O x i m e t e r
Address:No.112 Qinhuang West Street, Economic
Zone, Qinhuangdao, Hebei Province, PEOPLE'S REPUBLIC OF CHINA
Tel: +86-335-8015430
Fax: +86-335-8015588
Technical support:+86-335-8015431
E-mail: cms@contecmed.com.cn
Website: http://www.contecmed.com
EC REPRESENTATIVE
Shanghai International Holding Corp. GmbH(Europe)
Address: Eiffestrasse 80, 20537, Hamburg, Germany
Tel:
4 9-40-2513175
Fax:
4 9-40-255726
E-mail: shholding@hotmail.com
CMS2.782.027(CE)ESS/1.9 1.4.01.01.573 2019.08
Dear Users, thank you very much for purchasing our product.
This Manual is written and compiled in accordance with the council directive
MDD93/42/EEC for medical devices and harmonized standards. The Manual is
written for the current Pulse Oximeter. In case of modifications and software
upgrades, the information contained in this document is subject to change without
notice.
The Manual describes, in accordance with the Pulse Oximeter's features and
requirements, main structure, functions, specifications, correct methods for
transportation, installation, usage, operation, repair, maintenance and storage, etc. as
well as the safety procedures to protect both the user and equipment. Refer to the
respective chapters for details.
Please read the Manual very carefully before using this equipment. These instructions
describe the operating procedures to be followed strictly, failure to follow these
instructions can cause measuring abnormality, equipment damage and personal injury.
The manufacturer is NOT responsible for the safety, reliability and performance
issues and any monitoring abnormality, personal injury and equipment damage due to
user's negligence of the operation instructions. The manufacturer's warranty service
does not cover such faults.
Owing to the forthcoming renovation, the specific products you received may not be
totally in accordance with the description of this User Manual. We would sincerely
regret for that.
This product is medical device, and can be used repeatedly. Its using life is 3 years.
WARNING:
The uncomfortable or painful feeling may appear if using the device
ceaselessly, especially for the microcirculation barrier patients. It is
recommended that the sensor should not be applied to the same finger for
over 2 hours.
For the individual patients, there should be a more prudent inspecting in
the placing process. The device can not be clipped on the edema and
tender tissue.
The light (the infrared is invisible) emitted from the device is harmful to
the eyes, so the user and the maintenance man, can not stare at the light.
Testee can not use enamel or other makeup.
Testee's fingernail can not be too long.
Please peruse the relative content about the clinical restrictions and
caution.
This device is not intended for treatment.
Caution: Federal law restricts this device to sale by or on the order of a
physician.
1 Safety
1.1 Instructions for Safe Operations
Check the main unit and all accessories periodically to make sure that there
is no visible damage that may affect patient's safety and monitoring
performance about cables and transducers. It is recommended that the
device should be inspected once a week at least. When there is obvious
damage, stop using the monitor.
Necessary maintenance must be performed by qualified service engineers
ONLY. Users are not permitted to maintain it by themselves.
The oximeter cannot be used together with devices not specified in User's
Manual.Only the accessory that appointed or recommendatory by
manufacture can be used with this device.
This product is calibrated before leaving factory.
1.2 Warnings
Explosive hazard—DO NOT use the oximeter in environment with
Contec Medical Systems Co., Ltd.
Instructions to User
T echnical Development

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Summary of Contents for Contec CMS50D

  • Page 1 CMS50D P u l s e O x i m e t e r Contec Medical Systems Co., Ltd. Address:No.112 Qinhuang West Street, Economic T echnical Development & Zone, Qinhuangdao, Hebei Province, PEOPLE’S REPUBLIC OF CHINA Tel: +86-335-8015430 Fax: +86-335-8015588 Technical support:+86-335-8015431 E-mail: cms@contecmed.com.cn...
  • Page 2 inflammable gas such as some ignitable anesthetic agents.  DO NOT use the oximeter while the testee measured by MRI and CT.  The person who is allergic to rubber can not use this device.  The disposal of scrap instrument and its accessories and packings(including battery, plastic bags, foams and paper boxes) should follow the local laws and regulations.
  • Page 3 2.3 Major Applications and Scope of Application The Pulse Oximeter can be used to measure human Hemoglobin Saturation and pulse rate through finger, and indicate the pulse intensity by the bar-display. The product is suitable for use in family, hospital (Ordinary sickroom), Oxygen Bar, social medical organizations and also the measure of saturation oxygen and pulse rate.
  • Page 4 Pulse Rate Measuring Range: 30 bpm ~ 250 bpm; Pulse Wave Display: columniation display and the waveform display. Power Requirements: 2×1.5V AAA alkaline battery (or using the rechargeable battery instead), adaptable range: 2.6V-3.6V. Power Consumption: Smaller than 30mA. Resolution: 1% for SpO and 1 bpm for Pulse Rate.
  • Page 5: Troubleshooting

    Let the patient’s finger put into the rubber cushions of the clip (make sure the finger is in the right position), and then clip the finger. Press the switch button once on front panel. Do not shake the finger and keep the patient at ease during the process. Meanwhile, human body is not recommended in movement status.
  • Page 6 Type BF Refer to instruction manual/booklet The pulse oxygen saturation(%) PRbpm Pulse rate (bpm) The battery voltage indication is deficient (change the battery in time avoiding the inexact measure) 1. no finger inserted 2. An indicator of signal inadequacy battery positive electrode battery cathode 1.Power switch 2.change direction of the screen...
  • Page 7 EQUIPMENT and SYSTEMS Guidance and manufacture’s declaration-electromagnetic immunity The CMS50D Pulse Oximeter is intended for use in the electromagnetic environment specified specified below. The the user of CMS50D Pulse Oximeter should assure that it is used in such an environment. Immunity...
  • Page 8 If the measured field strength in the location in which The CMS50D Pulse Oximeter is used exceeds the applicable RF compliance level above, the CMS50D Pulse Oximeter should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the CMS50D Pulse Oximeter.