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CONTEC CMS5100 Patient Monitor


Brief introduction

CMS5100 Patient Monitor adopts Oscillometry for NIBP measuring, Photoelectric Oxyhemoglobin Inspection Technology combining Capacity Pulse Scanning & Recording Technology for SpO2 measuring. Systolic Pressure(SYS), Diastolic Pressure(DIA), Mean Pressure(MAP), SpO2 and Pulse rate(PR) can be accurately measured.

Compact appearance, comprehensive functions, simple and convenient operation, which is applicable for hospitals, community medical treatment and family.


Features

■Be applicable for adult, pediatric and neonatal for all-round monitoring, easy operation and high cost performance.

■Be applicable for medicine, surgery, operating room, ICU/CCU, emergency room, obstetrics and gynecology, pediatrics.

Built-in rechargeable Li-polymer battery for uninterrupted monitoring.

■Compact and flexible appearance, easy for carrying and be suitable for indoor and outdoor(in ambulance) monitoring.

■With user-friendly interface.

■Display with 2.8'' (320×240) color TFT LCD and red and yellow highlight LED.

■Visual and audible alarm for Systolic Pressure(SYS), Diastolic Pressure(DIA), Mean Pressure(MAP), SpO2 and Pulse rate(PR), and upper and lower limit of alarm can be set.

■Unique Flash memory, storage for up to 2000 NIBP data and 30000 SpO2 data.

■Convenient and quick in inquiring measurement data, review for NIBP trend graph within 24-hour and SpO2 and Pulse rate(PR) trend graph within 20-hour.


Performance

NIBP monitoring

■Measurement method: Oscillometry

■Measurement mode: manual/auto/continuous.

■Auto measurement interval: adjustable from 1 to 90 minutes.

■Resolution: 1mmHg.

■Accuracy: Maximum Mean deviation≤±5mmHg, Maximum Standard deviation≤8mmHg.

■Self-check function.

■Overpressure protection: double protection for software and hardware.


Accessories

A power cord

A power adapter

A SpO2 probe

An adult NIBP cuff

An extending tube for blood pressure


Physical characteristic

Dimension for product: 190(L)×162(W)×240(H)mm

Weight: 1.6kg

Dimension for packaging: 402(L)×228(W)×320(H)mm


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The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If the item is subject to FDA regulation, we will verify your status as an authorized purchaser of this item before shipping of the item.

The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG)with the code 197923, and certified by FDA of United States and CE,TUV of Europe. The  Fingertip Pulse Oximeter that is FDA 510K Approved

International Buyer--Please note:

Import duties,Taxes are not included in the item price.These charges are buyers' responsibility.

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