Description

Introductions:

The device acquires functions that including synchronous sampling of conventional 12-lead ECG data and 3-lead vector ECG data, various forms of analysis and diagnosis, report output and other functions. As an integrated ECG analysis system, the devic can reflect the movement of user’s heart timely and accurately. The device is applicable for ECG examination in medical and health institutions at all levels, providing accurate and reliable basis for diagnosis.


Features

1. Compact and portable design for Recorder, support Wilson and Frank lead system, with lead-off indicator light

2. Adopt real-time sampling, display and store mode, it has many functions, such as QRS wave analyzing in real-time, heart rate calculating and real-time printing, and provides multiple filter methods to avoid from baseline drift and interference.

3. Adopt advanced ECG analysis arithmetic, more perfect for the computer to seek points, and obtain reliable auto-recognizing sort of arrhythmia, which makes the analyzing report and conclusion more valuable.

4. ECG waveform is displayed using anti-aliasing technology clearly and intelligently, lead position can be adjusted, which solves the problem of overlapping waveform caused by baseline drift or high amplitude waveform.

5. High sampling frequency (1000Hz) ensures no distortion of ECG waveform. High resolution in display and printout guarantees the details of ECG waveform.

6. Provide dozens of sync and continuous display and print mode, including 6×2, 3×4, 3×4+2, etc. Auxiliary tool, such as superposed waveform analysis, electronic scale and editable terminology database, etc., brings much more convenient for diagnosis and clinical application.

7. Multiple analysis function, including: conventional 12-lead ECG, Frequency Cardiogram (FCG), High Frequency ECG, QT internal dispersion analysis, Heart Rate Variability (HRV) analysis, myocardium ischemia (STLE) analysis, Heart rate turbulence (HRT) analysis, Pacing ECG analysis, Vector Cardiogram (VCG), Time Vector Cardiogram (TVCG) and SAECG etc.

8. The “shortcut print” function can preview or print the whole analysis reports, and save them in PC with multimedia format (BMP, PNG, PDF or JPG format) according to factual need

9. Support calling external procedures to obtain patient information of unknown origin, export HL7 aECG standard format ECG data, print electronic report and send notice to external procedure, convenience for systems docking with hospital HIS, PACS and others.


Performance

HR display range: 30bpm~300bpm, error: 30bpm~100bpm, ±1bpm; 100bpm~ 300bpm, ±1%.

Sampling frequency: max. 1000Hz

Sampling accuracy: max. 24 bits

Lead: Standard 12 leads

Input loop current:≤ 0.1μA

CMRR: >60dB, >100dB (with filter)

Amplitude frequency characteristic: set 10Hz as benchmark, 0.05Hz~150Hz (-3dB~+0.4dB)

Noise level: ≤15μVp-p

Safety type: Class II Type CF with defibrillation protection 


Accessories

Ground wire 1pc

ECG Workstation patch cord 2pcs

ECG Workstation data transmission line 1pc

ECG Workstation lead cable 1pc

Limb electrode clamp 1 set (4pcs)

Chest electrode 1 set (6pcs)

User manual 1pc

lead wire clip 1pc(2pcs)


Physical Characteristic

Operational environment

a) Environment temperature: 5℃~ 40℃

b) Relative humidity: 25%~ 95% (no condensation)

c) Power supply: USB DC 5V

d) Atmospheric pressure: 700hPa~1060hPa

Storage environment

a) Environment temperature: -40℃~+55℃

b) Relative humidity: ≤95%HR

c) Atmospheric pressure: 500hPa~1060hPa

Shipping

    1. Clearance: we will ship your item to your confirmed address.
    2. Buyers’ responsibility to pay duties,taxes and other extra charges by the government in your country.

Terms of Sale

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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. 
If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA’s Center for Devices and Radiological Health.
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

About Us

Contec Medical Systems Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.

Contact Us

Contact Name:Tessy Zhang; Whatsapp/Mobile:+86-18716007715;