Digital 3 Channel ECG Machine EKG Monitor 12 Leads electrocardiograph+Software

Description

Test Item
ECG300G 3 Channel ECG Machine
USB+
PC software+Printer
Description
Introduction
ECG300G is an Electrocardiograph which can collect 12-lead ECG signal and print waveform by the thermal printing system. It features in, recording and displaying ECG waveform in AUTO/Manual mode, measuring and diagnosing ECG waveform parameters automatically, prompting for “Lead off” and “Lack of paper”, multi-language interface, AC/DC, selecting any rhythm lead, case database management.
Function
1)Sync collection for 12-lead ECG, adopt digital signal processing technology and get high-quality ECG waveform via power frequency filter, baseline filter and EMG filter of ECG signal.
2)Display of 3/6/12-lead ECG, print mode, sensitivity, paper speed and filter state, etc. on one screen, convenient for contrastively diagnosing.
3)Multiply printing modes and formats, including manual, auto 4×3, auto 3×4+1, auto 3×4, auto 2×6+1, auto 2×6, auto 3-2+1, auto 3-2, auto 1×12+1, auto 1×12, rhythm 4, rhythm 3 and rhythm 2, etc. Waveform length printed can be adjusted, and with time print function, which meets different requirements.
4)With the functions of auto-analysis and auto-diagnosis for routine ECG parameters, provide measurement results and auto-diagnosis conclusion for HR, P-R interval, P Duration, QRS Duration, T Duration, Q-T interval, Q-Tc, P Axis, QRS Axis, T Axis, R(V5), S(V1), R(V5)+S(V1), etc. which reduces the doctor’s burden.
5)Built-in memory stores up to 1000 cases, convenient for case review and statistic.
6)Multi-language(Chinese, English, Spanish, Turkish, Polish, Italian, French, German, Portuguese, Kazakstan, Russian, Ukrainian, Serbian and Slovenian) interface and report.
Performance
Input mode: floating and defibrillation protection
Frequency response: 0.05Hz ~ 150Hz(-3dB~+0.4dB)
CMRR: >60dB, >100dB(add filter)
Time constant:≥ 3.2s
Patient leak current: <10µA
Calibration voltage: 1mV
Sensitivity: 2.5, 5, 10, 20, 40 mm/mV ±5%, standard sensitivity: 10mm/mV±2%
Noise level: <15µVp-p
Input circuit current: ≤50nA
Input impedance: ≥50MΩ
Sampling accuracy: 12-bit
Safety classification: class I, type CF and defibrillation-proof applied part
Recording mode: thermal printing system
Auto record: set record according to auto record format and mode, automatically switching leads, measuring and analyzing.
Rhythm record: set record according to rhythm record format and mode, automatically measuring and analyzing.
Manual record: set record according to record format, manually switching leads.
Measurement parameters: HR, P-R interval, P Duration, QRS Duration, T Duration, Q-T interval, Q-Tc, P Axis, QRS Axis, T Axis, R(V5), S(V1), R(V5)+S(V1)
Paper size: 80mm(W)×20m(L)
Sampling frequency: 1000Hz
EMG interference filter: 25Hz/35Hz (-3dB)
Power frequency filter: AC 50Hz/60Hz(-20dB)
Paper speed:
Auto: 25, 50mm/s, ±5%
Rhythm: 25, 50mm/s, ±5%
Manual: 5, 6.25, 10, 12.5, 25, 50mm/s, ±5%
Power supply:
AC: 100V~240V(50/60Hz)
DC: 7.4V/3500mAh rechargeable lithium battery
Fuse specification: two AC time lag fuse(φ5×20mm), T1.6AL250V
Waterproof degree: IPX0
Working mode: continuous working
Accessories
A lead cable
A limb electrode
A chest electrode
A thermal recording paper
A power cord
An earth wire
A user manual
ECG-Sync software+USB cable
Physical characteristic
Working environment
Temperature: 5℃~40℃
Relative humidity: 25%~95%(non-condensing)
Atmospheric pressure: 700hPa~1060hPa
Transport and storage environment
Temperature: -40℃~+55℃
Relative humidity: ≤95%
Atmospheric pressure: 500hPa~1060hPa
Dimension: 315mm(L) × 215mm(W) × 77mm(H)
Weigh: 1.6Kg
Payment
1.Paypal account
Shipping
Clearance: we will ship your item to your confirmed address.
Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
Terms of Sale
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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; Email:[email protected]
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Only English user guide, if you need any other language, please contact us!
Only English user guide, if you need any other language, please contact us!