CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new

CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new

CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new
CONTEC Auto Digital 3 Channel ECG EKG Machine 12 Lead electrocardiograph E3M new


$459.0 Buy It Now or Best Offer
free,30-Day Returns





Seller Store contecmedsys
() %,

Location: qinhuangdao
Ships to: US,
Item: 176316821822

Return shipping will be paid by:Buyer
All returns accepted:Returns Accepted
Item must be returned within:60 Days
Refund will be given as:Money Back
Return policy details:
CONTEC:CONTEC
MPN:Does Not Apply
Number of Channels:3
ECG & EKG Machine Type:Electrocardiograph
Intended Use/Discipline:Biological Laboratory,Dental Laboratory,Emergency Medicine
Operation:Digital
E3m:E3m
Country/Region of Manufacture:China

electrocardiograma ECG machine E3M Introduction E3M is a kind of electrocardiograph, which is able to sample 12 leads ECG signals simultaneously and print out the ECG waveform with thermal printing system. Its functions are as follows: recording and displaying ECG waveform in auto/manual mode; measuring ECG waveform parameters automatically, and automatic analysis and diagnosis; pacing ECG detection; prompt for electrode-off and out of paper; optional interface languages(Chinese/English, etc.); built-in lithium battery, powered either by AC or DC; arbitrarily select the rhythm lead to conveniently observe abnormal heart rate; case database management, etc. 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 1/3/6/12-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, etc. Waveform length printed can be adjusted, and with timed print function, which meets different requirements. 4)With the functions of auto-analysis and auto-diagnosis for routine ECG parameters, which reduces the doctor’s burden. 5)Build-in memory, which is convenient for doctor to review case and statistic. 6)Multi- language(Chinese, English) interface and report. 7)Optional ECG-Sync software, connect with PC by USB2.0 interface to form a ECG workstation, import real-time data to the software for analyzing and report printing, and old cases stored in Electrocardiograph can be uploaded to PC. 8)Power supply: AC/DC and built-in rechargeable lithium battery, which meets the requirements of visiting a patient at home and body examination. Performance Input way: Floating and defibrillation protection Lead: Standard 12 leads Patient leakage current: <10µA Input impedance: ≥100MΩ(1Hz) Frequency response:0.01~150 Hz(-3 dB) Time constant: ≥3.2s CMRR: >123 dB Filter: power frequency(AC50/60 Hz), myoelectricity(25 Hz/35 Hz (-3 dB)), baseline drift filter Recording way: Thermal printing system Specification of recording paper: 80 mm(W)×20 m(L) high-speed thermal paper Time base selection(paper speed):6.25 mm/s, 12.5 mm/s, 25 mm/s, 50 mm/s, error: ±5% Gain control(sensitivity): 2.5, 5, 10, 20 mm/mV, accuracy is ±2%; Standard sensitivity: 10 mm/mV±0.2 mm/mV Auto record: record setup according to auto record format and mode, automatically change leads, automatically measure and analyze. Rhythm record: record setup according to rhythm record format and mode, automatically measure and analyze. Manual record: record according to manual record format. 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) amplitude, S(V1) amplitude, R(V5)+S(V1) amplitude Product safety type: Class I type CF defibrillation-proof applied part Polarization resistance voltage: ±950mV Noise level: ≤12 µVp-p ECG signal input sampling frequency: 32 kHz Waveform data processing sampling frequency: 1 kHz Sampling precision: 24-bit The minimum detection signal: 10 Hz, 20 µV(peak-peak value) deflected sinusoidal signal can be detected Accuracy of input signal: ±5 % Amplitude quantization: ≤5µV/LSB Interchannel time deviation: <100 µs Calibration voltage:1 mV±2 % Input circuit current:≤0.01 uA 50Hz interference suppression filter:≥20 dB Pacing detection channel: all leads Power supply: AC: 100V~240V(50/60Hz) DC: 7.4V/5000mAh rechargeable lithium battery Degree of protection against ingress of liquid: IPX0 Working mode: continuous working Accessories Standard configuration: A lead cable A limb electrode A chest electrode A thermal recording paper A power cord An earth wire A user manual Physical characteristic Working environment Temperature: 5℃~40℃ Relative humidity: 25%~95%(non-condensing) Atmospheric pressure: 700 hPa~1060 hPa Transport and storage environment Temperature: -20 ℃~+55 ℃ Relative humidity: ≤95% Atmospheric pressure: 500 hPa~1060 hPa Dimension: 315mm(L)×200mm(W)×77mm(H) Net weight: 1.5Kg Buy safe products 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 Agent in the world! We are looking for partners in the world now! Do you want to become our agent in you conutry? Join US! Skype:xuebox3 contec.med.mary at hotmail.com Only English User Manual,Please contact us if you need other language version.thank you

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