3Sync analysis for 12-lead, which ensures that QRS waveform can be found accurately, and no distortion. 4With more than 10 templatessuch as atrial premature beat, ventricular premature beat, long interval, atrial fibrillation, etc.
And many user-defined modules, which can almost distinguish any kind of pathologic waveforms. 5Flexible analysis channel selection function, which ensures that any channels can be selected as the main analysis channel. 6Flexible atrial fibrillation analysis, which ensures that physicians can use the whole or segmented AUTO/manual analysis, more accurate in atrial fibrillation analysis. 7All pacemakerssuch as AAI, VVI, DDD etc. Can be analyzed by the powerful pacemaker analysis function.8With many pacing analysis templates, such as "Dual chamber pacing", "Atrial pacing", "Ventricular pacing", "Ventricular Pseudofusion" and "Ventricular asynchronous pacing", etc. 9Single or full-lead ECG in any time bucket can be reviewed by the fast review analysis function. 10With analysis functions for 5-minute, 1-hour and 24-hour heart rate variability. 11One-key print, convenient and fast to print the reports. 13Abnormal ST can be analyzed according to the whole and event by the advanced ST segment analysis and total load of myocardial ischemia, which can help the doctors comprehensively judge myocardial ischemia. 14The risk of sleep breath pause can be predicted by the unique "Sleep breath pause syndrome"analysis function. 15The death risk in patients with myocardial infarction can be predicted by the "HRT" analysis function. 16"T-Wave alternation" is an important index to predict the malignant arrhythmia and sudden cardiac death.
17With QTD(QT dispersion), VCG(vector cardiogram), VLP(ventricular late potential) and TVCG(time vector cardiogram) analysis modules, more v. Power supply: two "AA" batteries. Gain accuracy: At all possible gain settings, the maximum amplitude error of the output is ±10%. Gain stability: One minute after energizing the device, the gain change in stable ambient conditions shall not exceed 3% over a 24h period.Frequency response: The amplitude response to sinusoidal signals within the frequency range 0.05Hz to 40Hz shall be between the +3dB to -3dB of the response at 5 Hz. Minimum measure signal: 50 µV. With the function in the presence of pacemaker pulses. Timing accuracy: the overall error during 24h shall not exceed 30s.
Food and Drug Administration and state and local regulatory agencies. 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. Only English user guide, if you need any other language, please contact me.
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