CONTEC 3-Channel 24hour ECG/EKG Holter Monitor Recorder Analyzer System+Software. TLC9803 Dynamic ECG Systems adopt 3-lead, which can continuously record ECG waveform for 24-hour and analyze ECG waveform by the PC software. It is applicable for use in medical institution and community. 1The recorder can real-time store ECG data for 24-hour. 2Arrhythmia analysis basing on MCSSTM and TMCATM can greatly reduce doctor's work.
3With 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. 4Flexible analysis channel selection function, which ensures that any channels can be selected as the main analysis channel.
5Flexible atrial fibrillation analysis, which ensures that physicians can use the whole or segmented AUTO/manual analysis, more accurate in atrial fibrillation analysis. 6All pacemakerssuch as AAI, VVI, DDD etc. Can be analyzed by the powerful pacemaker analysis function. 7With many pacing analysis templates, such as "Dual chamber pacing", "Atrial pacing", "Ventricular pacing", "Ventricular Pseudofusion" and "Ventricular asynchronous pacing", etc.
8Single or full-lead ECG in any time bucket can be reviewed by the fast review analysis function. 9With analysis functions for 5-minute, 1-hour and 24-hour heart rate variability. 10One-key print, convenient and fast to print the reports. 12The risk of sleep breath pause can be predicted by the unique "Sleep breath pause syndrome"analysis function. 13The death risk in patients with myocardial infarction can be predicted by the "HRT" analysis function.14"T-Wave alternation" is an important index to predict the malignant arrhythmia and sudden cardiac death. Power supply: two "AA" batteries. Low-frequency characteristics: time constant=3.2s. Polarizing voltage: ±300mV, sensitivity: =±10%. Minimum measure signal: 50 µV p-p. Dimension: 111mm(L) × 60mm(W) × 25mm(H). Weight: about 105g(without batteries). Food and Drug Administration and state and local regulatory agencies. 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. Note: For your earlier and safer to receive the item, please leave us your detailed address and telephone number.100% satisfaction is our goal! If you have a defective item, you want to return or discount. International Buyers - Please Note. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\ECG & EKG Machines". The seller is "contecmedical" and is located in this country: CN.
This item can be shipped to North, South, or Latin America, all countries in Europe, all countries in continental Asia, Australia.