Image 1 - US Seller 24h Holter Monitor 3-Channel ECG/EKG System Machine,Pacemaker Analyzer
Image 61 - TLC9803 Dynamic 24hour 3-channel ECG Holter Monitor,Software ​Analysis,US Seller
Image 51 - TLC9803 Dynamic 24hour 3-channel ECG Holter Monitor,Software ​Analysis,US Seller

TLC9803 Dynamic ECG Holter

PC Software download

Introduction

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.


Function

1)The recorder can real-time store ECG data for 24-hour.

2)Arrhythmia analysis basing on MCSSTM and TMCATM can greatly reduce doctor’s work.

3)With more than 10 templates(such 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.

4)Flexible analysis channel selection function, which ensures that any channels can be selected as the main analysis channel.

5)Flexible atrial fibrillation analysis, which ensures that physicians can use the whole or segmented AUTO/manual analysis, more accurate in atrial fibrillation analysis.

6)All pacemakers(such as AAI, VVI, DDD etc.) can be analyzed by the powerful pacemaker analysis function. 

7)With many pacing analysis templates, such as “Dual chamber pacing”, “Atrial pacing”, “Ventricular pacing”, “Ventricular Pseudofusion” and “Ventricular asynchronous pacing”, etc.

8)Single or full-lead ECG in any time bucket can be reviewed by the fast review analysis function.

9)With analysis functions for 5-minute, 1-hour and 24-hour heart rate variability.

10)One-key print, convenient and fast to print the reports.

11)Perfect case management function.

12)The risk of sleep breath pause can be predicted by the unique "Sleep breath pause syndrome"analysis function.

13)The 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


Performance

Lead: 3-lead

Record time: ≥24-hour

Power supply: two “AA” alkaline batteries

Interface: USB2.0

Sampling accuracy: 24bit

Sampling frequency: 250Hz

Dynamic range: 10mV

Input impedance: ≥10MΩ

CMR: ≥60dB

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.

System noise: ≤50µVp-p

Multichannel crosstalk: ≤0.2mV

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.



Accessories

Lead cable (1 set)

ECG electrode (1 bag)

USB cable(1)

Software download

Bag(1)

User manual(1)


Physical characteristic

Dimension: 111mm(L) × 61mm(W) × 25mm(H)

Weight: about 105g(without batteries)


Shipping

1. For your earlier and safer to receive the item, please leave us your detail address and telephone number.
2. Your item will be sent via Air mail within 48 hours after payment is received. 
   

3. As the usual way, buyer is responsible for the duties, taxes or other VAT or extra charges from the import countries.
4.All items will be shipped to buyer's PayPal address. Please confirm your PayPal address is correct before purchase.


 International Buyers - Please Note:
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* Please check with your country's customs office to determine what these additional cost will be prior to bidding/buying.


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.
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


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