TLC5007 FDA 24hrs 3-Lead color EKG Holter ECG Recorder Monitor Software Analyzer For Sale

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

Record time: 24-hour
Power supply: two “AA” batteries
Interface: USB2.0
Calibration voltage: 1mV±5%
Noise level: ≤30μV
CMRR: ≥60dB
Low-frequency characteristics: time constant≥3.2s
Scan speed: 25mm/s±5%
Polarizing voltage: ±300mV, sensitivity: ≤±10%
Minimum measure signal: 50 µV p-p

ECG electrode (1 bag)
USB cable(1)
Bag(1)
User manual(1)

Dimension: 111mm(L) × 60mm(W) × 25mm(H)
Weight: about 105g(without 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.

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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Return - After service

We offer 60 days return policy. 100% satisfaction is our goal!

1.All items are brand new ,with 1 years warranty.

2.If you have a defective item, you want to return or discount. Please contact us within 2 days from you receive the item.

3.We will refund the money to you when we get the return items or replace item for you.

4. All return items must be returned with its original package and accessories. Customer is responsible for shipping charges on returned items.

Contec Medical Systems focusing on research, manufacture and distribution of medical instruments,was founded in 1992 as a high-tech company.At present there are more than 1200 employees in our company.Our product line covers a wide range of 13 categories.Most of the domestic hospitals are our customers.Contec hopes to cooperate with international companies to supply more innovative design and advanced technology products.We sincerely welcome you to become one of our global partners.We are looking forward to establishing a successful business relationship with you.

ContactPerson:Vivian English User Manual,Please contact us if you need other language manual.