Mini Portable Digital 12-channel 12-Lead Electrocardiograph ECG EKG Machine FDA

Description

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Description:
Features:
12 channel digital ECG machine with interpretation
Simultaneous acquisition of 12-lead ECG signal
Manual/Auto/Arrhythmia analysis modes
Real time ECG, 20 patients cases
Alphabetic keyboard for patient info
Multiple printing modes
320x240 graphic, 5.7 inch LCD
High resolution thermal printing system
High resolution digital filter
Built-in USB or RS232, optional PC-ECG software
AC/DC power, built-in rechargeable Ni-MH battery
Light weight, portable, convenient for use
Specification:
Safety standard
IEC60601-1 class I, type CF
Lead
Standard 12 Leads, Lead change automatically
Resolution
12 bit / 1000Hz
Operation mode
Manual/Auto/Analysis modes
Filter
AC, EMG filter
Drift filter
Anti-drift system
Input circuit
Floating; Protection against Defibrillator effect
CMRR
>100dB (with filter)
Input circuit current
<0.1μA
Input impedance
≥50ΜΩ
Calibrating voltage
1mV±3%
Frequency response
0.05Hz~160Hz (IEC)
Time constant
>3.2seconds
Noise level
≤15Vp-p
Threshold
≤20μV
Sensitivity
Auto 2.5, 5, 10, 20, 40mm/mV
Recording system
High resolution thermal printer
Paper speed
25, 50mm/s±3%
Recording paper
210/216mmx20m, roll/fold paper
Power supply
AC: 220V / 110V, 50/60Hz
DC: 14.4V rechargeable NI-Ion battery (4400mAh)
LCD display
320x240 graphic, 5.7 inch LCD
Dimensions
285×265×72mm
Weight
3.8kg
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FDA declaration
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.And This item has been cleaned and treated according to the manufacturer's instructions. (The seller’s name: Christine  City: Beijing  State: Beijing    Country: China   Telephone number: 86-10-81290069). This item has been cleaned and treated according to the manufacturer's instructions.
The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606.
The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number
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K132989
The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number
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K180353
The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number
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K141973
massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number
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K161892
Payment
We accept PayPal only. We will ship out the item after receiving cleared payment.
Shipping
A complete and correct shipping address is essential.
Customers with shipping addresses outside of the U.S. are responsible for all duties and import taxes. Please contact your customs for information
Return Policy
All items are in brand new condition unless specified.
Contact Us
We are the manufacturer and distributor of Dental equipments for more than 10 years. Any questions, please contact us through eBay message or e-mail,We will reply to you within 48 hours.