Portable laptop machine Color Doppler Diagnostic Ultrasound Scanner Convex Probe

Description

CONTEC Color Doppler Ultrasonic Dignostic System CMS1700A + 3.5Mhz Convex Probe
Introduction
CMS1700A is a color Doppler ultrasonic diagnostic device with high resolution, which has a powerful computer processing platform. The system is mainly suitable for the diagnosis of abdomen, heart, peripheral vessels, breast, obstetrics and gynecology, small organs, urology, muscle, incretion and pediatrics, etc. It adopts Doppler ultrasound imaging technology, advanced image processing technology (such as digital beam-forming technology, tissue harmonic imaging (THI), image speckle suppression, etc.) and digital integrated graphic management system, and the internal professional measurement software package can fully meet the clinic diagnostic requirement.
Features1)Color Doppler (CF), color power Doppler imaging (PDI).
2)Pulse spectrum Doppler (PW).
3)B+CF (Dual Images)
4)B+CF/PDI/DPDI+PW (Triplex)
5)Linear array deflection/trapezoid imaging.(optional)
6)Anatomic M-mode imaging.(optional)
7)space compounding imaging
8)Tissue harmonic imaging (THI).
9)Wide scene imaging.(optional)
10)Puncture enhanced.(optional)
Performance
1)Display depth: ≥ 300 mm
2)Extended interface: VIDEO interface, S-VIDEO interface, RJ-45 interface, USB interface, VGA interface.
Safety
Type of protection against electric shock: class Ⅰ equipment
Degree of protection against electric shock: type B applied part
Operating voltage: AC 100 V~240 V
Operating frequency: 50 Hz/60 Hz
Power consumption: ≤ 100 VA
Accessories
One abdominal probe (3.5 MHz)
One User Manual
One power cord
One adapter
Physical characteristic
Dimension: 370 mm (L) × 360 mm (W) × 80 mm (H)
Weight: 6.5 kg
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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
International Buyer--Please note:
Import duties,Taxes are not included in the item price.These charges are buyers' responsibility
We are the manufacturer of medical equipment for 17 years, the following are our main products:
ECG /  ECG holter   EEG / EEG Holter      B-ultrasound
Patient Monitor      Fetal doppler             Fetal Monitor
Spo2 Monitor          Stethoscope              Medical Image...
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Only English User Manual,Please contact us if you need other language version.thank you