Portable Ultrasound Scanner Color Doppler Diagnostic System Machine+Convex Probe

  
Color Doppler Ultrasound Scanner CMS1700A. 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. 1 Color Doppler (CF), color power Doppler imaging (PDI). 2 Pulse spectrum Doppler (PW). 3 B+CF Color double-frame real-time imaging.

4 Linear array deflection/trapezoid imaging, contrast imaging. 7 Tissue harmonic imaging (THI). 1 Display depth: = 300 mm.

2 Sync implementation of three modes (B+CFM/PDI+PWD). 3 Extended interface: VIDEO interface, S-VIDEO interface, RJ-45 interface, USB interface, VGA interface.

Type of protection against electric shock: class? Degree of protection against electric shock: type B applied part.

Operating voltage: AC 100 V240 V. Operating frequency: 50 Hz/60 Hz. Power consumption: = 100 VA.

One convex probe (3.5 MHz). Dimension: 370 mm (L) × 360 mm (W) × 80 mm (H). 1 examination of abdominal tissues including: liver, gallbladder, spleen, pancreas, kidney, uterus, bladder, prostate, etc. 2 assessment of fetal growth and fetal maturity in obstetric diagnosis. Be mainly used for examination of heart and abdominal tissues. Be mainly used for examination of rectum. Be mainly used for gynecological examination. Be mainly used for neonate, musculoskeletal system, peripheral vessels, small organs breast, thyroid, testis, etc.

Included for REFERENCE: The sale of this item may be subject to regulation by the U. Food and Drug Administration and state and local regulatory agencies.

If the item is subject to FDA regulation, we will. 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. International Buyers - Please Note. Copmany:CONTEC Medical Systems CO. 112 Qinhuang West Ave, Qinhuangdao City, 066004 China.