Handheld Color Doppler Ultrasonic Diagnostic System Digital ultrasound machine

  
Portable Color Doppler laptop Digital B-Ultrasound machine 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. 1Color Doppler (CF), color power Doppler imaging (PDI). 3B+CF Color double-frame real-time imaging. 4Linear array deflection/trapezoid imaging, contrast imaging.

2Sync implementation of three modes (B+CFM/PDI+PWD). 3Extended interface: VIDEO interface, S-VIDEO interface, RJ-45 interface, USB interface, VGA interface. SafetyType 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. Dimension: 370 mm (L) × 360 mm (W) × 80 mm (H).

1 Convex probe Be mainly used for. 1examination of abdominal tissues including: liver, gallbladder, spleen, pancreas, kidney, uterus, bladder, prostate, etc.

2assessment of fetal growth and fetal maturity in obstetric diagnosis. 2 Microconvex probe(optional) Be mainly used for examination of heart and abdominal tissues. 3 Transrectal probe(optional) Be mainly used for examination of rectum. 4 endo-vaginale probe(optional) Be mainly used for gynecological examination.

5 Linear Probe(optional) Be mainly used for neonate, musculoskeletal system, peripheral vessels, small organs breast, thyroid, testis, etc. 1Contain rich software packages, which can fully meet the requirements of clinical diagnosis. 3Sync implementation of three modes (B+CFM/PDI+PWD). Food and Drug Administration and state and local regulatory agencies. 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. 100% satisfaction is our goal! We are looking forward to establishing a successful business relationship with you.