CMS1700B Portable color Doppler ultrasound scanner with abdominal probe
Introduction

This is a high-resolution color Doppler ultrasound diagnostic device with a powerful computer processing platform. This system is mainly suitable for the diagnosis of abdomen, heart, peripheral blood vessels, breast, obstetrics and gynecology, small organs, urology, muscle, endocrine, and pediatrics. It adopts Doppler ultrasound imaging technology, advanced image processing techniques such as digital beamforming, tissue harmonic imaging (THI), image speckle suppression, etc., and a digital integrated graphic management system. The internal professional measurement software package can fully meet clinical diagnostic requirements.



feature

1) Color Doppler (CF) and Color Power Doppler Imaging (PDI).
2) Pulse spectrum Doppler (PW),
3) Continuous wave Doppler (CW).
4) B+CF (dual image)
5) B+CF/PDI/DPI+PW (Triple)
6) 3D and 4D imaging. Optional
7) Advanced phased array cardiac imaging technology and a complete software package for cardiac measurement functions.
8) Convex array extended imaging.
9) Linear array deflection/trapezoidal imaging.
10) Anatomy M-mode imaging. Optional
11) Space composite imaging
12) Organizational harmonic imaging (THI).
13) Contrast agent imaging. Optional
14) Wide scene imaging. Optional
15) Puncture enhancement. Optional


performance

1) Display depth: ≥ 300mm

2) Expansion interfaces: video interface, S-Video interface, RJ-45 interface, USB interface, VGA interface.

safety

Ø Anti electric shock type: Class I equipment

Ø Anti electric shock level: Class B application components

Operating voltage: AC 100V~240V

Operating frequency: 50 Hz/60 Hz

Ø Power consumption: ≤ 100VA

accessories

An abdominal probe
A user manual

One power cord

An adapter

physical properties

Dimensions: 370mm in length, 360mm in width, and 80mm in height

Weight: 6.5 kilograms

Purchase security products
The following disclaimer from the US Food and Drug Administration applies to all healthcare categories listed on eBay for reference only: The sale of this product may be regulated by the US Food and Drug Administration as well as state and local regulatory agencies. If the product is regulated by the US Food and Drug Administration, we will verify your identity as the authorized purchaser of the product before shipping.
The fingertip pulse oximeter has been registered with the Australian Therapeutic Goods Registry (ARTG) with code 197923 and has obtained certifications from the US Food and Drug Administration and European CE and TUV. Fingertip pulse oximeter approved by the US Food and Drug Administration 510K