Introduction
CMS600P2PLUS-VET is a B-Ultrasound Diagnostic System with high resolution and PW Doppler. The system is mainly suitable for the ultrasonic examination of canine,feline, ovine, bovine,equine, Ilama, goat,swine,dolphin,etc. It adopts 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.
Function
15 Inch TFT Display
Portable design
Built-in lithium battery, the device can work continuously for up to 2h after fully charged.
Store the patient data by 128 G hard disk.
Advanced Digital Beam Forming (DBF) technology.
Real time Dynamic Aperture (RDA)
Tissue Harmonic Imaging (TH)
Pulse wave Doppler (PW)
Space Compounding Imaging.
OB measurement: EDD and GA for Bovine, equine, ovine, canine,feline, goat, swine and lama.Automatically calculate backfat and lean percentage of swine.
Working mode: B, 2B, 4B, B/M, M, PW
optional : Trolley
Performance
Scan depth: 250 mm max
Extended interface: two probe interfaces, two USB interfaces, one VIDEO interface, one S-VIDEO interface, RJ-45 interface, one VGA interface.
Type of probe: Convex Probe, Micro Convex Probe, Trans-Rectal Probe,Trans-Vaginal Probe, Linear Probe
Safety
Type of protection against electric shock: class 1 equipment
Degree of protection against electric shock: type BF applied part
Operating voltage: AC 100 V ~ 240V
Operating frequency: 50 Hz/60 Hz
Power consumption:≤100 VA
Accessories
One Linear probe (7.5 MHz)
One User Manual
One power cord
One adapter
Buy safe product
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