ambulatory blood pressure monitor

CMS600P2 PLUS Ultrasound Scanner with Linear Probe

FDA Certificated

Description

1.Introduction
CMS600P2PLUS is a B-Ultrasound Diagnostic System with high resolution and PW Doppler. The system is mainly suitable for the ultrasonic examination of abdomen, obstetrics and gynecology, small organs, urology, 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.
 Functions
15 Inch TFT Display
Portable design
Built-in lithium battery, the device can work continuously for up to 2 h 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 (THI)
Pulse wave Doppler (PW)
Space Compounding Imaging.
Working mode: B, 2B, 4B, B/M, M, PW
Software packages: routine, abdomen, obstetrics, gynecology, vessels, small organ, urology, etc.
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 Ⅰ equipment
 Degree of protection against electric shock: type BF applied part
 Operating voltage: AC 100 V ~ 240 V
 Operating frequency: 50 Hz/60 Hz
 Power consumption: ≤ 100 VA
 Accessories
 One  Linear probe
 One User Manual
 One power cord
 One adapter
 Physical characteristic
Dimension: 370 mm (L) × 360 mm (W) × 80 mm (H)
Weight: 6.5 k g

Payment

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Shipping

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Terms of Sale

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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. If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health.
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.

About Us

Contec Medical Systems Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.

Contact Us

Please contact us through eBay Message, we are on line to reply your message within 24 hours.
Whatsapp/Wechat:+86 18716007715

We only have the English Manual in the standard package, If you need any other language Manual, please contact us freelyibay365