+3D Portable Digital Ultrasound Scanner LAPTOP Machine Convex Transducer CE USA For Sale

+3D Portable Digital Ultrasound Scanner LAPTOP Machine Convex Transducer CE USA


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+3D Portable Digital Ultrasound Scanner LAPTOP Machine Convex Transducer CE USA:
$1,269

CAREJOY

Details

Description:

Features For Ultrasound Scanner:

High-frequency beam-former to ensure best resolution of the image

8steps for TGC and digital over-all Gain grasp the high-quality image

Whole-course real-time continuous dynamic focusing and aperture obtains high-resolution and picture in picture in

Super professional software packages to have the scanner widely used in ObstetricsGynecoloyg,Urology, Cardiology ,Small parts.

Easy for operators with the comfortable application and professional software package.

It is the best choice for clinical diagnosis,because it makes clinic diagnostic more convenient and effective.

Specification For Ultrasound Scanner:

Screen Size

10.4inch

Display Mode

B, B+B, B+M, M, 4B

Image gray scale

256 scale

Cine loop

≥500 Frame

Image storage

64Frame

Scale Angle

Adjustable

Scan depth

40mm~240mm

Image flip

Image Process

GAMA,Image Smoothen.THI,Histogram,Zoom

Focus

Focus Number,Focus position,Focus space

Measure

Character display

Output report

4 types

USB port

USB2.0

Power consumption

200VA

Size

Packing list:

1×Main Unit

1×96 elements R60, 3.5MHz multi-frequency convex probe

1×Lilon battery

1×Power adapter(AC110V~240V,2A,50/60Hz)

1×OperationManual
1X3D external Ultrasound image working station

****Optional *****

96 elements L40, 7.5MHz multi-frequency Linear probe
96 elements R13, 6.5MHz multi-frequency Transvaginal Probe
96 elements R20, 5.0MHz multi-frequency Micro-convex probe
96 elements L40, 7.5MHz multi-frequency Rectal probe
Video thermal recorder (Original Sony UP-897MD)

PAYMENT

1.Weaccept payment

FDADisclaimer

The Fingertip Pulse-Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 136606, and certified by FDA of United States (Premarket Submission Number (510K): K073454 Listing Number: D045684, K082641 Listing Number: D064765, K090671 Listing Number: D078664); and CE Approved, TUV of Europe (Cert.No. : G1 10 02 50972 013). You can consult with the FDA's Center for Devices and Radiological Health: www.fda.gov/cdrh/devadvice/; Phone number: 800.638.2041;

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Notes:

Warranty:

ABOUTUS

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  • On Mar-08-18 at 19:28:24 PST, seller added the following information:



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