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Ultra sound, basic unit, ALOKA 500

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last updated : 2018/12/31
Code Description Budget Price Ship. weight Ship. vol.
XMEQULSOA5
ULTRA SOUND BASIC UNIT, ALOKA 500, w/convex probe 3.5Mhz on request 0kg 0 Add
XMEQULSOA5G05
ULTRASOUND COUPLING GEL, 5 Lt CH 8.05 5.22kg 7,125L Add
XMEQULSOA5G05D
(ultra sound Aloka 500), DISPENSER, to fit gel container 5l CH 10.24 0.1kg 4,224L Add
XMEQULSOA5PC05
(ultra sound Aloka 500) PROBE CONVEX, 5Mhz, vaginal CH 4,489.45 0kg 0 Add
Item to be justified
XMEQULSOA5PC35
(ultra sound Aloka 500) PROBE CONVEX, 3.5Mhz, standard CH 2,599.08 0kg 0 Add
Item to be justified
XMEQULSOA5PC75
(ultra sound Aloka 500) PROBE CONVEX, 7.5Mhz, small parts CH 4,122.20 0kg 0 Add
Item to be justified
XMEQULSOA5PL05
(ultra sound Aloka 500) PROBE LINEAR, 5Mhz, paediatric CH 4,721.79 0kg 0 Add
Item to be justified
XMEQULSOA5PV
(ultra sound Aloka 500) PRINTER, VIDEO CH 857.23 0kg 0 Add
Item to be justified
XMEQULSOA5PVP
(ultra sound Aloka 500, printer video) PAPER, roll CH 8.45 0kg 0 Add
Item to be justified
XMEQULSOA5SF
(ultra sound Aloka 500) SWITCH FOOT, for freezing picture CH 213.60 0kg 0 Add
Item to be justified
XMEQULSOA5T
(ultra sound Aloka 500) TROLLEY, with wheels CH 725.05 0kg 0 Add
Item to be justified

General information

Portable appliance used for diagnostic imaging in obstetric, gynaecology, paediatrics and general surgery.

Used by trained personal. Depending on local conditions an uninterruptible power supply (UPS) should be used to protect the device from power outs, surges and fluctuations.

Specifications

Complies with WHO specifications governing EUG (ultrasound for general use)

 

Component:

ULTRA SOUND BASIC UNIT, ALOKA 500, with convex probe 3.5Mhz.

 

1 scanner, ultrasound portable system, main unit with accessories.

 

1 standard electronic convex sector probe: frequency 3.5MHz, scanning angle 60°, radius 60mm.

 

1 ultrasonic gel 5-litre container.

 

1 dispenser for ultrasonic gel.

 

1 operating manual: English and French

 

1 service manual: English and French

Specifications:

Portable high-performance ultrasound system, main unit.

 

Compact and lightweight, easy to carry.

 

Size WHD 29x32x25cm, weight: 10kg

 

Monitor with screen: simple controls, straight-forward operation.

 

Scanning method: electronic convex sector probe, electronic linear.

 

Imaging display modes: B, dual B, M, and B and M.

 

Imaging technologies: dynamic frequency imaging, multi-stage focusing and aperture control.

 

Image gray-scale: 64 levels.

 

Depth range selection: convex sector image and linear image, 3 steps.

 

Image orientation: lateral and vertical inversion (in B mode).

Measurement and analysis:

Calibre control: trackball.

 

On B-mode image: distance, area and circumference via ellipse or trace method; and volume, ratio, gestational age, foetal weight, angle.

 

Gestational table: user programmable.

 

On M-mode: velocity, time interval, depth, heart rate, LV function.

Characters & graphics:

Patient information, annotation area, body mark display.

 

Automatic display: date and time, focal-point setting, image orientation mark, image scrolled position, distance scale mark, M-mode time mark, and grey scale for calibration.

 

Selectable On/Off automatic display: gain setting, near gain setting, far gain setting, probe frequency, and puncture guide line.

 

Viewing monitor: 7-inch diagonal monitor with non-reflexion filter.

 

Video output: 625 lines per frame.

 

Power requirement: 220/240V ±10%, 50/60Hz, approximately 160VA.

Environmental requirements:

In operation: temperature -10 to +40°C, relative humidity 30 to 85% non-condensing.

 

In storage: temperature -10 to +50°C, relative humidity 10 to 90% non-condensing.

Packaging and labelling:

Primary packaging: unit of use

 

Scanner ultrasound, individually wrapped in a plastic film with manufacturer’s instruction for use, spare parts and accessories (including list of). Supplied with clear instructions for use and diagrams for assembly. Must be multilingual: English, French and Spanish, others when available.

Other requirement:

Conforms to Medical Device Directive, Council Directive 93/42/EEC and has CE mark and reference number of notifying body.

Safety regulation:

Complies with IEC 601-1 Class1, type BF