6PA Phased Array Wireless Ultrasound Probe

Product Details

6PA Phased Array Wireless Ultrasound Probe

6PA

6PA phased array wireless probe: 192 elements, 2.2-3.6 MHz, depth 90-200 mm, scan angle 80 degrees, imaging modes including CW.

Brand: SonoStar
Price: On request
Probe frequency: 2.2-3.6 MHz
Connection: Wireless - built-in WiFi hotspot in the probe; phone, tablet or Windows PC receives the images, with no dependence on the WiFi available on site
Charging: Wired charging
Category: Handheld Ultrasound

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Product overview

The 6PA is a phased array wireless ultrasound probe using electronic array scanning, with 192 elements and 32 channels. The host is built into the probe, and images travel over its own WiFi to a phone, tablet or Windows PC, so the unit does not depend on the WiFi available on site.

The frequency is 2.2-3.6 MHz with scanning depth adjustable across 90 / 130 / 160 / 200 mm and a scan angle of 80 degrees. The low frequency penetrates the chest wall, which suits assessment of cardiac function and blood volume, and chest work such as pericardial effusion.

Imaging covers B, B/M, Color, PDI, PW and CW with a gain range of 30-105 dB, and gain, focus, pulse inversion harmonic imaging and noise reduction are adjustable. In-plane needle guidance lines and out-of-plane guidance are supported. The battery is rated at 2600 mAh. The probe measures 135 x 40 x 25 mm and weighs 120 g.

Technical specifications

Specifications for this model

Item	Data
Probe frequency	2.2-3.6 MHz
Scanning depth	90 / 130 / 160 / 200 mm, adjustable
Scanning method	Electronic phased array scanning
Elements	192
Channels	32
Scan angle	80 degrees
Imaging modes	B, B/M, Color, PDI, PW, CW
Gain	30-105 dB
Image adjustment	Gain, focus, pulse inversion harmonic imaging, noise reduction
Battery life	2 hours
Battery capacity	2600 mAh
Frame rate	18 f/s
Charging	Wired charging
Noise reduction	0 / 1 / 2 / 3 / 4
Needle guidance	In-plane guidance line; out-of-plane guidance with automatic vessel measurement
Cine review	Manual and automatic, playback frame count 100 / 200 / 500 / 1000
Measurements	Distance, area, circumference, heart rate
Image storage	jpg, mp4, DICOM
Connection	WiFi or USB cable
WiFi type	802.11n / 2.4 GHz / 5 GHz dual band, 450 Mbps
Software platforms	iOS
Dimensions	135 x 40 x 25 mm
Weight	120 g

Common to the series

Item	Data
Gain range	30-105 dB
Noise reduction	5 levels: 0 / 1 / 2 / 3 / 4
Dynamic range	40 / 50 / 60 / 70 / 80 / 90 / 100 / 110
Image transmission	Built-in WiFi in the probe; does not depend on the WiFi available on site
Devices	Phone, tablet or Windows PC (Windows software supplied)

Specifications updated 2026-11-01

Typical applications

The application scenarios on this page describe the device based on its technical data and configuration. The actual scope of application is the one stated in the product registration certificate. Follow your institution's procedures and the instructions for use.

Setting / department	Typical use	Configuration note
Cardiology	Assessment of cardiac structure and function, blood volume assessment	Phased array with low-frequency penetration
Emergency and ICU	Chest examination such as pericardial effusion, and needle guidance	Low frequency penetrates the chest wall
Anaesthetics	Peri-operative cardiac monitoring	Phased array probe

Usage and selection notes

The 6PA belongs to the phased array cardiac series: low frequency penetrates the chest wall, which suits assessment of cardiac function and blood volume, and chest work such as pericardial effusion. This is the configuration for cardiac work; please confirm the selection with our product department.

The data on this page is taken from the product technical documentation and the figures are unchanged.

For contraindications and precautions, refer to the instructions for use. The device must be operated by a licensed physician with the relevant qualifications.
The technical data on this page is taken from the product technical documentation; where it has been updated, the latest version applies. The listed departments and application scenarios describe the device based on its technical data, and the actual scope of application is the one stated in the product registration certificate. This page makes no claim about clinical outcome and does not constitute clinical guidance.