Model note · Ultrasound

GE LOGIQ E10 general imaging ultrasound system

Name: GE LOGIQ E10 general imaging ultrasound system
Brand: LOGIQ

The LOGIQ E10 is GE HealthCare's premium general imaging cart based ultrasound system, used for abdominal, vascular, obstetric, small parts, cardiac and other work. It uses GE's cSound imaging engine and supports elastography, shear wave, contrast, 3D/4D and attenuation imaging. It is a Track 3 system under FDA acoustic output rules.

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The model

Maker, model and type.

Maker: GE Medical Systems Ultrasound and Primary Care Diagnostics (GE HealthCare)
Model: LOGIQ E10 general imaging ultrasound system (model 530000E10)
Device type: Ultrasound
Main document: Open the public document

Key specifications

What the public record says.

Item	Value	Source
Console dimensions	585 mm wide, 900.9 mm deep, 1300 mm high (GE sheet; 510(k) gives 991 mm deep)	Source
Weight	126 kg	Source
Electrical	100 to 240 VAC, 50/60 Hz, maximum 0.9 kVA with peripherals	Source
Probe ports	4 active probe ports	Source
Displays	22 inch OLED monitor, 1920 x 1080; 12.1 inch touch screen	Source
Storage	Integrated 1 TB HDD and 128 GB SSD	Source
Beamformer	cSound Imageformer, stated as 11,750,000 channels	Source
Physiological inputs	ECG, PCG and AUX, one channel each	Source
Imaging modes	B, M, PW, CW, Color, Color M, Power Doppler, harmonics, coded pulse, 3D/4D, strain and shear wave elastography, attenuation imaging	Source
FDA clearance	K231966, product code IYN, November 2023 (Track 3)	Source

Recalls

Known FDA recalls.

Z-0588-20192018-09-14
Potential undetected over temperature condition on TEE probes used with LOGIQ E10, possible burn injury.
FDA record

Safety

Safety warnings from the record.

An overheating TEE probe can burn the oesophagus; only use TEE probes on corrected systems. Source
Acoustic output is displayed and must stay within FDA Track 3 limits; the 510(k) states the system's levels are below them. Source

Sources

Where this note comes from.

Not covered: The LOGIQ E10 Basic Service Manual (direction 5750007-1EN and later) exists but was not opened, so system error messages, diagnostics, PM steps and FRU part numbers are missing. The specification sheet is a GE document hosted by a distributor and its depth figure differs from the 510(k). The manufacturerUrl is GE HealthCare's home page.

BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.

Ultrasound