GE LOGIQ V2

Target SDGs

Market Suggested Retail Price

$4,700.00

Target Users (Target Impact Group)

Small and Medium-sized Enterprises, Public Sector Agencies

Distributors / Implementing Organizations

GE Healthcare, National Ultrasound, Innovative Medical Technologies

Competitive Landscape

Direct competitors include Clarius Ultrasound, Healcerion Sonon 300C, dDopp, and GE VScan Pocket Ultrasound.

Regions

Worldwide

Manufacturing/Building Method

The LOGIQ V2 is currently manufactured in China.

Intellectural Property Type

Patent

User Provision Model

Customers can fill out the contact form on the GE Healthcare website to request a quote. The product is also sold through "National Ultrasound" and "Innovative Medical Technologies". The Logiq V2 can also be purchased at regional and local manufacturer offices.

Distributions to Date Status

Between 101-1,000 units have been distributed. The exact amount of units distributed is unknown.

Design Specifications

The LOGIQ V2 produces high quality images using CrossXBeam (Spatial Compounding), SRI HD (Speckle Reduction Imaging in High Definition), and Coded Harmonics. The system includes workflow features such as Raw Data for post-processing of images, Automatic Optimization, Virtual Convex, and B-Steer, which maneuvers the ultrasound beam for better visualization of the needle (available on linear probes). The system includes SonoBiometry software that allows for automatic measurement of key fetal biometry measurements. The system also includes ScanCoach, a reference tool that can be used during living imaging that displays reference images, animations, and schematics to guide the proper probe placement.

The system can function via wall electrical supply or with a rechargeable battery. The battery life is 45 minutes and the charging time is 2.5 hours. The LOGIQ V2 system is compatible with 7 ultrasound probes that each have different frequency bandwidths and clinical applications.

Proprietary software is included with the system and is available in 14 different languages. Key functionality of the software include operation system, database server, conversion reports into PDF format, data export and import with CD/DVD.

Dimensions: 120x368x396mm;
Weight: 6kg
Temperature/humidity requirements :10-40°C/30-80% RH

Technical Support

Training is provided by a manufacturer representative. The extent of the training providing depends on the user's current knowledge of ultrasound. The system is also equipped with on-board training modules that provide information on settings, operation, connectivity, and maintenance. This feature can be used in areas without internet access.

The user can perform daily routine maintenance on the system with guidance from the on-board training modules. The system requires yearly on-site maintenance by manufacturer technicians or authorized service providers.

Purchase of the device includes a 3 year warranty that includes probes, parts, and labor.

Replacement Components

Spare parts can be purchased from GE or its authorized service providers if the system is no longer covered under warranty.^{Interview with representative}

Lifecycle

The estimated lifetime of the device is 5-10 years.

Manufacturer Specified Performance Parameters

Unknown.

Vetted Performance Status

Unknown.

Safety

Unknown.

Complementary Technical Systems

Unknown.

Academic Research and References

Compliance with regulations

AAMI/ANSI ES60601-1, IEC60601-1-2, IEC60601-2-37, NEMA UD 3, ISO10993-1, NEMA UD 2, ISO14971, NEMA Digital Imaging and Communications in Medicine (DICOM) Set (Radiology), MDS2, CE Marked, FDA 510(k), TUV certified, Japan MHLW, IHE compliant

Evaluation methods

The system has undergone usability testing with clinicians to evaluate ease of use. Other quality assurance measurements that were applied include risk analysis, requirements reviews, design reviews, testing on unit level (module verification), integration testing (system verification), performance testing, safety testing, and stimulated use testing. The technical capability of the equipment for intended objectives has been thoroughly evaluated both in the restricted laboratory environment and unrestricted field environment by GE Healthcare.

Clinical usability studies are being conducted in different institutional settings in Europe, USA, ASEAN, and Japan. (Interview with representative)

Other Information

Designers should also investigate additional guidelines, such as the WHO Manual of diagnostic ultrasound. Designers should also take social factors into consideration, such as the use of ultrasounds for gender-biased sex selection in some parts of the world.