Ge Yokogawa Medical Systems, Ltd

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Address: Tachihi Bldg No.2 6-1-3 Sakae-cho Tachikawa-shi, Tokyo 190-8586, Japan
Phone: +81-(0422)-534-1370 | Fax: +81-(0422)-534-1372 | Map/Directions >>

Profile: Ge Yokogawa Medical Systems, Ltd provides test and measuring instruments. Our flexray signal analyser captures the desired flexray bus signal by specifying combinations of trigger bit conditions of the frame start, payload preamble, null frame, sync frame, startup frame indicators, frame ID, cycle count and (Payload) data.

FDA Registration Number: 9612283
US Agent: Kirsten Hood / Ge Healthcare
Phone: +1-(262)-501-2034 E-Mail:

8 Products/Services (Click for related suppliers)

• Calibrators

• Computed Tomography X-Ray System (FDA Code: JAK / 892.1750)

A computed tomography x-ray system is a diagnostic x-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same axial plane taken at different angles. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Diagnostic Ultrasonic Transducer (FDA Code: ITX / 892.1570)

A diagnostic ultrasonic transducer is a device made of a piezoelectric material that converts electrical signals into acoustic signals and acoustic signals into electrical signals and intended for use in diagnostic ultrasonic medical devices. Accessories of this generic type of device may include transmission media for acoustically coupling the transducer to the body surface, such as acoustic gel, paste, or a flexible fluid container.

• Nuclear Magnetic Resonance Imaging System (FDA Code: LNH / 892.1000)

A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).

• Specialty Magnetic Resonance Coil (FDA Code: MOS / 892.1000)

• Thermometers

• Ultrasonic Puls-Echo Scanner (FDA Code: IYO / 892.1560)

An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Ultrasonic Pulsed Doppler Imaging System (FDA Code: IYN / 892.1550)

An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.