Profile: Biosound Esaote, Inc. produces medical ultrasound systems for multiple specialities. We are an ISO 9001, CE MARK certified company. We offer products such as MyLabr70 X Vision, MyLabr50 X Vision, MyLabr40, and MyLabr 30Gold, MyLabr 25Gold & MyLabr 20Plus. The MyLabr 30 CV ultrasound system is an evolutionary step in ultrasound technology. Weighing less than 19 pounds, it is the first compact ultrasound system to deliver premium console performanceOur MyLab™50 offers premium performance for cardiac and general imaging ultrasound scanning. Our transducers are designed using advanced manufacturing processes that allow a wide bandwidth to be achieved.
The company was founded in 1979, has revenues of USD 25-50 Million, has ~80 employees.
FDA Registration Number: 1826555
21 Products/Services (Click for related suppliers)
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• Abdominal Ultrasonic Scanner |
• Complete Echocardiography Systems |
• Contract Manufacturers |
• 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. |
• Echocardiograph (FDA Code: DXK / 870.2330) An echocardiograph is a device that uses ultrasonic energy to create images of cardiovascular structures. It includes phased arrays and two-dimensional scanners. |
• Electrocardiograph (FDA Code: DPS / 870.2340) An electrocardiograph is a device used to process the electrical signal transmitted through two or more electrocardiograph electrodes and to produce a visual display of the electrical signal produced by the heart. |
• Medical Imaging |
• Medical Imaging Kits |
• Medical Ultrasound Devices |
• Mobile Obstetrical/Gynecological Ultrasonic Scanner |
• 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). |
• Portable Echocardiography Systems |
• Radiological Digital Image Communication System (FDA Code: LMD / 892.2020) A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol. |
• Radiological Image Processing System (FDA Code: LLZ / 892.2050) A picture archiving and communications system is a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital processing of medical images. Its hardware components may include workstations, digitizers, communications devices, computers, video monitors, magnetic, optical disk, or other digital data storage devices, and hardcopy devices. The software components may provide functions for performing operations related to image manipulation, enhancement, compression or quantification. |
• Small Parts Ultrasonic Scanner |
• Specialty Magnetic Resonance Coil (FDA Code: MOS / 892.1000) |
• 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. |
• Ultrasound Transducers |
• Ultrasounds |
• Ultrasounds |