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Neuromag Ltd.


Address: Elimaenkatu 22-A, Helsinki Media 00040, Finland
Phone: +358-(756)-24012 | Map/Directions >>
 
 

Profile: Neuromag Ltd. manufactures magnetoencephalographs.

FDA Registration Number: 9680891
US Agent: Thomas Valentine / Elekta Inc.
Phone: +1-(770)-670-2548  Fax: +1-(770)-729-1585  E-Mail:

18 Products/Services (Click for related suppliers)  
• Data Processing Module for Clinical use (FDA Code: JQP / 862.2100)
A calculator/data processing module for clinical use is an electronic device intended to store, retrieve, and process laboratory data.
• Depth Electrodes (FDA Code: GZL / 882.1330)
A depth electrode is an electrode used for temporary stimulation of, or recording electrical signals at, subsurface levels of the brain.
• 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.
• Electroencephalographs (FDA Code: GWQ / 882.1400)
An electroencephalograph is a device used to measure and record the electrical activity of the patient's brain obtained by placing two or more electrodes on the head.
• Medical Charged-Particle Radiotherapy Unit (FDA Code: LHN / 892.5050)
A medical charged-particle radiation therapy system is a device that produces by acceleration high energy charged particles (e.g., electrons and protons) intended for use in radiation therapy. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts, and accessories.
• Medical Linear Accelerator (FDA Code: IYE / 892.5050)
• Neurological Stereotaxic Instrument (FDA Code: HAW / 882.4560)
A stereotaxic instrument is a device consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal cord, or other part of the nervous system.
• Powered Radiation Therapy Couch (FDA Code: JAI / 892.5770)
A powered radiation therapy patient support assembly is an electrically powered adjustable couch intended to support a patient during radiation therapy.
• Radiation Therapy Beam Shaping Block (FDA Code: IXI / 892.5710)
A radiation therapy beam-shaping block is a device made of a highly attenuating material (such as lead) intended for medical purposes to modify the shape of a beam from a radiation therapy source.
• Radiation Therapy Simulation System (FDA Code: KPQ / 892.5840)
A radiation therapy simulation system is a fluoroscopic or radiographic x-ray system intended for use in localizing the volume to be exposed during radiation therapy and confirming the position and size of the therapeutic irradiation field produced. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts, and accessories.
• Radiation Therapy Treatment Planning System (FDA Code: MUJ / 892.5050)
• Radiofrequency Lesion Generator (FDA Code: GXD / 882.4400)
A radiofrequency lesion generator is a device used to produce lesions in the nervous system or other tissue by the direct application of radiofrequency currents to selected sites.
• Radiographic Head Holder (FDA Code: IWY / 892.1920)
A radiographic head holder is a device intended to position the patient's head during a radiographic procedure.
• Radiological Digital Image Storage Device (FDA Code: LMB / 892.2010)
A medical image storage device is a device that provides electronic storage and retrieval functions for medical images. Examples include devices employing magnetic and optical discs, magnetic tape, and digital memory.
• 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.
• Radionuclide Radiation Therapy System (FDA Code: IWB / 892.5750)
A radionuclide radiation therapy system is a device intended to permit an operator to administer gamma radiation therapy, with the radiation source located at a distance from the patient's body. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts (including beam-limiting devices), and accessories.
• Stationary Top Radiographic Table (FDA Code: IXQ / 892.1980)
A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be electrically powered.
• Table Operating Room Accessories (FDA Code: FWZ / 878.4950)
A manual operating table and accessories and a manual operating chair and accessories are nonpowered devices, usually with movable components, intended to be used to support a patient during diagnostic examinations or surgical procedures.

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