Profile: Siemens Medical Solutions - OCS Heidelberg is a manufacturer of multi-leaf collimator. The multi-leaf collimator is used in radiation therapy dose delivery.
28 Products/Services (Click for related suppliers)
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| • Angiographic X-Ray System (FDA Code: IZI / 892.1600) An angiographic x-ray system is a device intended for radiologic visualization of the heart, blood vessels, or lymphatic system during or after injection of a contrast medium. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. |
| • 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 X-Ray Beam Limiting Device (FDA Code: KPW / 892.1610) A diagnostic x-ray beam-limiting device is a device such as a collimator, a cone, or an aperture intended to restrict the dimensions of a diagnostic x-ray field by limiting the size of the primary x-ray beam. |
| • Diagnostic X-Ray High Voltage Generator (FDA Code: IZO / 892.1700) A diagnostic x-ray high voltage generator is a device that is intended to supply and control the electrical energy applied to a diagnostic x-ray tube for medical purposes. This generic type of device may include a converter that changes alternating current to direct current, filament transformers for the x-ray tube, high voltage switches, electrical protective devices, or other appropriate elements. |
| • Diagnostic X-Ray Tube Housing Assembly (FDA Code: ITY / 892.1760) A diagnostic x-ray tube housing assembly is an x-ray generating tube encased in a radiation-shielded housing that is intended for diagnostic purposes. This generic type of device may include high voltage and filament transformers or other appropriate components. |
| • Image-Intensified Fluoroscopic X-Ray System (FDA Code: JAA / 892.1650) An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. |
| • Mammographic X-Ray System (FDA Code: IZH / 892.1710) A mammographic x-ray system is a device intended to be used to produce radiographs of the breast. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. |
| • Mammographic X-Ray System Full Field Digital (FDA Code: MUE / 892.1715) A full-field digital mammography system is a device intended to produce planar digital x-ray images of the entire breast. This generic type of device may include digital mammography acquisition software, full-field digital image receptor, acquisition workstation, automatic exposure control, image processing and reconstruction programs, patient and equipment supports, component parts, and accessories. |
| • Medical Linear Accelerator (FDA Code: IYE / 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. |
| • Mobile Fluoroscopic X-Ray System (FDA Code: IZL / 892.1720) A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. |
| • Mobile X-Ray System (FDA Code: IZL / 892.1720) |
| • 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). |
| • Nuclear Magnetic Resonance Spectroscopic System (FDA Code: LNI / 892.1000) |
| • Powered Non-Tilting Radiographic Table (FDA Code: IZZ / 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. |
| • 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. |
| • Programmable Diagnostic Computer (FDA Code: DQK / 870.1425) A programmable diagnostic computer is a device that can be programmed to compute various physiologic or blood flow parameters based on the output from one or more electrodes, transducers, or measuring devices; this device includes any associated commercially supplied programs. |
| • 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 Treatment Planning System (FDA Code: MUJ / 892.5050) |
| • Radiologic Table (FDA Code: KXJ / 892.1980) |
| • 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 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. |
| • Remote-Controlled Radionuclide Applicator System (FDA Code: JAQ / 892.5700) A remote controlled radionuclide applicator system is an electromechanical or pneumatic device intended to enable an operator to apply, by remote control, a radionuclide source into the body or to the surface of the body for radiation therapy. This generic type of device may include patient and equipment supports, component parts, treatment planning computer programs, and accessories. |
| • Solid State X-Ray Imager (FDA Code: MQB / 892.1680) An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. |
| • Stationary Top Radiographic Table (FDA Code: IXQ / 892.1980) |
| • Stationary X-Ray System (FDA Code: KPR / 892.1680) |
| • Tilting Radiographic Table (FDA Code: IXR / 892.1980) |
| • Urological Extracorporeal Shock-wave Lithotriptor (FDA Code: LNS / 876.5990) An extracorporeal shock wave lithotripter is a device that focuses ultrasonic shock waves into the body to noninvasively fragment urinary calculi within the kidney or ureter. The primary components of the device are a shock wave generator, high voltage generator, control console, imaging/localization system, and patient table. Prior to treatment, the urinary stone is targeted using either an integral or stand-alone localization/imaging system. Shock waves are typically generated using electrostatic spark discharge (spark gap), electromagnetically repelled membranes, or piezoelectric crystal arrays, and focused onto the stone with either a specially designed reflector, dish, or acoustic lens. The shock waves are created under water within the shock wave generator, and are transferred to the patient's body using an appropriate acoustic interface. After the stone has been fragmented by the focused shock waves, the fragments pass out of the body with the patient's urine. |