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Biotronik (BIOTRONIK SE & Co. KG; [1] [2] Biotronik Worldwide) is a limited partnership [1] multi-national cardiovascular biomedical research and technology company, headquartered in Berlin, Germany. The company offers equipment for diagnosis, treatment, and therapy support in the areas of cardiac rhythm management, electrophysiology , and ...
An MRI robot is a medical robot capable of operating within a magnetic resonance imaging (MRI) scanner for the purpose of performing or assisting in image-guided interventions (IGI). IGI are commonly performed manually by physicians operating instruments, such as needles, based on medical images and are used in most medical fields, particularly ...
It was designed to function within the environment of 1.5 and 3.0 tesla intraoperative MRI systems. As neuroArm is MR-compatible, stereotaxy can be performed inside the bore of the magnet with near real-time image guidance. NeuroArm possesses the dexterity to perform microsurgery, outside of the MRI system.
MR-Safe – The device or implant is completely non-magnetic, non-electrically conductive, and non-RF reactive, eliminating all of the primary potential threats during an MRI procedure. MR-Conditional – A device or implant that may contain magnetic, electrically conductive, or RF-reactive components that is safe for operations in proximity to ...
New devices are able to store a total of 60 minutes of recordings on their memory. Thirty minutes is reserved for automatic storage of arrhythmias according to preprogrammed criteria. The remaining 30 minutes can be divided into a selectable number of slots for storage of manually triggered retrograde recordings as an answer to symptoms ...
DICOM is used worldwide to store, exchange, and transmit medical images.DICOM has been central to the development of modern radiological imaging: DICOM incorporates standards for imaging modalities such as radiography, ultrasonography, computed tomography (CT), magnetic resonance imaging (MRI), and radiation therapy.
The ISO 10993 set entails a series of standards for evaluating the biocompatibility of medical devices to manage biological risk. These documents were preceded by the Tripartite agreement and is a part of the international harmonisation of the safe use evaluation of medical devices. [1]
The term "phantom" describes an object that is designed to resemble human tissue and can be evaluated, analyzed or manipulated to study the performance of a medical device. Phantoms are created using a digital file that is rendered through magnetic resonance imaging (MRI) or computer-aided design (CAD).