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Astm fstandard practice for marking medical devices and other items for safety in the magnetic resonance environment significance and use medical devices and other items have caused serious injuries and death for patients and other individuals in the mr environment. This has also been published by iec as standard iec 62570: [ 15] users should update all safety markings in line with the latest version of astm international. Which defines “ an item which poses unacceptable risks. 1 interactions of medical devices and other items with the mr environment has resulted in serious injuries and death of patients and other individuals. 1 this practice applies to medical devices and other items that are anticipated to enter the magnetic resonance ( mr) environment. Standard practice for marking medical devices and other items for safety in the magnetic resonance environment. Based on the results of your assessment, you should label your medical device as mr safe, mr unsafe, or mr conditional, and include the appropriate symbol from astm f2503 and/ or the corresponding term in your labeling. Astm international’ s standard f2503 [ 14] for the marking of devices brought into the mr environment should be used. Note 1: “ medical devices and other items” will be referred to as “ items” for the remainder of this practice.
00 want this as a site license? Adapted from astm f2503- 20. Astm fstandard practice for marking medical devices and other items for safety in the magnetic resonance environment significance and use 4.
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