ASTM-F2119 › Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants
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Scope
1.1 This test method characterizes the distortion and signal loss artifacts produced in a magnetic resonance (MR) image by a passive implant (implant that functions without the supply of electrical or external power). Anything not established to be MR-Safe or MR-Conditional is excluded.
1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.4 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Significance and Use
5.1 This test method provides a quantified measure of the image artifact produced under a standard set of scanning conditions.
5.2 This test method applies only to passive implants that have been established to be MR-Safe or MR-Conditional.
Keywords
image artifact; implant; metals for surgical implants; MR compatibility; MRI (magnetic resonance imaging); MR safety;
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13.01 (Medical and Surgical Materials and Devices)
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Document Number
ASTM-F2119-24
Revision Level
2024 EDITION
Status
Current
Modification Type
Reinstated
Publication Date
May 17, 2024
Document Type
Test Method
Page Count
4 pages
Committee Number
F04.15