ASTM F2119-07(2013) - 1.3.2013 | ||||||||
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. | ||||||||
1. 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. | ||||||||
2. Referenced Documents | ||||||||
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