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

F2213-17

Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment

F2182-19e2

Standard Test Method for Measurement of Radio Frequency Induced Heating On or Near Passive Implants During Magnetic Resonance Imaging (Includes all amendments and changes 4/7/2020).

F2503-23e1

Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment (Includes all amendments and changes 10/24/2023).

F2052-21

Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment