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ASTM F2119

Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants

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Organization: ASTM
Publication Date: 1 September 2007
Status: inactive
Page Count: 4
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40
scope:

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.

Document History

ASTM F2119
September 1, 2007
Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants
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...
ASTM F2119
September 1, 2007
Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants
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...
ASTM F2119
June 10, 2001
Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants
Scope 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...

References

This document references:
ASTM F2052 - Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment
Published by ASTM on September 15, 2015
This test method covers the measurement of the magnetically induced displacement force produced by static magnetic field gradients on medical devices and the comparison of that force to the weight of...
This document references:
ASTM F2182 - Standard Test Method for Measurement of Radio Frequency Induced Heating On or Near Passive Implants During Magnetic Resonance Imaging
Published by ASTM on September 15, 2019
This test method covers measurement of radio frequency (RF)-induced heating on or near a passive medical implant within a phantom during magnetic resonance imaging (MRI). The test method does not...
This document references:
ASTM F2182 - Standard Test Method for Measurement of Radio Frequency Induced Heating On or Near Passive Implants During Magnetic Resonance Imaging
Published by ASTM on September 15, 2019
This test method covers measurement of radio frequency (RF)-induced heating on or near a passive medical implant within a phantom during magnetic resonance imaging (MRI). The test method does not...
This document references:
ASTM F2213 - Standard Test Method for Measurement of Magnetically Induced Torque on Medical Devices in the Magnetic Resonance Environment
Published by ASTM on September 1, 2017
This test method covers the measurement of the magnetically induced torque produced by the static magnetic field in the magnetic resonance environment on medical devices and the comparison of that...
This document references:
ASTM F2503 - Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment
Published by ASTM on February 1, 2020
This international standard applies to the practice of marking of items that might be used in the magnetic resonance (MR) environment. The purpose of this practice is to mark items that might be...
This document is referenced by:
ISO TS 10974 - Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device
Published by ISO on April 1, 2018
intended to be used in patients who undergo a magnetic resonance scan in 1,5 T, cylindrical (circular or elliptical cross-section) bore, whole body MR scanners operating at approximately 64 MHz with...
This document is referenced by:
SN EN ISO 25539-3 - Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
Published by SNV on March 1, 2012
This part of ISO 25539 specifies requirements for vena cava filters, based upon current medical knowledge. With regard to safety, it gives requirements for intended performance, design attributes,...
This document is referenced by:
EN ISO 25539-3 - Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
Published by CEN on December 1, 2011
This part of ISO 25539 specifies requirements for vena cava filters, based upon current medical knowledge. With regard to safety, it gives requirements for intended performance, design attributes,...
This document is referenced by:
BS EN ISO 25539-2 - Cardiovascular implants - Endovascular devices Part 2: Vascular stents
Published by BSI on October 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 25539-3 - Cardiovascular implants - Endovascular devices Part 3: Vena cava filters
Published by BSI on March 31, 2012
A description is not available for this item.
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