ASTM-F2119 Historical Revision Information
Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants

ASTM-F2119 - 2007 R13 EDITION - CANCELLED
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Standard Test Method for Evaluation of MR Image Artifacts from Passive Implants (Withdrawn 2022)
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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.

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; MRI (magnetic resonance imaging); MR compatibility; MR safety

To find similar documents by ASTM Volume:

13.01 (Medical and Surgical Materials and Devices)

To find similar documents by classification:

11.040.40 (Implants for surgery, prosthetics and orthotics Including pacemakers Ophthalmic implants, see 11.040.70)

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Document Number

ASTM-F2119-07(2013)

Revision Level

2007 R13 EDITION

Status

Cancelled

Modification Type

Withdrawn

Publication Date

March 15, 2013

Document Type

Test Method

Page Count

4 pages

Committee Number

F04.15