ASTM-F2052 Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment

ASTM-F2052 - 2021 EDITION - CURRENT
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Standard Test Method for Measurement of Magnetically Induced Displacement Force on Medical Devices in the Magnetic Resonance Environment
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Scope

1.1 This test method covers the measurement of the magnetically induced displacement force produced by static magnetic field gradients (spatial field gradient) on medical devices and the comparison of that force to the weight of the medical device.

1.2 This test method does not address other possible safety issues which include, but are not limited to: issues of magnetically induced torque, radiofrequency (RF) heating, induced heating, acoustic noise, interaction among devices, and the functionality of the device and the magnetic resonance (MR) system.

1.3 This test method is intended for devices that can be suspended from a string. Devices which cannot be suspended from a string are not covered by this test method. The weight of the string from which the device is suspended during the test must be less than 1 % of the weight of the tested device.

1.4 This test method shall be carried out in a horizontal bore MR system with a static magnetic field oriented horizontally and parallel to the MR system bore.

1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.6 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.

1.7 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 is one of those required to determine if the presence of a medical device may cause injury to individuals during an MR examination or in the MR environment. Other safety issues which should be addressed include, but may not be limited to: magnetically induced torque (see Test Method F2213) and radiofrequency (RF) heating (see Test Method F2182). The terms and icons in Practice F2503 should be used to mark the device for safety in the magnetic resonance environment.

5.2 If the maximum magnetically induced displacement force for the specified magnetic field conditions (see Appendix X3) is less than the force on the device due to gravity (its weight), it is assumed that any risk imposed by the application of the magnetically induced force is no greater than any risk imposed by normal daily activity in the Earth’s gravitational field. This statement does not constitute an acceptance criterion; it is provided as a conservative reference point. It is possible that a greater magnetically induced displacement force can be acceptable and would not harm a patient or other individual in a specific case.

Note 2: For instance, in the case of an implanted device that is or could be subjected to a magnetic displacement force greater than the force due to gravity, the location of the implant, surrounding tissue properties, and means of fixation within the body may be considered. For a non-implanted device with a magnetically induced force greater than the gravitational force, consideration should be given to mitigate the projectile risk which may include fixing or tethering the device or excluding it from the MR environment so that it does not become a projectile.

5.3 The maximum static magnetic field strength and spatial field gradient vary for different MR systems. Appendix X3 provides guidance for calculating the allowable static magnetic field strength and spatial field gradient.

5.4 This test method alone is not sufficient for determining if a device is safe in the MR environment.

Keywords

medical device; metals (for surgical implants and medical devices); MRI (magnetic resonance imaging); 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-F2052-21

Revision Level

2021 EDITION

Status

Current

Modification Type

Revision

Publication Date

Jan. 17, 2022

Document Type

Test Method

Page Count

10 pages

Committee Number

F04.15