ASTM F2503-08 - 1.10.2008
 
Significance and Use

Medical devices and other items have caused serious injuries and death for patients and other individuals in the MR environment.

This practice provides a uniform system for marking to indicate the MR conditions that have been determined to be acceptable for a medical device or other item. It provides simple visual icons and terms which are intended to reduce injuries and other mishaps that occur when items that pose hazards in the MR environment are brought into the MR environment.

 
1. Scope
p id="s00002">1.1 This practice covers the marking of medical devices and other items to indicate their safety in the magnetic resonance (MR) environment.

1.2 The purpose of this practice is to (1) recommend that items that may be brought into the MR environment be permanently marked to indicate the MR environment to which a specific item may safely be exposed, and (2) recommend information that should be included in the marking. It is recognized that direct marking on the item is not practical for implants and certain other medical devices. Where direct marking is not practical, this practice recommends that the marking be included in the labeling and on patient information cards (see 7.1).

1.3 Image artifact is not considered to be a safety issue and so is not addressed in this practice (see X1.5).

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

1.5 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 and health practices and determine the applicability of regulatory limitations prior to use.

 
2. Referenced Documents

IEC 60601-2-33

Medical Electrical Equipment--Part 2-33: Particular Requirements for the Safety of Magnetic Resonance Equipment for Medical Diagnosis Available from International Electrotechnical Commission (IEC), 3, rue de Varemb, P.O. Box 131, CH-1211 Geneva 20, Switzerland, http://www.iec.ch.

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).

F2052-21

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

F2119-07

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

ISO 14971

Medical Devices--Application of Risk Management to Medical Devices Available from American National Standards Institute (ANSI), 25 W. 43rd St., 4th Floor, New York, NY 10036, http://www.ansi.org.

ISO/IEC Guide 51

Safety Aspects--Guidelines for their Inclusion in Standards

ISO TS 10974

Assessment of the Safety of Magnetic Resonance Imaging for Patients with an Active Implantable Medical Device