IEC 62570:2014

Overview

IEC 62570:2014 is an international standard that establishes the standard practice for marking medical devices and other items intended for use in the magnetic resonance (MR) environment. Developed by IEC Technical Committee 62, in collaboration with ASTM, this standard integrates the unmodified text of ASTM F2503-13 to provide a clear, uniform approach for labeling devices that may be exposed to magnetic resonance imaging (MRI) settings. The main purpose is to enhance safety by defining permanent markings, including specific terms and icons, for items that might present hazards or require special handling in the MR environment.

This standard addresses the need for clear communication to clinicians, technicians, and safety personnel regarding the compatibility and safety conditions for medical devices within MR environments. Importantly, MRI image artifacts caused by such devices are not considered safety hazards and therefore are not covered by this standard.

Key Topics

• Scope and Purpose
  IEC 62570 specifies how to mark medical and other devices that may be introduced into MR environments. It applies to devices used within the spatial reach of the MR magnetic field including static magnetic fields, gradient fields, and radiofrequency fields.

• Marking Requirements
  The standard mandates permanent markings using standard terms such as:

  • MR Safe – indicating no known hazards in MR environment
  • MR Conditional – indicating safety only under specified conditions
  • MR Unsafe – indicating known hazards in the MR environment
    These terms are supplemented by symbols and additional safety information describing the conditions under which the device may be used safely.

• Assessment of Hazards
  The standard refers to evaluating potential magnetically induced displacement forces, torques, and RF-induced heating to determine appropriate MR classification. These assessments are critical for ensuring device safety and usability within varying strengths and configurations of MRI machines.

• Terminology
  Clear definitions are provided for terms such as magnetically induced displacement force, hazard, MR environment, and items that might interact with MR equipment. This promotes consistent understanding among manufacturers, users, and regulatory bodies.

• Safety Communication
  IEC 62570 highlights the importance of clear labeling to convey risk information, ensuring that users are aware of any required restrictions or conditions such as maximum magnetic field strength, SAR limits, and device configurations.

Applications

• Medical Device Manufacturing
  Manufacturers utilize IEC 62570 to label devices intended for use near MRI scanners, such as implants, tools, monitors, and accessories, ensuring adherence to international safety standards.

• Hospital and Clinical Settings
  Healthcare professionals rely on devices marked according to IEC 62570 to prevent accidents or malfunctions triggered by the powerful MR magnetic fields, thereby safeguarding patients and staff.

• Regulatory Compliance
  Marking practices outlined in the standard help meet regulatory requirements globally, facilitating market access and improving device traceability regarding MR safety.

• Risk Management
  Organizations implement IEC 62570 markings as part of broader risk mitigation strategies when integrating new devices into MR environments, protecting against unintended electromagnetic interactions.

Related Standards

IEC 62570 references and complements several related standards to create a comprehensive safety framework:

• ASTM F2052 – Measurement of magnetically induced displacement forces
• ASTM F2119 – Evaluation of MR image artifacts from passive implants
• ASTM F2182 – Measurement of RF-induced heating on or near passive implants
• ASTM F2213 – Measurement of magnetically induced torque on devices
• IEC 60601-2-33 – Particular requirements for safety of MR equipment for medical diagnosis
• ISO 14971 – Application of risk management to medical devices
• ISO/IEC Guide 51 – Guidelines on safety aspects inclusion in standards
• ISO TS 10974 – Assessment of MR safety for active implantable medical devices

These interconnected standards collectively ensure comprehensive safety, performance, and risk evaluation for medical devices used in MR environments.

Keywords: MR safety, medical device marking, IEC 62570, magnetic resonance environment, MRI safety standards, MR conditional, MR safe, MR unsafe, medical device labeling, magnetically induced torque, RF-induced heating, magnetic displacement force, diagnostic imaging equipment.