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SRPS EN IEC 62570:2026

Standard practice for marking medical devices and other items for safety in the magnetic resonance environment

Jul 31, 2026

General information

60.60     Jul 31, 2026

ISS

N062

European Norm

11.040.50     11.040.55  

English  

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Scope

IEC 62570:2025 applies to medical devices and other items that are anticipated to enter the magnetic resonance (MR) environment.

This document specifies the marking of items anticipated to enter the MR environment by means of terms and icons, and recommends information that should be included in the labeling.

MR image artifacts are not in the scope of the mandatory portions of this practice because they do not present a direct safety issue resulting from specific characteristics of the MR examination.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Life cycle

PREVIOUSLY

PUBLISHED
SRPS EN 62570:2016

NOW

PUBLISHED
SRPS EN IEC 62570:2026
60.60 Standard published
Jul 31, 2026

Related project

Adopted from EN IEC 62570:2025 IDENTICAL

Adopted from IEC 62570:2025 ED2 IDENTICAL