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SRPS EN 62570:2016

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

Jan 29, 2016

General information

60.60     Jan 29, 2016

ISS

N062

European Norm

11.040.55     11.040.50  

English  

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Scope

IEC 62570:2014 applies to the practice of marking of items that might be used in the magnetic resonance (MR) environment. The purpose of this practice is to mark items that might be brought into the MR environment and to recommend information that should be included in the marking. The standard specifies the permanent marking of items, which are used in an MR environment, by means of terms and icons. MR image artifacts are not considered to be a performance issue and so are not addressed in this international standard practice. IEC 62570 is integrating the unmodified text of ASTM F2503-13. It has been developed by subcommittee 62B: Diagnostic imaging equipment, of IEC technical committee 62: Medical equipment in medical practice, in collaboration with ASTM.

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

NOW

PUBLISHED
SRPS EN 62570:2016
60.60 Standard published
Jan 29, 2016

REVISED BY

PROJECT
naSRPS EN IEC 62570:2025

Related project

Adopted from EN 62570:2015