EN IEC 60601-2-33:2024

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis EN IEC 60601-2-33:2024

Publication date:   Nov 14, 2024

General information

60.60 Standard published   Sep 20, 2024

CENELEC

CLC/TC 62 Electrical equipment in medical practice

European Norm

11.040.55   Diagnostic equipment

Buying

Published

Language in which you want to receive the document.

Scope

This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MAGNETIC RESONANCE (MR) EQUIPMENT and MAGNETIC RESONANCE (MR) SYSTEMS.
NOTE Where ME EQUIPMENT and ME SYSTEMS are used in the clause headings, this is to be understood to indicate MR EQUIPMENT and MR SYSTEMS.
This document does not cover the application of MR EQUIPMENT beyond the INTENDED USE.
If a clause or subclause is specifically intended to be applicable to MR EQUIPMENT only, or to MR SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to MR EQUIPMENT and to MR SYSTEMS, as relevant.
This document does not formulate additional specific requirements for MR EQUIPMENT or MR SYSTEMS used in INTERVENTIONAL MR EXAMINATIONS.

Life cycle

NOW

PUBLISHED
EN IEC 60601-2-33:2024
60.60 Standard published
Sep 20, 2024