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EVS-EN IEC 61326-2-6:2025

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical electrical equipment

General information

Valid from 01.09.2025
Base Documents
IEC 61326-2-6:2025; EN IEC 61326-2-6:2025
Directives or regulations
None

Standard history

Status
Date
Type
Name
Amendment
EN IEC 61326-2-6:2025/prAA:2025
01.09.2025
Main
15.06.2021
Main

IEC 61326-2-6 applies to the basic safety and essential performance of in vitro diagnostic medical electrical equipment (IVD MEE). IEC 61326-2-6 applies to the basic safety and essential performance of IVD MEE in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted by IVD MEE. Basic safety with regard to electromagnetic disturbances is applied to all IVD MEE.

This edition includes the following significant technical changes with respect to the previous edition:

- Update of the document with respect to test levels and documentation.

IEC 61326-2-6:2025 text has been approved in Europe as EN IEC 61326-2-6:2025 without any changes.

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