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SRPS EN IEC 61326-2-6:2021

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

Jun 30, 2021

General information

60.60     Jun 30, 2021

ISS

N065

European Norm

17.220     25.040.40     33.100     17.220.20     33.100.20  

English  

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Scope

<!-- NEW! -->IEC 61326-2-6:2020 is available as <a href="https://webstore.iec.ch/publication/67814">IEC 61326-2-6:2020 RLV</a> which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.</br></br>IEC 61326-2-6:2020 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for IN VITRO DIAGNOSTIC (IVD) MEDICAL EQUIPMENT, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.

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.

98/79/EC

In vitro diagnostic medical devices

Directive 98/79/EC
2014/30/EU

Directive 2014/30/EU of the European Parliament and of the Council of 26 February 2014 on the harmonisation of the laws of the Member States relating to electromagnetic compatibility (recast)

Directive 2014/30/EU

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN 61326-2-6:2013

NOW

PUBLISHED
SRPS EN IEC 61326-2-6:2021
60.60 Standard published
Jun 30, 2021

REVISED BY

PROJECT
dnaSRPS EN IEC 61326-2-6:2025

Related project

Adopted from EN IEC 61326-2-6:2021

Adopted from IEC 61326-2-6:2020 ED3 IDENTICAL