Standard

NEK IEC 61326-2-6:2020

Oct 2020 Withdrawn

Note: This standard has a new edition: NEK IEC 61326-2-6:2025

Corrigenda and amendments are bought separately.

Language English

Services Read Online (No printing ) kr 1 303,00 Printed and bound Delivery time: 5-10 days kr 1 629,00

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Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment Withdrawn NEK IEC 61326-2-6:2020 RLV Redline Publication date: Oct 2020 Language: English Services: Read Online (No printing ), Printed and bound

There are no available corrigendum or amendments for this standard. Any future corrigendum and amendments will be added automatically for subscribers.

Abstract

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.

Document information

Standard from NEK
Published: 28 October 2020
Withdrawn: 18 June 2025
Edition: 3.0
Version: 1
Document type: NAT
ISBN:

ICS 17.220.20
ICS 25.040.40
ICS 33.100.20

Product Relations

Replaced by: NEK IEC 61326-2-6:2025
Replaces: NEK IEC 61326-2-6:2012
Adopted from: IEC 61326-2-6:2020

NEK IEC 61326-2-6:2020

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NEK IEC 61326-2-6:2025