Back

EVS-EN 61326-2-6:2013

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2012)

General information

Withdrawn from 15.06.2021
Base Documents
IEC 61326-2-6:2012; EN 61326-2-6:2013
ICS Groups
17.220 Electricity. Magnetism. Electrical and magnetic measurements 25.040.40 Industrial process measurement and control 33.100 Electromagnetic compatibility (EMC)
Directives or regulations
None

Standard history

Status
Date
Type
Name
15.06.2021
Main
EVS-EN IEC 61326-2-6:2021
04.07.2013
Main
EVS-EN 61326-2-6:2013
Main
EVS-EN 61326-2-6:2006
In addition to the scope of IEC 61326-1, this part of IEC 61326 series specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic medical equipment, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.

Required fields are indicated with *

*
*
*
PDF
15.86 € incl tax
Paper
15.86 € incl tax
Browse standard from 2.44 € incl tax
Standard monitoring
English (PDF 213 KB)

Related products

Main

EVS-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
Newest version Valid from 15.06.2021
Main

EVS-EN IEC 61326-1:2021

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Newest version Valid from 20.07.2021
Main

EVS-EN 61326-1:2013

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Withdrawn from 20.07.2021
Main

EVS-EN 61508-3:2010

Functional safety of electrical/electronic/programmable electronic safety-related systems - Part 3: Software requirements
Newest version Valid from 06.09.2010

Customers who bought this item also bought

Main

EVS-EN 61326-1:2013

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Withdrawn from 20.07.2021
Main

EVS-EN 61010-2-101:2017

Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for laboratory equipment for in vitro diagnostic (IVD) medical equipment
Withdrawn from 01.12.2022
Main

EVS-EN 61010-1:2010

Safety requirements for electrical equipment for measurement, control and laboratory use - Part 1: General requirements
Newest version Valid from 06.12.2010
Main

EVS-EN ISO 18113-3:2011

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
Withdrawn from 01.07.2024

Standards designation

EVS Estonian standard
EN European standard (published by an CEN or CENELEC)
EN ISO International standard adopted as an European standard
ISO International Organization for Standardization’s standard
IEC International Electrotechnical Commission’s standard
HD CENELEC’s harmonisation document
   
EVS-EN European standard implemented in Estonia
EVS-EN ISO International standard adopted in Europe and implemented in Estonia
EVS-EN ISO/IEC International standard/International electrotechnical standard adopted in Europe and implemented in Estonia
EVS-IEC International electrotechnical standard implemented in Estonia
EVS-ISO International standard implemented in Estonia
   
A, AMD amedment
+A a full standard plus the amendment
/A only amendment
COR, AC corrigendum
+COR a full standard plus the corrigendum
NA national annex
+NA a full standard plus the national annex
/NA only national annex
TS technical specification
TR technical report
CWA agreement, developed by a CEN or CENELEC
prEVS-EN (etc) draft standard
   
et the standard is in Estonian only
en the standard is in English only
et-en the standard is in Parallel text Estonian-English