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IEC 61326-2-6

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

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Organization: IEC
Publication Date: 1 July 2012
Status: inactive
Page Count: 26
ICS Code (Electromagnetic compatibility (EMC)): 33.100
ICS Code (Electrical and electronic testing): 19.080
ICS Code (Electricity. Magnetism. Electrical and magnetic measurements): 17.220
ICS Code (Industrial process measurement and control): 25.040.40
scope:

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.

Document History

IEC 61326-2-6
October 1, 2020
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
In addition to the scope of IEC 61326-1, this part of IEC 61326 specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for IN VITRO DIAGNOSTIC (IVD) MEDICAL...
IEC 61326-2-6
July 1, 2012
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
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...
IEC 61326-2-6
September 1, 2007
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic...
IEC 61326-2-6
December 1, 2005
Electrical equipment for measurement, control and laboratory use – EMC requirements – Part 2-6: Particular requirements – In vitro diagnostic (IVD) medical equipment
In addition to the scope of International Standard IEC 61326-1, this part specifies minimum requirements for immunity and emissions regarding electromagnetic compatibility for in vitro diagnostic...

References

This document references:
ISO 18113-1 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
Published by ISO on December 15, 2009
This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This part of ISO...
This document references:
ISO 14971 - Medical devices - Application of risk management to medical devices
Published by ISO on December 1, 2019
This document specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The process...
This document references:
ANSI C63.18 - Recommended Practice for an on-Site, Ad Hoc Test Method for Estimating Electrimagnetic Immunity of Medical Devices to Radiated Radio-Frequency (RF) Emissions from RF Transmitters
Published by IEEE on January 1, 2014
This recommended practice is a guide to evaluating the electromagnetic immunity of medical devices to radiated radio-frequency (RF) emissions from common RF transmitters (e.g., two-way radios;...
This document is referenced by:
IEC 60794-2-42 - Optical fibre cables - Part 2-42: Indoor optical fibre cables - Product specification for simplex and duplex cables with A4 fibres
Published by IEC on April 1, 2008
This part of IEC 60794 covers simplex and duplex optical fibre cables containing A4 fibres for indoor use. The requirements of the sectional specification IEC 60794-2 are applicable to cables covered...
This document is referenced by:
18113-3 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
Published by ISO on October 1, 2022
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use. This document also applies to apparatus and...
This document is referenced by:
18113-5 - In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
Published by ISO on October 1, 2022
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for self-testing. This document is also applicable to apparatus and...
This document is referenced by:
IEC 61010-2-020 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-020: Particular requirements for laboratory centrifuges
Published by IEC on May 1, 2016
Equipment included in scope This part of IEC 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used....
This document is referenced by:
IEC 61010-2-020 REDLINE - Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-020: Particular requirements for laboratory centrifuges
Published by IEC on May 1, 2016
Equipment included in scope This part of IEC 61010 specifies general safety requirements for the following types of electrical equipment and their accessories, wherever they are intended to be used....
This document is referenced by:
IEC 61326-1 - Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Published by IEC on October 1, 2020
This part of IEC 61326 specifies requirements for immunity and emissions regarding electromagnetic compatibility (EMC) for electrical equipment, operating from a supply or battery of less than 1 000...
This document is referenced by:
IEC 61326-1 - Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Published by IEC on October 1, 2020
This part of IEC 61326 specifies requirements for immunity and emissions regarding electromagnetic compatibility (EMC) for electrical equipment, operating from a supply or battery of less than 1 000...
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