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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 September 2007
Status: inactive
Page Count: 1
ICS Code (Electromagnetic compatibility (EMC)): 33.100
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 International Standard IEC 61326-1, this part 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:
AAMI TIR18 - Guidance on electromagnetic compatibility of medical devices in healthcare facilities
Published by AAMI on January 1, 2010
Introduction and scope Because the performance of electronic medical devices can be disrupted by electromagnetic (EM) energy, patient safety can potentially be put at increased risk because of the...
This document is referenced by:
IEC 61298-3 - Process measurement and control devices – General methods and procedures for evaluating performance – Part 3: Tests for the effects of influence quantities
Published by IEC on October 1, 2008
This part of IEC 61298 specifies general methods and procedures for conducting tests and reporting on the functional and performance characteristics of process measurement and control devices. The...
This document is referenced by:
SN EN ISO 18113-5 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
Published by SNV on May 1, 2012
This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for self-testing. This part of ISO 18113 also applies to apparatus and equipment intended...
This document is referenced by:
IEC 62598 - Nuclear instrumentation – Constructional requirements and classification of radiometric gauges
Published by IEC on March 1, 2011
This International Standard applies to the manufacture and installation of electrical measuring systems and instruments utilizing radioactive sources (radiometric gauges, hereinafter called gauges)....
This document is referenced by:
EN 60204-33 - Safety of machinery - Electrical equipment of machines - Part 33: Requirements for semiconductor fabrication equipment
Published by CENELEC on March 1, 2011
This part of IEC 60204 applies to electrical and electronic equipment associated with semiconductor fabrication equipment for the manufacture, measurement, assembly, and test of semiconductors. NOTE...
This document is referenced by:
UL 61010-1 - UL Standard for Safety Electrical Equipment For Measurement, Control, and Laboratory Use; Part 1: General Requirements
Published by UL on May 11, 2012
Equipment included in scope This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical...
This document is referenced by:
BS EN ISO 18113-3 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) Part 3: In vitro diagnostic instruments for professional use
Published by BSI on November 30, 2011
A description is not available for this item.
This document is referenced by:
BS EN ISO 18113-5 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
Published by BSI on November 30, 2011
A description is not available for this item.
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