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CEI EN 61326-2-6 : 2014

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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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

Available format(s)

Hardcopy , PDF

Language(s)

English - Italian

Published date

01-01-2014

Superseded date

11-04-2022

£39.63
Excluding VAT
Summarise this standard

1 Scope
2 Normative references
3 Terms and definitions
4 General
5 EMC test plan
6 Immunity requirements
7 Emission requirements
8 Test results and test report
9 Instructions for use
Annex A (normative) - Immunity test requirements
                      for portable test and measurement
                      equipment powered by battery or
                      from the circuit being measured
Bibliography
Annex ZA (normative) - Normative references to
                       international publications with their
                       corresponding European publications
Annex ZZ (informative) - Coverage of Essential
                         Requirements of EC Directives

Describes 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.

Committee
CT 65
DevelopmentNote
Classificazione CEI 65-102. To be used in conjunction with CEI EN 61326-1. (02/2007) Supersedes CEI EN 61326. (05/2008)
DocumentType
Standard
Pages
28
PublisherName
Comitato Elettrotecnico Italiano
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
EN 61326-2-6:2013 Identical
IEC 61326-2-6:2012 Identical

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A newer version of this standard is available.

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£39.63
Excluding VAT