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BS EN IEC 61326-2-6:2021

$102.76

Electrical equipment for measurement, control and laboratory use. EMC requirements – Particular requirements. In vitro diagnostic (IVD) medical equipment

Published By Publication Date Number of Pages
BSI 2021 22
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IEC 61326-2-6:2020 is available as IEC 61326-2-6:2020 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.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.

PDF Catalog

PDF Pages PDF Title
2 undefined
5 Annex ZA(normative)Normative references to international publicationswith their corresponding European publications
7 English
CONTENTS
8 FOREWORD
10 1 Scope
2 Normative references
3 Terms and definitions
12 4 General
5 EMC test plan
5.1 General
5.2 Configuration of EUT during testing
5.3 Operation conditions of EUT during testing
5.4 Specification of functional performance
5.5 Test description
6 Immunity requirements
6.1 Conditions during the tests
13 6.2 Immunity test requirements
14 Table 101 – Immunity test requirements for equipment intended to be used in professional healthcare facility environment
15 Table 102 – Immunity test requirements for equipment intended to be used in a home healthcare environment
16 6.3 Random aspects
6.4 Performance criteria
Table 103 – Immunity test requirements for equipment intended to be used in a home healthcare environment
17 7 Emission requirements
8 Test results and test report
9 Instructions for use
19 Annex A (normative) Immunity test requirements for portable test and measurement equipment powered by battery or from the circuit being measured
20 Annex B (informative) Guide for analysis and assessment for electromagnetic compatibility
21 Bibliography
BS EN IEC 61326-2-6:2021
$102.76