I.S. EN IEC 61326-2-6:2021
Current
The latest, up-to-date edition.
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2020)
Hardcopy , PDF
English
02-07-2021
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FOREWORD
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
Annex B (informative) Guide for analysis and assessment for electromagnetic
compatibility
Bibliography
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 EQUIPMENT, taking into account the particularities and specific aspects of this electrical equipment and their electromagnetic environment.
| Committee |
TC 65
|
| DocumentType |
Standard
|
| ISBN |
978-2-8322-8983-9
|
| Pages |
46
|
| ProductNote |
The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| IEC 61326-2-6:2020 | Identical |
| EN IEC 61326-2-6:2021 | Identical |
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