CEI EN IEC 61326-2-6:2022
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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
Published date
01-03-2022
Publisher
Superseded date
22-10-2025
Superseded by
€59.54
Excluding VAT
This Standard specifies the particular requirements regarding electromagnetic compatibility (EMC) for electrical equipment for measurement, control and laboratory use, in relation to medical equipment for in vitro diagnostics (IVD).
| Committee |
CT 65
|
| DocumentType |
Standard
|
| ISBN |
978-2-8322-8983-9
|
| Pages |
26
|
| PublisherName |
Comitato Elettrotecnico Italiano
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| IEC 61326-2-6:2020 | Identical |
| EN IEC 61326-2-6:2021 | Identical |
| ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
| IEEE/ANSI C63.18-2014 | American National Standard Recommended Practice for an On-Site, Ad Hoc Test Method for Estimating Electromagnetic Immunity of Medical Devices to Radiated Radio-Frequency (RF) Emissions from RF Transmitters |
| IEC 60601-1-2:2001+AMD1:2004 CSV | Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic compatibility - Requirements and tests |
| AAMI TIR18:2010 | GUIDANCE ON ELECTROMAGNETIC COMPATIBILITY OF MEDICAL DEVICES IN HEALTHCARE FACILITIES |
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