CEI EN IEC 61326-2-6:2022
Superseded
View Superseded by
Electrical equipment for measurement, control and laboratory use -EMC requirements Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment
Hardcopy , PDF
English
03-01-2022
10-22-2025
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Superseded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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