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prEN IEC 60601-2-33:2021

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis

Üldinfo
Kavand
Alusdokumendid
IEC 60601-2-33 Ed.4.0; prEN IEC 60601-2-33:2021
Tegevusala (ICS grupid)
11.040.55 Diagnostikaseadmed
Direktiivid või määrused
puuduvad
Standardi ajalugu
Staatus
Kuupäev
Tüüp
Nimetus
01.04.2019
Põhitekst + muudatus
06.12.2016
Muudatus
04.04.2016
Parandus
06.10.2015
Muudatus
08.06.2015
Muudatus
02.11.2011
Muudatus
06.12.2010
Põhitekst
06.12.2010
Parandus
This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS. NOTE Where ME EQUIPMENT and ME SYSTEMS are used in the clause headings, this is to be understood to indicate MR EQUIPMENT and MR SYSTEMS. This document does not cover the application of MR EQUIPMENT beyond the INTENDED USE. If a clause or subclause is specifically intended to be applicable to MR EQUIPMENT only, or to MR SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to MR EQUIPMENT and to MR SYSTEMS, as relevant. This document does not formulate additional specific requirements for MR EQUIPMENT or MR SYSTEMS used in INTERVENTIONAL MR EXAMINATIONS.
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