Norm

IEC 60601-2-33:2010+A1:2013+A2:2015 en

Medische elektrische toestellen - Deel 2-33: Bijzondere eisen voor de veiligheid van magnetische-resonantie apparatuur voor medische diagnostiek

623,18

Over deze norm

Status Definitief
Aantal pagina's 58
Commissie Medische elektrische toestellen
Gepubliceerd op 01-06-2015
Taal Engels
IEC 60601-2-33+A1+A2 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MR EQUIPMENT and MR SYSTEMS, hereafter referred to also as ME EQUIPMENT. This standard does not cover the application of MR EQUIPMENT beyond the INTENDED USE. If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME 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 ME EQUIPMENT and to ME SYSTEMS, as relevant. The standard does not formulate specific requirements for MR EQUIPMENT or MR SYSTEMS used in INTERVENTIONAL MR EXAMINATIONS.

Details

ICS-code 11.040.55
Nederlandse titel Medische elektrische toestellen - Deel 2-33: Bijzondere eisen voor de veiligheid van magnetische-resonantie apparatuur voor medische diagnostiek
Engelse titel Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
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