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MSZ EN IEC 60522-1:2021

Dokumentumazonosító

677153

Cím

Gyógyászati villamos készülékek. Diagnosztikai röntgenberendezések. 1. rész: A minőség-egyenértékű szűrés és az állandó szűrés meghatározása (IEC 60522-1:2020)

Angol cím

Medical electrical equipment. Diagnostic X-rays. Part 1: Determination of quality equivalent filtration and permanent filtration (IEC 60522-1:2020)

Alkalmazási terület

This document applies to X-RAY TUBE ASSEMBLIES and to FILTERING MATERIAL, in medical diagnostic applications up to a HIGH VOLTAGE of 150 kV. For HIGH VOLTAGES greater than 50 kV, this document applies to X-RAY TUBE ASSEMBLIES with tungsten or tungsten-alloy TARGETS only. NOTE 1 The FILTERING MATERIAL in the X-RAY BEAM can be removable or irremovable; it can be positioned in any orientation or can have any shape (e.g. tapering thickness) – although usually plane-parallel material, perpendicular to the REFERENCE AXIS is applied. Examples of FILTERING MATERIALS are ADDED FILTERS, a PATIENT table (in case of an under-table X-RAY TUBE ASSEMBLY), materials in the BEAM LIMITING DEVICE, or a breast COMPRESSION DEVICE. NOTE 2 The methodology and statement of compliance given in this document is for flat FILTERS only, but the methodology can be used for any kind of non-flat FILTER. In that case further data are included in order to produce useful results, e.g. field size, geometry/position of FILTER, etc. This document defines the concept of PERMANENT FILTRATION of X-RAY TUBE ASSEMBLIES, and it defines the term FILTERING MATERIAL. Methods are given to determine the PERMANENT FILTRATION of an X-RAY TUBE ASSEMBLY and for determining the QUALITY EQUIVALENT FILTRATION of FILTERING MATERIALS. It contains requirements for statements of compliance of X-RAY TUBE ASSEMBLIES in ACCOMPANYING DOCUMENTS and for markings on X-RAY TUBE ASSEMBLIES, and for indications and statements of compliance of FILTERING MATERIAL. NOTE 3 This document does not contain requirements for any specific values of PERMANENT FILTRATION. For X-RAY EQUIPMENT used for diagnostic purposes, FILTRATION requirements are given in e.g. IEC 60601-1-3:2008 and IEC 60601-1-3:2008/AMD1:2013 or in the applicable particular standard. NOTE 4 The method of determination described in this document is suitable as a type test. It is not intended as a test to be applied by the USER.

ICS

11.040.50 Röntgenkészülékek

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2021-07-01

Forrás

idt EN IEC 60522-1:2021; idt IEC 60522-1:2020

Előd

MSZ EN 60522:1999

Utód

Módosítás

SZK-közlemények

Kapcsolódó európai jogszabály

A szabvány

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