Hivatkozási szám

MSZ EN 60601-2-43:2011

Dokumentumazonosító

150887

Cím

Gyógyászati villamos készülékek. 2-43. rész: Intervenciós röntgenberendezések alapvető biztonságra és lényeges működésre vonatkozó kiegészítő követelményei (IEC 60601-2-43:2010)

Angol cím

Medical electrical equipment. Part 2-43: Particular requirements for basic safety and essential performance of X-ray equipment for interventional procedures (IEC 60601-2-43:2010)

Alkalmazási terület

Clause 1 of the general standard1) applies, except as follows: 201.1.1 * Scope Replacement: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, hereafter referred to as INTERVENTIONAL X-RAY EQUIPMENT. Its scope excludes, in particular: – equipment for RADIOTHERAPY; – equipment for COMPUTED TOMOGRAPHY; – ACCESSORIES intended to be introduced into the PATIENT; – mammographic X-RAY EQUIPMENT; – dental X-RAY EQUIPMENT. NOTE 1 Examples of RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, for which the use of INTERVENTIONAL X-RAY EQUIPMENT complying with this standard is recommended, are given in Annex AA. NOTE 2 Specific requirements for magnetic navigation devices, and for the use of INTERVENTIONAL X-RAY EQUIPMENT in an operating room environment were not considered in this particular standard; therefore no specific requirements have been developed for these devices or uses. In any case, such devices or uses remain under the general clause requirements. NOTE 3 INTERVENTIONAL X-RAY EQUIPMENT when used in cross-sectional imaging mode (sometimes described as CT-like mode or cone-beam CT) is covered by this particular standard and not by IEC 60601-2-44 [2]2. Additional requirements for operation in CT-like mode or cone-beam CT were not considered in the present standard. INTERVENTIONAL X-RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES, which does not include a PATIENT SUPPORT as part of the system, is exempt from the PATIENT SUPPORT provisions of this standard. If a clause or subclause is specifically intended to be applicable to INTERVENTIONAL X-RAY 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 INTERVENTIONAL X-RAY EQUIPMENT and to ME SYSTEMS, as relevant. NOTE 4 See also 4.2 of the general standard. Túl hosszú

ICS

11.040.50 Röntgenkészülékek

37.040.25 Röntgenfilmek

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2011-01-01

A visszavonás napja

2026-01-09

Forrás

idt EN 60601-2-43:2010/AC:2014; idt EN 60601-2-43:2010; idt IEC 60601-2-43:2010

Előd

MSZ EN 60601-2-43:2001, MSZ EN 60601-2-54:2010

Utód

MSZ EN IEC 60601-2-43:2023

Módosítás

MSZ EN 60601-2-43:2010/A1:2018, MSZ EN 60601-2-43:2010/A2:2020

Kiegészítő információk

SZK-közlemények

2014/10: Helyesbítés; 2018/09: Helyesbítés

Kapcsolódó európai jogszabály

93/42/EGK A TANÁCS 93/42/EGK IRÁNYELVE (1993. június 14.) az orvostechnikai eszközökről (MDV93)

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