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SRPS EN 60601-1-3:2009

Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment

Oct 28, 2009
95.99 Withdrawal of Standard   Aug 27, 2012

General information

95.99     Aug 27, 2012

ISS

N062

European Norm

13.280     11.040.50  

English  

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Scope

This collateral standard applies to X-ray equipment and to subassemblies of such equipment, where radiological images of a human patient are used for diagnosis, planning or guidance of medical procedures. The object of this collateral standard is to establish general requirements for protection against X-radiation in X-ray equipment, in order that the irradiation of the human patient, the operator, staff and members of the public can be kept as low as reasonably achievable, without jeopardizing the benefit of the radiological procedure. Particular standards may specify their appropriate values and/or measures for general requirements specified in this collateral standard. The implementation of the general requirements or the reference to the particular standard instead, shall be justified in the risk management process. This collateral standard considers radiation protection aspects related to X-radiation only. Requirements for the control of the electrical energy used to generate X-radiation, which is also an important aspect of radiation protection, are included in IEC 60601-1 and in particular standards for the safety and essential performance of the equipment concerned. This document cancels and replaces the first edition of IEC 60601-1-3, published in 1994 (which replaced IEC 407 issued in 1973). It constitutes a technical revision. This edition has been restructured and aligned to IEC 60601-1(2005) and focussed on general requirements for RADIATION PROTECTION that apply to all diagnostic X-RAY EQUIPMENT. Requirements particular to specific equipment have been removed and will be covered in particular standards. For a description of the changes, see the mapping in Annex C.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Harmonized

Life cycle

NOW

WITHDRAWN
SRPS EN 60601-1-3:2009
95.99 Withdrawal of Standard
Aug 27, 2012

REVISED BY

PUBLISHED
SRPS EN 60601-1-3:2012

Related project

Adopted from EN 60601-1-3:2008

Regulation

"Сл. гласник РС" бр. 92/2020 Правилник о боверавању мерних уређаја који су саставни део неонаталних и педијатријских инкубатора и реанимационих топлих столова