BAS EN 60601-2-54:2012
Medicinska električna oprema – Dio 2-54: posebni zahtjevi za osnovnu sigurnost i esencijalne performance rendgenske opreme za radiografiju i radioskopiju
Опште информације
Статус: Важећи
Број страна: 74
Језик: Енглески
Издање: 1.
Метода усвајања: Proglašavanje
Датум објаве: 16.11.2012
Технички комитет:
Директива:
93/42/EEC, Медицинска средства
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Апстракт
IEC 60601-2-54:2009 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems intended to be used for projection radiography and radioscopy. The minimum safety requirements specified in this particular standard are considered to provide for a practical degree of safety in the operation of ME equipment for radiography and radioscopy. Requirements for additional provisions for ME equipment for interventional applications are covered by IEC 60601-2-43. IEC 60601-2-54:2009 has been developed for use with the third edition of IEC 60601-1 (2005) and its collateral standards.
IEC 60601-2-54:2009 is about type testing of X-ray systems. For the type test of a given product only one particular standard applies. Thus, IEC 60601-2-28 cannot be used in the type test according to IEC 60601-2-54:2009. The system aspects of the X-ray source integrated into X-ray systems are covered by IEC 60601-2-54:2009.
IEC 60601-2-32 and IEC 60601-2-7, which had been written for use with the second edition of IEC 60601-1 (1988), cannot be used with the third edition of IEC 60601-1 (2005) and IEC 60601-2-54.
The contents of the corrigenda of March 2010 and June 2011 have been included in this copy.
Животни циклус
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Изворни документ и степен усаглашености
- EN 60601-2-54:2009, идентичан
- IEC 60601-2-54:2009, идентичан