CEI EN 60601-2-11 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- CEI EN 60601-2-11 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment
- 11
- CEI EN 60601-2-11 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment
- 11.040
- CEI EN 60601-2-11 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment
- 11.040.60
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- IEC 61010-1 Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 1: General requirements - Edition 3.0; Incorporates Corrigendum 1: 05/2011 and Corrigendum 2: 10/2013 (Applies to French Text Only); Includes Interpretation 1: 02/2013
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- IEC CISPR 16-2-3 Specification for radio disturbance and immunity measuring apparatus and methods – Part 2-3: Methods of measurement of disturbances and immunity – Radiated disturbance measurements - Edition 3.2 Consolidated Reprint
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- Картотека зарубежных и международных стандартов
Comitato Elettrotecnico Italiano
Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of gamma beam therapy equipment
N EN 60601-2-11
Annotation
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of GAMMA BEAM THERAPY EQUIPMENT, including MULTI-SOURCE STEREOTACTIC RADIOTHERAPY equipment, hereafter referred to as ME EQUIPMENT.
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.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard.
NOTE See also 4.2 of the general standard.
Автоматический перевод:
Медицинская Часть 2 электрооборудования: Конкретные требования для основной безопасности и существенной производительности гамма оборудования для лучевой терапии
Этот Международный стандарт относится к BASIC SAFETY и ESSENTIAL PERFORMANCE GAMMA BEAM THERAPY EQUIPMENT, включая МУЛЬТИ-SOURCE STEREOTACTIC оборудование RADIOTHERAPY, в дальнейшем именуемый ME EQUIPMENT.



