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ÖVE/ÖNORM EN 60601-2-26:2016-03
Medical electrical equipment -- Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs (IEC 60601-2-26:2012) (english version)
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Разработчик:
Зарубежные/ON
ICS:
11.040.55 Diagnostic. Including medical monitoring equipment, medical thermometers and related materials / Диагностическое оборудование. Включая медицинскую контрольную аппаратуру, медицинские термометры и связанные с ними материалы11.040.99 Other medical equipment / Медицинское оборудование прочее
Описание
201.1 Scope, object and related standards
Clause 1 of the general standard1 applies, except as follows:
201.1.1 * Scope
Replacement:
This particular standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of
ELECTROENCEPHALOGRAPHS (EEG) as defined in 201.3.63, hereafter referred to as
ME EQUIPMENT. This standard is applicable to ME EQUIPMENT used in a clinical environment
(e.g., hospital, physician’s office, etc.).
This standard does not cover requirements for other equipment used in
electroencephalography such as:
– phono-photic stimulators;
– electroencephalographic telemetry;
– EEG data storage and retrieval;
– ME EQUIPMENT particularly intended for monitoring during electro-convulsive therapy;
– ambulatory electroencephalographic recorders.
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.