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Normas BSI – AENOR
BS EN 60601-2-47:2001, IEC 60601-2-47:2001

BS EN 60601-2-47:2001, IEC 60601-2-47:2001

Medical electrical equipment. Particular requirements for safety. Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems

Fecha Anulación:
2018-07-17 /Withdrawn
Comité:
CH/62/4
Equivalencias internacionales:

IEC 60601-2-47:2001

Relación con otras normas BSI:

Reemplazada por: BS EN 60601-2-47:2015

Resumen:
Specifies the particular safety requirements for ambulatory electrocardiographic systems. Within the scope of this standard are systems of the following types: a) systems that provide continuous recording and continuous analysis of the ECG allowing full re-analysis giving essentially similar results. The systems may first record and store the ECG and analyse it later on a separate unit, or record and analyse the ECG simultaneously. The type of storage media used is irrelevant with regard to this standard; b) systems that provide continuous analysis and only partial or limited recording not allowing a full re-analysis of the ECG. The safety aspects of this standard apply to all types of systems falling in one of the above- mentioned categories.
Keywords:
Measuring instruments, Performance, Electrical medical equipment, Electrocardiographs, Safety measures, Electrical equipment, Safety engineering, Electrical safety, Electronic equipment and components, Medical equipment
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Formato digital

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