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sklademVydáno: 1995-10-15
BS EN 61266:1995 Ultrasonics. Hand-held probe Doppler foetal heartbeat detectors. Performance requirements and methods of measurement and reporting

BS EN 61266:1995

Ultrasonics. Hand-held probe Doppler foetal heartbeat detectors. Performance requirements and methods of measurement and reporting

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Označení normy:BS EN 61266:1995
Počet stran:28
Vydáno:1995-10-15
ISBN:0 580 24579 9
Status:Standard
Popis

BS EN 61266:1995


This standard BS EN 61266:1995 Ultrasonics. Hand-held probe Doppler foetal heartbeat detectors. Performance requirements and methods of measurement and reporting is classified in these ICS categories:
  • 11.040.55 Diagnostic equipment

This International Standard IEC 1266 establishes:

  • methods of measurement of performance of a complete ultrasonic hand-held Doppler foetal heartbeat detector (hereinafter referred to as “equipment”);

  • requirements for the performance of equipment;

  • requirements for the reporting of the performance of existing equipment;

  • requirements for the declaration by manufacturers in accompanying literature of aspects of the performance of equipment.

This International Standard is applicable to ultrasonic Doppler foetal heartbeat detectors which generate a single ultrasound beam and consist of a hand-held probe which is applied to the maternal abdomen to obtain information on foetal heart activity by means of the Doppler method using continuous wave (c.w.) or quasi-continuous wave ultrasound. This standard, however, currently does not cover the continuous monitoring devices which generate more than one ultrasound beam and are usually of the type utilising a similar principle of operation but using a flat probe strapped to the patient.

This International Standard is not an equipment design standard.


Applies to detectors which generate a single continuous wave or quasi-continuous wave ultrasonic beam. It does not cover continuous monitoring devices which generate more than one ultrasound beam and use a flat standard probe strapped to a patient. This standard is not an equipment design standard.