IEC 60645-7:2025
Electroacoustics - Audiometric equipment - Part 7: Instruments for the measurement of auditory evoked potentials
Electroacoustics - Audiometric equipment - Part 7: Instruments for the measurement of auditory evoked potentials
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Количество страниц:
- 20
- Дата публикации:
- 22 августа 2025 г.
- Издание:
- IEC IS 60645 edition 2 version 1
- ICS:
- 17.140.50
IEC 60645-7:2025 applies to instruments designed for the measurement of auditory evoked potentials from the inner ear, the auditory nerve, and the brainstem, evoked by either acoustic or vibratory stimuli of short duration. This document defines the characteristics to be specified by the manufacturer, specifies performance requirements for two types of instruments (screening and diagnostic/clinical), and specifies the functions to be provided on these types. It also specifies a means of describing the physical characteristics, in terms of electrical waveforms, of audiometric reference and test signals of short duration used with auditory evoked potential equipment and other equipment (e.g. otoacoustic emission instruments), and methods for their measurement. The purpose of this document is to ensure that measurements made under comparable test conditions with different instruments complying with this document will be consistent. This document is not intended to restrict development or incorporation of new features, nor to discourage innovative approaches. Evoked response measurement using the application of electric stimuli to a subject is beyond the scope of this document.
Abstract
Overview
IEC 60645-7:2025 - "Electroacoustics - Audiometric equipment - Part 7: Instruments for the measurement of auditory evoked potentials" specifies requirements for instruments that measure auditory evoked potentials (AEPs) from the inner ear, auditory nerve and brainstem, evoked by short-duration acoustic or vibratory stimuli. The standard defines manufacturer-declared characteristics, performance requirements for two instrument classes (screening and diagnostic/clinical), stimulus and reference-signal descriptions (electrical waveforms), calibration and measurement methods, and verification of measurement uncertainty. The document is designed to ensure consistent, comparable AEP measurements across compliant instruments while allowing innovation. Note: AEPs evoked by applied electrical stimulation are outside the scope.
Key topics and technical requirements
- Instrument classes: performance and functional requirements for screening and diagnostic/clinical AEP instruments.
- Measuring system: units, measurement ranges and time resolution for AEP recordings.
- Stimulus system: general requirements and supported stimulus types (clicks, tone-bursts, broadband and octave‑band chirps, and vibratory stimuli of short duration).
- Reference signals: electrical waveform definitions and measurement methods for reference click, tone-burst, broadband chirp and octave‑band chirps.
- Test quality assurance: recording conditions, automated response detection, and quality estimates to support reliable results.
- Calibration & measurement: procedures for short‑duration signals and periodic calibration requirements, including maximum permitted expanded uncertainty of measurement (Umax).
- Presentation & documentation: required presentation of results and documentation of test conditions, parameters and outcomes.
- General requirements: marking, instruction manuals, safety, immunity to power/RF fields, warm‑up, and environmental/voltage-variation performance.
- Conformity demonstration: methods to show compliance (tolerance vs acceptance limits and uncertainty considerations).
Practical applications and users
IEC 60645-7:2025 is intended for:
- Manufacturers of audiometric and AEP measurement systems (product specification and design verification).
- Clinical engineers and medical device test laboratories performing calibration and conformity testing.
- Audiology clinics and hospitals using screening or diagnostic AEP instruments for objective hearing assessment.
- Regulators and procurement teams defining performance criteria for medical audiometric equipment.
The standard helps ensure reproducible AEP recordings for newborn hearing screening, neuro‑audiological assessment and clinical diagnostic workflows when acoustic or vibratory short‑duration stimuli are used.
Related standards
Key normative references include IEC 60601‑1, IEC 60645‑1, the IEC 60318 series (head/ear simulators and couplers), ISO 389‑6 (reference thresholds for short‑duration test signals) and ISO/IEC Guide 98‑3 (GUM: uncertainty of measurement).
Технические детали
- Технический комитет
- TC 29 - Electroacoustics
- SKU
- IEC 60645-7:2025
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