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  • Abstract:
    This part of IEC 60118 covers relevant EMC phenomena for hearing aids. Hearing aid immunity to high frequency fields originating from digital wireless devices such as mobile phones was originally identified as the most relevant EMC phenomena impacting hearing aids.
  • Document number:
    DIN EN IEC 60118-13; VDE 0750-11
  • Issuing date:
    2021-03-01
  • Document type:
    Norm
  • Title:
    Electroacoustics - Hearing aids - Part 13: Requirements and methods of measurement for electromagnetic immunity to mobile digital wireless devices (IEC 60118-13:2019); German version EN IEC 60118-13:2020
  • Replaces:
    DIN EN 60118-13(2012-02); DIN IEC 60118-13(2018-04)
  • Author:
    German Commission for Electrical, Electronic and Information Technologies of DIN and VDE
  • Search term:
    Acoustics; CE marking; Definitions; Digital; Electrical engineering; Electroacoustics; Electromagnetic; Electromagnetic compatibility; Electromagnetism; EMC; Environment; Environmental conditions; Features; Field strength (electric); Frequencies; Frequency ranges; Functions; Hearing aids; High frequencies; Immunity; Interference rejections; Limits (mathematics); Measuring techniques; Measuring uncertainty; Mobile radio systems; Noise sources; Operation; Performance; Specification (approval); Telephones; Test signals; Testing; Transmission characteristics; Wireless
  • Application areas:
    09.05 Medizinische Geräte und Instrumente
  • Hazards:
    AB Terminologische Festlegungen in Normen mit Arbeitsschutzbezug; GH Elektrische, magnetische und elektromagnetische Felder; KE Belastungen durch Funktionsstörungen an Arbeitsmitteln (Ausfall, Bruch, fehlerhafte Montage, Softwarefehler, Störung der Energieversorgung)
  • ICS:
    11.180.15 Aids for deaf and hearing impaired people
  • Price:
    62,88 EUR
  • Cross references:
    IEC 60118-0 (2015-06)<S>; IEC 60318-5 (2006-08)<G>; IEC 61000-4-3 (2020-09)<G>; IEC 61000-4-20 (2022-02)<G>; DIN EN 60118-0 (2016-09); DIN EN IEC 60118-4 (2018-08); DIN EN 60118-7 (2006-08); DIN EN 60118-15 (2012-12); DIN EN 60318-5 (2007-04); DIN EN 61000-4-2 (2009-12); DIN EN 61000-4-8 (2010-11); DIN EN 61000-4-20 (2011-07); CISPR 11 (2015-06); IEC 60118-4 (2014-12); IEC 60118-7 (2005-10); IEC 60118-15 (2012-02); IEC 60601-1-2 (2014-02); IEC 60601-2-66 (2019-10); IEC 61000-4-2 (2008-12); IEC 61000-4-8 (2009-09); DIN EN 60601-1-2 (2022-01); DIN EN IEC 60601-2-66 (2020-09); DIN EN IEC 61000-4-3 (2021-11); ANSI C 63.19 (2019); IEEE C 63.19 (2019); EUV 2017/745 (2017-04-05)
  • Identical with:
    EN IEC 60118-13(2020-04)<IDT>; IEC 60118-13(2019-10)<IDT>
  • Legislation:
    93/42/EWG (1993-06-14)<H>; Medizinprodukterichtlinie; EUB 2021/610 (2021-04-14)
  • Update flag:
    Unchanged