Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment (IEC 62D/1847/CDV:2021); German and English version EN 60601-2-6:2015/prA2:2021

Medical electrical equipment - Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment (IEC 62D/1856/CDV:2021); German and English version EN IEC 60601-2-75:2019/prA1:2021

Medical electrical equipment - Part 2-45: Particular requirements for the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices (IEC 62B/1271/CDV:2022); German and English version EN 60601-2-45:2011/prA2:2022

Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy (IEC 62B/1251/CDV:2021); German and English version prEN IEC 60601-2-54:2021

Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment (IEC 62D/1931/CDV:2022); German and English version EN IEC 60601-2-83:2020/prA1:2022

Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery (IEC 62D/1914/CD:2021); Text in German and English

Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use (IEC 76/696/CD:2021); Text in German and English

Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 62D/1944/CDV:2022); German and English version EN IEC 60601-2-2:2018/prA1:2022

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1 (ISO 15223-1:2021/DAM 1:2024); German and English version EN ISO 15223-1:2021/prA1:2024