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DIN EN ISO/IEEE 11073-10471
Health informatics - Device interoperability - Part 10471: Personal health device communication - Device specialization - Independent living activity hub (ISO/IEEE FDIS 11073-10471:2024); English version prEN ISO IEEE 11073-10471:2024
DIN EN ISO/IEEE 11073-10472
Health informatics - Device interoperability - Part 10472: Personal health device communication - Device specialization - Medication monitor (ISO/IEEE FDIS 11073-10472:2024); English version prEN ISO/IEEE 11073-10472:2024
prEN ISO/IEEE 11073-10701
Health informatics - Device interoperability - Part 10701: Point-of-Care Medical Device Communication - Metric Provisioning by Participants in a Service-Oriented Device Connectivity (SDC) System (ISO/IEEE FDIS 11073-10701:2024)
DIN EN IEC 60601-2-19
Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators (IEC 60601-2-19:2020 + AMD1:2023); German version EN IEC 60601-2-19:2021 + A1:2023
DIN EN IEC 80601-2-71
Medical electrical equipment - Part 2-71: Particular requirements for the basic safety and essential performance of functional near-infrared spectroscopy (NIRS) equipment (IEC 62D/2062/CDV:2023); German and English version prEN IEC 80601-2-71:2023
DIN EN IEC 60601-2-21
Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers (IEC 60601-2-21:2020 + AMD1:2023); German version EN IEC 60601-2-21:2021 + A1:2023
DIN EN IEC 60601-2-20
Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators (IEC 60601-2-20:2020 + AMD1:2023); German version EN IEC 60601-2-20:2020 + A1:2023
DIN EN IEC 80601-2-26
Medical electrical equipment - Part 2-26: Particular requirements for the basic safety and essential performance of electroencephalographs (IEC 80601-2-26:2019 + COR1:2021 + AMD1:2024); German version EN IEC 80601-2-26:2020 + AC:2021 + A1:2024
ISO/AWI TS 19844-2
Health informatics - Identification of medicinal products (IDMP) - Implementation guidelines for ISO 11238 for data elements and structures for the unique identification and exchange of regulated information on substances - Part 2: ISO 11238 implementation guidelines for chemical substances
DIN EN IEC 60601-2-76
Medical electrical equipment - Part 2-76: Particular requirements for the basic safety and essential performance of low energy ionized gas haemostasis equipment (IEC 60601-2-76:2018 + AMD1:2023); German version EN IEC 60601-2-76:2019 + A1:2023
