Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment (IEC 61010-2-101:2018, modified); German version EN IEC 61010-2-101:2022 + A11:2022
Edition 2023-12

Health software - Software life cycle processes (IEC 62A/1235/CDV:2018); German and English version prEN 62304:2018
Edition 2018-06

Medical device software - Software life-cycle processes (IEC 62304:2006 + A1:2015); German version EN 62304:2006 + Cor.:2008 + A1:2015
Edition 2016-10

Health informatics - Device interoperability - Part 20701: Point-of-care medical device communication - Service-oriented medical device exchange architecture and protocol binding (ISO/IEEE 11073-20701:2020); English version EN ISO 11073-20701:2020
Edition 2020-07

Health informatics - Device interoperability - Part 20701: Point-of-care medical device communication - Service oriented medical device exchange architecture and protocol binding
Edition 2020-03

Medical device software - Software life cycle processes
Edition 2006-05

Medical device software - Software life cycle processes
Edition 2015-06

Health informatics - Device interoperability - Part 20701: Point-of-care medical device communication - Service oriented medical device exchange architecture and protocol binding (ISO/IEEE 11073-20701:2020)
Edition 2020-07-01

Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
Edition 2008-12-01

Active implantable medical devices - Part 2-3: Particular requirements for cochlear and auditory brainstem implant systems (german version)
Edition 2010-09-01