Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2024
Edition 2024-09

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022); German version EN ISO 18113-1:2024
Edition 2024-10

Microbiology of the food chain - Method validation - Part 2: Protocol for the validation of alternative (proprietary) methods against a reference method (ISO 16140-2:2016 + Amd 1:2024); German version EN ISO 16140-2:2016 + A1:2024
Edition 2025-07

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices; German version EN 556-2:2024
Edition 2025-01

Requirements for professional profiles related to personal data processing and protection; German version EN 17740:2023
Edition 2024-04

Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German version EN ISO 17664-2:2023
Edition 2024-04

Gas infrastructure - Pipelines for maximum operating pressure over 16 bar - Functional requirements; German version EN 1594:2024
Edition 2024-05

Non-active surgical implants - General requirements (ISO 14630:2024); German version EN ISO 14630:2024
Edition 2025-03

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing; German version EN 14180:2025
Edition 2025-08

Medical laboratories - Concepts and specifications for the design, development, implementation and use of laboratory-developed tests (ISO 5649:2024); German version EN ISO 5649:2024
Edition 2025-04