In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media
General requirements for in vitro diagnostic medical devices for self-testing
Performance evaluation of in vitro diagnostic medical devices
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
Medical device software - Software life-cycle processes
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019)
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)
53,361 cadenas de referencia distintas indexadas a partir de instantáneas de fuentes oficiales accesadas el 19 de octubre de 2026. Incluye ediciones anteriores. El índice y las colecciones de publicadores tienen una cobertura diferente. Ver fuentes y cobertura.