Sterilization of health care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
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Sterilization of health care products — Radiation Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
€225.00
Manufacture of cell-based health care products — Control of microbial risks during processing Amendment 1
€21.00
Sterilization of health care products — Chemical indicators
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001
€56.17
Sterilization of medical devices - Information to be provided by the manufacturer for the reprocessing of resterilizable devices (ISO/DIS 17664:2001); German version prEN ISO 17664:2001
€77.20
Sterilization of medical devices - Requirements for terminally sterilized medical devices to be labelled "Sterile" (includes Amendment A1:1998); German version EN 556:1994 + A1:1998
€48.79
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998); German version EN ISO 11737-2:2000
Corrigenda to DIN EN 552:1994-11 (EN 552:1994/A1:1999)
€0.00
Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices Amendment 1
Aseptic processing of health care products - Part 2: Sterilizing filtration - Amendment 1 (ISO 13408-2:2018/DAM 1:2025); German and English version EN ISO 13408-2:2018/prA1:2025
Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
Sterilization of health care products — Chemical indicators — Part 1: General requirements
