NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 11138-7 [CURRENT] references following documents:
Document number | Edition | Title |
---|---|---|
DIN EN ISO 11138-1 | 2017-07 | Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2017); German version EN ISO 11138-1:2017 More |
DIN EN ISO 11138-2 | 2017-07 | Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2017); German version EN ISO 11138-2:2017 More |
DIN EN ISO 11138-3 | 2017-07 | Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017); German version EN ISO 11138-3:2017 More |
DIN EN ISO 11138-4 | 2017-07 | Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017); German version EN ISO 11138-4:2017 More |
DIN EN ISO 11138-5 | 2017-07 | Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2017); German version EN ISO 11138-5:2017 More |
DIN EN ISO 14937 | 2010-03 | 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 (ISO 14937:2009); German version EN ISO 14937:2009 More |
DIN EN ISO 18472 | 2018-11 | Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2018); German version EN ISO 18472:2018 More |
DIN EN ISO 19011 | 2018-10 | Guidelines for auditing management systems (ISO 19011:2018); German and English version EN ISO 19011:2018 More |
DIN EN ISO 20857 | 2013-08 | Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010); German version EN ISO 20857:2013 More |
DIN EN ISO 9001 | 2015-11 | Quality management systems - Requirements (ISO 9001:2015); German and English version EN ISO 9001:2015 More |