NA 027
DIN Standards Committee Optics and Precision Mechanics
DIN EN ISO 22442-3 [CURRENT] referenced in following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN ISO 11135 | 2020-04 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018); German version EN ISO 11135:2014 + A1:2019 More |
| DIN EN ISO 11137-1 | 2020-04 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd.1:2013 + Amd.2:2018); German version EN ISO 11137-1:2015 + A2:2019 More |
| DIN EN ISO 13408-5 | 2011-09 | Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006); German version EN ISO 13408-5:2011 More |
| DIN EN ISO 14534 | 2015-08 | Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011); German version EN ISO 14534:2015 More |
| DIN EN ISO 14630 | 2013-03 | Non-active surgical implants - General requirements (ISO 14630:2012); German version EN ISO 14630:2012 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 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 22442-2 | 2021-04 | Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020); German version EN ISO 22442-2:2020 More |
| DIN EN ISO 5840-1 | 2021-05 | Cardiovascular implants - Cardiac valve prostheses - Part 1: General requirements (ISO 5840-1:2021); German version EN ISO 5840-1:2021 More |
| DIN ISO 13022 | 2014-06 | Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012) More |
