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DIN EN ISO 11137-1 [Withdrawn] referenced in following documents:

Document number Edition Title
VDI 2083 Blatt 21 2019-10 Cleanroom technology - Cleanliness of medical devices in the manufacturing process More 
DIN EN ISO 11070 2019-04 Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014 + Amd 1:2018); German version EN ISO 11070:2014 + A1:2018 More 
DIN EN ISO 11137-3 2017-11 Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017); German version EN ISO 11137-3:2017 More 
DIN EN ISO 11139 2019-05 Sterilization of health care products - Vocabulary of terms used in sterilization and related equipment and process standards (ISO 11139:2018); German and English version EN ISO 11139:2018 More 
DIN EN ISO 1135-3 2017-05 Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016); German version EN ISO 1135-3:2017 More 
DIN EN ISO 1135-4 2016-06 Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015); German version EN ISO 1135-4:2015 More 
DIN EN ISO 1135-5 2016-06 Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015); German version EN ISO 1135-5:2015 More 
DIN EN ISO 13408-1 2015-12 Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013); German version EN ISO 13408-1:2015 More 
DIN EN ISO 13408-2 2018-06 Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018); German version EN ISO 13408-2:2018 More 
DIN EN ISO 15378 2018-04 Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017); German version EN ISO 15378:2017 More