DIN EN ISO 14160 PDF

Published Date: 11/01/2021

Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2020)

Published Date: 05/01/2018

Draft Document - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2018); German and English version prEN ISO 14160:2018

Published Date: 10/01/2011

Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2011)

Published Date: 04/01/2009

Draft Document - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO/DIS 14160:2009); German version prEN ISO 14160:2009

Published Date: 06/01/1998

Sterilization of single-use medical devices incorporating materials of animal origin - Validation and routine control of sterilization by liquid chemical sterilants (ISO 14160:1998); German version EN ISO 14160:1998

Published Date: 11/01/2019

Sterilization of health care products - Biological indicators - Part 7: Guidance for the selection, use and interpretation of results (ISO 11138-7:2019)

Published Date: 09/01/2011

Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)

Published Date: 07/01/2022

Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018 + Amd 1:2022) (includes Amendment :2022)

Published Date: 08/01/2013

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)

Published Date: 05/01/2017

Additive manufacturing - General principles - Terminology (ISO/ASTM 52900:2015)

Published Date: 12/16/2021

Additive manufacturing - General principles - Fundamentals and vocabulary (ISO/ASTM 52900:2021)

Published Date: 01/01/2019

Additive manufacturing - General principles - Requirements for purchased AM parts (ISO/ASTM 52901:2017)

Published Date: 12/01/2019

Additive manufacturing - Test artifacts - Geometric capability assessment of additive manufacturing systems (ISO/ASTM 52902:2019)

Published Date: 03/25/2021

Additive manufacturing - Material extrusion-based additive manufacturing of plastic materials - Part 1: Feedstock materials (ISO/ASTM 52903-1:2020)

Published Date: 11/16/2020

Additive manufacturing — Material extrusion based additive manufacturing of plastic materials — Part 2: Process equipment (ISO/ASTM 52903-2:2020)