DIN EN ISO 5173 PDF

Published Date: 05/01/2023

Destructive tests on welds in metallic materials - Bend tests (ISO 5173:2023)

Published Date: 03/01/2021

Draft Document - Destructive tests on welds in metallic materials - Bend tests (ISO/DIS 5173:2021); German and English version prEN ISO 5173:2021

Published Date: 05/01/2017

Draft Document - Destructive tests on welds in metallic materials - Bend tests (ISO/DIS 5173:2017); German and English version prEN ISO 5173:2017

Published Date: 02/01/2012

Destructive tests on welds in metallic materials - Bend tests (ISO 5173:2009 + Amd 1:2011); German version EN ISO 5173:2010 + A1:2011

Published Date: 07/01/2011

Draft Document - Destructive tests on welds in metallic materials - Bend tests - AMENDMENT 1 (ISO 5173:2009/FDAM 1:2011); German version EN ISO 5173:2010/FprA1:2011

Published Date: 08/01/2010

Destructive tests on welds in metallic materials - Bend tests (ISO 5173:2009)

Published Date: 10/01/2009

Draft Document - Destructive tests on welds in metallic materials - Bend tests (ISO 5173:2009); German version FprEN ISO 5173:2009

Published Date: 06/01/2018

Metallic materials - Method of test for the determination of quasistatic fracture toughness of welds (ISO 15653:2018)

Published Date: 01/01/2012

Aerospace series - Weldments and brazements for aerospace structures - Joints of metallic materials by laser beam welding - Quality of weldments; German and English version EN 4678:2011

Published Date: 11/01/2018

Non-destructive testing of welds - Time-of-flight diffraction technique (TOFD) - Acceptance levels (ISO 15626:2018)

Published Date:

Guidelines Relating to the Application of: The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices

Published Date: 03/01/1998

Guidelines Relating to the Demarcation Between 90/385/EEC on Active Implatable Medical Devices, 93/42/EEC on Medical Devices,65/65/EEC Relating to Medicinal Products & Related Directives

Published Date: 04/01/1994

Guidelines Relating to the Application of : The Council Directive 90/385/EEC on Active Implantable Medical Devices and The Council Directive 93/42/EEC on Medical Devices