DIN EN ISO 10993-15 PDF

Published Date: 07/01/2023

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019)

Published Date: 05/01/2018

Draft Document - Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO/DIS 10993-15:2018); German and English version prEN ISO 10993-15:2018

Published Date: 10/01/2009

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); German version EN ISO 10993-15:2009

Published Date: 11/01/2001

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000); English version of DIN EN ISO 10993-15

Published Date: 12/01/2020

Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

Published Date: 10/01/2009

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)

Published Date: 05/01/2021

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)

Published Date: 01/01/1998

Americans With Disabilities Act Accessibility Guidelines Manual (ADAAG)

Published Date: 09/01/1992

Published Date: 06/01/1999

Published Date: 02/01/2000

Published Date: 05/01/1994

Published Date: 11/01/1995