Standards STN - Slovak standards - Page 6841

Biological evaluation of medical devices. Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)

WITHDRAWN published on 1.5.2003

Biological evaluation of medical devices. Part 16: Toxicokinetic study design for degradation products and leachables

WITHDRAWN published on 1.6.2001

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

WITHDRAWN published on 1.1.2004

Biological evaluation of medical devices. Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)

WITHDRAWN published on 1.4.2004

Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)

WITHDRAWN published on 1.12.2005

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)

Standard published on 1.2.2015

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)

Change published on 1.3.2020

Sterilization of medical devices. Validation and routine control of ethylene oxide sterilization

WITHDRAWN published on 1.12.1999

Sterilization of health care products. Ethylene oxide. Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 1135-1:2007)

WITHDRAWN published on 1.12.2007

Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008)

WITHDRAWN published on 1.11.2008