Standards STN - Slovak standards - Page 6898

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WITHDRAWN published on 1.4.2004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WITHDRAWN published on 1.12.2005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WITHDRAWN published on 1.12.1999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WITHDRAWN published on 1.12.2007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WITHDRAWN published on 1.11.2008

Sterilization of medical devices. Validation and routine control of sterilization by irradiation

Standard published on 1.10.1999

Sterilization of medical devices. Validation and routine control of sterilization by irradiation

Change published on 1.6.2001

Sterilization of medical devices. Validation and routine control of sterilization by irradiation

Change published on 1.12.2002