Standards STN - Slovak standards - Page 6859

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)

WITHDRAWN published on 1.5.2008

Biological evaluation of medical devices. Part 13: Identification and quantification of degradation products from polymeric medical devices

WITHDRAWN published on 1.7.2001

Biological evaluation of medical devices. Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)

WITHDRAWN published on 1.4.2003

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WITHDRAWN published on 1.5.2003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WITHDRAWN published on 1.6.2001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WITHDRAWN published on 1.1.2004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WITHDRAWN published on 1.4.2004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WITHDRAWN published on 1.12.2005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