AS ISO 10993.3:2002
$27.30
Biological evaluation of medical devices – Tests for genotoxicity, carcinogenicity and reproductive toxicity
| Published By | Publication Date | Number of Pages |
| AS | 2002-06-28 | 16 |
Specifies the requirements for tests of genotoxicity, carcinogenicity and reproductive toxicity for biological evaluation of medical devices.
Related products
-
ISO 10993-7:2008
Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals Published By Publication…
-
AS ISO 10993.5:2002
Biological evaluation of medical devices – Tests for in vitro cytotoxicity Published By Publication Date…
-
ISO 10993-12:2012
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials Published By…
-
AS ISO 10993.7:2003
Biological evaluation of medical devices – Ethylene oxide sterilization residuals Published By Publication Date Number…
-
ISO/TS 10993-20:2006
Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of…
-
BS EN ISO 10993-4:2002:2006 Edition
Biological evaluation of medical devices – Selection of tests for interactions with blood Published By…
-
ISO 10993-1:2009
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management…
-
AS ISO 10993.4:2003
Biological evaluation of medical devices – Selection of tests for interactions with blood Published By…
-
ISO 10993-4:2002
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood…
-
AS ISO 10993.12:2004
Biological evaluation of medical devices – Sample preparation and reference materials Published By Publication Date…
-
AS ISO 10993.14:2003
Biological evaluation of medical devices – Identification and quantification of degradation products from ceramics Published…
-
ISO 10993-18:2005
Biological evaluation of medical devices — Part 18: Chemical characterization of materials Published By Publication…
-
ISO 10993-9:2009
Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential…
-
AS ISO 10993.13:2002
Biological evaluation of medical devices – Identification and quantification of degradation products from polymeric medical…
-
AS ISO 10993.10:2003
Biological evaluation of medical devices – Tests for irritation and delayed type hypersensitivity Published By…
-
CAN/CSA-ISO 10993.11-F98 (C2002):2000 Edition
Évaluation biologique des dispositifs médicaux – Partie 11: Essais de toxicité systémique Published By Publication…
-
AS ISO 10993.8:2003
Biological evaluation of medical devices – Selection and qualification of reference materials for biological tests…
-
ISO 10993-11:2006
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity Published By Publication…
-
ISO 10993-8:2000
Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for…
-
AS ISO 10993.6:2002
Biological evaluation of medical devices – Tests for local effects after implantation Published By Publication…
-
ISO 10993-6:2007
Biological evaluation of medical devices — Part 6: Tests for local effects after implantation Published…
-
AS ISO 10993.15:2003
Biological evaluation of medical devices – Identification and quantification of degradation products from metals and…
-
ISO 10993-17:2002
Évaluation biologique des dispositifs médicaux — Partie 17: Établissement des limites admissibles des substances relargables…
-
AS ISO 10993.16:2002
Biological evaluation of medical devices – Toxicokinetic study design for degradation products and leachables Published…
-
ISO 19933:2007
Space systems — Format for spacecraft launch environment test report Published By Publication Date Number…
-
AS ISO 10993.1:2002
Biological evaluation of medical devices – Evaluation and testing Published By Publication Date Number of…
-
AS ISO 14990.3:2022
Earth-moving machinery – Electrical safety of machines utilizing electric drives and related components and systems…
-
ISO 10993-14:2001
Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from…
-
AS ISO 6993.3:2007 (R2017)
Buried, high-impact poly(vinyl chloride) (PVC-HI) piping systems for the supply of gaseous fuels – Fittings…
-
ISO 10993-15:2000
Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from…
-
ISO 10993-2:2006
Évaluation biologique des dispositifs médicaux — Partie 2: Exigences relatives à la protection des animaux…
-
AS ISO 10993.9:2002
Biological evaluation of medical devices – Framework for identification and quantification of potential degradation products…
-
ISO 10993-3:2003
Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity…
-
AS ISO 10993.17:2004
Biological evaluation of medical devices – Establishment of allowable limits for leachable substances Published By…
-
ISO 10993-18:2020
Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within…
-
ISO 10993-4:2002/Amd 1:2006
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood…
-
ISO 10993-5:2009
Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity Published By…
-
AS ISO 10993.11:2002
Biological evaluation of medical devices – Tests for systemic toxicity Published By Publication Date Number…
-
BS EN ISO 10993-10:2002:2006 Edition
Biological evaluation of medical devices – Tests for irritation and delayed-type hypersensitivity Published By Publication…
-
AS ISO/IEC 20943.3:2005
Information technology – Procedures for achieving metadata registry content consistency – Value domains Published By…
