DIN EN ISO 10993-18:2009-08

Superseded

Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005); German version EN ISO 10993-18:2009

Available format(s)

Hardcopy , PDF

Superseded date

03-15-2021

Language(s)

English, German

Published date

08-01-2009

Publisher

German Institute for Standardisation (Deutsches Institut für Normung)

DocumentType	Standard
Pages	27
PublisherName	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Superseded
SupersededBy	DIN EN ISO 10993-18:2021-03
Supersedes	DIN EN ISO 10993-18:2005-10

Standards	Relationship
UNI EN ISO 10993-18 : 2009	Identical
SN EN ISO 10993-18 : 2009	Identical
BS EN ISO 10993-18:2009	Identical
NS EN ISO 10993-18 : 2009	Identical
NF EN ISO 10993-18 : 2009	Identical
EN ISO 10993-18:2009	Identical
ISO 10993-18:2005	Identical
NBN EN ISO 10993-18 : 2009	Identical
UNE-EN ISO 10993-18:2009	Identical
I.S. EN ISO 10993-18:2009	Identical
NEN EN ISO 10993-18 : 2009	Identical
ONORM EN ISO 10993-18 : 2009	Identical

VDI 5703:2015-09	Systematical development for a model-based testing of medical devices
DIN EN ISO 10993-3:2015-02	BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY AND REPRODUCTIVE TOXICITY (ISO 10993-3:2014)
DIN EN ISO 10993-1:2010-04	Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009)
DIN EN ISO 10993-10:2014-10	Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)

EN 12442-3 : 2000	ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 3: VALIDATION OF THE ELIMINATION AND/OR INACTIVATION OF VIRUSES AND TRANSMISSIBLE AGENTS
ISO 5725-1:1994	Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions
ISO 5832-1:2016	Implants for surgery — Metallic materials — Part 1: Wrought stainless steel
ISO 10993-13:2010	Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
DIN EN ISO 14971:2013-04	MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007)
ISO 10993-2:2006	Biological evaluation of medical devices — Part 2: Animal welfare requirements
EN 455-3:2015	Medical gloves for single use - Part 3: Requirements and testing for biological evaluation
ISO 10993-14:2001	Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
ISO 10993-17:2002	Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 10993-9:2009	Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
EN 12442-1 : 2000	ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 1: ANALYSIS AND MANAGEMENT OF RISK
ISO 14971:2007	Medical devices Application of risk management to medical devices
DIN EN ISO 10993-17:2009-08	Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
EN 12442-2 : 2000	ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 2: CONTROLS ON SOURCING, COLLECTION AND HANDLING