DIN EN ISO 10993-15:2009-10

Superseded

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

Available format(s)

Hardcopy , PDF

Superseded date

07-01-2023

Language(s)

English, German

Published date

10-01-2009

Publisher

German Institute for Standardisation (Deutsches Institut für Normung)

DocumentType	Standard
Pages	21
PublisherName	German Institute for Standardisation (Deutsches Institut für Normung)
Status	Superseded
SupersededBy	DIN EN ISO 10993-15:2023-07
Supersedes	DIN EN ISO 10993-15 E : 2001 DIN EN ISO 10993-15:2001-11

Standards	Relationship
ONORM EN ISO 10993-15 : 2009	Identical
SN EN ISO 10993-15 : 2009	Identical
NF EN ISO 10993-15 : 2009	Identical
UNI EN ISO 10993-15 : 2009	Identical
EN ISO 10993-15:2009	Identical
BS EN ISO 10993-15:2009	Identical
NS EN ISO 10993-15 : 2009	Identical
I.S. EN ISO 10993-15:2009	Identical
UNE-EN ISO 10993-15:2009	Identical
NBN EN ISO 10993-15 : 2009	Identical
NEN EN ISO 10993-15 : 2009	Identical

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)
DIN EN ISO 10993-9:2010-04	Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)

ISO 10993-16:2017	Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables
NFS 91 141 : 1997	BIODEGRADABILITY OF DENTAL METAL ALLOYS - STANDARDIZATION OF ELECTROCHEMICAL TESTS
ISO 10993-13:2010	Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
ISO 3585:1998	Borosilicate glass 3.3 Properties
ISO 10271:2011	Dentistry Corrosion test methods for metallic materials
ISO 10993-14:2001	Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
DIN EN ISO 10993-16:2016-04 (Draft)	BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 16: TOXICOKINETIC STUDY DESIGN FOR DEGRADATION PRODUCTS AND LEACHABLES (ISO 10993-16:2017)
DIN EN ISO 8044:2015-12	CORROSION OF METALS AND ALLOYS - BASIC TERMS AND DEFINITIONS (ISO 8044:2015)
DIN EN ISO 10993-12:2012-10	Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)
ISO 10993-12:2012	Biological evaluation of medical devices Part 12: Sample preparation and reference materials
ISO 8044:2015	Corrosion of metals and alloys Basic terms and definitions
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
ISO 3696:1987	Water for analytical laboratory use — Specification and test methods
DIN ISO 3696:1991-06	WATER FOR ANALYTICAL LABORATORY USE - SPECIFICATION AND TEST METHODS
DIN EN ISO 10993-14:2009-08	Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
DIN EN ISO 10993-9:2010-04	Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)
DIN EN ISO 10993-13:2010-11	Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)