EN ISO 10993-15:2009
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)
21-03-2010
10-06-2009
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Degradation test methods
4.1 General
4.2 Prerequisites
5 Reagent and sample preparation
5.1 Sample documentation
5.2 Test solution (electrolyte)
5.3 Preparation of test samples
6 Electrochemical tests
6.1 Apparatus
6.2 Sample preparation
6.3 Test conditions
6.4 Potentiodynamic measurements
6.5 Potentiostatic measurements
7 Immersion test
7.1 Apparatus
7.2 Sample preparation
7.3 Immersion test procedure
8 Analysis
9 Test report
Annex A (informative) - Schematic diagram of the
electrochemical measuring circuit
Annex B (informative) - Schematic drawing of an
electrolytic cell
Annex C (informative) - Examples of alternative
electrolytes for the electrochemical tests
Bibliography
Annex ZA (informative) - Relationship between this European
Standard and the Essential Requirements of
EU Directive 93/42/EEC on Medical Devices
Gives guidance on general requirements for the design of tests for identifying and quantifying degradation products from finished metallic medical devices or corresponding material samples finished as ready for clinical use.
Committee |
CEN/TC 206
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Withdrawn
|
Standards | Relationship |
DS EN ISO 10993-15 : 2009 | Identical |
ONORM EN ISO 10993-15 : 2009 | Identical |
DIN EN ISO 10993-15:2009-10 | Identical |
SN EN ISO 10993-15 : 2009 | Identical |
NF EN ISO 10993-15 : 2009 | Identical |
PN EN ISO 10993-15 : 2009 | Identical |
UNI 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 |
SS-EN ISO 10993-15 : 2009 | Identical |
NBN EN ISO 10993-15 : 2009 | Identical |
NEN EN ISO 10993-15 : 2009 | Identical |
ISO 10993-15:2000 | Identical |
I.S. EN ISO 7198:2017 | CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - VASCULAR PROSTHESES - TUBULAR VASCULAR GRAFTS AND VASCULAR PATCHES (ISO 7198:2016) |
BS EN ISO 25539-1:2017 | Cardiovascular implants. Endovascular devices Endovascular prostheses |
I.S. EN ISO 25539-1:2017 | CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 1: ENDOVASCULAR PROSTHESES (ISO 25539-1:2017) |
EN ISO 7198:2017 | Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016) |
UNE-EN ISO 7198:2017 | Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016) |
BS EN ISO 7198:2017 | Cardiovascular implants and extracorporeal systems. Vascular prostheses. Tubular vascular grafts and vascular patches |
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 |
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 |
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