EN ISO 9693-1:2012
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Dentistry - Compatibility testing - Part 1: Metal-ceramic systems (ISO 9693-1:2012)
31-08-2012
15-02-2012
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Sampling
6 Test methods
7 Test report
Bibliography
ISO 9693-1:2012 specifies test methods for determining the compatibility of metallic and ceramic materials used for dental restorations by testing the composite structure.The requirements given in ISO 9693-1:2012 are applicable to metallic materials and ceramics when used in combination, and are not applicable to either metallic materials or ceramics when used alone.
| Committee |
CEN/TC 55
|
| DevelopmentNote |
Supersedes EN ISO 9693, (03/2012)
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| ISO 9693-1:2012 | Identical |
| NF EN ISO 9693-1 : 2012 | Identical |
| NBN EN ISO 9693-1 : 2012 | Identical |
| NEN EN ISO 9693-1 : 2012 | Identical |
| NS EN ISO 9693-1 : 2012 | Identical |
| I.S. EN ISO 9693-1:2012 | Identical |
| PN EN ISO 9693-1 : 2012 | Identical |
| SN EN ISO 9693-1 : 2012 | Identical |
| UNI EN ISO 9693-1 : 2012 | Identical |
| UNE-EN ISO 9693-1:2012 | Identical |
| BS EN ISO 9693-1:2012 | Identical |
| DIN EN ISO 9693-1:2012-06 | Identical |
| BS EN ISO 17892-6:2017 | Identical |
| ISO 6872:2015 | Dentistry — Ceramic materials |
| ISO 6892-1:2016 | Metallic materials Tensile testing Part 1: Method of test at room temperature |
| ISO 7405:2008 | Dentistry Evaluation of biocompatibility of medical devices used in dentistry |
| ISO 1942:2009 | Dentistry Vocabulary |
| ISO 22674:2016 | Dentistry — Metallic materials for fixed and removable restorations and appliances |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
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