EN ISO 3107:2011
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.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 - Zinc oxide/eugenol cements and zinc oxide/non-eugenol cements (ISO 3107:2011)
30-09-2011
01-03-2011
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Classification
5 Requirements
6 Sampling
7 Test methods
8 Marking, labelling and packaging
Bibliography
ISO 3107:2011 specifies requirements for non-water-based zinc oxide/eugenol cements suitable for use in restorative dentistry for temporary cementation, for bases and as temporary restorations.ISO 3107:2011 also specifies requirements for non-eugenol cements containing zinc oxide and aromatic oils suitable for temporary cementation.
| Committee |
CEN/TC 55
|
| DevelopmentNote |
Supersedes EN 23107. (10/2004)
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| ONORM EN ISO 3107 : 2011 | Identical |
| DS EN ISO 3107 : 2011 | Identical |
| NF EN ISO 3107 : 2011 | Identical |
| NEN EN ISO 3107 : 2011 | Identical |
| SN EN ISO 3107:2011 | Identical |
| ISO 3107:2011 | Identical |
| UNE-EN ISO 3107:2011 | Identical |
| DIN EN ISO 3107:2011-06 | Identical |
| NBN EN ISO 3107 : 2011 | Identical |
| BS EN ISO 3107:2011 | Identical |
| PN EN ISO 3107 : 2011 | Identical |
| NS EN ISO 3107 : 2011 | Identical |
| UNI EN ISO 3107 : 2011 | Identical |
| I.S. EN ISO 3107:2011 | Identical |
| 08/30184612 DC : DRAFT SEP 2008 | BS EN 1641 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
| DIN EN 1641:2010-02 | Dentistry - Medical devices for dentistry - Materials |
| I.S. EN 1641:2009 | DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
| UNI EN 1641 : 2010 | DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
| BS EN 1641:2004 | Dentistry. Medical devices for dentistry. Materials |
| EN 1641:2009 | Dentistry - Medical devices for dentistry - Materials |
| ISO 7405:2008 | Dentistry Evaluation of biocompatibility of medical devices used in dentistry |
| ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
| ISO 1942:2009 | Dentistry Vocabulary |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 3696:1987 | Water for analytical laboratory use — Specification and test methods |
| ISO 2590:1973 | General method for the determination of arsenic Silver diethyldithiocarbamate photometric method |
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