EN ISO 3107:2011
Withdrawn
Withdrawn
Dentistry - Zinc oxide/eugenol cements and zinc oxide/non-eugenol cements (ISO 3107:2011)
Published date
03-01-2011
Publisher
Withdrawn date
09-30-2011
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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Withdrawn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 |
| DS EN ISO 3107 : 2011 | Identical |
| NF EN ISO 3107 : 2011 | Identical |
| NEN EN ISO 3107 : 2011 | Identical |
| 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 |
| I.S. EN ISO 3107:2011 | Identical |
| UNE-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 |
| 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 |
Summarise
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