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Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Dentistry — Zinc oxide/eugenol cements and zinc oxide/non-eugenol cements
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
15-09-2022
French, English
23-02-2011
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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.
| DevelopmentNote |
Supersedes ISO 3106 (04/2001) Supersedes ISO/DIS 3107. (02/2011)
|
| DocumentType |
Standard
|
| Pages |
11
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ONORM EN ISO 3107 : 2011 | Identical |
| DS EN ISO 3107 : 2011 | Identical |
| NF EN ISO 3107 : 2011 | Identical |
| NBN EN ISO 3107 : 2011 | Identical |
| NEN EN ISO 3107 : 2011 | Identical |
| NS EN ISO 3107 : 2011 | Identical |
| I.S. EN ISO 3107:2011 | Identical |
| PN EN ISO 3107 : 2011 | Identical |
| SN EN ISO 3107:2011 | Identical |
| UNI EN ISO 3107 : 2011 | Identical |
| UNE-EN ISO 3107:2011 | Identical |
| BS EN ISO 3107:2011 | Identical |
| EN ISO 3107:2011 | Identical |
| ADA 30 : 2013 | Identical |
| DIN EN ISO 3107:2011-06 | Identical |
| DIN 13924-1 : 1978 | Similar to |
| UNE-EN 23107:1992 | Identical |
| DIN EN 23107:1992-05 | Corresponds |
| NS ISO 3107 : 1ED 1992 | Identical |
| I.S. EN 23107:1992 | Identical |
| EN 23107 : 1991 | Identical |
| NEN ISO 3107 : 1992 | Identical |
| BS 7214:1989 | Identical |
| CSA Z349.16 TO Z349.28 : M92 | Identical |
| 15/30328959 DC : 0 | BS ISO 16142-2 - MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 2: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
| ANSI/AAMI/ISO 16142-1:2016 | MEDICAL DEVICES - RECOGNIZED ESSENTIAL PRINCIPLES OF SAFETY AND PERFORMANCE OF MEDICAL DEVICES - PART 1: GENERAL ESSENTIAL PRINCIPLES AND ADDITIONAL SPECIFIC ESSENTIAL PRINCIPLES FOR ALL NON-IVD MEDICAL DEVICES AND GUIDANCE ON THE SELECTION OF STANDARDS |
| DIN EN 1641:2010-02 | Dentistry - Medical devices for dentistry - Materials |
| I.S. EN 1641:2009 | DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
| ISO 16142-1:2016 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
| BS ISO 16142-1:2016 | Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
| PD 6502:1982 | Guide to the use of dental 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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