EN ISO 6877:2006
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Dentistry - Root-canal obturating points (ISO 6877:2006)
28-09-2021
01-04-2006
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
4.1 Points
4.2 Biocompatibility
4.3 Length
4.4 Size designation and taper
4.5 Physical integrity
4.6 Radio-opacity
4.7 Colour coding
5 Procurement of samples
6 Test methods
6.1 Test conditions
6.2 Visual examination
6.3 Length
6.4 Size designation
6.5 Physical integrity
6.6 Radio-opacity for polymeric points
7 Packaging
8 Marking and information to be supplied by manufacturer
Bibliography
ISO 6877:2006 specifies the dimensions and compositional requirements for prefabricated metal or polymeric points or cones suitable for use in the obturation of the dental root-canal, but not for support of a coronal restoration. It also specifies numerical systems and a colour coding system for designating the sizes.Dental root-canal obturating points are marketed sterilized or unsterilized. ISO 6877:2006 covers the physical attributes expected of such products as supplied. Requirements for sterility are not included, and any claim that the product is sterile is the responsibility of the manufacturer.
Committee |
CEN/TC 55
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
NF EN ISO 6877 : 2006 | Identical |
DIN EN ISO 6877:2006-07 | Identical |
NBN EN ISO 6877 : 2006 | Identical |
NEN EN ISO 6877 : 2006 | Identical |
BS EN ISO 6877:2006 | Identical |
ISO 6877:2006 | Identical |
UNI EN ISO 6877 : 2006 | Identical |
I.S. EN ISO 6877:2006 | Identical |
UNE-EN ISO 6877:2007 | Identical |
NS EN ISO 6877 : 2ED 2006 | Identical |
PN EN ISO 6877 : 2008 | Identical |
SN EN ISO 6877 : 2006 | Identical |
ONORM EN ISO 6877 : 2006 | Identical |
UNE-EN ISO 6877:2006 | Identical |
08/30184612 DC : DRAFT SEP 2008 | BS EN 1641 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
02/563832 DC : DRAFT SEP 2002 | 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 3665:2011 | Photography Intra-oral dental radiographic film and film packets Manufacturer specifications |
ISO 8601:2004 | Data elements and interchange formats Information interchange Representation of dates and times |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 3630-1:2008 | Dentistry Root-canal instruments Part 1: General requirements and test methods |
ISO 15223:2000 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |
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