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  • EN ISO 6877:2006

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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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    Dentistry - Root-canal obturating points (ISO 6877:2006)

    Available format(s): 

    Superseded date:  28-09-2021

    Language(s): 

    Published date:  01-04-2006

    Publisher:  Comite Europeen de Normalisation

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    Table of Contents - (Show below) - (Hide below)

    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

    Abstract - (Show below) - (Hide below)

    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.

    General Product Information - (Show below) - (Hide below)

    Committee CEN/TC 55
    Document Type Standard
    Publisher Comite Europeen de Normalisation
    Status Superseded
    Superseded By

    Standards Referenced By This Book - (Show below) - (Hide below)

    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

    Standards Referencing This Book - (Show below) - (Hide below)

    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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