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  • BS EN ISO 3630-4:2009

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    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 instruments Auxiliary instruments

    Available format(s):  Hardcopy, PDF

    Superseded date:  23-08-2023

    Language(s):  English

    Published date:  31-07-2009

    Publisher:  British Standards Institution

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    Scope - (Show below) - (Hide below)

    This part of ISO3630 specifies requirements and test methods for hand-held or mechanically operated instruments for performing root canal procedures not cited in ISO3630-1, 3630-2, 3630-3 or 3630-5.

    This part of ISO3630 specifies requirements for size, product designation, safety considerations, instructions and labelling.

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    Committee CH/106/4
    Development Note Supersedes 08/30168812 DC. (07/2009) Reviewed and confirmed by BSI, February 2015. (01/2015)
    Document Type Standard
    Publisher British Standards Institution
    Status Superseded
    Superseded By
    Supersedes

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

    ISO 1797-2:1992 Dental rotary instruments Shanks Part 2: Shanks made of plastics
    ISO 6360-2:2004 Dentistry — Number coding system for rotary instruments — Part 2: Shapes
    ISO 6360-5:2007 Dentistry — Number coding system for rotary instruments — Part 5: Specific characteristics of root-canal instruments
    ISO 6360-1:2004 Dentistry — Number coding system for rotary instruments — Part 1: General characteristics
    ISO 1797-1:2011 Dentistry Shanks for rotary instruments Part 1: Shanks made of metals
    ISO 1942:2009 Dentistry Vocabulary
    ISO 3630-2:2013 Dentistry — Endodontic instruments — Part 2: Enlargers
    ISO 3630-1:2008 Dentistry Root-canal instruments Part 1: General requirements and test methods
    ISO 15223-1:2016 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
    ISO 17664:2017 Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices
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