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I.S. EN ISO 3630-5:2011

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by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 - ENDODONTIC INSTRUMENTS - PART 5: SHAPING AND CLEANING INSTRUMENTS (ISO 3630-5:2011)

Available format(s)

Hardcopy , PDF

Withdrawn date

31-03-2021

Superseded by

I.S. EN ISO 3630-5:2020

Language(s)

English

Published date

01-01-2011

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.


Dates of withdrawal of national standards are available from NSAI.

€28.00
Excluding VAT

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Classification
5 Requirements
6 Sampling
7 Testing
8 Designation, marking, and identification
9 Packaging
10 Instructions for use
11 Labelling
Bibliography

Describes requirements for size, marking, product designation, safety considerations, labelling and packaging.

DocumentType
Standard
Pages
21
PublisherName
National Standards Authority of Ireland
Status
Withdrawn
SupersededBy

Standards Relationship
ISO 3630-5:2011 Identical
EN ISO 3630-5:2011 Identical

ISO 1797-2:1992 Dental rotary instruments Shanks Part 2: Shanks made of plastics
ISO 7405:2008 Dentistry Evaluation of biocompatibility of medical devices used in dentistry
ISO 1797-1:2011 Dentistry Shanks for rotary instruments Part 1: Shanks made of metals
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 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

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