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BS EN ISO 21563:2013

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by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. Hydrocolloid impression materials

Available format(s)

Hardcopy , PDF

Superseded date

15-09-2021

Superseded by

BS EN ISO 21563:2021

Language(s)

English

Published date

31-08-2013

$669.38
Including GST where applicable

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Classification of agar hydrocolloid impression materials
5 Requirements - Characteristics and properties
6 Pre-test planning approaches
7 Test methods
8 Requirements - Labelling and instructions for use
Annex A (normative) - Figures illustrating instruments and
        accessories used in tests
Annex B (informative) - Tear test specimen preparation steps
        for an optional gripping method
Bibliography

Provides the requirements and tests for helping determine whether the elastic aqueous agar and alginate hydrocolloid dental impression materials, as prepared for retail marketing, are of the quality needed for their intended purposes.

Committee
CH/106/2
DevelopmentNote
Supersedes BS 4269-2(1991), BS EN ISO 13716, BS EN ISO 1564 & 11/30227250 DC. (09/2013)
DocumentType
Standard
Pages
56
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

Standards Relationship
EN ISO 21563:2013 Identical
ISO 21563:2013 Identical

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 21067:2007 Packaging 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 6873:2013 Dentistry — Gypsum products
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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