I.S. EN ISO 10650:2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 - POWERED POLYMERIZATION ACTIVATORS (ISO 10650:2015)
Hardcopy , PDF
05-11-2018
English
01-01-2015
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National Foreword
European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Classification
5 Requirements
6 Sampling
7 Test methods
8 Information to be supplied by the manufacturer
9 Marking
10 Packaging
Bibliography
Provides requirements and test methods for powered Polymerization activators in the 385 nm - 515 nm wavelength region intended for chairside use in polymerization of dental polymer-based materials.
| DevelopmentNote |
Supersedes I.S. EN ISO 10650-1 & I.S. EN ISO 10650-2. (10/2015)
|
| DocumentType |
Standard
|
| Pages |
32
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| EN ISO 10650:2015 | Identical |
| ISO 10650:2015 | Identical |
| IEC 60601-2-57:2011 | Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use |
| IEC 80601-2-60:2012 | Medical electrical equipment - Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| ISO 1942:2009 | Dentistry Vocabulary |
| IEC 62471:2006 | Photobiological safety of lamps and lamp systems |
| ISO 9687:2015 | Dentistry — Graphical symbols for dental equipment |
| 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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