BS ISO 16840-10:2014
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Wheelchairs. Resistance to ignition of non-integrated seat and back support cushions Requirements and test methods
Hardcopy , PDF
14-06-2021
English
31-12-2014
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Principle
5 Health and safety of test personnel
6 Apparatus
7 Test procedure
8 Requirements
9 Test report
10 Disclosure of results
Annex A (informative) - Design of a heat source as
a surrogate cigarette device
Annex B (normative) - Conditioning of outer cover
materials by washing and drying procedures
Bibliography
Describes requirements and test methods to assess the resistance to ignition by smouldering cigarette equivalent of non-integrated components of a wheelchair intended to protect tissue integrity.
Committee |
CH/173/1
|
DevelopmentNote |
Supersedes 14/30280574 DC. (12/2014)
|
DocumentType |
Standard
|
Pages |
24
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
ISO 16840-10:2014 | Identical |
ISO 7176-15:1996 | Wheelchairs — Part 15: Requirements for information disclosure, documentation and labelling |
EN 1021-1:2014 | Furniture - Assessment of the ignitability of upholstered furniture - Part 1: Ignition source smouldering cigarette |
ISO 7176-16:2012 | Wheelchairs Part 16: Resistance to ignition of postural support devices |
ISO 10993-10:2010 | Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 554:1976 | Standard atmospheres for conditioning and/or testing — Specifications |
ISO 8191-1:1987 | Furniture — Assessment of the ignitability of upholstered furniture — Part 1: Ignition source: smouldering cigarette |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
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