DIN EN ISO 11199-3:2005-07
Current
The latest, up-to-date edition.
WALKING AIDS MANIPULATED BY BOTH ARMS - REQUIREMENTS AND TEST METHODS - PART 3: WALKING TABLES
Hardcopy , PDF
English
01-01-2005
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Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
4.1 Stability
4.2 Brakes
4.3 Mechanical durability
4.4 Manoeuvrability
4.5 Handgrip
4.6 Leg section and tip
4.7 Adjusting devices
4.8 Resting seat
4.9 Materials and finish
4.10 Marking and labelling
5 Test methods
5.1 General
5.2 Sampling, sequence of tests and inspection
5.3 Determination of dimensions and mass
5.4 Forward stability test
5.5 Backward stability test
5.6 Sideways stability test
5.7 Accessory equipment
5.8 Brake test
5.9 Resting seat test
5.10 Static strength test
5.11 Fatigue test
5.12 Final inspection
6 Information supplied by the manufacturer
6.1 General
6.2 Information marked on the product and/or accessories
6.3 Documentation
7 Test report
Annex A (informative) Supplementary information
Bibliography
Defines requirements and methods of testing the static stability, braking capabilities, static strength and fatigue of walking tables without accessory equipment, unless specified in the particular test procedure. Also provides requirements relating to safety, ergonomics and performance, marking, labelling and information supplied by the manufacturer.
| DocumentType |
Standard
|
| Pages |
29
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Current
|
| Standards | Relationship |
| BS EN ISO 11199-3:2005 | Identical |
| SN EN ISO 11199-3 : 2005 | Identical |
| NF EN ISO 11199-3 : 2005 | Identical |
| EN ISO 11199-3:2005 | Identical |
| I.S. EN ISO 11199-3:2005 | Identical |
| UNI EN ISO 11199-3 : 2005 | Identical |
| ISO 11199-3:2005 | Identical |
| NBN EN ISO 11199-3 : 2005 | Identical |
| NEN EN ISO 11199-3 : 2005 | Identical |
| NS EN ISO 11199-3 : 1ED 2005 | Identical |
| UNE-EN ISO 11199-3:2005 | Identical |
| EN 12182:2012 | Assistive products for persons with disability - General requirements and test methods |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO/IEC Guide 37:2012 | Instructions for use of products by consumers |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 9999:2016 | Assistive products for persons with disability Classification and terminology |
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