EN ISO 16201:2006
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Technical aids for disabled persons - Environmental control systems for daily living (ISO 16201:2006)
30-04-2007
01-10-2006
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
4.1 Risk management
4.2 Information supplied by the manufacturer
4.3 Materials
5 Functional requirements and test methods
5.1 General
5.2 Design
5.3 User interface
5.4 Controlled functions
6 Technical safety requirements and test methods
Annex A (informative) Guidance notes
Annex ZA (informative) Relationship between this European
Standard and the Essential Requirements
of EU Directive 93/42/EEC
ISO 16201:2006 specifies functional and technical requirements and test methods for environmental control systems intended for use to alleviate or compensate for a disability. Such systems are also known as electronic aids to daily living.The aim of ISO 16201:2006 is to provide safety requirements and recommendations for manufacturers of such environmental control systems.Target devices are not covered by ISO 16201:2006. Technical requirements for items of equipment connected within the system are to be covered by their own specific standards, e.g. adjustable beds.
| Committee |
CEN/TC 293
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Withdrawn
|
| Standards | Relationship |
| SN EN ISO 16201:2007 | Identical |
| NS EN ISO 16201 : 1ED 2007 | Identical |
| NF EN ISO 16201 : 2007 | Identical |
| UNI EN ISO 16201 : 2007 | Identical |
| DIN EN ISO 16201:2006-12 | Identical |
| ISO 16201:2006 | Identical |
| I.S. EN ISO 16201:2006 | Identical |
| PN EN ISO 16201 : 2007 | Identical |
| UNE-EN ISO 16201:2007 | Identical |
| NBN EN ISO 16201 : 2006 | Identical |
| BS EN ISO 16201:2006 | Identical |
| NEN EN ISO 16201 : 2006 | Identical |
| IEC 60950-1:2005+AMD1:2009+AMD2:2013 CSV | Information technology equipment - Safety - Part 1: General requirements |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| IEC 60825-1:2014 | Safety of laser products - Part 1: Equipment classification and requirements |
| IEC 60529:1989+AMD1:1999+AMD2:2013 CSV | Degrees of protection provided by enclosures (IP Code) |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| IEC 60601-1-1:2000 | Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
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