EN ISO 16201:2006
Withdrawn
Technical aids for disabled persons - Environmental control systems for daily living (ISO 16201:2006)
10-01-2006
04-30-2007
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Withdrawn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 |
| NS EN ISO 16201 : 1ED 2007 | Identical |
| NF 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 |
| NBN EN ISO 16201 : 2006 | Identical |
| BS EN ISO 16201:2006 | Identical |
| NEN EN ISO 16201 : 2006 | Identical |
| UNE-EN ISO 16201:2007 | 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 |