I.S. EN 1865-1:2010
Withdrawn
PATIENT HANDLING EQUIPMENT USED IN ROAD AMBULANCES - PART 1: GENERAL STRETCHER SYSTEMS AND PATIENT HANDLING EQUIPMENT
Hardcopy , PDF
English
08-16-2010
06-13-2015
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
5 Test methods
6 Marking
Annex ZA (informative) - Relationship between this
European Standard and the Essential
Requirements of EU Directive 93/42/EEC
concerning Medical Devices
Bibliography
Specifies minimum requirements for the design and performance of stretchers and other patient handling equipment used in road ambulances for the handling and carrying of patients.
| DevelopmentNote |
Supersedes I.S. EN 1865. (08/2010) 2010 Edition Re-Issued in June 2015 & incorporates AMD 1 2015. (06/2015)
|
| DocumentType |
Standard
|
| Pages |
38
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Withdrawn
|
| Supersedes |
| Standards | Relationship |
| EN 1865-1:2010+A1:2015 | Identical |
| DIN EN 1865-1:2010-12 | Equivalent |
| BS EN 1865-1 : 2010 | Equivalent |
| EN 1865-1:2010 | Equivalent |
| EN 1021-1:2014 | Furniture - Assessment of the ignitability of upholstered furniture - Part 1: Ignition source smouldering cigarette |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| EN 597-1:2015 | Furniture - Assessment of the ignitability of mattresses and upholstered bed bases - Part 1: Ignition source smouldering cigarette |
| EN ISO 14971:2012 | Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
| EN 1789:2007+A2:2014 | Medical vehicles and their equipment - Road ambulances |
| ISO 14971:2007 | Medical devices — Application of risk management to medical devices |
| 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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