EN 60601-1-9:2008/A1:2013
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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MEDICAL ELECTRICAL EQUIPMENT - PART 1-9: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR ENVIRONMENTALLY CONSCIOUS DESIGN (IEC 60601-1-9:2007/A1:2013)
17-09-2020
12-01-2013
FOREWORD
INTRODUCTION
1 Scope, object and related standards
2 Normative references
3 Terms and definitions
4 Protection of the ENVIRONMENT
Annex A (informative) - General guidance and rationale
Annex B (informative) - Guide to marking and labelling
requirements for ME EQUIPMENT
Annex ZA (normative) - Normative references to international
publications with their corresponding European
publications
Annex ZZ (informative) - Coverage of Essential Requirements of
EC Directives
Bibliography
Index of defined terms used in this collateral standard
Pertains to the reduction of adverse ENVIRONMENTAL IMPACTS of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT.
Committee |
TC 62
|
DocumentType |
Standard
|
PublisherName |
European Committee for Standards - Electrical
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
CEI EN 60601-1/A1 : 2014 | Identical |
CEI EN 60601-1-9 / A1 : 2016 | Identical |
SN EN 60601-1-9:2008+A1:2013 | Identical |
UNE-EN 60601-1-9:2008 | Identical |
IEC 60601-1-9:2007+AMD1:2013 CSV | Identical |
NF EN 60601-1-9 : 2008 AMD 1 2014 | Identical |
NBN EN 60601-1-9 : 2008 AMD 1 2014 | Identical |
NEN EN IEC 60601-1-9 : 2008 AMD 1 2013 | Identical |
I.S. EN 60601-1-9:2008 | Identical |
PN EN 60601-1-9 : 2008 AMD 1 2014 | Identical |
DIN EN 60601-1-9 : 2014 | Identical |
VDE 0750-1-9 : 2014 | Identical |
BS EN 60601-1-9 : 2008 | Identical |
OVE/ONORM EN 60601-1-9 : 2014 | Identical |
BS EN 60601-1-9:2008+A1:2013 | Identical |
BS EN 60601-1-11:2015 | Medical electrical equipment General requirements for basic safety and essential performance. Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |
EN 60601-2-39:2008/A11:2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-39: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PERITONEAL DIALYSIS EQUIPMENT (IEC 60601-2-39:2007) |
I.S. EN 60601-2-39:2008 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-39: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PERITONEAL DIALYSIS EQUIPMENT (IEC 60601-2-39:2007 (EQV)) |
PREN 12182 : 2009-06 | ASSISTIVE PRODUCTS FOR PERSONS WITH DISABILITY - GENERAL REQUIREMENTS AND TEST METHODS |
DIN EN 12182:2012-07 | Assistive products for persons with disability - General requirements and test methods |
I.S. EN 12182:2012 | ASSISTIVE PRODUCTS FOR PERSONS WITH DISABILITY - GENERAL REQUIREMENTS AND TEST METHODS |
VDE 0750-2-64 : 2018 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-64: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LIGHT ION BEAM MEDICAL ELECTRICAL EQUIPMENT |
DIN EN 60601-2-64 : 2018 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-64: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LIGHT ION BEAM MEDICAL ELECTRICAL EQUIPMENT |
09/30201992 DC : 0 | BS EN 12182 - ASSISTIVE PRODUCTS FOR PERSONS WITH DISABILITY - GENERAL REQUIREMENTS AND TEST METHODS |
UNI EN 12182 : 2012 | ASSISTIVE PRODUCTS FOR PERSONS WITH DISABILITY - GENERAL REQUIREMENTS AND TEST METHODS |
BS EN 60601-2-39:2008 | Medical electrical equipment Particular requirements for basic safety and essential performance of peritoneal dialysis equipment |
BS EN 12182:2012 | Assistive products for persons with disability. General requirements and test methods |
EN 60601-1-11:2015 | Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment |
EN 12182:2012 | Assistive products for persons with disability - General requirements and test methods |
IEC GUIDE 109:2012 | Environmental aspects - Inclusion in electrotechnical product standards |
IEC GUIDE 113:2000 | Materials declaration questionnaires - Basic guidelines |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO 14021:2016 | Environmental labels and declarations — Self-declared environmental claims (Type II environmental labelling) |
ISO/TR 14062:2002 | Environmental management Integrating environmental aspects into product design and development |
ISO 14001:2015 | Environmental management systems — Requirements with guidance for use |
IEC PAS 61906:2005 | Procedure for the declaration of materials in products of the electrotechnical and electronic industry |
ISO 14040:2006 | Environmental management Life cycle assessment Principles and framework |
IEC GUIDE 114:2005 | Environmentally conscious design - Integrating environmental aspects into design and development of electrotechnical products |
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