AAMI TIR65 : 2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
SUSTAINABILITY OF MEDICAL DEVICES - ELEMENTS OF A RESPONSIBLE PRODUCT LIFE CYCLE
Hardcopy , PDF
15-02-2023
English
04-11-2015
Important note : Users cannot be edited or removed once added to your Multi user PDF.
Glossary of equivalent standards
Committee representation
Introduction
1 Scope
2 Normative references
3 Informative references
4 Definitions
5 Social sustainability
6 Economic sustainability
7 Environmental sustainability
8 Conclusions
Annexes
A - Chemicals of concern references
B - Sustainable product development tools
C - Appendix of acronyms
D - Manufacturer life cycle case studies
E - User life cycle case studies
Bibliography
Describes sustainability considerations during the product design, supply chain, manufacturing, acquisition, use, and end of life of medical devices, taking into account the life cycle impacts of the product.
| DocumentType |
Standard
|
| ISBN |
1-57020-602-3
|
| Pages |
44
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Superseded
|
| SupersededBy |
| OHSAS 18001:2007 | Occupational health and safety management systems. Requirements |
| AAMI ISO TIR 11139 : 2006 | STERILIZATION OF HEALTH CARE PRODUCTS - VOCABULARY |
| ISO 50001:2011 | Energy management systems Requirements with guidance for use |
| ISO Guide 82:2014 | Guidelines for addressing sustainability in standards |
| ISO 14044:2006 | Environmental management Life cycle assessment Requirements and guidelines |
| ISO 14001:2015 | Environmental management systems — Requirements with guidance for use |
| 2012/19/EU : 2012 COR 1 2015 | DIRECTIVE 2012/19/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 4 JULY 2012 ON WASTE ELECTRICAL AND ELECTRONIC EQUIPMENT (WEEE) (RECAST) |
| AAMI TIR 12 : 2010 | DESIGNING, TESTING, AND LABELING REUSABLE MEDICAL DEVICES FOR REPROCESSING IN HEALTH CARE FACILITIES: A GUIDE FOR MEDICAL DEVICE MANUFACTURERS |
| ASTM D 6868 : 2017 : REDLINE | Standard Specification for Labeling of End Items that Incorporate Plastics and Polymers as Coatings or Additives with Paper and Other Substrates Designed to be Aerobically Composted in Municipal or Industrial Facilities |
| ANSI/AAMI EQ89:2015 | GUIDANCE FOR THE USE OF MEDICAL EQUIPMENT MAINTENANCE STRATEGIES AND PROCEDURES |
| ISO 11607-1:2006 | Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
| AAMI ST91 : 2015 | FLEXIBLE AND SEMI-RIGID ENDOSCOPE PROCESSING IN HEALTH CARE FACILITIES |
| ISO 14040:2006 | Environmental management Life cycle assessment Principles and framework |
| IEC 60601-1-9:2007+AMD1:2013 CSV | Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
| IEC 62474:2012 | Material declaration for products of and for the electrotechnical industry |
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