{"id":198186,"date":"2024-10-19T12:36:59","date_gmt":"2024-10-19T12:36:59","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/aami-tir65-2015\/"},"modified":"2024-10-25T05:10:09","modified_gmt":"2024-10-25T05:10:09","slug":"aami-tir65-2015","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/aami\/aami-tir65-2015\/","title":{"rendered":"AAMI TIR65 2015"},"content":{"rendered":"
Highlights sustainability considerations during the product design and manufacturing, acquisition and use, and end of life of medical devices, taking into account the life cycle impacts of the product.<\/p>\n
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
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1<\/td>\n | AAMI TIR65:2015, Sustainability of medical devices\u2014Elements of a responsible product life cycle <\/td>\n<\/tr>\n | ||||||
3<\/td>\n | Title page <\/td>\n<\/tr>\n | ||||||
4<\/td>\n | AAMI Technical Information Report Copyright information <\/td>\n<\/tr>\n | ||||||
5<\/td>\n | Contents <\/td>\n<\/tr>\n | ||||||
6<\/td>\n | Glossary of equivalent standards <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Committee representation <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 1 Scope 2 Normative references 3 Informative references <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | 4 Definitions <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 5 Social sustainability 5.1 Corporate responsibility 5.2 Employee management 5.3 Supply chain <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 5.4 External engagement 6 Economic sustainability 6.1 Extended supply chain 6.2 Total cost of ownership (TCO) <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 6.3 Measurement and disclosure of material sustainability topics 7 Environmental sustainability 7.1 Manufacturer <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 7.1.1 Product design minimization\/ simplicity 7.1.2 Raw materials and selection 7.1.2.1 Chemical assessment <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 7.1.2.2 Renewable and nonrenewable resources 7.1.2.3 Recycled materials 7.1.3 Manufacturing 7.1.3.1 Environmental, health, and safety management system <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 7.1.3.2 Energy management 7.1.3.3 Renewable energy 33F <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 7.1.3.4 Air quality and emissions management 34F 7.1.3.5 Water management <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 7.1.3.5.1 Water usage 7.1.3.5.2 Water reuse and recycling 7.1.3.5.3 Pollution to water37F 7.1.3.6 Chemical\/ resource management <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 7.1.3.7 Waste management 7.1.4 Packaging system 7.1.4.1 Minimize packaging 7.1.4.2 Raw materials <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 7.1.4.3 Design for end of life 7.1.4.4 Distribution packaging 7.1.5 Distribution 7.1.5.1 Mode of transportation <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | Figure 1 \u2013 Transportation Emissions by Type 7.1.5.2 Distribution efficiency 7.1.6 Use 7.1.6.1 Disclosure of environmental attributes <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | 7.1.6.2 User guide 7.1.6.3 Manufacturer recommended cleaning chemicals 7.1.6.4 Energy intensity, for electrical medical devices only 7.1.6.5 Consumables including accessories <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | 7.1.6.6 Water usage 7.1.6.7 Medical gas usage 7.1.6.8 Waste generation during use 7.1.6.9 Storage required, physical or electronic 7.1.7 End of life <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | 7.1.7.1 Recyclability 7.1.7.2 Compostability 7.1.7.3 Hazardous waste 7.1.7.4 Take-back programs <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | 7.2 User and\/or purchaser 7.2.1 Procurement 7.2.1.1 Medical device selection and acquisition 7.2.1.2 Training 7.2.1.3 Warehouse, distribution center, and other transportation <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | 7.2.2 Use of all medical devices 7.2.2.1 Routine maintenance, if applicable 7.2.2.2 Repair, if applicable 7.2.2.3 Consumables, if applicable 7.2.2.4 Medical gas usage, if applicable <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | 7.2.2.5 Water management, if applicable 7.2.2.6 Energy management, if applicable 7.2.3 Use of sterile medical devices 7.2.3.1 Single-use disposable medical devices <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | 7.2.3.2 Reprocessing (multi-use medical devices) 7.2.3.3 Reprocessing single-use medical devices 7.2.4 End of life <\/td>\n<\/tr>\n | ||||||
33<\/td>\n | 7.2.4.1 Reuse, repair, refurbishment, and upgrades 7.2.4.2 Recycling, general 7.2.4.3 Recycling, electronic waste <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | 7.2.4.4 Take-back programs 7.2.4.5 Donation and redeployment 8 Conclusions <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | Annex A: Chemicals of concern references <\/td>\n<\/tr>\n | ||||||
37<\/td>\n | Annex B: Sustainable product development tools <\/td>\n<\/tr>\n | ||||||
39<\/td>\n | Annex C: Appendix of acronyms <\/td>\n<\/tr>\n | ||||||
40<\/td>\n | Annex D: Manufacturer life cycle case studies <\/td>\n<\/tr>\n | ||||||
41<\/td>\n | Annex E: User life cycle case studies <\/td>\n<\/tr>\n | ||||||
42<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" AAMI TIR65:2015 – Technical Information Report Sustainability of medical devices – Elements of a responsible product life cycle<\/b><\/p>\n |