ISO/TC 150/JWG 1 - Joint ISO/TC 150 - ISO/TC 261 WG: Additive manufacturing in surgical implant applications
GT mixte ISO/TC 150 - ISO/TC 261 "Additive manufacturing in surgical implant applications "
General Information
Frequently Asked Questions
ISO/TC 150/JWG 1 is a Technical Committee within the International Organization for Standardization (ISO). It is named "Joint ISO/TC 150 - ISO/TC 261 WG: Additive manufacturing in surgical implant applications". This committee has published 1 standards.
ISO/TC 150/JWG 1 develops ISO standards in the area of Information technology. Currently, there are 1 published standards from this technical committee.
The International Organization for Standardization (ISO) is an independent, non-governmental international organization that develops and publishes international standards. Founded in 1947 and headquartered in Geneva, Switzerland, ISO brings together experts from 170+ member countries to share knowledge and develop voluntary, consensus-based standards that support innovation and provide solutions to global challenges.
A Technical Committee (TC) in ISO is a group of experts responsible for developing international standards in a specific technical area. TCs are composed of national member body delegates and work through consensus to create standards that meet global industry needs. Each TC may have subcommittees (SCs) and working groups (WGs) for specialized topics.
This document identifies factors that affect the safety and performance of surgical implants due to the fact that these implants are manufactured additively. This document applies to non-active implants manufactured additively, including custom-made implants and patient-matched implants. This document also applies to instrumentation for use in association with non-active surgical implants manufactured by additive manufacturing (AM). While this document is not intended to apply to active implants, certain clauses or subclauses of this document can potentially still be used in the context of active implants. This document identifies factors which are either unique to additively manufactured implants or which require additional consideration for additively manufactured implants. These factors have not always been included within existing implant specific standards. This document is not applicable to implants which contain or incorporate tissues or cells, or their derivates, of animal or human origin.
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