ISO/TR 14283:2018
Current
The latest, up-to-date edition.
Implants for surgery Essential principles of safety and performance
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
English
01-03-2018
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ISO/TR 14283:2017 provides fundamental principles for the design and manufacture of active or non-active implants in order that each implant can achieve its intended purpose.
ISO/TR 14283:2017 is often the case that instruments and other equipment are used in association with implants. These devices might be useful or even essential for the safe implantation and/or use of the implants. This document applies to implants, however, it also applies to associated instruments and equipment to the extent that the design and manufacture of the implants is intended to ensure the safe combination and use of the implants with such devices.
Requirements for the safe operation and use of associated instruments and equipment are contained in other standards.
| DocumentType |
Technical Report
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| Pages |
20
|
| ProductNote |
THIS STANDARD ALSO REFERS TO GHTF/AHWG-UDI/N2R3 2011,GHTF/SG1/N044 2008,GHTF/SG1/N055 2009,GHTF/SG1/N68 2012,GHTF/SG1/N70 2011, GHTF/SG1/N71 2012,GHTF/SG1/N78 2012,GHTF/SG5/N1R8 2007,GHTF/SG5/N2R8 2007, GHTF/SG5/N3 2010,
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| PublisherName |
International Organization for Standardization
|
| Status |
Current
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| Supersedes |
| Standards | Relationship |
| IS/ISO/TR 14283 : 2018 | Identical |
| PD ISO/TR 14283:2018 | Identical |
| ISO 14160:2011 | Sterilization of health care products Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives Requirements for characterization, development, validation and routine control of a sterilization process for medical devices |
| ISO 11135:2014 | Sterilization of health-care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
| ISO 16142-1:2016 | Medical devices — Recognized essential principles of safety and performance of medical devices — Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards |
| ISO 14937:2009 | Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
| ISO 14630:2012 | Non-active surgical implants — General requirements |
| ISO 16061:2015 | Instrumentation for use in association with non-active surgical implants General requirements |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO 14155:2011 | Clinical investigation of medical devices for human subjects Good clinical practice |
| 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 |
| ISO 17664:2017 | Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
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