
ISO 14630:2012 - Non-active surgical implants — General …
ISO 14630:2012 specifies general requirements for non-active surgical implants. ISO 14630:2012 is not applicable to dental implants, dental restorative materials, transendodontic and …
ISO 14630:2012 (en), Non-active surgical implants — General …
This fourth edition cancels and replaces the third edition (ISO 14630:2008), which has been technically revised. Introduction This International Standard provides a method of addressing …
ISO 14630:2012(E) Introduction This International Standard provides a method of addressing the fundamental principles outlined in ISO/TR 14283 as they apply to non-active surgical implants. …
ISO 14630 was prepared by Technical Committee ISO/TC 150, Implants for surgery. This fifth edition cancels and replaces the fourth edition (ISO 14630:2012), which has been technically …
ISO 14630:2024(en) Introduction There are three levels of standards dealing with non-active surgical implants and related instrumentation. For the implants themselves, they are as …
ISO 14630 was prepared by Technical Committee ISO/TC 150, Implants for surgery. This second edition cancels and replaces the first edition (ISO 14630:1997), which has been technically …
EN ISO 14630:2024 - Non-active surgical implants - iTeh Standards
2024年12月17日 · EN ISO 14630:2024 - This document specifies general requirements for non-active surgical implants, hereafter referred to as implants. This document is not applicable to …
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CEN - EN ISO 14630 - Non-active surgical implants - General ...
However, the application of a quality management system, such as that described in ISO 13485, might be appropriate to help ensure that the implant achieves its intended performance. …
ISO 14630:2024 - Non-active surgical implants — General …
However, many regulatory authorities require the application of a quality management system, such as that described in ISO 13485, to ensure that the implant achieves its intended …
BS EN ISO 14630:2024 - Non-active surgical implants. General ...
However, many regulatory authorities require the application of a quality management system, such as that described in ISO 13485, to ensure that the implant achieves its intended …