prBAS EN ISO 21535:2025
Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants
General information
Status:Project
Number of pages:39
Adoption method:Proglašavanje
Language:engleski
Edition:2.
Realization date:08.10.2024
Forseen date for next stage code:09.10.2024
Technical committee:BAS/TC 25, Healthcare
Directives:
2017/745, Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC
ICS:
11.040.40, Implants for surgery, prosthetics and orthotics
Abstract
This document specifies requirements for hip-joint replacement implants. With regard to safety, this document specifies requirements for intended performance, design attributes, materials, design evaluation, manufacture, sterilization, packaging, information supplied by the manufacturer and methods of test.
This document applies to both total and partial hip joint replacement implants. It applies to components made of metallic and non-metallic materials.
This document applies to a wide variety of hip replacement implants, but for some specific hip replacement implant types, some considerations, not specifically covered in this document, can be applicable. Further details are given in 7.2.1.2.
The requirements which are specified in this document are not intended to require the re-design or re-testing of implants which have been legally marketed and for which there is a history of sufficient and safe clinical use. For such implants, compliance with this document can be demonstrated by providing evidence of the implant’s sufficient and safe clinical use.
Lifecycle
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Original document and degree of correspondence
EN ISO 21535:2024, identical
ISO 21535:2023, identical
Relation to BAS standards
Work material
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