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EVS-EN ISO 21536:2024

Mitteaktiivsed kirurgilised implantaadid. Liigeste endoproteesid. Erinõuded põlveliigese endoproteesidele

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Kehtiv alates 01.08.2024
Alusdokumendid
ISO 21536:2023; EN ISO 21536:2024
Direktiivid või määrused
puuduvad

Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
01.08.2024
Põhitekst
01.04.2014
Muudatus
03.12.2009
Põhitekst
This document specifies requirements for knee-joint replacement implants. Regarding 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 knee joint replacement implants. It applies to these replacements both with and without the replacement of the patella-femoral joint. It applies to components made of metallic and non-metallic materials.
This document applies to a wide variety of knee replacement implants, but for some specific knee 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.

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Põhitekst

EVS-EN ISO 21535:2024

Mitteaktiivsed kirurgilised implantaadid. Liigeste endoproteesid. Erinõuded puusaliigese endoproteesidele
Uusim versioon Kehtiv alates 01.08.2024