Skip to main content
Tagasi

ISO 21535:2023

Non-active surgical implants — Joint replacement implants — Specific requirements for hip-joint replacement implants

Üldinfo

Kehtiv alates 05.07.2023
Direktiivid või määrused
puuduvad

Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
05.07.2023
Põhitekst
16.11.2016
Muudatus
26.09.2007
Põhitekst
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.

Nõutud väljad on tähistatud *

*
*
*
PDF
197,98 € koos KM-ga
Paber
197,98 € koos KM-ga
Standardi monitooring

Teised on ostnud veel

Põhitekst

EVS-EN ISO 16061:2021

Instruments for use in association with non-active surgical implants - General requirements (ISO 16061:2021)
Uusim versioon Kehtiv alates 15.04.2021
Põhitekst

EVS-EN ISO 17664-1:2021

Tervishoiutoodete töötlemine. Meditsiiniseadme tootja esitatav teave meditsiiniseadmete töötlemiseks. Osa 1: Kriitilised ja poolkriitilised meditsiiniseadmed
Uusim versioon Kehtiv alates 16.09.2021
Muudatus

EVS-EN ISO 11137-2:2015/A1:2023

Tervishoiutoodete steriliseerimine. Kiirgus. Osa 2: Steriliseerimisdoosi määramine
Kehtiv alates 02.05.2023
Põhitekst

EVS-EN ISO 17664-2:2023

Tervishoiutoodete töötlemine. Meditsiiniseadme tootja esitatav teave meditsiiniseadmete töötlemiseks. Osa 2: Mittekriitilised meditsiiniseadmed
Uusim versioon Kehtiv alates 29.12.2023