Skip to main content
Tagasi

EVS-EN ISO 10993-2:2022

Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)

Üldinfo

Kehtiv alates 01.12.2022
Alusdokumendid
ISO 10993-2:2022; EN ISO 10993-2:2022
Direktiivid või määrused
puuduvad

Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
01.12.2022
Põhitekst
07.09.2006
Põhitekst
This document specifies the minimum requirements to be satisfied to ensure and demonstrate that proper provision has been made for the welfare of animals used in animal tests to assess the biocompatibility of materials used in medical devices. It is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical devices, or that of the medical devices themselves.
This document makes recommendations and offers guidance intended to facilitate future further reductions in the overall number of animals used, refinement of test methods to reduce or eliminate pain or distress in animals, and the replacement of animal tests by other scientifically valid means not requiring animal tests.
This document applies to tests performed on living vertebrate animals, other than man, to establish the biocompatibility of materials or medical devices.
This document does not apply to tests performed on invertebrate animals and other lower forms; nor (other than with respect to provisions relating to species, source, health status, and care and accommodation) does it apply to testing performed on isolated tissues and organs taken from vertebrate animals that have been euthanized.

Nõutud väljad on tähistatud *

*
*
*
PDF
19,52 € koos KM-ga
PDF redline
25,38 € koos KM-ga
Paber
19,52 € koos KM-ga
Sirvi standardit alates 2,44 € koos KM-ga
Standardi monitooring

Teised on ostnud veel

Põhitekst

EVS-EN ISO 10993-10:2023

Meditsiiniseadmete bioloogiline hindamine. Osa 10: Naha sensibiliseerimise katsed
Uusim versioon Kehtiv alates 01.03.2023
Põhitekst

EVS-EN ISO 10993-3:2014

Meditsiiniseadmete bioloogiline hindamine. Osa 3: Testid geenitoksiliste, kantserogeensete ja reproduktiivsete toksiinide määramiseks
Uusim versioon Kehtiv alates 07.11.2014
Põhitekst

EVS-EN ISO 10993-9:2021

Meditsiiniseadmete bioloogiline hindamine. Osa 9: Potentsiaalsete degradatsioonisaaduste tuvastamise ja koguselise kindlaksmääramise raamistik
Uusim versioon Kehtiv alates 15.10.2021
Põhitekst

EVS-EN ISO 10993-23:2021

Meditsiiniseadmete bioloogiline hindamine. Osa 23: Kontaktärrituskatsed
Uusim versioon Kehtiv alates 15.04.2021