prEN ISO 10993-2
Biologinis medicinos priemonių įvertinimas. 2 dalis. Gyvūnų gerovės reikalavimai (ISO/DIS 10993-2:2024)
Standarto projektas Viešoji apklausaProjekto etapai
1. Decision on WI Proposal
2. Projektas
3. Viešoji apklausa
Nuo 2024-11-19
iki 2025-01-18
4. Closure of enquiry
5. Submission to Formal Vote
Organizacija
CEN Europos standartizacijos komitetasICS
11.100.20 - Biologinis medicinos priemonių įvertinimasTechnikos komitetas
TK 32 SveikataUžsienio technikos komitetas
CEN/TC 206Komentarų skaičius
0Komentavimo pradžia
2024-11-19Taikymo sritis
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.Ryšiai
Pakeis
LST EN ISO 10993-2:2023
Biologinis medicinos priemonių įvertinimas. 2 dalis. Gyvūnų gerovės reikalavimai (ISO/FDIS 10993-2:2022)