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NF EN ISO 10993-16, S99-501-16 (12/2017)

Biological evaluation of medical devices - Part 16 : Toxicokinetic study design for degradation products and leachables

Summary

DI 90/385/CE 20/06/1990 Directive concernant le rapprochement des législations des états membres relatives aux dispositifs médicaux implantables actifs.

Notes

Édition bilingue FR,EN

Technical characteristics

Publisher Association Française de Normalisation (AFNOR)
Publication Date 12/01/2017
Release Date 12/01/2017
Page Count 28
EAN ---
ISBN ---
Weight (in grams) ---