Publikuar
ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
                WITHDRAWN
                                    ISO 10993-11:2006
                            
                    PUBLISHED
                    ISO 10993-11:2017
                    90.92
                                        Standard to be revised
                    18 pri 2023
                
                IN_DEVELOPMENT
                                    ISO/DIS 10993-11
                            
Vlerësimi biologjik i pajisjeve mjekësore - Pjesa 11: Testet për toksicitetin sistemik (ISO 10993-11:2017)
60.60 Standard published