nsBAS EN ISO 21535:2025
Neaktivni hirurški implantati – Zamjenski implantati za zglobove - Posebni zahtjevi za zamjenske implantate zgloba kuka
Opće informacije
                    Status:Projekt                
                
                    Broj stranica:35                
                
                    Metoda usvajanja:Proglašavanje                
            
                    Jezik:engleski                
                
                                    
                        Izdanje:2.                    
                                
                    Nadnevak realizacije:13.10.2025                
            
                    Predviđeni nadnevak naredne faze:12.12.2025                
                            
                    Tehnički komitet:BAS/TC 25, Zdravstvena skrb                
            Direktive:
                    
                                                    2017/745, Uredba (EU) o medicinskim sredstvima
                                            
                ICS:
                    
                                                    11.040.40, Implantati za hirurgiju, protetiku i ortotiku
                                            
                Apstrakt
                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.            
        Životni ciklus
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        Izvorni dokument i stepen usklađenosti
                        EN ISO 21535:2024, identičan
                    
                                    
                        ISO 21535:2023, identičan
                    
                
            Veza sa BAS standardima
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