ANSI/AAMI/ISO TIR/(R) Medical devices — Guidance on the application of ISO. Approved 27 June by. AAMI. Registered application of ISO Dispositifs médicaux — Directives relatives à l’ISO REPORT. ISO/TR. First edition. Reference number. REPORT. ISO/TR. First edition. Reference number. ISO/TR (E). This is a preview – click here to buy the full publication.
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Experience shows that manufacturers have difficulty with the practical implementation of some clauses in the medical devices risk 2497 standard BS EN ISO This published document is the UK implementation of an international Technical Report.
It supplies guidance on tackling specific clauses in the standard. This is not an overall guidance document on the implementation of BS EN ISObut it will 244971 manufacturers in the development, implementation and maintenance of risk management for a wide variety medical devices including: Worldwide Standards We can source any standard from anywhere in the world.
PD ISO/TR Medical devices. Guidance on the application of ISO
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PD ISO/TR 24971:2013
Guidance on the application of ISO Status: Click to learn more. Overview Product Details What is this published document about?
Who is this published document for? It provides guidance to help manufacturers and other users of the standard: Your basket is empty.
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The faster, easier way to work with standards. Application of risk management to medical devices BS 42971 You may experience issues viewing this site in Internet Explorer 9, 10 or Please download Chrome or Firefox or view our browser tips.
Accept and continue Learn more about the cookies we use and how to change your settings. Sets of data, Electrical medical equipment, Information exchange, Data processing, Medical equipment, Terminology, Data handling, Thesauri, Data representation, Data structures, Medical instruments, Databases, Classification systems, Data organization.