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Class 1 devices : Case studies in medical devices design /

The Case Studies in Medical Devices Design series consists of practical, applied case studies relating to medical device design in industry. These titles complement Ogrodnik's Medical Device Design and will assist engineers with applying the theory in practice. The case studies presented direct...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Ogrodnik, Peter J. (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Academic Press, [2015]
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Ogrodnik, Peter J.,  |e author. 
245 1 0 |a Class 1 devices :  |b Case studies in medical devices design /  |c Peter J. Ogrodnik. 
246 3 |a Class one devices 
246 3 |a Case studies in medical devices design 
264 1 |a Amsterdam :  |b Academic Press,  |c [2015] 
264 4 |c �2015 
300 |a 1 online resource :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
347 |a text file 
504 |a Includes bibliographical references. 
588 0 |a Online resource; title from PDF title page (EBSCO, viewed December 13, 2014). 
520 |a The Case Studies in Medical Devices Design series consists of practical, applied case studies relating to medical device design in industry. These titles complement Ogrodnik's Medical Device Design and will assist engineers with applying the theory in practice. The case studies presented directly relate to Class I, Class IIa, Class IIb and Class III medical devices. Designers and companies who wish to extend their knowledge in a specific discipline related to their respective class of operation will find any or all of these titles a great addition to their library. Class 1 Devices is a companion text to Medical Devices Design: Innovation from Concept to Market. The intention of this book, and its sister books in the series, is to support the concepts presented in Medical Devices Design through case studies. In the context of this book the case studies consider Class I (EU) and 510(k) exempt (FDA) . This book covers classifications, the conceptual and embodiment phase, plus design from idea to PDS. 
505 0 0 |g 1.  |t Introduction --  |g 1.1.  |t Reminder concerning classification --  |g 1.2.  |t A reminder concerning the importance of design rigour (or design control) --  |g 1.3.  |t A reminder concerning understanding the problem --  |g 1.4.  |t A reminder concerning a team/holistic approach --  |g 1.5.  |t A reminder concerning costs --  |g 1.6.  |t Introduction to the case studies --  |g 1.6.1.  |t Comments Concerning the Case Studies --  |g 1.7.  |t Hints to enable you to understand the text --  |g 2.  |t Classification --  |g 2.1.  |t Introduction --  |g 2.1.1.  |t Timing --  |g 2.2.  |t FDA classification --  |g 2.2.1.  |t Keywords --  |g 2.3.  |t EU MDD classification --  |g 2.4.  |t Your turn --  |g 3.  |t Taking the Design from Idea to PDS --  |g 3.1.  |t Introduction --  |g 3.2.  |t Developing the specification --  |g 3.2.1.  |t The Need --  |g 3.2.2.  |t The PDS --  |g 3.2.3.  |t Customer Section --  |g 3.2.4.  |t Regulatory and Statutory Section --  |g 3.2.5.  |t Technical Section and Performance Section --  |g 3.2.6.  |t Sales Section --  |g 3.2.7.  |t Manufacturing Section --  |g 3.2.8.  |t Packaging and Transportation Section --  |g 3.2.9.  |t Environmental Section --  |g 4.  |t Conceptual Phase --  |g 4.1.  |t A reminder about space --  |g 4.2.  |t The relationship with your product design specification (PDS) --  |g 4.3.  |t Solution selection --  |g 4.3.1.  |t Initial Screening (optional) --  |g 4.3.2.  |t Detailed Selection (Essential) --  |g 4.4.  |t Summary --  |g 5.  |t Embodiment Phase --  |g 5.1.  |t A reminder about this phase --  |g 5.2.  |t Initial embodiment -- or first prototype phase --  |g 5.2.1.  |t Detailed Drawings and Specifications of Components --  |g 5.2.2.  |t Calculations/Simulations Demonstrating Performance and Quality in Design --  |g 5.2.2.1.  |t FMEA --  |g 5.2.2.2.  |t Optimisation --  |g 5.2.2.3.  |t Design for X --  |g 5.2.2.4.  |t Validation and Verification --  |g 5.2.2.5.  |t Design for Manufacture --  |g 5.3.  |t Prototype to final design --  |g 5.3.1.  |t Link Between this Stage and the Previous Stage --  |g 5.3.2.  |t Detailed Drawings and Specifications --  |g 5.3.2.1.  |t A Reminder About Logging Modifications --  |g 5.3.2.2.  |t Transition from FMEA to Risk Analysis (RA) --  |g 5.3.2.3.  |t Essential Requirements (Especially for EU) --  |g 5.3.2.4.  |t Validation, Verification and Clinical Evaluation --  |g 5.3.2.5.  |t IFUs, Labelling, Other Instructions and Markings --  |g 5.4.  |t Summary --  |g 6.  |t The Home Run --  |g 6.1.  |t A summary of activity --  |g 6.2.  |t The technical file --  |g 6.3.  |t A note about manufacturing --  |g 6.4.  |t A note about post market surveillance (PMS) --  |g 6.5.  |t The final furlong --  |g 6.5.1.  |t EU --  |g 6.5.2.  |t FDA --  |g 6.6.  |t Continual improvement. 
650 0 |a Medical instruments and apparatus  |x Design and construction. 
650 2 |a Analytical, Diagnostic and Therapeutic Techniques and Equipment 
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650 2 |a Equipment Design  |0 (DNLM)D004867 
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650 2 |a Equipment and Supplies  |0 (DNLM)D004864 
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650 7 |a Medical instruments and apparatus  |x Design and construction.  |2 fast  |0 (OCoLC)fst01014206 
655 2 |a Case Reports  |0 (DNLM)D002363 
655 7 |a Case studies.  |2 fast  |0 (OCoLC)fst01423765 
655 7 |a Case studies.  |2 lcgft 
655 7 |a �Etudes de cas.  |2 rvmgf  |0 (CaQQLa)RVMGF-000001726 
776 0 8 |i Print version:  |a Ogrodnik, Peter J.  |t Class 1 devices : case studies in medical devices design.  |d London, [England] ; San Diego, California : Academic Press, �2015  |h viii, 104 pages  |z 9780128000281  |w (OCoLC)904423763 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128000281  |z Texto completo