Medical Device Design

Innovation from Concept to Market

Peter J. Ogrodnik (Autor)

Buch | Softcover

625 Seiten

2026 | 3rd edition
Academic Press Inc (Verlag)
978-0-443-40318-7 (ISBN)

Noch nicht erschienen (ca. Februar 2026)
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Medical Device Design: Innovation from Concept to Market, Third Edition provides the bridge between engineering design and medical device development. The book clearly explains the process of medical device development - from very early stages of conceptualization to commercialization on the global market. It addresses medical devices' regulatory (FDA and EU) requirements, shows the essential methodologies medical designers must understand to ensure their products meet requirements, and brings together proven design protocols, enabling engineers and medical device manufacturers to rapidly bring new products to the marketplace.

This book is suitable for professional engineers, both new and experienced, as well as students taking a course in medical device design.

Professor Ogrodnik is a Chartered Mechanical Engineer, a Member of the Institution of Engineering Designers and a Fellow (regional) of the Royal Society of Medicine, an Honorary Consultant at the Royal Stoke University Hospital. For over 20 years he has conducted research into optimising the treatment of tibial fractures. Using this research base he has enhanced the application of engineering design principles to the solution of medical devices, his book Medical Devices Design is a core text in core R&D departments. He has founded two medical devices companies (one manufactures and sells medical devices to the NHS and beyond) and is named inventor on numerous patents. He was a founding director of the University spinout Intelligent Orthopaedics Ltd, and is a founding partner of Metaphysis LLP. Through this corporate involvement Professor Ogrodnik has an understanding of the realities of applied research for industry; for example he was a member of the AWM Healthcare Technologies cluster opportunity group.

1. Introduction
2. Classifying Medical Devices
3.. The Design Process
4. Implementing Design Procedures
5. Developing Your Product Design Specification
6. Generating Ideas and Concepts
7. Quality in Design
8. Design Realization/Detailed Design
9. Evaluation Chapter 10. Manufacturing Supply Chain
11. Labelling and Instructions for Use
12. Postmarket Surveillance Chapter 13 Sustainability and Resilient systems
14. Protecting Your IP
15. Exploiting IP
16. Obtaining Regulatory Approval to Market
16. Active medical devices
17. Software in Medical Devices
18 AI in Medical Devices

Appendix
A. Useful Websites FDA Medical Devices
B. Tables
C. ISO 14971 Annex C Pre–Risk Analysis Questionnaire Appendix
D. Generic Codes for Class I Medical Devices (MHRA)FDA Class I and II Exempt Devices
E. Basic Materials Properties for Materials Selection E.1 Density E.2 Stress and Strain

Erscheint lt. Verlag	1.2.2026
Verlagsort	San Diego
Sprache	englisch
Maße	191 x 235 mm
Themenwelt	Medizin / Pharmazie ► Physiotherapie / Ergotherapie ► Orthopädie
	Technik ► Medizintechnik
	Technik ► Umwelttechnik / Biotechnologie
ISBN-10	0-443-40318-X / 044340318X
ISBN-13	978-0-443-40318-7 / 9780443403187
Zustand	Neuware