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  • Medical Device Design: Innovation from Concept to Market

    Medical Device Design by Ogrodnik, Peter J.;

    Innovation from Concept to Market

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      • The discount is only available for 'Alert of Favourite Topics' newsletter recipients.
      • Publisher's listprice EUR 142.99
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        59 305 Ft (56 481 Ft + 5% VAT)
      • Discount 10% (cc. 5 931 Ft off)
      • Discounted price 53 375 Ft (50 833 Ft + 5% VAT)

    59 305 Ft

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    Why don't you give exact delivery time?

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    Product details:

    • Edition number 3
    • Publisher Elsevier Science
    • Date of Publication 1 April 2026

    • ISBN 9780443403187
    • Binding Paperback
    • No. of pages625 pages
    • Size 235x191 mm
    • Language English
    • 700

    Categories

    Long description:

    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.

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    Table of Contents:

    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

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