Medical Devices with Embedded Sensor Systems: Design and Development Methodology for Start-Ups

Author:

Arandia Nerea1ORCID,Garate Jose Ignacio2ORCID,Mabe Jon1ORCID

Affiliation:

1. Tekniker, Basque Research and Technology Alliance (BRTA), 20600 Eibar, Spain

2. Department of Electronics Technology, University of the Basque Country (UPV/EHU), 48080 Bilbao, Spain

Abstract

Embedded systems have become a key technology for the evolution of medical devices. However, the regulatory requirements that must be met make designing and developing these devices challenging. As a result, many start-ups attempting to develop medical devices fail. Therefore, this article presents a methodology to design and develop embedded medical devices while minimising the economic investment during the technical risk stages and encouraging customer feedback. The proposed methodology is based on the execution of three stages: Development Feasibility, Incremental and Iterative Prototyping, and Medical Product Consolidation. All this is completed in compliance with the applicable regulations. The methodology mentioned above is validated through practical use cases in which the development of a wearable device for monitoring vital signs is the most relevant. The presented use cases sustain the proposed methodology, for the devices were successfully CE marked. Moreover, ISO 13485 certification is obtained by following the proposed procedures.

Funder

Centre for Industrial Technological Development

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Biochemistry,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference67 articles.

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3. European Council and Parliament (2017). Regulation

4. (EU) 2017/746 of the European Parliament and of the Council on in vitro diagnostic medical devices. Off. J. Eur. Union, L 117, 1-157.

5. European Commision (2023, February 17). Transitional Provisions for Certain Medical Devices and In Vitro Diagnostic Medical Devices European Parliament Legislative Resolution of 16 February 2023 on the Proposal for a Regulation of the European Parliament and of the Council Amending Regulations (EU) 2017/745 and (EU) 2017/746 as Regards the Transitional Provisions for Certain Medical Devices and In Vitro Diagnostic Medical Devices (COM(2023)0010–C9-0003/2023–2023/0005(COD)), Available online: https://www.europarl.europa.eu/doceo/document/TA-9-2023-0052_EN.html.

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