Abstract

Assessing products prior to remanufacture is an important part of the remanufacturing process, ensuring that unsuitable cores are removed at an early stage to avoid unnecessary processing. In particular, understanding the economic cost of remanufacturing a product can be an important aspect of the assessment, especially for businesses operating in low volumes and on high value products, where the risk associated with unexpected costs or failure to complete remanufacture are much greater. Estimating these costs can however be difficult, as important information required to make a prediction is often uncertain, such as the product design, its condition and also the understanding of the resource requirements for remanufacture. Within this research a method has been developed to estimate the economic cost and risks of conducting a remanufacturing activity to a product when information is uncertain. Summation of the individual activities can then be conducted to determine the economic cost and risks of the entire remanufacturing process. The method utilises a combination of case based reasoning and probability theory to identify similarities between historical data records and the product under assessment, to predict the cost and risks of remanufacture. In particular this method enables cost estimation when important product information is missing including the manufacturer, model or condition. Additionally estimates can be made when exact historical information is not present, which can be useful to business remanufacturing bespoke or rare products. The method is then implemented within a service oriented architecture and functionally demonstrated using an example of an independent wind turbine gearbox remanufacturer.

Highlights

  • It is difficult for many developing countries to access medical equipment necessary for healthcare

  • This paper proposes a definition for medical equipment remanufacture

  • The medical equipment sector is one crucial area where its practice would yield tremendous benefits contributing to the sustainable development goals of health and poverty alleviation

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Summary

Introduction

It is difficult for many developing countries to access medical equipment necessary for healthcare. The model is primarily useful in resolving ethical, liability, environmental and cost issues associated with reusing single-use medical devices While these papers address medical equipment remanufacturing from various perspectives, none has reported the manner in which it is practised in the industry, especially from the perspective of fulfilling regulatory requirements which determine medical equipment market entry. This paper intends to analyse the EU and US regulatory perspectives with respect to medical equipment remanufacturing or related practices and to propose a definition for remanufacturing which can help to achieve the goal of increasing access to functional medical equipment in developing countries. This is important as current approaches are unsustainable. The European remanufacturing network market studies show that many developing countries are destinations for used medical equipment sold ‘as is’ or following poorly conducted recovery process [18], a situation which has contributed to the abundance of poor quality medical equipment that either cannot be put to use or would no longer be safe

Methods
Training and optional continuing education programme
10 This will help prolong the period of use of the medical equipment
10 To ensure that finished products are of high quality
Conclusion
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