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PUBLISHER: Mordor Intelligence | PRODUCT CODE: 391440

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PUBLISHER: Mordor Intelligence | PRODUCT CODE: 391440

Europe Single-use Medical Device Reprocessing Market - Segmented by Devices Type and Geography - Growth, Trends, and Forecasts (2022 - 2027)

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The Europe Single-Use Medical Device (SUD) reprocessing market is anticipated to grow at a CAGR of 6.1% over the forecast period. Rising clinical urgency to minimize the generation of medical waste in healthcare settings and hospitals is among the key factors driving market growth.

The lowering of the overall cost of healthcare through the reprocessing of single-use devices is the primary factor driving this market. In Germany, reprocessing has been regulated for over a decade with a large number of hospitals showing significant cost savings. It has been strictly subjected to monitoring and surveillance by public authorities and the European Union (EU)-accredited notified body. Similarly, in the United Kingdom, the Medicines and Healthcare products Regulatory Agency (MHRA) legalized the use and manufacture of reprocessed single-use medical devices for use. In addition, it helps insurers and hospitals for better management and reduced healthcare costs with the improvement of the healthcare system.

Along with cost reduction, it also results in environmental sustainability. SUD reprocessing is one of the top healthcare supply chain strategies used to reduce costs and optimize resources. The aforementioned factors are anticipated to contribute towards the development of industry in the immediate future. However, the lack of dedicated SUD reprocessing facilities in emerging markets is currently a huge opportunity for this market, while the unauthorized overuse of reprocessed SUDs in emerging markets is currently the major challenge faced by this market.

Key Market Trends

Sequential Compression Sleeves by Class II Device Segment is Poised to Register Robust Growth

  • Sequential compression sleeves are designed to increase venous blood flow in patients with deep vein thrombosis and pulmonary embolism. Compression sleeves are considered reusable, as they can withstand the necessary cleaning and sterilization process.​
  • The quality of device and physical characteristics are not likely to be affected by reprocessing and the device remains safe and effective for its intended use. Hospitals are believed to save USD 300,000 by reprocessing compression sleeves. Compression sleeves account for the greatest volume of overall business of SUDs reprocessing. ​
  • Stryker is the leading provider of reprocessed compression sleeve devices. The company's reprocessed compression devices such as are intended for use in preventing deep vein thrombosis, reducing post-operative pain and swelling, enhancing blood circulation, and reducing wound healing time.​ Medline also offers reprocessed compression sleeves such as Kendall SCD Compression Sleeves

Competitive Landscape

The Europe Single-use Medical Device Reprocessing Market is moderately competitive and consists of several major players. In terms of market share, a few of the major players currently dominate the market. The major market players include Hygia, Medline ReNewal, NEScientific, ReNu Medical, SterilMed among others.

Additional Benefits:

  • The market estimate (ME) sheet in Excel format
  • 3 months of analyst support
Product Code: 51252

TABLE OF CONTENTS

1 INTRODUCTION

  • 1.1 Study Deliverables
  • 1.2 Study Assumptions
  • 1.3 Scope of the Study

2 RESEARCH METHODOLOGY

3 EXECUTIVE SUMMARY

4 MARKET DYNAMICS

  • 4.1 Market Overview
  • 4.2 Market Drivers
    • 4.2.1 Cost Savings Through Reprocessing Single-use Devices
    • 4.2.2 Regulatory Pressure to Reduce Volume of Medical Waste
  • 4.3 Market Restraints
    • 4.3.1 Potential of Material Alteration and Cross Infection with Reprocessed Device
    • 4.3.2 Preconceived Notions Regarding the Quality of Reprocessed Single-use Medical Devices (SUDs)
  • 4.4 Porter's Five Forces Analysis
    • 4.4.1 Bargaining Power of Suppliers
    • 4.4.2 Bargaining Power of Buyers/Consumers
    • 4.4.3 Bargaining Power of Suppliers
    • 4.4.4 Threat of Substitute Products
    • 4.4.5 Intensity of Competitive Rivalry

5 MARKET SEGMENTATION

  • 5.1 By Device Type
    • 5.1.1 Class I Devices
      • 5.1.1.1 Laparoscopic Graspers
      • 5.1.1.2 Scalpels
      • 5.1.1.3 Tourniquet Cuffs
      • 5.1.1.4 Other Class I Devices
    • 5.1.2 Class II Devices
      • 5.1.2.1 Pulse Oximeter Sensors
      • 5.1.2.2 Sequential Compression Sleeves
      • 5.1.2.3 Catheters and Guidewires
      • 5.1.2.4 Other Class II Devices
  • 5.2 Geography
    • 5.2.1 Europe
      • 5.2.1.1 United Kingdom
      • 5.2.1.2 Germany
      • 5.2.1.3 France
      • 5.2.1.4 Italy
      • 5.2.1.5 Spain
      • 5.2.1.6 Rest of Europe

6 COMPETITIVE LANDSCAPE

  • 6.1 Company Profiles
    • 6.1.1 Hygia
    • 6.1.2 Medline Industries Inc.
    • 6.1.3 NEScientific
    • 6.1.4 ReNu Medical (Arjo)
    • 6.1.5 Sterilmed Inc. (Johnson & Johnson)
    • 6.1.6 Stryker Corporation
    • 6.1.7 SureTek Medical
    • 6.1.8 Vanguard

7 MARKET OPPORTUNITIES AND FUTURE TRENDS

Have a question?
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Jeroen Van Heghe

Manager - EMEA

+32-2-535-7543

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Christine Sirois

Manager - Americas

+1-860-674-8796

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