-

European Vascular Access Devices & Accessories Market, 2020-2026 - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Vascular Access Devices and Accessories Market Report Suite: Europe 2020-2026 - Medsuite" report has been added to ResearchAndMarkets.com's offering.

The European vascular access market was valued at 1.7 billion in 2019. This is expected to increase over the forecast period at a CAGR of 1.7% to reach 1.9 billion.

Market growth is expected to be limited by pricing pressures across Europe. European healthcare facilities often trend towards lower-cost products, which forces many competitors to lower their prices. Furthermore, preferences for high cost, premium-priced versions of products, such as those with antimicrobial coatings, is still developing in many markets. As such, premiums on many of these devices are still being kept low and, therefore, there is not a significant upward force on the market from conversion to these products.

On the other hand, the market is benefitting from increased conversion towards safety devices that prevent needle-stick injuries. This trend is having a particularly strong effect in the PIVC and syringe and needle markets, which represent a sizable portion of the total vascular access market in Europe. Europe-wide legislation encouraging the use of safety devices implemented in 2013 and early 2014 has been transposed in all countries included in this report.

This report suite on the European market for vascular access devices and accessories includes implantable ports, port needles, central venous catheters (CVCs), peripherally inserted central catheters (PICCs), peripheral intravenous catheters (PIVCs), midline catheters, dialysis catheters, catheter securement devices and syringes and needles. Vascular access ultrasound devices, tip-placement systems, antibacterial catheter patches and catheter caps are analyzed separately in a series of appendices.

Key Topics Covered

1. Introduction

2. Disease Overview

3. Product Assessment

4. European Vascular Access Devices and Accessories Market Overview

5. Country Profiles

6. Procedure Numbers

7. Implantable Port Market

8. Port Needle Market

9. Central Venous Catheter Market

10. Peripherally Inserted Central Catheter Market

11. Peripheral Intravenous Catheter Market

Companies Mentioned

  • 3M
  • Access Scientific
  • AngioDynamics
  • Applied Medical Technology
  • Argon Medical
  • Artsana
  • B. Braun
  • Baxter International
  • Becton Dickinson
  • Bionic
  • C. R. Bard
  • Cardinal Health
  • Centurion Medical
  • Codan
  • Cook Medical
  • Covidien
  • DeRoyal
  • Deltamed
  • Districlass Medical
  • Edwards Lifesciences
  • Fannin
  • Fresenius
  • GlucoRx
  • Greiner Bio-One
  • HEKA Healthcare
  • Interrad Medical
  • Investindustrial
  • Johnson & Johnson
  • Joline
  • Kimal
  • M.C. Johnson
  • Medcomp
  • Medikit
  • Medline Industries
  • Medtronic
  • Neo Medical
  • Nipro Medical
  • Nostix, LLC
  • Nova Medical
  • Novico
  • Novo Nordisk
  • Owen Mumford
  • PFM Medical
  • Pentaferte
  • Rays
  • Roche
  • Romedex
  • SFM
  • Safety Syringes Inc.
  • Sentra Medical
  • Smith & Nephew
  • Smiths Medical
  • Sonosite, Inc.
  • TIDI Products
  • Teleflex
  • Terumo
  • Troge
  • V-Tech
  • Vascular Pathways, Inc.
  • VigMed
  • Vygon
  • Ypsomed

For more information about this report visit https://www.researchandmarkets.com/r/fqnkml

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Research and Markets


Release Versions

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

More News From Research and Markets

Computer System Validation (CSV) Training Course: Regulations Impacting Your Systems and Hands-on Practice Writing Validation Documents (Jan 27th - Jan 29th, 2026 & On-Demand) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Jan 27th - Jan 29th, 2026)" training has been added to ResearchAndMarkets.com's offering. A course designed to completely immerse you in computer system validation. This course delivers comprehension of the regulations impacting your systems and hands-on practice writing validation documents. You will leave ready to lead efficient, effective, inspection- ready validation projects. Registration Includes: Checklist of...

Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions Webinar - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions (January 15, 2026)" training has been added to ResearchAndMarkets.com's offering. This expert-led 3-hour webinar provides a comprehensive introduction to the key regulatory pathways for medical device submissions in the US market. The regulation and control of new or substantially changed medical devices for sale in the US is based on the 510(k), PMA or DeNovo submission process. This w...

Medical Devices: Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) Course: Developing Effective Post Market Surveillance and Complaint Handling Systems Training - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course (Jan 22nd - Jan 23rd, 2026)" training has been added to ResearchAndMarkets.com's offering. What are U.S. FDA CGMP expectations/requirements for Post Market Surveillance and Complaint Handling? This seminar will examine Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), as well as appropriate articles / Annexes of the EU's MDR, which require manu...
Back to Newsroom