Market revenue in 2023 | USD 39.4 million |
Market revenue in 2030 | USD 58.2 million |
Growth rate | 5.7% (CAGR from 2023 to 2030) |
Largest segment | Central venous catheter (cvcs) |
Fastest growing segment | Peripherally Inserted Central Catheter (PICCs) |
Historical data | 2017 - 2022 |
Base year | 2023 |
Forecast period | 2024 - 2030 |
Quantitative units | Revenue in USD million |
Market segmentation | Short Peripheral Intravenous Catheter (Short PIVCs), Huber Needles, Midline Catheters, Peripherally Inserted Central Catheter (PICCs), Central Venous Catheter (CVCs), Dialysis Catheters, Implantable Ports |
Key market players worldwide | Teleflex Inc, BD, B. Braun, Smiths Group PLC, Cook Medical, AngioDynamics Inc, Medtronic PLC, Terumo Corp |
No credit card required*
Name | Profile | # Employees | HQ | Website |
---|
The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to vascular access devices market will help companies and investors design strategic landscapes.
Central venous catheter (cvcs) was the largest segment with a revenue share of 33.5% in 2023. Horizon Databook has segmented the France vascular access devices market based on short peripheral intravenous catheter (short pivcs), huber needles, midline catheters, peripherally inserted central catheter (piccs), central venous catheter (cvcs), dialysis catheters, implantable ports covering the revenue growth of each sub-segment from 2017 to 2030.
The National Agency for the Safety of Medicines and Health Products in France (ANSM) is the authorized body responsible for governing the import and market entrance of medical devices in the country. Manufacturers must receive CE certification before marketing any medical devices, including Active Implantable Medical Devices (AIMD) and In Vitro Diagnostic Medical Devices (IVDDM).
The market entrant must submit the devices to a compliance evaluation with the crucial standards outlined in the relevant European directives to apply for the CE marking. The Public Health Code in France incorporates these European regulations.
The CE mark is a necessity for all medical devices before they may be marketed in France. A Representative or Authorized Representative must be chosen in the case of a non-European Manufacturer.
Horizon Databook provides a detailed overview of country-level data and insights on the France vascular access devices market, including forecasts for subscribers. This country databook contains high-level insights into France vascular access devices market from 2017 to 2030, including revenue numbers, major trends, and company profiles.
Sign up and get instant basic access to databook, upgrade
when ready, or enjoy our
free plan indefinitely.
Included in Horizon account