Market revenue in 2023 | USD 18.7 million |
Market revenue in 2030 | USD 21.1 million |
Growth rate | 1.7% (CAGR from 2023 to 2030) |
Largest segment | Short peripheral intravenous catheter (short pivcs) |
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 |
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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.
Short peripheral intravenous catheter (short pivcs) was the largest segment with a revenue share of 40.64% in 2024. Horizon Databook has segmented the Brazil 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 2018 to 2030.
The Brazilian Health Surveillance Agency oversees the regulation of all medical equipment in Brazil. All devices are required by ANVISA to undergo a device registration process. To submit technical data to ANVISA, non-Brazilian producers must do so through a local Brazilian Registration Holder (BRH) domiciled in Brazil.
Manufacturers can submit to a single audit under the Medical Device Single Audit Program (MDSAP) to satisfy the QMS/GMP criteria of several Regulatory Authorities (RAs). ANVISA uses the program's outputs, including the reports, to inform its premarket and post market assessment procedures.
When necessary, it offers crucial data that is anticipated to enhance regulatory technical review of these challenges. Medical Device Single Audit Program (MDSAP) Audits are carried out by Auditing Organizations (AO), such as BSI, who are permitted to audit in accordance with Medical Device Single Audit Program (MDSAP) regulations by the participating Authorized Representative.
Horizon Databook provides a detailed overview of country-level data and insights on the Brazil vascular access devices market, including forecasts for subscribers. This country databook contains high-level insights into Brazil vascular access devices market from 2018 to 2030, including revenue numbers, major trends, and company profiles.
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